PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
29964784-0	2016	[Adsorption Cd2+ from Solution by EDTA-modified Silicate Nanoparticles].	Edetic Acid	34-38	CD2 molecule	Homo sapiens	12-15
27875876-1	2016	We present novel means to hyperpolarize deuterium nuclei in 13CD2 groups at cryogenic temperatures.	Deuterium	40-49	CD2 molecule	Homo sapiens	62-65
27628907-7	2016	As a consequence, a reductive cyclization of the starting materials is favored in CD2 Cl2 solutions as shown for two beta-(3-iodopropoxy)-substituted tetronates, which underwent in dichloromethane almost exclusive reduction, but gave predominantly the cyclization products in CD2 Cl2 .	beta-(3-iodopropoxy)-substituted tetronates	117-160	CD2 molecule	Homo sapiens	82-85
27628907-7	2016	As a consequence, a reductive cyclization of the starting materials is favored in CD2 Cl2 solutions as shown for two beta-(3-iodopropoxy)-substituted tetronates, which underwent in dichloromethane almost exclusive reduction, but gave predominantly the cyclization products in CD2 Cl2 .	beta-(3-iodopropoxy)-substituted tetronates	117-160	CD2 molecule	Homo sapiens	276-279
27628907-7	2016	As a consequence, a reductive cyclization of the starting materials is favored in CD2 Cl2 solutions as shown for two beta-(3-iodopropoxy)-substituted tetronates, which underwent in dichloromethane almost exclusive reduction, but gave predominantly the cyclization products in CD2 Cl2 .	Methylene Chloride	181-196	CD2 molecule	Homo sapiens	82-85
27593346-2	2016	Here, we present a systematic investigation of cation-exchange reactions that involve the displacement of Mn2+ from CdSe nanocrystals by Cd2+ or In3+.	Manganese(2+)	106-110	CD2 molecule	Homo sapiens	137-140
27593346-6	2016	Despite their very different kinetics, indistinguishable diffusion barriers of ED   1.1 eV are found for both reactions (In3+ and Cd2+).	in3+	121-125	CD2 molecule	Homo sapiens	130-133
27934318-5	2016	The compound features the first 3D NCS cadmium molybdotellurite with 1D 4- and 6-MR channels and a polar structure originating from the TeO3 groups, MoO4 groups, and displacements of d10 Cd2+ cations.	cadmium molybdotellurite	39-63	CD2 molecule	Homo sapiens	187-190
27766856-0	2016	Measuring and Reporting Electrical Conductivity in Metal-Organic Frameworks: Cd2(TTFTB) as a Case Study.	Metals	51-56	CD2 molecule	Homo sapiens	77-80
27766856-0	2016	Measuring and Reporting Electrical Conductivity in Metal-Organic Frameworks: Cd2(TTFTB) as a Case Study.	ttftb	81-86	CD2 molecule	Homo sapiens	77-80
27766856-5	2016	Here, we use the anisotropic semiconducting framework Cd2(TTFTB) (TTFTB4- = tetrathiafulvalene tetrabenzoate) to benchmark several common methods available for measuring electrical properties in MOFs.	ttftb	58-63	CD2 molecule	Homo sapiens	54-57
27766856-5	2016	Here, we use the anisotropic semiconducting framework Cd2(TTFTB) (TTFTB4- = tetrathiafulvalene tetrabenzoate) to benchmark several common methods available for measuring electrical properties in MOFs.	ttftb4	66-72	CD2 molecule	Homo sapiens	54-57
27766856-5	2016	Here, we use the anisotropic semiconducting framework Cd2(TTFTB) (TTFTB4- = tetrathiafulvalene tetrabenzoate) to benchmark several common methods available for measuring electrical properties in MOFs.	tetrathiafulvalene tetrabenzoate	76-108	CD2 molecule	Homo sapiens	54-57
27766856-7	2016	Consistent results emerge only when these factors are strictly controlled and the morphology and anisotropy of the Cd2(TTFTB) single-crystal devices are taken into account.	ttftb	119-124	CD2 molecule	Homo sapiens	115-118
27808109-1	2016	We derive structural and binding energy trends for twenty amino acids, their dipeptides, and their interactions with the divalent cations Ca2+, Ba2+, Sr2+, Cd2+, Pb2+, and Hg2+.	Dipeptides	77-87	CD2 molecule	Homo sapiens	156-159
29964784-0	2016	[Adsorption Cd2+ from Solution by EDTA-modified Silicate Nanoparticles].	Silicates	48-56	CD2 molecule	Homo sapiens	12-15
29964784-2	2016	In order to improve the Cd2+ adsorption ability, the EDTA-modified nSiO2 nanoparticles were prepared by grafting method and characterized by TEM, N2 adsorption-desorption, FTIR, and TGA.	Edetic Acid	53-57	CD2 molecule	Homo sapiens	24-27
27373667-2	2016	The reaction mechanism was extrapolated from a deuteration experiment with CD2=S(O)(CD3)2.	s(o)(cd3)2	79-89	CD2 molecule	Homo sapiens	75-78
29964784-12	2016	The Cd2+ adsorption decreased from 0.433 to 0.294 mmol g-1, when NaCl concentration varied from 0 to 100 mmol L-1.	Sodium Chloride	65-69	CD2 molecule	Homo sapiens	4-7
29964784-13	2016	The desorption of Cd2+ from the EDTA-nSiO2 nanoparticles was carried out with distilled water, 0.1 mol L-1 NaCl and 0.1 mol L-1 HCl.	Edetic Acid	32-36	CD2 molecule	Homo sapiens	18-21
29964784-13	2016	The desorption of Cd2+ from the EDTA-nSiO2 nanoparticles was carried out with distilled water, 0.1 mol L-1 NaCl and 0.1 mol L-1 HCl.	nsio2	37-42	CD2 molecule	Homo sapiens	18-21
29964784-13	2016	The desorption of Cd2+ from the EDTA-nSiO2 nanoparticles was carried out with distilled water, 0.1 mol L-1 NaCl and 0.1 mol L-1 HCl.	Water	88-93	CD2 molecule	Homo sapiens	18-21
29964784-13	2016	The desorption of Cd2+ from the EDTA-nSiO2 nanoparticles was carried out with distilled water, 0.1 mol L-1 NaCl and 0.1 mol L-1 HCl.	l-1 nacl	103-111	CD2 molecule	Homo sapiens	18-21
29964784-13	2016	The desorption of Cd2+ from the EDTA-nSiO2 nanoparticles was carried out with distilled water, 0.1 mol L-1 NaCl and 0.1 mol L-1 HCl.	l-1 hcl	124-131	CD2 molecule	Homo sapiens	18-21
29964784-14	2016	The maximum Cd2+ desorption of 94.36% was obtained at 0.1 mol L-1 HCl.	l-1 hcl	62-69	CD2 molecule	Homo sapiens	12-15
29964784-16	2016	This study indicated that the EDTA-nSiO2 is an effective engineering nanomaterial that could be used in Cd2+ adsorption.	Edetic Acid	30-34	CD2 molecule	Homo sapiens	104-107
29964784-16	2016	This study indicated that the EDTA-nSiO2 is an effective engineering nanomaterial that could be used in Cd2+ adsorption.	nsio2	35-40	CD2 molecule	Homo sapiens	104-107
28344264-0	2016	Determination of Cd2+ and Pb2+ Based on Mesoporous Carbon Nitride/Self-Doped Polyaniline Nanofibers and Square Wave Anodic Stripping Voltammetry.	cyanogen	51-65	CD2 molecule	Homo sapiens	17-20
28344264-0	2016	Determination of Cd2+ and Pb2+ Based on Mesoporous Carbon Nitride/Self-Doped Polyaniline Nanofibers and Square Wave Anodic Stripping Voltammetry.	polyaniline	77-88	CD2 molecule	Homo sapiens	17-20
27454933-4	2016	The catalytic activity of CD2 from both species exhibited broad substrate specificity, whereas that of CD1 was highly specific for substrates bearing C-terminal acetyllysine residues.	N-epsilon-Acetyl-L-lysine	161-173	CD2 molecule	Homo sapiens	26-29
27341440-1	2016	Rice plants accumulate cadmium (Cd2+) within the grain, increasing the danger of human exposure.	Cadmium	23-30	CD2 molecule	Homo sapiens	32-35
27038580-1	2016	A metal-organic complex [Cd2(L)(N3)4] DMF was prepared by the reaction of Cd(NO3)2 4H2O, NaN3 and ligand L (L: 1,4-bis(bis(3,5-dimethyl-1H-pyrazol-1-yl)methyl)benzene) in a DMF system.	Metals	2-7	CD2 molecule	Homo sapiens	25-28
27038580-1	2016	A metal-organic complex [Cd2(L)(N3)4] DMF was prepared by the reaction of Cd(NO3)2 4H2O, NaN3 and ligand L (L: 1,4-bis(bis(3,5-dimethyl-1H-pyrazol-1-yl)methyl)benzene) in a DMF system.	cadmium nitrate	74-87	CD2 molecule	Homo sapiens	25-28
27038580-1	2016	A metal-organic complex [Cd2(L)(N3)4] DMF was prepared by the reaction of Cd(NO3)2 4H2O, NaN3 and ligand L (L: 1,4-bis(bis(3,5-dimethyl-1H-pyrazol-1-yl)methyl)benzene) in a DMF system.	Sodium Azide	89-93	CD2 molecule	Homo sapiens	25-28
27038580-1	2016	A metal-organic complex [Cd2(L)(N3)4] DMF was prepared by the reaction of Cd(NO3)2 4H2O, NaN3 and ligand L (L: 1,4-bis(bis(3,5-dimethyl-1H-pyrazol-1-yl)methyl)benzene) in a DMF system.	1,4-bis(bis(3,5-dimethyl-1h-pyrazol-1-yl)methyl)benzene	111-166	CD2 molecule	Homo sapiens	25-28
27038580-1	2016	A metal-organic complex [Cd2(L)(N3)4] DMF was prepared by the reaction of Cd(NO3)2 4H2O, NaN3 and ligand L (L: 1,4-bis(bis(3,5-dimethyl-1H-pyrazol-1-yl)methyl)benzene) in a DMF system.	Dimethylformamide	38-41	CD2 molecule	Homo sapiens	25-28
26865636-1	2016	The alpha-(1 2) branching sucrase DeltaN123-GBD-CD2 is a transglucosylase belonging to glycoside hydrolase family 70 (GH70) that catalyzes the transfer ofd-glucosyl units from sucroseto dextrans or gluco-oligosaccharides via the formation of alpha-(1 2) glucosidic linkages.	sucroseto dextrans	176-194	CD2 molecule	Homo sapiens	48-51
26865636-1	2016	The alpha-(1 2) branching sucrase DeltaN123-GBD-CD2 is a transglucosylase belonging to glycoside hydrolase family 70 (GH70) that catalyzes the transfer ofd-glucosyl units from sucroseto dextrans or gluco-oligosaccharides via the formation of alpha-(1 2) glucosidic linkages.	gluco-oligosaccharides	198-220	CD2 molecule	Homo sapiens	48-51
26865636-1	2016	The alpha-(1 2) branching sucrase DeltaN123-GBD-CD2 is a transglucosylase belonging to glycoside hydrolase family 70 (GH70) that catalyzes the transfer ofd-glucosyl units from sucroseto dextrans or gluco-oligosaccharides via the formation of alpha-(1 2) glucosidic linkages.	-(1 2) glucosidic	247-264	CD2 molecule	Homo sapiens	48-51
26865636-2	2016	The first structures of DeltaN123-GBD-CD2 in complex withd-glucose, isomaltosyl, or isomaltotriosyl residues were solved.	Glucose	58-66	CD2 molecule	Homo sapiens	38-41
31973329-1	2015	5-(3",4"-Dicarboxylphenoxy)isophthalic acid (H4 L1) and 5-(2",3"-dicarboxylphenoxy)isophthalic acid (H4 L2) were reacted with Cd2+ salt with/without the assistance of N-donor ligands, creating five 3D CdII coordination polymers [Cd2 (L1)(H2 O)5 ] H2 O (1), [Cd2 (L1)(bpe)(H2 O)] (bpe=1,2-bis(4-pyridyl)ethene; 2), [Cd2 (L1)(bpa)(H2 O)] (bpa=1,2-bis(4-pyridyl)ethane; 3), [Cd2 (L1)(bpp)] (bpp=1,3-bis(4-pyridyl)propane; 4), and [Cd2 (L2)(bpp)2 (H2 O)2 ] H2 O (5).	isophthalate	0-43	CD2 molecule	Homo sapiens	126-129
27148732-0	2016	Enhanced selectivity and capacity of clinoptilolite for Cd2+ removal from aqueous solutions by incorporation of magnetite nanoparticles and surface modification with cysteine.	Cysteine	166-174	CD2 molecule	Homo sapiens	56-59
27398533-1	2016	A colorimetric assay has been developed for detection of Cd2+ utilizing DL-mercaptosuccinic acid-modified gold nanoparticles (MSA-AuNPs).	2-thiomalic acid	72-96	CD2 molecule	Homo sapiens	57-60
27398533-2	2016	The method showed good selectivity for Cd2+ over other metal ions.	Metals	55-60	CD2 molecule	Homo sapiens	39-42
26647830-6	2016	These results were recapitulated in T-cells activated with anti-CD2, anti-CD3 and anti-CD28 by direct activation of the GCN2 kinase with tryptophanol.	tryptophanol	137-149	CD2 molecule	Homo sapiens	64-67
27148732-0	2016	Enhanced selectivity and capacity of clinoptilolite for Cd2+ removal from aqueous solutions by incorporation of magnetite nanoparticles and surface modification with cysteine.	clinoptilolite	37-51	CD2 molecule	Homo sapiens	56-59
31973329-1	2015	5-(3",4"-Dicarboxylphenoxy)isophthalic acid (H4 L1) and 5-(2",3"-dicarboxylphenoxy)isophthalic acid (H4 L2) were reacted with Cd2+ salt with/without the assistance of N-donor ligands, creating five 3D CdII coordination polymers [Cd2 (L1)(H2 O)5 ] H2 O (1), [Cd2 (L1)(bpe)(H2 O)] (bpe=1,2-bis(4-pyridyl)ethene; 2), [Cd2 (L1)(bpa)(H2 O)] (bpa=1,2-bis(4-pyridyl)ethane; 3), [Cd2 (L1)(bpp)] (bpp=1,3-bis(4-pyridyl)propane; 4), and [Cd2 (L2)(bpp)2 (H2 O)2 ] H2 O (5).	isophthalate	0-43	CD2 molecule	Homo sapiens	229-232
31973329-1	2015	5-(3",4"-Dicarboxylphenoxy)isophthalic acid (H4 L1) and 5-(2",3"-dicarboxylphenoxy)isophthalic acid (H4 L2) were reacted with Cd2+ salt with/without the assistance of N-donor ligands, creating five 3D CdII coordination polymers [Cd2 (L1)(H2 O)5 ] H2 O (1), [Cd2 (L1)(bpe)(H2 O)] (bpe=1,2-bis(4-pyridyl)ethene; 2), [Cd2 (L1)(bpa)(H2 O)] (bpa=1,2-bis(4-pyridyl)ethane; 3), [Cd2 (L1)(bpp)] (bpp=1,3-bis(4-pyridyl)propane; 4), and [Cd2 (L2)(bpp)2 (H2 O)2 ] H2 O (5).	isophthalate	0-43	CD2 molecule	Homo sapiens	229-232
31973329-1	2015	5-(3",4"-Dicarboxylphenoxy)isophthalic acid (H4 L1) and 5-(2",3"-dicarboxylphenoxy)isophthalic acid (H4 L2) were reacted with Cd2+ salt with/without the assistance of N-donor ligands, creating five 3D CdII coordination polymers [Cd2 (L1)(H2 O)5 ] H2 O (1), [Cd2 (L1)(bpe)(H2 O)] (bpe=1,2-bis(4-pyridyl)ethene; 2), [Cd2 (L1)(bpa)(H2 O)] (bpa=1,2-bis(4-pyridyl)ethane; 3), [Cd2 (L1)(bpp)] (bpp=1,3-bis(4-pyridyl)propane; 4), and [Cd2 (L2)(bpp)2 (H2 O)2 ] H2 O (5).	isophthalate	0-43	CD2 molecule	Homo sapiens	229-232
31973329-1	2015	5-(3",4"-Dicarboxylphenoxy)isophthalic acid (H4 L1) and 5-(2",3"-dicarboxylphenoxy)isophthalic acid (H4 L2) were reacted with Cd2+ salt with/without the assistance of N-donor ligands, creating five 3D CdII coordination polymers [Cd2 (L1)(H2 O)5 ] H2 O (1), [Cd2 (L1)(bpe)(H2 O)] (bpe=1,2-bis(4-pyridyl)ethene; 2), [Cd2 (L1)(bpa)(H2 O)] (bpa=1,2-bis(4-pyridyl)ethane; 3), [Cd2 (L1)(bpp)] (bpp=1,3-bis(4-pyridyl)propane; 4), and [Cd2 (L2)(bpp)2 (H2 O)2 ] H2 O (5).	isophthalate	0-43	CD2 molecule	Homo sapiens	229-232
31973329-1	2015	5-(3",4"-Dicarboxylphenoxy)isophthalic acid (H4 L1) and 5-(2",3"-dicarboxylphenoxy)isophthalic acid (H4 L2) were reacted with Cd2+ salt with/without the assistance of N-donor ligands, creating five 3D CdII coordination polymers [Cd2 (L1)(H2 O)5 ] H2 O (1), [Cd2 (L1)(bpe)(H2 O)] (bpe=1,2-bis(4-pyridyl)ethene; 2), [Cd2 (L1)(bpa)(H2 O)] (bpa=1,2-bis(4-pyridyl)ethane; 3), [Cd2 (L1)(bpp)] (bpp=1,3-bis(4-pyridyl)propane; 4), and [Cd2 (L2)(bpp)2 (H2 O)2 ] H2 O (5).	isophthalate	0-43	CD2 molecule	Homo sapiens	229-232
31973329-1	2015	5-(3",4"-Dicarboxylphenoxy)isophthalic acid (H4 L1) and 5-(2",3"-dicarboxylphenoxy)isophthalic acid (H4 L2) were reacted with Cd2+ salt with/without the assistance of N-donor ligands, creating five 3D CdII coordination polymers [Cd2 (L1)(H2 O)5 ] H2 O (1), [Cd2 (L1)(bpe)(H2 O)] (bpe=1,2-bis(4-pyridyl)ethene; 2), [Cd2 (L1)(bpa)(H2 O)] (bpa=1,2-bis(4-pyridyl)ethane; 3), [Cd2 (L1)(bpp)] (bpp=1,3-bis(4-pyridyl)propane; 4), and [Cd2 (L2)(bpp)2 (H2 O)2 ] H2 O (5).	isophthalate	56-99	CD2 molecule	Homo sapiens	126-129
31973329-1	2015	5-(3",4"-Dicarboxylphenoxy)isophthalic acid (H4 L1) and 5-(2",3"-dicarboxylphenoxy)isophthalic acid (H4 L2) were reacted with Cd2+ salt with/without the assistance of N-donor ligands, creating five 3D CdII coordination polymers [Cd2 (L1)(H2 O)5 ] H2 O (1), [Cd2 (L1)(bpe)(H2 O)] (bpe=1,2-bis(4-pyridyl)ethene; 2), [Cd2 (L1)(bpa)(H2 O)] (bpa=1,2-bis(4-pyridyl)ethane; 3), [Cd2 (L1)(bpp)] (bpp=1,3-bis(4-pyridyl)propane; 4), and [Cd2 (L2)(bpp)2 (H2 O)2 ] H2 O (5).	isophthalate	56-99	CD2 molecule	Homo sapiens	229-232
31973329-1	2015	5-(3",4"-Dicarboxylphenoxy)isophthalic acid (H4 L1) and 5-(2",3"-dicarboxylphenoxy)isophthalic acid (H4 L2) were reacted with Cd2+ salt with/without the assistance of N-donor ligands, creating five 3D CdII coordination polymers [Cd2 (L1)(H2 O)5 ] H2 O (1), [Cd2 (L1)(bpe)(H2 O)] (bpe=1,2-bis(4-pyridyl)ethene; 2), [Cd2 (L1)(bpa)(H2 O)] (bpa=1,2-bis(4-pyridyl)ethane; 3), [Cd2 (L1)(bpp)] (bpp=1,3-bis(4-pyridyl)propane; 4), and [Cd2 (L2)(bpp)2 (H2 O)2 ] H2 O (5).	isophthalate	56-99	CD2 molecule	Homo sapiens	229-232
31973329-1	2015	5-(3",4"-Dicarboxylphenoxy)isophthalic acid (H4 L1) and 5-(2",3"-dicarboxylphenoxy)isophthalic acid (H4 L2) were reacted with Cd2+ salt with/without the assistance of N-donor ligands, creating five 3D CdII coordination polymers [Cd2 (L1)(H2 O)5 ] H2 O (1), [Cd2 (L1)(bpe)(H2 O)] (bpe=1,2-bis(4-pyridyl)ethene; 2), [Cd2 (L1)(bpa)(H2 O)] (bpa=1,2-bis(4-pyridyl)ethane; 3), [Cd2 (L1)(bpp)] (bpp=1,3-bis(4-pyridyl)propane; 4), and [Cd2 (L2)(bpp)2 (H2 O)2 ] H2 O (5).	isophthalate	56-99	CD2 molecule	Homo sapiens	229-232
31973329-1	2015	5-(3",4"-Dicarboxylphenoxy)isophthalic acid (H4 L1) and 5-(2",3"-dicarboxylphenoxy)isophthalic acid (H4 L2) were reacted with Cd2+ salt with/without the assistance of N-donor ligands, creating five 3D CdII coordination polymers [Cd2 (L1)(H2 O)5 ] H2 O (1), [Cd2 (L1)(bpe)(H2 O)] (bpe=1,2-bis(4-pyridyl)ethene; 2), [Cd2 (L1)(bpa)(H2 O)] (bpa=1,2-bis(4-pyridyl)ethane; 3), [Cd2 (L1)(bpp)] (bpp=1,3-bis(4-pyridyl)propane; 4), and [Cd2 (L2)(bpp)2 (H2 O)2 ] H2 O (5).	isophthalate	56-99	CD2 molecule	Homo sapiens	229-232
31973329-1	2015	5-(3",4"-Dicarboxylphenoxy)isophthalic acid (H4 L1) and 5-(2",3"-dicarboxylphenoxy)isophthalic acid (H4 L2) were reacted with Cd2+ salt with/without the assistance of N-donor ligands, creating five 3D CdII coordination polymers [Cd2 (L1)(H2 O)5 ] H2 O (1), [Cd2 (L1)(bpe)(H2 O)] (bpe=1,2-bis(4-pyridyl)ethene; 2), [Cd2 (L1)(bpa)(H2 O)] (bpa=1,2-bis(4-pyridyl)ethane; 3), [Cd2 (L1)(bpp)] (bpp=1,3-bis(4-pyridyl)propane; 4), and [Cd2 (L2)(bpp)2 (H2 O)2 ] H2 O (5).	isophthalate	56-99	CD2 molecule	Homo sapiens	229-232
26344428-8	2015	Synta 66 inhibited CD2/3/28 induced IL-2, IL-7, IL-13 & IFNUpsilon in a concentration-dependent manner in healthy and severe asthma donors, with over 60% inhibition observed for all cytokines.	synta	0-5	CD2 molecule	Homo sapiens	19-22
26617434-8	2015	Once inside the covellite particles, Cd2+ and Hg2+ cations engaged in exchange reactions, pushing the expelled Cu+ ions toward the not-yet exchanged regions in the same particles, or out to the solution, from where they could be recaptured by other covellite nanoparticles/domains.	cupric sulfide	16-25	CD2 molecule	Homo sapiens	37-40
26617434-8	2015	Once inside the covellite particles, Cd2+ and Hg2+ cations engaged in exchange reactions, pushing the expelled Cu+ ions toward the not-yet exchanged regions in the same particles, or out to the solution, from where they could be recaptured by other covellite nanoparticles/domains.	Copper	111-114	CD2 molecule	Homo sapiens	37-40
26617434-8	2015	Once inside the covellite particles, Cd2+ and Hg2+ cations engaged in exchange reactions, pushing the expelled Cu+ ions toward the not-yet exchanged regions in the same particles, or out to the solution, from where they could be recaptured by other covellite nanoparticles/domains.	cupric sulfide	249-258	CD2 molecule	Homo sapiens	37-40
26344428-8	2015	Synta 66 inhibited CD2/3/28 induced IL-2, IL-7, IL-13 & IFNUpsilon in a concentration-dependent manner in healthy and severe asthma donors, with over 60% inhibition observed for all cytokines.	Adenosine Monophosphate	55-58	CD2 molecule	Homo sapiens	19-22
26375382-3	2015	The rate constants for the various metal-retaining intermediates (Cd(i), intermediate with i Cd2+ ions attached) differ by >3 orders of magnitude: Cd4< Cd3< Cd2< Cd1~ Cd6 < Cd7 < Cd5.	Metals	35-40	CD2 molecule	Homo sapiens	93-96
26375382-3	2015	The rate constants for the various metal-retaining intermediates (Cd(i), intermediate with i Cd2+ ions attached) differ by >3 orders of magnitude: Cd4< Cd3< Cd2< Cd1~ Cd6 < Cd7 < Cd5.	Metals	35-40	CD2 molecule	Homo sapiens	166-169
26206156-3	2015	The mu-oxo-bridged secondary building unit, {Cd2 (mu-OCO)2 }, guides the parallel alignment of bpNDI (N,N"-di(4-pyridyl)-1,4,5,8-naphthalenediimide) acceptor linkers, which are tethered with bpdc (bpdcH2 =4,4"-biphenyldicarboxylic acid) linkers of another entangled net in the framework, resulting in photochromic behaviour through inter-net electron transfer.	oxo	7-10	CD2 molecule	Homo sapiens	45-48
26291380-8	2015	The 1,1-HCl and 1,1-HF reactions are observed via the CD2 CDF and CD2 CDCl products formed from isomerization of the CD3CF and CD3CCl carbenes.	cd3cf	117-122	CD2 molecule	Homo sapiens	54-57
26291380-8	2015	The 1,1-HCl and 1,1-HF reactions are observed via the CD2 CDF and CD2 CDCl products formed from isomerization of the CD3CF and CD3CCl carbenes.	cd3cf	117-122	CD2 molecule	Homo sapiens	66-69
26291380-8	2015	The 1,1-HCl and 1,1-HF reactions are observed via the CD2 CDF and CD2 CDCl products formed from isomerization of the CD3CF and CD3CCl carbenes.	cd3ccl carbenes	127-142	CD2 molecule	Homo sapiens	54-57
26291380-8	2015	The 1,1-HCl and 1,1-HF reactions are observed via the CD2 CDF and CD2 CDCl products formed from isomerization of the CD3CF and CD3CCl carbenes.	cd3ccl carbenes	127-142	CD2 molecule	Homo sapiens	66-69
26301920-3	2015	In this study, we first synthesized an amphiphilic beta-cyclodextrin (beta-CD) dimer that consists of one hydrophobic ibuprofen (Ibu) and two hydrophilic beta-CD moieties (i.e., Ibu-CD2).	betadex	51-68	CD2 molecule	Homo sapiens	182-185
26301920-3	2015	In this study, we first synthesized an amphiphilic beta-cyclodextrin (beta-CD) dimer that consists of one hydrophobic ibuprofen (Ibu) and two hydrophilic beta-CD moieties (i.e., Ibu-CD2).	betadex	70-77	CD2 molecule	Homo sapiens	182-185
26301920-5	2015	The host-guest interaction of Ibu-CD2 induced the formation of branched supramolecular polymers (SPs) in pure water, whereas the hydrophilic-hydrophobic interaction generated spherical or irregular micelles in water/organic mixtures.	Polymers	87-95	CD2 molecule	Homo sapiens	34-37
26301920-5	2015	The host-guest interaction of Ibu-CD2 induced the formation of branched supramolecular polymers (SPs) in pure water, whereas the hydrophilic-hydrophobic interaction generated spherical or irregular micelles in water/organic mixtures.	Sodium phenolsulfonate	97-100	CD2 molecule	Homo sapiens	34-37
26301920-5	2015	The host-guest interaction of Ibu-CD2 induced the formation of branched supramolecular polymers (SPs) in pure water, whereas the hydrophilic-hydrophobic interaction generated spherical or irregular micelles in water/organic mixtures.	Water	110-115	CD2 molecule	Homo sapiens	34-37
26301920-5	2015	The host-guest interaction of Ibu-CD2 induced the formation of branched supramolecular polymers (SPs) in pure water, whereas the hydrophilic-hydrophobic interaction generated spherical or irregular micelles in water/organic mixtures.	Water	210-215	CD2 molecule	Homo sapiens	34-37
26301920-6	2015	The SP size increased with the increase in Ibu-CD2 concentration in pure water.	sp	4-6	CD2 molecule	Homo sapiens	47-50
26301920-6	2015	The SP size increased with the increase in Ibu-CD2 concentration in pure water.	Water	73-78	CD2 molecule	Homo sapiens	47-50
26291380-8	2015	The 1,1-HCl and 1,1-HF reactions are observed via the CD2 CDF and CD2 CDCl products formed from isomerization of the CD3CF and CD3CCl carbenes.	1,1-hcl	4-11	CD2 molecule	Homo sapiens	54-57
26291380-8	2015	The 1,1-HCl and 1,1-HF reactions are observed via the CD2 CDF and CD2 CDCl products formed from isomerization of the CD3CF and CD3CCl carbenes.	1,1-hcl	4-11	CD2 molecule	Homo sapiens	66-69
26291380-8	2015	The 1,1-HCl and 1,1-HF reactions are observed via the CD2 CDF and CD2 CDCl products formed from isomerization of the CD3CF and CD3CCl carbenes.	,1-hf	17-22	CD2 molecule	Homo sapiens	54-57
26291380-8	2015	The 1,1-HCl and 1,1-HF reactions are observed via the CD2 CDF and CD2 CDCl products formed from isomerization of the CD3CF and CD3CCl carbenes.	,1-hf	17-22	CD2 molecule	Homo sapiens	66-69
26206156-3	2015	The mu-oxo-bridged secondary building unit, {Cd2 (mu-OCO)2 }, guides the parallel alignment of bpNDI (N,N"-di(4-pyridyl)-1,4,5,8-naphthalenediimide) acceptor linkers, which are tethered with bpdc (bpdcH2 =4,4"-biphenyldicarboxylic acid) linkers of another entangled net in the framework, resulting in photochromic behaviour through inter-net electron transfer.	bpndi (n,n"-di(4-pyridyl)-1,4,	95-125	CD2 molecule	Homo sapiens	45-48
26150356-2	2015	A combination of desolvation and cycloaddition reactions has been employed to synthesise a 3D coordination polymer (CP) from 1D CP [Cd(bdc)(4-spy)2 (H2 O)] 2 H2 O 2 DMF (bdc=1,4-benzenedicarboxylate, 4-spy=4-styrylpyridine) presumably via a 2D layered structure, [Cd2 (bdc)2 (4-spy)4 ].	Polymers	107-114	CD2 molecule	Homo sapiens	264-274
26206156-3	2015	The mu-oxo-bridged secondary building unit, {Cd2 (mu-OCO)2 }, guides the parallel alignment of bpNDI (N,N"-di(4-pyridyl)-1,4,5,8-naphthalenediimide) acceptor linkers, which are tethered with bpdc (bpdcH2 =4,4"-biphenyldicarboxylic acid) linkers of another entangled net in the framework, resulting in photochromic behaviour through inter-net electron transfer.	5,8-naphthalenediimide	125-147	CD2 molecule	Homo sapiens	45-48
26206156-3	2015	The mu-oxo-bridged secondary building unit, {Cd2 (mu-OCO)2 }, guides the parallel alignment of bpNDI (N,N"-di(4-pyridyl)-1,4,5,8-naphthalenediimide) acceptor linkers, which are tethered with bpdc (bpdcH2 =4,4"-biphenyldicarboxylic acid) linkers of another entangled net in the framework, resulting in photochromic behaviour through inter-net electron transfer.	bpdc	191-195	CD2 molecule	Homo sapiens	45-48
26150356-2	2015	A combination of desolvation and cycloaddition reactions has been employed to synthesise a 3D coordination polymer (CP) from 1D CP [Cd(bdc)(4-spy)2 (H2 O)] 2 H2 O 2 DMF (bdc=1,4-benzenedicarboxylate, 4-spy=4-styrylpyridine) presumably via a 2D layered structure, [Cd2 (bdc)2 (4-spy)4 ].	cd(bdc	132-138	CD2 molecule	Homo sapiens	264-274
26150356-2	2015	A combination of desolvation and cycloaddition reactions has been employed to synthesise a 3D coordination polymer (CP) from 1D CP [Cd(bdc)(4-spy)2 (H2 O)] 2 H2 O 2 DMF (bdc=1,4-benzenedicarboxylate, 4-spy=4-styrylpyridine) presumably via a 2D layered structure, [Cd2 (bdc)2 (4-spy)4 ].	Dimethylformamide	165-168	CD2 molecule	Homo sapiens	264-274
26206156-3	2015	The mu-oxo-bridged secondary building unit, {Cd2 (mu-OCO)2 }, guides the parallel alignment of bpNDI (N,N"-di(4-pyridyl)-1,4,5,8-naphthalenediimide) acceptor linkers, which are tethered with bpdc (bpdcH2 =4,4"-biphenyldicarboxylic acid) linkers of another entangled net in the framework, resulting in photochromic behaviour through inter-net electron transfer.	bpdch2	197-203	CD2 molecule	Homo sapiens	45-48
26206156-3	2015	The mu-oxo-bridged secondary building unit, {Cd2 (mu-OCO)2 }, guides the parallel alignment of bpNDI (N,N"-di(4-pyridyl)-1,4,5,8-naphthalenediimide) acceptor linkers, which are tethered with bpdc (bpdcH2 =4,4"-biphenyldicarboxylic acid) linkers of another entangled net in the framework, resulting in photochromic behaviour through inter-net electron transfer.	4,4'-biphenyldicarboxylic acid	205-235	CD2 molecule	Homo sapiens	45-48
25990730-0	2015	Rational evolution of Cd2+-specific DNAzymes with phosphorothioate modified cleavage junction and Cd2+ sensing.	Parathion	50-66	CD2 molecule	Homo sapiens	22-25
26592037-7	2015	The former was attributed to the interaction between Cd2 and --OH groups by chemical binding to form inner-sphere complexes in ATP and the attachment between Cd2+ and the defect sites in ATP framework.	attapulgite	127-130	CD2 molecule	Homo sapiens	53-65
26592037-7	2015	The former was attributed to the interaction between Cd2 and --OH groups by chemical binding to form inner-sphere complexes in ATP and the attachment between Cd2+ and the defect sites in ATP framework.	attapulgite	127-130	CD2 molecule	Homo sapiens	53-56
26592037-7	2015	The former was attributed to the interaction between Cd2 and --OH groups by chemical binding to form inner-sphere complexes in ATP and the attachment between Cd2+ and the defect sites in ATP framework.	attapulgite	187-190	CD2 molecule	Homo sapiens	53-65
26592037-7	2015	The former was attributed to the interaction between Cd2 and --OH groups by chemical binding to form inner-sphere complexes in ATP and the attachment between Cd2+ and the defect sites in ATP framework.	attapulgite	187-190	CD2 molecule	Homo sapiens	53-56
26373084-2	2015	The heterostructures were achieved by a two-step method where CdS nanorods were prepared in the first step, acting as the substrates inducing successive cation exchange reaction between Cd2+ and Ag+ ion.	Cadmium	62-65	CD2 molecule	Homo sapiens	186-189
25765909-7	2015	Hoechst staining assay indicated that compound T11 can cause morphological changes and induce apoptosis of HCT-116 cells.	hoechst	0-7	CD2 molecule	Homo sapiens	47-50
25817651-2	2015	Spectral results revealed that PCA forms 1:2 drug-CD2 inclusion complexes with CDs.	Cadmium	79-82	CD2 molecule	Homo sapiens	50-53
25915900-5	2015	CD2v-AP-1 binding was independent of CD2v glycosylation and occurred on the carboxy-terminal part of CD2v, where a canonical di-Leu motif previously reported to mediate AP-1 binding in eukaryotic cells, was identified.	di-leu	125-131	CD2 molecule	Homo sapiens	0-3
25803003-0	2015	A novel polynorbornene-based chemosensor for the fluorescence sensing of Zn2+ and Cd2+ and subsequent detection of pyrophosphate in aqueous solutions.	polynorbornen	8-22	CD2 molecule	Homo sapiens	82-85
29056654-1	2015	The transition metal ion cadmium (Cd2+) is a significant environmental contaminant.	Metals	15-20	CD2 molecule	Homo sapiens	34-37
25893518-5	2015	For Cd2+ they were mainly pH and, to a lesser extent, Mn oxides and clay content.	mn oxides	54-63	CD2 molecule	Homo sapiens	4-7
29056654-1	2015	The transition metal ion cadmium (Cd2+) is a significant environmental contaminant.	Cadmium	25-32	CD2 molecule	Homo sapiens	34-37
32262913-1	2015	Throughout the years, reported intracellular H2O2 sensors just focused on unrelated measurements of intracellular H2O2 generated from the stimulus of Cd2+, ascorbic acid (AA) etc., leading to difficulty in data interpretation.	Hydrogen Peroxide	45-49	CD2 molecule	Homo sapiens	150-153
32262913-1	2015	Throughout the years, reported intracellular H2O2 sensors just focused on unrelated measurements of intracellular H2O2 generated from the stimulus of Cd2+, ascorbic acid (AA) etc., leading to difficulty in data interpretation.	Hydrogen Peroxide	114-118	CD2 molecule	Homo sapiens	150-153
25875164-4	2015	In the present study we applied the real-time NMR method to analyze the catalytic activity of CD2 toward DNA oligonucleotides containing a nucleotide analog at a single or multiple positions.	Oligonucleotides	109-125	CD2 molecule	Homo sapiens	94-97
25450655-11	2015	In the 20  kyphosis model, the higher CPS values showed bimodal peaks at T6 and T7 in the midthoracic spine and at T10 and T11 in the two superior adjacent vertebrae.	cps	38-41	CD2 molecule	Homo sapiens	123-126
25875164-6	2015	It was also shown that the sugar or base moieties of the nucleotides outside this 5 nucleotide recognition sequence are also relevant as to CD2"s activity.	Sugars	27-32	CD2 molecule	Homo sapiens	140-143
25875164-7	2015	Analyses involving DNA oligonucleotides having two CCC hotspots linked by a long sequence of either deoxyribonucleotides, ribonucleotides or abasic deoxyribonucleotides suggested that the phosphate backbone is required for CD2 to slide along the DNA strand and to exert the 3" 5" polarity.	Phosphates	188-197	CD2 molecule	Homo sapiens	223-226
25875164-9	2015	This is most likely the result of alleviation of sliding due to a decrease in the affinity of CD2 with the phosphate backbone at high salt concentrations.	Phosphates	107-116	CD2 molecule	Homo sapiens	94-97
25875164-9	2015	This is most likely the result of alleviation of sliding due to a decrease in the affinity of CD2 with the phosphate backbone at high salt concentrations.	Salts	134-138	CD2 molecule	Homo sapiens	94-97
25311520-1	2015	The interaction of Cd(II) with the non-steroidal anti-inflammatory drug diclofenac sodium (Dic) leads to the formation of the complex [Cd2(L)41.5(MeOH)2(H2O)]n(L = Dic), 1, which has been isolated and structurally characterized by X-ray crystallography.	cd(ii)	19-25	CD2 molecule	Homo sapiens	135-138
25311520-1	2015	The interaction of Cd(II) with the non-steroidal anti-inflammatory drug diclofenac sodium (Dic) leads to the formation of the complex [Cd2(L)41.5(MeOH)2(H2O)]n(L = Dic), 1, which has been isolated and structurally characterized by X-ray crystallography.	Diclofenac	72-89	CD2 molecule	Homo sapiens	135-138
25614390-6	2015	Such restriction was not observed in cell adhesion mediated by the mutant of physiological adhesion protein CD2, which lacked its cytoplasmic domain and was unable to connect to cytoplasmic actin filaments, but had a similar affinity for its ligand compared with the chol-gelatin-cell membrane interaction.	chol	267-271	CD2 molecule	Homo sapiens	108-111
25311520-1	2015	The interaction of Cd(II) with the non-steroidal anti-inflammatory drug diclofenac sodium (Dic) leads to the formation of the complex [Cd2(L)41.5(MeOH)2(H2O)]n(L = Dic), 1, which has been isolated and structurally characterized by X-ray crystallography.	Diclofenac	91-94	CD2 molecule	Homo sapiens	135-138
25311520-1	2015	The interaction of Cd(II) with the non-steroidal anti-inflammatory drug diclofenac sodium (Dic) leads to the formation of the complex [Cd2(L)41.5(MeOH)2(H2O)]n(L = Dic), 1, which has been isolated and structurally characterized by X-ray crystallography.	Methanol	146-150	CD2 molecule	Homo sapiens	135-138
25311520-1	2015	The interaction of Cd(II) with the non-steroidal anti-inflammatory drug diclofenac sodium (Dic) leads to the formation of the complex [Cd2(L)41.5(MeOH)2(H2O)]n(L = Dic), 1, which has been isolated and structurally characterized by X-ray crystallography.	Water	153-156	CD2 molecule	Homo sapiens	135-138
26676004-8	2015	Below this threshold value, the Cd2+ and Pb2+ ions are uptaken simultaneously due to the abundance of Cd2+ ions and the availability of adsorption sites at very low Pb2+ molar ratios.	Lead	41-45	CD2 molecule	Homo sapiens	102-105
25431256-1	2015	A luminescent cadmium-pamoate metal-organic framework, [Cd2 (PAM)2 (dpe)2 (H2 O)2 ] 0.5(dpe) (1), has been synthesized under hydrothermal conditions by using pi-electron-rich ligands 4,4"-methylenebis(3-hydroxy-2-naphthalenecarboxylic acid) (H2 PAM) and 1,2-di(4-pyridyl)ethylene (dpe).	cadmium-pamoate	14-29	CD2 molecule	Homo sapiens	56-59
25431256-1	2015	A luminescent cadmium-pamoate metal-organic framework, [Cd2 (PAM)2 (dpe)2 (H2 O)2 ] 0.5(dpe) (1), has been synthesized under hydrothermal conditions by using pi-electron-rich ligands 4,4"-methylenebis(3-hydroxy-2-naphthalenecarboxylic acid) (H2 PAM) and 1,2-di(4-pyridyl)ethylene (dpe).	Metals	30-35	CD2 molecule	Homo sapiens	56-59
25431256-1	2015	A luminescent cadmium-pamoate metal-organic framework, [Cd2 (PAM)2 (dpe)2 (H2 O)2 ] 0.5(dpe) (1), has been synthesized under hydrothermal conditions by using pi-electron-rich ligands 4,4"-methylenebis(3-hydroxy-2-naphthalenecarboxylic acid) (H2 PAM) and 1,2-di(4-pyridyl)ethylene (dpe).	dpe	68-71	CD2 molecule	Homo sapiens	56-59
25431256-1	2015	A luminescent cadmium-pamoate metal-organic framework, [Cd2 (PAM)2 (dpe)2 (H2 O)2 ] 0.5(dpe) (1), has been synthesized under hydrothermal conditions by using pi-electron-rich ligands 4,4"-methylenebis(3-hydroxy-2-naphthalenecarboxylic acid) (H2 PAM) and 1,2-di(4-pyridyl)ethylene (dpe).	pamoic acid	183-240	CD2 molecule	Homo sapiens	56-59
25431256-1	2015	A luminescent cadmium-pamoate metal-organic framework, [Cd2 (PAM)2 (dpe)2 (H2 O)2 ] 0.5(dpe) (1), has been synthesized under hydrothermal conditions by using pi-electron-rich ligands 4,4"-methylenebis(3-hydroxy-2-naphthalenecarboxylic acid) (H2 PAM) and 1,2-di(4-pyridyl)ethylene (dpe).	4,4'-Vinylenedipyridine	254-279	CD2 molecule	Homo sapiens	56-59
25431256-1	2015	A luminescent cadmium-pamoate metal-organic framework, [Cd2 (PAM)2 (dpe)2 (H2 O)2 ] 0.5(dpe) (1), has been synthesized under hydrothermal conditions by using pi-electron-rich ligands 4,4"-methylenebis(3-hydroxy-2-naphthalenecarboxylic acid) (H2 PAM) and 1,2-di(4-pyridyl)ethylene (dpe).	dpe	88-91	CD2 molecule	Homo sapiens	56-59
25302775-0	2015	TQPHEN (N,N,N",N"-tetrakis(2-quinolylmethyl)-1,2-phenylenediamine) derivatives as highly selective fluorescent probes for Cd2+.	tqphen	0-6	CD2 molecule	Homo sapiens	122-125
25413113-0	2015	Nanoparticles of KFeP2O7 implanted on silica gel beads for Cd2+ ion adsorption.	kfep2o7	17-24	CD2 molecule	Homo sapiens	59-62
25413113-0	2015	Nanoparticles of KFeP2O7 implanted on silica gel beads for Cd2+ ion adsorption.	Silica Gel	38-48	CD2 molecule	Homo sapiens	59-62
25413113-1	2015	Nanoparticles of iron and potassium diphosphate (KFeP2O7) implanted in silica gel beads (SiO2) have been investigated as an alternative adsorbent for removing Cd2+ ions from aqueous solutions.	Iron	17-21	CD2 molecule	Homo sapiens	159-162
25413113-1	2015	Nanoparticles of iron and potassium diphosphate (KFeP2O7) implanted in silica gel beads (SiO2) have been investigated as an alternative adsorbent for removing Cd2+ ions from aqueous solutions.	tetrapotassium pyrophosphate	26-47	CD2 molecule	Homo sapiens	159-162
25413113-1	2015	Nanoparticles of iron and potassium diphosphate (KFeP2O7) implanted in silica gel beads (SiO2) have been investigated as an alternative adsorbent for removing Cd2+ ions from aqueous solutions.	kfep2o7	49-56	CD2 molecule	Homo sapiens	159-162
25051461-0	2014	Specific binding of Zn2+, Cd2+ and Ni2+ ions by a cyclic four-cysteinyl peptide.	cyclic four-cysteinyl peptide	50-79	CD2 molecule	Homo sapiens	26-29
24935191-0	2014	Conversion of waste FGD gypsum into hydroxyapatite for removal of Pb2+ and Cd2+ from wastewater.	Durapatite	36-50	CD2 molecule	Homo sapiens	75-78
24969429-7	2014	Ligand addition generally strongly reduced hydrated Cd (Cd(2+)) concentration in soil solution through Cd complexation.	Cadmium	52-54	CD2 molecule	Homo sapiens	56-62
24969429-8	2014	Dissociation of Cd complex ([Formula: see text]) could not compensate for this reduction, which greatly lowered Cd(2+) symplastic uptake by roots.	Cadmium	16-18	CD2 molecule	Homo sapiens	112-118
24398472-1	2014	Three phenothiazine-triphenylamine-based organic dyes (CD-1, CD-2 and CD-3) are designed based on the dye WD-8.	phenothiazine-triphenylamine	6-34	CD2 molecule	Homo sapiens	61-65
25244843-0	2014	[Effect of SDS on the adsorption of Cd2+ onto amphoteric modified bentonites].	dodecylsulfonic acid	11-14	CD2 molecule	Homo sapiens	36-39
25244843-1	2014	Under different modified ratios, temperatures, pH and ionic strengths, the effect of sodium dodecyl sulfonate (SDS) on the adsorption of Cd2+ onto bentonites which modified with amphoteric modifier dodecyl dimethyl betaine (BS-12) was studied by batch experiments, and the adsorption mechanism was also discussed.	dodecylsulfonic acid	85-109	CD2 molecule	Homo sapiens	137-140
25244843-1	2014	Under different modified ratios, temperatures, pH and ionic strengths, the effect of sodium dodecyl sulfonate (SDS) on the adsorption of Cd2+ onto bentonites which modified with amphoteric modifier dodecyl dimethyl betaine (BS-12) was studied by batch experiments, and the adsorption mechanism was also discussed.	dodecylsulfonic acid	111-114	CD2 molecule	Homo sapiens	137-140
25244843-1	2014	Under different modified ratios, temperatures, pH and ionic strengths, the effect of sodium dodecyl sulfonate (SDS) on the adsorption of Cd2+ onto bentonites which modified with amphoteric modifier dodecyl dimethyl betaine (BS-12) was studied by batch experiments, and the adsorption mechanism was also discussed.	dodecyl dimethyl betaine	198-222	CD2 molecule	Homo sapiens	137-140
25244843-6	2014	The adsorption of Cd2+ on bentonites decreases with ionic strength rise, but the effect of ionic strength can be reduced with an increase of SDS modified ratio also.	dodecylsulfonic acid	141-144	CD2 molecule	Homo sapiens	18-21
25244843-8	2014	When the SDS modified ratio is lower than 100% CEC, the adsorption of Cd2+ on modified bentonites is a process with characteristics of both enthalpy increment and entropy increment, while the SDS modified ratio is equal to or higher than 100% CEC, the adsorption of Cd2+ on modified bentonites becomes a process of enthalpy decrement and entropy increment.	dodecylsulfonic acid	9-12	CD2 molecule	Homo sapiens	70-73
24367995-0	2014	Structural characterization of Cd2+ complexes in solution with DMSA and DMPS.	Succimer	63-67	CD2 molecule	Homo sapiens	31-34
24367995-0	2014	Structural characterization of Cd2+ complexes in solution with DMSA and DMPS.	Unithiol	72-76	CD2 molecule	Homo sapiens	31-34
24890988-0	2014	Switchable and selective detection of Zn2+ or Cd2+ in living cells based on 3"-O-substituted arrangement of benzoxazole-derived fluorescent probes.	Benzoxazoles	108-119	CD2 molecule	Homo sapiens	46-49
25244843-8	2014	When the SDS modified ratio is lower than 100% CEC, the adsorption of Cd2+ on modified bentonites is a process with characteristics of both enthalpy increment and entropy increment, while the SDS modified ratio is equal to or higher than 100% CEC, the adsorption of Cd2+ on modified bentonites becomes a process of enthalpy decrement and entropy increment.	dodecylsulfonic acid	192-195	CD2 molecule	Homo sapiens	70-73
24720997-0	2014	Square wave anodic stripping voltammetric determination of Cd2+ and Pb2+ at bismuth-film electrode modified with electroreduced graphene oxide-supported thiolated thionine.	Bismuth	76-83	CD2 molecule	Homo sapiens	59-62
24720997-0	2014	Square wave anodic stripping voltammetric determination of Cd2+ and Pb2+ at bismuth-film electrode modified with electroreduced graphene oxide-supported thiolated thionine.	graphene oxide	128-142	CD2 molecule	Homo sapiens	59-62
24720997-0	2014	Square wave anodic stripping voltammetric determination of Cd2+ and Pb2+ at bismuth-film electrode modified with electroreduced graphene oxide-supported thiolated thionine.	thiolated thionine	153-171	CD2 molecule	Homo sapiens	59-62
24380377-1	2014	Substitution of -CD2- at the reactive centers of linoleic and linolenic acids reduces the rate of abstraction of D by a tocopheryl radical by as much as 36-fold, compared to the abstraction of H from a corresponding -CH2- center.	Linoleic Acid	49-57	CD2 molecule	Homo sapiens	17-20
24346307-1	2014	The 3-D coordination polymer with the basic formula Cd2(TCNQ)3.5(H2O)2 is the first instance of the coexistence of the bridging modes mu2, mu3 and mu4 for TCNQ in one network.	Polymers	21-28	CD2 molecule	Homo sapiens	52-55
24346307-1	2014	The 3-D coordination polymer with the basic formula Cd2(TCNQ)3.5(H2O)2 is the first instance of the coexistence of the bridging modes mu2, mu3 and mu4 for TCNQ in one network.	Hydrogen Peroxide	65-70	CD2 molecule	Homo sapiens	52-55
24346307-1	2014	The 3-D coordination polymer with the basic formula Cd2(TCNQ)3.5(H2O)2 is the first instance of the coexistence of the bridging modes mu2, mu3 and mu4 for TCNQ in one network.	tetracyanoquinodimethane	56-60	CD2 molecule	Homo sapiens	52-55
24380377-1	2014	Substitution of -CD2- at the reactive centers of linoleic and linolenic acids reduces the rate of abstraction of D by a tocopheryl radical by as much as 36-fold, compared to the abstraction of H from a corresponding -CH2- center.	tocopheryl radical	120-138	CD2 molecule	Homo sapiens	17-20
24519575-0	2014	The synthesis of (14)C-labeled, (13)CD2-labeled saxagliptin, and its (13)CD2-labeled 5-hydroxy metabolite.	saxagliptin	48-59	CD2 molecule	Homo sapiens	36-39
24519575-5	2014	By following similar synthetic routes, 580.0 mg of (13)CD2-labeled saxagliptin and 153.1 mg of (13)CD2-labeled 5-hydroxysaxagliptin metabolite were prepared.	5-hydroxysaxagliptin	111-131	CD2 molecule	Homo sapiens	99-102
24380377-1	2014	Substitution of -CD2- at the reactive centers of linoleic and linolenic acids reduces the rate of abstraction of D by a tocopheryl radical by as much as 36-fold, compared to the abstraction of H from a corresponding -CH2- center.	Linolenic Acids	62-77	CD2 molecule	Homo sapiens	17-20
24123641-6	2013	A site-specific glycoform profile variation was obtained by comparing the glycoform profile of CH2 and 13 CD2 glycopeptides.	Glycopeptides	110-123	CD2 molecule	Homo sapiens	106-109
24853041-4	2014	This paper comments on different sensing strategies with QD for the most toxic heavy metal ions (i.e., cadmium, Cd2+; mercury, Hg2+; and lead, Pb2+).	Metals	85-90	CD2 molecule	Homo sapiens	112-115
24982998-0	2014	The effect of chloride and sulfate ions on the adsorption of Cd2+ on clay and sandy loam Egyptian soils.	Chlorides	14-22	CD2 molecule	Homo sapiens	61-64
24982998-0	2014	The effect of chloride and sulfate ions on the adsorption of Cd2+ on clay and sandy loam Egyptian soils.	Sulfates	27-34	CD2 molecule	Homo sapiens	61-64
32261092-2	2013	The CdS-capped TiO2 was obtained by immersing TiO2 nanoparticles into separate Cd2+ and S2- solutions successively 10 times.	Cadmium	4-7	CD2 molecule	Homo sapiens	79-82
24113906-0	2013	An OFF-ON chemosensor for biological and environmental applications: sensing Cd2+ in water using catanionic vesicles and in living cells.	Water	85-90	CD2 molecule	Homo sapiens	77-80
24555377-3	2013	It was indicated that soluble extracellular carbohydrates may help the bacteria to enhance resistance to Cd2+, and insoluble EPS could contribute to Cd2+ removal effectively.	Carbohydrates	44-57	CD2 molecule	Homo sapiens	105-108
24555377-3	2013	It was indicated that soluble extracellular carbohydrates may help the bacteria to enhance resistance to Cd2+, and insoluble EPS could contribute to Cd2+ removal effectively.	eps	125-128	CD2 molecule	Homo sapiens	149-152
24555377-4	2013	The FTIR spectra showed that the peaks of amide and carboxyl were main functional groups for Cd2+ adsorption.	Amides	42-47	CD2 molecule	Homo sapiens	93-96
24555377-4	2013	The FTIR spectra showed that the peaks of amide and carboxyl were main functional groups for Cd2+ adsorption.	carboxyl	52-60	CD2 molecule	Homo sapiens	93-96
32261092-2	2013	The CdS-capped TiO2 was obtained by immersing TiO2 nanoparticles into separate Cd2+ and S2- solutions successively 10 times.	titanium dioxide	15-19	CD2 molecule	Homo sapiens	79-82
23981228-7	2013	Complex 1 exchanges with D2C CD2 with concomitant release of H2C CH2.	d2c	25-28	CD2 molecule	Homo sapiens	29-32
28788340-1	2013	Carbon from jatropha seed hull (JC) was prepared to study the adsorption of cadmium ions (Cd2+) from aqueous solutions under various experimental conditions.	Carbon	0-6	CD2 molecule	Homo sapiens	90-93
28788340-1	2013	Carbon from jatropha seed hull (JC) was prepared to study the adsorption of cadmium ions (Cd2+) from aqueous solutions under various experimental conditions.	Cadmium	76-83	CD2 molecule	Homo sapiens	90-93
28788340-4	2013	A kinetic study proved that the mechanism of Cd2+ adsorption on JC followed a three steps process, confirmed by an intraparticle diffusion model: rapid adsorption of metal ions, a transition phase, and nearly flat plateau section.	Metals	166-171	CD2 molecule	Homo sapiens	45-48
23981228-7	2013	Complex 1 exchanges with D2C CD2 with concomitant release of H2C CH2.	H2C	61-64	CD2 molecule	Homo sapiens	29-32
24237148-4	2013	The findings of this work show that Cd2+ and Zn2+ selectively inhibit the Mn2+-induced error-prone DNA polymerase activity in extracts of cells from human and mouse tissues.	Manganese(2+)	74-78	CD2 molecule	Homo sapiens	36-39
24237148-7	2013	Thus, we have shown that in some cases low concentrations of Cd2+ can display a positive influence on cells, whereas it is widely acknowledged that this metal is not a necessary microelement and is toxic for organisms.	Metals	153-158	CD2 molecule	Homo sapiens	61-64
23663663-0	2013	Multimeric and differential binding of CIN85/CD2AP with two atypical proline-rich sequences from CD2 and Cbl-b*.	Proline	69-76	CD2 molecule	Homo sapiens	45-48
23837645-2	2013	Three unimolecular processes are in competition with collisional deactivation of CH2FCD2Cl; HCl and DF elimination to give CHF CD2 and CH2 CDCl plus isomerization to give CH2ClCD2F by the interchange of F and Cl atoms.	Hydrochloric Acid	92-95	CD2 molecule	Homo sapiens	85-88
23837645-2	2013	Three unimolecular processes are in competition with collisional deactivation of CH2FCD2Cl; HCl and DF elimination to give CHF CD2 and CH2 CDCl plus isomerization to give CH2ClCD2F by the interchange of F and Cl atoms.	ch2 cdcl	135-143	CD2 molecule	Homo sapiens	85-88
23837645-2	2013	Three unimolecular processes are in competition with collisional deactivation of CH2FCD2Cl; HCl and DF elimination to give CHF CD2 and CH2 CDCl plus isomerization to give CH2ClCD2F by the interchange of F and Cl atoms.	ch2clcd2f	171-180	CD2 molecule	Homo sapiens	85-88
23837645-3	2013	The Cl/F interchange reaction was observed, and the rate constant was assigned from measurement of CHCl CD2 as a product, which is formed by HF elimination from CH2ClCD2F.	Fluorine	7-8	CD2 molecule	Homo sapiens	104-107
23837645-3	2013	The Cl/F interchange reaction was observed, and the rate constant was assigned from measurement of CHCl CD2 as a product, which is formed by HF elimination from CH2ClCD2F.	ch2clcd2f	161-170	CD2 molecule	Homo sapiens	104-107
23663663-2	2013	Using NMR, isothermal titration calorimetry and small-angle X-ray scattering methods, we have characterized several binding modes of the N-terminal SH3 domain (SH3A) of CD2AP and CIN85 with two natural atypical proline-rich regions in CD2 (cluster of differentiation 2) and Cbl-b (Casitas B-lineage lymphoma), and compared these data with previous studies and published crystal structures.	Proline	211-218	CD2 molecule	Homo sapiens	169-172
23400297-0	2013	Aqueous synthesis of sulfonate-functionalized 1,2,4-triazole ligands and their 2D Cd2+ coordination networks: crystal structure and photoluminescent properties.	sulfonate	21-30	CD2 molecule	Homo sapiens	82-85
23499788-5	2013	To test this hypothesis, we have synthesized three novel Cd-containing complexes: [Cd2(C12H12O2N)4(H2O)2] 2H2O (Cd1), [Cd2(C11H10O2N)4(H2O)2] 2H2O (Cd2) and [Cd(C7H4N2O2)(C8H6O2)2] 2H2O (Cd3), by using these three ligands.	Cadmium	57-59	CD2 molecule	Homo sapiens	83-86
24027999-0	2013	[Adsorption of Cd2+ ions in aqueous by diamine-modified ordered mesoporous SBA-15 particles].	Diamines	39-46	CD2 molecule	Homo sapiens	15-18
24027999-0	2013	[Adsorption of Cd2+ ions in aqueous by diamine-modified ordered mesoporous SBA-15 particles].	SBA-15	75-81	CD2 molecule	Homo sapiens	15-18
24027999-9	2013	The adsorption capacity of Cd2+ was 0.9 mmol x g(-1) which is comparable to the adsorption capacity of various adsorbents reported in the literature, and 0.1 mol x L(-1) HCl could remove nearly 93% Cd2+ from 2N-SBA-15 particles.	Hydrochloric Acid	170-173	CD2 molecule	Homo sapiens	27-30
24027999-9	2013	The adsorption capacity of Cd2+ was 0.9 mmol x g(-1) which is comparable to the adsorption capacity of various adsorbents reported in the literature, and 0.1 mol x L(-1) HCl could remove nearly 93% Cd2+ from 2N-SBA-15 particles.	Hydrochloric Acid	170-173	CD2 molecule	Homo sapiens	198-201
24027999-9	2013	The adsorption capacity of Cd2+ was 0.9 mmol x g(-1) which is comparable to the adsorption capacity of various adsorbents reported in the literature, and 0.1 mol x L(-1) HCl could remove nearly 93% Cd2+ from 2N-SBA-15 particles.	SBA-15	211-217	CD2 molecule	Homo sapiens	27-30
24027999-11	2013	The study indicated that the diamine -modified ordered mesoporous material SBA-15 is a potential sorbent which could be used for the aqueous Cd2+ removal.	Diamines	29-36	CD2 molecule	Homo sapiens	141-144
24027999-11	2013	The study indicated that the diamine -modified ordered mesoporous material SBA-15 is a potential sorbent which could be used for the aqueous Cd2+ removal.	SBA-15	75-81	CD2 molecule	Homo sapiens	141-144
23499788-5	2013	To test this hypothesis, we have synthesized three novel Cd-containing complexes: [Cd2(C12H12O2N)4(H2O)2] 2H2O (Cd1), [Cd2(C11H10O2N)4(H2O)2] 2H2O (Cd2) and [Cd(C7H4N2O2)(C8H6O2)2] 2H2O (Cd3), by using these three ligands.	Cadmium	57-59	CD2 molecule	Homo sapiens	119-122
23499788-5	2013	To test this hypothesis, we have synthesized three novel Cd-containing complexes: [Cd2(C12H12O2N)4(H2O)2] 2H2O (Cd1), [Cd2(C11H10O2N)4(H2O)2] 2H2O (Cd2) and [Cd(C7H4N2O2)(C8H6O2)2] 2H2O (Cd3), by using these three ligands.	Cadmium	57-59	CD2 molecule	Homo sapiens	119-122
23532210-0	2013	A selective turn-on fluorescent probe for Cd2+ based on a boron difluoride beta-dibenzoyl dye and its application in living cells.	boron difluoride beta-dibenzoyl dye	58-93	CD2 molecule	Homo sapiens	42-45
23400297-0	2013	Aqueous synthesis of sulfonate-functionalized 1,2,4-triazole ligands and their 2D Cd2+ coordination networks: crystal structure and photoluminescent properties.	1,2,4-triazole	46-60	CD2 molecule	Homo sapiens	82-85
23658623-3	2013	Here, we showed curcumin-mediated regulation of CD2/CD3/CD28-initiated CD4(+) T cell activation in vitro.	Curcumin	16-24	CD2 molecule	Homo sapiens	48-51
23914530-4	2013	When the original pH of water was 5.0, the concentrations of Cd2+ in samples were 19-58 times higher than the national standard limit, and when the original pH of water were 6.0, 7.0, 8.0 and 9.0, respectively, the concentrations of Cd2+ in samples varied from below to 11 times higher than the national standard limit.	Water	24-29	CD2 molecule	Homo sapiens	61-64
23914530-5	2013	The release of cadmium from the flocs was higher in the disturbed water, with the concentrations of Cd2+ in most samples higher than 5.0 microg x L(-1), and the highest was double of the national standard limit.	Cadmium	15-22	CD2 molecule	Homo sapiens	100-103
23914530-5	2013	The release of cadmium from the flocs was higher in the disturbed water, with the concentrations of Cd2+ in most samples higher than 5.0 microg x L(-1), and the highest was double of the national standard limit.	Water	66-71	CD2 molecule	Homo sapiens	100-103
23658623-5	2013	We found that curcumin suppresses CD2/CD3/CD28-initiated CD4(+) T cell activation by inhibiting cell proliferation, differentiation and cytokine production.	Curcumin	14-22	CD2 molecule	Homo sapiens	34-37
23658623-6	2013	On the other hand, curcumin attenuated the spontaneous decline of CD69 expression and indirectly increased expression of CCR7, L-selectin and Transforming growth factor-beta1 (TGF-beta1) at the late phase of CD2/CD3/CD28-initiated T cell activation.	Curcumin	19-27	CD2 molecule	Homo sapiens	208-211
23658623-9	2013	CONCLUSIONS/SIGNIFICANCE: Curcumin not merely blocks, but regulates CD2/CD3/CD28-initiated CD4(+) T cell activation by augmenting CD69, CCR7, L-selectin and TGF-beta1 expression followed by regulatory T cell generation.	Curcumin	26-34	CD2 molecule	Homo sapiens	68-71
23289094-0	2013	Thiol-ene chemistry guided preparation of thiolated polymeric nanocomposite for anodic stripping voltammetric analysis of Cd2+ and Pb2+.	2,3-Dihydrothiophene	0-9	CD2 molecule	Homo sapiens	122-125
23544576-0	2013	Branching pattern of gluco-oligosaccharides and 1.5kDa dextran grafted by the alpha-1,2 branching sucrase GBD-CD2.	gluco-oligosaccharides	21-43	CD2 molecule	Homo sapiens	110-113
23544576-0	2013	Branching pattern of gluco-oligosaccharides and 1.5kDa dextran grafted by the alpha-1,2 branching sucrase GBD-CD2.	Dextrans	55-62	CD2 molecule	Homo sapiens	110-113
23544576-1	2013	GBD-CD2, an engineered sucrose-acting enzyme of glycoside hydrolase family 70, transfers D-glucopyranosyl (D-Glcp) units from sucrose onto dextrans or gluco-oligosaccharides (GOS) through the formation of alpha-(1 2) linkages leading to branched products of interest for health, food and cosmetic applications.	Sucrose	23-30	CD2 molecule	Homo sapiens	4-7
23544576-1	2013	GBD-CD2, an engineered sucrose-acting enzyme of glycoside hydrolase family 70, transfers D-glucopyranosyl (D-Glcp) units from sucrose onto dextrans or gluco-oligosaccharides (GOS) through the formation of alpha-(1 2) linkages leading to branched products of interest for health, food and cosmetic applications.	d-glucopyranosyl	89-105	CD2 molecule	Homo sapiens	4-7
23544576-1	2013	GBD-CD2, an engineered sucrose-acting enzyme of glycoside hydrolase family 70, transfers D-glucopyranosyl (D-Glcp) units from sucrose onto dextrans or gluco-oligosaccharides (GOS) through the formation of alpha-(1 2) linkages leading to branched products of interest for health, food and cosmetic applications.	Glucose	107-113	CD2 molecule	Homo sapiens	4-7
23544576-1	2013	GBD-CD2, an engineered sucrose-acting enzyme of glycoside hydrolase family 70, transfers D-glucopyranosyl (D-Glcp) units from sucrose onto dextrans or gluco-oligosaccharides (GOS) through the formation of alpha-(1 2) linkages leading to branched products of interest for health, food and cosmetic applications.	Sucrose	126-133	CD2 molecule	Homo sapiens	4-7
23544576-1	2013	GBD-CD2, an engineered sucrose-acting enzyme of glycoside hydrolase family 70, transfers D-glucopyranosyl (D-Glcp) units from sucrose onto dextrans or gluco-oligosaccharides (GOS) through the formation of alpha-(1 2) linkages leading to branched products of interest for health, food and cosmetic applications.	Dextrans	139-147	CD2 molecule	Homo sapiens	4-7
23544576-1	2013	GBD-CD2, an engineered sucrose-acting enzyme of glycoside hydrolase family 70, transfers D-glucopyranosyl (D-Glcp) units from sucrose onto dextrans or gluco-oligosaccharides (GOS) through the formation of alpha-(1 2) linkages leading to branched products of interest for health, food and cosmetic applications.	gluco-oligosaccharides	151-173	CD2 molecule	Homo sapiens	4-7
23544576-1	2013	GBD-CD2, an engineered sucrose-acting enzyme of glycoside hydrolase family 70, transfers D-glucopyranosyl (D-Glcp) units from sucrose onto dextrans or gluco-oligosaccharides (GOS) through the formation of alpha-(1 2) linkages leading to branched products of interest for health, food and cosmetic applications.	D-Glucitol-1,6-bisphosphate	175-178	CD2 molecule	Homo sapiens	4-7
23544576-2	2013	Structural characterization of the branched products obtained from sucrose and pure GOS of degree of polymerization (DP) 4 or DP 5 revealed that highly alpha-(1 2) branched and new molecular structures can be synthesized by GBD-CD2.	Sucrose	67-74	CD2 molecule	Homo sapiens	228-231
23522108-0	2013	Fabrication and application of a new modified electrochemical sensor using nano-silica and a newly synthesized Schiff base for simultaneous determination of Cd2+, Cu2+ and Hg2+ ions in water and some foodstuff samples.	Silicon Dioxide	80-86	CD2 molecule	Homo sapiens	157-160
23522108-0	2013	Fabrication and application of a new modified electrochemical sensor using nano-silica and a newly synthesized Schiff base for simultaneous determination of Cd2+, Cu2+ and Hg2+ ions in water and some foodstuff samples.	Schiff Bases	111-122	CD2 molecule	Homo sapiens	157-160
23522108-0	2013	Fabrication and application of a new modified electrochemical sensor using nano-silica and a newly synthesized Schiff base for simultaneous determination of Cd2+, Cu2+ and Hg2+ ions in water and some foodstuff samples.	Water	185-190	CD2 molecule	Homo sapiens	157-160
23165407-0	2013	Simple naphthalimide-based fluorescent sensor for highly sensitive and selective detection of Cd2+ and Cu2+ in aqueous solution and living cells.	Naphthalimides	7-20	CD2 molecule	Homo sapiens	94-97
23457703-0	2013	A highly efficient PET switch on-off-on fluorescence receptor based on calix[4]arene for the selective recognition of Cd2+ and Sr2+.	calix(4)arene	71-84	CD2 molecule	Homo sapiens	118-121
23457703-0	2013	A highly efficient PET switch on-off-on fluorescence receptor based on calix[4]arene for the selective recognition of Cd2+ and Sr2+.	strontium cation	127-131	CD2 molecule	Homo sapiens	118-121
23359487-5	2013	In contrast, two different coordination polymers, Cd-2 and Cd-3, were obtained from mechanochemical reactions of CNacacH with Cd(OAc)(2) 2 H(2)O at M/L ratios of 1:1 and 1:2, respectively.	Polymers	40-48	CD2 molecule	Homo sapiens	50-54
23359487-5	2013	In contrast, two different coordination polymers, Cd-2 and Cd-3, were obtained from mechanochemical reactions of CNacacH with Cd(OAc)(2) 2 H(2)O at M/L ratios of 1:1 and 1:2, respectively.	cnacach	113-120	CD2 molecule	Homo sapiens	50-54
23359487-5	2013	In contrast, two different coordination polymers, Cd-2 and Cd-3, were obtained from mechanochemical reactions of CNacacH with Cd(OAc)(2) 2 H(2)O at M/L ratios of 1:1 and 1:2, respectively.	cd(oac)	126-133	CD2 molecule	Homo sapiens	50-54
23032481-0	2012	Simple pyrazoline and pyrazole "turn on" fluorescent sensors selective for Cd2+ and Zn2+ in MeCN.	pyrazoline	7-17	CD2 molecule	Homo sapiens	75-78
23646543-1	2013	CdS nanobubbles and Cd-DMS nanosheets have been prepared by a solvothermal method from a solution of Cd2+ in dimethyl sulfoxide in the absence of elemental S. A formation mechanism for the nanobubble morphology arising during the CdS nanocrystal growth has been proposed, based on the results of transmission electron microscopy and photoluminescence spectrophotometry.	Cadmium	0-3	CD2 molecule	Homo sapiens	101-104
23841333-2	2013	Among the eight possible glutathione binding sites, only two are determined as groups that interact with the Cd2+ ion.	Glutathione	25-36	CD2 molecule	Homo sapiens	109-112
23841333-3	2013	Analysis of vibrational spectra and 13C and 1H NMR spectra revealed that thiol and glutamyl"s carboxylic groups are groups that cooperate in interaction with Cd2+ ions.	13c	36-39	CD2 molecule	Homo sapiens	158-161
23841333-3	2013	Analysis of vibrational spectra and 13C and 1H NMR spectra revealed that thiol and glutamyl"s carboxylic groups are groups that cooperate in interaction with Cd2+ ions.	Hydrogen	44-46	CD2 molecule	Homo sapiens	158-161
23841333-3	2013	Analysis of vibrational spectra and 13C and 1H NMR spectra revealed that thiol and glutamyl"s carboxylic groups are groups that cooperate in interaction with Cd2+ ions.	Sulfhydryl Compounds	73-78	CD2 molecule	Homo sapiens	158-161
23841333-4	2013	The coordination of Cd2+ with those groups was supported by the application of auxiliary molecules (D-penicillamine, glycine, cysteine and glutamic acid dipeptides, mercaptosuccinic acid and N-acetyl-L-cysteine).	Penicillamine	100-115	CD2 molecule	Homo sapiens	20-23
23841333-4	2013	The coordination of Cd2+ with those groups was supported by the application of auxiliary molecules (D-penicillamine, glycine, cysteine and glutamic acid dipeptides, mercaptosuccinic acid and N-acetyl-L-cysteine).	Glycine	117-124	CD2 molecule	Homo sapiens	20-23
23841333-4	2013	The coordination of Cd2+ with those groups was supported by the application of auxiliary molecules (D-penicillamine, glycine, cysteine and glutamic acid dipeptides, mercaptosuccinic acid and N-acetyl-L-cysteine).	Cysteine	126-134	CD2 molecule	Homo sapiens	20-23
23841333-4	2013	The coordination of Cd2+ with those groups was supported by the application of auxiliary molecules (D-penicillamine, glycine, cysteine and glutamic acid dipeptides, mercaptosuccinic acid and N-acetyl-L-cysteine).	glutamic acid dipeptides	139-163	CD2 molecule	Homo sapiens	20-23
23841333-4	2013	The coordination of Cd2+ with those groups was supported by the application of auxiliary molecules (D-penicillamine, glycine, cysteine and glutamic acid dipeptides, mercaptosuccinic acid and N-acetyl-L-cysteine).	2-thiomalic acid	165-186	CD2 molecule	Homo sapiens	20-23
23841333-4	2013	The coordination of Cd2+ with those groups was supported by the application of auxiliary molecules (D-penicillamine, glycine, cysteine and glutamic acid dipeptides, mercaptosuccinic acid and N-acetyl-L-cysteine).	Acetylcysteine	191-210	CD2 molecule	Homo sapiens	20-23
23841333-6	2013	Concentration-dependent measurements of Cd2+ ions showed that the optimal stoichiometry of coordination with the glutathione molecule is 1:1.	Glutathione	113-124	CD2 molecule	Homo sapiens	40-43
23841333-7	2013	The analysis of 3J (Halpha, H(N)) coupling constants and conformational sensitive bands in the glutathione vibrational spectra suggest that interaction with Cd2+ ions significantly alters glutathione backbone conformation.	Glutathione	95-106	CD2 molecule	Homo sapiens	157-160
23841333-7	2013	The analysis of 3J (Halpha, H(N)) coupling constants and conformational sensitive bands in the glutathione vibrational spectra suggest that interaction with Cd2+ ions significantly alters glutathione backbone conformation.	Glutathione	188-199	CD2 molecule	Homo sapiens	157-160
23841340-0	2013	Theoretical model for the prediction of the stability of Co2+, Ni2+, Cu2+, Zn2+, and Cd2+ mono-complexes with monocarboxylic acids based on 3chi(v) connectivity index.	monocarboxylic acids	110-130	CD2 molecule	Homo sapiens	85-88
23841340-1	2013	The quadratic model for the prediction of stability constants of transition metal (Co2+, Ni2+, Cu2+, Zn2+, and Cd2+) complexes with four monocarboxylic amino acids (methanoic, ethanoic, propanoic, and butanoic) was developed.	monocarboxylic amino acids	137-163	CD2 molecule	Homo sapiens	111-114
23841340-1	2013	The quadratic model for the prediction of stability constants of transition metal (Co2+, Ni2+, Cu2+, Zn2+, and Cd2+) complexes with four monocarboxylic amino acids (methanoic, ethanoic, propanoic, and butanoic) was developed.	methanoic	165-174	CD2 molecule	Homo sapiens	111-114
23841340-1	2013	The quadratic model for the prediction of stability constants of transition metal (Co2+, Ni2+, Cu2+, Zn2+, and Cd2+) complexes with four monocarboxylic amino acids (methanoic, ethanoic, propanoic, and butanoic) was developed.	ethanoic	166-174	CD2 molecule	Homo sapiens	111-114
24061378-2	2012	Further, the stability constants of the 1 M2+ complexes in water-saturated nitrobenzene were calculated; they were found to increase in the series of Cu2+ < Ba2+ < Zn2+ < Ni2+ < UO22+ < Co2+ < Mn2+ < Cd2+ < Ca2+ < Pb2+.	Water	59-64	CD2 molecule	Homo sapiens	221-224
24061378-2	2012	Further, the stability constants of the 1 M2+ complexes in water-saturated nitrobenzene were calculated; they were found to increase in the series of Cu2+ < Ba2+ < Zn2+ < Ni2+ < UO22+ < Co2+ < Mn2+ < Cd2+ < Ca2+ < Pb2+.	nitrobenzene	75-87	CD2 molecule	Homo sapiens	221-224
24061378-2	2012	Further, the stability constants of the 1 M2+ complexes in water-saturated nitrobenzene were calculated; they were found to increase in the series of Cu2+ < Ba2+ < Zn2+ < Ni2+ < UO22+ < Co2+ < Mn2+ < Cd2+ < Ca2+ < Pb2+.	cupric ion	150-154	CD2 molecule	Homo sapiens	221-224
24061378-2	2012	Further, the stability constants of the 1 M2+ complexes in water-saturated nitrobenzene were calculated; they were found to increase in the series of Cu2+ < Ba2+ < Zn2+ < Ni2+ < UO22+ < Co2+ < Mn2+ < Cd2+ < Ca2+ < Pb2+.	N-methyl-valyl-amiclenomycin	160-164	CD2 molecule	Homo sapiens	221-224
24061378-2	2012	Further, the stability constants of the 1 M2+ complexes in water-saturated nitrobenzene were calculated; they were found to increase in the series of Cu2+ < Ba2+ < Zn2+ < Ni2+ < UO22+ < Co2+ < Mn2+ < Cd2+ < Ca2+ < Pb2+.	Zinc	170-174	CD2 molecule	Homo sapiens	221-224
24061378-2	2012	Further, the stability constants of the 1 M2+ complexes in water-saturated nitrobenzene were calculated; they were found to increase in the series of Cu2+ < Ba2+ < Zn2+ < Ni2+ < UO22+ < Co2+ < Mn2+ < Cd2+ < Ca2+ < Pb2+.	Nickel(2+)	180-184	CD2 molecule	Homo sapiens	221-224
24061378-2	2012	Further, the stability constants of the 1 M2+ complexes in water-saturated nitrobenzene were calculated; they were found to increase in the series of Cu2+ < Ba2+ < Zn2+ < Ni2+ < UO22+ < Co2+ < Mn2+ < Cd2+ < Ca2+ < Pb2+.	uo22+	190-195	CD2 molecule	Homo sapiens	221-224
24061378-2	2012	Further, the stability constants of the 1 M2+ complexes in water-saturated nitrobenzene were calculated; they were found to increase in the series of Cu2+ < Ba2+ < Zn2+ < Ni2+ < UO22+ < Co2+ < Mn2+ < Cd2+ < Ca2+ < Pb2+.	Cobalt(2+)	201-205	CD2 molecule	Homo sapiens	221-224
24061378-2	2012	Further, the stability constants of the 1 M2+ complexes in water-saturated nitrobenzene were calculated; they were found to increase in the series of Cu2+ < Ba2+ < Zn2+ < Ni2+ < UO22+ < Co2+ < Mn2+ < Cd2+ < Ca2+ < Pb2+.	Manganese(2+)	211-215	CD2 molecule	Homo sapiens	221-224
24061378-2	2012	Further, the stability constants of the 1 M2+ complexes in water-saturated nitrobenzene were calculated; they were found to increase in the series of Cu2+ < Ba2+ < Zn2+ < Ni2+ < UO22+ < Co2+ < Mn2+ < Cd2+ < Ca2+ < Pb2+.	Lead	241-245	CD2 molecule	Homo sapiens	221-224
22973059-5	2012	In the absence of other permeant ions (Ca2+ and Na+ replaced by N-methyl-d-glucamine), Cd2+ carried sizable inward currents through Ca(v)3.1 channels (210 +- 20 pA at -60 mV with 2 mM Cd2+).	Meglumine	64-84	CD2 molecule	Homo sapiens	87-90
23646543-1	2013	CdS nanobubbles and Cd-DMS nanosheets have been prepared by a solvothermal method from a solution of Cd2+ in dimethyl sulfoxide in the absence of elemental S. A formation mechanism for the nanobubble morphology arising during the CdS nanocrystal growth has been proposed, based on the results of transmission electron microscopy and photoluminescence spectrophotometry.	Dimethyl Sulfoxide	109-127	CD2 molecule	Homo sapiens	101-104
23140570-1	2012	Hybrid dendritic-linear block copolymers based on a 4-arm poly(ethylene glycol) (PEG) core were synthesized using an accelerated AB2/CD2 dendritic growth approach through orthogonal amine/epoxy and thiol-yne chemistries.	copolymers	30-40	CD2 molecule	Homo sapiens	133-136
23140570-1	2012	Hybrid dendritic-linear block copolymers based on a 4-arm poly(ethylene glycol) (PEG) core were synthesized using an accelerated AB2/CD2 dendritic growth approach through orthogonal amine/epoxy and thiol-yne chemistries.	Polyethylene Glycols	81-84	CD2 molecule	Homo sapiens	133-136
23032481-0	2012	Simple pyrazoline and pyrazole "turn on" fluorescent sensors selective for Cd2+ and Zn2+ in MeCN.	pyrazole	22-30	CD2 molecule	Homo sapiens	75-78
23032481-0	2012	Simple pyrazoline and pyrazole "turn on" fluorescent sensors selective for Cd2+ and Zn2+ in MeCN.	acetonitrile	92-96	CD2 molecule	Homo sapiens	75-78
23233994-1	2012	The role of layered double hydroxide (LDH) in the protection of herring testis DNA from heavy metals Cd2+ and Pb2+ was studied by X-ray diffraction ( XRD) spectra, Fourier transform infrared (FTIR) spectra, Scanning Electron Microscopy (SEM), Cyclic Voltammetry and Ultraviolet Spectrometry.	hydroxide ion	27-36	CD2 molecule	Homo sapiens	101-104
23233994-9	2012	The results showed that, on the one hand, both Cd2+ and Pb2+ were absorbed on the external surface of LDH for immobilization, on the other hand, the layer of LDH provided ideal space for DNA by the action of protecting DNA molecules from Cd2+ and Pb2+.	Lead	56-60	CD2 molecule	Homo sapiens	238-241
23233994-9	2012	The results showed that, on the one hand, both Cd2+ and Pb2+ were absorbed on the external surface of LDH for immobilization, on the other hand, the layer of LDH provided ideal space for DNA by the action of protecting DNA molecules from Cd2+ and Pb2+.	Lead	247-251	CD2 molecule	Homo sapiens	47-50
22946557-0	2012	Exploring the molecular mechanism of stabilization of the adhesion domains of human CD2 by N-glycosylation.	Nitrogen	91-92	CD2 molecule	Homo sapiens	84-87
22946557-8	2012	and indicates that enthalpy and entropy may both contribute to the stabilization of human CD2 by N-glycosylation.	Nitrogen	97-98	CD2 molecule	Homo sapiens	90-93
22934785-0	2012	Cd2+ complexation with P(CH2OH)3, OP(CH2OH)3, and (HOCH2)2PO2(-): coordination in solution and coordination polymers.	(hoch2)2po2	50-61	CD2 molecule	Homo sapiens	0-3
22934785-0	2012	Cd2+ complexation with P(CH2OH)3, OP(CH2OH)3, and (HOCH2)2PO2(-): coordination in solution and coordination polymers.	Polymers	108-116	CD2 molecule	Homo sapiens	0-3
23035480-3	2012	The molar ratio of TGA/Cd2+ in solutions and the concentration of starting materials play important roles in creating the NCs with a large size for long PL peak wavelength and decreased surface defects for a target of a high PLQY.	2-mercaptoacetate	19-22	CD2 molecule	Homo sapiens	23-26
22771214-4	2012	External Cd2+ enhances the rate of C-type inactivation in an cysteine mutant (Y82C) via metal-bridge formation.	Cysteine	61-69	CD2 molecule	Homo sapiens	9-12
23120985-2	2012	It was established that Fe3+ in a form of free ion at concentration of 30 mg/l also stimulates both the reduction of chlorate by A. thermotoleranticus C-1 and the growth of biomass, Cd2+ Pb2+ and Mn2+ do not practically affect the process velocity or stimulate it a little, Cu2+ and Zn2+ lower the reduction rate of C10(3)- 2.5-3 times, under these conditions the biomass growth is inhibited more weakly than the reduction rate.	ferric sulfate	24-28	CD2 molecule	Homo sapiens	182-185
22834792-0	2012	Cd2+ complex of a triazole-based calix[4]arene conjugate as a selective fluorescent chemosensor for Cys.	Triazoles	18-26	CD2 molecule	Homo sapiens	0-3
22834792-0	2012	Cd2+ complex of a triazole-based calix[4]arene conjugate as a selective fluorescent chemosensor for Cys.	calix(4)arene	33-46	CD2 molecule	Homo sapiens	0-3
22834792-0	2012	Cd2+ complex of a triazole-based calix[4]arene conjugate as a selective fluorescent chemosensor for Cys.	Cysteine	100-103	CD2 molecule	Homo sapiens	0-3
22619211-0	2012	A mild one-step process from graphene oxide and Cd2+ to a graphene-CdSe quantum dot nanocomposite with enhanced photoelectric properties.	cdse	67-71	CD2 molecule	Homo sapiens	48-51
22771214-4	2012	External Cd2+ enhances the rate of C-type inactivation in an cysteine mutant (Y82C) via metal-bridge formation.	Metals	88-93	CD2 molecule	Homo sapiens	9-12
22771214-6	2012	Tandem dimer and tandem tetramer constructs of equivalent cysteine mutants in KcsA and Shaker K+ channels demonstrate that these Cd2+ metal bridges are formed only between adjacent subunits.	Cysteine	58-66	CD2 molecule	Homo sapiens	129-132
22613180-10	2012	The findings extend the evidence suggesting a link between As3+ and Cd2+ exposure and neuroendocrine differentiation in tumors.	as3+	59-63	CD2 molecule	Homo sapiens	68-71
22674831-0	2012	Multiparametric assessment of Cd2+ cytotoxicity using MTT-based microfluidic image cytometry.	monooxyethylene trimethylolpropane tristearate	54-57	CD2 molecule	Homo sapiens	30-33
23343930-5	2012	The biodegradable PEG polymer coating could protect QDs from being exposed to the intracellular environment and restrained the release of toxic Cd2(+).	peg polymer	18-29	CD2 molecule	Homo sapiens	144-147
22634534-13	2012	Larger and further studies are required to validate CD2 as a marker of cisplatin resistance.	Cisplatin	71-80	CD2 molecule	Homo sapiens	52-55
22802697-4	2012	Adding hydrocortisone (HDC) and stromal cells greatly increases the frequency of c-kit(+) BM cells that give rise to CD2(+)CD8(+) NK cells.	Hydrocortisone	7-21	CD2 molecule	Homo sapiens	117-120
22499396-0	2012	A novel quinoline-based two-photon fluorescent probe for detecting Cd2+ in vitro and in vivo.	quinoline	8-17	CD2 molecule	Homo sapiens	67-70
22529353-0	2012	Histidine pairing at the metal transport site of mammalian ZnT transporters controls Zn2+ over Cd2+ selectivity.	Histidine	0-9	CD2 molecule	Homo sapiens	95-98
22529353-0	2012	Histidine pairing at the metal transport site of mammalian ZnT transporters controls Zn2+ over Cd2+ selectivity.	Metals	25-30	CD2 molecule	Homo sapiens	95-98
22529353-0	2012	Histidine pairing at the metal transport site of mammalian ZnT transporters controls Zn2+ over Cd2+ selectivity.	Zinc	85-89	CD2 molecule	Homo sapiens	95-98
22262856-2	2012	It was constructed by rational truncation of GBD-CD2, which harbors the second catalytic domain of DSR-E. Like GBD-CD2, this variant displays alpha-(1 2) branching activity when incubated with sucrose as glucosyl donor and (oligo-)dextran as acceptor, transferring glucosyl residues to the acceptor via a ping-pong bi-bi mechanism.	Sucrose	193-200	CD2 molecule	Homo sapiens	49-52
22262856-7	2012	Subsite +1 analysis revealed three residues (Ala-2249, Gly-2250, and Phe-2214) that are specific to DeltaN(123)-GBD-CD2.	Glycine	55-58	CD2 molecule	Homo sapiens	116-119
22428526-0	2012	Adsorption of Cd2+ on carboxyl-terminated superparamagnetic iron oxide nanoparticles.	carboxyl	22-30	CD2 molecule	Homo sapiens	14-17
22428526-0	2012	Adsorption of Cd2+ on carboxyl-terminated superparamagnetic iron oxide nanoparticles.	ferric oxide	60-70	CD2 molecule	Homo sapiens	14-17
22262856-2	2012	It was constructed by rational truncation of GBD-CD2, which harbors the second catalytic domain of DSR-E. Like GBD-CD2, this variant displays alpha-(1 2) branching activity when incubated with sucrose as glucosyl donor and (oligo-)dextran as acceptor, transferring glucosyl residues to the acceptor via a ping-pong bi-bi mechanism.	Sucrose	193-200	CD2 molecule	Homo sapiens	115-118
22262856-7	2012	Subsite +1 analysis revealed three residues (Ala-2249, Gly-2250, and Phe-2214) that are specific to DeltaN(123)-GBD-CD2.	Phenylalanine	69-72	CD2 molecule	Homo sapiens	116-119
22262856-2	2012	It was constructed by rational truncation of GBD-CD2, which harbors the second catalytic domain of DSR-E. Like GBD-CD2, this variant displays alpha-(1 2) branching activity when incubated with sucrose as glucosyl donor and (oligo-)dextran as acceptor, transferring glucosyl residues to the acceptor via a ping-pong bi-bi mechanism.	(oligo-)dextran	223-238	CD2 molecule	Homo sapiens	49-52
22262856-2	2012	It was constructed by rational truncation of GBD-CD2, which harbors the second catalytic domain of DSR-E. Like GBD-CD2, this variant displays alpha-(1 2) branching activity when incubated with sucrose as glucosyl donor and (oligo-)dextran as acceptor, transferring glucosyl residues to the acceptor via a ping-pong bi-bi mechanism.	(oligo-)dextran	223-238	CD2 molecule	Homo sapiens	115-118
22262856-6	2012	Residues forming subsite -1, involved in binding the glucosyl residue of sucrose and catalysis, are strictly conserved in both GTF180-DeltaN and DeltaN(123)-GBD-CD2.	Sucrose	73-80	CD2 molecule	Homo sapiens	161-164
22262856-7	2012	Subsite +1 analysis revealed three residues (Ala-2249, Gly-2250, and Phe-2214) that are specific to DeltaN(123)-GBD-CD2.	Alanine	45-48	CD2 molecule	Homo sapiens	116-119
24371564-3	2012	The identified CD2f isoforms of the ginbuna carp (caauCD2f) exhibited high sequence similarity to the mammalian CD2 subsets CD48, CD244, and CD319, but it was difficult to classify them into their respective mammalian CD2f based on sequence similarity, the presence of an immunoreceptor tyrosine-based switch motif (ITSM), and phylogenetic tree analysis.	Tyrosine	287-295	CD2 molecule	Homo sapiens	15-18
22047918-0	2012	Removal of Cd2+ from contaminated water by nano-sized aragonite mollusk shell and the competition of coexisting metal ions.	Water	34-39	CD2 molecule	Homo sapiens	11-14
22047918-0	2012	Removal of Cd2+ from contaminated water by nano-sized aragonite mollusk shell and the competition of coexisting metal ions.	Metals	112-117	CD2 molecule	Homo sapiens	11-14
22295784-1	2011	The photoluminescence property of CdS/PAMAM nanocomposites in water at different ratio of Cd2+ to PAMAM(r) was studied by fluorescence emission spectrum, and the according mechanism was explored.	Cadmium	34-37	CD2 molecule	Homo sapiens	90-93
21967556-1	2012	Identification of Hb A2-Melbourne [delta43(CD2)Glu Lys] in Thai individuals.	Lysine	51-54	CD2 molecule	Homo sapiens	43-46
22295784-1	2011	The photoluminescence property of CdS/PAMAM nanocomposites in water at different ratio of Cd2+ to PAMAM(r) was studied by fluorescence emission spectrum, and the according mechanism was explored.	pamam	38-43	CD2 molecule	Homo sapiens	90-93
22295784-1	2011	The photoluminescence property of CdS/PAMAM nanocomposites in water at different ratio of Cd2+ to PAMAM(r) was studied by fluorescence emission spectrum, and the according mechanism was explored.	Water	62-67	CD2 molecule	Homo sapiens	90-93
22295784-4	2011	The strength of the frontier fluorescence emission peak became weaker and weaker, and at last disappeared with the enhancement of the ratio of Cd2+ to PAMAM; the strength of the latter fluorescence emission peak became stronger, which indicates that the electron at valence band of N atom in amines of dendrimers was transferred to CdS QDs.	pamam	151-156	CD2 molecule	Homo sapiens	143-146
22295784-4	2011	The strength of the frontier fluorescence emission peak became weaker and weaker, and at last disappeared with the enhancement of the ratio of Cd2+ to PAMAM; the strength of the latter fluorescence emission peak became stronger, which indicates that the electron at valence band of N atom in amines of dendrimers was transferred to CdS QDs.	Nitrogen	282-283	CD2 molecule	Homo sapiens	143-146
22295784-4	2011	The strength of the frontier fluorescence emission peak became weaker and weaker, and at last disappeared with the enhancement of the ratio of Cd2+ to PAMAM; the strength of the latter fluorescence emission peak became stronger, which indicates that the electron at valence band of N atom in amines of dendrimers was transferred to CdS QDs.	Amines	292-298	CD2 molecule	Homo sapiens	143-146
22295784-4	2011	The strength of the frontier fluorescence emission peak became weaker and weaker, and at last disappeared with the enhancement of the ratio of Cd2+ to PAMAM; the strength of the latter fluorescence emission peak became stronger, which indicates that the electron at valence band of N atom in amines of dendrimers was transferred to CdS QDs.	Cadmium	332-335	CD2 molecule	Homo sapiens	143-146
22164125-5	2011	In samples containing ruminant fat (butter and various confectioneries), vaccenic acid (t11-C18:1, t11) predominated, while in foods containing industrially hydrogenated fats, elaidic acid (trans-9, t9-) and t10-C18:1 were the major trans isomers..	11-octadecenoic acid	73-86	CD2 molecule	Homo sapiens	88-91
21683516-3	2011	Resveratrol inhibited growth and induced cellular differentiation, as demonstrated by morphological changes and elevated expression of T cell differentiation markers CD2, CD3, and CD8.	Resveratrol	0-11	CD2 molecule	Homo sapiens	166-169
22164125-5	2011	In samples containing ruminant fat (butter and various confectioneries), vaccenic acid (t11-C18:1, t11) predominated, while in foods containing industrially hydrogenated fats, elaidic acid (trans-9, t9-) and t10-C18:1 were the major trans isomers..	11-octadecenoic acid	73-86	CD2 molecule	Homo sapiens	99-102
22164125-8	2011	The t9/t11 index could be used as an indicator to determine ruminant fat.Practical applications: A number of studies provide evidence that a high TFA intake, particularly of industrial origin, adversely affects human health.	Trans Fatty Acids	146-149	CD2 molecule	Homo sapiens	7-10
22164125-15	2011	Therefore, the t9/t11 index imparts important information on the source of TFA in processed foods.	Trans Fatty Acids	75-78	CD2 molecule	Homo sapiens	18-21
24062116-0	2011	Flow Injection Potentiometric Determination of Cd2+ Ions Using a Coated Graphite Plasticized PVC-Membrane Electrode Based on 1, 3-Bis(2-cyanobenzene)triazene.	Graphite	72-80	CD2 molecule	Homo sapiens	47-50
24062116-0	2011	Flow Injection Potentiometric Determination of Cd2+ Ions Using a Coated Graphite Plasticized PVC-Membrane Electrode Based on 1, 3-Bis(2-cyanobenzene)triazene.	1, 3-bis(2-cyanobenzene)triazene	125-157	CD2 molecule	Homo sapiens	47-50
24062116-1	2011	1, 3-Bis(2-cyanobenzene)triazene, L, was used as a suitable ionophore for the fabrication of a new PVC-based polymeric membrane coated graphite electrode for selective sensing of Cd2+ ion.	1, 3-bis(2-cyanobenzene)triazene	0-32	CD2 molecule	Homo sapiens	179-182
24062116-1	2011	1, 3-Bis(2-cyanobenzene)triazene, L, was used as a suitable ionophore for the fabrication of a new PVC-based polymeric membrane coated graphite electrode for selective sensing of Cd2+ ion.	Graphite	135-143	CD2 molecule	Homo sapiens	179-182
24062116-2	2011	The electrode exhibited a selective linear Nernstian response to Cd2+ ion at an optimal pH range of 6-9 with a limit of detection of 8.0 x 10-6 M and a fast response time of about 2 s. The electrode was used as a proper detection system in flow-injection potentiometry of cadmium ion and resulted in well defined peaks for cadmium ions with stable baseline, excellent reproducibility and high sampling rates of over 100 injections per hour.	Cadmium	272-279	CD2 molecule	Homo sapiens	65-68
24062116-2	2011	The electrode exhibited a selective linear Nernstian response to Cd2+ ion at an optimal pH range of 6-9 with a limit of detection of 8.0 x 10-6 M and a fast response time of about 2 s. The electrode was used as a proper detection system in flow-injection potentiometry of cadmium ion and resulted in well defined peaks for cadmium ions with stable baseline, excellent reproducibility and high sampling rates of over 100 injections per hour.	Cadmium	323-330	CD2 molecule	Homo sapiens	65-68
21504230-12	2011	The enzymes mainly expressed in the liver and gastrointestinal tract, GSTA1-1, T1-1, and M1-1, seemed to be mainly involved in the MC-LR detoxification after oral exposure, whereas P1-1 kinetics and location in the skin suggest a role related to dermal exposure.	Lawrencium	134-136	CD2 molecule	Homo sapiens	79-83
20546866-5	2011	The four other antibodies tested (anti-CD2, CD4, CD8 and CD21) were compatible with zinc salts-based fixation and cryopreservation.	zinc salts	84-94	CD2 molecule	Homo sapiens	39-42
21293259-6	2011	In addition, CD14, CD2, and CD56 detections on MCs showed greater sensitivity by FCA than by IHCA.	mcs	47-50	CD2 molecule	Homo sapiens	19-22
21623697-6	2011	This study examines the effects of exposures to concentrations of TBBPA (i.e., that were able to decrease the binding capacity of NK cells) on the expression of cell-surface proteins (CD2, CD11a, CD16, CD18, and CD56) that are needed for NK cells to bind target cells.	tetrabromobisphenol A	66-71	CD2 molecule	Homo sapiens	184-187
21504230-9	2011	In the present work, the MC-LR conjugation with GSH catalyzed by five recombinant human GSTs (A1-1, A3-3, M1-1, P1-1, and T1-1) has been characterized for the first time.	cyanoginosin LR	25-30	CD2 molecule	Homo sapiens	122-126
21396912-3	2011	One of four endogenous cysteines facing the cytoplasm contributes to a high-affinity site for inhibition by internal Cd2(+).	Cysteine	23-32	CD2 molecule	Homo sapiens	117-120
21504230-9	2011	In the present work, the MC-LR conjugation with GSH catalyzed by five recombinant human GSTs (A1-1, A3-3, M1-1, P1-1, and T1-1) has been characterized for the first time.	Glutathione	48-51	CD2 molecule	Homo sapiens	122-126
21504230-12	2011	The enzymes mainly expressed in the liver and gastrointestinal tract, GSTA1-1, T1-1, and M1-1, seemed to be mainly involved in the MC-LR detoxification after oral exposure, whereas P1-1 kinetics and location in the skin suggest a role related to dermal exposure.	Microcystins	131-133	CD2 molecule	Homo sapiens	79-83
21711888-4	2011	We proposed that the strong binding between Cd2+ and halide ions reduced the reactivity of the precursors, decreased the nuclei formed in the nucleation stage, and led to the high concentration of precursor in the growth stage, resulting in the increase of size and phase transformation of CdS nanocrystals.	halide	53-59	CD2 molecule	Homo sapiens	44-47
21396912-5	2011	This mode of action causes the tethering of the N-terminus to CD loop in the stimulus-sensing domain, suggesting that their conformational changes participate in gating and Cd2(+) inhibits Kir3.2 by trapping the conformation in the closed state like "inverse agonist".	Cadmium	62-64	CD2 molecule	Homo sapiens	173-176
20843600-0	2010	Ageing and structural effects on the sorption characteristics of Cd2+ by clinoptilolite and Y-type zeolite studied using isotope exchange technique.	clinoptilolite	73-87	CD2 molecule	Homo sapiens	65-68
20833258-1	2011	The CD48 molecule is a glycosyl-phosphatidyl-inositol (GPI)-anchored cell-surface protein of the CD2 family of molecules.	Glycosylphosphatidylinositols	23-53	CD2 molecule	Homo sapiens	97-100
20833258-1	2011	The CD48 molecule is a glycosyl-phosphatidyl-inositol (GPI)-anchored cell-surface protein of the CD2 family of molecules.	Glycosylphosphatidylinositols	55-58	CD2 molecule	Homo sapiens	97-100
21421124-0	2011	Probing the coordination behavior of Hg2+, CH3Hg+, and Cd2+ towards mixtures of two biological thiols by HPLC-ICP-AES.	Sulfhydryl Compounds	95-101	CD2 molecule	Homo sapiens	55-58
21790050-3	2011	The effects of pH, chelating agent dosage, and other heavy metal ions on the performance of PBD in Cd2+ removal from water are investigated.	Water	117-122	CD2 molecule	Homo sapiens	99-102
21790050-9	2011	If Cd2+ co-exists with Pb2+ and Cu2+, the affinity of the chelating agent with these three heavy metal ions was in the order of: Cu2+ > Pb2+ > Cd2+.	Lead	23-27	CD2 molecule	Homo sapiens	3-6
21790050-9	2011	If Cd2+ co-exists with Pb2+ and Cu2+, the affinity of the chelating agent with these three heavy metal ions was in the order of: Cu2+ > Pb2+ > Cd2+.	Lead	23-27	CD2 molecule	Homo sapiens	149-152
21790050-9	2011	If Cd2+ co-exists with Pb2+ and Cu2+, the affinity of the chelating agent with these three heavy metal ions was in the order of: Cu2+ > Pb2+ > Cd2+.	cupric ion	32-36	CD2 molecule	Homo sapiens	3-6
21790050-9	2011	If Cd2+ co-exists with Pb2+ and Cu2+, the affinity of the chelating agent with these three heavy metal ions was in the order of: Cu2+ > Pb2+ > Cd2+.	cupric ion	32-36	CD2 molecule	Homo sapiens	149-152
21790050-9	2011	If Cd2+ co-exists with Pb2+ and Cu2+, the affinity of the chelating agent with these three heavy metal ions was in the order of: Cu2+ > Pb2+ > Cd2+.	Metals	97-102	CD2 molecule	Homo sapiens	3-6
21790050-9	2011	If Cd2+ co-exists with Pb2+ and Cu2+, the affinity of the chelating agent with these three heavy metal ions was in the order of: Cu2+ > Pb2+ > Cd2+.	Metals	97-102	CD2 molecule	Homo sapiens	149-152
21790050-9	2011	If Cd2+ co-exists with Pb2+ and Cu2+, the affinity of the chelating agent with these three heavy metal ions was in the order of: Cu2+ > Pb2+ > Cd2+.	cupric ion	129-133	CD2 molecule	Homo sapiens	3-6
21790050-9	2011	If Cd2+ co-exists with Pb2+ and Cu2+, the affinity of the chelating agent with these three heavy metal ions was in the order of: Cu2+ > Pb2+ > Cd2+.	Lead	139-143	CD2 molecule	Homo sapiens	3-6
20813844-5	2010	IL-2-activated NK cells cultured in the absence of 2B4/CD48 or CD2/CD58 interactions were severely impaired for their ability to induce intracellular calcium mobilization and subsequent ERK activation upon tumor target exposure, suggesting that the early signaling pathway of NK receptors leading to impaired cytolysis and interferon (IFN)-gamma secretion was inhibited.	Calcium	150-157	CD2 molecule	Homo sapiens	63-66
20849150-8	2010	Polymorphic hGST T1-1 did not show any activity in catalyzing GSH conjugation of reactive clozapine metabolites.	Clozapine	90-99	CD2 molecule	Homo sapiens	17-21
20849150-4	2010	In the present study, we studied the ability of four recombinant human GSTs (hGST A1-1, hGST M1-1, hGST P1-1, and hGST T1-1) to catalyze the GSH conjugation of reactive metabolites of clozapine, formed in vitro by human and rat liver microsomes and drug-metabolizing P450 BM3 mutant, P450 102A1M11H.	Glutathione	141-144	CD2 molecule	Homo sapiens	119-123
20189851-0	2010	First detection of Hb Hornchurch (beta43(CD2) Glu-Lys) in a Chinese.	Lysine	50-53	CD2 molecule	Homo sapiens	41-44
20825031-2	2010	The performance of the MFC-type biotoxicity detector was evaluated with the synthetic water containing heavy metals of Cd2+ and Cu2+.	Water	86-91	CD2 molecule	Homo sapiens	119-122
20455852-2	2010	However, this signaling pathway also plays a role in normal adult tissues and in carcinogenesis, including cadmium (Cd2+) induced nephrocarcinogenesis, which is the topic of this review.	Cadmium	107-114	CD2 molecule	Homo sapiens	116-119
20455852-7	2010	The nephrotoxic metal Cd2+ causes renal cancer in humans.	Metals	16-21	CD2 molecule	Homo sapiens	22-25
19854665-0	2010	First principle study towards the influence of Cd2+ on the morphology of sodium chloride.	Sodium Chloride	73-88	CD2 molecule	Homo sapiens	47-50
20545173-4	2010	The experimental results showed that under the optimal adsorption conditions, the pH of adsorbate solution was 5-6, static adsorption time was 1.5-2 h, and adsorption procedure was carried out at room temperature, polyacrylonitrile as adsorbent has high adsorption capacity (mg x g(-1)) for Cu2+, Pb2+, Cd2+ and Zn2+, which can reach 26.6, 45.2, 39.7 and 32.5 separately.	polyacrylonitrile	214-231	CD2 molecule	Homo sapiens	303-306
19453575-5	2010	This study was designed to utilize flow cytometric immunophenotyping to characterize effects of regular blood transfusion, and high serum ferritin levels because of irregular use of iron chelation therapy on T lymphocytes (CD2, CD3, CD4 and CD8), B lymphocytes (CD19) and natural killer cells (CD56) and zinc levels in the blood of patients with thalassemia major (n = 49) and healthy normal controls (n = 60) in Kuwait.	Iron	182-186	CD2 molecule	Homo sapiens	223-226
19841038-7	2010	These results indicate that while the ILT2/HLA-G interaction leads to the inhibition of NK-cell functions, it displays differential effects on cytoskeleton reorganization and CD2 localization at the NK-cell synapse.-Favier, B., LeMaoult, J., Lesport, E., Carosella, E. D. ILT2/HLA-G interaction impairs NK-cell functions through the inhibition of the late but not the early events of the NK-cell-activating synapse.	carosella	255-264	CD2 molecule	Homo sapiens	175-178
20051780-7	2010	Bisulfite sequencing of CD10 type 1 and 2 promoters showed that more than 84% of the cytosine-phosphate-guanine (CpG) dinucleotides identified were methylated in all 3 CD10-negative infant ALL samples with MLL/AF4.	hydrogen sulfite	0-9	CD2 molecule	Homo sapiens	24-41
20051780-7	2010	Bisulfite sequencing of CD10 type 1 and 2 promoters showed that more than 84% of the cytosine-phosphate-guanine (CpG) dinucleotides identified were methylated in all 3 CD10-negative infant ALL samples with MLL/AF4.	cytosine-phosphate-guanine (cpg) dinucleotides	85-131	CD2 molecule	Homo sapiens	24-41
19640638-0	2009	Novel PVC-membrane potentiometric sensors based on a recently synthesized sulfur-containing macrocyclic diamide for Cd2+ ion.	Sulfur	74-80	CD2 molecule	Homo sapiens	116-119
21462709-9	2010	Adversely, the removal of ANT was decreased with Cd2+ under the addition of EDCD, this was due to the fact that Cd2+ enhanced the polarity of EDCD molecule and inhibited the complexation between ANT and EDCD.	anthracene	26-29	CD2 molecule	Homo sapiens	49-52
21462709-9	2010	Adversely, the removal of ANT was decreased with Cd2+ under the addition of EDCD, this was due to the fact that Cd2+ enhanced the polarity of EDCD molecule and inhibited the complexation between ANT and EDCD.	anthracene	26-29	CD2 molecule	Homo sapiens	112-115
21462709-9	2010	Adversely, the removal of ANT was decreased with Cd2+ under the addition of EDCD, this was due to the fact that Cd2+ enhanced the polarity of EDCD molecule and inhibited the complexation between ANT and EDCD.	ethylene-diamine-beta-cyclodextrin	76-80	CD2 molecule	Homo sapiens	49-52
21462709-9	2010	Adversely, the removal of ANT was decreased with Cd2+ under the addition of EDCD, this was due to the fact that Cd2+ enhanced the polarity of EDCD molecule and inhibited the complexation between ANT and EDCD.	ethylene-diamine-beta-cyclodextrin	76-80	CD2 molecule	Homo sapiens	112-115
21462709-9	2010	Adversely, the removal of ANT was decreased with Cd2+ under the addition of EDCD, this was due to the fact that Cd2+ enhanced the polarity of EDCD molecule and inhibited the complexation between ANT and EDCD.	ethylene-diamine-beta-cyclodextrin	142-146	CD2 molecule	Homo sapiens	49-52
21462709-9	2010	Adversely, the removal of ANT was decreased with Cd2+ under the addition of EDCD, this was due to the fact that Cd2+ enhanced the polarity of EDCD molecule and inhibited the complexation between ANT and EDCD.	ethylene-diamine-beta-cyclodextrin	142-146	CD2 molecule	Homo sapiens	112-115
21462709-9	2010	Adversely, the removal of ANT was decreased with Cd2+ under the addition of EDCD, this was due to the fact that Cd2+ enhanced the polarity of EDCD molecule and inhibited the complexation between ANT and EDCD.	anthracene	195-198	CD2 molecule	Homo sapiens	49-52
21462709-9	2010	Adversely, the removal of ANT was decreased with Cd2+ under the addition of EDCD, this was due to the fact that Cd2+ enhanced the polarity of EDCD molecule and inhibited the complexation between ANT and EDCD.	anthracene	195-198	CD2 molecule	Homo sapiens	112-115
21462709-9	2010	Adversely, the removal of ANT was decreased with Cd2+ under the addition of EDCD, this was due to the fact that Cd2+ enhanced the polarity of EDCD molecule and inhibited the complexation between ANT and EDCD.	ethylene-diamine-beta-cyclodextrin	142-146	CD2 molecule	Homo sapiens	49-52
21462709-9	2010	Adversely, the removal of ANT was decreased with Cd2+ under the addition of EDCD, this was due to the fact that Cd2+ enhanced the polarity of EDCD molecule and inhibited the complexation between ANT and EDCD.	ethylene-diamine-beta-cyclodextrin	142-146	CD2 molecule	Homo sapiens	112-115
21462709-2	2010	The results showed that GluCD and EDCD were powerful complexant for ANT and Cd2+.	glutamic acid-beta-cyclodextrin	24-29	CD2 molecule	Homo sapiens	76-79
21462709-2	2010	The results showed that GluCD and EDCD were powerful complexant for ANT and Cd2+.	ethylene-diamine-beta-cyclodextrin	34-38	CD2 molecule	Homo sapiens	76-79
21462709-4	2010	GluCD resulted in approximately 90% complexation of Cd2+ while 70% complexation was observed for EDCD.	glutamic acid-beta-cyclodextrin	0-5	CD2 molecule	Homo sapiens	52-55
21462709-5	2010	Simultaneously, GluCD and EDCD could greatly enhance the elution removal of ANT and Cd2+ from soil.	glutamic acid-beta-cyclodextrin	16-21	CD2 molecule	Homo sapiens	84-87
21462709-5	2010	Simultaneously, GluCD and EDCD could greatly enhance the elution removal of ANT and Cd2+ from soil.	ethylene-diamine-beta-cyclodextrin	26-30	CD2 molecule	Homo sapiens	84-87
21462709-6	2010	GluCD resulted in the highest elution efficiency of ANT and Cd2+.	glutamic acid-beta-cyclodextrin	0-5	CD2 molecule	Homo sapiens	60-63
21462709-7	2010	With the addition of 10 g/L GluCD, 53.5% of ANT and 85.6% of Cd2+ were eluted, respectively.	glutamic acid-beta-cyclodextrin	28-33	CD2 molecule	Homo sapiens	61-64
19640638-0	2009	Novel PVC-membrane potentiometric sensors based on a recently synthesized sulfur-containing macrocyclic diamide for Cd2+ ion.	Diamide	104-111	CD2 molecule	Homo sapiens	116-119
19635351-0	2009	Sodium polyacrylate as a binding agent in diffusive gradients in thin-films technique for the measurement of Cu2+ and Cd2+ in waters.	carbopol 940	0-19	CD2 molecule	Homo sapiens	118-121
21099036-1	2010	A highly electroactive material [Mo2(OAc)2(H2-calix[4]arene)] is used as a neutral carrier for Cd2+ ions in this paper.	mo2(oac)2	33-42	CD2 molecule	Homo sapiens	95-98
21099036-1	2010	A highly electroactive material [Mo2(OAc)2(H2-calix[4]arene)] is used as a neutral carrier for Cd2+ ions in this paper.	h2-calix[4]arene)	43-60	CD2 molecule	Homo sapiens	95-98
21099036-5	2010	Electrode sensor has distinguishable ability for Cd2+ ion with regard to several alkali, alkaline earth, transition and heavy metal ions.	Metals	126-131	CD2 molecule	Homo sapiens	49-52
21099036-6	2010	It was used in direct potentiometry as an indicator electrode, in the potentiometric titration of 10-3 M Cd2+ solution against 10-2 M of ethylenediaminetetraacetic acid (EDTA).	Edetic Acid	137-168	CD2 molecule	Homo sapiens	105-108
21099036-6	2010	It was used in direct potentiometry as an indicator electrode, in the potentiometric titration of 10-3 M Cd2+ solution against 10-2 M of ethylenediaminetetraacetic acid (EDTA).	Edetic Acid	170-174	CD2 molecule	Homo sapiens	105-108
19664997-1	2009	We have previously expressed hexa-histidine-tagged human glutathione transferase GST T1-1 at very high levels in an Escherichia colilacZ mutagenicity assay strain.	His-His-His-His-His-His	29-43	CD2 molecule	Homo sapiens	85-89
20088201-6	2009	The anaerobic incubation of the raw material led to an increase in adsorption capacities towards metal ions, which were multiplied by around 2.0 for Zn2+ and 2.3 for Cd2+.	Metals	97-102	CD2 molecule	Homo sapiens	166-169
19968107-3	2009	The results show that single heavy metal biological toxicity is in the order: Hg2+ > Cu2+ > Cd2+ > As5+ > Pb2+ > Cr6+; Two, three and four heavy metal mixture experiments show synergism primarily, antagonism is in minority.	Metals	35-40	CD2 molecule	Homo sapiens	98-101
19968111-3	2009	Results indicated that the adsorption rate of heavy metal ions on the EAF slag was relatively high, and the sorption rate followed the order Cd2+ > Pb2+ > Cu2+.	Metals	52-57	CD2 molecule	Homo sapiens	141-144
19968111-3	2009	Results indicated that the adsorption rate of heavy metal ions on the EAF slag was relatively high, and the sorption rate followed the order Cd2+ > Pb2+ > Cu2+.	cupric ion	161-165	CD2 molecule	Homo sapiens	141-144
19968111-5	2009	Adsorption isotherm experiment showed that adsorption isotherm of heavy metal ions on slag fitted Langmuir model, and the maximum adsorption capacity of Cu2+, Cd2+ and Pb2+ was 0.101, 0.058 and 0.120 mmol x g(-1), respectively.	Metals	72-77	CD2 molecule	Homo sapiens	159-162
19968111-5	2009	Adsorption isotherm experiment showed that adsorption isotherm of heavy metal ions on slag fitted Langmuir model, and the maximum adsorption capacity of Cu2+, Cd2+ and Pb2+ was 0.101, 0.058 and 0.120 mmol x g(-1), respectively.	Lead	168-172	CD2 molecule	Homo sapiens	159-162
19664997-2	2009	Ethylene dibromide (EDB), which is activated by GST T1-1, produces a potent response in the mutation assay.	Ethylene Dibromide	0-18	CD2 molecule	Homo sapiens	52-56
19664997-2	2009	Ethylene dibromide (EDB), which is activated by GST T1-1, produces a potent response in the mutation assay.	Ethylene Dibromide	20-23	CD2 molecule	Homo sapiens	52-56
19848157-3	2009	Phthalic acid (0.6 mM) enhanced Cd2+ adsorption onto ferrihydrite (due to surface ternary complex formation) butinhibited Cd2 adsorption onto bacteria to the same extent as predicted by Cd-phthalate solution complex formation constants, implying no significant surface ternary interaction occurred in this system.	phthalic acid	0-13	CD2 molecule	Homo sapiens	32-35
19477102-0	2009	Adsorption of Cu2+ and Cd2+ from aqueous solution by mercapto-acetic acid modified orange peel.	2-mercaptoacetate	53-73	CD2 molecule	Homo sapiens	23-26
19477102-1	2009	The present article describes the adsorption behaviors of Cu2+ and Cd2+ on mercapto-acetic acid modified orange peel.	2-mercaptoacetate	75-95	CD2 molecule	Homo sapiens	67-70
19477102-6	2009	Maximum adsorption capacities of Cu2+ and Cd2+ on the mercapto-acetic acid modified orange peel were found to be 70.67 and 136.05 mg/g, respectively.	2-mercaptoacetate	54-74	CD2 molecule	Homo sapiens	42-45
19848157-3	2009	Phthalic acid (0.6 mM) enhanced Cd2+ adsorption onto ferrihydrite (due to surface ternary complex formation) butinhibited Cd2 adsorption onto bacteria to the same extent as predicted by Cd-phthalate solution complex formation constants, implying no significant surface ternary interaction occurred in this system.	phthalic acid	0-13	CD2 molecule	Homo sapiens	122-125
19848157-3	2009	Phthalic acid (0.6 mM) enhanced Cd2+ adsorption onto ferrihydrite (due to surface ternary complex formation) butinhibited Cd2 adsorption onto bacteria to the same extent as predicted by Cd-phthalate solution complex formation constants, implying no significant surface ternary interaction occurred in this system.	ferric oxyhydroxide	53-65	CD2 molecule	Homo sapiens	32-35
19848157-5	2009	By adding a generic reaction to the model for the interaction between ferrihydrite and the bacteria, the adsorption of Cd2+ onto Comamonas spp.-ferrihydrite was accurately predicted and Cd2+ distribution and speciation in systems containing ferrihydrite, Comamonas spp., and H2Lp could be predicted.	ferric oxyhydroxide	70-82	CD2 molecule	Homo sapiens	119-122
19848157-5	2009	By adding a generic reaction to the model for the interaction between ferrihydrite and the bacteria, the adsorption of Cd2+ onto Comamonas spp.-ferrihydrite was accurately predicted and Cd2+ distribution and speciation in systems containing ferrihydrite, Comamonas spp., and H2Lp could be predicted.	ferric oxyhydroxide	70-82	CD2 molecule	Homo sapiens	186-189
19619128-6	2009	A catalytically inactive form of CD2-P110alpha (R1130P), on the other hand, prevented the dexamethasone-induced activation of SGK1, but did not inhibit the activation of pGL3-KR1.	Dexamethasone	90-103	CD2 molecule	Homo sapiens	33-36
19619128-7	2009	However, expression of SGK1-S422D or CD2-P110alpha enhanced the transcriptional responses to maximally effective concentrations of dexamethasone and this effect occurred with no change in EC50.	Dexamethasone	131-144	CD2 molecule	Homo sapiens	37-40
19403143-0	2009	Simultaneous adsorption of Cd2+ and phenol on modified N-doped carbon nanotubes: experimental and DFT studies.	Carbon	63-69	CD2 molecule	Homo sapiens	27-30
19652789-0	2009	Triazole-ester modified silver nanoparticles: click synthesis and Cd2+ colorimetric sensing.	triazole-ester	0-14	CD2 molecule	Homo sapiens	66-69
19652789-1	2009	Triazole-ester modified silver nanoparticles were designed and synthesized through click chemistry, which provided a highly selective colorimetric sensor for Cd2+.	triazole-ester	0-14	CD2 molecule	Homo sapiens	158-161
19719190-0	2009	Ratiometric Zn2+ fluorescent sensor and new approach for sensing Cd2+ by ratiometric displacement.	Zinc	12-16	CD2 molecule	Homo sapiens	65-68
19562195-2	2009	Alkaline earth metal ions Mg2+, Ca2+, trivalent Al3+, La3+ and divalent transition metal ions Ni2+, Cu2+, Cd2+ and Hg2+ have been selected in this study and the results are compared with previous studies on the effects of Zn2+ on the EIS of DNA films.	Metals	15-20	CD2 molecule	Homo sapiens	106-109
19562195-2	2009	Alkaline earth metal ions Mg2+, Ca2+, trivalent Al3+, La3+ and divalent transition metal ions Ni2+, Cu2+, Cd2+ and Hg2+ have been selected in this study and the results are compared with previous studies on the effects of Zn2+ on the EIS of DNA films.	Metals	83-88	CD2 molecule	Homo sapiens	106-109
19562195-2	2009	Alkaline earth metal ions Mg2+, Ca2+, trivalent Al3+, La3+ and divalent transition metal ions Ni2+, Cu2+, Cd2+ and Hg2+ have been selected in this study and the results are compared with previous studies on the effects of Zn2+ on the EIS of DNA films.	Nickel(2+)	94-98	CD2 molecule	Homo sapiens	106-109
19659100-1	2009	A quantitative comparison between experiment and theory is presented, which shows that all ions of the Suzuki structure on (001) surfaces of Mg2+ or Cd2+ doped NaCl crystals can be identified despite the tip-surface distance, differences in impurity chemistry, and surface termination.	Sodium Chloride	160-164	CD2 molecule	Homo sapiens	149-152
19293260-5	2009	Reductions in CD4(+) and CD8(+) cell count numbers in response to therapy were seen in all patients, but in those patients developing EBV-LPD a significantly greater reduction in natural killer (NK) cell number and CD2 expression on T cells was seen.	ebv-lpd	134-141	CD2 molecule	Homo sapiens	215-218
19131354-10	2009	One (p.K301M) produced a lysine to methionine change in the third interactive SH3 domain (position 301) and resulted in the defective CD2-CD2AP interaction and clustering; the other (c.1573delAGA) caused the deletion of the glutamic acid in position 525 in the COOH-terminal region of binding with nephrin and was associated with down-modulation of CD2AP, podocin and nephrin glomerular expression.	Methionine	35-45	CD2 molecule	Homo sapiens	134-137
19131354-10	2009	One (p.K301M) produced a lysine to methionine change in the third interactive SH3 domain (position 301) and resulted in the defective CD2-CD2AP interaction and clustering; the other (c.1573delAGA) caused the deletion of the glutamic acid in position 525 in the COOH-terminal region of binding with nephrin and was associated with down-modulation of CD2AP, podocin and nephrin glomerular expression.	Glutamic Acid	224-237	CD2 molecule	Homo sapiens	134-137
19452064-0	2009	Multinuclear Cd2, Cd3 and 1-D framework structures of Cd(II) Schiff base complexes.	cd(ii) schiff base	54-72	CD2 molecule	Homo sapiens	13-16
19469470-7	2009	X-ray diffraction spectra of as prepared samples indicated that silver occupies an interstitial position, while for annealed samples, Ag+ ions get oxidized to Ag2+ and substituted for Cd2+ in the CdS lattice.	Cadmium	196-199	CD2 molecule	Homo sapiens	184-187
19269450-2	2009	In this work, two beta-cyclodextrin (beta-CD) bonded stationary phases for reversed-phase HPLC, including 1, 12-dodecyldiol linked beta-CD stationary phase (CD1) and olio (ethylene glycol) (OEG) linked beta-CD stationary phase (CD2), have been synthesized via click chemistry.	betadex	37-44	CD2 molecule	Homo sapiens	228-231
19177362-6	2009	Subsequently, OptGraft is used to guide the transfer of a calcium-binding pocket from thermitase protein (PDB: 1thm) into the first domain of CD2 protein (PDB:1hng).	Calcium	58-65	CD2 molecule	Homo sapiens	142-145
19101683-0	2009	Electrolyte ion effects on Cd2+ binding at Al2O3 surface: specific synergism versus bulk effects.	Aluminum Oxide	43-48	CD2 molecule	Homo sapiens	27-30
19402500-4	2009	Under these conditions, separation of Cd2+ and recovery of SDS are 98.0% and 58.1%, respectively.	Sodium Dodecyl Sulfate	59-62	CD2 molecule	Homo sapiens	38-41
19402500-5	2009	And the efficiency of reclaimed SDS for removing Cd2+ is 80.2%.	Sodium Dodecyl Sulfate	32-35	CD2 molecule	Homo sapiens	49-52
19402500-7	2009	Under these conditions, separation of Cd2+ and recovery of SDS are 90.1% and 60.5%, respectively.	Sodium Dodecyl Sulfate	59-62	CD2 molecule	Homo sapiens	38-41
19402500-8	2009	And the efficiency of reclaimed SDS for removing Cd2+ is 79.4%.	Sodium Dodecyl Sulfate	32-35	CD2 molecule	Homo sapiens	49-52
27877265-2	2009	On the basis of the effects of the ratio of PAC to PEG, neutralization degree, heavy-metal ion concentration, and temperature on the adsorption behavior of PAC/PEG IPN hydrogel toward Ni2 +, Cr3 + and Cd2 +, the preparation conditions were optimized.	Polyethylene Glycols	160-163	CD2 molecule	Homo sapiens	201-204
27877265-2	2009	On the basis of the effects of the ratio of PAC to PEG, neutralization degree, heavy-metal ion concentration, and temperature on the adsorption behavior of PAC/PEG IPN hydrogel toward Ni2 +, Cr3 + and Cd2 +, the preparation conditions were optimized.	ipn	164-167	CD2 molecule	Homo sapiens	201-204
18780324-0	2009	Luminescent sensor for Cd2+, Hg2+ and Ag+ in water based on a sulphur-containing receptor: quantitative binding-softness relationship.	Water	45-50	CD2 molecule	Homo sapiens	23-26
19204290-1	2009	The folding energetics of the mono-N-glycosylated adhesion domain of the human immune cell receptor cluster of differentiation 2 (hCD2ad) were studied systematically to understand the influence of the N-glycan on the folding energy landscape.	mono-n-octyl phthalate	30-36	CD2 molecule	Homo sapiens	130-134
19204290-1	2009	The folding energetics of the mono-N-glycosylated adhesion domain of the human immune cell receptor cluster of differentiation 2 (hCD2ad) were studied systematically to understand the influence of the N-glycan on the folding energy landscape.	n-glycan	201-209	CD2 molecule	Homo sapiens	130-134
19320163-3	2009	We measured the Donnan potential and partitioning of Cd2+ in alginate gel as a function of ionic strength in the range 1-100 mM.	Alginates	61-69	CD2 molecule	Homo sapiens	53-56
19320163-5	2009	The total Cd(II) concentration in the gel correlates approximately linearly with the free [Cd2+]gel.	cd(ii)	10-16	CD2 molecule	Homo sapiens	91-94
19187636-15	2009	In CT scans of ASA detection, the mean CT values in the aorta at the arch and at T11 were 360 and 358 HU, respectively, whereas in CT scans without ASA detection, the CT values in the aorta at the arch and at T11 were lower (P < 0.05), 297 and 317 HU, respectively.	Aspirin	15-18	CD2 molecule	Homo sapiens	81-84
19187636-15	2009	In CT scans of ASA detection, the mean CT values in the aorta at the arch and at T11 were 360 and 358 HU, respectively, whereas in CT scans without ASA detection, the CT values in the aorta at the arch and at T11 were lower (P < 0.05), 297 and 317 HU, respectively.	Aspirin	15-18	CD2 molecule	Homo sapiens	209-212
18488146-4	2008	Special attention was paid to the complexation with Cd2+, a well known toxic metal ion.	Metals	77-82	CD2 molecule	Homo sapiens	52-55
19053674-2	2008	Observed pressure -induced variations in CD2 and N-D stretching modes indicate significant changes in the hydrogen-bonding interactions.	Hydrogen	106-114	CD2 molecule	Homo sapiens	41-44
18817447-0	2008	A pyrenyl-appended triazole-based calix[4]arene as a fluorescent sensor for Cd2+ and Zn2+.	pyrenyl-appended	2-18	CD2 molecule	Homo sapiens	76-79
18817447-0	2008	A pyrenyl-appended triazole-based calix[4]arene as a fluorescent sensor for Cd2+ and Zn2+.	Triazoles	19-27	CD2 molecule	Homo sapiens	76-79
18817447-0	2008	A pyrenyl-appended triazole-based calix[4]arene as a fluorescent sensor for Cd2+ and Zn2+.	calix(4)arene	34-47	CD2 molecule	Homo sapiens	76-79
18488146-6	2008	Rhod-5N was found to be highly selective of Cd2+ over those interfering cations except Pb2+.	Lead	87-91	CD2 molecule	Homo sapiens	44-47
18379773-4	2008	The cGMP dose response and blockage by TEA+ and Cd2+ were instead significantly different in CNGA1 and CNGA1cys-free channels, but not in CNGA1 and CNGA1tandem channels.	Cyclic GMP	4-8	CD2 molecule	Homo sapiens	48-51
18766973-7	2008	Finally, pre-incubation of CTL with CD2 antibodies led to an Fc-dependent redistribution of CD2 into TC-induced synapses and restored IFN-gamma production by CMV-specific CTL.	Technetium	101-103	CD2 molecule	Homo sapiens	36-39
18766973-7	2008	Finally, pre-incubation of CTL with CD2 antibodies led to an Fc-dependent redistribution of CD2 into TC-induced synapses and restored IFN-gamma production by CMV-specific CTL.	Technetium	101-103	CD2 molecule	Homo sapiens	92-95
18558110-1	2008	This paper describes the fabrication, characterisation and the application of a Nafion/2,2"-bipyridyl/bismuth composite film-coated glassy carbon electrode (NC(Bpy)BiFE) for the anodic stripping voltammetric determination of trace metal ions (Zn2+, Cd2+ and Pb2+).	perfluorosulfonic acid	80-86	CD2 molecule	Homo sapiens	249-252
18558110-1	2008	This paper describes the fabrication, characterisation and the application of a Nafion/2,2"-bipyridyl/bismuth composite film-coated glassy carbon electrode (NC(Bpy)BiFE) for the anodic stripping voltammetric determination of trace metal ions (Zn2+, Cd2+ and Pb2+).	2,2'-Dipyridyl	87-101	CD2 molecule	Homo sapiens	249-252
18558110-1	2008	This paper describes the fabrication, characterisation and the application of a Nafion/2,2"-bipyridyl/bismuth composite film-coated glassy carbon electrode (NC(Bpy)BiFE) for the anodic stripping voltammetric determination of trace metal ions (Zn2+, Cd2+ and Pb2+).	Bismuth	102-109	CD2 molecule	Homo sapiens	249-252
18558110-5	2008	With a 2 min deposition time in the presence of oxygen, linear calibration curves were obtained in a wide concentration range (about 2-0.001 microM) with detection limits of 8.6 nM (0.56 microg dm(-3)) for Zn2+, 1.1 nM (0.12 microg dm(-3)) for Cd2+ and 0.37 nM (0.077 microg dm(-3)) for Pb(2+).	Oxygen	48-54	CD2 molecule	Homo sapiens	244-247
18558110-5	2008	With a 2 min deposition time in the presence of oxygen, linear calibration curves were obtained in a wide concentration range (about 2-0.001 microM) with detection limits of 8.6 nM (0.56 microg dm(-3)) for Zn2+, 1.1 nM (0.12 microg dm(-3)) for Cd2+ and 0.37 nM (0.077 microg dm(-3)) for Pb(2+).	Zinc	206-210	CD2 molecule	Homo sapiens	244-247
18379773-5	2008	Cd2+ blocked irreversibly the mutant channel A406C in the absence of cGMP.	Cyclic GMP	69-73	CD2 molecule	Homo sapiens	0-3
18077090-1	2008	A 3D coordination polymer of cadmium(II) hydrazine azide, [Cd2(N2H4)2(N3)4]n, was synthesized and characterized by elemental analysis and Fourier transform infrared (FT-IR) spectrum.	Polymers	18-25	CD2 molecule	Homo sapiens	59-62
18077090-1	2008	A 3D coordination polymer of cadmium(II) hydrazine azide, [Cd2(N2H4)2(N3)4]n, was synthesized and characterized by elemental analysis and Fourier transform infrared (FT-IR) spectrum.	cadmium(ii) hydrazine azide	29-56	CD2 molecule	Homo sapiens	59-62
18359184-8	2008	Taken together, these findings suggest that Cd2+ enhanced the cytotoxicity of EGCG to PC-3 cells by up-regulating the 67LR and the mitochondria-mediated apoptosis pathway.	epigallocatechin gallate	78-82	CD2 molecule	Homo sapiens	44-47
18442233-0	2008	Cd2+-induced conformational change of a synthetic metallopeptide: slow metal binding followed by a slower conformational change.	Metals	50-55	CD2 molecule	Homo sapiens	0-3
18442233-2	2008	The addition of Cd2+ results in the incorporation of 2 equiv of metal ion, which is accompanied by a conformational change of the peptide, as observed by circular dichroism (CD) spectroscopy.	Metals	64-69	CD2 molecule	Homo sapiens	16-19
18359184-0	2008	Investigations of the cytotoxicity of epigallocatechin-3-gallate against PC-3 cells in the presence of Cd2+ in vitro.	epigallocatechin gallate	38-64	CD2 molecule	Homo sapiens	103-106
18160217-1	2008	The purpose of this study was to investigate the use of foam fractionation to recover valuable surfactant (SDS) and metal ion (Cd2+) in the permeate of micellar-enhanced ultrafiltration (MEUF).	Metals	116-121	CD2 molecule	Homo sapiens	127-130
18160217-3	2008	When the concentrations of surfactant (SDS) and metal ion (Cd2+) in the feed solution were 500 mg/L and 10 mg/L, an enrichment ratio of 3.1 was achieved for SDS along with 52% removal fraction, as well as 99.35% Cd2+ was removed, after optimization of different process parameters.	Metals	48-53	CD2 molecule	Homo sapiens	59-62
18160217-3	2008	When the concentrations of surfactant (SDS) and metal ion (Cd2+) in the feed solution were 500 mg/L and 10 mg/L, an enrichment ratio of 3.1 was achieved for SDS along with 52% removal fraction, as well as 99.35% Cd2+ was removed, after optimization of different process parameters.	Sodium Dodecyl Sulfate	157-160	CD2 molecule	Homo sapiens	59-62
18261755-1	2008	Cadmium (Cd2+) is a heavy metal ion known to have a long biological half-life in humans.	Cadmium	0-7	CD2 molecule	Homo sapiens	9-12
18359184-5	2008	The results showed that both EGCG and Cd2+ suppressed viability and clonegenecity of PC-3 cells, and the suppression effect was enhanced when EGCG added with Cd2+.	epigallocatechin gallate	29-33	CD2 molecule	Homo sapiens	158-161
18359184-5	2008	The results showed that both EGCG and Cd2+ suppressed viability and clonegenecity of PC-3 cells, and the suppression effect was enhanced when EGCG added with Cd2+.	epigallocatechin gallate	142-146	CD2 molecule	Homo sapiens	38-41
18359184-5	2008	The results showed that both EGCG and Cd2+ suppressed viability and clonegenecity of PC-3 cells, and the suppression effect was enhanced when EGCG added with Cd2+.	epigallocatechin gallate	142-146	CD2 molecule	Homo sapiens	158-161
18359184-7	2008	We also found that EGCG and Cd2+ directly interacted with mitochondrial, and the mixture of EGCG and Cd2+ (EGCG+Cd2+) significantly caused loss of the mitochondrial membrane potential, decrease of the ATP content and activation of caspase-9 compared with EGCG treated alone.	Adenosine Triphosphate	201-204	CD2 molecule	Homo sapiens	28-31
18359184-7	2008	We also found that EGCG and Cd2+ directly interacted with mitochondrial, and the mixture of EGCG and Cd2+ (EGCG+Cd2+) significantly caused loss of the mitochondrial membrane potential, decrease of the ATP content and activation of caspase-9 compared with EGCG treated alone.	Adenosine Triphosphate	201-204	CD2 molecule	Homo sapiens	101-104
18359184-7	2008	We also found that EGCG and Cd2+ directly interacted with mitochondrial, and the mixture of EGCG and Cd2+ (EGCG+Cd2+) significantly caused loss of the mitochondrial membrane potential, decrease of the ATP content and activation of caspase-9 compared with EGCG treated alone.	Adenosine Triphosphate	201-204	CD2 molecule	Homo sapiens	101-104
18407645-1	2008	The direct coupling of a variety of amides with CH2 Cl2 or CD2 Cl2 promoted by TiCl 4/Mg/THF provides an extremely simple, practical, selective, and efficient approach for the construction of methyl ketones.	Amides	36-42	CD2 molecule	Homo sapiens	59-62
18407645-1	2008	The direct coupling of a variety of amides with CH2 Cl2 or CD2 Cl2 promoted by TiCl 4/Mg/THF provides an extremely simple, practical, selective, and efficient approach for the construction of methyl ketones.	titanium tetrachloride	79-85	CD2 molecule	Homo sapiens	59-62
18407645-1	2008	The direct coupling of a variety of amides with CH2 Cl2 or CD2 Cl2 promoted by TiCl 4/Mg/THF provides an extremely simple, practical, selective, and efficient approach for the construction of methyl ketones.	Magnesium	86-88	CD2 molecule	Homo sapiens	59-62
18407645-1	2008	The direct coupling of a variety of amides with CH2 Cl2 or CD2 Cl2 promoted by TiCl 4/Mg/THF provides an extremely simple, practical, selective, and efficient approach for the construction of methyl ketones.	tetrahydrofuran	89-92	CD2 molecule	Homo sapiens	59-62
18407645-1	2008	The direct coupling of a variety of amides with CH2 Cl2 or CD2 Cl2 promoted by TiCl 4/Mg/THF provides an extremely simple, practical, selective, and efficient approach for the construction of methyl ketones.	Acetone	192-206	CD2 molecule	Homo sapiens	59-62
18261755-1	2008	Cadmium (Cd2+) is a heavy metal ion known to have a long biological half-life in humans.	Metals	26-31	CD2 molecule	Homo sapiens	9-12
18036605-0	2008	Adsorption of Pb2+, Zn2+, and Cd2+ from waters by amorphous titanium phosphate.	titanium phosphate	60-78	CD2 molecule	Homo sapiens	30-33
18184015-2	2008	The measurements are based on CdS quantum dot labels of the secondary aptamer, which were determined with a novel solid-contact Cd2+-selective polymer membrane electrode after dissolution with hydrogen peroxide.	Cadmium	30-33	CD2 molecule	Homo sapiens	128-131
18184015-2	2008	The measurements are based on CdS quantum dot labels of the secondary aptamer, which were determined with a novel solid-contact Cd2+-selective polymer membrane electrode after dissolution with hydrogen peroxide.	Polymers	143-150	CD2 molecule	Homo sapiens	128-131
18184015-2	2008	The measurements are based on CdS quantum dot labels of the secondary aptamer, which were determined with a novel solid-contact Cd2+-selective polymer membrane electrode after dissolution with hydrogen peroxide.	Hydrogen Peroxide	193-210	CD2 molecule	Homo sapiens	128-131
18160350-7	2008	The interaction of Cd2+ and Ni2+ causes conformational changes, destabilizing the double helix, which can enable the action of other oxidative agents on DNA.	Nickel(2+)	28-32	CD2 molecule	Homo sapiens	19-22
17706343-0	2008	A comparative study on Pb2+, Zn2+ and Cd2+ sorption onto zirconium phosphate supported by a cation exchanger.	zirconium phosphate	57-76	CD2 molecule	Homo sapiens	38-41
18234058-5	2008	When compared to PBT, LPT show an increased activation of the phosphoinositide 3/protein kinase B/glycogen synthase kinase 3beta (PI3-kinase/AKT/GSK-3beta) pathway in response to CD2 stimulation.	CIS-(AMMINE)(CYCLOHEXYLAMINE)PLATINUM(II) COMPLEX	22-25	CD2 molecule	Homo sapiens	179-182
18468120-3	2008	We systematically investigated the effect of synthesis conditions on the optical properties of the L-cysteine hydrochloride-stabilized CdSe nanocrystals, and found that different sizes of CdSe nanocrystals can be obtained by changing the pH value, the molar ratio of L-cysteine hydrochloride to Cd2+, or the refluxing time.	Cysteine	99-123	CD2 molecule	Homo sapiens	295-298
18468120-5	2008	We observed an obvious blue-shift of the absorption and photoluminescence peak position by varying the molar ratio of L-Cys to Cd2+ from 3.5:1 to 2:1 at the same pH value.	Cysteine	118-123	CD2 molecule	Homo sapiens	127-130
18287277-0	2008	Rational design of a novel calcium-binding site adjacent to the ligand-binding site on CD2 increases its CD48 affinity.	Calcium	27-34	CD2 molecule	Homo sapiens	87-90
17948990-3	2007	The structure of [Cd3(H2O)3((O3PCH2)2NH-CH2C6H4-COOH)2].11H2O is built up of cadmium phosphonate layers connected by water-mediated hydrogen bonds between aryl-carboxylic acid groups and water molecules coordinated to Cd2+ ions of adjacent layers (C-OH...H2O...H2O-Cd2+).	cd3(h2o)3	18-27	CD2 molecule	Homo sapiens	218-221
18399206-1	2008	Reaction of a rigid triangular ligand 2,4,6-tris[4-(1H-imidazole-1-yl)phenyl]-1,3,5-triazine (TIPT) with Cd2+ ions affordedrare non-interpenetrating CdI2-type networks which display high thermostability and potential porosity; the topological character of the CdI2-type networks have been analyzed in comparison with three common uniform (4,4), (6,3) and (3,6) plane nets.	2,4,6-tris[4-(1h-imidazole-1-yl)phenyl]-1,3,5-triazine	38-92	CD2 molecule	Homo sapiens	105-108
18399206-1	2008	Reaction of a rigid triangular ligand 2,4,6-tris[4-(1H-imidazole-1-yl)phenyl]-1,3,5-triazine (TIPT) with Cd2+ ions affordedrare non-interpenetrating CdI2-type networks which display high thermostability and potential porosity; the topological character of the CdI2-type networks have been analyzed in comparison with three common uniform (4,4), (6,3) and (3,6) plane nets.	Titanium tetraisopropanolate	94-98	CD2 molecule	Homo sapiens	105-108
18399206-1	2008	Reaction of a rigid triangular ligand 2,4,6-tris[4-(1H-imidazole-1-yl)phenyl]-1,3,5-triazine (TIPT) with Cd2+ ions affordedrare non-interpenetrating CdI2-type networks which display high thermostability and potential porosity; the topological character of the CdI2-type networks have been analyzed in comparison with three common uniform (4,4), (6,3) and (3,6) plane nets.	CdI2	149-153	CD2 molecule	Homo sapiens	105-108
18481799-4	2008	Upon complexation with heavy metal ions such as Pb2+ and Cd2+, a red shift of the one- and two-photon excitation spectra was observed in the absorption and emission spectra.	Metals	29-34	CD2 molecule	Homo sapiens	57-60
18481799-4	2008	Upon complexation with heavy metal ions such as Pb2+ and Cd2+, a red shift of the one- and two-photon excitation spectra was observed in the absorption and emission spectra.	Lead	48-52	CD2 molecule	Homo sapiens	57-60
18481799-5	2008	Furthermore, enhancement of the electron-withdrawing character of the phosphane oxide resulted in a significant enhancement of the two-photon absorption cross-section, leading to the first biphotonic Cd2+ sensors combining high affinity for Cd2+, large two-photon absorption cross-sections, and significant enhancement of the two-photon excited fluorescence in the presence of the cation.	phosphane oxide	70-85	CD2 molecule	Homo sapiens	200-203
18481799-5	2008	Furthermore, enhancement of the electron-withdrawing character of the phosphane oxide resulted in a significant enhancement of the two-photon absorption cross-section, leading to the first biphotonic Cd2+ sensors combining high affinity for Cd2+, large two-photon absorption cross-sections, and significant enhancement of the two-photon excited fluorescence in the presence of the cation.	phosphane oxide	70-85	CD2 molecule	Homo sapiens	241-244
17948990-3	2007	The structure of [Cd3(H2O)3((O3PCH2)2NH-CH2C6H4-COOH)2].11H2O is built up of cadmium phosphonate layers connected by water-mediated hydrogen bonds between aryl-carboxylic acid groups and water molecules coordinated to Cd2+ ions of adjacent layers (C-OH...H2O...H2O-Cd2+).	cd3(h2o)3	18-27	CD2 molecule	Homo sapiens	265-268
17948990-3	2007	The structure of [Cd3(H2O)3((O3PCH2)2NH-CH2C6H4-COOH)2].11H2O is built up of cadmium phosphonate layers connected by water-mediated hydrogen bonds between aryl-carboxylic acid groups and water molecules coordinated to Cd2+ ions of adjacent layers (C-OH...H2O...H2O-Cd2+).	((o3pch2)2nh-ch2c6h4	27-47	CD2 molecule	Homo sapiens	218-221
17948990-3	2007	The structure of [Cd3(H2O)3((O3PCH2)2NH-CH2C6H4-COOH)2].11H2O is built up of cadmium phosphonate layers connected by water-mediated hydrogen bonds between aryl-carboxylic acid groups and water molecules coordinated to Cd2+ ions of adjacent layers (C-OH...H2O...H2O-Cd2+).	((o3pch2)2nh-ch2c6h4	27-47	CD2 molecule	Homo sapiens	265-268
18422129-2	2008	The results show that the sulfur atoms in thiourea molecules coordinate with Cd2+ ions on the surface of the nanocrystals.	Sulfur	26-32	CD2 molecule	Homo sapiens	77-80
18422129-2	2008	The results show that the sulfur atoms in thiourea molecules coordinate with Cd2+ ions on the surface of the nanocrystals.	Thiourea	42-50	CD2 molecule	Homo sapiens	77-80
18817066-4	2008	The single Cd2+ and Pb2+ treatments significantly inhibited dehydrogenase activities at concentrations in excess of 20 micromol/L Cd2+ and 80 micromol/L Pb2+, respectively.	Lead	20-24	CD2 molecule	Homo sapiens	130-133
18817066-4	2008	The single Cd2+ and Pb2+ treatments significantly inhibited dehydrogenase activities at concentrations in excess of 20 micromol/L Cd2+ and 80 micromol/L Pb2+, respectively.	Lead	153-157	CD2 molecule	Homo sapiens	11-14
18817066-6	2008	At the same time, the combined treatment of Cd2+ and Pb2+ significantly inhibited dehydrogenase activities at all five concentrations studied and the lowest combined concentration was 1.25 micromol/L Cd2+ and 5 micromol/L Pb2+.	Lead	53-57	CD2 molecule	Homo sapiens	200-203
18817066-6	2008	At the same time, the combined treatment of Cd2+ and Pb2+ significantly inhibited dehydrogenase activities at all five concentrations studied and the lowest combined concentration was 1.25 micromol/L Cd2+ and 5 micromol/L Pb2+.	Lead	222-226	CD2 molecule	Homo sapiens	44-47
18817066-8	2008	On the other hand, polysaccharide contents varied unpredictably with the increasing concentrations of Cd2+ and Pb2+ and extended experimental time.	Polysaccharides	19-33	CD2 molecule	Homo sapiens	102-105
19092216-0	2008	Modeling Cd2+ sorption onto ferrihydrite in the presence of phthalic acid.	ferric oxyhydroxide	28-40	CD2 molecule	Homo sapiens	9-12
19092216-0	2008	Modeling Cd2+ sorption onto ferrihydrite in the presence of phthalic acid.	phthalic acid	60-73	CD2 molecule	Homo sapiens	9-12
17948990-3	2007	The structure of [Cd3(H2O)3((O3PCH2)2NH-CH2C6H4-COOH)2].11H2O is built up of cadmium phosphonate layers connected by water-mediated hydrogen bonds between aryl-carboxylic acid groups and water molecules coordinated to Cd2+ ions of adjacent layers (C-OH...H2O...H2O-Cd2+).	Carbonic Acid	48-54	CD2 molecule	Homo sapiens	218-221
17948990-3	2007	The structure of [Cd3(H2O)3((O3PCH2)2NH-CH2C6H4-COOH)2].11H2O is built up of cadmium phosphonate layers connected by water-mediated hydrogen bonds between aryl-carboxylic acid groups and water molecules coordinated to Cd2+ ions of adjacent layers (C-OH...H2O...H2O-Cd2+).	Carbonic Acid	48-54	CD2 molecule	Homo sapiens	265-268
18024392-6	2007	The growth-inhibitory effects of dasatinib in HMC-1 cells were found to be associated with a decrease in expression of CD2 and CD63.	Dasatinib	33-42	CD2 molecule	Homo sapiens	119-122
17948990-3	2007	The structure of [Cd3(H2O)3((O3PCH2)2NH-CH2C6H4-COOH)2].11H2O is built up of cadmium phosphonate layers connected by water-mediated hydrogen bonds between aryl-carboxylic acid groups and water molecules coordinated to Cd2+ ions of adjacent layers (C-OH...H2O...H2O-Cd2+).	11h2o	56-61	CD2 molecule	Homo sapiens	218-221
17948990-3	2007	The structure of [Cd3(H2O)3((O3PCH2)2NH-CH2C6H4-COOH)2].11H2O is built up of cadmium phosphonate layers connected by water-mediated hydrogen bonds between aryl-carboxylic acid groups and water molecules coordinated to Cd2+ ions of adjacent layers (C-OH...H2O...H2O-Cd2+).	11h2o	56-61	CD2 molecule	Homo sapiens	265-268
17948990-3	2007	The structure of [Cd3(H2O)3((O3PCH2)2NH-CH2C6H4-COOH)2].11H2O is built up of cadmium phosphonate layers connected by water-mediated hydrogen bonds between aryl-carboxylic acid groups and water molecules coordinated to Cd2+ ions of adjacent layers (C-OH...H2O...H2O-Cd2+).	Water	22-25	CD2 molecule	Homo sapiens	218-221
17948990-3	2007	The structure of [Cd3(H2O)3((O3PCH2)2NH-CH2C6H4-COOH)2].11H2O is built up of cadmium phosphonate layers connected by water-mediated hydrogen bonds between aryl-carboxylic acid groups and water molecules coordinated to Cd2+ ions of adjacent layers (C-OH...H2O...H2O-Cd2+).	Water	22-25	CD2 molecule	Homo sapiens	265-268
17948990-3	2007	The structure of [Cd3(H2O)3((O3PCH2)2NH-CH2C6H4-COOH)2].11H2O is built up of cadmium phosphonate layers connected by water-mediated hydrogen bonds between aryl-carboxylic acid groups and water molecules coordinated to Cd2+ ions of adjacent layers (C-OH...H2O...H2O-Cd2+).	Water	58-61	CD2 molecule	Homo sapiens	218-221
17948990-3	2007	The structure of [Cd3(H2O)3((O3PCH2)2NH-CH2C6H4-COOH)2].11H2O is built up of cadmium phosphonate layers connected by water-mediated hydrogen bonds between aryl-carboxylic acid groups and water molecules coordinated to Cd2+ ions of adjacent layers (C-OH...H2O...H2O-Cd2+).	Water	58-61	CD2 molecule	Homo sapiens	265-268
18225653-0	2007	[The nature of different influence of Cd2+ ions on the conformation of three-stranded polyU-polyA-polyU and polyI-polyA-polyI in aqueous solution].	polyu-polya-polyu	86-103	CD2 molecule	Homo sapiens	38-41
18225653-0	2007	[The nature of different influence of Cd2+ ions on the conformation of three-stranded polyU-polyA-polyU and polyI-polyA-polyI in aqueous solution].	polyi-polya-polyi	108-125	CD2 molecule	Homo sapiens	38-41
18225653-1	2007	The methods of UV (DUV) spectroscopy and thermal denaturation were used to study the effect of Cd2+ ions on the conformational equilibrium of three-stranded (A21, A2U) and single-stranded (poly U, poly A and poly I) polynucleotides in aqueous solutions containing 0.1 M Na+ (pH 7).	Polynucleotides	216-231	CD2 molecule	Homo sapiens	95-98
18225653-4	2007	It is supposed that, during the formation of metallized A2I, Cd2+ ions form bridges between the adenine and hypoxanthine of its homopolynucleotide circuits, being arranged inside the triple helix.	Adenine	96-103	CD2 molecule	Homo sapiens	61-64
18225653-4	2007	It is supposed that, during the formation of metallized A2I, Cd2+ ions form bridges between the adenine and hypoxanthine of its homopolynucleotide circuits, being arranged inside the triple helix.	Hypoxanthine	108-120	CD2 molecule	Homo sapiens	61-64
17705397-0	2007	A water-soluble "switching on" fluorescent chemosensor of selectivity to Cd2+.	Water	2-7	CD2 molecule	Homo sapiens	73-76
17705397-2	2007	This fluorescent chemosensor exhibits its selectivity to Cd2+ among a series of cations in HEPES buffer solution.	HEPES	91-96	CD2 molecule	Homo sapiens	57-60
17705397-4	2007	The mechanistic selectivity and sensitivity of compound 1 to Cd2+ was discussed on the basis of fluorescence, 1H NMR, and mass spectroscopic results.	Hydrogen	110-112	CD2 molecule	Homo sapiens	61-64
17475644-3	2007	To probe the metal-binding properties of this motif, we used an established grafting approach and engineered the 12-residue Ca(2+)-coordinating loop into a non-Ca(2+)-binding scaffold protein, CD2.	Metals	13-18	CD2 molecule	Homo sapiens	193-196
17974251-4	2007	Two-constant equation was the best model to describe the sorption kinetics of Cd2+ and Pb2+, Elovich equation was the second, and the worst was first-order dynamics equation.	Lead	87-91	CD2 molecule	Homo sapiens	78-81
17974251-7	2007	In test soils, the desorption rates of Cd2+ and Pb2+ increased with increasing initial concentrations of Cd2+ and Pb2+, but decreased with increasing duration of desorpion.	Lead	48-52	CD2 molecule	Homo sapiens	105-108
17974251-7	2007	In test soils, the desorption rates of Cd2+ and Pb2+ increased with increasing initial concentrations of Cd2+ and Pb2+, but decreased with increasing duration of desorpion.	Lead	114-118	CD2 molecule	Homo sapiens	39-42
17974251-7	2007	In test soils, the desorption rates of Cd2+ and Pb2+ increased with increasing initial concentrations of Cd2+ and Pb2+, but decreased with increasing duration of desorpion.	desorpion	162-171	CD2 molecule	Homo sapiens	39-42
17685497-0	2007	Hydrogen migration and vinylidene pathway for formation of methane in the 193 nm photodissociation of propene: CH3CH=CH2 and CD3CD=CD2.	Hydrogen	0-8	CD2 molecule	Homo sapiens	131-134
17685497-0	2007	Hydrogen migration and vinylidene pathway for formation of methane in the 193 nm photodissociation of propene: CH3CH=CH2 and CD3CD=CD2.	ethen-1,1-diyl	23-33	CD2 molecule	Homo sapiens	131-134
17685497-0	2007	Hydrogen migration and vinylidene pathway for formation of methane in the 193 nm photodissociation of propene: CH3CH=CH2 and CD3CD=CD2.	Methane	59-66	CD2 molecule	Homo sapiens	131-134
17685497-0	2007	Hydrogen migration and vinylidene pathway for formation of methane in the 193 nm photodissociation of propene: CH3CH=CH2 and CD3CD=CD2.	propylene	102-109	CD2 molecule	Homo sapiens	131-134
17685497-0	2007	Hydrogen migration and vinylidene pathway for formation of methane in the 193 nm photodissociation of propene: CH3CH=CH2 and CD3CD=CD2.	cd3cd	125-130	CD2 molecule	Homo sapiens	131-134
17386421-0	2007	Voltammetric determination of Cd2+ based on the bifunctionality of single-walled carbon nanotubes-Nafion film.	Carbon	81-87	CD2 molecule	Homo sapiens	30-33
17467737-2	2007	U5-52K binds to the CD2 receptor via its GYF-domain specifically recognizing a proline-rich motif on the cytoplasmic surface of the receptor.	Proline	79-86	CD2 molecule	Homo sapiens	20-23
17381157-1	2007	In a neutral aqueous environment, a new ratiometric Cd2+ fluorescent sensor 1a can successfully discriminate Cd2+ from Zn2+ by undergoing two different internal charge transfer (ICT) processes, and the high selectivity of sensor 1a to Cd2+ over some other metals was also observed.	Zinc	119-123	CD2 molecule	Homo sapiens	52-55
17220479-0	2007	CD2 and TCR synergize for the activation of phospholipase Cgamma1/calcium pathway at the immunological synapse.	Calcium	66-73	CD2 molecule	Homo sapiens	0-3
17220479-2	2007	We investigated the contribution of the accessory molecule CD2 to the activation of phospholipase Cgamma1 (PLCgamma1)/calcium pathway in antigen-stimulated T cells.	Calcium	118-125	CD2 molecule	Homo sapiens	59-62
17279683-1	2007	Several studies suggested that the cytotoxic effects of quantum dots (QDs) may be mediated by cadmium ions (Cd2+) released from the QDs cores.	Cadmium	94-101	CD2 molecule	Homo sapiens	108-111
17279683-2	2007	The objective of this work was to assess the intracellular Cd2+ concentration in human breast cancer MCF-7 cells treated with cadmium telluride (CdTe) and core/shell cadmium selenide/zinc sulfide (CdSe/ZnS) nanoparticles capped with mercaptopropionic acid (MPA), cysteamine (Cys), or N-acetylcysteine (NAC) conjugated to cysteamine.	cadmium telluride	126-143	CD2 molecule	Homo sapiens	59-62
17279683-2	2007	The objective of this work was to assess the intracellular Cd2+ concentration in human breast cancer MCF-7 cells treated with cadmium telluride (CdTe) and core/shell cadmium selenide/zinc sulfide (CdSe/ZnS) nanoparticles capped with mercaptopropionic acid (MPA), cysteamine (Cys), or N-acetylcysteine (NAC) conjugated to cysteamine.	cadmium telluride	145-149	CD2 molecule	Homo sapiens	59-62
17279683-2	2007	The objective of this work was to assess the intracellular Cd2+ concentration in human breast cancer MCF-7 cells treated with cadmium telluride (CdTe) and core/shell cadmium selenide/zinc sulfide (CdSe/ZnS) nanoparticles capped with mercaptopropionic acid (MPA), cysteamine (Cys), or N-acetylcysteine (NAC) conjugated to cysteamine.	cadmium selenide	166-182	CD2 molecule	Homo sapiens	59-62
17279683-2	2007	The objective of this work was to assess the intracellular Cd2+ concentration in human breast cancer MCF-7 cells treated with cadmium telluride (CdTe) and core/shell cadmium selenide/zinc sulfide (CdSe/ZnS) nanoparticles capped with mercaptopropionic acid (MPA), cysteamine (Cys), or N-acetylcysteine (NAC) conjugated to cysteamine.	zinc sulfide	183-195	CD2 molecule	Homo sapiens	59-62
17279683-2	2007	The objective of this work was to assess the intracellular Cd2+ concentration in human breast cancer MCF-7 cells treated with cadmium telluride (CdTe) and core/shell cadmium selenide/zinc sulfide (CdSe/ZnS) nanoparticles capped with mercaptopropionic acid (MPA), cysteamine (Cys), or N-acetylcysteine (NAC) conjugated to cysteamine.	cdse	197-201	CD2 molecule	Homo sapiens	59-62
17279683-2	2007	The objective of this work was to assess the intracellular Cd2+ concentration in human breast cancer MCF-7 cells treated with cadmium telluride (CdTe) and core/shell cadmium selenide/zinc sulfide (CdSe/ZnS) nanoparticles capped with mercaptopropionic acid (MPA), cysteamine (Cys), or N-acetylcysteine (NAC) conjugated to cysteamine.	Zinc	202-205	CD2 molecule	Homo sapiens	59-62
17243837-7	2007	The reaction coordinates of the ribozyme reaction in TS, RC1-CD1 and RC4-CD2, are 2.35 and 2.33 A, respectively, compared to 2.37 and 2.36 A in water.	Water	144-149	CD2 molecule	Homo sapiens	69-76
17639938-1	2007	The influence of Ni2+, Cd2+ and Cu2+ on electron transport system (ETS) activity of anaerobic 2-chlorophenon degradation sludge, as well as the effect of acclimation on microbial resistance to metallic toxicity, was investigated.	2-chlorophenon	94-108	CD2 molecule	Homo sapiens	23-26
17639938-3	2007	The relative strength of inhibition was Ni2+ > Cd2+ > Cu2+ and was mainly dependent on the metallic ion concentration in solution.	Nickel(2+)	40-44	CD2 molecule	Homo sapiens	50-53
17639938-3	2007	The relative strength of inhibition was Ni2+ > Cd2+ > Cu2+ and was mainly dependent on the metallic ion concentration in solution.	cupric ion	60-64	CD2 molecule	Homo sapiens	50-53
17639938-7	2007	The relative amelioration of microbial resistance was Ni2+ > Cd2+ > Cu2+.	Nickel(2+)	54-58	CD2 molecule	Homo sapiens	64-67
17639938-7	2007	The relative amelioration of microbial resistance was Ni2+ > Cd2+ > Cu2+.	cupric ion	74-78	CD2 molecule	Homo sapiens	64-67
17291025-8	2007	Cd2+ shows a lesser diffusion coefficient compared to that of Pb2+ despite its smaller atomic radius, indicating a more persistent first coordination shell for the cadmium(II) ion, a result confirmed with calculations of the mean residence time of water molecules in the first coordination shell.	Cadmium	164-171	CD2 molecule	Homo sapiens	0-3
17291025-8	2007	Cd2+ shows a lesser diffusion coefficient compared to that of Pb2+ despite its smaller atomic radius, indicating a more persistent first coordination shell for the cadmium(II) ion, a result confirmed with calculations of the mean residence time of water molecules in the first coordination shell.	Water	248-253	CD2 molecule	Homo sapiens	0-3
17279683-2	2007	The objective of this work was to assess the intracellular Cd2+ concentration in human breast cancer MCF-7 cells treated with cadmium telluride (CdTe) and core/shell cadmium selenide/zinc sulfide (CdSe/ZnS) nanoparticles capped with mercaptopropionic acid (MPA), cysteamine (Cys), or N-acetylcysteine (NAC) conjugated to cysteamine.	3-Mercaptopropionic Acid	233-255	CD2 molecule	Homo sapiens	59-62
17279683-2	2007	The objective of this work was to assess the intracellular Cd2+ concentration in human breast cancer MCF-7 cells treated with cadmium telluride (CdTe) and core/shell cadmium selenide/zinc sulfide (CdSe/ZnS) nanoparticles capped with mercaptopropionic acid (MPA), cysteamine (Cys), or N-acetylcysteine (NAC) conjugated to cysteamine.	mpa	257-260	CD2 molecule	Homo sapiens	59-62
17279683-2	2007	The objective of this work was to assess the intracellular Cd2+ concentration in human breast cancer MCF-7 cells treated with cadmium telluride (CdTe) and core/shell cadmium selenide/zinc sulfide (CdSe/ZnS) nanoparticles capped with mercaptopropionic acid (MPA), cysteamine (Cys), or N-acetylcysteine (NAC) conjugated to cysteamine.	Cysteamine	263-273	CD2 molecule	Homo sapiens	59-62
17279683-2	2007	The objective of this work was to assess the intracellular Cd2+ concentration in human breast cancer MCF-7 cells treated with cadmium telluride (CdTe) and core/shell cadmium selenide/zinc sulfide (CdSe/ZnS) nanoparticles capped with mercaptopropionic acid (MPA), cysteamine (Cys), or N-acetylcysteine (NAC) conjugated to cysteamine.	Cysteamine	275-278	CD2 molecule	Homo sapiens	59-62
17279683-2	2007	The objective of this work was to assess the intracellular Cd2+ concentration in human breast cancer MCF-7 cells treated with cadmium telluride (CdTe) and core/shell cadmium selenide/zinc sulfide (CdSe/ZnS) nanoparticles capped with mercaptopropionic acid (MPA), cysteamine (Cys), or N-acetylcysteine (NAC) conjugated to cysteamine.	Acetylcysteine	284-300	CD2 molecule	Homo sapiens	59-62
17279683-2	2007	The objective of this work was to assess the intracellular Cd2+ concentration in human breast cancer MCF-7 cells treated with cadmium telluride (CdTe) and core/shell cadmium selenide/zinc sulfide (CdSe/ZnS) nanoparticles capped with mercaptopropionic acid (MPA), cysteamine (Cys), or N-acetylcysteine (NAC) conjugated to cysteamine.	Acetylcysteine	302-305	CD2 molecule	Homo sapiens	59-62
17279683-2	2007	The objective of this work was to assess the intracellular Cd2+ concentration in human breast cancer MCF-7 cells treated with cadmium telluride (CdTe) and core/shell cadmium selenide/zinc sulfide (CdSe/ZnS) nanoparticles capped with mercaptopropionic acid (MPA), cysteamine (Cys), or N-acetylcysteine (NAC) conjugated to cysteamine.	Cysteamine	321-331	CD2 molecule	Homo sapiens	59-62
17279683-3	2007	The Cd2+ concentration determined by a Cd2+-specific cellular assay was below the assay detection limit (<5 nM) in cells treated with CdSe/ZnS QDs, while in cells incubated with CdTe QDs, it ranged from approximately 30 to 150 nM, depending on the capping molecule.	cdse	137-141	CD2 molecule	Homo sapiens	4-7
17279683-3	2007	The Cd2+ concentration determined by a Cd2+-specific cellular assay was below the assay detection limit (<5 nM) in cells treated with CdSe/ZnS QDs, while in cells incubated with CdTe QDs, it ranged from approximately 30 to 150 nM, depending on the capping molecule.	cdse	137-141	CD2 molecule	Homo sapiens	39-42
17279683-3	2007	The Cd2+ concentration determined by a Cd2+-specific cellular assay was below the assay detection limit (<5 nM) in cells treated with CdSe/ZnS QDs, while in cells incubated with CdTe QDs, it ranged from approximately 30 to 150 nM, depending on the capping molecule.	Zinc	142-145	CD2 molecule	Homo sapiens	4-7
17279683-3	2007	The Cd2+ concentration determined by a Cd2+-specific cellular assay was below the assay detection limit (<5 nM) in cells treated with CdSe/ZnS QDs, while in cells incubated with CdTe QDs, it ranged from approximately 30 to 150 nM, depending on the capping molecule.	Zinc	142-145	CD2 molecule	Homo sapiens	39-42
17279683-3	2007	The Cd2+ concentration determined by a Cd2+-specific cellular assay was below the assay detection limit (<5 nM) in cells treated with CdSe/ZnS QDs, while in cells incubated with CdTe QDs, it ranged from approximately 30 to 150 nM, depending on the capping molecule.	cadmium telluride	181-185	CD2 molecule	Homo sapiens	4-7
17279683-3	2007	The Cd2+ concentration determined by a Cd2+-specific cellular assay was below the assay detection limit (<5 nM) in cells treated with CdSe/ZnS QDs, while in cells incubated with CdTe QDs, it ranged from approximately 30 to 150 nM, depending on the capping molecule.	cadmium telluride	181-185	CD2 molecule	Homo sapiens	39-42
17279683-6	2007	Confocal laser scanning microscopy of CdTe QDs-treated cells imaged with organelle-specific dyes revealed significant lysosomal damage attributable to the presence of Cd2+ and of reactive oxygen species (ROS), which can be formed via Cd2+-specific cellular pathways and/or via CdTe-triggered photoxidative processes involving singlet oxygen or electron transfer from excited QDs to oxygen.	cadmium telluride	38-42	CD2 molecule	Homo sapiens	167-170
17279683-6	2007	Confocal laser scanning microscopy of CdTe QDs-treated cells imaged with organelle-specific dyes revealed significant lysosomal damage attributable to the presence of Cd2+ and of reactive oxygen species (ROS), which can be formed via Cd2+-specific cellular pathways and/or via CdTe-triggered photoxidative processes involving singlet oxygen or electron transfer from excited QDs to oxygen.	cadmium telluride	38-42	CD2 molecule	Homo sapiens	234-237
17279683-6	2007	Confocal laser scanning microscopy of CdTe QDs-treated cells imaged with organelle-specific dyes revealed significant lysosomal damage attributable to the presence of Cd2+ and of reactive oxygen species (ROS), which can be formed via Cd2+-specific cellular pathways and/or via CdTe-triggered photoxidative processes involving singlet oxygen or electron transfer from excited QDs to oxygen.	Reactive Oxygen Species	179-202	CD2 molecule	Homo sapiens	234-237
17279683-6	2007	Confocal laser scanning microscopy of CdTe QDs-treated cells imaged with organelle-specific dyes revealed significant lysosomal damage attributable to the presence of Cd2+ and of reactive oxygen species (ROS), which can be formed via Cd2+-specific cellular pathways and/or via CdTe-triggered photoxidative processes involving singlet oxygen or electron transfer from excited QDs to oxygen.	Reactive Oxygen Species	204-207	CD2 molecule	Homo sapiens	234-237
17279683-7	2007	In summary, CdTe QDs induce cell death via mechanisms involving both Cd2+ and ROS accompanied by lysosomal enlargement and intracellular redistribution.	cadmium telluride	12-16	CD2 molecule	Homo sapiens	69-72
17386421-0	2007	Voltammetric determination of Cd2+ based on the bifunctionality of single-walled carbon nanotubes-Nafion film.	perfluorosulfonic acid	98-104	CD2 molecule	Homo sapiens	30-33
17680181-10	2007	RESULTS: TcPO(2) increased significantly after spinal anesthesia only at T11, and was increased by oxygen administration at both T3 and T11.	Trichloroepoxypropane	9-13	CD2 molecule	Homo sapiens	73-76
16939420-4	2007	The AMP moiety of ATP binds at the ATP-binding site, and a Cd2+ ion binds at the active site and in a position to interact with the beta- and gamma-phosphates of ATP.	Adenosine Triphosphate	35-38	CD2 molecule	Homo sapiens	59-62
16939420-4	2007	The AMP moiety of ATP binds at the ATP-binding site, and a Cd2+ ion binds at the active site and in a position to interact with the beta- and gamma-phosphates of ATP.	beta- and gamma-phosphates	132-158	CD2 molecule	Homo sapiens	59-62
16939420-4	2007	The AMP moiety of ATP binds at the ATP-binding site, and a Cd2+ ion binds at the active site and in a position to interact with the beta- and gamma-phosphates of ATP.	Adenosine Triphosphate	35-38	CD2 molecule	Homo sapiens	59-62
17680181-10	2007	RESULTS: TcPO(2) increased significantly after spinal anesthesia only at T11, and was increased by oxygen administration at both T3 and T11.	Trichloroepoxypropane	9-13	CD2 molecule	Homo sapiens	136-139
17680181-10	2007	RESULTS: TcPO(2) increased significantly after spinal anesthesia only at T11, and was increased by oxygen administration at both T3 and T11.	Oxygen	99-105	CD2 molecule	Homo sapiens	136-139
17680181-11	2007	The increase of tcPO(2) after oxygen administration was larger at T3 than T11, without any differences in absolute values.	Trichloroepoxypropane	16-20	CD2 molecule	Homo sapiens	74-77
17680181-11	2007	The increase of tcPO(2) after oxygen administration was larger at T3 than T11, without any differences in absolute values.	Oxygen	30-36	CD2 molecule	Homo sapiens	74-77
16941565-1	2006	The cytoplasmic region of the CD2 receptor of lymphocytes contains proline-rich motifs, which are involved in T cell activation and interleukin-2 production.	Proline	67-74	CD2 molecule	Homo sapiens	30-33
17969635-3	2007	The results indicated that the Cd2+ could be efficiently removed using MnO2 loaded D301 resin in the pH range of 3-8 from aqueous solutions with the co-existence of high concentration of alkali and alkaline-earth metals ions.	manganese dioxide	71-75	CD2 molecule	Homo sapiens	31-34
17969635-3	2007	The results indicated that the Cd2+ could be efficiently removed using MnO2 loaded D301 resin in the pH range of 3-8 from aqueous solutions with the co-existence of high concentration of alkali and alkaline-earth metals ions.	benzoxonium chloride	83-87	CD2 molecule	Homo sapiens	31-34
17885889-1	2007	The soluble E-receptor (SER) of lymphocytes that is related to CD2 was detected in human plasma and serum using immunoelectrophoresis with sheep antiserum.	Serine	24-27	CD2 molecule	Homo sapiens	63-66
16989853-0	2006	Study of the selection mechanism of heavy metal (Pb2+, Cu2+, Ni2+, and Cd2+) adsorption on clinoptilolite.	clinoptilolite	91-105	CD2 molecule	Homo sapiens	71-74
16989853-1	2006	The study was carried out on the sorption of heavy metals (Ni2+, Cu2+, Pb2+, and Cd2+) under static conditions from single- and multicomponent aqueous solutions by raw and pretreated clinoptilolite.	clinoptilolite	183-197	CD2 molecule	Homo sapiens	81-84
16989853-6	2006	The maximum sorption capacity toward Cd2+ is determined as 4.22 mg/g at an initial concentration of 80 mg/L and toward Pb2+, Cu2+, and Ni2+ as 27.7, 25.76, and 13.03 mg/g at 800 mg/L.	Lead	119-123	CD2 molecule	Homo sapiens	37-40
16989853-6	2006	The maximum sorption capacity toward Cd2+ is determined as 4.22 mg/g at an initial concentration of 80 mg/L and toward Pb2+, Cu2+, and Ni2+ as 27.7, 25.76, and 13.03 mg/g at 800 mg/L.	cupric ion	125-129	CD2 molecule	Homo sapiens	37-40
16989853-6	2006	The maximum sorption capacity toward Cd2+ is determined as 4.22 mg/g at an initial concentration of 80 mg/L and toward Pb2+, Cu2+, and Ni2+ as 27.7, 25.76, and 13.03 mg/g at 800 mg/L.	Nickel(2+)	135-139	CD2 molecule	Homo sapiens	37-40
17256349-2	2006	GMA-IDA chelating groups which are grafted onto the poly(propylene) fibers are the coordination sites for chelating Cd+2, on which nano-sized CdS nanocrystals grew.	Polypropylenes	52-67	CD2 molecule	Homo sapiens	116-120
16753198-0	2006	Characterization of H+ and Cd2+ binding properties of the bacterial exopolysaccharides.	exopolysaccharides	68-86	CD2 molecule	Homo sapiens	27-30
16928378-3	2006	Of the three cations investigated, Ni2+ had the highest sorption affinity, followed by Cd2+ and Co2+.	Nickel(2+)	35-39	CD2 molecule	Homo sapiens	87-90
17102865-5	2006	However, the Cd2+ complex with [17](DBF)N2O2 exhibits the highest value of stability constant for the whole series of metal ions studied, indicating that this ligand reveals a remarkable selectivity for cadmium(II) in the presence of all the metal ions studied, except copper(II), indicating that this ligand reveals a remarkable selectivity for cadmium(II) in the presence of the mentioned metal ions.	[17](dbf)n2o2	31-44	CD2 molecule	Homo sapiens	13-16
17102865-5	2006	However, the Cd2+ complex with [17](DBF)N2O2 exhibits the highest value of stability constant for the whole series of metal ions studied, indicating that this ligand reveals a remarkable selectivity for cadmium(II) in the presence of all the metal ions studied, except copper(II), indicating that this ligand reveals a remarkable selectivity for cadmium(II) in the presence of the mentioned metal ions.	Metals	118-123	CD2 molecule	Homo sapiens	13-16
17102865-5	2006	However, the Cd2+ complex with [17](DBF)N2O2 exhibits the highest value of stability constant for the whole series of metal ions studied, indicating that this ligand reveals a remarkable selectivity for cadmium(II) in the presence of all the metal ions studied, except copper(II), indicating that this ligand reveals a remarkable selectivity for cadmium(II) in the presence of the mentioned metal ions.	Cadmium	203-210	CD2 molecule	Homo sapiens	13-16
17102865-5	2006	However, the Cd2+ complex with [17](DBF)N2O2 exhibits the highest value of stability constant for the whole series of metal ions studied, indicating that this ligand reveals a remarkable selectivity for cadmium(II) in the presence of all the metal ions studied, except copper(II), indicating that this ligand reveals a remarkable selectivity for cadmium(II) in the presence of the mentioned metal ions.	Metals	242-247	CD2 molecule	Homo sapiens	13-16
17102865-5	2006	However, the Cd2+ complex with [17](DBF)N2O2 exhibits the highest value of stability constant for the whole series of metal ions studied, indicating that this ligand reveals a remarkable selectivity for cadmium(II) in the presence of all the metal ions studied, except copper(II), indicating that this ligand reveals a remarkable selectivity for cadmium(II) in the presence of the mentioned metal ions.	Copper	269-275	CD2 molecule	Homo sapiens	13-16
17102865-5	2006	However, the Cd2+ complex with [17](DBF)N2O2 exhibits the highest value of stability constant for the whole series of metal ions studied, indicating that this ligand reveals a remarkable selectivity for cadmium(II) in the presence of all the metal ions studied, except copper(II), indicating that this ligand reveals a remarkable selectivity for cadmium(II) in the presence of the mentioned metal ions.	Cadmium	346-353	CD2 molecule	Homo sapiens	13-16
17102865-5	2006	However, the Cd2+ complex with [17](DBF)N2O2 exhibits the highest value of stability constant for the whole series of metal ions studied, indicating that this ligand reveals a remarkable selectivity for cadmium(II) in the presence of all the metal ions studied, except copper(II), indicating that this ligand reveals a remarkable selectivity for cadmium(II) in the presence of the mentioned metal ions.	Metals	242-247	CD2 molecule	Homo sapiens	13-16
17102865-7	2006	The Cd2+ ion fits exactly inside the macrocyclic cavity exhibiting coordination number eight by coordination to all the donor atoms of the ligand, and additionally to two oxygen atoms from one nitrate anion and one oxygen atom from a water molecule.	Oxygen	171-177	CD2 molecule	Homo sapiens	4-7
17102865-7	2006	The Cd2+ ion fits exactly inside the macrocyclic cavity exhibiting coordination number eight by coordination to all the donor atoms of the ligand, and additionally to two oxygen atoms from one nitrate anion and one oxygen atom from a water molecule.	punky blue	193-206	CD2 molecule	Homo sapiens	4-7
17102865-7	2006	The Cd2+ ion fits exactly inside the macrocyclic cavity exhibiting coordination number eight by coordination to all the donor atoms of the ligand, and additionally to two oxygen atoms from one nitrate anion and one oxygen atom from a water molecule.	Oxygen	215-221	CD2 molecule	Homo sapiens	4-7
17102865-7	2006	The Cd2+ ion fits exactly inside the macrocyclic cavity exhibiting coordination number eight by coordination to all the donor atoms of the ligand, and additionally to two oxygen atoms from one nitrate anion and one oxygen atom from a water molecule.	Water	234-239	CD2 molecule	Homo sapiens	4-7
16914250-6	2006	Entry via Zn2+, Fe2+, and Ca2+ transporters is the molecular basis of Cd2+ uptake into plant cells.	Zinc	10-14	CD2 molecule	Homo sapiens	70-73
16850851-5	2006	Compared with the total adsorption, the desorptive percentage of the adsorped Cd2+ in the phaeozem and burozem was in a low extent, which was ranged within rate of 9.0% and 15.1% respectively.	burozem	103-110	CD2 molecule	Homo sapiens	78-81
17144258-3	2006	Batch sorption analyses have confirmed that the Al-substituted 11 A tobermorite-bearing product is an effective sorbent for Co2+, Cd2+ and Zn2+ ions from acidified aqueous media.	Aluminum	48-50	CD2 molecule	Homo sapiens	130-133
17144258-3	2006	Batch sorption analyses have confirmed that the Al-substituted 11 A tobermorite-bearing product is an effective sorbent for Co2+, Cd2+ and Zn2+ ions from acidified aqueous media.	tobermorite	68-79	CD2 molecule	Homo sapiens	130-133
16721869-3	2006	In 1, the Cd1, Cd3, and Cd4 atoms are all pentacoordinate, while the Cd2 atom is coordinated by four oxygen atoms from three phosphonate ligands and two nitrogen atoms from the chelating phen in a distorted octahedral geometry.	Oxygen	101-107	CD2 molecule	Homo sapiens	69-72
16721869-3	2006	In 1, the Cd1, Cd3, and Cd4 atoms are all pentacoordinate, while the Cd2 atom is coordinated by four oxygen atoms from three phosphonate ligands and two nitrogen atoms from the chelating phen in a distorted octahedral geometry.	Nitrogen	153-161	CD2 molecule	Homo sapiens	69-72
16724074-5	2006	Transfection of PBMC with constructs containing the -179G or -179T site revealed CD2-mediated enhancement of the -179T compared to -179G allele, although, in LPMC, a similar level of expression was detected.	lpmc	158-162	CD2 molecule	Homo sapiens	81-84
16709846-4	2006	PreBCR complexes retained in the TGN or shunted from the TGN to lysosomes were as or 50% as active as the corresponding wild-type preBCRs in directing preBCR-dependent events, including CD2 and CD22 expression and proliferation in primary pro-B cells.	Arsenic	79-81	CD2 molecule	Homo sapiens	186-189
17059770-16	2006	The expression of CD2 is higher in M4Eo.	m4eo	35-39	CD2 molecule	Homo sapiens	18-21
16621248-0	2006	Cu2+, Cd2+ and Pb2+ adsorption from aqueous solutions by pyrite and synthetic iron sulphide.	pyrite	57-63	CD2 molecule	Homo sapiens	6-9
16621248-0	2006	Cu2+, Cd2+ and Pb2+ adsorption from aqueous solutions by pyrite and synthetic iron sulphide.	ferrous sulfide	78-91	CD2 molecule	Homo sapiens	6-9
16808486-3	2006	In this paper, the decomposition of Cd2+ complex with 4-(2-pyridylazo)resorcinol has been tested, and its decomposition kinetics has been studied.	4-(2-pyridylazo)resorcinol	54-80	CD2 molecule	Homo sapiens	36-39
16732662-3	2006	Four moieties of the DPPC molecule are probed by BBSFG: the terminal methyl (CD3) groups of the tails, the methylene (CD2) groups of the tails, the choline methyls (CH3) in the headgroup, and the phosphate in the headgroup.	1,2-Dipalmitoylphosphatidylcholine	21-25	CD2 molecule	Homo sapiens	118-121
16488017-0	2006	Selective transport of Pb2+ and Cd2+ across a phospholipid bilayer by a cyclohexanemonocarboxylic acid-capped 15-crown-5 ether.	Phospholipids	46-58	CD2 molecule	Homo sapiens	32-35
16608287-2	2006	Uncoated Qdots made of core/shell CdSe/ZnS are toxic to cells because of the release of Cd2+ ions into the cellular environment.	cdse	34-38	CD2 molecule	Homo sapiens	88-91
16608287-2	2006	Uncoated Qdots made of core/shell CdSe/ZnS are toxic to cells because of the release of Cd2+ ions into the cellular environment.	Zinc	39-42	CD2 molecule	Homo sapiens	88-91
16548613-2	2006	The principle is based on a combination of top-down and bottom-up approaches in which a transmission electron microscope grid is placed on a poly(vinylpyrrolidone) film containing Cd2+ ions, which is then exposed to H2S gas.	Povidone	141-163	CD2 molecule	Homo sapiens	180-183
16548613-2	2006	The principle is based on a combination of top-down and bottom-up approaches in which a transmission electron microscope grid is placed on a poly(vinylpyrrolidone) film containing Cd2+ ions, which is then exposed to H2S gas.	Hydrogen Sulfide	216-219	CD2 molecule	Homo sapiens	180-183
16488017-0	2006	Selective transport of Pb2+ and Cd2+ across a phospholipid bilayer by a cyclohexanemonocarboxylic acid-capped 15-crown-5 ether.	cyclohexanemonocarboxylic acid-capped	72-109	CD2 molecule	Homo sapiens	32-35
16488017-0	2006	Selective transport of Pb2+ and Cd2+ across a phospholipid bilayer by a cyclohexanemonocarboxylic acid-capped 15-crown-5 ether.	15-crown-5	110-126	CD2 molecule	Homo sapiens	32-35
16488017-1	2006	A cyclohexanemonocarboxylic acid-capped 15-crown-5 ether was synthesized and found to be effective as an ionophore for Pb2+ and Cd2+, transporting them across a phospholipid bilayer membrane.	cyclohexanemonocarboxylic acid	2-32	CD2 molecule	Homo sapiens	128-131
16283201-2	2006	Introduction ofa cadmium (Cd2+)-binding site in the external vestibule of Kv2.1 (drk1), allowed us to functionally characterize a binding site for external monovalent cations.	Cadmium	17-24	CD2 molecule	Homo sapiens	26-29
16283201-4	2006	Point mutations identified the highly conserved aspartate residue immediately following the selectivity filter as a critical determinant of the antagonism between external K+ and Cd2+ ions.	Aspartic Acid	48-57	CD2 molecule	Homo sapiens	179-182
16283201-7	2006	Reducing the Rb+ conductance by mutating the selectivity filter to the sequence found inKv4.1, also significantly reduced the effectiveness ofRb+ ions to antagonize Cd2+ inhibition, thereby implicating the selectivity filter as the site at which K+ions exert their antagonistic effect on Cd2+ block.	Rubidium	13-16	CD2 molecule	Homo sapiens	165-168
16283201-7	2006	Reducing the Rb+ conductance by mutating the selectivity filter to the sequence found inKv4.1, also significantly reduced the effectiveness ofRb+ ions to antagonize Cd2+ inhibition, thereby implicating the selectivity filter as the site at which K+ions exert their antagonistic effect on Cd2+ block.	Rubidium	13-16	CD2 molecule	Homo sapiens	288-291
16488017-1	2006	A cyclohexanemonocarboxylic acid-capped 15-crown-5 ether was synthesized and found to be effective as an ionophore for Pb2+ and Cd2+, transporting them across a phospholipid bilayer membrane.	15-crown-5	40-56	CD2 molecule	Homo sapiens	128-131
16488017-1	2006	A cyclohexanemonocarboxylic acid-capped 15-crown-5 ether was synthesized and found to be effective as an ionophore for Pb2+ and Cd2+, transporting them across a phospholipid bilayer membrane.	Phospholipids	161-173	CD2 molecule	Homo sapiens	128-131
16488017-3	2006	Data obtained at pH 7.0 using this system, show that the synthetic ionophore transports divalent cations with the selectivity sequence Pb2+ > Cd2+ >> Zn2+ > Mn2+ > Co2+ > Ni2+ > Ca2+ > Sr2+.	Lead	135-139	CD2 molecule	Homo sapiens	145-148
16488017-3	2006	Data obtained at pH 7.0 using this system, show that the synthetic ionophore transports divalent cations with the selectivity sequence Pb2+ > Cd2+ >> Zn2+ > Mn2+ > Co2+ > Ni2+ > Ca2+ > Sr2+.	Zinc	159-163	CD2 molecule	Homo sapiens	145-148
16488017-3	2006	Data obtained at pH 7.0 using this system, show that the synthetic ionophore transports divalent cations with the selectivity sequence Pb2+ > Cd2+ >> Zn2+ > Mn2+ > Co2+ > Ni2+ > Ca2+ > Sr2+.	Manganese(2+)	169-173	CD2 molecule	Homo sapiens	145-148
16488017-3	2006	Data obtained at pH 7.0 using this system, show that the synthetic ionophore transports divalent cations with the selectivity sequence Pb2+ > Cd2+ >> Zn2+ > Mn2+ > Co2+ > Ni2+ > Ca2+ > Sr2+.	Cobalt(2+)	179-183	CD2 molecule	Homo sapiens	145-148
16488017-3	2006	Data obtained at pH 7.0 using this system, show that the synthetic ionophore transports divalent cations with the selectivity sequence Pb2+ > Cd2+ >> Zn2+ > Mn2+ > Co2+ > Ni2+ > Ca2+ > Sr2+.	Nickel(2+)	189-193	CD2 molecule	Homo sapiens	145-148
16488017-3	2006	Data obtained at pH 7.0 using this system, show that the synthetic ionophore transports divalent cations with the selectivity sequence Pb2+ > Cd2+ >> Zn2+ > Mn2+ > Co2+ > Ni2+ > Ca2+ > Sr2+.	strontium cation	209-213	CD2 molecule	Homo sapiens	145-148
16488017-8	2006	The high selectivity for Pb2+ and Cd2+ displayed by the cyclohexanecarboxylic acid-capped 15-crown-5 ether suggests potential applications of this ionophore for the treatment of Pb and Cd intoxication, and removal of these heavy metals from wastewater.	cyclohexanecarboxylic acid	56-82	CD2 molecule	Homo sapiens	34-37
16488017-8	2006	The high selectivity for Pb2+ and Cd2+ displayed by the cyclohexanecarboxylic acid-capped 15-crown-5 ether suggests potential applications of this ionophore for the treatment of Pb and Cd intoxication, and removal of these heavy metals from wastewater.	15-crown-5	90-106	CD2 molecule	Homo sapiens	34-37
16450024-5	2006	Following alternating droplet generation, the channel geometry allows the exclusive fusion of alternate droplets with concomitant rapid mixing and produces supersaturated solution of Cd2+ and S2- ions to form CdS nanoparticles in each fused droplet.	Cadmium	209-212	CD2 molecule	Homo sapiens	183-186
16458199-1	2006	Cadmium (Cd2+) is a highly toxic metal that affects the endocrine system.	Cadmium	0-7	CD2 molecule	Homo sapiens	9-12
16458199-1	2006	Cadmium (Cd2+) is a highly toxic metal that affects the endocrine system.	Metals	33-38	CD2 molecule	Homo sapiens	9-12
16458199-2	2006	We have previously shown that Cd2+ induces caspase-3 activation and apoptosis of anterior pituitary cells and that endogenous nitric oxide (NO) protects these cells from Cd2+.	Nitric Oxide	126-138	CD2 molecule	Homo sapiens	170-173
16458199-5	2006	Cd2+-induced apoptosis was mitochondrial dependent since cyclosporin A protected the cells from this metal.	Cyclosporine	57-70	CD2 molecule	Homo sapiens	0-3
16458199-5	2006	Cd2+-induced apoptosis was mitochondrial dependent since cyclosporin A protected the cells from this metal.	Metals	101-106	CD2 molecule	Homo sapiens	0-3
16458199-6	2006	Inhibition of NO synthesis with 0.5 mM L-NAME increased the effect of Cd2+ on MMP, whereas the NO donor DETANONOate (0.1 mM) reduced it.	NG-Nitroarginine Methyl Ester	39-45	CD2 molecule	Homo sapiens	70-73
16458199-7	2006	Cd2+ increased the production of reactive oxygen species (ROS) as measured by flow cytometry.	Reactive Oxygen Species	33-56	CD2 molecule	Homo sapiens	0-3
16458199-7	2006	Cd2+ increased the production of reactive oxygen species (ROS) as measured by flow cytometry.	Reactive Oxygen Species	58-61	CD2 molecule	Homo sapiens	0-3
16458199-10	2006	The action of Cd2+ on mitochondrial integrity was ROS dependent.	Reactive Oxygen Species	50-53	CD2 molecule	Homo sapiens	14-17
16458199-12	2006	Cd2+-induced increase in ROS generation was reduced by DETANONOate.	Reactive Oxygen Species	25-28	CD2 molecule	Homo sapiens	0-3
16458199-12	2006	Cd2+-induced increase in ROS generation was reduced by DETANONOate.	2,2'-(hydroxynitrosohydrazono)bis-ethanamine	55-66	CD2 molecule	Homo sapiens	0-3
16343515-0	2006	Direct fluorescence detection of Pb2+ and Cd2+ by high-performance liquid chromatography using 1-(4-aminobenzyl)ethylenediamine-N,N,N",N"-tetraacetate as a pre-column derivatizing agent.	1-(4-aminobenzyl)ethylenediamine-N,N,N',N'-tetraacetate	95-150	CD2 molecule	Homo sapiens	42-45
16343515-1	2006	A highly sensitive HPLC with direct fluorescent detection (lambda(ex) = 235 nm, lambda(em) = 355 nm) was developed for Pb2+ and Cd2+ complexes with an aromatic polyaminocarboxylate, 1-(4-aminobenzyl)ethylenediamine-N,N,N",N"-tetraacetate as a pre-column derivatizing agent.	aromatic polyaminocarboxylate	151-180	CD2 molecule	Homo sapiens	128-131
16343515-1	2006	A highly sensitive HPLC with direct fluorescent detection (lambda(ex) = 235 nm, lambda(em) = 355 nm) was developed for Pb2+ and Cd2+ complexes with an aromatic polyaminocarboxylate, 1-(4-aminobenzyl)ethylenediamine-N,N,N",N"-tetraacetate as a pre-column derivatizing agent.	1-(4-aminobenzyl)ethylenediamine-N,N,N',N'-tetraacetate	182-237	CD2 molecule	Homo sapiens	128-131
16266835-7	2006	Complementary studies with Cd2+ ions cause perturbations to 1H NMR spectra that are strikingly similar to that observed for Zn2+.	Hydrogen	60-62	CD2 molecule	Homo sapiens	27-30
16266835-7	2006	Complementary studies with Cd2+ ions cause perturbations to 1H NMR spectra that are strikingly similar to that observed for Zn2+.	Zinc	124-128	CD2 molecule	Homo sapiens	27-30
17206012-1	2006	An 1H NMR (nuclear magnetic resonance) spectroscopic structural analysis of Cd2+ complexes formed with the pentapeptide phytochelatin, (NH3)+-(gamma-Glu-Cys)2-Gly-COO- (PC2), at a pH of 7.5 showed that the two thiol groups of the Cys residues and either the carbonyl or amide group of the peptide bond between Glu1 and Cys1 act as possible donor groups in the complexes at Cd2+/PC2 ratios up to 0.4.	Hydrogen	3-5	CD2 molecule	Homo sapiens	76-79
16280379-1	2006	Cadmium (Cd2+) is known to cause a selective disruption of the filamentous actin cytoskeleton in the smooth muscle-like renal mesangial cell.	Cadmium	0-7	CD2 molecule	Homo sapiens	9-12
16341850-1	2006	A novel and low-cost optical sensor for the naked eye detection of Cd2+ in aqueous media based on mesoporous silica containing 4-(2-pyridylazo)resorcinol (PAR) as a probe molecule anchored by N-trimethoxysilylpropyl-N,N,N-trimethylammonium chloride (TMAC) was prepared.	Silicon Dioxide	109-115	CD2 molecule	Homo sapiens	67-70
16341850-1	2006	A novel and low-cost optical sensor for the naked eye detection of Cd2+ in aqueous media based on mesoporous silica containing 4-(2-pyridylazo)resorcinol (PAR) as a probe molecule anchored by N-trimethoxysilylpropyl-N,N,N-trimethylammonium chloride (TMAC) was prepared.	4-(2-pyridylazo)resorcinol	127-153	CD2 molecule	Homo sapiens	67-70
16341850-1	2006	A novel and low-cost optical sensor for the naked eye detection of Cd2+ in aqueous media based on mesoporous silica containing 4-(2-pyridylazo)resorcinol (PAR) as a probe molecule anchored by N-trimethoxysilylpropyl-N,N,N-trimethylammonium chloride (TMAC) was prepared.	4-(2-pyridylazo)resorcinol	155-158	CD2 molecule	Homo sapiens	67-70
16341850-1	2006	A novel and low-cost optical sensor for the naked eye detection of Cd2+ in aqueous media based on mesoporous silica containing 4-(2-pyridylazo)resorcinol (PAR) as a probe molecule anchored by N-trimethoxysilylpropyl-N,N,N-trimethylammonium chloride (TMAC) was prepared.	trimethyl-(3-(trimethoxysilyl)propyl)ammonium	192-248	CD2 molecule	Homo sapiens	67-70
16341850-1	2006	A novel and low-cost optical sensor for the naked eye detection of Cd2+ in aqueous media based on mesoporous silica containing 4-(2-pyridylazo)resorcinol (PAR) as a probe molecule anchored by N-trimethoxysilylpropyl-N,N,N-trimethylammonium chloride (TMAC) was prepared.	trimethyl-(3-(trimethoxysilyl)propyl)ammonium	250-254	CD2 molecule	Homo sapiens	67-70
16341850-4	2006	The intensity of the Cd-PAR complex varies linearly with the Cd2+ concentration, from zero to 1.78x10(-7) mol dm(-3).	cd-par	21-27	CD2 molecule	Homo sapiens	61-64
16341850-5	2006	The detection and quantification limits for the method when determining Cd2+ were 1.75x10(-8) and 5.77x10(-8) mol dm(-3), respectively, with a correlation coefficient of 0.99.	dm	114-116	CD2 molecule	Homo sapiens	72-75
17206012-1	2006	An 1H NMR (nuclear magnetic resonance) spectroscopic structural analysis of Cd2+ complexes formed with the pentapeptide phytochelatin, (NH3)+-(gamma-Glu-Cys)2-Gly-COO- (PC2), at a pH of 7.5 showed that the two thiol groups of the Cys residues and either the carbonyl or amide group of the peptide bond between Glu1 and Cys1 act as possible donor groups in the complexes at Cd2+/PC2 ratios up to 0.4.	Amides	270-275	CD2 molecule	Homo sapiens	76-79
17206012-1	2006	An 1H NMR (nuclear magnetic resonance) spectroscopic structural analysis of Cd2+ complexes formed with the pentapeptide phytochelatin, (NH3)+-(gamma-Glu-Cys)2-Gly-COO- (PC2), at a pH of 7.5 showed that the two thiol groups of the Cys residues and either the carbonyl or amide group of the peptide bond between Glu1 and Cys1 act as possible donor groups in the complexes at Cd2+/PC2 ratios up to 0.4.	phytochelatin 2	378-381	CD2 molecule	Homo sapiens	76-79
17206012-3	2006	The manner in which Cd2+ forms complexes with PC2 is distinctly different from Zn2+ and might account for the role of phytochelatin in Cd2+ detoxification.	phytochelatin 2	46-49	CD2 molecule	Homo sapiens	20-23
17206012-3	2006	The manner in which Cd2+ forms complexes with PC2 is distinctly different from Zn2+ and might account for the role of phytochelatin in Cd2+ detoxification.	phytochelatin 2	46-49	CD2 molecule	Homo sapiens	135-138
17206012-4	2006	Electron absorption spectrometry demonstrated that the Cd2+ complexes are coordinated in a tetrahedral fashion by four thiol groups and that several sulfur atoms might bridge Cd2+ ions, resulting in the formation of polynuclear complexes.	Sulfhydryl Compounds	119-124	CD2 molecule	Homo sapiens	55-58
17206012-4	2006	Electron absorption spectrometry demonstrated that the Cd2+ complexes are coordinated in a tetrahedral fashion by four thiol groups and that several sulfur atoms might bridge Cd2+ ions, resulting in the formation of polynuclear complexes.	Sulfur	149-155	CD2 molecule	Homo sapiens	55-58
17206012-4	2006	Electron absorption spectrometry demonstrated that the Cd2+ complexes are coordinated in a tetrahedral fashion by four thiol groups and that several sulfur atoms might bridge Cd2+ ions, resulting in the formation of polynuclear complexes.	Sulfur	149-155	CD2 molecule	Homo sapiens	175-178
17206012-1	2006	An 1H NMR (nuclear magnetic resonance) spectroscopic structural analysis of Cd2+ complexes formed with the pentapeptide phytochelatin, (NH3)+-(gamma-Glu-Cys)2-Gly-COO- (PC2), at a pH of 7.5 showed that the two thiol groups of the Cys residues and either the carbonyl or amide group of the peptide bond between Glu1 and Cys1 act as possible donor groups in the complexes at Cd2+/PC2 ratios up to 0.4.	Ammonia	135-141	CD2 molecule	Homo sapiens	76-79
17206012-1	2006	An 1H NMR (nuclear magnetic resonance) spectroscopic structural analysis of Cd2+ complexes formed with the pentapeptide phytochelatin, (NH3)+-(gamma-Glu-Cys)2-Gly-COO- (PC2), at a pH of 7.5 showed that the two thiol groups of the Cys residues and either the carbonyl or amide group of the peptide bond between Glu1 and Cys1 act as possible donor groups in the complexes at Cd2+/PC2 ratios up to 0.4.	phytochelatin 2	169-172	CD2 molecule	Homo sapiens	76-79
17206012-1	2006	An 1H NMR (nuclear magnetic resonance) spectroscopic structural analysis of Cd2+ complexes formed with the pentapeptide phytochelatin, (NH3)+-(gamma-Glu-Cys)2-Gly-COO- (PC2), at a pH of 7.5 showed that the two thiol groups of the Cys residues and either the carbonyl or amide group of the peptide bond between Glu1 and Cys1 act as possible donor groups in the complexes at Cd2+/PC2 ratios up to 0.4.	Sulfhydryl Compounds	210-215	CD2 molecule	Homo sapiens	76-79
17206012-1	2006	An 1H NMR (nuclear magnetic resonance) spectroscopic structural analysis of Cd2+ complexes formed with the pentapeptide phytochelatin, (NH3)+-(gamma-Glu-Cys)2-Gly-COO- (PC2), at a pH of 7.5 showed that the two thiol groups of the Cys residues and either the carbonyl or amide group of the peptide bond between Glu1 and Cys1 act as possible donor groups in the complexes at Cd2+/PC2 ratios up to 0.4.	Cysteine	153-156	CD2 molecule	Homo sapiens	76-79
16515197-1	2005	The study on the thermodynamics and kinetics of Cd2+ adsorption in phaeozem and burozem showed that within the test range, Cd2+ adsorption was increased with its increasing initial concentration, and phaeozem had a much higher Cd2+ adsorption capacity than burozem.	phaeozem	67-75	CD2 molecule	Homo sapiens	48-51
16183644-4	2005	In the present study, we report the three-dimensional solution structures of the three CDs (CD1, CD2, and CD3) using a variety of triple resonance NMR experiments.	cds	87-90	CD2 molecule	Homo sapiens	97-100
16515197-1	2005	The study on the thermodynamics and kinetics of Cd2+ adsorption in phaeozem and burozem showed that within the test range, Cd2+ adsorption was increased with its increasing initial concentration, and phaeozem had a much higher Cd2+ adsorption capacity than burozem.	phaeozem	67-75	CD2 molecule	Homo sapiens	123-126
16515197-1	2005	The study on the thermodynamics and kinetics of Cd2+ adsorption in phaeozem and burozem showed that within the test range, Cd2+ adsorption was increased with its increasing initial concentration, and phaeozem had a much higher Cd2+ adsorption capacity than burozem.	phaeozem	67-75	CD2 molecule	Homo sapiens	123-126
16515197-1	2005	The study on the thermodynamics and kinetics of Cd2+ adsorption in phaeozem and burozem showed that within the test range, Cd2+ adsorption was increased with its increasing initial concentration, and phaeozem had a much higher Cd2+ adsorption capacity than burozem.	burozem	80-87	CD2 molecule	Homo sapiens	123-126
16515197-1	2005	The study on the thermodynamics and kinetics of Cd2+ adsorption in phaeozem and burozem showed that within the test range, Cd2+ adsorption was increased with its increasing initial concentration, and phaeozem had a much higher Cd2+ adsorption capacity than burozem.	burozem	80-87	CD2 molecule	Homo sapiens	123-126
16515197-1	2005	The study on the thermodynamics and kinetics of Cd2+ adsorption in phaeozem and burozem showed that within the test range, Cd2+ adsorption was increased with its increasing initial concentration, and phaeozem had a much higher Cd2+ adsorption capacity than burozem.	phaeozem	200-208	CD2 molecule	Homo sapiens	48-51
16515197-1	2005	The study on the thermodynamics and kinetics of Cd2+ adsorption in phaeozem and burozem showed that within the test range, Cd2+ adsorption was increased with its increasing initial concentration, and phaeozem had a much higher Cd2+ adsorption capacity than burozem.	burozem	257-264	CD2 molecule	Homo sapiens	123-126
16515197-1	2005	The study on the thermodynamics and kinetics of Cd2+ adsorption in phaeozem and burozem showed that within the test range, Cd2+ adsorption was increased with its increasing initial concentration, and phaeozem had a much higher Cd2+ adsorption capacity than burozem.	burozem	257-264	CD2 molecule	Homo sapiens	123-126
16515197-2	2005	When the Cd2+ concentration in adsorption equilibrium was 20 mg x kg(-1), the amount of adsorbed Cd2+ was 1 485.2 mg x kg(-1) in phaeozem, but 700.6 mg x kg(-1) in burozem.	phaeozem	129-137	CD2 molecule	Homo sapiens	9-12
16515197-2	2005	When the Cd2+ concentration in adsorption equilibrium was 20 mg x kg(-1), the amount of adsorbed Cd2+ was 1 485.2 mg x kg(-1) in phaeozem, but 700.6 mg x kg(-1) in burozem.	phaeozem	129-137	CD2 molecule	Homo sapiens	97-100
16515197-2	2005	When the Cd2+ concentration in adsorption equilibrium was 20 mg x kg(-1), the amount of adsorbed Cd2+ was 1 485.2 mg x kg(-1) in phaeozem, but 700.6 mg x kg(-1) in burozem.	burozem	164-171	CD2 molecule	Homo sapiens	9-12
16515197-2	2005	When the Cd2+ concentration in adsorption equilibrium was 20 mg x kg(-1), the amount of adsorbed Cd2+ was 1 485.2 mg x kg(-1) in phaeozem, but 700.6 mg x kg(-1) in burozem.	burozem	164-171	CD2 molecule	Homo sapiens	97-100
16515197-4	2005	The maximum adsorption of Cd2+ in phaeozem and burozem was 5939.3 and 2 790 mg x kg(-1), respectively, according to Langmuir formulation.	burozem	47-54	CD2 molecule	Homo sapiens	26-29
16515197-8	2005	Under low concentrations of Cd2+, the decrease of its adsorption rate with time was more quickly in phaeozem than in burozem.	burozem	117-124	CD2 molecule	Homo sapiens	28-31
16853468-8	2005	At neutral pH, L1 fluorescence decreases upon addition of Zn2+ or Cd2+ because of a formation of metal-anthracene pi complex.	metal-anthracene	97-113	CD2 molecule	Homo sapiens	66-69
16215756-10	2005	The analytical performance of bismuth-film electrodes for anodic stripping voltammetry of heavy metals was evaluated for non-deaerated solutions containing Cd2+, Pb2+, and Zn2+ ions.	Bismuth	30-37	CD2 molecule	Homo sapiens	156-159
16215756-12	2005	Linear calibration plots were obtained for Cd2+ in acidified tap water at concentrations ranging from 2 x 10(-8) to 1 x 10(-7) mol L(-1) and from 1 x 10(-7) to 1 x 10(-6) mol L(-1) with relative standard deviations of 5% (n = 15) at the 1 x 10(-7) mol L(-1) level.	Water	65-70	CD2 molecule	Homo sapiens	43-46
16124830-1	2005	The sterically crowded isoindoline pincer ligand, 6"-MeLH, prepared by condensation of 4-methyl-2-aminopyridine and phthalonitrile, exhibits very different reaction chemistry with Cd2+, Zn2+, and Pd2+.	2-(3-hydroxypropyl)isoindoline-1,3-dione	23-34	CD2 molecule	Homo sapiens	180-183
16178910-7	2005	The CR rate of CD2- APL was 87.0% while that of CD2+ APL was 50 %.	Chromium	4-6	CD2 molecule	Homo sapiens	15-18
16177091-0	2005	Phosphotyrosine binding-mediated oligomerization of downstream of tyrosine kinase (Dok)-1 and Dok-2 is involved in CD2-induced Dok phosphorylation.	Phosphotyrosine	0-15	CD2 molecule	Homo sapiens	115-118
16177091-7	2005	Moreover, in CD2-stimulated Jurkat cells, Dok-1 coimmunoprecipitates with tyrosine-phosphorylated Dok-2.	Tyrosine	74-82	CD2 molecule	Homo sapiens	13-16
32397051-5	2005	The results of experiments and calculations lead us to the conclusion that the observed Cd2+ emission bands are due to the triplet-singlet transitions from the Cd s-states to the nearest fluorine ions.	Fluorine	187-195	CD2 molecule	Homo sapiens	88-91
16190751-5	2005	The 12-amino acid synthetic cyclic peptides effectively blocked the interaction between CD2 and CD58 proteins as demonstrated by E-rosetting and heterotypic adhesion assays.	12-amino acid	4-17	CD2 molecule	Homo sapiens	88-91
16190751-5	2005	The 12-amino acid synthetic cyclic peptides effectively blocked the interaction between CD2 and CD58 proteins as demonstrated by E-rosetting and heterotypic adhesion assays.	Peptides, Cyclic	28-43	CD2 molecule	Homo sapiens	88-91
16217830-4	2005	For example, in comparison with single CD1, dual CDs can enhance Deltamu and alpha up to the maximum value when enantiomers migrate with the same order in CD1 and CD2, and have the value of rho > 1.0, where rho is the enantioselectivity ratio for CD2 to CD1, while worse Deltamu and alpha are obtained for enantiomers with rho < 1.0.	Cadmium	49-52	CD2 molecule	Homo sapiens	163-166
16217830-4	2005	For example, in comparison with single CD1, dual CDs can enhance Deltamu and alpha up to the maximum value when enantiomers migrate with the same order in CD1 and CD2, and have the value of rho > 1.0, where rho is the enantioselectivity ratio for CD2 to CD1, while worse Deltamu and alpha are obtained for enantiomers with rho < 1.0.	Cadmium	49-52	CD2 molecule	Homo sapiens	250-253
16124830-1	2005	The sterically crowded isoindoline pincer ligand, 6"-MeLH, prepared by condensation of 4-methyl-2-aminopyridine and phthalonitrile, exhibits very different reaction chemistry with Cd2+, Zn2+, and Pd2+.	6"-melh	50-57	CD2 molecule	Homo sapiens	180-183
16124830-1	2005	The sterically crowded isoindoline pincer ligand, 6"-MeLH, prepared by condensation of 4-methyl-2-aminopyridine and phthalonitrile, exhibits very different reaction chemistry with Cd2+, Zn2+, and Pd2+.	2-amino-4-picoline	87-111	CD2 molecule	Homo sapiens	180-183
16124830-1	2005	The sterically crowded isoindoline pincer ligand, 6"-MeLH, prepared by condensation of 4-methyl-2-aminopyridine and phthalonitrile, exhibits very different reaction chemistry with Cd2+, Zn2+, and Pd2+.	1,2-benzenedicarbonitrile	116-130	CD2 molecule	Homo sapiens	180-183
16124830-1	2005	The sterically crowded isoindoline pincer ligand, 6"-MeLH, prepared by condensation of 4-methyl-2-aminopyridine and phthalonitrile, exhibits very different reaction chemistry with Cd2+, Zn2+, and Pd2+.	PALLADIUM ION	196-200	CD2 molecule	Homo sapiens	180-183
16124830-3	2005	This isoindoline binds to Cd2+ as a charge-neutral, zwitterionic, bidentate ligand using imine and pyridine nitrogen atoms to form the eight-coordinate fluxional complex, Cd(6"-MeLH)2(NO3)2.	2-(3-hydroxypropyl)isoindoline-1,3-dione	5-16	CD2 molecule	Homo sapiens	26-29
16124830-3	2005	This isoindoline binds to Cd2+ as a charge-neutral, zwitterionic, bidentate ligand using imine and pyridine nitrogen atoms to form the eight-coordinate fluxional complex, Cd(6"-MeLH)2(NO3)2.	Imines	89-94	CD2 molecule	Homo sapiens	26-29
16124830-3	2005	This isoindoline binds to Cd2+ as a charge-neutral, zwitterionic, bidentate ligand using imine and pyridine nitrogen atoms to form the eight-coordinate fluxional complex, Cd(6"-MeLH)2(NO3)2.	pyridine	99-107	CD2 molecule	Homo sapiens	26-29
16124830-3	2005	This isoindoline binds to Cd2+ as a charge-neutral, zwitterionic, bidentate ligand using imine and pyridine nitrogen atoms to form the eight-coordinate fluxional complex, Cd(6"-MeLH)2(NO3)2.	Nitrogen	108-116	CD2 molecule	Homo sapiens	26-29
16124830-3	2005	This isoindoline binds to Cd2+ as a charge-neutral, zwitterionic, bidentate ligand using imine and pyridine nitrogen atoms to form the eight-coordinate fluxional complex, Cd(6"-MeLH)2(NO3)2.	cd(6"-melh)2(no3)2	171-189	CD2 molecule	Homo sapiens	26-29
15914164-3	2005	Equilibrium and kinetic adsorption data showed that ETS-10 displays a high selectivity toward one metal in a two-component or a three-component system with an affinity order of Pb2+ > Cd2+ > Cu2+.	ETS-10	52-58	CD2 molecule	Homo sapiens	187-190
16153116-1	2005	The Pb and Cd binding capacity of alginates were quantified by the determination of their complex stability constants and the concentration of complexing sites using H+, Pb2+, or Cd2+ selective electrodes in both static and dynamic titrations.	Alginates	34-43	CD2 molecule	Homo sapiens	179-182
16027135-3	2005	Ex vivo, the CD2-/lo cells can proliferate (carboxyfluorescein diacetate succinimidyl ester analysis) independently from exogenous stimulation, respond to CD3-mediated stimulation with significantly greater proliferation than the autologous mature cells and their subsets are inducible to undergo in vitro a developmental sequence similar to that reported for the phenotypically similar thymic populations.	5-(6)-carboxyfluorescein diacetate succinimidyl ester	44-91	CD2 molecule	Homo sapiens	13-16
16041429-0	2005	Axial bis(terpyridoxy)phosphorus(V) porphyrin: modulation of PET and EET by Zn2+ or Cd2+ ions.	bis(terpyridoxy)phosphorus	6-32	CD2 molecule	Homo sapiens	84-87
16041429-0	2005	Axial bis(terpyridoxy)phosphorus(V) porphyrin: modulation of PET and EET by Zn2+ or Cd2+ ions.	Porphyrins	36-45	CD2 molecule	Homo sapiens	84-87
15914164-0	2005	Competitive adsorption of Pb2+, Cu2+, and Cd2+ ions on microporous titanosilicate ETS-10.	titanosilicate	67-81	CD2 molecule	Homo sapiens	42-45
15914164-0	2005	Competitive adsorption of Pb2+, Cu2+, and Cd2+ ions on microporous titanosilicate ETS-10.	ETS-10	82-88	CD2 molecule	Homo sapiens	42-45
16477530-9	2005	Tail-current analysis reveals a differential effect of Cd2+ on Ca(v)3.3 channels, which can not close while the pore is occupied with this metal cation.	Metals	139-144	CD2 molecule	Homo sapiens	55-58
15892121-0	2005	Phase equilibrium in poly(rA).poly(rU) complexes with Cd2+ and Mg2+ ions, studied by ultraviolet, infrared, and vibrational circular dichroism spectroscopy.	Poly A	21-29	CD2 molecule	Homo sapiens	54-57
15892121-0	2005	Phase equilibrium in poly(rA).poly(rU) complexes with Cd2+ and Mg2+ ions, studied by ultraviolet, infrared, and vibrational circular dichroism spectroscopy.	Poly U	30-38	CD2 molecule	Homo sapiens	54-57
15892121-4	2005	poly(rU) at [Mg2+],[Cd2+]/[P] = 0.3.	Poly U	0-8	CD2 molecule	Homo sapiens	20-23
15892121-7	2005	poly(rU) has a triple point ([Cd2+] approximately 10(-4)M) at which the helix-coil (2 --> 1) transition is replaced with a disproportion transition 2AU --> A2U + poly(rA) (2 --> 3) and the subsequent destruction of the triple helix (3 --> 1).	Poly A	0-4	CD2 molecule	Homo sapiens	30-33
15892121-7	2005	poly(rU) has a triple point ([Cd2+] approximately 10(-4)M) at which the helix-coil (2 --> 1) transition is replaced with a disproportion transition 2AU --> A2U + poly(rA) (2 --> 3) and the subsequent destruction of the triple helix (3 --> 1).	Radium	173-175	CD2 molecule	Homo sapiens	30-33
15892121-10	2005	At [Me2+] approximately 10(-3) M, the temperature interval of A2U stability is not less than 20 degrees C. In the case of Cd2+, it increases with the rise of ion concentration due to the decrease of T(m) (2-->3).	me2+	4-8	CD2 molecule	Homo sapiens	122-125
15892121-11	2005	The T(m) (3-->1) value is practically unchanged up to [Cd2+] approximately 10(-3)M. Differences between diagrams for Mg(2+) and Cd2+ result from the various kinds of ion binding to poly(rA).poly-(rU) and poly(rA).	Magnesium	120-122	CD2 molecule	Homo sapiens	58-61
15892121-11	2005	The T(m) (3-->1) value is practically unchanged up to [Cd2+] approximately 10(-3)M. Differences between diagrams for Mg(2+) and Cd2+ result from the various kinds of ion binding to poly(rA).poly-(rU) and poly(rA).	Radium	189-191	CD2 molecule	Homo sapiens	58-61
15892121-11	2005	The T(m) (3-->1) value is practically unchanged up to [Cd2+] approximately 10(-3)M. Differences between diagrams for Mg(2+) and Cd2+ result from the various kinds of ion binding to poly(rA).poly-(rU) and poly(rA).	Radium	189-191	CD2 molecule	Homo sapiens	131-134
15892121-11	2005	The T(m) (3-->1) value is practically unchanged up to [Cd2+] approximately 10(-3)M. Differences between diagrams for Mg(2+) and Cd2+ result from the various kinds of ion binding to poly(rA).poly-(rU) and poly(rA).	Radium	212-214	CD2 molecule	Homo sapiens	58-61
15892121-11	2005	The T(m) (3-->1) value is practically unchanged up to [Cd2+] approximately 10(-3)M. Differences between diagrams for Mg(2+) and Cd2+ result from the various kinds of ion binding to poly(rA).poly-(rU) and poly(rA).	Radium	212-214	CD2 molecule	Homo sapiens	131-134
16134227-0	2005	Post-chemiluminescence behaviour of Ni2+, Mg2+, Cd2+ and Zn2+ in the potassium ferricyanide-luminol reaction.	potassium ferricyanide	69-91	CD2 molecule	Homo sapiens	48-51
16134227-0	2005	Post-chemiluminescence behaviour of Ni2+, Mg2+, Cd2+ and Zn2+ in the potassium ferricyanide-luminol reaction.	Luminol	92-99	CD2 molecule	Homo sapiens	48-51
16134227-1	2005	A new chemiluminescence (CL) reaction was observed when Ni2+, Mg2+, Cd2+ or Zn2+ was injected into the reaction mixture after the finish of the CL reaction of alkaline luminol and potassium ferricyanide.	Nickel(2+)	56-60	CD2 molecule	Homo sapiens	68-71
16134227-1	2005	A new chemiluminescence (CL) reaction was observed when Ni2+, Mg2+, Cd2+ or Zn2+ was injected into the reaction mixture after the finish of the CL reaction of alkaline luminol and potassium ferricyanide.	alkaline luminol	159-175	CD2 molecule	Homo sapiens	68-71
16134227-1	2005	A new chemiluminescence (CL) reaction was observed when Ni2+, Mg2+, Cd2+ or Zn2+ was injected into the reaction mixture after the finish of the CL reaction of alkaline luminol and potassium ferricyanide.	potassium ferricyanide	180-202	CD2 molecule	Homo sapiens	68-71
15863054-1	2005	Theoretical and experimental evidence of a weak M(z)(R) dipole transition moment between the X(1)0g+ ground and (3)1u(5(3)P1) excited states in Cd2 is presented.	(r) dipole	52-62	CD2 molecule	Homo sapiens	144-147
15917089-5	2005	The CaM-CD2-III-5G-52 has stronger affinities to Ca(2+), Tb(3+) and La(3+) than CaM-CD2-IV-5G-52, indicating differential intrinsic metal-binding affinities of the EF-loops.	Terbium	57-59	CD2 molecule	Homo sapiens	8-11
15917089-5	2005	The CaM-CD2-III-5G-52 has stronger affinities to Ca(2+), Tb(3+) and La(3+) than CaM-CD2-IV-5G-52, indicating differential intrinsic metal-binding affinities of the EF-loops.	Metals	132-137	CD2 molecule	Homo sapiens	8-11
15683365-1	2005	GST (glutathione transferase) T1-1 plays an important role in the biotransformation of halogenated alkanes, which are used in large quantities as solvents and occur as environmental pollutants.	Alkanes	99-106	CD2 molecule	Homo sapiens	30-34
15683365-2	2005	Many reactions that are catalysed by GST T1-1 qualify as detoxification processes, but some reactions with dihalogenated alkanes lead to reactive products more toxic than the substrates.	Alkanes	121-128	CD2 molecule	Homo sapiens	41-45
15683365-4	2005	Human GST T1-1 activity is considerably lower with halogenated hydrocarbons and some related substrates.	Hydrocarbons	63-75	CD2 molecule	Homo sapiens	10-14
15683365-5	2005	Human GST T1-1 is polymorphic with a frequent null phenotype, suggesting that it is advantageous, under some circumstances, to lack the functional enzyme, which catalyses GSH conjugations that may cause bioactivation.	Glutathione	171-174	CD2 molecule	Homo sapiens	10-14
15683365-7	2005	The replacement of Trp234 in human GST T1-1 by arginine, found in the rodent enzyme, enhanced the alkyltransferase activity by an order of magnitude with a series of homologous iodoalkanes and some typical GST substrates.	Arginine	47-55	CD2 molecule	Homo sapiens	39-43
15683365-7	2005	The replacement of Trp234 in human GST T1-1 by arginine, found in the rodent enzyme, enhanced the alkyltransferase activity by an order of magnitude with a series of homologous iodoalkanes and some typical GST substrates.	iodoalkanes	177-188	CD2 molecule	Homo sapiens	39-43
15683365-8	2005	The specific activity of the alternative mutant Trp234-->Lys was lower than for the parental human GST T1-1 with many substrates, showing that a positive charge is not sufficient for increased activity.	Lysine	60-63	CD2 molecule	Homo sapiens	106-110
15792476-4	2005	The structure of Cd complex 2 consists of double layers, and a unique bond was found between the Cd2+ cation and a Cl atom of clodronate.	Cadmium	17-19	CD2 molecule	Homo sapiens	97-100
15941036-5	2005	From the analysis of the CD2 stretching and CD2 rocking bands information about the conformational order at a specific deuterated methylene segment is available.	deuterated methylene	119-139	CD2 molecule	Homo sapiens	25-28
15941036-5	2005	From the analysis of the CD2 stretching and CD2 rocking bands information about the conformational order at a specific deuterated methylene segment is available.	deuterated methylene	119-139	CD2 molecule	Homo sapiens	44-47
15941036-6	2005	Here, the CD2 rocking band data are used to determine the amount of gauche conformers at the deuterated carbon positions C-4 and C-6, and C-12.	Carbon	104-110	CD2 molecule	Homo sapiens	10-13
15913136-1	2005	A chloroform membrane system containing a given mixture of ketoconazole and oleic acid was applied for the uphill transport of Cd2+ ions as CdI42-.	Chloroform	2-12	CD2 molecule	Homo sapiens	127-130
15913136-1	2005	A chloroform membrane system containing a given mixture of ketoconazole and oleic acid was applied for the uphill transport of Cd2+ ions as CdI42-.	Ketoconazole	59-71	CD2 molecule	Homo sapiens	127-130
15913136-1	2005	A chloroform membrane system containing a given mixture of ketoconazole and oleic acid was applied for the uphill transport of Cd2+ ions as CdI42-.	Oleic Acid	76-86	CD2 molecule	Homo sapiens	127-130
15913136-1	2005	A chloroform membrane system containing a given mixture of ketoconazole and oleic acid was applied for the uphill transport of Cd2+ ions as CdI42-.	cdi42	140-145	CD2 molecule	Homo sapiens	127-130
15913136-4	2005	The selectivity and efficiency of Cd2+ transport from an aqueous solution containing other cations, such as Co2+, Cr3+, Ni2+, Fe2+, Mn2+, Pd2+ and Zn2+ ions, were investigated.	Cobalt(2+)	108-112	CD2 molecule	Homo sapiens	34-37
15913136-4	2005	The selectivity and efficiency of Cd2+ transport from an aqueous solution containing other cations, such as Co2+, Cr3+, Ni2+, Fe2+, Mn2+, Pd2+ and Zn2+ ions, were investigated.	Nickel(2+)	120-124	CD2 molecule	Homo sapiens	34-37
15913136-4	2005	The selectivity and efficiency of Cd2+ transport from an aqueous solution containing other cations, such as Co2+, Cr3+, Ni2+, Fe2+, Mn2+, Pd2+ and Zn2+ ions, were investigated.	ammonium ferrous sulfate	126-130	CD2 molecule	Homo sapiens	34-37
15913136-4	2005	The selectivity and efficiency of Cd2+ transport from an aqueous solution containing other cations, such as Co2+, Cr3+, Ni2+, Fe2+, Mn2+, Pd2+ and Zn2+ ions, were investigated.	Manganese(2+)	132-136	CD2 molecule	Homo sapiens	34-37
15913136-4	2005	The selectivity and efficiency of Cd2+ transport from an aqueous solution containing other cations, such as Co2+, Cr3+, Ni2+, Fe2+, Mn2+, Pd2+ and Zn2+ ions, were investigated.	PALLADIUM ION	138-142	CD2 molecule	Homo sapiens	34-37
15913136-4	2005	The selectivity and efficiency of Cd2+ transport from an aqueous solution containing other cations, such as Co2+, Cr3+, Ni2+, Fe2+, Mn2+, Pd2+ and Zn2+ ions, were investigated.	Zinc	147-151	CD2 molecule	Homo sapiens	34-37
15792476-4	2005	The structure of Cd complex 2 consists of double layers, and a unique bond was found between the Cd2+ cation and a Cl atom of clodronate.	Clodronic Acid	126-136	CD2 molecule	Homo sapiens	97-100
15721369-7	2005	The Zn(2+) coordination residues of the C-terminal catalytic domain (CD2) were not required for encapsidation but were essential for cytidine deaminase activity and the antiviral effect.	Zinc	4-10	CD2 molecule	Homo sapiens	69-72
15795762-1	2005	A novel two-dimensional coordination polymer containing infinite, coherently pitched single and triple helical motifs is formed by the self-assembly of Cd2+, succinate, water and a bipyridyl ligand.	Polymers	37-44	CD2 molecule	Homo sapiens	152-155
15871276-12	2005	Moreover, the fat and oil phases produced during this method act as chelating agents to catch metal ions with an order of recovery of Cu2+ > Zn2+ > Cd2+ and Zn2+ > Cu2+ > Cd2+, respectively.	Metals	94-99	CD2 molecule	Homo sapiens	154-157
15871276-12	2005	Moreover, the fat and oil phases produced during this method act as chelating agents to catch metal ions with an order of recovery of Cu2+ > Zn2+ > Cd2+ and Zn2+ > Cu2+ > Cd2+, respectively.	Metals	94-99	CD2 molecule	Homo sapiens	183-186
15871276-12	2005	Moreover, the fat and oil phases produced during this method act as chelating agents to catch metal ions with an order of recovery of Cu2+ > Zn2+ > Cd2+ and Zn2+ > Cu2+ > Cd2+, respectively.	cupric ion	134-138	CD2 molecule	Homo sapiens	154-157
15871276-12	2005	Moreover, the fat and oil phases produced during this method act as chelating agents to catch metal ions with an order of recovery of Cu2+ > Zn2+ > Cd2+ and Zn2+ > Cu2+ > Cd2+, respectively.	Zinc	144-148	CD2 molecule	Homo sapiens	154-157
15844555-1	2005	The separation of transition metal Ni2+, Cu2+, Co2+, Zn2+, Cd2+ and Fe3+ in methanol was investigated by using different types of organic acids as complexing agents.	Methanol	76-84	CD2 molecule	Homo sapiens	59-62
15595812-6	2004	It is also shown that Cd2+ activation of photoluminescence does not occur when Mg2+ ions are added to similar QD solutions, indicating potential of these block copolymer-stabilized QDs as Cd2+-selective sensors.	copolymer	160-169	CD2 molecule	Homo sapiens	22-25
15660125-2	2005	In this study, we show that the heavy metal Cd2+ over-rides both mechanisms to enable rapid Met4-dependent induction of metabolic networks needed for production of the antioxidant and Cd2+-chelating agent glutathione.	Metals	38-43	CD2 molecule	Homo sapiens	44-47
15660125-2	2005	In this study, we show that the heavy metal Cd2+ over-rides both mechanisms to enable rapid Met4-dependent induction of metabolic networks needed for production of the antioxidant and Cd2+-chelating agent glutathione.	Metals	38-43	CD2 molecule	Homo sapiens	184-187
15660125-2	2005	In this study, we show that the heavy metal Cd2+ over-rides both mechanisms to enable rapid Met4-dependent induction of metabolic networks needed for production of the antioxidant and Cd2+-chelating agent glutathione.	Glutathione	205-216	CD2 molecule	Homo sapiens	44-47
15660125-2	2005	In this study, we show that the heavy metal Cd2+ over-rides both mechanisms to enable rapid Met4-dependent induction of metabolic networks needed for production of the antioxidant and Cd2+-chelating agent glutathione.	Glutathione	205-216	CD2 molecule	Homo sapiens	184-187
15757339-5	2005	Atentative complexation/ electrochemical model is proposed for when both metal ions, Cd2+ and Zn2+, compete toward complexation, and some of the corresponding equilibrium constants are estimated.	Metals	73-78	CD2 molecule	Homo sapiens	85-88
15757339-5	2005	Atentative complexation/ electrochemical model is proposed for when both metal ions, Cd2+ and Zn2+, compete toward complexation, and some of the corresponding equilibrium constants are estimated.	Zinc	94-98	CD2 molecule	Homo sapiens	85-88
15792301-7	2005	The distribution coefficient (kd) of Cd in the soil decreased exponentially with increasing Cd2+ loading.	Cadmium	37-39	CD2 molecule	Homo sapiens	92-95
15598440-3	2005	Culture supernatant from peripheral blood mononuclear cells (PBMC) stimulated with anti-CD3 plus anti-CD2 antibodies effectively induced the expression of E-selectin, ICAM-1 and VCAM-1 on HMVEC, and treatment with FK506 down-regulated their expression.	Tacrolimus	214-219	CD2 molecule	Homo sapiens	102-105
16173063-2	2005	We have previously shown that Cd uptake in these cells involves both the free cation Cd2+ and chlorocomplex (CdCln(2-n)) species.	Cadmium	30-32	CD2 molecule	Homo sapiens	85-88
15595812-6	2004	It is also shown that Cd2+ activation of photoluminescence does not occur when Mg2+ ions are added to similar QD solutions, indicating potential of these block copolymer-stabilized QDs as Cd2+-selective sensors.	copolymer	160-169	CD2 molecule	Homo sapiens	188-191
15544625-0	2004	The anti-CD2 monoclonal antibody BTI-322 generates unresponsiveness by activation-associated T cell depletion.	LO-CD2a	33-40	CD2 molecule	Homo sapiens	9-12
15544625-1	2004	The antihuman CD2 MoAb BTI-322 (Lo-CD2a) effectively inhibits T cell responses in vitro to allogeneic cells, which is followed by unresponsiveness to the original stimulator in secondary stimulation.	LO-CD2a	23-30	CD2 molecule	Homo sapiens	14-17
15257038-3	2004	BTI-322 and its humanized form have been shown to mediate in vitro antibody-dependent cell-mediated cytotoxicity (ADCC) against CD2 cells through the activation of monocytes or natural killer (NK) cells.	LO-CD2a	0-7	CD2 molecule	Homo sapiens	128-131
15528362-9	2004	AG490, a tyrosine kinase inhibitor affecting Jak proteins, inhibits CD2-mediated IFN-gamma mRNA expression, secretion, and nucleoprotein binding to the IFN-gamma STAT5 site in a dose-dependent fashion.	alpha-cyano-(3,4-dihydroxy)-N-benzylcinnamide	0-5	CD2 molecule	Homo sapiens	68-71
15341838-3	2004	The adsorption of Zn2+ is speeded up by the presence of Cd2+ and Hg2+ ions provided that the concentration of these two ions is high as compared to the concentration of Zn2+.	Zinc	18-22	CD2 molecule	Homo sapiens	56-59
15341838-3	2004	The adsorption of Zn2+ is speeded up by the presence of Cd2+ and Hg2+ ions provided that the concentration of these two ions is high as compared to the concentration of Zn2+.	Zinc	169-173	CD2 molecule	Homo sapiens	56-59
15264817-0	2004	Differential binding of Mg2+, Zn2+, and Cd2+ at two sites in a hammerhead ribozyme motif, determined by 15N NMR.	15n	104-107	CD2 molecule	Homo sapiens	40-43
15264817-2	2004	The 15N NMR chemical shifts of the labeled N7s monitored during addition of Mg2+, Cd2+, and Zn2+ showed the same preference for binding at G10.1 over G16.2 for each metal.	15n	4-7	CD2 molecule	Homo sapiens	82-85
15264817-2	2004	The 15N NMR chemical shifts of the labeled N7s monitored during addition of Mg2+, Cd2+, and Zn2+ showed the same preference for binding at G10.1 over G16.2 for each metal.	4-(4-fluorophenyl)-2-methyl-6-(5-piperidinopentyloxy)pyrimidine hydrochloride	43-46	CD2 molecule	Homo sapiens	82-85
15264817-2	2004	The 15N NMR chemical shifts of the labeled N7s monitored during addition of Mg2+, Cd2+, and Zn2+ showed the same preference for binding at G10.1 over G16.2 for each metal.	Metals	165-170	CD2 molecule	Homo sapiens	82-85
15248738-4	2004	The transcription process of organogel fibers into CdS nanofibers was investigated, and it was found that Cd2+ ions were coated on the organogel fibers by the interaction with ester groups of 4, which might lead to the change of the arrangement of the organogelator and seemed to serve as nucleation sites for metalization.	Cadmium	51-54	CD2 molecule	Homo sapiens	106-109
15248738-4	2004	The transcription process of organogel fibers into CdS nanofibers was investigated, and it was found that Cd2+ ions were coated on the organogel fibers by the interaction with ester groups of 4, which might lead to the change of the arrangement of the organogelator and seemed to serve as nucleation sites for metalization.	Esters	176-181	CD2 molecule	Homo sapiens	106-109
15522710-7	2004	The aim of this study is to prepare ion-imprinted polymers, which can be used for the selective removal of Cd2+ ions from Cd2+-overdosed human plasma.	Polymers	50-58	CD2 molecule	Homo sapiens	107-110
15522710-7	2004	The aim of this study is to prepare ion-imprinted polymers, which can be used for the selective removal of Cd2+ ions from Cd2+-overdosed human plasma.	Polymers	50-58	CD2 molecule	Homo sapiens	122-125
15522710-10	2004	After that, the template (i.e., Cd2+ ions) were removed using 0.1 M thiourea solution.	Thiourea	68-76	CD2 molecule	Homo sapiens	32-35
15522710-14	2004	The relative selectivity coefficients of imprinted beads for Cd2+/Pb2+ and Cd2+/Zn2+ were 7.8 and 1683 times greater than non-imprinted matrix, respectively.	Lead	66-70	CD2 molecule	Homo sapiens	61-64
15522710-14	2004	The relative selectivity coefficients of imprinted beads for Cd2+/Pb2+ and Cd2+/Zn2+ were 7.8 and 1683 times greater than non-imprinted matrix, respectively.	Zinc	80-84	CD2 molecule	Homo sapiens	75-78
15454286-1	2004	Cadmium (Cd2+) is a potent toxic metal for both plants and animals.	Cadmium	0-7	CD2 molecule	Homo sapiens	9-12
15454286-1	2004	Cadmium (Cd2+) is a potent toxic metal for both plants and animals.	Metals	33-38	CD2 molecule	Homo sapiens	9-12
15454286-4	2004	Nitric oxide (NO) synthesis is affected by Cd2+ in several systems.	Nitric Oxide	0-12	CD2 molecule	Homo sapiens	43-46
15454286-8	2004	Here we show that DETA NONOate ((Z)-1-[2 (2-aminoethyl)-N-(2-ammonioethyl)amino]diazen-1-ium-1,2-diolate), a long-term NO donor, at concentrations below 0.5 mM, reduces nuclear condensation and fragmentation and reverses the decrease in cellular activity induced by Cd2+.	2,2'-(hydroxynitrosohydrazono)bis-ethanamine	18-30	CD2 molecule	Homo sapiens	266-269
15454286-8	2004	Here we show that DETA NONOate ((Z)-1-[2 (2-aminoethyl)-N-(2-ammonioethyl)amino]diazen-1-ium-1,2-diolate), a long-term NO donor, at concentrations below 0.5 mM, reduces nuclear condensation and fragmentation and reverses the decrease in cellular activity induced by Cd2+.	(z)-1-[2 (2-aminoethyl)-n-(2-ammonioethyl)amino]diazen-1-ium-1,2-diolate	32-104	CD2 molecule	Homo sapiens	266-269
15293396-1	2004	A rapid and sensitive method was developed to determine trace levels of Cd2+ ions in an aqueous medium by flame atomic absorption spectrometry, using on-line preconcentration in a mini-column packed with 100 mg of 2-aminothiazol modified silica gel (SiAT).	2-AMINOTHIAZOLE	214-228	CD2 molecule	Homo sapiens	72-75
15293396-1	2004	A rapid and sensitive method was developed to determine trace levels of Cd2+ ions in an aqueous medium by flame atomic absorption spectrometry, using on-line preconcentration in a mini-column packed with 100 mg of 2-aminothiazol modified silica gel (SiAT).	Silica Gel	238-248	CD2 molecule	Homo sapiens	72-75
15293396-3	2004	The preconcentrated Cd2+ ions were directly eluted from the column to the spectrometer"s nebulizer-burner system using 100 microL of 2 mol L(-1) hydrochloric acid.	Hydrochloric Acid	145-162	CD2 molecule	Homo sapiens	20-23
15158384-2	2004	A Cd2+ ion-selective electrode was used to generate high-resolution metal sorption data as a function of increasing pH.	Metals	68-73	CD2 molecule	Homo sapiens	2-5
15131114-7	2004	The ability of cysteine side chains at the 2" and -2" positions to coordinate Cd2+ in both the native open and closed states of the channel suggests that the cytoplasmic selectivity filter of 5-HT(3A) receptors maintains a narrow pore during channel gating.	Cysteine	15-23	CD2 molecule	Homo sapiens	78-81
15515950-3	2004	Percents of desorption amounts of Cd2+ calculated were 70%-100% in red soil and goethite, and 25%-50% in latosols and kaolinite.	goethite	80-88	CD2 molecule	Homo sapiens	34-37
15515950-3	2004	Percents of desorption amounts of Cd2+ calculated were 70%-100% in red soil and goethite, and 25%-50% in latosols and kaolinite.	latosols	105-113	CD2 molecule	Homo sapiens	34-37
15515950-3	2004	Percents of desorption amounts of Cd2+ calculated were 70%-100% in red soil and goethite, and 25%-50% in latosols and kaolinite.	Kaolin	118-127	CD2 molecule	Homo sapiens	34-37
15515950-4	2004	Parabolic diffusion could describe Cd2+ desorption kinetics in latosols and not suitable for red soil and goethite and kaolinite.	latosols	63-71	CD2 molecule	Homo sapiens	35-38
15515950-10	2004	The affinity of edge hydroxyl to Cd2+ would lead to the difference of Cd2+ desorption rate and amounts.	Hydroxyl Radical	21-29	CD2 molecule	Homo sapiens	33-36
15515950-10	2004	The affinity of edge hydroxyl to Cd2+ would lead to the difference of Cd2+ desorption rate and amounts.	Hydroxyl Radical	21-29	CD2 molecule	Homo sapiens	70-73
15041686-2	2004	Dichroism measurements of single, isotopically enhanced vibrational modes (e.g., Amide I 13C=18O or Gly CD2 stretching modes) can yield precise orientational restraints for the monomer helix protomer that can be used as refinement constraints in model building of the entire helical bundle.	Glycine	100-103	CD2 molecule	Homo sapiens	104-107
15984241-5	2004	The catalytic activity of PFTDA can be neutralized, however, simply by the addition of multivalent metallic ions such as Cd2+ to form saltlike complexes with PFTDA; the rate of 2-D sol-gel processes can thus be easily regulated by a minute amount of PFTDA and/or Cd2+ added into the reaction system.	pftda	26-31	CD2 molecule	Homo sapiens	121-124
15984241-5	2004	The catalytic activity of PFTDA can be neutralized, however, simply by the addition of multivalent metallic ions such as Cd2+ to form saltlike complexes with PFTDA; the rate of 2-D sol-gel processes can thus be easily regulated by a minute amount of PFTDA and/or Cd2+ added into the reaction system.	pftda	26-31	CD2 molecule	Homo sapiens	263-266
15984241-5	2004	The catalytic activity of PFTDA can be neutralized, however, simply by the addition of multivalent metallic ions such as Cd2+ to form saltlike complexes with PFTDA; the rate of 2-D sol-gel processes can thus be easily regulated by a minute amount of PFTDA and/or Cd2+ added into the reaction system.	pftda	158-163	CD2 molecule	Homo sapiens	121-124
15984241-5	2004	The catalytic activity of PFTDA can be neutralized, however, simply by the addition of multivalent metallic ions such as Cd2+ to form saltlike complexes with PFTDA; the rate of 2-D sol-gel processes can thus be easily regulated by a minute amount of PFTDA and/or Cd2+ added into the reaction system.	pftda	158-163	CD2 molecule	Homo sapiens	263-266
15984241-5	2004	The catalytic activity of PFTDA can be neutralized, however, simply by the addition of multivalent metallic ions such as Cd2+ to form saltlike complexes with PFTDA; the rate of 2-D sol-gel processes can thus be easily regulated by a minute amount of PFTDA and/or Cd2+ added into the reaction system.	pftda	158-163	CD2 molecule	Homo sapiens	121-124
15984241-5	2004	The catalytic activity of PFTDA can be neutralized, however, simply by the addition of multivalent metallic ions such as Cd2+ to form saltlike complexes with PFTDA; the rate of 2-D sol-gel processes can thus be easily regulated by a minute amount of PFTDA and/or Cd2+ added into the reaction system.	pftda	158-163	CD2 molecule	Homo sapiens	263-266
15113199-2	2004	Here for the first time we measured the strength of such a bond, using vibrational frequency shifts of a dimeric and nondimeric variants of GPA containing a Gly CD2 label.	Glycine	157-160	CD2 molecule	Homo sapiens	161-164
15969157-0	2004	Binding of Cd2+ to self-assembled bilayers bearing pyridine terminal groups: attenuated total reflection Fourier transform infrared spectroscopic studies.	pyridine	51-59	CD2 molecule	Homo sapiens	11-14
15969157-1	2004	Various aspects of the adsorption of Cd2+ on self-assembled monolayers (SAMs) of 4-heptadecylpyridine (HDpy) and 7-tridecyl-4-methyl-1,10-bipyridine (TMbipy) supported on an octadecylsilane (ODS)-modified Ge prism have been examined both ex situ (dry) and in situ (in the presence of aqueous solutions) using attenuated total reflection Fourier transform infrared spectroscopy.	SAMS Peptide	72-76	CD2 molecule	Homo sapiens	37-40
15969157-1	2004	Various aspects of the adsorption of Cd2+ on self-assembled monolayers (SAMs) of 4-heptadecylpyridine (HDpy) and 7-tridecyl-4-methyl-1,10-bipyridine (TMbipy) supported on an octadecylsilane (ODS)-modified Ge prism have been examined both ex situ (dry) and in situ (in the presence of aqueous solutions) using attenuated total reflection Fourier transform infrared spectroscopy.	4-heptadecylpyridine	81-101	CD2 molecule	Homo sapiens	37-40
15969157-1	2004	Various aspects of the adsorption of Cd2+ on self-assembled monolayers (SAMs) of 4-heptadecylpyridine (HDpy) and 7-tridecyl-4-methyl-1,10-bipyridine (TMbipy) supported on an octadecylsilane (ODS)-modified Ge prism have been examined both ex situ (dry) and in situ (in the presence of aqueous solutions) using attenuated total reflection Fourier transform infrared spectroscopy.	hdpy	103-107	CD2 molecule	Homo sapiens	37-40
15969157-1	2004	Various aspects of the adsorption of Cd2+ on self-assembled monolayers (SAMs) of 4-heptadecylpyridine (HDpy) and 7-tridecyl-4-methyl-1,10-bipyridine (TMbipy) supported on an octadecylsilane (ODS)-modified Ge prism have been examined both ex situ (dry) and in situ (in the presence of aqueous solutions) using attenuated total reflection Fourier transform infrared spectroscopy.	7-tridecyl-4-methyl-1,10-bipyridine	113-148	CD2 molecule	Homo sapiens	37-40
15969157-2	2004	In direct analogy with the behavior found for a variety of genuine pyridine (py) and bipyridine (bipy) metal ion complexes, Cd2+ binding to both SAMs led to shifts in the skeletal vibrational modes of the corresponding uncoordinated ligands in the region 1650-1400 cm(-1), toward higher energies.	pyridine	67-75	CD2 molecule	Homo sapiens	124-127
15969157-2	2004	In direct analogy with the behavior found for a variety of genuine pyridine (py) and bipyridine (bipy) metal ion complexes, Cd2+ binding to both SAMs led to shifts in the skeletal vibrational modes of the corresponding uncoordinated ligands in the region 1650-1400 cm(-1), toward higher energies.	pyridine	67-69	CD2 molecule	Homo sapiens	124-127
15969157-2	2004	In direct analogy with the behavior found for a variety of genuine pyridine (py) and bipyridine (bipy) metal ion complexes, Cd2+ binding to both SAMs led to shifts in the skeletal vibrational modes of the corresponding uncoordinated ligands in the region 1650-1400 cm(-1), toward higher energies.	2,2'-Dipyridyl	85-95	CD2 molecule	Homo sapiens	124-127
15969157-2	2004	In direct analogy with the behavior found for a variety of genuine pyridine (py) and bipyridine (bipy) metal ion complexes, Cd2+ binding to both SAMs led to shifts in the skeletal vibrational modes of the corresponding uncoordinated ligands in the region 1650-1400 cm(-1), toward higher energies.	2,2'-Dipyridyl	85-89	CD2 molecule	Homo sapiens	124-127
15969157-2	2004	In direct analogy with the behavior found for a variety of genuine pyridine (py) and bipyridine (bipy) metal ion complexes, Cd2+ binding to both SAMs led to shifts in the skeletal vibrational modes of the corresponding uncoordinated ligands in the region 1650-1400 cm(-1), toward higher energies.	Metals	103-108	CD2 molecule	Homo sapiens	124-127
15252635-0	2004	Aminoacid N-substituted 1,4,7-triazacyclononane and 1,4,7,10-tetraazacyclododecane Zn2+, Cd2+ and Cu2+ complexes.	cyclen	52-82	CD2 molecule	Homo sapiens	89-92
15252635-8	2004	The 1H and 13C NMR spectra of the ligands are consistent with formation of a predominant Zn2+ and Cd2+ Delta or Lambda diastereomer.	Hydrogen	4-6	CD2 molecule	Homo sapiens	98-101
15252635-8	2004	The 1H and 13C NMR spectra of the ligands are consistent with formation of a predominant Zn2+ and Cd2+ Delta or Lambda diastereomer.	13c	11-14	CD2 molecule	Homo sapiens	98-101
15242227-1	2004	Optimisation of process parameters for adsorption of metal ions viz., Cu2+, Cd2+ and Ni2+ ions on Straw Carbon (SC) was carried out by using Box-Behnken statistics and analysis of variance methods.	Metals	53-58	CD2 molecule	Homo sapiens	76-79
15242227-1	2004	Optimisation of process parameters for adsorption of metal ions viz., Cu2+, Cd2+ and Ni2+ ions on Straw Carbon (SC) was carried out by using Box-Behnken statistics and analysis of variance methods.	Carbon	104-110	CD2 molecule	Homo sapiens	76-79
15242227-4	2004	The optimum process parameters for maximum adsorption of Ni2+, Cu2+ and Cd2+ were obtained by this procedure.	Nickel(2+)	57-61	CD2 molecule	Homo sapiens	72-75
15743078-4	2004	Furthermore, we have demonstrated for the first time using in situ SFG measurement that the interfacial molecular structure at the LB bilayer of stearic acid on the hydrophilic substrates significantly change with immersion in the water subphase containing Cd2+ cation while such a structural change has not been observed in the water subphase without Cd2+.	stearic acid	145-157	CD2 molecule	Homo sapiens	257-260
15030479-9	2004	Taken together, these observations suggest that the protein-protein interaction between the n-sulfur protein hinge region and the cytochrome b extramembranous cd2 helix is important for maintaining the structure of the hinge region and, by consequence, the movement of the headgroup and the integrity of the enzyme.	Sulfur	94-100	CD2 molecule	Homo sapiens	159-162
15743078-0	2004	Cd2+-induced interfacial structural changes of Langmuir-Blodgett films of stearic acid on solid substrates: a sum frequency generation study.	stearic acid	74-86	CD2 molecule	Homo sapiens	0-3
15743078-3	2004	The SFG spectra in air are virtually identical and are independent of the odd-even property and thickness (1-12) of the LB films, indicating that the even-numbered LB film changes its surface structure after passing through the interface between the water subphase and air, especially when the Cd2+ cation was included in the water subphase.	lb	164-166	CD2 molecule	Homo sapiens	294-297
15743078-4	2004	Furthermore, we have demonstrated for the first time using in situ SFG measurement that the interfacial molecular structure at the LB bilayer of stearic acid on the hydrophilic substrates significantly change with immersion in the water subphase containing Cd2+ cation while such a structural change has not been observed in the water subphase without Cd2+.	lb bilayer	131-141	CD2 molecule	Homo sapiens	257-260
15743078-4	2004	Furthermore, we have demonstrated for the first time using in situ SFG measurement that the interfacial molecular structure at the LB bilayer of stearic acid on the hydrophilic substrates significantly change with immersion in the water subphase containing Cd2+ cation while such a structural change has not been observed in the water subphase without Cd2+.	lb bilayer	131-141	CD2 molecule	Homo sapiens	352-355
15743078-4	2004	Furthermore, we have demonstrated for the first time using in situ SFG measurement that the interfacial molecular structure at the LB bilayer of stearic acid on the hydrophilic substrates significantly change with immersion in the water subphase containing Cd2+ cation while such a structural change has not been observed in the water subphase without Cd2+.	stearic acid	145-157	CD2 molecule	Homo sapiens	352-355
15743078-4	2004	Furthermore, we have demonstrated for the first time using in situ SFG measurement that the interfacial molecular structure at the LB bilayer of stearic acid on the hydrophilic substrates significantly change with immersion in the water subphase containing Cd2+ cation while such a structural change has not been observed in the water subphase without Cd2+.	Water	231-236	CD2 molecule	Homo sapiens	257-260
15743078-4	2004	Furthermore, we have demonstrated for the first time using in situ SFG measurement that the interfacial molecular structure at the LB bilayer of stearic acid on the hydrophilic substrates significantly change with immersion in the water subphase containing Cd2+ cation while such a structural change has not been observed in the water subphase without Cd2+.	Water	231-236	CD2 molecule	Homo sapiens	352-355
15743078-4	2004	Furthermore, we have demonstrated for the first time using in situ SFG measurement that the interfacial molecular structure at the LB bilayer of stearic acid on the hydrophilic substrates significantly change with immersion in the water subphase containing Cd2+ cation while such a structural change has not been observed in the water subphase without Cd2+.	Water	329-334	CD2 molecule	Homo sapiens	257-260
15743078-5	2004	These results clearly indicate that a reorganization process takes place on the surface of the stearic acid bilayer induced by the Cd2+ cation.	stearic acid	95-107	CD2 molecule	Homo sapiens	131-134
15743078-6	2004	The electrostatic interaction between the carboxylate headgroup of stearic acid via the Cd2+ cation seems to play an important role in the surface reorganization process both in air and in solution.	carboxylate	42-53	CD2 molecule	Homo sapiens	88-91
15743078-6	2004	The electrostatic interaction between the carboxylate headgroup of stearic acid via the Cd2+ cation seems to play an important role in the surface reorganization process both in air and in solution.	stearic acid	67-79	CD2 molecule	Homo sapiens	88-91
14753790-1	2004	A simple and fast method for simultaneous separation of nine metal cations Ni2+, Cu2+, Co2+, Zn2+ Cd2+, K+, Na+, Mg2+ and Ca2+, and NH4+ in methanol is reported.	Metals	61-66	CD2 molecule	Homo sapiens	98-101
14753790-1	2004	A simple and fast method for simultaneous separation of nine metal cations Ni2+, Cu2+, Co2+, Zn2+ Cd2+, K+, Na+, Mg2+ and Ca2+, and NH4+ in methanol is reported.	Zinc	93-97	CD2 molecule	Homo sapiens	98-101
14753790-1	2004	A simple and fast method for simultaneous separation of nine metal cations Ni2+, Cu2+, Co2+, Zn2+ Cd2+, K+, Na+, Mg2+ and Ca2+, and NH4+ in methanol is reported.	magnesium ion	113-117	CD2 molecule	Homo sapiens	98-101
14753790-1	2004	A simple and fast method for simultaneous separation of nine metal cations Ni2+, Cu2+, Co2+, Zn2+ Cd2+, K+, Na+, Mg2+ and Ca2+, and NH4+ in methanol is reported.	Methanol	140-148	CD2 molecule	Homo sapiens	98-101
15454689-7	2004	MHC class II and CD2 single and double positive subpopulations exist, and their expression is also modulated in different doses of T11TS.	t11ts	131-136	CD2 molecule	Homo sapiens	17-20
14727918-6	2004	The relative efficacy of adduct formation was G > T > A >> C. The four DNA nucleosides were also reacted with the dihalomethanes CH(2)Cl(2) and CH(2)Br(2) in the presence of glutathione (GSH) and GSH S-transferases from bacteria (DM11), rat (GST 5-5), and human (GST T1-1) under conditions that produce mutations in bacteria.	Nucleosides	87-98	CD2 molecule	Homo sapiens	279-283
14727918-6	2004	The relative efficacy of adduct formation was G > T > A >> C. The four DNA nucleosides were also reacted with the dihalomethanes CH(2)Cl(2) and CH(2)Br(2) in the presence of glutathione (GSH) and GSH S-transferases from bacteria (DM11), rat (GST 5-5), and human (GST T1-1) under conditions that produce mutations in bacteria.	dihalomethanes	126-140	CD2 molecule	Homo sapiens	279-283
14727918-10	2004	The relative efficiency of adduct formation by GSH transferases was rat 5-5 > human T1-1 > bacterial DM11, showing that human GSH transferase T1-1 can form dihalomethane adducts under the conditions used.	dihalomethane	162-175	CD2 molecule	Homo sapiens	87-91
14727918-10	2004	The relative efficiency of adduct formation by GSH transferases was rat 5-5 > human T1-1 > bacterial DM11, showing that human GSH transferase T1-1 can form dihalomethane adducts under the conditions used.	dihalomethane	162-175	CD2 molecule	Homo sapiens	148-152
31394621-1	2004	Cadmium (Cd2+) is an ubiquitous toxic metal with apoptotic and genotoxic effects, which has been involved in a variety of pathological conditions inducing disturbance of the immune system.	Cadmium	0-7	CD2 molecule	Homo sapiens	9-12
31394621-1	2004	Cadmium (Cd2+) is an ubiquitous toxic metal with apoptotic and genotoxic effects, which has been involved in a variety of pathological conditions inducing disturbance of the immune system.	Metals	38-43	CD2 molecule	Homo sapiens	9-12
31394621-2	2004	In the present study we treated the Fas-expressed human immature T-cell line CCRF-CEM with 10muM Cd2+ for 6h or 24h.	ammonium ferrous sulfate	36-39	CD2 molecule	Homo sapiens	97-100
31394621-2	2004	In the present study we treated the Fas-expressed human immature T-cell line CCRF-CEM with 10muM Cd2+ for 6h or 24h.	2-chloroethyl methyl sulfide	82-85	CD2 molecule	Homo sapiens	97-100
31394621-3	2004	We found that pretreatment of the cells with Cd2+ for 24h inhibited apoptosis induced by Fas-ligation with the CH-11 antibody, in contrast to pretreatment for 6h.	ammonium ferrous sulfate	89-92	CD2 molecule	Homo sapiens	45-48
31394621-3	2004	We found that pretreatment of the cells with Cd2+ for 24h inhibited apoptosis induced by Fas-ligation with the CH-11 antibody, in contrast to pretreatment for 6h.	4-dimethylamino-3',4'-dimethoxychalcone	111-116	CD2 molecule	Homo sapiens	45-48
31394621-6	2004	The Fas down-regulation induced by Cd2+ seems to be responsible for the carcinogenic and the immunomodulatory effects of that metal.	Metals	126-131	CD2 molecule	Homo sapiens	35-38
15055942-6	2004	In alkaline conditions, the catalytic effects of Cu2+ or Cd2+ were accelerated and Cu2+ was found to be a more effective catalyst than Cd2+.	cupric ion	49-53	CD2 molecule	Homo sapiens	135-138
15055942-6	2004	In alkaline conditions, the catalytic effects of Cu2+ or Cd2+ were accelerated and Cu2+ was found to be a more effective catalyst than Cd2+.	cupric ion	83-87	CD2 molecule	Homo sapiens	57-60
15055942-6	2004	In alkaline conditions, the catalytic effects of Cu2+ or Cd2+ were accelerated and Cu2+ was found to be a more effective catalyst than Cd2+.	cupric ion	83-87	CD2 molecule	Homo sapiens	135-138
15137640-1	2004	Carbon nanotubes prepared by catalytic chemical vapor deposition of hydrocarbon at 650 degrees C show good adsorption capability of Pb2+, Cu2+ and Cd2+ ions from aqueous solution after oxidized with concentrated nitric acid at 140 degrees C for 1 h. The specific surface area and particle size distribution of the as-grown and oxidized CNTs were studied by BET method and laser particle analyzer.	Carbon	0-6	CD2 molecule	Homo sapiens	147-150
15137640-1	2004	Carbon nanotubes prepared by catalytic chemical vapor deposition of hydrocarbon at 650 degrees C show good adsorption capability of Pb2+, Cu2+ and Cd2+ ions from aqueous solution after oxidized with concentrated nitric acid at 140 degrees C for 1 h. The specific surface area and particle size distribution of the as-grown and oxidized CNTs were studied by BET method and laser particle analyzer.	Hydrocarbons	68-79	CD2 molecule	Homo sapiens	147-150
15137640-1	2004	Carbon nanotubes prepared by catalytic chemical vapor deposition of hydrocarbon at 650 degrees C show good adsorption capability of Pb2+, Cu2+ and Cd2+ ions from aqueous solution after oxidized with concentrated nitric acid at 140 degrees C for 1 h. The specific surface area and particle size distribution of the as-grown and oxidized CNTs were studied by BET method and laser particle analyzer.	Nitric Acid	212-223	CD2 molecule	Homo sapiens	147-150
14612578-7	2003	Thus the process of CD2, CD11a, CD11b, and F-actin accumulation in the pSMAC and perforin accumulation in the central SMAC of the NKIS are sequential processes with distinct cytoskeletal requirements.	psmac	71-76	CD2 molecule	Homo sapiens	20-23
14658918-6	2003	The second cadmium ion (Cd2) in this compound lies below the plane of three nitrogen atoms, N(6), N(8), and N(9).	Cadmium	11-18	CD2 molecule	Homo sapiens	24-27
14658918-6	2003	The second cadmium ion (Cd2) in this compound lies below the plane of three nitrogen atoms, N(6), N(8), and N(9).	Nitrogen	76-84	CD2 molecule	Homo sapiens	24-27
12902148-10	2003	The results indicated that the exposure of NK cells to 1.5 microM DBT for 24 h decreased the expression of CD2, CD11a, CD16, CD11c.	di-n-butyltin	66-69	CD2 molecule	Homo sapiens	107-110
14499349-3	2003	Cd2+ increased [3H]thymidine uptake and cell number twofold.	Tritium	16-18	CD2 molecule	Homo sapiens	0-3
14499349-3	2003	Cd2+ increased [3H]thymidine uptake and cell number twofold.	Thymidine	19-28	CD2 molecule	Homo sapiens	0-3
14499349-4	2003	Cd2+ elevated intracellular IP3, cytosolic-free Ca2+, phosphorylated MEK1/2, ERK1/2, p38 MAPK and JNK two- to threefold.	Inositol 1,4,5-Trisphosphate	28-31	CD2 molecule	Homo sapiens	0-3
14499349-7	2003	Cd2+-induced increased uptake of [3H]thymidine was abolished by translational and transcriptional inhibitors, and Ca2+ channel blockers.	[3h]thymidine	33-46	CD2 molecule	Homo sapiens	0-3
14596396-2	2003	Because Cd2+ is often found with Zn2+ in the environment and can form fluorescent complexes with chelating fluorophores, a potentially important property of chemosensors for Zn2+ is their selectivity for Zn2+ over Cd2+.	Zinc	33-37	CD2 molecule	Homo sapiens	8-11
14596396-2	2003	Because Cd2+ is often found with Zn2+ in the environment and can form fluorescent complexes with chelating fluorophores, a potentially important property of chemosensors for Zn2+ is their selectivity for Zn2+ over Cd2+.	Zinc	174-178	CD2 molecule	Homo sapiens	8-11
14596396-2	2003	Because Cd2+ is often found with Zn2+ in the environment and can form fluorescent complexes with chelating fluorophores, a potentially important property of chemosensors for Zn2+ is their selectivity for Zn2+ over Cd2+.	Zinc	174-178	CD2 molecule	Homo sapiens	214-217
14596396-2	2003	Because Cd2+ is often found with Zn2+ in the environment and can form fluorescent complexes with chelating fluorophores, a potentially important property of chemosensors for Zn2+ is their selectivity for Zn2+ over Cd2+.	Zinc	174-178	CD2 molecule	Homo sapiens	8-11
14596396-2	2003	Because Cd2+ is often found with Zn2+ in the environment and can form fluorescent complexes with chelating fluorophores, a potentially important property of chemosensors for Zn2+ is their selectivity for Zn2+ over Cd2+.	Zinc	174-178	CD2 molecule	Homo sapiens	214-217
14596396-3	2003	The Zn2+ or Cd2+ complexes of 1 gave an emission band from the 1:1 complex, but the fluorescence intensity for Cd2+ was a half of that for Zn2+.	Zinc	4-8	CD2 molecule	Homo sapiens	111-114
14596396-3	2003	The Zn2+ or Cd2+ complexes of 1 gave an emission band from the 1:1 complex, but the fluorescence intensity for Cd2+ was a half of that for Zn2+.	Zinc	139-143	CD2 molecule	Homo sapiens	12-15
14599205-1	2003	We present an STM study of self-assembled monolayers of 2,3,6,7,10,11-undecalkoxy-substituted triphenylene (T11) at the n-tetradecane/Au(111) interface under ambient conditions.	2,3,6,7,10,11-undecalkoxy-substituted triphenylene	56-106	CD2 molecule	Homo sapiens	108-111
14599205-1	2003	We present an STM study of self-assembled monolayers of 2,3,6,7,10,11-undecalkoxy-substituted triphenylene (T11) at the n-tetradecane/Au(111) interface under ambient conditions.	n-tetradecane	120-133	CD2 molecule	Homo sapiens	108-111
14599205-1	2003	We present an STM study of self-assembled monolayers of 2,3,6,7,10,11-undecalkoxy-substituted triphenylene (T11) at the n-tetradecane/Au(111) interface under ambient conditions.	Gold	134-136	CD2 molecule	Homo sapiens	108-111
14599205-3	2003	Three alkyl chains of each T11 molecule align along the 110 direction of the underlying Au(111) substrate.	Gold	88-90	CD2 molecule	Homo sapiens	27-30
14599205-4	2003	The association of T11 in molecular pairs appears to result from a substrate-induced mechanism governed by the strong anisotropic interaction between T11 alkyl chains and Au(111).	Gold	171-173	CD2 molecule	Homo sapiens	19-22
14599205-4	2003	The association of T11 in molecular pairs appears to result from a substrate-induced mechanism governed by the strong anisotropic interaction between T11 alkyl chains and Au(111).	Gold	171-173	CD2 molecule	Homo sapiens	150-153
14603992-2	2003	Iron disturbed CD2 expression on T-cells, cell-mediated immunity by Th1 cells and monocyte functions including phagocytosis and natural killer activity.	Iron	0-4	CD2 molecule	Homo sapiens	15-18
12974764-6	2003	LPMC isolated from CD patients produced significantly less TGF-beta1 than controls when stimulated via CD2 plus CD28 pathways (P = 0.001)] conversely, in UC patients increased production of TGF-beta1 compared to controls was observed (P = 0.0005).	lpmc	0-4	CD2 molecule	Homo sapiens	103-106
12432541-2	2002	Eight alkali, alkaline earth metal ions and ammonium could be separated in less than 4 min with detection limits in the order of 5 x 10(-8) M. The heavy metals Mn2+, Pb2+, Cd2+ Fe2+, Zn2+, Co2+, Cu2+ and Ni2+ could also be successfully resolved with a 10 mM 2-(N-morpholino)ethanesulfonic acid/DL-histidine (MES/His)-buffer.	Ammonium Compounds	44-52	CD2 molecule	Homo sapiens	172-175
12948123-0	2003	Application of a poly(4-styrenesulfonate) liquid binding layer for measurement of Cu2+ and Cd2+ with the diffusive gradients in thin-films technique.	poly(4-styrenesulfonate)	17-41	CD2 molecule	Homo sapiens	91-94
12785848-2	2003	We have introduced a de novo designed calcium-binding site into the framework of a non-calcium-binding protein, domain 1 of CD2.	Calcium	38-45	CD2 molecule	Homo sapiens	124-127
12785848-2	2003	We have introduced a de novo designed calcium-binding site into the framework of a non-calcium-binding protein, domain 1 of CD2.	Calcium	87-94	CD2 molecule	Homo sapiens	124-127
12523935-0	2003	Cystic fibrosis transmembrane conductance regulator: the NBF1+R (nucleotide-binding fold 1 and regulatory domain) segment acting alone catalyses a Co2+/Mn2+/Mg2+-ATPase activity markedly inhibited by both Cd2+ and the transition-state analogue orthovanadate.	Vanadates	244-257	CD2 molecule	Homo sapiens	205-208
12530983-2	2003	Here, we show that antigen-induced formation of T cell:APC conjugates and synapses is abrogated in WASp-deficient T cells and that CD2 engagement evokes interactions between the proline-rich region required for WASp translocation to the synapse and the PSTPIP1 adaptor SH3 domain and between the PSTPIp1 coiled-coil domain and both CD2 and another CD2-binding adaptor, CD2AP.	Proline	178-185	CD2 molecule	Homo sapiens	131-134
12743166-2	2003	The mutations of the aspartate residues to glutamate induce changes in the conduction properties, enhance Cd2+ and proton affinities, and modify the activation curve of the channel.	Aspartic Acid	21-30	CD2 molecule	Homo sapiens	106-109
12743166-2	2003	The mutations of the aspartate residues to glutamate induce changes in the conduction properties, enhance Cd2+ and proton affinities, and modify the activation curve of the channel.	Glutamic Acid	43-52	CD2 molecule	Homo sapiens	106-109
12731040-4	2003	Both PBMC and LPMC exhibit enhanced secretion and transactivation of the -2.7 kb IFN-gamma promoter region following CD2 signaling, but the IFN-gamma STAT-binding region (within the first intron) serves as an orientation-independent enhancer of promoter activity only in LPMC.	lpmc	14-18	CD2 molecule	Homo sapiens	117-120
12731040-6	2003	In LPMC, but not PBMC, CD2 mediates binding of STAT1 and STAT4 to the IFN-gamma intronic element.	lpmc	3-7	CD2 molecule	Homo sapiens	23-26
12731040-7	2003	Unstimulated LMPC exhibit low levels of phosphotyrosine-STAT4 and STAT1 and phosphoserine-STAT1, which increase substantially following CD2 activation.	1-Myristoyl-sn-glycero-3-phosphocholine	13-17	CD2 molecule	Homo sapiens	136-139
12530983-2	2003	Here, we show that antigen-induced formation of T cell:APC conjugates and synapses is abrogated in WASp-deficient T cells and that CD2 engagement evokes interactions between the proline-rich region required for WASp translocation to the synapse and the PSTPIP1 adaptor SH3 domain and between the PSTPIp1 coiled-coil domain and both CD2 and another CD2-binding adaptor, CD2AP.	Proline	178-185	CD2 molecule	Homo sapiens	332-335
12530983-2	2003	Here, we show that antigen-induced formation of T cell:APC conjugates and synapses is abrogated in WASp-deficient T cells and that CD2 engagement evokes interactions between the proline-rich region required for WASp translocation to the synapse and the PSTPIP1 adaptor SH3 domain and between the PSTPIp1 coiled-coil domain and both CD2 and another CD2-binding adaptor, CD2AP.	Proline	178-185	CD2 molecule	Homo sapiens	332-335
12426371-2	2002	In T cells, the CD2BP2 adaptor binds two membrane-proximal proline-rich motifs in the CD2 cytoplasmic tail via its GYF domain, thereby regulating interleukin-2 production.	Proline	59-66	CD2 molecule	Homo sapiens	16-19
12426371-5	2002	NMR analysis shows that the Fyn but not the Lck tyrosine kinase SH3 domain competes with CD2BP2 GYF-domain binding to the same CD2 proline-rich sequence in vitro.	Proline	131-138	CD2 molecule	Homo sapiens	89-92
12426371-6	2002	To test the in vivo significance of this competition, we used co-immunoprecipitation experiments and found that CD2BP2 is the ligand of the membrane-proximal proline-rich tandem repeat of CD2 in detergent-soluble membrane compartments, but is replaced by Fyn SH3 after CD2 is translocated into lipid rafts upon CD2 ectodomain clustering.	Proline	158-165	CD2 molecule	Homo sapiens	112-115
12426371-6	2002	To test the in vivo significance of this competition, we used co-immunoprecipitation experiments and found that CD2BP2 is the ligand of the membrane-proximal proline-rich tandem repeat of CD2 in detergent-soluble membrane compartments, but is replaced by Fyn SH3 after CD2 is translocated into lipid rafts upon CD2 ectodomain clustering.	Proline	158-165	CD2 molecule	Homo sapiens	188-191
12426371-6	2002	To test the in vivo significance of this competition, we used co-immunoprecipitation experiments and found that CD2BP2 is the ligand of the membrane-proximal proline-rich tandem repeat of CD2 in detergent-soluble membrane compartments, but is replaced by Fyn SH3 after CD2 is translocated into lipid rafts upon CD2 ectodomain clustering.	Proline	158-165	CD2 molecule	Homo sapiens	188-191
12432541-2	2002	Eight alkali, alkaline earth metal ions and ammonium could be separated in less than 4 min with detection limits in the order of 5 x 10(-8) M. The heavy metals Mn2+, Pb2+, Cd2+ Fe2+, Zn2+, Co2+, Cu2+ and Ni2+ could also be successfully resolved with a 10 mM 2-(N-morpholino)ethanesulfonic acid/DL-histidine (MES/His)-buffer.	ammonium ferrous sulfate	177-181	CD2 molecule	Homo sapiens	172-175
12141485-8	2002	Furthermore, the free Ni2+ or Cd2+ concentrations could be modulated by the addition of a strong chelating agent (e.g., EDTA), resulting in reduced deleterious effects.	Edetic Acid	120-124	CD2 molecule	Homo sapiens	30-33
12416880-4	2002	Thiols in the HPLC effluent compete for complexation of the Cd2+, resulting in a decrease in the fluorescence response.	Sulfhydryl Compounds	0-6	CD2 molecule	Homo sapiens	60-63
12384940-6	2002	RESULTS: Lovastatin induced a 15-fold rise in IL-1beta secretion by normal anti-CD2 + CD28-stimulated cells (P < 0.001).	Lovastatin	9-19	CD2 molecule	Homo sapiens	80-83
12163161-2	2002	Stimulation of tyrosine phosphorylation and activation of ITK by the T-cell antigen receptor, CD28 and CD2 requires the presence of the Src family kinase Lck in T-cells.	Tyrosine	15-23	CD2 molecule	Homo sapiens	94-97
12445125-3	2002	At higher Cd2+ concentrations, a Cd2+ -dependent decrease in leaf conductance and CO2 uptake was observed despite the photosynthetic apparatus appeared not to be affected as probed by fluorescence measurements.	N2,N6-bis(4-(2-aminoethoxy)quinolin-2-yl)-4-((4-fluorobenzyl)oxy)pyridine-2,6-dicarboxamide	82-85	CD2 molecule	Homo sapiens	10-13
12445125-3	2002	At higher Cd2+ concentrations, a Cd2+ -dependent decrease in leaf conductance and CO2 uptake was observed despite the photosynthetic apparatus appeared not to be affected as probed by fluorescence measurements.	N2,N6-bis(4-(2-aminoethoxy)quinolin-2-yl)-4-((4-fluorobenzyl)oxy)pyridine-2,6-dicarboxamide	82-85	CD2 molecule	Homo sapiens	33-36
12445125-6	2002	However, the Cd2+-induced stomatal closure was likely ABA-independent, since a 5-day treatment with 50 micro m Cd2+ did not affect the plant relative water content.	alisol B 23-acetate	54-57	CD2 molecule	Homo sapiens	13-16
12445125-7	2002	Additionally, a similar Cd2+-induced stomatal closure was observed in the ABA insensitive mutant abi1-1.	alisol B 23-acetate	74-77	CD2 molecule	Homo sapiens	24-27
12445125-11	2002	In conclusion, we propose that Cd2+ affects guard cell regulation in an ABA-independent manner by entering the cytosol via Ca2+ channels.	alisol B 23-acetate	72-75	CD2 molecule	Homo sapiens	31-34
12227513-4	2002	This competitive adsorption shows that the presence of Cd2+ has not an important effect on Cu2+ adsorption, whereas a dramatic decrease is observed on the adsorption of Cd2+ in the presence of Cu2+.	cupric ion	193-197	CD2 molecule	Homo sapiens	169-172
12133935-5	2002	cAMP-primed CD45RA cells had a phenotype characteristic of memory/effector T lymphocytes, as they showed an up-regulated expression of CD2, CD44, and CD11a molecules, while the levels of CD62L Ag were down-regulated.	Cyclic AMP	0-4	CD2 molecule	Homo sapiens	135-138
12147347-2	2002	We have successfully engineered a series of model proteins, each containing a single EF-hand loop but with increasing numbers of Gly residues linking the EF-hand loop to a scaffold protein, cluster of differentiation 2 (CD2), to obtain the site-specific calcium-binding ability of a protein with EF-hand motifs without the interference of cooperativity.	Glycine	129-132	CD2 molecule	Homo sapiens	220-223
12147347-2	2002	We have successfully engineered a series of model proteins, each containing a single EF-hand loop but with increasing numbers of Gly residues linking the EF-hand loop to a scaffold protein, cluster of differentiation 2 (CD2), to obtain the site-specific calcium-binding ability of a protein with EF-hand motifs without the interference of cooperativity.	Calcium	254-261	CD2 molecule	Homo sapiens	220-223
12147347-3	2002	Loop III of calmodulin with two Gly linkers in CD2 (CaM-CD2-III-5G) has metal affinities with K(d) values of 1.86 x 10(-4) and 5.8 x 10(-5) M for calcium and lanthanum, respectively.	Calcium	146-153	CD2 molecule	Homo sapiens	47-50
12147347-3	2002	Loop III of calmodulin with two Gly linkers in CD2 (CaM-CD2-III-5G) has metal affinities with K(d) values of 1.86 x 10(-4) and 5.8 x 10(-5) M for calcium and lanthanum, respectively.	Calcium	146-153	CD2 molecule	Homo sapiens	52-66
12147347-3	2002	Loop III of calmodulin with two Gly linkers in CD2 (CaM-CD2-III-5G) has metal affinities with K(d) values of 1.86 x 10(-4) and 5.8 x 10(-5) M for calcium and lanthanum, respectively.	Lanthanum	158-167	CD2 molecule	Homo sapiens	47-50
12147347-3	2002	Loop III of calmodulin with two Gly linkers in CD2 (CaM-CD2-III-5G) has metal affinities with K(d) values of 1.86 x 10(-4) and 5.8 x 10(-5) M for calcium and lanthanum, respectively.	Lanthanum	158-167	CD2 molecule	Homo sapiens	52-66
12147347-4	2002	The oligomeric states of the CD2 variants were examined by pulsed-field-gradient nuclear magnetic resonance (PFG NMR).	pfg	109-112	CD2 molecule	Homo sapiens	29-32
12147347-5	2002	The diffusion coefficient values of CD2 variants are about 11.1 x 10(-7) cm(2)/s both in the presence and absence of metal ions, which are the same as that of wild-type CD2.	Metals	117-122	CD2 molecule	Homo sapiens	36-39
12200539-1	2002	To understand the key determinants in calcium-binding affinity, a calcium-binding site with pentagonal bipyramid geometry was designed into a non-calcium-binding protein, domain 1 of CD2.	Calcium	38-45	CD2 molecule	Homo sapiens	183-186
12200539-1	2002	To understand the key determinants in calcium-binding affinity, a calcium-binding site with pentagonal bipyramid geometry was designed into a non-calcium-binding protein, domain 1 of CD2.	Calcium	66-73	CD2 molecule	Homo sapiens	183-186
12200539-1	2002	To understand the key determinants in calcium-binding affinity, a calcium-binding site with pentagonal bipyramid geometry was designed into a non-calcium-binding protein, domain 1 of CD2.	bipyramid	103-112	CD2 molecule	Homo sapiens	183-186
12200539-1	2002	To understand the key determinants in calcium-binding affinity, a calcium-binding site with pentagonal bipyramid geometry was designed into a non-calcium-binding protein, domain 1 of CD2.	Calcium	66-73	CD2 molecule	Homo sapiens	183-186
12200539-4	2002	The addition of protein concentration to Tb(III) solution results in a large enhancement of Tb(III) fluorescence due to energy transfer between terbium ions and aromatic residues in CD2-D1.	tb(iii)	41-48	CD2 molecule	Homo sapiens	182-185
12200539-4	2002	The addition of protein concentration to Tb(III) solution results in a large enhancement of Tb(III) fluorescence due to energy transfer between terbium ions and aromatic residues in CD2-D1.	tb(iii)	92-99	CD2 molecule	Homo sapiens	182-185
12200539-4	2002	The addition of protein concentration to Tb(III) solution results in a large enhancement of Tb(III) fluorescence due to energy transfer between terbium ions and aromatic residues in CD2-D1.	Terbium	144-151	CD2 molecule	Homo sapiens	182-185
11999076-3	2002	Cd2+ sorption is controlled by sample BET surface area, which shows a direct dependence on the hydroxyapatite crystallite dimensions.	Durapatite	95-109	CD2 molecule	Homo sapiens	0-3
12045262-5	2002	In contrast, CD2 activation induced modest PBT but vigorous LPT cycling.	(E)-2-(pent-3-en-1-yn-1-yl)thiophene	43-46	CD2 molecule	Homo sapiens	13-16
12045262-7	2002	LPTs failed to upregulate cyclin-dependent kinase 4 and cyclin D3, but Rb phosphorylation and cyclin A and B1 upregulation were induced by CD2 engagement.	Rubidium	71-73	CD2 molecule	Homo sapiens	139-142
12045262-9	2002	CD2-activated LPTs displayed a striking upregulation of p53, whose blockade by antisense oligonucleotides accelerated their S phase transit time to that of CD3-activated PBTs.	Oligonucleotides	89-105	CD2 molecule	Homo sapiens	0-3
12045262-9	2002	CD2-activated LPTs displayed a striking upregulation of p53, whose blockade by antisense oligonucleotides accelerated their S phase transit time to that of CD3-activated PBTs.	pbts	170-174	CD2 molecule	Homo sapiens	0-3
11984520-2	2002	METHODS: RA(+), RO(+) PBT, and LPT were activated with CD3, CD2, and CD28 antibodies, and caspase activity, apoptosis, and proliferation were measured by a fluorometric assay, DNA content, and thymidine incorporation, respectively.	ro(+) pbt	16-25	CD2 molecule	Homo sapiens	60-63
11984520-2	2002	METHODS: RA(+), RO(+) PBT, and LPT were activated with CD3, CD2, and CD28 antibodies, and caspase activity, apoptosis, and proliferation were measured by a fluorometric assay, DNA content, and thymidine incorporation, respectively.	CIS-(AMMINE)(CYCLOHEXYLAMINE)PLATINUM(II) COMPLEX	31-34	CD2 molecule	Homo sapiens	60-63
11941315-9	2002	p38 MAPK phosphorylation of CD2(+) T cells occurred on serine residues.	Serine	55-61	CD2 molecule	Homo sapiens	28-31
11948788-6	2002	Using the established method, we have designed de novo calcium-binding sites into the scaffold of non-calcium-binding proteins CD2 and Rop.	Calcium	55-62	CD2 molecule	Homo sapiens	127-130
11948788-6	2002	Using the established method, we have designed de novo calcium-binding sites into the scaffold of non-calcium-binding proteins CD2 and Rop.	Calcium	102-109	CD2 molecule	Homo sapiens	127-130
12102281-5	2002	Computed tomography (CT) and magnetic resonance imaging (MRI) of the thoracic spine showed calcium-density masses that were in contact with the neural arches and bulged into the spinal canal at T5/T6, T7/T8, T9/T10, and T10/T11.	Calcium	91-98	CD2 molecule	Homo sapiens	224-227
11844490-0	2002	A facile regio- and stereoselective synthesis of mannose octasaccharide of the N-glycan in human CD2 and mannose hexasaccharide antigenic factor 13b.	mannose octasaccharide	49-71	CD2 molecule	Homo sapiens	97-100
11996368-0	2002	Study of Cd2+ complexation by the glutathione fragments Cys-Gly (CG) and gamma-Glu-Cys (gamma-EC) by differential pulse polarography.	Glutathione	34-45	CD2 molecule	Homo sapiens	9-12
11996368-0	2002	Study of Cd2+ complexation by the glutathione fragments Cys-Gly (CG) and gamma-Glu-Cys (gamma-EC) by differential pulse polarography.	cysteinylglycine	56-63	CD2 molecule	Homo sapiens	9-12
11996368-0	2002	Study of Cd2+ complexation by the glutathione fragments Cys-Gly (CG) and gamma-Glu-Cys (gamma-EC) by differential pulse polarography.	cysteinylglycine	65-67	CD2 molecule	Homo sapiens	9-12
11996368-0	2002	Study of Cd2+ complexation by the glutathione fragments Cys-Gly (CG) and gamma-Glu-Cys (gamma-EC) by differential pulse polarography.	gamma-glutamylcysteine	73-86	CD2 molecule	Homo sapiens	9-12
11996368-2	2002	The simultaneous analysis of the titration of peptide with metal and of metal with peptide allowed the resolution of the Cd2+/Cys-Gly system, whereas in the analysis of the Cd2+/gamma-Glu-Cys system the analysis of a single titration experiment was sufficient.	Metals	72-77	CD2 molecule	Homo sapiens	121-124
11996368-2	2002	The simultaneous analysis of the titration of peptide with metal and of metal with peptide allowed the resolution of the Cd2+/Cys-Gly system, whereas in the analysis of the Cd2+/gamma-Glu-Cys system the analysis of a single titration experiment was sufficient.	Cysteine	126-129	CD2 molecule	Homo sapiens	121-124
11996368-2	2002	The simultaneous analysis of the titration of peptide with metal and of metal with peptide allowed the resolution of the Cd2+/Cys-Gly system, whereas in the analysis of the Cd2+/gamma-Glu-Cys system the analysis of a single titration experiment was sufficient.	Glycine	130-133	CD2 molecule	Homo sapiens	121-124
11996368-3	2002	The analysis of the shape of the resulting pure voltammograms and concentration profiles of the resolved components suggested the presence of two different types of bound Cd2+ in the two systems considered, that could be attributed to Cd2+ bound to one or two sulfur atoms to form complexes of stoichiometry 1:1 and 1:2. respectively.	Sulfur	260-266	CD2 molecule	Homo sapiens	171-174
11951988-4	2002	The negative deltarHthetam and deltarSthetam values are observed for the binding reaction of Cd2+ ion and BSA, suggesting that the binding reaction is mainly enthalpy-driven and the entropy is unfavorable for it.	deltarhthetam	13-26	CD2 molecule	Homo sapiens	93-96
11951988-4	2002	The negative deltarHthetam and deltarSthetam values are observed for the binding reaction of Cd2+ ion and BSA, suggesting that the binding reaction is mainly enthalpy-driven and the entropy is unfavorable for it.	deltarsthetam	31-44	CD2 molecule	Homo sapiens	93-96
11844490-1	2002	A highly concise and effective synthesis of the mannose octasaccharide of the N-linked glycan in the adhesion domain of human CD2 was achieved via TMSOTf-promoted selective 6-glycosylation of a trisaccharide 4,6-diol acceptor with a pentasaccharide donor, followed by deprotection.	mannose octasaccharide	48-70	CD2 molecule	Homo sapiens	126-129
11844490-1	2002	A highly concise and effective synthesis of the mannose octasaccharide of the N-linked glycan in the adhesion domain of human CD2 was achieved via TMSOTf-promoted selective 6-glycosylation of a trisaccharide 4,6-diol acceptor with a pentasaccharide donor, followed by deprotection.	n-linked glycan	78-93	CD2 molecule	Homo sapiens	126-129
11844490-1	2002	A highly concise and effective synthesis of the mannose octasaccharide of the N-linked glycan in the adhesion domain of human CD2 was achieved via TMSOTf-promoted selective 6-glycosylation of a trisaccharide 4,6-diol acceptor with a pentasaccharide donor, followed by deprotection.	Trisaccharides	194-207	CD2 molecule	Homo sapiens	126-129
11844490-1	2002	A highly concise and effective synthesis of the mannose octasaccharide of the N-linked glycan in the adhesion domain of human CD2 was achieved via TMSOTf-promoted selective 6-glycosylation of a trisaccharide 4,6-diol acceptor with a pentasaccharide donor, followed by deprotection.	4,6-diol	208-216	CD2 molecule	Homo sapiens	126-129
11844490-1	2002	A highly concise and effective synthesis of the mannose octasaccharide of the N-linked glycan in the adhesion domain of human CD2 was achieved via TMSOTf-promoted selective 6-glycosylation of a trisaccharide 4,6-diol acceptor with a pentasaccharide donor, followed by deprotection.	pentasaccharide	233-248	CD2 molecule	Homo sapiens	126-129
11844490-0	2002	A facile regio- and stereoselective synthesis of mannose octasaccharide of the N-glycan in human CD2 and mannose hexasaccharide antigenic factor 13b.	n-glycan	79-87	CD2 molecule	Homo sapiens	97-100
11803035-2	2002	Cd2+ and Zn2+ react with apo-MT to form metal-thiolate bonds in reactions that are complete within milliseconds and which are pH-dependent.	metal-thiolate	40-54	CD2 molecule	Homo sapiens	0-3
11841793-1	2002	A member of the Theta class of human glutathione transferases (GST T1-1) was found to display the greatest catalytic activity towards the cytostatic drug 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU) of the GSTs studied.	Carmustine	154-190	CD2 molecule	Homo sapiens	67-71
11841793-1	2002	A member of the Theta class of human glutathione transferases (GST T1-1) was found to display the greatest catalytic activity towards the cytostatic drug 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU) of the GSTs studied.	Carmustine	192-196	CD2 molecule	Homo sapiens	67-71
11841793-3	2002	From the 12 enzymes examined, only GST M2-2, GST M3-3 and GST T1-1 had significant activities with BCNU.	Carmustine	99-103	CD2 molecule	Homo sapiens	62-66
11739187-10	2001	In addition, stimulation of neoplastic MCs through T11-3 and a second CD2 epitope resulted in histamine release.	Histamine	94-103	CD2 molecule	Homo sapiens	70-73
11808652-0	2002	Electron paramagnetic resonance parameters of V2+ ions in both Cd2+ sites of CsCdCl3 crystal.	cscdcl3	77-84	CD2 molecule	Homo sapiens	63-66
12003149-1	2002	The interactions of Cd2+ with silica and calcite were observed through laboratory dynamic experiments.	Silicon Dioxide	30-36	CD2 molecule	Homo sapiens	20-23
12003149-3	2002	Chromatographic column experiments show that Cd2+ sorption on silica can be considered as a reversible equilibrate reaction which depends on water composition and pH.	Silicon Dioxide	62-68	CD2 molecule	Homo sapiens	45-48
12003149-3	2002	Chromatographic column experiments show that Cd2+ sorption on silica can be considered as a reversible equilibrate reaction which depends on water composition and pH.	Water	141-146	CD2 molecule	Homo sapiens	45-48
12003149-4	2002	For a porous medium composed by a mixture of silica and calcite, the Cd2+ migration behaviours are predominantly controlled by calcite.	Silicon Dioxide	45-51	CD2 molecule	Homo sapiens	69-72
11792427-6	2002	CD2 crosslinking markedly induced tyrosine phosphorylation of Cbl associated with Grb2 or CrkL, Shc and LAT, compared with IL-2 stimulation.	Tyrosine	34-42	CD2 molecule	Homo sapiens	0-3
11792427-9	2002	Furthermore, CD2 crosslinking, but not IL-2 stimulation, markedly induced tyrosine phosphorylation of LAT.	Tyrosine	74-82	CD2 molecule	Homo sapiens	13-16
11792427-10	2002	Thus, tyrosine phosphorylation of different adapter proteins and consequent interactions between signaling molecules described here may explain the molecular mechanisms of the additive effects of IL-2 stimulation and CD2 crosslinking on NK cell activation.	Tyrosine	6-14	CD2 molecule	Homo sapiens	217-220
11763042-3	2001	Moreover, the adsorption of both Cd2+ and Mn2+ to living cells and dry cells, was dependent on the metal concentrations, and fitted the Freundlich adsorption isotherm.	Metals	99-104	CD2 molecule	Homo sapiens	33-36
11553620-6	2001	While CD2-induced p62(dok) tyrosine phosphorylation was independent of both the p36/38 membrane adapter protein linker of activated T cells (LAT) and the ZAP70/Syk family of kinases, it was dependent upon the Src family of kinases including Lck and Fyn.	Tyrosine	27-35	CD2 molecule	Homo sapiens	6-9
11553620-7	2001	We find further that CD2 engagement induced the association of tyrosine-phosphorylated p62(dok) to Crk-L.	Tyrosine	63-71	CD2 molecule	Homo sapiens	21-24
11763042-6	2001	Polysaccharide extracts of this organism adsorbed high amounts of both Cd2+ (I15-425 microgmg(-1)) and Mn2+ (473-906 microgmg(-1)).	Polysaccharides	0-14	CD2 molecule	Homo sapiens	71-74
11763448-6	2001	It was found that hard Lewis acid type metal cations such as K+ and Mg2+, and borderline or soft metal cations such as Zn2+, Cu2+, and Cd2+ exhibit clearly different binding activity toward peptide-lipid monolayers.	Lewis Acids	23-33	CD2 molecule	Homo sapiens	135-138
11763448-6	2001	It was found that hard Lewis acid type metal cations such as K+ and Mg2+, and borderline or soft metal cations such as Zn2+, Cu2+, and Cd2+ exhibit clearly different binding activity toward peptide-lipid monolayers.	Metals	39-44	CD2 molecule	Homo sapiens	135-138
11763448-6	2001	It was found that hard Lewis acid type metal cations such as K+ and Mg2+, and borderline or soft metal cations such as Zn2+, Cu2+, and Cd2+ exhibit clearly different binding activity toward peptide-lipid monolayers.	magnesium ion	68-72	CD2 molecule	Homo sapiens	135-138
11763448-6	2001	It was found that hard Lewis acid type metal cations such as K+ and Mg2+, and borderline or soft metal cations such as Zn2+, Cu2+, and Cd2+ exhibit clearly different binding activity toward peptide-lipid monolayers.	Metals	97-102	CD2 molecule	Homo sapiens	135-138
11763448-6	2001	It was found that hard Lewis acid type metal cations such as K+ and Mg2+, and borderline or soft metal cations such as Zn2+, Cu2+, and Cd2+ exhibit clearly different binding activity toward peptide-lipid monolayers.	Zinc	119-123	CD2 molecule	Homo sapiens	135-138
11763448-6	2001	It was found that hard Lewis acid type metal cations such as K+ and Mg2+, and borderline or soft metal cations such as Zn2+, Cu2+, and Cd2+ exhibit clearly different binding activity toward peptide-lipid monolayers.	cupric ion	125-129	CD2 molecule	Homo sapiens	135-138
11691852-2	2001	From an integration library consisting of cells transformable by the insulin-like growth factor 1 (IGF-1), a collection of neomycin resistant (Neo(R)) clones was obtained; 86% also expressed the CD2 cell surface antigen.	Neomycin	123-131	CD2 molecule	Homo sapiens	195-198
11809931-3	2001	In addition, calcium binding to the engineered CD2 variants does not result in a significant change from native CD2 conformation.	Calcium	13-20	CD2 molecule	Homo sapiens	47-50
11809931-4	2001	The CD2 variant with two Gly linkers has been shown to have the strongest metal binding affinity to Ca(II) and La(III).	Glycine	25-28	CD2 molecule	Homo sapiens	4-7
11809931-4	2001	The CD2 variant with two Gly linkers has been shown to have the strongest metal binding affinity to Ca(II) and La(III).	Metals	74-79	CD2 molecule	Homo sapiens	4-7
11809931-4	2001	The CD2 variant with two Gly linkers has been shown to have the strongest metal binding affinity to Ca(II) and La(III).	Diazepam	111-118	CD2 molecule	Homo sapiens	4-7
11716369-3	2001	Using a CdS/AgS ion selective electrode to measure [Cd2+] in physiological saline solution at pH 7.4, we show that Fe2+ promotes Cd2+ binding to citrate thereby decreasing the availability of free Cd2+.	Cadmium	8-11	CD2 molecule	Homo sapiens	129-132
12914063-4	2001	Thereafter, the fatty acid film is immersed in cadmium sulfate solution and Cd2+ ions entrapped in the lipid matrix by electrostatic complexation with the carboxylate ions of the fatty acid molecules.	Fatty Acids	16-26	CD2 molecule	Homo sapiens	76-79
12914063-4	2001	Thereafter, the fatty acid film is immersed in cadmium sulfate solution and Cd2+ ions entrapped in the lipid matrix by electrostatic complexation with the carboxylate ions of the fatty acid molecules.	carboxylate	155-166	CD2 molecule	Homo sapiens	76-79
12914063-4	2001	Thereafter, the fatty acid film is immersed in cadmium sulfate solution and Cd2+ ions entrapped in the lipid matrix by electrostatic complexation with the carboxylate ions of the fatty acid molecules.	Fatty Acids	179-189	CD2 molecule	Homo sapiens	76-79
12914063-5	2001	The final step involves reaction of the entrapped Cd2+ ions with Na2S, leading to the in situ generation of cadmium sulfide nanoparticles within the patterned lipid matrix.	sodium sulfide	65-69	CD2 molecule	Homo sapiens	50-53
12914063-5	2001	The final step involves reaction of the entrapped Cd2+ ions with Na2S, leading to the in situ generation of cadmium sulfide nanoparticles within the patterned lipid matrix.	cadmium sulfide	108-123	CD2 molecule	Homo sapiens	50-53
11555388-3	2001	CD26 costimulates both the CD3 and the CD2 dependent T-cell activation and tyrosine phosphorylation of TCR/CD3 signal transduction pathway proteins.	Tyrosine	75-83	CD2 molecule	Homo sapiens	0-3
11716369-3	2001	Using a CdS/AgS ion selective electrode to measure [Cd2+] in physiological saline solution at pH 7.4, we show that Fe2+ promotes Cd2+ binding to citrate thereby decreasing the availability of free Cd2+.	Cadmium	8-11	CD2 molecule	Homo sapiens	129-132
11716369-3	2001	Using a CdS/AgS ion selective electrode to measure [Cd2+] in physiological saline solution at pH 7.4, we show that Fe2+ promotes Cd2+ binding to citrate thereby decreasing the availability of free Cd2+.	Silver	12-15	CD2 molecule	Homo sapiens	129-132
11716369-3	2001	Using a CdS/AgS ion selective electrode to measure [Cd2+] in physiological saline solution at pH 7.4, we show that Fe2+ promotes Cd2+ binding to citrate thereby decreasing the availability of free Cd2+.	Silver	12-15	CD2 molecule	Homo sapiens	129-132
11716369-3	2001	Using a CdS/AgS ion selective electrode to measure [Cd2+] in physiological saline solution at pH 7.4, we show that Fe2+ promotes Cd2+ binding to citrate thereby decreasing the availability of free Cd2+.	Sodium Chloride	75-81	CD2 molecule	Homo sapiens	52-55
11716369-3	2001	Using a CdS/AgS ion selective electrode to measure [Cd2+] in physiological saline solution at pH 7.4, we show that Fe2+ promotes Cd2+ binding to citrate thereby decreasing the availability of free Cd2+.	ammonium ferrous sulfate	115-119	CD2 molecule	Homo sapiens	52-55
11716369-3	2001	Using a CdS/AgS ion selective electrode to measure [Cd2+] in physiological saline solution at pH 7.4, we show that Fe2+ promotes Cd2+ binding to citrate thereby decreasing the availability of free Cd2+.	ammonium ferrous sulfate	115-119	CD2 molecule	Homo sapiens	129-132
11716369-3	2001	Using a CdS/AgS ion selective electrode to measure [Cd2+] in physiological saline solution at pH 7.4, we show that Fe2+ promotes Cd2+ binding to citrate thereby decreasing the availability of free Cd2+.	ammonium ferrous sulfate	115-119	CD2 molecule	Homo sapiens	129-132
11716369-3	2001	Using a CdS/AgS ion selective electrode to measure [Cd2+] in physiological saline solution at pH 7.4, we show that Fe2+ promotes Cd2+ binding to citrate thereby decreasing the availability of free Cd2+.	Citric Acid	145-152	CD2 molecule	Homo sapiens	129-132
11716369-3	2001	Using a CdS/AgS ion selective electrode to measure [Cd2+] in physiological saline solution at pH 7.4, we show that Fe2+ promotes Cd2+ binding to citrate thereby decreasing the availability of free Cd2+.	Citric Acid	145-152	CD2 molecule	Homo sapiens	129-132
11716369-4	2001	This suggests the formation of high molecular weight Cd2+-Fe2+-citrate complexes.	fe2+-citrate	58-70	CD2 molecule	Homo sapiens	53-56
11407316-6	2001	In a comparative study with steroids (alclometasone dipropionate and betamethason valerate) in anti-CD3/CD2 system, tacrolimus and both steroids inhibited Th1 cytokines (IL-2, IFN-gamma), Th2 cytokines (IL-4, IL-5) and IL-3, GM-CSF (produced by both Th1 and Th2).	alclometasone dipropionate	38-64	CD2 molecule	Homo sapiens	104-107
12947673-6	2001	The method was successfully applied to determinate trace amounts of Cu2+, Pb2+, Cd2+ and Mn2+ species in drinking water and environment water samples.	Water	114-119	CD2 molecule	Homo sapiens	80-83
11407316-6	2001	In a comparative study with steroids (alclometasone dipropionate and betamethason valerate) in anti-CD3/CD2 system, tacrolimus and both steroids inhibited Th1 cytokines (IL-2, IFN-gamma), Th2 cytokines (IL-4, IL-5) and IL-3, GM-CSF (produced by both Th1 and Th2).	betamethason valerate	69-90	CD2 molecule	Homo sapiens	104-107
11407316-6	2001	In a comparative study with steroids (alclometasone dipropionate and betamethason valerate) in anti-CD3/CD2 system, tacrolimus and both steroids inhibited Th1 cytokines (IL-2, IFN-gamma), Th2 cytokines (IL-4, IL-5) and IL-3, GM-CSF (produced by both Th1 and Th2).	Steroids	136-144	CD2 molecule	Homo sapiens	104-107
11273651-3	2001	Using the native mGluR1 and CD2-mGluR1 chimeric molecules, as well as their C-terminal truncations and mutants, we identified an endoplasmic reticulum (ER) retention signal Arg-Arg-Lys-Lys within the C-terminal sequence of mGluR1b.	Arginine	177-180	CD2 molecule	Homo sapiens	28-31
11376005-5	2001	Structural integrity of rafts is necessary for CD2-stimulated elevation of intracellular free calcium and tyrosine phosphorylation of cellular substrates.	Calcium	94-101	CD2 molecule	Homo sapiens	47-50
11376005-5	2001	Structural integrity of rafts is necessary for CD2-stimulated elevation of intracellular free calcium and tyrosine phosphorylation of cellular substrates.	Tyrosine	106-114	CD2 molecule	Homo sapiens	47-50
11376005-6	2001	Whereas murine CD2 contains two membrane-proximal intracellular cysteines, partitioning CD2 into cholesterol-rich lipid rafts constitutively, human CD2 has no cytoplasmic cysteines.	Cholesterol	97-108	CD2 molecule	Homo sapiens	88-91
11376005-7	2001	Mapping studies using CD2 point mutation, deletion, and chimeric molecules suggest that conformational change in the CD2 ectodomain participates in inducible raft association and excludes the membrane-proximal N-linked glycans, the transmembrane segment, and the CD2 cytoplasmic region (residues 8-117) as necessary for translocation.	n-linked glycans	210-226	CD2 molecule	Homo sapiens	117-120
11376005-7	2001	Mapping studies using CD2 point mutation, deletion, and chimeric molecules suggest that conformational change in the CD2 ectodomain participates in inducible raft association and excludes the membrane-proximal N-linked glycans, the transmembrane segment, and the CD2 cytoplasmic region (residues 8-117) as necessary for translocation.	n-linked glycans	210-226	CD2 molecule	Homo sapiens	117-120
11254695-2	2001	In T cells, the two members that are predominantly expressed, p56(dok) and p62(dok), are tyrosine phosphorylated upon CD2 or CD28 stimulation, but not upon CD3 ligation.	Tyrosine	89-97	CD2 molecule	Homo sapiens	118-121
11513145-7	2001	CS1 is a novel member of the CD2 subset that contains two of the unique tyrosine motifs present in 2B4 and SLAM.	Tyrosine	72-80	CD2 molecule	Homo sapiens	29-32
11393227-1	2001	An 1-(pyridylazo)-2-naphthol modified glassy carbon electrode has been investigated as sensor for the measurement of trace levels of Cd2+.	1-(pyridylazo)-2-naphthol	3-28	CD2 molecule	Homo sapiens	133-136
11393227-1	2001	An 1-(pyridylazo)-2-naphthol modified glassy carbon electrode has been investigated as sensor for the measurement of trace levels of Cd2+.	Carbon	45-51	CD2 molecule	Homo sapiens	133-136
11393227-2	2001	Cd2+ is deposited on the surface of a PAN modified glassy carbon electrode at -1.10 V (vs. SCE) via forming Cd2+-PAN and subsequent reduction at the electrode.	Carbon	58-64	CD2 molecule	Homo sapiens	0-3
11393227-2	2001	Cd2+ is deposited on the surface of a PAN modified glassy carbon electrode at -1.10 V (vs. SCE) via forming Cd2+-PAN and subsequent reduction at the electrode.	Carbon	58-64	CD2 molecule	Homo sapiens	108-111
11298136-9	2001	The results obtained during a three year period in the proliferation assays show an impaired PMA (phorbol myristate acetate) activation in specific T lymphocyte activation pathways (CD69, CD26, CD28, CD3, PHA, PWM and Con A mediated) but not in others (CD2, ionomycin, and Ig surface receptor).	Tetradecanoylphorbol Acetate	98-123	CD2 molecule	Homo sapiens	188-191
11273651-3	2001	Using the native mGluR1 and CD2-mGluR1 chimeric molecules, as well as their C-terminal truncations and mutants, we identified an endoplasmic reticulum (ER) retention signal Arg-Arg-Lys-Lys within the C-terminal sequence of mGluR1b.	Arginine	173-176	CD2 molecule	Homo sapiens	28-31
11285908-8	2001	Results show the measured stability constants follow the order (from strongest to weakest): Al3+ > Cu2+ > Pb2+ > Cd2+ > Zn2+ > Fe3+ > Hg2+ > Ca2+ > Co2+ > Ni2+ > Mn2+ > Mg2+ > K+.	Mercuric cation	152-156	CD2 molecule	Homo sapiens	122-125
11347608-7	2001	The affinity of PAA for Cd2+ increased strongly with pH.	carbopol 940	16-19	CD2 molecule	Homo sapiens	24-27
11285908-8	2001	Results show the measured stability constants follow the order (from strongest to weakest): Al3+ > Cu2+ > Pb2+ > Cd2+ > Zn2+ > Fe3+ > Hg2+ > Ca2+ > Co2+ > Ni2+ > Mn2+ > Mg2+ > K+.	Cobalt(2+)	172-176	CD2 molecule	Homo sapiens	122-125
11285908-8	2001	Results show the measured stability constants follow the order (from strongest to weakest): Al3+ > Cu2+ > Pb2+ > Cd2+ > Zn2+ > Fe3+ > Hg2+ > Ca2+ > Co2+ > Ni2+ > Mn2+ > Mg2+ > K+.	Nickel(2+)	182-186	CD2 molecule	Homo sapiens	122-125
11285908-8	2001	Results show the measured stability constants follow the order (from strongest to weakest): Al3+ > Cu2+ > Pb2+ > Cd2+ > Zn2+ > Fe3+ > Hg2+ > Ca2+ > Co2+ > Ni2+ > Mn2+ > Mg2+ > K+.	Manganese(2+)	192-196	CD2 molecule	Homo sapiens	122-125
11285908-8	2001	Results show the measured stability constants follow the order (from strongest to weakest): Al3+ > Cu2+ > Pb2+ > Cd2+ > Zn2+ > Fe3+ > Hg2+ > Ca2+ > Co2+ > Ni2+ > Mn2+ > Mg2+ > K+.	magnesium ion	202-206	CD2 molecule	Homo sapiens	122-125
11166460-5	2001	RESULTS: Stimulation of CD2 on primary T lymphocytes leads to the tyrosine phosphorylation, nuclear translocation, and DNA binding of STAT1.	Tyrosine	66-74	CD2 molecule	Homo sapiens	24-27
11328568-0	2001	Expression of CD2 and activation markers on blood T-helper cell subsets in patients with transfusional iron overload.	Iron	103-107	CD2 molecule	Homo sapiens	14-17
11328568-4	2001	When investigating whether this difference could be due to the iron overload we found the number of CD2 BS closely related to the iron saturation of serum transferrin (TfS) (R2 = 0.78, P < 0.001).	Iron	63-67	CD2 molecule	Homo sapiens	100-103
11328568-4	2001	When investigating whether this difference could be due to the iron overload we found the number of CD2 BS closely related to the iron saturation of serum transferrin (TfS) (R2 = 0.78, P < 0.001).	Iron	130-134	CD2 molecule	Homo sapiens	100-103
11215815-5	2000	Our results demonstrate that DMSO induces cell growth inhibition, cell phenotype changes, with down-regulation of CD2 and CD7, and increases in alpha/beta or gamma/delta TCR chains led by TdT, RAG-1 and RAG-2 activity.	Dimethyl Sulfoxide	29-33	CD2 molecule	Homo sapiens	114-117
11399323-6	2000	CD2 crosslinking results in the marked tyrosine phosphorylation of Cbl in an antibody concentration- and time-dependent manner.	Tyrosine	39-47	CD2 molecule	Homo sapiens	0-3
11399323-9	2000	In addition, we demonstrate that CrkL associates with a large portion of tyrosine phosphorylated Cbl after CD2 stimulation of NK3.3 cells.	Tyrosine	73-81	CD2 molecule	Homo sapiens	107-110
11399323-10	2000	In contrast to constitutive Cbl association with Grb2, tyrosine phosphorylated Cbl interacts with CrkL via its SH2 domain only after CD2 stimulation.	Tyrosine	55-63	CD2 molecule	Homo sapiens	133-136
11032778-2	2000	In this study, spectrofluorimetric experiments in free solution, using Fluo-3 and Fura-2, showed that Zn2+ and Cd2+ enhanced the probe signal, Cu2+ quenched it, and Hg2+ had no effect.	Fluo-3	71-77	CD2 molecule	Homo sapiens	111-114
11133830-2	2001	Engagement of human CD2 by mitogenic pairs of anti-CD2 mAb induces tyrosine phosphorylation of a number of intracellular proteins including a 120 kDa phosphoprotein that we identify as the proto-oncogene c-Cbl.	Tyrosine	67-75	CD2 molecule	Homo sapiens	20-23
11133830-2	2001	Engagement of human CD2 by mitogenic pairs of anti-CD2 mAb induces tyrosine phosphorylation of a number of intracellular proteins including a 120 kDa phosphoprotein that we identify as the proto-oncogene c-Cbl.	Tyrosine	67-75	CD2 molecule	Homo sapiens	51-54
11133830-7	2001	In Syk(-) Jurkat T cells stably expressing wild-type ZAP-70, CD2 stimulation induced only a minimal increase in ZAP-70 tyrosine phosphorylation.	Tyrosine	119-127	CD2 molecule	Homo sapiens	61-64
11962255-5	2001	On the other hand, our results indicate that apoptosis induced by CD2 samples could also be associated with high levels of arginine deiminase activity, which in turn was able to downregulate polyamine synthesis in Jurkat cells.	Polyamines	191-200	CD2 molecule	Homo sapiens	66-69
11093160-9	2000	In untransformed human peripheral blood T lymphocytes, these phosphatases function through a cyclosporin A/FK506-resistant co-stimulatory signaling pathway which is common for the accessory receptors CD2 and CD28.	Cyclosporine	93-106	CD2 molecule	Homo sapiens	200-203
11093160-9	2000	In untransformed human peripheral blood T lymphocytes, these phosphatases function through a cyclosporin A/FK506-resistant co-stimulatory signaling pathway which is common for the accessory receptors CD2 and CD28.	Tacrolimus	107-112	CD2 molecule	Homo sapiens	200-203
11093148-0	2000	Priming of CD2-induced p62Dok tyrosine phosphorylation by CD3 in Jurkat T cells.	Tyrosine	30-38	CD2 molecule	Homo sapiens	11-14
11093148-2	2000	Beside common biochemical events, we previously showed that a 62-kDa protein associated with PLCgamma-1 and p21RasGAP was specifically tyrosine phosphorylated after CD2 stimulation in Jurkat T cells.	Tyrosine	135-143	CD2 molecule	Homo sapiens	165-168
11093148-4	2000	Mainly, we showed that p62Dok tyrosine phosphorylation was strengthened by the functional interplay between CD3 and CD2.	Tyrosine	30-38	CD2 molecule	Homo sapiens	116-119
11093148-6	2000	Kinetic studies indicated that a short treatment with anti-CD3 was sufficient to amplify the CD2-induced tyrosine phosphorylation of p62Dok.	Tyrosine	105-113	CD2 molecule	Homo sapiens	93-96
11093148-7	2000	By contrast, CD2-induced PLCgamma-1 tyrosine phosphorylation and calcium response progressively diminished.	Tyrosine	36-44	CD2 molecule	Homo sapiens	13-16
11093148-7	2000	By contrast, CD2-induced PLCgamma-1 tyrosine phosphorylation and calcium response progressively diminished.	Calcium	65-72	CD2 molecule	Homo sapiens	13-16
11093148-8	2000	Finally, enhanced amounts of tyrosine phosphorylated p62Dok were recruited to p21RasGAP and PLCgamma-1 after CD2 stimulation in CD3-activated cells.	Tyrosine	29-37	CD2 molecule	Homo sapiens	109-112
11032778-2	2000	In this study, spectrofluorimetric experiments in free solution, using Fluo-3 and Fura-2, showed that Zn2+ and Cd2+ enhanced the probe signal, Cu2+ quenched it, and Hg2+ had no effect.	Fura-2	82-88	CD2 molecule	Homo sapiens	111-114
11032778-2	2000	In this study, spectrofluorimetric experiments in free solution, using Fluo-3 and Fura-2, showed that Zn2+ and Cd2+ enhanced the probe signal, Cu2+ quenched it, and Hg2+ had no effect.	cupric ion	143-147	CD2 molecule	Homo sapiens	111-114
11032778-2	2000	In this study, spectrofluorimetric experiments in free solution, using Fluo-3 and Fura-2, showed that Zn2+ and Cd2+ enhanced the probe signal, Cu2+ quenched it, and Hg2+ had no effect.	Mercuric cation	165-169	CD2 molecule	Homo sapiens	111-114
11032778-4	2000	Digital imaging of living mussel haemocytes loaded with Fura-2/AM or Fluo-3/AM showed that Hg2+, Cu2+ and Cd2+ induced a rise in probe fluorescence, whereas up to 200 microM Zn2+ had no effect.	Fura-2	56-62	CD2 molecule	Homo sapiens	106-109
11032778-4	2000	Digital imaging of living mussel haemocytes loaded with Fura-2/AM or Fluo-3/AM showed that Hg2+, Cu2+ and Cd2+ induced a rise in probe fluorescence, whereas up to 200 microM Zn2+ had no effect.	Fluo-3	69-75	CD2 molecule	Homo sapiens	106-109
11032778-4	2000	Digital imaging of living mussel haemocytes loaded with Fura-2/AM or Fluo-3/AM showed that Hg2+, Cu2+ and Cd2+ induced a rise in probe fluorescence, whereas up to 200 microM Zn2+ had no effect.	Zinc	174-178	CD2 molecule	Homo sapiens	106-109
11032778-6	2000	Probe calibration yielded [Ca2+]i values characteristic of resting levels in control and Zn2+-exposed cells, and, as expected, indicated Ca2+ homeostasis impairment in cells exposed to Cd2+, Cu2+ and Hg2+.	Zinc	89-93	CD2 molecule	Homo sapiens	185-188
11032778-6	2000	Probe calibration yielded [Ca2+]i values characteristic of resting levels in control and Zn2+-exposed cells, and, as expected, indicated Ca2+ homeostasis impairment in cells exposed to Cd2+, Cu2+ and Hg2+.	Mercuric cation	200-204	CD2 molecule	Homo sapiens	185-188
12541706-6	2000	The detection limits of the four metal ions in 5 microL injection solution were Cd2+ 0.02 ng, Pb2+ 0.02 ng, Cu2+ 0.02 ng, and Zn2+ 0.12 ng, and the linear ranges were Cd2+ 8 ng-1.5 micrograms, Pb2+ 8 ng-3.0 micrograms, Cu2+ 8 ng-5.0 micrograms, and Zn2+ 50 ng-10 micrograms in 10 mL reaction solution.	Metals	33-38	CD2 molecule	Homo sapiens	80-83
10979964-4	2000	Following ligation of CD2 on the surface of the Jurkat T-cell line and human purified T cells, LAT was tyrosine phosphorylated and shown to associate in vivo with a number of other tyrosine phosphorylated proteins including PLCgamma-1, Grb-2, and SLP-76.	Tyrosine	103-111	CD2 molecule	Homo sapiens	22-25
10979964-4	2000	Following ligation of CD2 on the surface of the Jurkat T-cell line and human purified T cells, LAT was tyrosine phosphorylated and shown to associate in vivo with a number of other tyrosine phosphorylated proteins including PLCgamma-1, Grb-2, and SLP-76.	Tyrosine	181-189	CD2 molecule	Homo sapiens	22-25
10979964-5	2000	Using Jurkat cell lines deficient in ZAP70/Syk (P116) or LAT (ANJ3) expression, CD2-dependent PLCgamma-1 and SLP-76 tyrosine phosphorylation required expression both of ZAP70 or Syk and of LAT.	Tyrosine	116-124	CD2 molecule	Homo sapiens	80-83
11034358-7	2000	CD2-induced proliferation as well as production of TNF-alpha and IFN-gamma was abrogated in ZAP-70-deficient T cells, whereas PMA plus ionomycin induced normal activation of these cells.	Ionomycin	135-144	CD2 molecule	Homo sapiens	0-3
12541706-1	2000	HPLC was used in the investigation of the reaction behavior of Cd2+, Pb2+, Cu2+ and Zn2+ with mesotetrakis (4-hydroxy-phenyl)porphine (THPP) and chromatographic behavior of their complexes.	cupric ion	75-79	CD2 molecule	Homo sapiens	63-66
12541706-1	2000	HPLC was used in the investigation of the reaction behavior of Cd2+, Pb2+, Cu2+ and Zn2+ with mesotetrakis (4-hydroxy-phenyl)porphine (THPP) and chromatographic behavior of their complexes.	Zinc	84-88	CD2 molecule	Homo sapiens	63-66
12541706-6	2000	The detection limits of the four metal ions in 5 microL injection solution were Cd2+ 0.02 ng, Pb2+ 0.02 ng, Cu2+ 0.02 ng, and Zn2+ 0.12 ng, and the linear ranges were Cd2+ 8 ng-1.5 micrograms, Pb2+ 8 ng-3.0 micrograms, Cu2+ 8 ng-5.0 micrograms, and Zn2+ 50 ng-10 micrograms in 10 mL reaction solution.	Metals	33-38	CD2 molecule	Homo sapiens	167-170
10968510-9	2000	After treatment with DTT, fluorescence intensity was significantly increased in CD16-positive granulocytes; it was reduced in CD2-positive lymphocytes, CD45-positive lymphocytes and CD14-positive monocytes (p < or = 0.001).	Dithiothreitol	21-24	CD2 molecule	Homo sapiens	126-129
12541706-1	2000	HPLC was used in the investigation of the reaction behavior of Cd2+, Pb2+, Cu2+ and Zn2+ with mesotetrakis (4-hydroxy-phenyl)porphine (THPP) and chromatographic behavior of their complexes.	mesotetrakis (4-hydroxy-phenyl)porphine	94-133	CD2 molecule	Homo sapiens	63-66
12541706-1	2000	HPLC was used in the investigation of the reaction behavior of Cd2+, Pb2+, Cu2+ and Zn2+ with mesotetrakis (4-hydroxy-phenyl)porphine (THPP) and chromatographic behavior of their complexes.	flopropione	135-139	CD2 molecule	Homo sapiens	63-66
12541706-2	2000	The reaction and chromatographic separation parameters were optimized and a method for the simultaneous determination of Cd2+, Pb2+, Cu2+ and Zn2+ by reversed-phase high performance liquid chromatography with THPP as pre-column derivatization reagent was established.	flopropione	209-213	CD2 molecule	Homo sapiens	121-124
10910919-2	2000	Anti-CD2 monoclonal antibody and staurosporine are such apoptosis inducers because they operate in the presence of broad-spectrum caspase inhibitors BOC-D.fmk and Z-VAD.fmk.	z-vad	163-168	CD2 molecule	Homo sapiens	5-8
10815800-7	2000	A Stat5-Ets protein complex was the major inducible DNA-binding complex bound to the human IL-2rE GASd/EBSd motif in long-term proliferating normal human T cells activated by CD2 and CD28.	ebsd	103-107	CD2 molecule	Homo sapiens	175-178
10994194-1	2000	The influence of the salt composition of casein-water-Cd(NO3)2 and defatted milk-Cd(NO3)2 systems on the partition of Cd2+ during acidic precipitation of casein was studied.	Salts	21-25	CD2 molecule	Homo sapiens	118-121
10812846-5	2000	The inhibition by Cd2+ was relieved by the addition of Zn2+ at much lower concentrations than that of Cd2+.	Zinc	55-59	CD2 molecule	Homo sapiens	18-21
11109620-1	2000	AIM: To elucidate the effects of combined therapy with glucocorticosteroids (GCS) and recombinant human interferon alpha or gamma (IFN) on proliferative responses of T-lymphocytes activated by various surface molecules (CD3 and CD2) in patients with SLE.	glucocorticosteroids	55-75	CD2 molecule	Homo sapiens	228-231
10741406-3	2000	Cofilin is dephosphorylated on phosphoserine residues following co-stimulation via accessory receptors such as CD2, CD4, CD8 or CD28, but not in response to TCR engagement alone.	Phosphoserine	31-44	CD2 molecule	Homo sapiens	111-114
10642604-2	2000	In the present work, gal-1 has been identified to be a ligand for the CD3-complex as well as for CD2 as detected by affinity chromatography of Jurkat T-cell lysates on gal-1 agarose and by binding of the biotinylated lectin to CD3 and CD2 immunoprecipitates on blots.	Sepharose	174-181	CD2 molecule	Homo sapiens	97-100
10642604-5	2000	Preincubation of Jurkat E6.1 cells with cholera toxin or with the protein tyrosine kinase inhibitor herbimycin A reduced the gal-1 induced calcium response whereas the increase in [Ca(2+)](i)stimulated by CD2 or CD3 monoclonal antibodies (mAbs) was completely inhibited.	herbimycin	100-112	CD2 molecule	Homo sapiens	205-208
10782569-1	2000	Humans are exposed occupationally and environmentally to metal aerosols including lead (Pb2+) and cadmium (Cd2+).	Metals	57-62	CD2 molecule	Homo sapiens	107-110
10782569-1	2000	Humans are exposed occupationally and environmentally to metal aerosols including lead (Pb2+) and cadmium (Cd2+).	Cadmium	98-105	CD2 molecule	Homo sapiens	107-110
10736969-5	2000	However, concomitant signaling through both CD2 and CD3 by plate-bound antibodies resulted in marked increases in CD69 expression on the T-cell surface and T-cell-cellular metabolism, as assessed by the ability of the cell to reduce 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxylmethoxyphenyl)-2-( 4-sulphophenyl)- 2H-tetrazolium (MTS) to formazen.	3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxylmethoxyphenyl)-2-( 4-sulphophenyl)- 2h-tetrazolium	233-325	CD2 molecule	Homo sapiens	44-47
10736969-5	2000	However, concomitant signaling through both CD2 and CD3 by plate-bound antibodies resulted in marked increases in CD69 expression on the T-cell surface and T-cell-cellular metabolism, as assessed by the ability of the cell to reduce 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxylmethoxyphenyl)-2-( 4-sulphophenyl)- 2H-tetrazolium (MTS) to formazen.	formazen	335-343	CD2 molecule	Homo sapiens	44-47
10736969-6	2000	In addition, simultaneous cross-linking of CD2 and CD3 caused a significant (P < 0.001) increase in phosphatidylinositol hydrolysis in resting T cells compared to stimulation with anti-CD3 mAb alone and anti-CD3 mAb plus anti-CD2 isotype control antibody.	Phosphatidylinositols	103-123	CD2 molecule	Homo sapiens	43-46
10736969-6	2000	In addition, simultaneous cross-linking of CD2 and CD3 caused a significant (P < 0.001) increase in phosphatidylinositol hydrolysis in resting T cells compared to stimulation with anti-CD3 mAb alone and anti-CD3 mAb plus anti-CD2 isotype control antibody.	Phosphatidylinositols	103-123	CD2 molecule	Homo sapiens	229-232
10640755-5	2000	Activation of LPMC via CD2-induced IFN-gamma secretion and a parallel up-regulation of mRNA expression.	lpmc	14-18	CD2 molecule	Homo sapiens	23-26
10640755-7	2000	Transfection of a -2.7-kb IFN-gamma promoter-reporter construct into PBL and LP mononuclear cells (LPMC) revealed significant promoter activity after CD2 activation, with additional transactivation after CD2/CD28 costimulation in PBL, but not in LPMC.	lpmc	99-103	CD2 molecule	Homo sapiens	150-153
10640755-7	2000	Transfection of a -2.7-kb IFN-gamma promoter-reporter construct into PBL and LP mononuclear cells (LPMC) revealed significant promoter activity after CD2 activation, with additional transactivation after CD2/CD28 costimulation in PBL, but not in LPMC.	lpmc	99-103	CD2 molecule	Homo sapiens	204-207
10640755-11	2000	Transfection of the proximal and distal AP-1-binding elements, as well as TRE/AP-1 constructs, revealed functional activation of AP-1 subsequent to CD2 signaling, with activation critical in PBL but diminished in LPMC.	lpmc	213-217	CD2 molecule	Homo sapiens	148-151
10430626-5	1999	Here we demonstrate that Lck and Fyn can be activated by proline motifs in the CD28 and CD2 proteins, respectively.	Proline	57-64	CD2 molecule	Homo sapiens	79-82
10586033-4	1999	In addition, this association was enhanced following independent ligation of the CD2, CD4, or CD28 costimulatory molecules, but not of CD5 or CD6 surface receptors, correlating to the induced tyrosine phosphorylation of Emt.	Tyrosine	192-200	CD2 molecule	Homo sapiens	81-84
10510361-8	1999	The failure of CD5 to become phosphorylated on tyrosine residues in the CD2 pathway has no parallel with the lack of use of zeta-chains in CD2 signaling; contrasting with comparable levels of association of CD2 or CD3 with CD5, zeta associates with CD2 only residually and is nevertheless slightly phosphorylated after CD2 stimulation.	Tyrosine	47-55	CD2 molecule	Homo sapiens	72-75
10529350-9	1999	The oligosaccharides located on the membrane proximal domains of CD2 and CD48 provide a scaffold to orient the binding faces, which leads to increased affinity.	Oligosaccharides	4-20	CD2 molecule	Homo sapiens	65-68
10477744-7	1999	Flow cytometric analysis demonstrates that mPEG-modification dramatically decreases antibody recognition of multiple molecules involved in essential cell:cell interactions, including both T-cell molecules (CD2, CD3, CD4, CD8, CD28, CD11a, CD62L) and antigen-presenting cell (APC) molecules (CD80, CD58, CD62L) likely preventing the initial adhesion and costimulatory events necessary for immune recognition and response.	monomethoxypolyethylene glycol	43-47	CD2 molecule	Homo sapiens	206-209
10456774-0	1999	Beta-lactam degradation catalysed by Cd2+ ion in methanol.	beta-Lactams	0-11	CD2 molecule	Homo sapiens	37-40
10456774-0	1999	Beta-lactam degradation catalysed by Cd2+ ion in methanol.	Methanol	49-57	CD2 molecule	Homo sapiens	37-40
10456774-1	1999	Kinetic schemes are established for degradation catalysed by Cd2+ ions in methanolic medium for penicillin G, penicillin V and cephalothin, a cephalosporin.	methanolic	74-84	CD2 molecule	Homo sapiens	61-64
10456774-1	1999	Kinetic schemes are established for degradation catalysed by Cd2+ ions in methanolic medium for penicillin G, penicillin V and cephalothin, a cephalosporin.	Penicillin G	96-108	CD2 molecule	Homo sapiens	61-64
10456774-1	1999	Kinetic schemes are established for degradation catalysed by Cd2+ ions in methanolic medium for penicillin G, penicillin V and cephalothin, a cephalosporin.	Penicillin V	110-122	CD2 molecule	Homo sapiens	61-64
10456774-1	1999	Kinetic schemes are established for degradation catalysed by Cd2+ ions in methanolic medium for penicillin G, penicillin V and cephalothin, a cephalosporin.	Cephalothin	127-138	CD2 molecule	Homo sapiens	61-64
10456774-1	1999	Kinetic schemes are established for degradation catalysed by Cd2+ ions in methanolic medium for penicillin G, penicillin V and cephalothin, a cephalosporin.	Cephalosporins	142-155	CD2 molecule	Homo sapiens	61-64
10411004-5	1999	The production of SE-induced chemokines was blocked partially by anti-DR and anti-CD2 antibodies.	Selenium	18-20	CD2 molecule	Homo sapiens	82-85
10404387-9	1999	To our knowledge, 3E10 is the first well characterized mAb specific for a subclass of polyproline-arg motif recognizing Sm B/B" and CD2 proteins.	polyproline	86-97	CD2 molecule	Homo sapiens	132-135
10404387-9	1999	To our knowledge, 3E10 is the first well characterized mAb specific for a subclass of polyproline-arg motif recognizing Sm B/B" and CD2 proteins.	Arginine	98-101	CD2 molecule	Homo sapiens	132-135
10233065-1	1999	The conventional formula for relating CD2 average order parameters <Sn> to average methylenic travel <Dn> is flawed when compared to molecular dynamics simulations of dipalmitoylphosphatidylcholine.	1,2-Dipalmitoylphosphatidylcholine	179-209	CD2 molecule	Homo sapiens	38-41
10404223-1	1999	T cell activation through the CD2 cell surface receptor is transmitted by proline-rich sequences within its cytoplasmic tail.	Proline	74-81	CD2 molecule	Homo sapiens	30-33
10404223-2	1999	A membrane-proximal proline-rich tandem repeat, involved in cytokine production, is recognized by the intracellular CD2 binding protein CD2BP2.	Proline	20-27	CD2 molecule	Homo sapiens	116-119
10404223-3	1999	We solved the solution structure of the CD2 binding domain of CD2BP2, which we name the glycine-tyrosine-phenylalanine (GYF) domain.	glycine-tyrosine-phenylalanine	88-118	CD2 molecule	Homo sapiens	40-43
10404223-3	1999	We solved the solution structure of the CD2 binding domain of CD2BP2, which we name the glycine-tyrosine-phenylalanine (GYF) domain.	METHYL 3-MERCAPTOPROPIONATE	120-123	CD2 molecule	Homo sapiens	40-43
10352279-6	1999	LPMC exhibited increased IL-2 production in response to CD28 costimulation, compared with cells activated through CD2 alone.	lpmc	0-4	CD2 molecule	Homo sapiens	56-59
10352279-8	1999	In contrast to transcriptional activation in PBMC, EMSA revealed that CD28 coligation of CD2-activated LPMC does not result in increased binding of trans-factors to the CD28RE, nor did Western blots detect changes in I-kappaBalpha or I-kappaBbeta levels following CD28 coligation.	lpmc	103-107	CD2 molecule	Homo sapiens	70-73
10612091-0	1999	[Myelin basic protein stimulation index of CD 2 cells in the course of steroid treatment].	Steroids	71-78	CD2 molecule	Homo sapiens	43-47
10612091-2	1999	After both treatments a decrease of myelin basic protein CD 2 lymphocyte stimulation index was observed, statistically significant after methyloprednisolone medication.	methyloprednisolone	137-156	CD2 molecule	Homo sapiens	57-61
10222100-1	1999	Adsorption isotherms have been determined for the intercalation of cadmium ions (Cd2+) into layered hydrophobized montmorillonite (HDP-M) and calumit (DBS-C) sheets dispersed in ethanol (1)-cyclohexane (2) mixtures.	Cadmium	67-74	CD2 molecule	Homo sapiens	81-84
10222100-2	1999	The amount of Cd2+ adsorbed depended strongly on the composition of the binary liquid; at an ethanol mole fraction of 0.05 (x1 = 0.05), 95% of the added Cd2+ is located in the ethanolic nanoreactor at the HDP-M (or DBS-C) surface.	Ethanol	93-100	CD2 molecule	Homo sapiens	14-17
10222100-2	1999	The amount of Cd2+ adsorbed depended strongly on the composition of the binary liquid; at an ethanol mole fraction of 0.05 (x1 = 0.05), 95% of the added Cd2+ is located in the ethanolic nanoreactor at the HDP-M (or DBS-C) surface.	dibromsalan	215-218	CD2 molecule	Homo sapiens	14-17
11969587-1	1999	The transport of fast electrons generated by a 1 ps, 20 J, 10(19) W cm(-2), 1 microm wavelength laser pulse through 70-250 microm thick deuterated polyethylene (CD2) targets is modeled with a Fokker-Planck hybrid code in r-z geometry.	deuterated polyethylene	136-159	CD2 molecule	Homo sapiens	161-164
10390059-2	1999	The toxicity scale of these metals found was Hg2+ > Cu2+ > Cd2+ > Pb2+.	cupric ion	55-59	CD2 molecule	Homo sapiens	65-68
10390059-2	1999	The toxicity scale of these metals found was Hg2+ > Cu2+ > Cd2+ > Pb2+.	Lead	75-79	CD2 molecule	Homo sapiens	65-68
10217297-3	1999	This increase was fully reversed by the Cd2+ chelator tetrakis(2-pyridylmethyl)ethylenediamine, indicating a cadmium influx into the cell.	SCHEMBL231091	54-94	CD2 molecule	Homo sapiens	40-43
10217297-3	1999	This increase was fully reversed by the Cd2+ chelator tetrakis(2-pyridylmethyl)ethylenediamine, indicating a cadmium influx into the cell.	Cadmium	109-116	CD2 molecule	Homo sapiens	40-43
10217297-5	1999	Concurrent application of nimodipine and omega-agatoxin IVA (200 nM) blocked Cd2+ permeation almost completely (88+/-5%), whereas omega-conotoxin MVIIC (2 microM) reduced dR/dt by 24+/-8%.	Nimodipine	26-36	CD2 molecule	Homo sapiens	77-80
10217297-7	1999	Stimulation with glutamate or NMDA and glycine also caused a rise of R in external Cd2+.	Glutamic Acid	17-26	CD2 molecule	Homo sapiens	83-86
10217297-7	1999	Stimulation with glutamate or NMDA and glycine also caused a rise of R in external Cd2+.	N-Methylaspartate	30-34	CD2 molecule	Homo sapiens	83-86
10217297-7	1999	Stimulation with glutamate or NMDA and glycine also caused a rise of R in external Cd2+.	Glycine	39-46	CD2 molecule	Homo sapiens	83-86
10217297-9	1999	NMDA-driven Cd2(+) entry was almost completely prevented by 1 mM Mg2+, 50 microM memantine, and 10 microM 5,7-dichlorokynurenic acid, suggesting a major contribution of NMDA-gated channels in glutamate-stimulated Cd2+ influx.	N-Methylaspartate	0-4	CD2 molecule	Homo sapiens	12-15
10217297-9	1999	NMDA-driven Cd2(+) entry was almost completely prevented by 1 mM Mg2+, 50 microM memantine, and 10 microM 5,7-dichlorokynurenic acid, suggesting a major contribution of NMDA-gated channels in glutamate-stimulated Cd2+ influx.	N-Methylaspartate	0-4	CD2 molecule	Homo sapiens	213-216
10217297-9	1999	NMDA-driven Cd2(+) entry was almost completely prevented by 1 mM Mg2+, 50 microM memantine, and 10 microM 5,7-dichlorokynurenic acid, suggesting a major contribution of NMDA-gated channels in glutamate-stimulated Cd2+ influx.	magnesium ion	65-69	CD2 molecule	Homo sapiens	12-15
10217297-9	1999	NMDA-driven Cd2(+) entry was almost completely prevented by 1 mM Mg2+, 50 microM memantine, and 10 microM 5,7-dichlorokynurenic acid, suggesting a major contribution of NMDA-gated channels in glutamate-stimulated Cd2+ influx.	Memantine	81-90	CD2 molecule	Homo sapiens	12-15
10217297-9	1999	NMDA-driven Cd2(+) entry was almost completely prevented by 1 mM Mg2+, 50 microM memantine, and 10 microM 5,7-dichlorokynurenic acid, suggesting a major contribution of NMDA-gated channels in glutamate-stimulated Cd2+ influx.	5,7-dichlorokynurenic acid	106-132	CD2 molecule	Homo sapiens	12-15
10217297-9	1999	NMDA-driven Cd2(+) entry was almost completely prevented by 1 mM Mg2+, 50 microM memantine, and 10 microM 5,7-dichlorokynurenic acid, suggesting a major contribution of NMDA-gated channels in glutamate-stimulated Cd2+ influx.	5,7-dichlorokynurenic acid	106-132	CD2 molecule	Homo sapiens	213-216
10217297-9	1999	NMDA-driven Cd2(+) entry was almost completely prevented by 1 mM Mg2+, 50 microM memantine, and 10 microM 5,7-dichlorokynurenic acid, suggesting a major contribution of NMDA-gated channels in glutamate-stimulated Cd2+ influx.	N-Methylaspartate	169-173	CD2 molecule	Homo sapiens	12-15
10217297-9	1999	NMDA-driven Cd2(+) entry was almost completely prevented by 1 mM Mg2+, 50 microM memantine, and 10 microM 5,7-dichlorokynurenic acid, suggesting a major contribution of NMDA-gated channels in glutamate-stimulated Cd2+ influx.	N-Methylaspartate	169-173	CD2 molecule	Homo sapiens	213-216
10217297-9	1999	NMDA-driven Cd2(+) entry was almost completely prevented by 1 mM Mg2+, 50 microM memantine, and 10 microM 5,7-dichlorokynurenic acid, suggesting a major contribution of NMDA-gated channels in glutamate-stimulated Cd2+ influx.	Glutamic Acid	192-201	CD2 molecule	Homo sapiens	12-15
10217297-10	1999	Moreover, perfusion with alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate caused a slow increase of R. These results suggest that Cd2+ permeates the cell membrane mainly through the same pathways of Ca2+ influx.	alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate	25-77	CD2 molecule	Homo sapiens	134-137
10201397-2	1999	Thiophilic metal ions such as Mn2+, Zn2+ or Cd2+ rescue the >10(3)-fold inhibitory effect of sulfur substitution of the 3"-oxygen leaving group but do not effectively rescue the effect of sulfur substitution of the nonbridging pro-Sp phosphoryl oxygen.	Sulfur	96-102	CD2 molecule	Homo sapiens	44-47
10201397-2	1999	Thiophilic metal ions such as Mn2+, Zn2+ or Cd2+ rescue the >10(3)-fold inhibitory effect of sulfur substitution of the 3"-oxygen leaving group but do not effectively rescue the effect of sulfur substitution of the nonbridging pro-Sp phosphoryl oxygen.	Metals	11-16	CD2 molecule	Homo sapiens	44-47
10201397-2	1999	Thiophilic metal ions such as Mn2+, Zn2+ or Cd2+ rescue the >10(3)-fold inhibitory effect of sulfur substitution of the 3"-oxygen leaving group but do not effectively rescue the effect of sulfur substitution of the nonbridging pro-Sp phosphoryl oxygen.	Oxygen	126-132	CD2 molecule	Homo sapiens	44-47
10201397-2	1999	Thiophilic metal ions such as Mn2+, Zn2+ or Cd2+ rescue the >10(3)-fold inhibitory effect of sulfur substitution of the 3"-oxygen leaving group but do not effectively rescue the effect of sulfur substitution of the nonbridging pro-Sp phosphoryl oxygen.	Sulfur	191-197	CD2 molecule	Homo sapiens	44-47
10201397-2	1999	Thiophilic metal ions such as Mn2+, Zn2+ or Cd2+ rescue the >10(3)-fold inhibitory effect of sulfur substitution of the 3"-oxygen leaving group but do not effectively rescue the effect of sulfur substitution of the nonbridging pro-Sp phosphoryl oxygen.	Oxygen	248-254	CD2 molecule	Homo sapiens	44-47
10201397-3	1999	We now show that the latter effect can be fully rescued by Zn2+ or Cd2+ using a phosphorodithioate substrate, in which both the 3"-oxygen and the pro-Sp oxygen are simultaneously substituted with sulfur.	phosphorodithioic acid	80-98	CD2 molecule	Homo sapiens	67-70
10201397-3	1999	We now show that the latter effect can be fully rescued by Zn2+ or Cd2+ using a phosphorodithioate substrate, in which both the 3"-oxygen and the pro-Sp oxygen are simultaneously substituted with sulfur.	3"-oxygen	128-137	CD2 molecule	Homo sapiens	67-70
10201397-3	1999	We now show that the latter effect can be fully rescued by Zn2+ or Cd2+ using a phosphorodithioate substrate, in which both the 3"-oxygen and the pro-Sp oxygen are simultaneously substituted with sulfur.	Sulfur	196-202	CD2 molecule	Homo sapiens	67-70
10049540-1	1999	In this paper we report the behavior of an amphiphilic polymer monolayer on pure water and Cd2+ subphase.	Polymers	55-62	CD2 molecule	Homo sapiens	91-94
10049540-3	1999	The introduction of Cd2+ ions in subphase had a marked effect on the process of the organization of the amphiphilic polymer at the air/water interface due to the association of Cd2+ ions with the hydrophilic network, which could be indicated by the pressure-area isotherms and Brewster Angle Microscopy.	Polymers	116-123	CD2 molecule	Homo sapiens	20-23
10049540-3	1999	The introduction of Cd2+ ions in subphase had a marked effect on the process of the organization of the amphiphilic polymer at the air/water interface due to the association of Cd2+ ions with the hydrophilic network, which could be indicated by the pressure-area isotherms and Brewster Angle Microscopy.	Polymers	116-123	CD2 molecule	Homo sapiens	177-180
10049540-3	1999	The introduction of Cd2+ ions in subphase had a marked effect on the process of the organization of the amphiphilic polymer at the air/water interface due to the association of Cd2+ ions with the hydrophilic network, which could be indicated by the pressure-area isotherms and Brewster Angle Microscopy.	Water	135-140	CD2 molecule	Homo sapiens	20-23
10029614-1	1999	BACKGROUND & AIMS: Normal human lamina propria lymphocytes manifest increased unstimulated apoptosis compared with peripheral lymphocytes, which are enhanced after stimulation via the CD2 activation pathway.	Adenosine Monophosphate	12-15	CD2 molecule	Homo sapiens	188-191
10087189-5	1999	In contrast, cAMP enhanced CD40L induced by CD2-mediated T cell activation or by calcium-dependent mechanisms.	Cyclic AMP	13-17	CD2 molecule	Homo sapiens	44-47
9890636-6	1999	An anti-CD2 antibody induced a strong ROS flux, suggesting that the CD2/LFA-3 interaction may be important in this regulation.	Reactive Oxygen Species	38-41	CD2 molecule	Homo sapiens	8-11
9880485-5	1999	This phenomenon may be partially explained by two amino acid replacements in the beta chains (CD2 Glu-43 --> Thr and G3 Glu-101 --> Val), which result in the loss of two negative charges at the alpha1beta2 interface and favors the dissociation into dimers.	Glutamic Acid	98-101	CD2 molecule	Homo sapiens	94-97
9880485-5	1999	This phenomenon may be partially explained by two amino acid replacements in the beta chains (CD2 Glu-43 --> Thr and G3 Glu-101 --> Val), which result in the loss of two negative charges at the alpha1beta2 interface and favors the dissociation into dimers.	Threonine	112-115	CD2 molecule	Homo sapiens	94-97
9880485-5	1999	This phenomenon may be partially explained by two amino acid replacements in the beta chains (CD2 Glu-43 --> Thr and G3 Glu-101 --> Val), which result in the loss of two negative charges at the alpha1beta2 interface and favors the dissociation into dimers.	Valine	138-141	CD2 molecule	Homo sapiens	94-97
10398339-1	1999	20-hydroxyecdysone (1 microM) was found to activate in vitro T-cell CD2 presentation, which is suppressed both in secondary immunodeficient persons and pharmacologically by increasing intracellular cAMP levels.	Ecdysterone	0-18	CD2 molecule	Homo sapiens	68-71
10398339-1	1999	20-hydroxyecdysone (1 microM) was found to activate in vitro T-cell CD2 presentation, which is suppressed both in secondary immunodeficient persons and pharmacologically by increasing intracellular cAMP levels.	Cyclic AMP	198-202	CD2 molecule	Homo sapiens	68-71
10053166-2	1999	For that purpose filter-grown Caco-2 and IEC-18 cells were apically exposed to 5 to 100 microM CdCl2 for 4 or 14 h. It was found that the effects of Cd2+ on the epithelial barrier were concentration- and time-dependent.	Cadmium Chloride	95-100	CD2 molecule	Homo sapiens	149-152
10053166-3	1999	The first detected effects of Cd2+ in Caco-2 cells after 4 h exposure were a decrease in transepithelial electrical resistance, increased permeabilities of mannitol and PEG-4000, and changes in intercellular localization of ZO-1, occludin, and e-cadherin.	Mannitol	156-164	CD2 molecule	Homo sapiens	30-33
10053166-3	1999	The first detected effects of Cd2+ in Caco-2 cells after 4 h exposure were a decrease in transepithelial electrical resistance, increased permeabilities of mannitol and PEG-4000, and changes in intercellular localization of ZO-1, occludin, and e-cadherin.	peg-4000	169-177	CD2 molecule	Homo sapiens	30-33
9862968-3	1999	Addition of low concentrations of several thiophilic metal ions, especially Cd2+, to these reactions is sufficient to fully restore the cleavage rate of the RPsubstrate without affecting cleavage rate of the all-oxygen or SPsubstrate.	Metals	53-58	CD2 molecule	Homo sapiens	76-79
9890636-6	1999	An anti-CD2 antibody induced a strong ROS flux, suggesting that the CD2/LFA-3 interaction may be important in this regulation.	Reactive Oxygen Species	38-41	CD2 molecule	Homo sapiens	68-71
9843450-12	1998	Kinetic studies revealed that inhibition by Cd2+ was competitive with respect to Mg2+ and noncompetitive with respect to MgATP.	magnesium ion	81-85	CD2 molecule	Homo sapiens	44-47
9843987-0	1998	Identification of a proline-binding motif regulating CD2-triggered T lymphocyte activation.	Proline	20-27	CD2 molecule	Homo sapiens	53-56
9862370-3	1998	Addition of various co-stimuli (phorbol 12-myristate 13-acetate or monoclonal antibodies to CD3 or CD2) increases the CD82-induced morphological alterations and, reciprocally, CD82 engagement synergizes with these stimuli to induce T cell activation as indicated by both primary tyrosine phosphorylation and IL-2 production.	Tetradecanoylphorbol Acetate	32-63	CD2 molecule	Homo sapiens	99-102
9862370-3	1998	Addition of various co-stimuli (phorbol 12-myristate 13-acetate or monoclonal antibodies to CD3 or CD2) increases the CD82-induced morphological alterations and, reciprocally, CD82 engagement synergizes with these stimuli to induce T cell activation as indicated by both primary tyrosine phosphorylation and IL-2 production.	Tyrosine	279-287	CD2 molecule	Homo sapiens	99-102
9893043-6	1998	CD2, but not CD3, cross-linking increased cAMP detected by competitive enzyme-linked immunosorbent assay (ELISA) approximately fourfold.	Cyclic AMP	42-46	CD2 molecule	Homo sapiens	0-3
9893043-10	1998	Both CD2 and CD3 cross-linking increased binding of nuclear proteins to a radiolabelled CRE oligonucleotide probe in electrophoretic mobility shift assays suggesting that lymphocyte activation enhances binding independently of phosphorylation of CREB at serine 133.	Oligonucleotides	92-107	CD2 molecule	Homo sapiens	5-8
9893043-10	1998	Both CD2 and CD3 cross-linking increased binding of nuclear proteins to a radiolabelled CRE oligonucleotide probe in electrophoretic mobility shift assays suggesting that lymphocyte activation enhances binding independently of phosphorylation of CREB at serine 133.	Serine	254-260	CD2 molecule	Homo sapiens	5-8
9834211-0	1998	A phase II study of BTI-322, a monoclonal anti-CD2 antibody, for treatment of steroid-resistant acute graft-versus-host disease.	LO-CD2a	20-27	CD2 molecule	Homo sapiens	47-50
9834211-1	1998	BTI-322, a rat monoclonal IgG2b directed against the CD2 antigen on T cells and natural killer (NK) cells, blocks primary and memory alloantigen proliferative responses in vitro.	LO-CD2a	0-7	CD2 molecule	Homo sapiens	53-56
9843450-12	1998	Kinetic studies revealed that inhibition by Cd2+ was competitive with respect to Mg2+ and noncompetitive with respect to MgATP.	Adenosine Triphosphate	121-126	CD2 molecule	Homo sapiens	44-47
9843450-13	1998	These results indicate that Cd2+ competes for a second metal-binding site.	Metals	55-60	CD2 molecule	Homo sapiens	28-31
9712768-1	1998	A biotinylated peptide covering a sequence of 21 amino acids (aa) from the erythrocyte binding antigen (EBA-175) of Plasmodium falciparum bound to human glycophorin A, an erythrocyte receptor for merozoites, as demonstrated by enzyme-linked immunosorbent assay (ELISA) and to erythrocytes as demonstrated by flow cytometry analysis.	Peptides	15-22	CD2 molecule	Homo sapiens	171-191
9829702-4	1998	Manual docking of known substrates and non-substrates has implicated potential candidates for the T1-1 catalytic residues involved in the dehalogenation and epoxide-ring opening activities.	Epoxy Compounds	157-164	CD2 molecule	Homo sapiens	98-102
9794375-9	1998	Thus, although CD3, CD28, and CD2 activate many of the same signaling molecules, they differed in their capacity to induce the tyrosine phosphorylation of HSI.	Tyrosine	127-135	CD2 molecule	Homo sapiens	20-23
9710614-0	1998	Identification of a proline-rich sequence in the CD2 cytoplasmic domain critical for regulation of integrin-mediated adhesion and activation of phosphoinositide 3-kinase.	Proline	20-27	CD2 molecule	Homo sapiens	49-52
9710614-6	1998	A proline-rich sequence, K-G-P-P-L-P (amino acids 299 to 305), is essential for CD2-mediated regulation of beta1 integrin activity.	Proline	2-9	CD2 molecule	Homo sapiens	80-83
9710614-6	1998	A proline-rich sequence, K-G-P-P-L-P (amino acids 299 to 305), is essential for CD2-mediated regulation of beta1 integrin activity.	k-g-p-p-l-p	25-36	CD2 molecule	Homo sapiens	80-83
9710614-10	1998	Mutation of the proline residues in the K-G-P-P-L-P motif to alanines prevented CD2-mediated activation of integrin function and PI 3-K activity but not mitogen-activated protein (MAP) kinase activity.	Proline	16-23	CD2 molecule	Homo sapiens	80-83
9710614-10	1998	Mutation of the proline residues in the K-G-P-P-L-P motif to alanines prevented CD2-mediated activation of integrin function and PI 3-K activity but not mitogen-activated protein (MAP) kinase activity.	Alanine	61-69	CD2 molecule	Homo sapiens	80-83
9710614-12	1998	These studies identify a proline-rich sequence in CD2 critical for PI 3-K-dependent regulation of beta1 integrin adhesion by CD2.	Proline	25-32	CD2 molecule	Homo sapiens	50-53
9710614-12	1998	These studies identify a proline-rich sequence in CD2 critical for PI 3-K-dependent regulation of beta1 integrin adhesion by CD2.	Proline	25-32	CD2 molecule	Homo sapiens	125-128
9768847-3	1998	We found that substituting cysteine at a particular position in the last transmembrane region (S6) of the homotetrameric Shaker K+ channel creates metal binding sites at which Cd2+ ions can bind with high affinity.	Cysteine	27-35	CD2 molecule	Homo sapiens	176-179
9768847-3	1998	We found that substituting cysteine at a particular position in the last transmembrane region (S6) of the homotetrameric Shaker K+ channel creates metal binding sites at which Cd2+ ions can bind with high affinity.	Metals	147-152	CD2 molecule	Homo sapiens	176-179
9558083-0	1998	Potent apoptotic signaling and subsequent unresponsiveness induced by a single CD2 mAb (BTI-322) in activated human peripheral T cells.	LO-CD2a	88-95	CD2 molecule	Homo sapiens	79-82
9768847-4	1998	The bound Cd2+ ions form a bridge between the introduced cysteine in one channel subunit and a native histidine in another subunit, and the bridge traps the gate in the open state.	Cysteine	57-65	CD2 molecule	Homo sapiens	10-13
9768847-4	1998	The bound Cd2+ ions form a bridge between the introduced cysteine in one channel subunit and a native histidine in another subunit, and the bridge traps the gate in the open state.	Histidine	102-111	CD2 molecule	Homo sapiens	10-13
9744815-7	1998	113Cd NMR spectra suggest a specific binding of Cd2+ ions to the RNA.	Cadmium, isotope of mass 113	0-5	CD2 molecule	Homo sapiens	48-51
9677430-9	1998	In addition, we found that the ability of the Fyn SH2 domain to precipitate tyrosine-phosphorylated proteins, including the CD3zeta chain, was enhanced after T cell stimulation with mitogenic pairs of CD2 mAbs.	Tyrosine	76-84	CD2 molecule	Homo sapiens	201-204
9677430-11	1998	We thus propose that stimulation through the CD2 receptor leads to the tyrosine phosphorylation of intracellular proteins, including CD3zeta itself, which in turn bind to the Fyn-SH2 domain, allowing the direct association of the Fyn SH3 domain with CD2 and the initiation of downstream signaling events.	Tyrosine	71-79	CD2 molecule	Homo sapiens	45-48
9677430-11	1998	We thus propose that stimulation through the CD2 receptor leads to the tyrosine phosphorylation of intracellular proteins, including CD3zeta itself, which in turn bind to the Fyn-SH2 domain, allowing the direct association of the Fyn SH3 domain with CD2 and the initiation of downstream signaling events.	Tyrosine	71-79	CD2 molecule	Homo sapiens	250-253
9726012-7	1998	Compared to the parent line, SJCEM808 had similar cytogenetic abnormalities, lower CD2, CD1, and CD10 expression, and negligible RAG-1 expression.	sjcem808	29-37	CD2 molecule	Homo sapiens	83-86
9710155-8	1998	The above results indicated that Raji cells were more sensitive to cadmium compared to both CCRF-CEM and Molt-3 cells, suggesting a differential Cd2+-induced apoptotic effect, which may disturb the immune system normal growth and development.	Cadmium	67-74	CD2 molecule	Homo sapiens	145-148
9678765-0	1998	Co-stimulation of T cells with CD2 augments TCR-CD3-mediated activation of protein tyrosine kinase p72syk, resulting in increased tyrosine phosphorylation of adapter proteins, Shc and Cbl.	Tyrosine	83-91	CD2 molecule	Homo sapiens	31-34
9678765-5	1998	Enhancement of tyrosine phosphorylation of Syk by CD2 co-stimulation was CD2 antibody concentration-dependent, and time course studies showed that CD2 co-stimulation enhanced Syk tyrosine phosphorylation by 30 s and through 5 min stimulation compared with the control.	Tyrosine	15-23	CD2 molecule	Homo sapiens	50-53
9678765-5	1998	Enhancement of tyrosine phosphorylation of Syk by CD2 co-stimulation was CD2 antibody concentration-dependent, and time course studies showed that CD2 co-stimulation enhanced Syk tyrosine phosphorylation by 30 s and through 5 min stimulation compared with the control.	Tyrosine	15-23	CD2 molecule	Homo sapiens	73-76
9678765-5	1998	Enhancement of tyrosine phosphorylation of Syk by CD2 co-stimulation was CD2 antibody concentration-dependent, and time course studies showed that CD2 co-stimulation enhanced Syk tyrosine phosphorylation by 30 s and through 5 min stimulation compared with the control.	Tyrosine	15-23	CD2 molecule	Homo sapiens	73-76
9678765-5	1998	Enhancement of tyrosine phosphorylation of Syk by CD2 co-stimulation was CD2 antibody concentration-dependent, and time course studies showed that CD2 co-stimulation enhanced Syk tyrosine phosphorylation by 30 s and through 5 min stimulation compared with the control.	Tyrosine	179-187	CD2 molecule	Homo sapiens	50-53
9678765-5	1998	Enhancement of tyrosine phosphorylation of Syk by CD2 co-stimulation was CD2 antibody concentration-dependent, and time course studies showed that CD2 co-stimulation enhanced Syk tyrosine phosphorylation by 30 s and through 5 min stimulation compared with the control.	Tyrosine	179-187	CD2 molecule	Homo sapiens	73-76
9678765-5	1998	Enhancement of tyrosine phosphorylation of Syk by CD2 co-stimulation was CD2 antibody concentration-dependent, and time course studies showed that CD2 co-stimulation enhanced Syk tyrosine phosphorylation by 30 s and through 5 min stimulation compared with the control.	Tyrosine	179-187	CD2 molecule	Homo sapiens	73-76
9678765-7	1998	Furthermore, CD2 co-stimulation with CD3 resulted in enhanced tyrosine phosphorylation of adapter proteins, such as Shc and Cbl, in an antibody concentration-dependent manner.	Tyrosine	62-70	CD2 molecule	Homo sapiens	13-16
9584138-8	1998	We propose that either the sialic acid moiety of glycophorins, predominantly glycophorin A, or a more complex interaction involving the glycophorin peptide backbone, is the erythrocyte receptor for adhesion to microgametes.	N-Acetylneuraminic Acid	27-38	CD2 molecule	Homo sapiens	173-193
9686569-0	1998	Serine 16 of stathmin as a cytosolic target for Ca2+/calmodulin-dependent kinase II after CD2 triggering of human T lymphocytes.	Serine	0-6	CD2 molecule	Homo sapiens	90-93
9701039-1	1998	Ligation of the CD2 co-stimulatory receptor on human T lymphocytes induces tyrosine phosphorylation and activation of the Tec-family tyrosine kinase, ITK.	Tyrosine	75-83	CD2 molecule	Homo sapiens	16-19
9666569-3	1998	Differential scanning calorimetry scans of solutions of the metal ion derivatives of Con A show that the thermodynamics of the unfolding transition for the cobalt and nickel substituted derivatives are the same as for Con A: they dissociate from tetramers into monomers as they unfold around 85 degrees C. The cadmium substituted Con A derivative, however, exhibits an additional transition around 93 degrees C which also appears following the addition of Cd2+ to the Con A solutions.	Metals	60-65	CD2 molecule	Homo sapiens	456-459
9666569-3	1998	Differential scanning calorimetry scans of solutions of the metal ion derivatives of Con A show that the thermodynamics of the unfolding transition for the cobalt and nickel substituted derivatives are the same as for Con A: they dissociate from tetramers into monomers as they unfold around 85 degrees C. The cadmium substituted Con A derivative, however, exhibits an additional transition around 93 degrees C which also appears following the addition of Cd2+ to the Con A solutions.	Cobalt	156-162	CD2 molecule	Homo sapiens	456-459
9666569-3	1998	Differential scanning calorimetry scans of solutions of the metal ion derivatives of Con A show that the thermodynamics of the unfolding transition for the cobalt and nickel substituted derivatives are the same as for Con A: they dissociate from tetramers into monomers as they unfold around 85 degrees C. The cadmium substituted Con A derivative, however, exhibits an additional transition around 93 degrees C which also appears following the addition of Cd2+ to the Con A solutions.	Nickel	167-173	CD2 molecule	Homo sapiens	456-459
9558083-5	1998	Less than 5 ng/ml of BTI-322, added at the beginning of culture, were able to eliminate within 4 days most CD3+ cells from OKT3- and IL-2-stimulated lymphocytes, the only cells remaining being CD16+CD2- NK cells.	LO-CD2a	21-28	CD2 molecule	Homo sapiens	198-201
9591360-2	1998	Binding of Ca2+ and Cd2+ resulted in fluorescence lifetime enhancements as compared to that of free Quin2 ("tau" = 0.9 ns).	Quin2	100-105	CD2 molecule	Homo sapiens	20-23
9650640-6	1998	CdCl2 (10 microM) caused an accumulation of c-fos mRNA over 30 min that was sustained for at least 8 h. Cycloheximide inhibits turnover of c-fos mRNA and shows a synergistic effect with Cd2+ on transcript levels.	Cycloheximide	104-117	CD2 molecule	Homo sapiens	186-189
9650640-9	1998	The MAPK kinase inhibitor PD98059 caused a marked decrease in the induction of c-fos by Cd2+, but did not eliminate the phenomenon completely.	2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one	26-33	CD2 molecule	Homo sapiens	88-91
9650640-6	1998	CdCl2 (10 microM) caused an accumulation of c-fos mRNA over 30 min that was sustained for at least 8 h. Cycloheximide inhibits turnover of c-fos mRNA and shows a synergistic effect with Cd2+ on transcript levels.	Cadmium Chloride	0-5	CD2 molecule	Homo sapiens	186-189
9485403-1	1998	The N-terminal domain of phosphoglycerate kinase (N-PGK) and domain 1 of the T-cell adhesion protein CD2 (CD2.d1) fold through rapidly formed and transiently populated intermediate states in reactions which have no kinetic complications arising from proline isomerization or disulfide bonding.	Proline	250-257	CD2 molecule	Homo sapiens	101-104
9490708-6	1998	In a second step, CPC can be further purged of contaminating T or B cells by incubation with lymphoid-specific magnetic microbeads (anti-CD2 and -CD7 to remove T cells; anti-CD19 to remove B cells) and elution through a type-D depletion column (composed of ferromagnetic fiber) inserted within a SuperMACS separator device (Miltenyi Biotech, Bergisch-Gladbach, Germany).	cpc	18-21	CD2 molecule	Homo sapiens	137-140
9562374-1	1998	Phosphorylation of the cAMP-response element binding protein CREB within 1 h of CD2 but not CD3 cross-linking of human PBMC was recently demonstrated.	Cyclic AMP	23-27	CD2 molecule	Homo sapiens	80-83
9848163-1	1998	The inhibiting effect of Pb2+, Zn2+ and Cd2+ on Mg(2+)-dependent superprecipitation and ATPase activity of myometrium actomyosin.	magnesium ion	48-54	CD2 molecule	Homo sapiens	40-43
9848163-2	1998	The inhibiting effect of heavy metals cations on the both processes satisfies the succession: Pb2+ > Zn2+ > Cd2+.	Lead	94-98	CD2 molecule	Homo sapiens	114-117
9848163-2	1998	The inhibiting effect of heavy metals cations on the both processes satisfies the succession: Pb2+ > Zn2+ > Cd2+.	Zinc	104-108	CD2 molecule	Homo sapiens	114-117
9485403-1	1998	The N-terminal domain of phosphoglycerate kinase (N-PGK) and domain 1 of the T-cell adhesion protein CD2 (CD2.d1) fold through rapidly formed and transiently populated intermediate states in reactions which have no kinetic complications arising from proline isomerization or disulfide bonding.	Proline	250-257	CD2 molecule	Homo sapiens	106-112
9485403-1	1998	The N-terminal domain of phosphoglycerate kinase (N-PGK) and domain 1 of the T-cell adhesion protein CD2 (CD2.d1) fold through rapidly formed and transiently populated intermediate states in reactions which have no kinetic complications arising from proline isomerization or disulfide bonding.	Disulfides	275-284	CD2 molecule	Homo sapiens	101-104
9485403-1	1998	The N-terminal domain of phosphoglycerate kinase (N-PGK) and domain 1 of the T-cell adhesion protein CD2 (CD2.d1) fold through rapidly formed and transiently populated intermediate states in reactions which have no kinetic complications arising from proline isomerization or disulfide bonding.	Disulfides	275-284	CD2 molecule	Homo sapiens	106-112
9486420-5	1998	These changes were studied using lipopolysaccharide (LPS)-induced and anti-CD2/anti-CD28 MoAb-stimulated cytokine release in whole blood and its modulation by dexamethasone.	Dexamethasone	159-172	CD2 molecule	Homo sapiens	75-78
9486420-10	1998	Moreover, since dexamethasone responsiveness of anti-CD2/anti-CD28 MoAb-induced IFN-gamma secretion in whole blood is not affected by exercise, it may suggest that exercise differentially affects monocytes and lymphocytes.	Dexamethasone	16-29	CD2 molecule	Homo sapiens	53-56
9417049-11	1998	A specific inhibitor of the MAPK kinases, PD98059, partially inhibited the induction of c-fos by Cd2+.	2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one	42-49	CD2 molecule	Homo sapiens	97-100
9530513-4	1998	The ions Zn2+, Co2+, and Cd2+ present in the medium at 50 microM concentration totally protect the erythrocytes against hemolysis induced by the compound (C3H7)3SnCl.	(c3h7)3sncl	154-165	CD2 molecule	Homo sapiens	25-28
9396720-4	1997	The valency of the multivalent cation was not as important, since tervalent lanthanides (Eu3+, Gd3+ and Tb3+) of ionic radius 106-109 pm induced similar levels (50-60%) of helix to those induced by Ca2+ and Cd2+ (ionic radii 109 and 114 pm respectively).	tb3+	104-108	CD2 molecule	Homo sapiens	207-210
9669212-5	1997	MTX resistance of Jurkat T cells in vitro was accompanied by significantly (P < 0.05) decreased expression of CD2, CD3, CD4, CD28, and CD69, IL-2 production, and MTX uptake assessed by cell association or disassociation of 3[H]-MTX or fluoresceinated MTX (FMTX), respectively.	Methotrexate	0-3	CD2 molecule	Homo sapiens	113-116
9548475-5	1997	Using a chimeric receptor composed of the cytoplasmic domain of the beta1 integrin subunit and the extracellular and transmembrane domains of the CD2 Ag, we demonstrate that the beta1 cytoplasmic domain is necessary and sufficient for inducing tyrosine phosphorylation of each of these three substrates in H9 T cells.	Tyrosine	244-252	CD2 molecule	Homo sapiens	146-149
9548475-6	1997	Analysis of a series of beta1 cytoplasmic domain truncations reveals that a truncation of only five amino acids from the carboxyl-terminal end of the beta1 cytoplasmic domain abrogates the ability of the CD2/beta1 chimera to activate tyrosine phosphorylation of HEF1, pp105, or pp115.	Tyrosine	234-242	CD2 molecule	Homo sapiens	204-207
9550432-4	1997	Increased IFN-gamma production was demonstrated in anti-CD2-stimulated LPMC cultured in TNF-alpha.	lpmc	71-75	CD2 molecule	Homo sapiens	56-59
9550432-6	1997	In all four patients who demonstrated clinical and endoscopic improvement, decreased numbers of LPMC producing IFN-gamma and TNF-alpha following CD2/CD28 activation paralleled improvement in disease activity over 8 wk.	lpmc	96-100	CD2 molecule	Homo sapiens	145-148
9389770-8	1997	Using this optimized ImmunoMax method, we were able to detect CD2, CD3, CD4, and CD5 with conventional monoclonal antibodies in formalin-fixed, paraffin-embedded tissue specimens of various lymphoid tissues.	Formaldehyde	128-136	CD2 molecule	Homo sapiens	62-65
9389770-8	1997	Using this optimized ImmunoMax method, we were able to detect CD2, CD3, CD4, and CD5 with conventional monoclonal antibodies in formalin-fixed, paraffin-embedded tissue specimens of various lymphoid tissues.	Paraffin	144-152	CD2 molecule	Homo sapiens	62-65
9365628-0	1997	CD2+, CD3+, and CD19+ depletion after a course of antithymocyte globulin for a steroid-resistant rejection.	Steroids	79-86	CD2 molecule	Homo sapiens	0-3
33863068-3	1997	The presence of Pb2+ and Sb3- in the media did however, amcliorate Cd2+ and Zn2+ toxicity in some circumstances.	amcliorate	56-66	CD2 molecule	Homo sapiens	67-70
33863068-5	1997	Zn2+ was found to significantly ameliorate the toxicity of Cd2+ to three of the four isolates tested.	Zinc	0-4	CD2 molecule	Homo sapiens	59-62
9356396-9	1997	Two components of ICa were identified by their sensitivity to either 50 mu M nifedipine or micromolar Cd2+.	isocyanic acid	18-21	CD2 molecule	Homo sapiens	102-105
33863068-0	1997	Toxic interactions of metal ions (Cd2+ , Pb2+ , Zn2+ and Sb3- ) on in vitro biomass production of ectomycorrhizal fungi.	Metals	22-27	CD2 molecule	Homo sapiens	34-37
33863068-3	1997	The presence of Pb2+ and Sb3- in the media did however, amcliorate Cd2+ and Zn2+ toxicity in some circumstances.	Lead(2+)	16-20	CD2 molecule	Homo sapiens	67-70
9341112-3	1997	The Rp-, but not Sp-, phosphorothioate reduces the cleavage rate by 10(3)-fold, and the rate can be fully restored by addition of low concentrations of Cd2+, a thiophilic metal ion.	Parathion	22-38	CD2 molecule	Homo sapiens	152-155
9341112-3	1997	The Rp-, but not Sp-, phosphorothioate reduces the cleavage rate by 10(3)-fold, and the rate can be fully restored by addition of low concentrations of Cd2+, a thiophilic metal ion.	Metals	171-176	CD2 molecule	Homo sapiens	152-155
9202170-15	1997	The increase in Quin-2 fluorescence after addition of excess CdCl2 indicates that, in our experimental conditions, Ca2+ tightly-bound to actin is partially (60-70%) replaced by Cd2+, forming Cd-actin.	Quin2	16-22	CD2 molecule	Homo sapiens	177-180
9341233-1	1997	The 98 residue C-terminal domain of the cell-surface receptor protein CD2 (CD2.D1) has a beta-sandwich fold belonging to the immunoglobulin superfamily but lacking the usual disulfide bridges.	Disulfides	174-183	CD2 molecule	Homo sapiens	70-73
9341233-1	1997	The 98 residue C-terminal domain of the cell-surface receptor protein CD2 (CD2.D1) has a beta-sandwich fold belonging to the immunoglobulin superfamily but lacking the usual disulfide bridges.	Disulfides	174-183	CD2 molecule	Homo sapiens	75-81
9341233-5	1997	The pattern of protected amides in the intermediate reveal that the essential features of the beta-sheet topology of CD2.D1 are defined early in the folding pathway, before the development of intimate side chain interactions characteristic of the native state.	Amides	25-31	CD2 molecule	Homo sapiens	117-123
9307035-0	1997	Evidence that human class Theta glutathione S-transferase T1-1 can catalyse the activation of dichloromethane, a liver and lung carcinogen in the mouse.	Methylene Chloride	94-109	CD2 molecule	Homo sapiens	58-62
9307035-4	1997	15 mg/l for the protein A fusion and 25 mg/l for the C-terminal polyhistidine-tagged GST T1-1.	polyhistidine	64-77	CD2 molecule	Homo sapiens	89-93
9307035-7	1997	Recombinant human GST T1-1 was found to exhibit glutathione peroxidase activity and could catalyse the reduction of cumene hydroperoxide.	cumene hydroperoxide	116-136	CD2 molecule	Homo sapiens	22-26
9307035-8	1997	In addition, recombinant human GST T1-1 was found to conjugate glutathione with dichloromethane, a pulmonary and hepatic carcinogen in the mouse.	Glutathione	63-74	CD2 molecule	Homo sapiens	35-39
9307035-8	1997	In addition, recombinant human GST T1-1 was found to conjugate glutathione with dichloromethane, a pulmonary and hepatic carcinogen in the mouse.	Methylene Chloride	80-95	CD2 molecule	Homo sapiens	35-39
9373455-10	1997	A negative relationship was found between GHR expression on CD2+ cells and height-SDS (r - 0.54, P < 0.0001) or BMI (r - 0.4, P < 0.015) in controls and short children, independent of their GH secretory status.	Sodium Dodecyl Sulfate	82-85	CD2 molecule	Homo sapiens	60-63
9247273-6	1997	At two of these sites, Cd2+ ions bind to the cysteines without affecting the energetics of gating; at a third site, Cd2+ binding holds the channel open.	Cysteine	45-54	CD2 molecule	Homo sapiens	23-26
9417495-4	1997	RESULTS: The main significant results of selenium substitution are: increased plasma-selenium, blood cell selenium, plasma-Gpx activity and left ventricular cardiac index as well as decreased plasma thyroxin, free thyroxin, reverse triiodthyronin, total cholesterol, mean erythrocyte and thrombocyte volume and lymphocytic CD2 expression.	Selenium	41-49	CD2 molecule	Homo sapiens	323-326
9341764-0	1997	CD2-mediated signaling in T cells lacking the zeta-chain-specific immune receptor tyrosine-based activation (ITAM) motif.	Tyrosine	82-90	CD2 molecule	Homo sapiens	0-3
9341764-3	1997	Here, we show that CD2-induced activation also functions in T cells which express zeta-chains lacking a functional immune-receptor tyrosine-based activation motif (ITAM).	Tyrosine	131-139	CD2 molecule	Homo sapiens	19-22
9233614-5	1997	Herbimycin, a protein tyrosine kinase (PTK) inhibitor, or wortmannin, a specific inhibitor of phosphatidylinositol 3-kinase (PI 3-K), inhibited completely or almost completely CD2- or CD16-mediated granular exocytosis, suggesting the involvement of protein tyrosine kinases and PI 3-K in both CD2- and CD16-mediated granular exocytosis.	herbimycin	0-10	CD2 molecule	Homo sapiens	176-179
9233614-5	1997	Herbimycin, a protein tyrosine kinase (PTK) inhibitor, or wortmannin, a specific inhibitor of phosphatidylinositol 3-kinase (PI 3-K), inhibited completely or almost completely CD2- or CD16-mediated granular exocytosis, suggesting the involvement of protein tyrosine kinases and PI 3-K in both CD2- and CD16-mediated granular exocytosis.	herbimycin	0-10	CD2 molecule	Homo sapiens	293-296
9233614-5	1997	Herbimycin, a protein tyrosine kinase (PTK) inhibitor, or wortmannin, a specific inhibitor of phosphatidylinositol 3-kinase (PI 3-K), inhibited completely or almost completely CD2- or CD16-mediated granular exocytosis, suggesting the involvement of protein tyrosine kinases and PI 3-K in both CD2- and CD16-mediated granular exocytosis.	Wortmannin	58-68	CD2 molecule	Homo sapiens	176-179
9233614-5	1997	Herbimycin, a protein tyrosine kinase (PTK) inhibitor, or wortmannin, a specific inhibitor of phosphatidylinositol 3-kinase (PI 3-K), inhibited completely or almost completely CD2- or CD16-mediated granular exocytosis, suggesting the involvement of protein tyrosine kinases and PI 3-K in both CD2- and CD16-mediated granular exocytosis.	Wortmannin	58-68	CD2 molecule	Homo sapiens	293-296
9233614-6	1997	We also observed that cross-linking of CD2 as well as CD16 enhances p72syk tyrosine kinase activity, and this enhancement correlated well with the increased tyrosine phosphorylation of several cellular proteins, including the adapter protein Shc.	Tyrosine	75-83	CD2 molecule	Homo sapiens	39-42
9233614-7	1997	Furthermore, we have observed that cross-linking of CD2 as well as CD16 enhances the PI 3-K activity associated with the tyrosine-phosphorylated cellular proteins and Shc.	Tyrosine	121-129	CD2 molecule	Homo sapiens	52-55
9202170-15	1997	The increase in Quin-2 fluorescence after addition of excess CdCl2 indicates that, in our experimental conditions, Ca2+ tightly-bound to actin is partially (60-70%) replaced by Cd2+, forming Cd-actin.	Cadmium Chloride	61-66	CD2 molecule	Homo sapiens	177-180
9012681-4	1997	Fourier transform infrared (FTIR) spectroscopy was used to monitor conformational order in the acyl chains of the incorporated phospholipid, as detected through the asymmetric CD2 stretching vibrations in the intact cells.	Phospholipids	127-139	CD2 molecule	Homo sapiens	176-179
9116293-8	1997	Thus, pediatric ALL patients treated on contemporary CCG protocols who present with CD2+ CD19+ biphenotypic leukemia generally have good treatment outcomes, due in part to their favorable presenting features.	cationic colloidal gold	53-56	CD2 molecule	Homo sapiens	84-87
9155647-9	1997	When phorbol 12-myristate 13-acetate (PMA) was added to the cells triggered with CD2 + 28mAbs, the responses examined were enhanced in both cord and adult blood with no significant differences between the groups.	Tetradecanoylphorbol Acetate	5-36	CD2 molecule	Homo sapiens	81-84
9155647-9	1997	When phorbol 12-myristate 13-acetate (PMA) was added to the cells triggered with CD2 + 28mAbs, the responses examined were enhanced in both cord and adult blood with no significant differences between the groups.	Tetradecanoylphorbol Acetate	38-41	CD2 molecule	Homo sapiens	81-84
9070896-2	1997	At physiological temperature the CD2 scissoring mode of the palmitic acid methylenes, and the CH2 rocking mode of the ceramide methylenes, are each split into two components.	Palmitic Acid	60-73	CD2 molecule	Homo sapiens	33-36
9070896-2	1997	At physiological temperature the CD2 scissoring mode of the palmitic acid methylenes, and the CH2 rocking mode of the ceramide methylenes, are each split into two components.	Ceramides	118-126	CD2 molecule	Homo sapiens	33-36
9070896-5	1997	The thermotropic behavior of the CD2 stretching vibrations demonstrates that conformational disordering of the palmitic acid commences at 42 degrees C with a transition midpoint of 50 degrees C. The CH2 stretching frequency indicates the ceramide chains remain ordered until 50 degrees C then disorder with a midpoint of 67 degrees C. The results provide a molecular characterization for the complex low temperature (10-40 degrees C) dynamic behavior suggested by recent 2H NMR experiments.	Palmitic Acid	111-124	CD2 molecule	Homo sapiens	33-36
9070896-5	1997	The thermotropic behavior of the CD2 stretching vibrations demonstrates that conformational disordering of the palmitic acid commences at 42 degrees C with a transition midpoint of 50 degrees C. The CH2 stretching frequency indicates the ceramide chains remain ordered until 50 degrees C then disorder with a midpoint of 67 degrees C. The results provide a molecular characterization for the complex low temperature (10-40 degrees C) dynamic behavior suggested by recent 2H NMR experiments.	Ceramides	238-246	CD2 molecule	Homo sapiens	33-36
9044850-0	1997	Down-regulation of prostate-specific antigen expression by finasteride through inhibition of complex formation between androgen receptor and steroid receptor-binding consensus in the promoter of the PSA gene in LNCaP cells.	Finasteride	59-70	CD2 molecule	Homo sapiens	141-175
9044850-8	1997	Binding of LNCaP cell nuclear proteins to SRBC was diminished when the cells were exposed to 25 microM finasteride, at which concentration 50% of both PSA mRNA and protein were inhibited.	Finasteride	103-114	CD2 molecule	Homo sapiens	42-46
9044850-10	1997	Our data indicate that inhibition of complex formation between SRBC and nuclear proteins due to the remarkable decrease in the level of androgen receptor plays a key role in the down-regulation of PSA gene expression by finasteride in LNCaP cells.	Finasteride	220-231	CD2 molecule	Homo sapiens	63-67
9160677-6	1997	In fact, we show that CD2 stimulation inhibits apoptosis by preventing the CD3-induced upregulation of Fas and Fas-L in a Fas-dependent experimental system.	ammonium ferrous sulfate	103-106	CD2 molecule	Homo sapiens	22-25
9130632-2	1997	Stimulation of either CD2 or T cell receptor (TCR)/CD3 on Tcells by monoclonal antibody-mediated cross-linking induced tyrosine phosphorylation of Itk, which was maximal as early as 1 min after stimulation.	Tyrosine	119-127	CD2 molecule	Homo sapiens	22-25
9070436-1	1997	We have used 15N NMR relaxation experiments to probe, for the glycosylated human CD2 adhesion domain, the overall molecular motion, as well as very fast nanosecond-picosecond (ns-ps) and slow millisecond-microsecond (ms-microsecond) internal motions.	15n	13-16	CD2 molecule	Homo sapiens	81-84
9070345-1	1997	The purpose of this study was to investigate the mechanism by which cadmium (Cd2+) crosses the intestinal epithelium using a Caco-2 cell model.	Cadmium	68-75	CD2 molecule	Homo sapiens	77-80
9070345-8	1997	Active transport was evaluated by examining the effect of 2,4-dinitrophenol, a metabolic inhibitor, on the transport of Cd2+.	2,4-Dinitrophenol	58-75	CD2 molecule	Homo sapiens	120-123
9070345-9	1997	These studies indicated that: (1) a portion of the overall transport of Cd2+ can be attributed to diffusion, (2) stimulation of calcium binding protein transcription by vit.	Calcium	128-135	CD2 molecule	Homo sapiens	72-75
9043953-3	1997	Increasing the concentration of intracellular GSH by means of N-acetyl-L-cysteine (NAC) and GSH ethyl ester (OEt) resulted in total protection against cell death, while inhibiting GSH synthesis with buthionine sulfoximine (BSO) greatly enhanced cell sensitivity to Fas and CD2 apoptotic signaling.	Ethane	109-112	CD2 molecule	Homo sapiens	273-276
9043953-0	1997	Thiol-mediated inhibition of FAS and CD2 apoptotic signaling in activated human peripheral T cells.	Sulfhydryl Compounds	0-5	CD2 molecule	Homo sapiens	37-40
9043953-3	1997	Increasing the concentration of intracellular GSH by means of N-acetyl-L-cysteine (NAC) and GSH ethyl ester (OEt) resulted in total protection against cell death, while inhibiting GSH synthesis with buthionine sulfoximine (BSO) greatly enhanced cell sensitivity to Fas and CD2 apoptotic signaling.	Glutathione	46-49	CD2 molecule	Homo sapiens	273-276
9043953-8	1997	These data suggest that GSH, the most abundant intracellular thiol antioxidant, may be important in counteracting Fas- and CD2-mediated apoptosis of T lymphocytes.	Glutathione	24-27	CD2 molecule	Homo sapiens	123-126
8975874-5	1996	Selection in G418-containing medium produced CTLLR8 transfectant clones that: (1) expressed chimeric Fc(epsilon) receptor as determined by flow cytometry; (2) bound human IgE antibodies with high affinity as determined by Scatchard analysis; (3) specifically rosetted IgE-coated SRBC; (4) lysed target cells in IgE-mediated ADCC and reverse ADCC assays; and (5) retarded tumor growth in a Winn assay.	antibiotic G 418	13-17	CD2 molecule	Homo sapiens	279-283
9172010-0	1996	Dexamethasone modulates CD2 expression.	Dexamethasone	0-13	CD2 molecule	Homo sapiens	24-27
9172010-2	1996	We studied the effect of dexamethasone (DEX) on the expression of CD2, an adhesion molecule involved in T-lymphocyte homing and activation.	Dexamethasone	25-38	CD2 molecule	Homo sapiens	66-69
9172010-2	1996	We studied the effect of dexamethasone (DEX) on the expression of CD2, an adhesion molecule involved in T-lymphocyte homing and activation.	Dexamethasone	40-43	CD2 molecule	Homo sapiens	66-69
9172010-3	1996	Results of flow cytometry analysis and immunoprecipitation with anti-CD2 monoclonal antibodies (mAbs) indicated that in vitro treatment with DEX augments CD2 expression in transformed T-cell lines.	Dexamethasone	141-144	CD2 molecule	Homo sapiens	69-72
9172010-3	1996	Results of flow cytometry analysis and immunoprecipitation with anti-CD2 monoclonal antibodies (mAbs) indicated that in vitro treatment with DEX augments CD2 expression in transformed T-cell lines.	Dexamethasone	141-144	CD2 molecule	Homo sapiens	154-157
9172010-5	1996	The DEX-induced CD2 augmentation was transient, peaked at days 1-2 and returned to the levels of untreated controls at days 3-4.	Dexamethasone	4-7	CD2 molecule	Homo sapiens	16-19
8906806-6	1996	In Jurkat cells, p56lck is required for CD3- or CD2-induced tyrosine phosphorylations and clearly activated after CD2 cross-linking.	Tyrosine	60-68	CD2 molecule	Homo sapiens	48-51
8972736-3	1996	The authors previously described N-linked sialic acid-containing carbohydrates associated with CD2 of the CD4+ tumour cell line Jurkat which induced tumour necrosis factor (TNF) secretion by human monocytes.	n-linked sialic acid	33-53	CD2 molecule	Homo sapiens	95-98
8972736-3	1996	The authors previously described N-linked sialic acid-containing carbohydrates associated with CD2 of the CD4+ tumour cell line Jurkat which induced tumour necrosis factor (TNF) secretion by human monocytes.	Carbohydrates	65-78	CD2 molecule	Homo sapiens	95-98
8972736-5	1996	Mannose-6-phosphate, an inhibitor of L-selectin binding, blocked CD2-induced TNF production whereas other ligands for L-selectin (the monomeric monoclonal antibody to L-selectin, DREG-200; inositol hexaphosphoric acid; heparin) amplified CD2-induced secretion of TNF.	mannose-6-phosphate	0-19	CD2 molecule	Homo sapiens	65-68
8906806-0	1996	Tyrosine phosphorylation and recruitment of ZAP-70 to the CD3-TCR complex are defective after CD2 stimulation.	Tyrosine	0-8	CD2 molecule	Homo sapiens	94-97
8972736-7	1996	Jurkat-CD2 is associated with sialyl Lewis X-related carbohydrates which differ in their expression or composition from that of the non-stimulatory CD2 from non-malignant T cells.	Carbohydrates	53-66	CD2 molecule	Homo sapiens	7-10
8972736-8	1996	Taken together the data presented in this report suggest that-at least in the case of Jurkat-CD2-L-selectin is involved in monocyte activation by tumour typical carbohydrate structures.	Carbohydrates	161-173	CD2 molecule	Homo sapiens	93-96
8906806-7	1996	However, we find that the CD3 complex, and especially its zeta-chain, are faintly tyrosine phosphorylated after CD2 triggering.	Tyrosine	82-90	CD2 molecule	Homo sapiens	112-115
8906806-8	1996	By contrast, CD2 induces PLCgamma-1 tyrosine phosphorylation as efficiently as CD3, with a correlated inositol phosphate production and intracellular calcium increase, and even a higher production of IL-2.	Tyrosine	36-44	CD2 molecule	Homo sapiens	13-16
8906806-8	1996	By contrast, CD2 induces PLCgamma-1 tyrosine phosphorylation as efficiently as CD3, with a correlated inositol phosphate production and intracellular calcium increase, and even a higher production of IL-2.	Inositol Phosphates	102-120	CD2 molecule	Homo sapiens	13-16
8906806-8	1996	By contrast, CD2 induces PLCgamma-1 tyrosine phosphorylation as efficiently as CD3, with a correlated inositol phosphate production and intracellular calcium increase, and even a higher production of IL-2.	Calcium	150-157	CD2 molecule	Homo sapiens	13-16
8906806-9	1996	Interestingly, the SH2 domains of PLCgamma-1 associate with ZAP-70 upon CD3 stimulation while they bind, in CD2-activated cells, to a heavily tyrosine-phosphorylated 62-kDa protein.	Tyrosine	142-150	CD2 molecule	Homo sapiens	108-111
8871052-6	1996	In three out of nine clones tested, the stimulation with anti-CD2/CD28/phorbol myristate acetate (PMA) induced a shift of the IFN-gamma/IL-4 ratio towards a Th2-type cytokine profile.	Tetradecanoylphorbol Acetate	71-96	CD2 molecule	Homo sapiens	62-65
8909290-8	1996	Interprotein metal exchange between Cu12-MT and Cd7MT leads to the net transfer of Cd2+ into the alpha-domain and Cu+ into the beta-domain.	Metals	13-18	CD2 molecule	Homo sapiens	83-86
8898024-1	1996	Heavy metal intoxication with Hg2+, Pb2+ and Cd2+ commonly leads to phosphaturia.	Metals	6-11	CD2 molecule	Homo sapiens	45-48
8898024-9	1996	In contrast to Hg2+, the inhibition of Ip by Cd2+ and Pb2+ was rapidly reversible upon washout.	ip	39-41	CD2 molecule	Homo sapiens	45-48
8991852-5	1996	CadA has been labeled with 32P from [alpha-32P] ATP and drives ATP-dependent Cd2+ (and Zn2+) uptake by inside-out membrane vesicles (equivalent to efflux from whole cells).	CADA	0-4	CD2 molecule	Homo sapiens	77-80
8991852-9	1996	The triple-polypeptide Czc (Cd2+, Zn2+ and Co2+) chemiosmotic efflux pump consists of inner membrane (CzcA), outer membrane (CzcC) and membrane-spanning (CzcB) proteins that together transport cations from the cytoplasm across the periplasmic space to the outside of the cell.	Carbon Dioxide	43-47	CD2 molecule	Homo sapiens	28-31
8943565-0	1996	CD2 signaling in T cells involves tyrosine phosphorylation and activation of the Tec family kinase, EMT/ITK/TSK.	Tyrosine	34-42	CD2 molecule	Homo sapiens	0-3
8943565-1	1996	Ligation of the CD2 cell surface glycoprotein expressed on T lymphocytes and NK cells induces protein tyrosine phosphorylation and activation of the Src kinases, LCK and FYN.	Tyrosine	102-110	CD2 molecule	Homo sapiens	16-19
8943565-2	1996	We show here that in Jurkat T leukemia cells and in peripheral blood T cells, CD2 stimulation also leads to tyrosine phosphorylation and activation of the Tec family kinase, EMT/ITK/TSK.	Tyrosine	108-116	CD2 molecule	Homo sapiens	78-81
9389074-1	1996	A continuous flow analysis system for the preconcentration of Cu2+ and/or Cd2+ in water was developed.	Water	82-87	CD2 molecule	Homo sapiens	74-77
8811891-3	1996	The complexation of Cd2+ by glutathione (GSH), in 0.13 m borate buffer at pH 9.5, was studied by differential pulse polarography (DPP) and multivariate curve resolution.	Glutathione	28-39	CD2 molecule	Homo sapiens	20-23
8811891-3	1996	The complexation of Cd2+ by glutathione (GSH), in 0.13 m borate buffer at pH 9.5, was studied by differential pulse polarography (DPP) and multivariate curve resolution.	Glutathione	41-44	CD2 molecule	Homo sapiens	20-23
8811891-3	1996	The complexation of Cd2+ by glutathione (GSH), in 0.13 m borate buffer at pH 9.5, was studied by differential pulse polarography (DPP) and multivariate curve resolution.	Borates	57-63	CD2 molecule	Homo sapiens	20-23
8871052-6	1996	In three out of nine clones tested, the stimulation with anti-CD2/CD28/phorbol myristate acetate (PMA) induced a shift of the IFN-gamma/IL-4 ratio towards a Th2-type cytokine profile.	Tetradecanoylphorbol Acetate	98-101	CD2 molecule	Homo sapiens	62-65
8837187-4	1996	METHODS: A 12-mL dose of 2% mepivacaine was injected at the T11 level posterior to the endothoracic fascia in 15 patients.	Mepivacaine	28-39	CD2 molecule	Homo sapiens	60-63
8685893-1	1996	Cadmium exposure produces depolymerization of the actin cytoskeleton in several cultured cell lines, and we have previously shown that in renal mesangial cells this effect is caused by picomolar concentrations of cytosolic Cd2+.	Cadmium	0-7	CD2 molecule	Homo sapiens	223-226
8660853-3	1996	A putative FAK-related phosphoprotein (fakB) was identified that is responsive to intracellular signals induced through ligation of antigen receptors on both T- and B-lymphocytes, and whose induced tyrosine phosphorylation is augmented by TCR costimulation through the adhesion/costimulatory receptors CD2 and CD4.	Tyrosine	198-206	CD2 molecule	Homo sapiens	302-305
8864569-5	1996	Besides Na+ and K+, several divalent cations were effective in the sequence: Ca2+ > Mn2+ > Ba2+ > Cd2+ > Mg2+ > Co2+ > Zn2+ > Ni2+.	Manganese(2+)	87-91	CD2 molecule	Homo sapiens	107-110
8864569-5	1996	Besides Na+ and K+, several divalent cations were effective in the sequence: Ca2+ > Mn2+ > Ba2+ > Cd2+ > Mg2+ > Co2+ > Zn2+ > Ni2+.	N-methyl-valyl-amiclenomycin	97-101	CD2 molecule	Homo sapiens	107-110
8864569-5	1996	Besides Na+ and K+, several divalent cations were effective in the sequence: Ca2+ > Mn2+ > Ba2+ > Cd2+ > Mg2+ > Co2+ > Zn2+ > Ni2+.	magnesium ion	117-121	CD2 molecule	Homo sapiens	107-110
8864569-5	1996	Besides Na+ and K+, several divalent cations were effective in the sequence: Ca2+ > Mn2+ > Ba2+ > Cd2+ > Mg2+ > Co2+ > Zn2+ > Ni2+.	Cobalt(2+)	127-131	CD2 molecule	Homo sapiens	107-110
8864569-5	1996	Besides Na+ and K+, several divalent cations were effective in the sequence: Ca2+ > Mn2+ > Ba2+ > Cd2+ > Mg2+ > Co2+ > Zn2+ > Ni2+.	Zinc	137-141	CD2 molecule	Homo sapiens	107-110
8864569-5	1996	Besides Na+ and K+, several divalent cations were effective in the sequence: Ca2+ > Mn2+ > Ba2+ > Cd2+ > Mg2+ > Co2+ > Zn2+ > Ni2+.	Nickel(2+)	147-151	CD2 molecule	Homo sapiens	107-110
8698315-5	1996	Two cases of nasal lymphomas with CD2+CD3(Leu4)-CD19-CD56+ phenotype were shown to express truncated 1.0-kb Tbeta and multiple unrearranged Tdelta transcripts with germline TCR beta, gamma, delta, and immunoglobulin heavy-chain joining region (JH) genes, consistent with NK cell lineage.	tbeta	108-113	CD2 molecule	Homo sapiens	34-37
8698315-6	1996	In contrast, one case of nasal lymphoma with CD2+CD3(Leu4)+CD8+CD19-CD56+ phenotype expressed full-length Talpha, Tbeta, and Tgamma transcripts rearranged TCR beta, gamma, and deleted TCR delta genes, indicating T-lineage, These results support the view that nasal lymphomas can separated into NK-cell and T-cell neoplasms, based on differences genotypic characteristics.	talpha	106-112	CD2 molecule	Homo sapiens	45-48
8698315-6	1996	In contrast, one case of nasal lymphoma with CD2+CD3(Leu4)+CD8+CD19-CD56+ phenotype expressed full-length Talpha, Tbeta, and Tgamma transcripts rearranged TCR beta, gamma, and deleted TCR delta genes, indicating T-lineage, These results support the view that nasal lymphomas can separated into NK-cell and T-cell neoplasms, based on differences genotypic characteristics.	tbeta	114-119	CD2 molecule	Homo sapiens	45-48
8617939-9	1996	Our data suggest that CD2 is a Fas-independent cell death pathway that might contribute directly to the elimination of T cells expanding during an immune reaction.	ammonium ferrous sulfate	31-34	CD2 molecule	Homo sapiens	22-25
8706670-9	1996	The spectroscopic characterization of Zn2+-substituted and Cd2+-substituted GIF (6-7 metal ions/protein) showed CD and MCD features at positions identical to those reported for the well-characterized mammalian Zn7-metallothionein and Cd7-metallothionein.	Metals	85-90	CD2 molecule	Homo sapiens	59-62
8706670-9	1996	The spectroscopic characterization of Zn2+-substituted and Cd2+-substituted GIF (6-7 metal ions/protein) showed CD and MCD features at positions identical to those reported for the well-characterized mammalian Zn7-metallothionein and Cd7-metallothionein.	Cadmium	112-114	CD2 molecule	Homo sapiens	59-62
8706670-9	1996	The spectroscopic characterization of Zn2+-substituted and Cd2+-substituted GIF (6-7 metal ions/protein) showed CD and MCD features at positions identical to those reported for the well-characterized mammalian Zn7-metallothionein and Cd7-metallothionein.	zn7-metallothionein	210-229	CD2 molecule	Homo sapiens	59-62
8617939-0	1996	CD2-induced apoptosis in activated human peripheral T cells: a Fas-independent pathway that requires early protein tyrosine phosphorylation.	Tyrosine	115-123	CD2 molecule	Homo sapiens	0-3
8617939-8	1996	Pretreating the cells with herbimycin A, before the addition of the apoptotic stimuli, almost completely inhibited CD2 transmembrane signaling of apoptosis, but left intact Fas-induced apoptosis.	herbimycin	27-39	CD2 molecule	Homo sapiens	115-118
8609406-0	1996	A carbohydrate structure associated with CD15 (Lewis x) on myeloid cells is a novel ligand for human CD2.	Carbohydrates	2-14	CD2 molecule	Homo sapiens	101-104
8609406-11	1996	Collectively, this study indicates that a CD15 (Lewis x)-associated carbohydrate structure(s), which has previously been shown to be a selectin ligand, also may function as an important CD2 ligand on myeloid cells.	Carbohydrates	68-80	CD2 molecule	Homo sapiens	186-189
8609406-3	1996	CD2L bound to a different region of CD2 than known ligands and was N-glycosylation dependent.	Nitrogen	67-68	CD2 molecule	Homo sapiens	0-3
8558013-6	1996	In contrast, cross-linking of a CD2/28 chimera containing a tyrosine to phenylalanine substitution in the YMNM motif did not result in increased adhesion to fibronectin and did not lead to association of the chimera with PI 3-K.	Tyrosine	60-68	CD2 molecule	Homo sapiens	32-35
8600461-14	1996	Cd2+ and Al3+ ions also inhibited the ability of TFIIIA to bind complementary single-stranded DNA and promote renaturation, as measured by Tris-phosphate agarose gel electrophoresis.	tris-phosphate agarose	139-161	CD2 molecule	Homo sapiens	0-3
8601217-2	1996	Mitogenic pairs of anti-CD2 monoclonal antibodies inhibited [3H]thymidine incorporation from 25 to 62% in CD2+ HTLV-I-infected lymphocytes.	Tritium	61-63	CD2 molecule	Homo sapiens	24-27
8601217-2	1996	Mitogenic pairs of anti-CD2 monoclonal antibodies inhibited [3H]thymidine incorporation from 25 to 62% in CD2+ HTLV-I-infected lymphocytes.	Tritium	61-63	CD2 molecule	Homo sapiens	106-109
8601217-4	1996	While cyclosporin A abrogated CD2-mediated proliferation in peripheral blood mononuclear cells, it had no effect on CD2-induced apoptosis in the HTLV-I-infected cell lines.	Cyclosporine	6-19	CD2 molecule	Homo sapiens	30-33
8636222-3	1996	We have studied the interaction of CD2 with LFA-3 in the contact area between Jurkat T lymphoblasts and planar phospholipid bilayers containing purified, fluorescently labeled LFA-3.	Phospholipids	111-123	CD2 molecule	Homo sapiens	35-38
8558013-6	1996	In contrast, cross-linking of a CD2/28 chimera containing a tyrosine to phenylalanine substitution in the YMNM motif did not result in increased adhesion to fibronectin and did not lead to association of the chimera with PI 3-K.	Phenylalanine	72-85	CD2 molecule	Homo sapiens	32-35
9328633-4	1996	The redox reaction between Cd2+ and receptor thiols may result in binding of the metal into stable (di)thiol-cadmium complexes rather than in the formation of disulfide and liberation of the reduced metal.	Sulfhydryl Compounds	45-51	CD2 molecule	Homo sapiens	27-30
9328633-4	1996	The redox reaction between Cd2+ and receptor thiols may result in binding of the metal into stable (di)thiol-cadmium complexes rather than in the formation of disulfide and liberation of the reduced metal.	Disulfides	159-168	CD2 molecule	Homo sapiens	27-30
9328633-4	1996	The redox reaction between Cd2+ and receptor thiols may result in binding of the metal into stable (di)thiol-cadmium complexes rather than in the formation of disulfide and liberation of the reduced metal.	Metals	199-204	CD2 molecule	Homo sapiens	27-30
9328633-4	1996	The redox reaction between Cd2+ and receptor thiols may result in binding of the metal into stable (di)thiol-cadmium complexes rather than in the formation of disulfide and liberation of the reduced metal.	Metals	81-86	CD2 molecule	Homo sapiens	27-30
9328633-4	1996	The redox reaction between Cd2+ and receptor thiols may result in binding of the metal into stable (di)thiol-cadmium complexes rather than in the formation of disulfide and liberation of the reduced metal.	dithiol	99-108	CD2 molecule	Homo sapiens	27-30
9328633-4	1996	The redox reaction between Cd2+ and receptor thiols may result in binding of the metal into stable (di)thiol-cadmium complexes rather than in the formation of disulfide and liberation of the reduced metal.	Cadmium	109-116	CD2 molecule	Homo sapiens	27-30
8551220-0	1996	The SH3 domain of p56lck binds to proline-rich sequences in the cytoplasmic domain of CD2.	Proline	34-41	CD2 molecule	Homo sapiens	86-89
8674140-13	1996	We conclude that depolymerization of F-actin by Cd2+ in smooth muscle and mesangial cells is metal-specific, Ca(2+)-independent, and accompanied by a depletion of total actin protein.	Metals	93-98	CD2 molecule	Homo sapiens	48-51
8674140-7	1996	However, it is this Cd2+ pool which is responsible for F-actin depolymerization because equal cellular concentrations of cadmium delivered as Cd-metallothionein have no effect.	Cadmium	121-128	CD2 molecule	Homo sapiens	20-23
8674140-7	1996	However, it is this Cd2+ pool which is responsible for F-actin depolymerization because equal cellular concentrations of cadmium delivered as Cd-metallothionein have no effect.	cd-metallothionein	142-160	CD2 molecule	Homo sapiens	20-23
8551220-7	1996	Thus, proline-rich sequences in the cytoplasmic domain of CD2 allow this transmembrane receptor to bind to the SH3 domain of p56lck.	Proline	6-13	CD2 molecule	Homo sapiens	58-61
8748652-2	1995	Frequency- and temperature-dependent T(-1)1 studies of lithium borate and thioborate glasses revealed that iron impurities cause frequency-independent relaxation and "shoulders" of the low-temperature slopes in high fields, whereas manganese produces enhanced relaxation peaks.	lithium borate	55-69	CD2 molecule	Homo sapiens	37-43
8557753-8	1995	A role for both protein kinase C and cytoskeletal rearrangements in CD2 regulation of integrin activity is also suggested, since a PKC inhibitor partially inhibits CD2-induced increases in beta 1 integrin function, and CD2 stimulation increases F-actin content in a wortmannin-sensitive manner.	Wortmannin	266-276	CD2 molecule	Homo sapiens	68-71
8557753-8	1995	A role for both protein kinase C and cytoskeletal rearrangements in CD2 regulation of integrin activity is also suggested, since a PKC inhibitor partially inhibits CD2-induced increases in beta 1 integrin function, and CD2 stimulation increases F-actin content in a wortmannin-sensitive manner.	Wortmannin	266-276	CD2 molecule	Homo sapiens	164-167
8557753-8	1995	A role for both protein kinase C and cytoskeletal rearrangements in CD2 regulation of integrin activity is also suggested, since a PKC inhibitor partially inhibits CD2-induced increases in beta 1 integrin function, and CD2 stimulation increases F-actin content in a wortmannin-sensitive manner.	Wortmannin	266-276	CD2 molecule	Homo sapiens	164-167
8540621-2	1995	Formation constants (log K) for the Cd2+ and Zn2+ complexes of PLC estimated by spectrophotometric titration were 8.0 +/- 0.8 and 9.5 +/- 0.5, respectively.	Zinc	45-49	CD2 molecule	Homo sapiens	36-39
8557753-5	1995	Antibody stimulation of CD2 expressed on HL60 transfectants resulted within minutes in increased beta 1-mediated adhesion to fibronectin and VCAM-1 at levels comparable to that obtained upon stimulation with the phorbol ester PMA.	Phorbol Esters	212-225	CD2 molecule	Homo sapiens	24-27
8557753-6	1995	A role for PI 3-K in CD2-mediated increases in beta 1 integrin function is suggested by: (a) the ability of the PI 3-K inhibitor wortmannin to completely inhibit CD2-induced increases in beta 1 integrin activity; (b) the association of PI 3-K with CD2; and (c) induced PI 3-K activity upon CD2 stimulation.	Wortmannin	129-139	CD2 molecule	Homo sapiens	21-24
8557753-6	1995	A role for PI 3-K in CD2-mediated increases in beta 1 integrin function is suggested by: (a) the ability of the PI 3-K inhibitor wortmannin to completely inhibit CD2-induced increases in beta 1 integrin activity; (b) the association of PI 3-K with CD2; and (c) induced PI 3-K activity upon CD2 stimulation.	Wortmannin	129-139	CD2 molecule	Homo sapiens	162-165
8557753-6	1995	A role for PI 3-K in CD2-mediated increases in beta 1 integrin function is suggested by: (a) the ability of the PI 3-K inhibitor wortmannin to completely inhibit CD2-induced increases in beta 1 integrin activity; (b) the association of PI 3-K with CD2; and (c) induced PI 3-K activity upon CD2 stimulation.	Wortmannin	129-139	CD2 molecule	Homo sapiens	162-165
8557753-6	1995	A role for PI 3-K in CD2-mediated increases in beta 1 integrin function is suggested by: (a) the ability of the PI 3-K inhibitor wortmannin to completely inhibit CD2-induced increases in beta 1 integrin activity; (b) the association of PI 3-K with CD2; and (c) induced PI 3-K activity upon CD2 stimulation.	Wortmannin	129-139	CD2 molecule	Homo sapiens	162-165
7491938-5	1995	Cd2+, La3+, and Gd3+ had biphasic effects on membrane conductance (Gm).	gm	67-69	CD2 molecule	Homo sapiens	0-3
8748652-2	1995	Frequency- and temperature-dependent T(-1)1 studies of lithium borate and thioborate glasses revealed that iron impurities cause frequency-independent relaxation and "shoulders" of the low-temperature slopes in high fields, whereas manganese produces enhanced relaxation peaks.	thioborate	74-84	CD2 molecule	Homo sapiens	37-43
8748652-2	1995	Frequency- and temperature-dependent T(-1)1 studies of lithium borate and thioborate glasses revealed that iron impurities cause frequency-independent relaxation and "shoulders" of the low-temperature slopes in high fields, whereas manganese produces enhanced relaxation peaks.	Iron	107-111	CD2 molecule	Homo sapiens	37-43
8748652-2	1995	Frequency- and temperature-dependent T(-1)1 studies of lithium borate and thioborate glasses revealed that iron impurities cause frequency-independent relaxation and "shoulders" of the low-temperature slopes in high fields, whereas manganese produces enhanced relaxation peaks.	Manganese	232-241	CD2 molecule	Homo sapiens	37-43
7542590-1	1995	The glycosylphosphatidylinositol (GPI)-anchored CD59 protein (human protectin) protects cells against complement-induced lysis, binds to CD2 and also transduces activation signals within T cells.	Glycosylphosphatidylinositols	4-32	CD2 molecule	Homo sapiens	137-140
8562067-7	1995	Amino acid analysis, Edman degradation, and FAB-MS identified T11 as the N-blocked decapeptide pyro-Gln-Pro-Val-Trp-Gln-Asp-Glu-Gly-Gln-Arg derived from the N-terminus of pZPC.	pyro-gln	95-103	CD2 molecule	Homo sapiens	62-65
8562067-7	1995	Amino acid analysis, Edman degradation, and FAB-MS identified T11 as the N-blocked decapeptide pyro-Gln-Pro-Val-Trp-Gln-Asp-Glu-Gly-Gln-Arg derived from the N-terminus of pZPC.	Proline	104-107	CD2 molecule	Homo sapiens	62-65
8562067-7	1995	Amino acid analysis, Edman degradation, and FAB-MS identified T11 as the N-blocked decapeptide pyro-Gln-Pro-Val-Trp-Gln-Asp-Glu-Gly-Gln-Arg derived from the N-terminus of pZPC.	Valine	108-111	CD2 molecule	Homo sapiens	62-65
8562067-7	1995	Amino acid analysis, Edman degradation, and FAB-MS identified T11 as the N-blocked decapeptide pyro-Gln-Pro-Val-Trp-Gln-Asp-Glu-Gly-Gln-Arg derived from the N-terminus of pZPC.	Tryptophan	112-115	CD2 molecule	Homo sapiens	62-65
8562067-7	1995	Amino acid analysis, Edman degradation, and FAB-MS identified T11 as the N-blocked decapeptide pyro-Gln-Pro-Val-Trp-Gln-Asp-Glu-Gly-Gln-Arg derived from the N-terminus of pZPC.	Glutamine	100-103	CD2 molecule	Homo sapiens	62-65
8562067-7	1995	Amino acid analysis, Edman degradation, and FAB-MS identified T11 as the N-blocked decapeptide pyro-Gln-Pro-Val-Trp-Gln-Asp-Glu-Gly-Gln-Arg derived from the N-terminus of pZPC.	Aspartic Acid	120-123	CD2 molecule	Homo sapiens	62-65
8562067-7	1995	Amino acid analysis, Edman degradation, and FAB-MS identified T11 as the N-blocked decapeptide pyro-Gln-Pro-Val-Trp-Gln-Asp-Glu-Gly-Gln-Arg derived from the N-terminus of pZPC.	Glutamic Acid	124-127	CD2 molecule	Homo sapiens	62-65
8562067-7	1995	Amino acid analysis, Edman degradation, and FAB-MS identified T11 as the N-blocked decapeptide pyro-Gln-Pro-Val-Trp-Gln-Asp-Glu-Gly-Gln-Arg derived from the N-terminus of pZPC.	Glycine	128-131	CD2 molecule	Homo sapiens	62-65
8562067-7	1995	Amino acid analysis, Edman degradation, and FAB-MS identified T11 as the N-blocked decapeptide pyro-Gln-Pro-Val-Trp-Gln-Asp-Glu-Gly-Gln-Arg derived from the N-terminus of pZPC.	Glutamine	116-119	CD2 molecule	Homo sapiens	62-65
8562067-7	1995	Amino acid analysis, Edman degradation, and FAB-MS identified T11 as the N-blocked decapeptide pyro-Gln-Pro-Val-Trp-Gln-Asp-Glu-Gly-Gln-Arg derived from the N-terminus of pZPC.	Arginine	136-139	CD2 molecule	Homo sapiens	62-65
8537235-0	1995	Hb A2-Agrinio [delta 43(CD2)Glu-->Gly(GAG-->GGG)]: a new delta chain variant detected in a Greek family.	Glutamic Acid	28-31	CD2 molecule	Homo sapiens	24-27
8537816-2	1995	In mammalian heart Na channels, this residue is substituted by cysteine, which results in low affinity for TTX/STX and enhanced sensitivity to block by Zn2+ and Cd2+.	Cysteine	63-71	CD2 molecule	Homo sapiens	161-164
7628605-2	1995	In D2O both HD and D2 are formed from CH2 = H4MPT and in H2O both HD and H2 from CD2 = H4MPT.	Water	57-60	CD2 molecule	Homo sapiens	81-84
7544493-0	1995	Conformation and function of the N-linked glycan in the adhesion domain of human CD2.	n-linked glycan	33-48	CD2 molecule	Homo sapiens	81-84
7544493-1	1995	The adhesion domain of human CD2 bears a single N-linked carbohydrate.	n-linked carbohydrate	48-69	CD2 molecule	Homo sapiens	29-32
7544493-2	1995	The solution structure of a fragment of CD2 containing the covalently bound high-mannose N-glycan [-(N-acetylglucosamine)2-(mannose)5-8] was solved by nuclear magnetic resonance.	mannose n-glycan [-(n-acetylglucosamine)2-(mannose	81-131	CD2 molecule	Homo sapiens	40-43
7544493-4	1995	Mutagenesis of all residues in the vicinity of the glycan suggests that the glycan is not a component of the CD2-CD58 interface; rather, the carbohydrate stabilizes the protein fold by counterbalancing an unfavorable clustering of five positive charges centered about lysine-61 of CD2.	Carbohydrates	141-153	CD2 molecule	Homo sapiens	281-284
7595664-2	1995	ACh release was stimulated in cutaneous pectoris nerve-muscle preparations by: (1) 1 mM Cd2+ in Ca(2+)-free medium for a period of 3 h, (2) 25 or 40 mM K+ in normal Ringer"s solution.	Acetylcholine	0-3	CD2 molecule	Homo sapiens	88-91
7595664-6	1995	In preparations stimulated with Cd2+ in Ca(2+)-free medium, the immunofluorescence was also observed in non Triton X-100 treated muscle fibres.	Octoxynol	108-120	CD2 molecule	Homo sapiens	32-35
7542590-1	1995	The glycosylphosphatidylinositol (GPI)-anchored CD59 protein (human protectin) protects cells against complement-induced lysis, binds to CD2 and also transduces activation signals within T cells.	Glycosylphosphatidylinositols	34-37	CD2 molecule	Homo sapiens	137-140
7769716-5	1995	An absolutely conserved histidine in CD2 has also been demonstrated by site-directed mutagenesis of the SCMV and HSV-1 enzymes to be essential for proteolytic activity and has been proposed to be a second member of the catalytic triad of this serine proteinase.	Histidine	24-33	CD2 molecule	Homo sapiens	37-40
7621876-7	1995	Additional CD2 cross-linking resulted in the tyrosine phosphorylation of distinct proteins.	Tyrosine	45-53	CD2 molecule	Homo sapiens	11-14
7769716-9	1995	Results of these experiments verified that HCMV CD3 serine (Ser-132) and CD2 histidine (His-63) are essential for proteolytic activity and identified a glutamic acid (Glu-122) within CD3 that is also essential for proteolytic activity and may be conserved among all herpesvirus assemblin homologs.	Histidine	77-86	CD2 molecule	Homo sapiens	73-76
7615011-0	1995	Involvement of cAMP in CD3 T cell receptor complex- and CD2-mediated apoptosis of human thymocytes.	Cyclic AMP	15-19	CD2 molecule	Homo sapiens	56-59
7769716-9	1995	Results of these experiments verified that HCMV CD3 serine (Ser-132) and CD2 histidine (His-63) are essential for proteolytic activity and identified a glutamic acid (Glu-122) within CD3 that is also essential for proteolytic activity and may be conserved among all herpesvirus assemblin homologs.	Histidine	88-91	CD2 molecule	Homo sapiens	73-76
7769716-10	1995	We suggest that CD3 Glu-122, CD3 Ser-132, and CD2 His-63 constitute the active-site triad of this serine proteinase.	Histidine	50-53	CD2 molecule	Homo sapiens	46-49
7615011-4	1995	Addition of Rp-cAMP also rescues thymocytes from activation-induced apoptosis following the ligation of surface CD3/T cell receptor complex or CD2 antigens.	Cyclic AMP	15-19	CD2 molecule	Homo sapiens	143-146
7767963-0	1995	The immature thymocyte is protected from N-methylnitrosourea-induced lymphoma by the human MGMT-CD2 transgene.	Methylnitrosourea	41-60	CD2 molecule	Homo sapiens	96-99
7628916-6	1995	The data obtained in vitro revealed that SMS may inhibit only the CD2-induced blastogenesis (in early and late interval after the use of PHA).	Samarium	41-44	CD2 molecule	Homo sapiens	66-69
7696499-6	1995	Depleting cells of cytoplasmic Ca2+, loading cells with dibutyric cAMP, and disrupting cellular microfilaments each partially reversed the effect of CD2-mediated activation on the lateral mobility of CD2.	Cyclic AMP	66-70	CD2 molecule	Homo sapiens	149-152
7739570-9	1995	Here we extend these studies to show that activation of both CD2 and the toxin receptor led to rapid tyrosine phosphorylation of three similar proteins.	Tyrosine	101-109	CD2 molecule	Homo sapiens	61-64
7890646-3	1995	NMR titration of the 111Cd-protein with EDTA showed that the ligand interacts preferentially and cooperatively with Cd2+ ions in the beta-domain cluster.	Edetic Acid	40-44	CD2 molecule	Homo sapiens	116-119
7890646-4	1995	NMR and ultrafiltration kinetic analysis of this reaction using 5.6 mM Cd2+ as 111Cd7-MT and 56 mM EDTA indicated that cadmium-EDTA formed less rapidly than 111Cd peak intensity declined.	cadmium-edta	119-131	CD2 molecule	Homo sapiens	71-74
7890646-5	1995	Spectrophotometric and gel filtration studies of the reaction with 20 microM Cd2+ as Cd7-MT with various concentrations of EDTA revealed biphasic kinetics with much larger rate constants than observed in the NMR experiments.	Edetic Acid	123-127	CD2 molecule	Homo sapiens	77-80
7890646-9	1995	The Cd4 domain reacted with EDTA with biphasic kinetics, in which one Cd2+ was removed rapidly with first-order kinetics, which were zero-order in EDTA.	Edetic Acid	28-32	CD2 molecule	Homo sapiens	70-73
7890646-9	1995	The Cd4 domain reacted with EDTA with biphasic kinetics, in which one Cd2+ was removed rapidly with first-order kinetics, which were zero-order in EDTA.	Edetic Acid	147-151	CD2 molecule	Homo sapiens	70-73
7849022-0	1995	Composition and sequence specific resonance assignments of the heterogeneous N-linked glycan in the 13.6 kDa adhesion domain of human CD2 as determined by NMR on the intact glycoprotein.	n-linked glycan	77-92	CD2 molecule	Homo sapiens	134-137
7849022-3	1995	This adhesion domain in human CD2 contains a single high-mannose N-glycan.	Mannose	57-64	CD2 molecule	Homo sapiens	30-33
7849022-3	1995	This adhesion domain in human CD2 contains a single high-mannose N-glycan.	n-glycan	65-73	CD2 molecule	Homo sapiens	30-33
7849022-5	1995	To better understand the structural aspects that regulate human CD2 adhesion functions, we had previously determined the solution structure of the protein part of the N-glycosylated adhesion domain of human CD2 (hu-sCD2(105); MW approximately 13.6 kDa) by NMR spectroscopy.	Nitrogen	167-168	CD2 molecule	Homo sapiens	64-67
7849022-5	1995	To better understand the structural aspects that regulate human CD2 adhesion functions, we had previously determined the solution structure of the protein part of the N-glycosylated adhesion domain of human CD2 (hu-sCD2(105); MW approximately 13.6 kDa) by NMR spectroscopy.	Nitrogen	167-168	CD2 molecule	Homo sapiens	207-210
7547686-5	1995	However, the alternative pathway of T cell activation through CD2/CD28 triggering was highly sensitive to DEX when naive cells were studied; in the case of memory cells, at least a 10-fold higher DEX concentration was needed to achieve a comparable inhibition.	Dexamethasone	106-109	CD2 molecule	Homo sapiens	62-65
7547686-5	1995	However, the alternative pathway of T cell activation through CD2/CD28 triggering was highly sensitive to DEX when naive cells were studied; in the case of memory cells, at least a 10-fold higher DEX concentration was needed to achieve a comparable inhibition.	Dexamethasone	196-199	CD2 molecule	Homo sapiens	62-65
7756555-5	1995	The smaller thiol reagent Cd2+ reacts with modified side chains that are also accessible to the larger (2-trimethylammoniumethyl)methanethiosulfate (MTSET) [corrected].	Sulfhydryl Compounds	12-17	CD2 molecule	Homo sapiens	26-29
7756555-5	1995	The smaller thiol reagent Cd2+ reacts with modified side chains that are also accessible to the larger (2-trimethylammoniumethyl)methanethiosulfate (MTSET) [corrected].	(2-trimethylammoniumethyl)methanethiosulfate	103-147	CD2 molecule	Homo sapiens	26-29
7756555-5	1995	The smaller thiol reagent Cd2+ reacts with modified side chains that are also accessible to the larger (2-trimethylammoniumethyl)methanethiosulfate (MTSET) [corrected].	MTSET	149-154	CD2 molecule	Homo sapiens	26-29
7662514-0	1995	Intracellular calcium levels are differentially regulated in T lymphocytes triggered by anti-CD2 and anti-CD3 monoclonal antibodies.	Calcium	14-21	CD2 molecule	Homo sapiens	93-96
7900519-5	1995	Responses to Ca2+ and oxytocin were significantly increased by exposure to cadmium in low concentration (10(-9) M-10(-8) M), whereas higher concentration of Cd2+ had inhibitory action.	Cadmium	75-82	CD2 molecule	Homo sapiens	157-160
7900519-7	1995	The increased responses to Ca2+ and oxytocin in the presence of low amounts of Cd2+ support a role of cadmium in mechanisms of preterm labor.	Cadmium	102-109	CD2 molecule	Homo sapiens	79-82
7696499-6	1995	Depleting cells of cytoplasmic Ca2+, loading cells with dibutyric cAMP, and disrupting cellular microfilaments each partially reversed the effect of CD2-mediated activation on the lateral mobility of CD2.	Cyclic AMP	66-70	CD2 molecule	Homo sapiens	200-203
7529232-4	1995	A form of human soluble CD2 (hsCD2) with single N-acetylglucosamine residues at each glycosylation site was produced by inhibiting glucosidase I with N-butyldeoxynojirimycin during expression in Chinese hamster ovary cells and digesting the expressed hsCD2 with endoglycosidase H. The ligand and antibody binding properties of this form of hsCD2 were indistinguishable from those of fully glycosylated hsCD2 as determined by surface plasmon resonance analyses.	Acetylglucosamine	48-67	CD2 molecule	Homo sapiens	24-27
7529282-6	1995	Antiphosphotyrosine (APT) immunoblotting revealed inducible substrate phosphorylation during CD2, but not CD3, ligation in whole LPLs, as well as LPL-derived T cell lines.	antiphosphotyrosine	0-19	CD2 molecule	Homo sapiens	93-96
7529282-6	1995	Antiphosphotyrosine (APT) immunoblotting revealed inducible substrate phosphorylation during CD2, but not CD3, ligation in whole LPLs, as well as LPL-derived T cell lines.	apt	21-24	CD2 molecule	Homo sapiens	93-96
8907637-0	1995	Improved detection of CD2 on formaldehyde-fixed non dehydrated cells.	Formaldehyde	29-41	CD2 molecule	Homo sapiens	22-25
8572506-2	1995	To estimate the influence of aryl group position on the immunostimulant properties of imidazo[2,1-b]thiazole derivatives, several compounds were obtained and tested, versus tetramisole hydrochloride, on the mobilisation of CD2 receptor by human T lymphocyte.	imidazo(2,1-b)thiazole	86-108	CD2 molecule	Homo sapiens	223-226
7821106-3	1995	Gastroesophageal reflux episodes were more frequent (P = 0.016) and gastroesophageal reflux indexes were greater (P < 0.010) after isosorbide dinitrate than after placebo in CD-2 group (N = 15) but not in healthy volunteers (N = 14) or CD-1 group (N = 9); six of seven CD-2 patients presenting with gastroesophageal reflux after isosorbide dinitrate had abnormal clearance of refluxate.	Isosorbide Dinitrate	134-154	CD2 molecule	Homo sapiens	177-181
7821106-3	1995	Gastroesophageal reflux episodes were more frequent (P = 0.016) and gastroesophageal reflux indexes were greater (P < 0.010) after isosorbide dinitrate than after placebo in CD-2 group (N = 15) but not in healthy volunteers (N = 14) or CD-1 group (N = 9); six of seven CD-2 patients presenting with gastroesophageal reflux after isosorbide dinitrate had abnormal clearance of refluxate.	Isosorbide Dinitrate	134-154	CD2 molecule	Homo sapiens	272-276
7821106-5	1995	In separate studies, 5 mg isosorbide dinitrate reduced the lower esophageal pressure (P < 0.01) in seven CD-2 patients.	Isosorbide Dinitrate	26-46	CD2 molecule	Homo sapiens	108-112
7956594-6	1994	Intravenous erythromycin markedly accelerated the gastric emptying (all three parameters studied) of solids (P < 0.01) in seven of nine patients with postsurgical gastroparesis [baseline T1/2 154 +/- 15 min; after intravenous erythromycin, T1/2 56 +/- 17 min (mean +/- SEM)].	Erythromycin	12-24	CD2 molecule	Homo sapiens	243-261
7824892-0	1995	Monocyte activation by tumour cells: a role for carbohydrate structures associated with CD2.	Carbohydrates	48-60	CD2 molecule	Homo sapiens	88-91
7824892-3	1995	Previous work in our laboratory suggested that carbohydrate moieties associated with the T cell adhesion molecule CD2 of Jurkat cells induce TNF-alpha secretion by human monocytes.	Carbohydrates	47-59	CD2 molecule	Homo sapiens	114-117
7824892-4	1995	In this study we present data indicating that the stimulatory capacity for TNF-alpha secretion is confined to carbohydrate moieties of tumour cell CD2.	Carbohydrates	110-122	CD2 molecule	Homo sapiens	147-150
8821628-9	1995	CD2-regulated decreases in R1-2 epitope expression correlated with increased cAMP and could be prevented by addition of high doses of IL-2 but was not affected by the addition of other cytokines.	Cyclic AMP	77-81	CD2 molecule	Homo sapiens	0-3
8866788-0	1995	Increased cAMP and cAMP-dependent protein kinase activity mediate anti-CD2 induced suppression of anti-CD3-driven interleukin-2 production and CD25 expression.	Cyclic AMP	10-14	CD2 molecule	Homo sapiens	71-74
8866788-0	1995	Increased cAMP and cAMP-dependent protein kinase activity mediate anti-CD2 induced suppression of anti-CD3-driven interleukin-2 production and CD25 expression.	Cyclic AMP	19-23	CD2 molecule	Homo sapiens	71-74
8866788-7	1995	Anti-CD2 increased cytoplasmic cAMP in a dose- and time-dependent manner.	Cyclic AMP	31-35	CD2 molecule	Homo sapiens	5-8
8866788-8	1995	Reagents that increased cytoplasmic cAMP such as forskolin, cholera toxin, and 3"-isobutyl-1-methylxanthine could mimic the inhibitory effect of anti-CD2 on anti-CD3-driven CD25 expression.	Cyclic AMP	36-40	CD2 molecule	Homo sapiens	150-153
8866788-8	1995	Reagents that increased cytoplasmic cAMP such as forskolin, cholera toxin, and 3"-isobutyl-1-methylxanthine could mimic the inhibitory effect of anti-CD2 on anti-CD3-driven CD25 expression.	Colforsin	49-58	CD2 molecule	Homo sapiens	150-153
8866788-8	1995	Reagents that increased cytoplasmic cAMP such as forskolin, cholera toxin, and 3"-isobutyl-1-methylxanthine could mimic the inhibitory effect of anti-CD2 on anti-CD3-driven CD25 expression.	1-Methyl-3-isobutylxanthine	79-107	CD2 molecule	Homo sapiens	150-153
8866788-10	1995	H8, a PKA antagonist, blocked the inhibitory effect of anti-CD2 on CD25 expression, further confirming the role of PKA in CD2-induced negative signaling.	N-(2-(methylamino)ethyl)-5-isoquinolinesulfonamide	0-2	CD2 molecule	Homo sapiens	60-63
8866788-10	1995	H8, a PKA antagonist, blocked the inhibitory effect of anti-CD2 on CD25 expression, further confirming the role of PKA in CD2-induced negative signaling.	N-(2-(methylamino)ethyl)-5-isoquinolinesulfonamide	0-2	CD2 molecule	Homo sapiens	67-70
8866788-12	1995	These findings show that increased cAMP and PKA activity mediate anti-CD2-induced suppression of anti-CD3-driven IL-2 production and CD25 expression, and provide mechanisms for anti-CD2-induced immunosuppression and inhibition of the cytokine syndrome associated with anti-CD3 treatment.	Cyclic AMP	35-39	CD2 molecule	Homo sapiens	70-73
8866788-12	1995	These findings show that increased cAMP and PKA activity mediate anti-CD2-induced suppression of anti-CD3-driven IL-2 production and CD25 expression, and provide mechanisms for anti-CD2-induced immunosuppression and inhibition of the cytokine syndrome associated with anti-CD3 treatment.	Cyclic AMP	35-39	CD2 molecule	Homo sapiens	133-136
7956594-7	1994	Oral erythromycin enhanced (P < 0.05) the gastric emptying rate (T1/2, area under the curve) in five of seven patients (baseline T1/2 146 +/- 16 min; after oral erythromycin, T1/2 87 +/- 20 min).	Erythromycin	5-17	CD2 molecule	Homo sapiens	178-192
7930601-4	1994	This implies a regulatory role for tyrosine phosphorylation in the induction of each function by CD2.	Tyrosine	35-43	CD2 molecule	Homo sapiens	97-100
7524094-4	1994	Costimulation of the T-cell antigen receptor (TCR/CD3) with either the CD2 or CD4 costimulatory receptors induced synergistic fakB tyrosine phosphorylation in normal human T cells.	Tyrosine	131-139	CD2 molecule	Homo sapiens	71-74
7930601-6	1994	First, immunoblotting total cellular extracts with an anti-phosphotyrosine mAb showed different patterns of tyrosine phosphorylation depending on the pair of CD2 mAbs used for stimulation.	Phosphotyrosine	59-74	CD2 molecule	Homo sapiens	158-161
7930601-6	1994	First, immunoblotting total cellular extracts with an anti-phosphotyrosine mAb showed different patterns of tyrosine phosphorylation depending on the pair of CD2 mAbs used for stimulation.	Tyrosine	66-74	CD2 molecule	Homo sapiens	158-161
7519476-8	1994	Analysis of intracellular signals transduced during T-ALL differentiation indicated that CD2-ligation induced Ca2+ influx and that the ligation of CD2 and IL-2R induced distinct tyrosine phosphorylation patterns.	Tyrosine	178-186	CD2 molecule	Homo sapiens	147-150
8000855-0	1994	Thymocytes bearing high-density T cell receptor and CD2 are selectively eliminated in cyclosporine-induced thymic atrophy.	Cyclosporine	86-98	CD2 molecule	Homo sapiens	52-55
8062258-2	1994	Previous studies have shown that single doses of MNU administered to adult mice induced thymic lymphomas in over 80% of mice, while transgenic mice expressing high levels of the human O6-alkylguanine-DNA alkyltransferase gene in the thymus (MGMT-CD2 transgenics) were protected from developing MNU-induced lymphomas.	Methylnitrosourea	49-52	CD2 molecule	Homo sapiens	246-249
7914908-1	1994	Two-dimensional gel electrophoresis of in vitro phosphorylated proteins coprecipitated by CD2 monoclonal antibody (mAb) from Brij58 lysates of resting human T lymphocytes and natural killer (NK) cells resulted in the identification of a novel 29/30-kD disulfide-linked dimer (pp29/30).	Disulfides	252-261	CD2 molecule	Homo sapiens	90-93
7981618-1	1994	p56lck, a src family protein tyrosine kinase interacts with several T cell receptors, like: CD4, CD8, CD2 and the beta-chain of the IL2, thereby receptors devoid of kinase activity may transduce signals via tyr phosphorylation.	Tyrosine	29-32	CD2 molecule	Homo sapiens	102-105
7526919-2	1994	In this study we examine the ability of tyrosine phosphorylated proteins from Jurkat T cells stimulated by CD2 or T cell receptor (TcR)-CD3 to interact with the src homology 2 (SH2) domains from p56lck (Lck).	Tyrosine	40-48	CD2 molecule	Homo sapiens	107-110
7909498-7	1994	Moreover, the modulation of CD26 resulted in an increase in anti-CD3-mediated cord T cell activation through an enhancement in intracellular calcium levels, IL-2 receptor expression, and IL-2 synthesis, whereas it had no effect on cord T cell activation induced by anti-CD2 or anti-CD2 plus exogenous IL-2.	Calcium	141-148	CD2 molecule	Homo sapiens	28-31
8162613-2	1994	Total melanoma gangliosides in micelles inhibited proliferation of peripheral blood mononuclear cells stimulated by various mitogens, modulated lymphocyte surface molecules CD2, CD3, CD4, CD5 and CD8 and inhibited the production of interleukin-1 beta (IL-1 beta), tumor necrosis factor alpha (TNF alpha) and IL-6 by stimulated adherent cells.	Gangliosides	15-27	CD2 molecule	Homo sapiens	173-176
7909604-4	1994	After T-cell stimulation with a phorbol ester, the force contributed by LFA-1 was drastically increased, while that of CD2 was unaffected.	Phorbol Esters	32-45	CD2 molecule	Homo sapiens	119-122
8208538-2	1994	In this study we examine the ability of tyrosine phosphorylated proteins from Jurkat T cells stimulated by CD2 or T cell receptor-CD3 to interact with the src homology 2 or src homology 3 domains from eight different proteins involved in signal transduction in lymphocytes: Vav, Shc, Nck, phosphatidylinositol-3-kinase, phospholipase C-gamma 1, Ras-GTPase activating protein, c-Crk and Grb2.	Tyrosine	40-48	CD2 molecule	Homo sapiens	107-110
8069676-0	1994	Cd2+ and Co2+ at micromolar concentrations stimulate catecholamine secretion by increasing the cytosolic free Ca2+ concentration in cat adrenal chromaffin cells.	Catecholamines	53-66	CD2 molecule	Homo sapiens	0-3
8069676-1	1994	Cd2+ and Co2+ at micromolar concentrations increased the cytosolic free Ca2+ concentration, which was measured by fura-2 microfluorometry, in cat adrenal chromaffin cells.	Fura-2	114-120	CD2 molecule	Homo sapiens	0-3
7909824-1	1994	Phosphorylation on serine residues of a 67-kDa cytoplasmic protein (p67) occurs as an early signaling event after stimulation of resting human T cells via CD2 but not via TCR/CD3.	Serine	19-25	CD2 molecule	Homo sapiens	155-158
8038379-1	1994	Substitution of a cysteine in the extracellular mouth of the pore of the Shaker-delta K+ channel permits allosteric inhibition of the channel by Zn2+ or Cd2+ ions at micromolar concentrations.	Cysteine	18-26	CD2 molecule	Homo sapiens	153-156
8039551-2	1994	In the present study, CEM-C12 cells were pretreated for 24 h with 1 microM Cd2+ and then challenged with toxic concentrations of this metal.	Metals	134-139	CD2 molecule	Homo sapiens	75-78
8039551-7	1994	Finally, verapamil, a calcium/potassium channel blocker displaced the dose-response curve for Cd2+ toxicity as well as metallothionein-IIA and heat shock protein 70 gene expression to higher Cd2+ concentrations.	Verapamil	9-18	CD2 molecule	Homo sapiens	94-97
8039551-7	1994	Finally, verapamil, a calcium/potassium channel blocker displaced the dose-response curve for Cd2+ toxicity as well as metallothionein-IIA and heat shock protein 70 gene expression to higher Cd2+ concentrations.	Verapamil	9-18	CD2 molecule	Homo sapiens	191-194
9910608-0	1994	Erratum: Fusion yields for carbon-cluster impact on CD2 targets	Carbon	27-33	CD2 molecule	Homo sapiens	52-55
8131214-2	1994	In the present work, iron (FeC6H5O7) and zinc (ZnCl2) were tested in comparison to nickel (NiCl2) and cobalt (CoCl2) for their effect on six different surface molecules known to be involved in recognition and activation processes, namely CD4, CD2, CD3, CD8, HLA-ABC, and HLA-DR. Iron was seen to down-modulate expression of the CD4 and the CD2 molecules on the surface of T-lymphocytes, as indicated by a decrease in the mean fluorescence intensity measured by FACS analysis.	Iron	21-25	CD2 molecule	Homo sapiens	243-246
8131214-2	1994	In the present work, iron (FeC6H5O7) and zinc (ZnCl2) were tested in comparison to nickel (NiCl2) and cobalt (CoCl2) for their effect on six different surface molecules known to be involved in recognition and activation processes, namely CD4, CD2, CD3, CD8, HLA-ABC, and HLA-DR. Iron was seen to down-modulate expression of the CD4 and the CD2 molecules on the surface of T-lymphocytes, as indicated by a decrease in the mean fluorescence intensity measured by FACS analysis.	Iron	21-25	CD2 molecule	Homo sapiens	340-343
8131214-2	1994	In the present work, iron (FeC6H5O7) and zinc (ZnCl2) were tested in comparison to nickel (NiCl2) and cobalt (CoCl2) for their effect on six different surface molecules known to be involved in recognition and activation processes, namely CD4, CD2, CD3, CD8, HLA-ABC, and HLA-DR. Iron was seen to down-modulate expression of the CD4 and the CD2 molecules on the surface of T-lymphocytes, as indicated by a decrease in the mean fluorescence intensity measured by FACS analysis.	zinc chloride	47-52	CD2 molecule	Homo sapiens	243-246
8131214-2	1994	In the present work, iron (FeC6H5O7) and zinc (ZnCl2) were tested in comparison to nickel (NiCl2) and cobalt (CoCl2) for their effect on six different surface molecules known to be involved in recognition and activation processes, namely CD4, CD2, CD3, CD8, HLA-ABC, and HLA-DR. Iron was seen to down-modulate expression of the CD4 and the CD2 molecules on the surface of T-lymphocytes, as indicated by a decrease in the mean fluorescence intensity measured by FACS analysis.	zinc chloride	47-52	CD2 molecule	Homo sapiens	340-343
7511258-0	1994	Anti-CD2 monoclonal antibodies synergize with FK506 but not with cyclosporine or rapamycin to induce tolerance.	Tacrolimus	46-51	CD2 molecule	Homo sapiens	5-8
7511258-15	1994	This suggests that FK506 acts at a different locus in allograft immunity compared with the other immunosuppressants and this may be related to the alternative CD2 T cell activation pathway.	Tacrolimus	19-24	CD2 molecule	Homo sapiens	159-162
7927512-7	1994	The increase of TNF-alpha mRNA by anti-CD2 and anti-CD3 was offset by the presence of TC, suggesting that TC supply a negative signal to the CTL resulting in degradation of the TNF-alpha mRNA.	Technetium	106-108	CD2 molecule	Homo sapiens	39-42
7908759-2	1993	We found that the addition of small concentrations (1-10 microM) of Cd2+ to the low calcium bathing Ringer reduced both the control EPP amplitude and the increase in EPP amplitude that normally occurs during repetitive stimulation under low quantal conditions.	Calcium	84-91	CD2 molecule	Homo sapiens	68-71
7509633-6	1994	The results indicate that the covalently coupled fatty acid is highly immobilized near the carboxyl terminus because double quadrupolar splittings and very low T1 values (4 ms) were found for the -CD2- deuterons at carbon atoms C2 and C3.	Fatty Acids	49-59	CD2 molecule	Homo sapiens	197-200
7509633-6	1994	The results indicate that the covalently coupled fatty acid is highly immobilized near the carboxyl terminus because double quadrupolar splittings and very low T1 values (4 ms) were found for the -CD2- deuterons at carbon atoms C2 and C3.	Carbon	215-221	CD2 molecule	Homo sapiens	197-200
7905298-0	1994	Induction of nuclear contour irregularity during T-cell activation via the T-cell receptor/CD3 complex and CD2 antigens in the presence of phorbol esters.	Phorbol Esters	139-153	CD2 molecule	Homo sapiens	107-110
8296322-2	1994	This study demonstrates a heterogeneous response to Cd2+ exposure in isolates from different individuals with some individuals nearly 3-times more sensitive to ionic cadmium exposure than others.	Cadmium	166-173	CD2 molecule	Homo sapiens	52-55
8296322-5	1994	This difference in response to Cd2+ may reflect a heterogeneous response within the human population to cadmium exposure.	Cadmium	104-111	CD2 molecule	Homo sapiens	31-34
7904541-4	1994	Thus, the inhibitors H-7, staurosporine, and genistein exerted a dose-dependent inhibition of CD2 up-regulation, CD25 expression, IL-2 production, and cellular proliferation.	1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine	21-24	CD2 molecule	Homo sapiens	94-97
7904541-4	1994	Thus, the inhibitors H-7, staurosporine, and genistein exerted a dose-dependent inhibition of CD2 up-regulation, CD25 expression, IL-2 production, and cellular proliferation.	Staurosporine	26-39	CD2 molecule	Homo sapiens	94-97
7904541-4	1994	Thus, the inhibitors H-7, staurosporine, and genistein exerted a dose-dependent inhibition of CD2 up-regulation, CD25 expression, IL-2 production, and cellular proliferation.	Genistein	45-54	CD2 molecule	Homo sapiens	94-97
8253745-4	1993	KCl-induced depolarization also stimulated a dose- and Ca(2+)-dependent [3H]serotonin release that in the GLC8 cell line was effectively inhibited by Ca2+ channel antagonists (Cd2+, nitrendipine, verapamil, omega-conotoxin GVIA, and omega-agatoxin IVA) and potentiated by the Ca2+ channel agonist BayK8644.	Potassium Chloride	0-3	CD2 molecule	Homo sapiens	176-179
8253745-4	1993	KCl-induced depolarization also stimulated a dose- and Ca(2+)-dependent [3H]serotonin release that in the GLC8 cell line was effectively inhibited by Ca2+ channel antagonists (Cd2+, nitrendipine, verapamil, omega-conotoxin GVIA, and omega-agatoxin IVA) and potentiated by the Ca2+ channel agonist BayK8644.	Serotonin	76-85	CD2 molecule	Homo sapiens	176-179
7908759-7	1993	The order of effectiveness in reducing stimulation-induced increases in EPP amplitude was: Cd2+ >>> Co2+,Zn2+ > Ni2+.	Cobalt(2+)	109-113	CD2 molecule	Homo sapiens	91-94
7908759-7	1993	The order of effectiveness in reducing stimulation-induced increases in EPP amplitude was: Cd2+ >>> Co2+,Zn2+ > Ni2+.	Nickel(2+)	124-128	CD2 molecule	Homo sapiens	91-94
8105887-0	1993	1H resonance assignments and secondary structure of the 13.6 kDa glycosylated adhesion domain of human CD2.	Hydrogen	0-2	CD2 molecule	Homo sapiens	103-106
7902214-0	1993	Regulation of CD2-mediated human T cell activation: anti-CD8 monoclonal antibodies inhibit CD2-mediated rise in intracellular calcium.	Calcium	126-133	CD2 molecule	Homo sapiens	14-17
7902214-0	1993	Regulation of CD2-mediated human T cell activation: anti-CD8 monoclonal antibodies inhibit CD2-mediated rise in intracellular calcium.	Calcium	126-133	CD2 molecule	Homo sapiens	91-94
7902214-2	1993	Activation of T cells by CD2 mAbs requires two mAbs directed against distinct CD2 epitopes and induces tyrosine phosphorylation, PI-PLC activity generating the second messengers, IP3 and DAG, and finally lymphokine secretion.	Tyrosine	103-111	CD2 molecule	Homo sapiens	25-28
7902214-2	1993	Activation of T cells by CD2 mAbs requires two mAbs directed against distinct CD2 epitopes and induces tyrosine phosphorylation, PI-PLC activity generating the second messengers, IP3 and DAG, and finally lymphokine secretion.	Tyrosine	103-111	CD2 molecule	Homo sapiens	78-81
7902214-2	1993	Activation of T cells by CD2 mAbs requires two mAbs directed against distinct CD2 epitopes and induces tyrosine phosphorylation, PI-PLC activity generating the second messengers, IP3 and DAG, and finally lymphokine secretion.	Inositol 1,4,5-Trisphosphate	179-182	CD2 molecule	Homo sapiens	25-28
7902214-2	1993	Activation of T cells by CD2 mAbs requires two mAbs directed against distinct CD2 epitopes and induces tyrosine phosphorylation, PI-PLC activity generating the second messengers, IP3 and DAG, and finally lymphokine secretion.	dag	187-190	CD2 molecule	Homo sapiens	25-28
7902214-2	1993	Activation of T cells by CD2 mAbs requires two mAbs directed against distinct CD2 epitopes and induces tyrosine phosphorylation, PI-PLC activity generating the second messengers, IP3 and DAG, and finally lymphokine secretion.	dag	187-190	CD2 molecule	Homo sapiens	78-81
7902214-6	1993	Furthermore, CD8 alpha-specific mAb inhibited the increase in intracellular ionized calcium mediated by CD2 mAbs in the CD8+ clone and in purified T cells.	Calcium	84-91	CD2 molecule	Homo sapiens	104-107
7693851-0	1993	Tyrosine phosphorylation and association with phospholipase C gamma-1 of the GAP-associated 62-kD protein after CD2 stimulation of Jurkat T cell.	Tyrosine	0-8	CD2 molecule	Homo sapiens	112-115
7693851-1	1993	Numerous substrates are tyrosine phosphorylated upon CD2 stimulation of human Jurkat T cells using a mitogenic pair of CD2 monoclonal antibodies, including the phospholipase C (PLC)gamma-1-p35/36 complex.	Tyrosine	24-32	CD2 molecule	Homo sapiens	53-56
7693851-1	1993	Numerous substrates are tyrosine phosphorylated upon CD2 stimulation of human Jurkat T cells using a mitogenic pair of CD2 monoclonal antibodies, including the phospholipase C (PLC)gamma-1-p35/36 complex.	Tyrosine	24-32	CD2 molecule	Homo sapiens	119-122
7693851-3	1993	We show, however, in this report that a 63-kD protein is specifically phosphorylated on tyrosine residues after ligation of the CD2 molecule.	Tyrosine	88-96	CD2 molecule	Homo sapiens	128-131
7693851-4	1993	The tyrosine phosphorylation of p63 can be induced independently of other substrates when using a single CD2 mAb recognizing the D66 epitope of the molecule.	Tyrosine	4-12	CD2 molecule	Homo sapiens	105-108
7693851-7	1993	Finally, we also show that a 62-kD protein coimmunoprecipitating with the p21ras GTPase activating protein (GAP) is heavily tyrosine phosphorylated only after CD2 stimulation.	Tyrosine	124-132	CD2 molecule	Homo sapiens	159-162
7907269-1	1993	PBMC proliferation in patients with SLE was assessed by incorporation of 3H-Tdr in an accessory cell-dependent response to anti-CD2 specific monoclonal antibody.	Tritium	73-75	CD2 molecule	Homo sapiens	128-131
8224653-7	1993	In vitro ethanol incubation of normal T lymphocytes resulted in rearrangement of the membrane CD45 antigen, favoring the expression of high-molecular-weight isoforms, and showed a poor blastogenic response to anti-CD3 and anti-CD2 with a decrease in intracellular Ca2+ mobilization and IP3 production.	Ethanol	9-16	CD2 molecule	Homo sapiens	227-230
7693851-5	1993	Importantly, this CD2-induced tyrosine phosphorylation of p63 can also occur in the absence of the CD3 zeta chain membrane expression, and is also distinct from the protein tyrosine kinases p56lck and p59fyn.	Tyrosine	30-38	CD2 molecule	Homo sapiens	18-21
8105887-2	1993	All CD2 adhesion functions are localized within the amino-terminal 105-residue domain, which contains a single high mannose N-glycan required for maintaining both the conformational stability and CD58 binding properties of the glycoprotein.	mannose n-glycan	116-132	CD2 molecule	Homo sapiens	4-7
8105887-3	1993	In order to better understand the structural basis for CD2-CD58-mediated adhesion and the critical role of the carbohydrate moiety in maintaining the functional stability of the molecule, we have determined the secondary structure of the N-glycosylated adhesion domain of human CD2 (hu-sCD2(105)) using NMR spectroscopy.	Nitrogen	238-239	CD2 molecule	Homo sapiens	55-58
8105887-3	1993	In order to better understand the structural basis for CD2-CD58-mediated adhesion and the critical role of the carbohydrate moiety in maintaining the functional stability of the molecule, we have determined the secondary structure of the N-glycosylated adhesion domain of human CD2 (hu-sCD2(105)) using NMR spectroscopy.	Nitrogen	238-239	CD2 molecule	Homo sapiens	278-281
8262550-4	1993	In addition, increased phosphorylation of CD27 in T-cell activation either via CD2 or CD3 pathways was strongly suppressed by a cyclic nucleotide-dependent kinase inhibitor, H-8, but only slightly by a protein kinase C inhibitor, staurosporine.	N-(2-(methylamino)ethyl)-5-isoquinolinesulfonamide	174-177	CD2 molecule	Homo sapiens	42-45
8399302-1	1993	In the presence as well as in the absence of calmodulin, Cd2+ inhibits the human erythrocyte plasma membrane Ca(2+)-ATPase activity non-competitively with Ki = 2 nM, whereas ATP-dependent Ca(2+)-transport across the red cell membrane was found to be inhibited competitively by Cd2+ (Verbost, P.M., Flik, G., Pang, P.K.T., Lock, R.A.C.	Adenosine Triphosphate	116-119	CD2 molecule	Homo sapiens	57-60
7903276-3	1993	With anti-CD3 or anti-CD2 activation the cells showed only a low (anti-CD3) or a moderate (anti-CD2) level of tyrosine phosphorylation of a 42,000 MW external signal-regulated kinase (ERK), which was accompanied by undetectable (anti-CD3) or low level (anti-CD2) IL-2 production.	Tyrosine	110-118	CD2 molecule	Homo sapiens	22-25
7903276-3	1993	With anti-CD3 or anti-CD2 activation the cells showed only a low (anti-CD3) or a moderate (anti-CD2) level of tyrosine phosphorylation of a 42,000 MW external signal-regulated kinase (ERK), which was accompanied by undetectable (anti-CD3) or low level (anti-CD2) IL-2 production.	Tyrosine	110-118	CD2 molecule	Homo sapiens	96-99
7903276-3	1993	With anti-CD3 or anti-CD2 activation the cells showed only a low (anti-CD3) or a moderate (anti-CD2) level of tyrosine phosphorylation of a 42,000 MW external signal-regulated kinase (ERK), which was accompanied by undetectable (anti-CD3) or low level (anti-CD2) IL-2 production.	Tyrosine	110-118	CD2 molecule	Homo sapiens	96-99
7903276-4	1993	In the presence of phorbol myristate acetate (PMA), large amounts of IL-2 were induced by both anti-CD3 and anti-CD2 stimulation, which was accompanied by strong concurrent tyrosine phosphorylation of the 42,000 MW ERK and a 100,000 MW protein.	Tetradecanoylphorbol Acetate	19-44	CD2 molecule	Homo sapiens	113-116
7903276-4	1993	In the presence of phorbol myristate acetate (PMA), large amounts of IL-2 were induced by both anti-CD3 and anti-CD2 stimulation, which was accompanied by strong concurrent tyrosine phosphorylation of the 42,000 MW ERK and a 100,000 MW protein.	Tetradecanoylphorbol Acetate	46-49	CD2 molecule	Homo sapiens	113-116
7903276-4	1993	In the presence of phorbol myristate acetate (PMA), large amounts of IL-2 were induced by both anti-CD3 and anti-CD2 stimulation, which was accompanied by strong concurrent tyrosine phosphorylation of the 42,000 MW ERK and a 100,000 MW protein.	Tyrosine	173-181	CD2 molecule	Homo sapiens	113-116
7691614-6	1993	Induction of apoptosis by anti-CD2 mAb was prevented by cyclosporine A and FK 506.	Cyclosporine	56-70	CD2 molecule	Homo sapiens	31-34
7691614-6	1993	Induction of apoptosis by anti-CD2 mAb was prevented by cyclosporine A and FK 506.	Tacrolimus	75-81	CD2 molecule	Homo sapiens	31-34
8262550-4	1993	In addition, increased phosphorylation of CD27 in T-cell activation either via CD2 or CD3 pathways was strongly suppressed by a cyclic nucleotide-dependent kinase inhibitor, H-8, but only slightly by a protein kinase C inhibitor, staurosporine.	Staurosporine	230-243	CD2 molecule	Homo sapiens	42-45
7915183-3	1993	Human CD2 domain 1 requires N-linked carbohydrate to maintain its native conformation and ability to bind CD58.	n-linked carbohydrate	28-49	CD2 molecule	Homo sapiens	6-9
7915183-9	1993	The model provides an explanation for the observed instability of deglycosylated human CD2, and allows residues that are important for CD58 binding to be differentiated from those affecting conformational stability via interactions with the glycan.	Polysaccharides	241-247	CD2 molecule	Homo sapiens	87-90
7915183-8	1993	CONCLUSION: Based on our results, we propose a model showing how the N-linked glycan might be positioned in the human CD2 domain 1 structure.	n-linked glycan	69-84	CD2 molecule	Homo sapiens	118-121
8509367-4	1993	Experimentally, accumulation of Cd2+ into vesicles could be driven by delta pH generated by either V-type ATPase or artificially using nigericin to exchange K+ and H+ in K(+)-loaded vesicles.	Nigericin	135-144	CD2 molecule	Homo sapiens	32-35
7688073-5	1993	As had been previously reported for Jurkat T cells, a qualitatively similar tyrosine phosphorylation response was induced upon CD2 or CD3 stimulation in each of the analysed T cell populations, suggesting that CD3 and CD2 share a common pathway of protein tyrosine kinase (PTK) activation.	Tyrosine	76-84	CD2 molecule	Homo sapiens	127-130
7688073-5	1993	As had been previously reported for Jurkat T cells, a qualitatively similar tyrosine phosphorylation response was induced upon CD2 or CD3 stimulation in each of the analysed T cell populations, suggesting that CD3 and CD2 share a common pathway of protein tyrosine kinase (PTK) activation.	Tyrosine	76-84	CD2 molecule	Homo sapiens	218-221
7688073-7	1993	ALL leukemia T cells (which express very low levels of CD45), both CD3 and CD2 stimulation induced only very weak protein tyrosyl phosphorylation.	cyclo(tyrosyl-tyrosyl)	122-129	CD2 molecule	Homo sapiens	75-78
7688073-10	1993	These results suggest that there is a common pathway of early PTK activation following CD3- or CD2-mediated stimulation in mature T cells, whether they express surface CD4 or CD8, and also that the PTK may be differently regulated in different T cell populations leading to different kinetics or intensity of tyrosyl phosphorylation.	cyclo(tyrosyl-tyrosyl)	309-316	CD2 molecule	Homo sapiens	95-98
8473296-10	1993	However, Cd2+ is a fairly specific inhibitor of 55Fe uptake by K562 cells (IC50 approximately 50 microM).	Iron-55	48-52	CD2 molecule	Homo sapiens	9-12
8099849-6	1993	When activated through the TCR/CD3 pathway, the CD2 pathway, or directly by the phorbol ester, PMA, the memory (CD26+) T cells showed an increased proliferative response that was inhibited by the pkC inhibitor, staurosporine.	Staurosporine	211-224	CD2 molecule	Homo sapiens	48-51
7688561-7	1993	Restimulation of the ASA+ activated T cells by triggering TCR-CD3 or CD2 induced proliferation and apoptosis in a fraction of the cells.	Aspirin	21-24	CD2 molecule	Homo sapiens	69-72
8098618-10	1993	In parallel, CD2 + CD28 activation triggered a significant intracellular thiol decrease, suggesting that oxygen radicals are involved in the signaling pathway of adhesion molecules.	Sulfhydryl Compounds	73-78	CD2 molecule	Homo sapiens	13-16
8098618-10	1993	In parallel, CD2 + CD28 activation triggered a significant intracellular thiol decrease, suggesting that oxygen radicals are involved in the signaling pathway of adhesion molecules.	Oxygen	105-111	CD2 molecule	Homo sapiens	13-16
7680961-2	1993	Here we show that active (phorbol myristate acetate, phorbol dibutyrate acetate, and mezerein) but not inactive (4 beta-phorbol) tumor-promoting agents inhibit the mAb-induced modulation of CD2 and CD5, but not CD3, without concomitant changes in the surface distribution of these antigens (such as capping).	Tetradecanoylphorbol Acetate	26-51	CD2 molecule	Homo sapiens	190-193
8100456-6	1993	In this latter case, CD28+ IL-2 stimulation was more sensitive to both forskolin and PKC inhibition than that of CD2 or CD3+ IL-2.	Colforsin	71-80	CD2 molecule	Homo sapiens	21-24
7680961-2	1993	Here we show that active (phorbol myristate acetate, phorbol dibutyrate acetate, and mezerein) but not inactive (4 beta-phorbol) tumor-promoting agents inhibit the mAb-induced modulation of CD2 and CD5, but not CD3, without concomitant changes in the surface distribution of these antigens (such as capping).	phorbol dibutyrate acetate	53-79	CD2 molecule	Homo sapiens	190-193
7680961-2	1993	Here we show that active (phorbol myristate acetate, phorbol dibutyrate acetate, and mezerein) but not inactive (4 beta-phorbol) tumor-promoting agents inhibit the mAb-induced modulation of CD2 and CD5, but not CD3, without concomitant changes in the surface distribution of these antigens (such as capping).	mezerein	85-93	CD2 molecule	Homo sapiens	190-193
7680961-2	1993	Here we show that active (phorbol myristate acetate, phorbol dibutyrate acetate, and mezerein) but not inactive (4 beta-phorbol) tumor-promoting agents inhibit the mAb-induced modulation of CD2 and CD5, but not CD3, without concomitant changes in the surface distribution of these antigens (such as capping).	phorbol	115-127	CD2 molecule	Homo sapiens	190-193
7680961-5	1993	Treatment with cytochalasin D (an agent that inhibits microfilament polymerization) but not colchicine (an agent that inhibits microtubule polymerization) reproduced the effect of TPA on the mAb-induced modulation of CD2, CD3, and CD5.	Cytochalasin D	15-29	CD2 molecule	Homo sapiens	217-220
7681075-2	1993	We have recently demonstrated that the interaction of CD2 with CD58 is dynamic: TCR stimulation or treatment with the phorbol ester PMA rapidly up-regulates CD2 ligand avidity, and this regulation requires the carboxyl-terminal asparagine residue of the CD2 cytoplasmic domain.	Phorbol Esters	118-131	CD2 molecule	Homo sapiens	54-57
7681075-2	1993	We have recently demonstrated that the interaction of CD2 with CD58 is dynamic: TCR stimulation or treatment with the phorbol ester PMA rapidly up-regulates CD2 ligand avidity, and this regulation requires the carboxyl-terminal asparagine residue of the CD2 cytoplasmic domain.	Phorbol Esters	118-131	CD2 molecule	Homo sapiens	157-160
7681075-2	1993	We have recently demonstrated that the interaction of CD2 with CD58 is dynamic: TCR stimulation or treatment with the phorbol ester PMA rapidly up-regulates CD2 ligand avidity, and this regulation requires the carboxyl-terminal asparagine residue of the CD2 cytoplasmic domain.	Phorbol Esters	118-131	CD2 molecule	Homo sapiens	157-160
7681075-2	1993	We have recently demonstrated that the interaction of CD2 with CD58 is dynamic: TCR stimulation or treatment with the phorbol ester PMA rapidly up-regulates CD2 ligand avidity, and this regulation requires the carboxyl-terminal asparagine residue of the CD2 cytoplasmic domain.	Asparagine	228-238	CD2 molecule	Homo sapiens	54-57
7681075-2	1993	We have recently demonstrated that the interaction of CD2 with CD58 is dynamic: TCR stimulation or treatment with the phorbol ester PMA rapidly up-regulates CD2 ligand avidity, and this regulation requires the carboxyl-terminal asparagine residue of the CD2 cytoplasmic domain.	Asparagine	228-238	CD2 molecule	Homo sapiens	157-160
7681075-2	1993	We have recently demonstrated that the interaction of CD2 with CD58 is dynamic: TCR stimulation or treatment with the phorbol ester PMA rapidly up-regulates CD2 ligand avidity, and this regulation requires the carboxyl-terminal asparagine residue of the CD2 cytoplasmic domain.	Asparagine	228-238	CD2 molecule	Homo sapiens	157-160
7681075-5	1993	TCR-initiated up-regulation of CD2 avidity requires the activity of both protein tyrosine kinases and protein kinase C. Agents which elevate intracellular levels of cAMP also up-regulate CD2 ligand avidity and act either distal to or independently of protein kinase C and protein tyrosine kinases.	Cyclic AMP	165-169	CD2 molecule	Homo sapiens	31-34
7681075-5	1993	TCR-initiated up-regulation of CD2 avidity requires the activity of both protein tyrosine kinases and protein kinase C. Agents which elevate intracellular levels of cAMP also up-regulate CD2 ligand avidity and act either distal to or independently of protein kinase C and protein tyrosine kinases.	Cyclic AMP	165-169	CD2 molecule	Homo sapiens	187-190
7681075-6	1993	Cell lines expressing single amino acid substitutions of the carboxyl-terminal asparagine of CD2 are incapable of avidity regulation by TCR signaling, PMA treatment, or elevation of intracellular cAMP levels, demonstrating that each of these stimuli utilizes a common structural element for regulating CD2 avidity.	Asparagine	79-89	CD2 molecule	Homo sapiens	93-96
7681075-6	1993	Cell lines expressing single amino acid substitutions of the carboxyl-terminal asparagine of CD2 are incapable of avidity regulation by TCR signaling, PMA treatment, or elevation of intracellular cAMP levels, demonstrating that each of these stimuli utilizes a common structural element for regulating CD2 avidity.	Asparagine	79-89	CD2 molecule	Homo sapiens	302-305
7681075-6	1993	Cell lines expressing single amino acid substitutions of the carboxyl-terminal asparagine of CD2 are incapable of avidity regulation by TCR signaling, PMA treatment, or elevation of intracellular cAMP levels, demonstrating that each of these stimuli utilizes a common structural element for regulating CD2 avidity.	Tetradecanoylphorbol Acetate	151-154	CD2 molecule	Homo sapiens	93-96
7681075-6	1993	Cell lines expressing single amino acid substitutions of the carboxyl-terminal asparagine of CD2 are incapable of avidity regulation by TCR signaling, PMA treatment, or elevation of intracellular cAMP levels, demonstrating that each of these stimuli utilizes a common structural element for regulating CD2 avidity.	Cyclic AMP	196-200	CD2 molecule	Homo sapiens	93-96
7681075-7	1993	The response to both cAMP and phorbol ester treatment distinguishes the regulation of CD2 avidity from that of a second major adhesion pathway, LFA-1 (CD11a/CD18)/ICAM-1 (CD54) and from that of the TCR coreceptor CD8.	Cyclic AMP	21-25	CD2 molecule	Homo sapiens	86-89
7681075-7	1993	The response to both cAMP and phorbol ester treatment distinguishes the regulation of CD2 avidity from that of a second major adhesion pathway, LFA-1 (CD11a/CD18)/ICAM-1 (CD54) and from that of the TCR coreceptor CD8.	Phorbol Esters	30-43	CD2 molecule	Homo sapiens	86-89
8096437-0	1993	Anti-CD2-induced tyrosine phosphorylation of T cell polypeptides is independent of the PMA-induced modification of p56lck.	Tyrosine	17-25	CD2 molecule	Homo sapiens	5-8
8324935-4	1993	Treatment with mycophenolate mofetil reduces rheumatoid factor titres, immunoglobulin (IgG, IgM, and IgA) levels, and the total number of T cells (CD2) in RA patient peripheral blood; in addition, lymphocyte mitogen responses are inhibited and delayed hypersensitivity skin test reactivity is decreased.	Mycophenolic Acid	15-36	CD2 molecule	Homo sapiens	147-150
7680330-12	1993	Double immunostaining with a CD2 monoclonal antibody demonstrated that labeling with HP-1H8 was predominantly associated with T-cell infiltration.	hp-1h8	85-91	CD2 molecule	Homo sapiens	29-32
8386451-5	1993	Simultaneous administration of 1 mM Cd2+ and 10 microM Ag+ to fibers voltage clamped with the double mannitol gap technique almost completely blocked the inward current.	Mannitol	101-109	CD2 molecule	Homo sapiens	36-39
8096558-0	1993	A CD2+ subset of non-malignant peripheral blood lymphocytes from patients with Sezary syndromes overexpress the low-molecular-weight GTP-binding protein Rab2.	Guanosine Triphosphate	133-136	CD2 molecule	Homo sapiens	2-5
8096437-2	1993	We find that with human peripheral T cells the serine phosphorylation of p56lck is independent of the more rapid tyrosine phosphorylation of other polypeptides via stimulation of the CD2 receptor with anti-CD2 (anti-T11(2) and anti-T11(3) mAb"s).	Serine	47-53	CD2 molecule	Homo sapiens	183-186
8096437-2	1993	We find that with human peripheral T cells the serine phosphorylation of p56lck is independent of the more rapid tyrosine phosphorylation of other polypeptides via stimulation of the CD2 receptor with anti-CD2 (anti-T11(2) and anti-T11(3) mAb"s).	Serine	47-53	CD2 molecule	Homo sapiens	206-209
8096437-4	1993	While polypeptides from resting T cells showed very low levels of endogenous tyrosine phosphorylation, incubation with anti-CD2 for periods as short as 30 sec resulted in the tyrosine phosphorylation of a 75-kDa polypeptide (p75).	Tyrosine	77-85	CD2 molecule	Homo sapiens	124-127
8096437-4	1993	While polypeptides from resting T cells showed very low levels of endogenous tyrosine phosphorylation, incubation with anti-CD2 for periods as short as 30 sec resulted in the tyrosine phosphorylation of a 75-kDa polypeptide (p75).	Tyrosine	175-183	CD2 molecule	Homo sapiens	124-127
8096437-6	1993	Preincubation of T cells with phenylarsine oxide amplified the anti-CD2-induced tyrosine phosphorylation of the p75 and revealed additional phosphotyrosine polypeptides of 120, 100, and 33 kDa.	oxophenylarsine	30-48	CD2 molecule	Homo sapiens	68-71
8096437-6	1993	Preincubation of T cells with phenylarsine oxide amplified the anti-CD2-induced tyrosine phosphorylation of the p75 and revealed additional phosphotyrosine polypeptides of 120, 100, and 33 kDa.	Tyrosine	80-88	CD2 molecule	Homo sapiens	68-71
8096437-11	1993	Whereas PMA with either anti-CD2 or Con A was required for mitogenesis, only anti-CD2 led to tyrosine phosphorylation, and only PMA induced the lck-shift.	Tyrosine	93-101	CD2 molecule	Homo sapiens	82-85
7680612-4	1993	Monoclonal antibody blocking experiments revealed that the contribution by CD2/LFA-3 is increased relative to that of LFA-1/ICAM-1 in conjugates between FLU+ B-LCL or NANAse-treated B-LCL and T cell clones.	nanase	167-173	CD2 molecule	Homo sapiens	75-78
8385519-8	1993	Only after three days of incubation with a mitogenic anti-CD2 MAb Lau-2.1.2, the PtdIns(4,5)P2-PLC activity increased in the particulate fraction of PBMN similar to ConA treatment.	Phosphatidylinositol 4,5-Diphosphate	81-94	CD2 molecule	Homo sapiens	58-61
7679705-3	1993	ChTX blocks T cell activation induced by signals (e.g., anti-CD2, anti-CD3, ionomycin) that elicit a rise in intracellular calcium ([Ca2+]i) by preventing the elevation of [Ca2+]i in a dose-dependent manner.	Charybdotoxin	0-4	CD2 molecule	Homo sapiens	61-64
7679705-3	1993	ChTX blocks T cell activation induced by signals (e.g., anti-CD2, anti-CD3, ionomycin) that elicit a rise in intracellular calcium ([Ca2+]i) by preventing the elevation of [Ca2+]i in a dose-dependent manner.	Calcium	123-130	CD2 molecule	Homo sapiens	61-64
8385519-8	1993	Only after three days of incubation with a mitogenic anti-CD2 MAb Lau-2.1.2, the PtdIns(4,5)P2-PLC activity increased in the particulate fraction of PBMN similar to ConA treatment.	pbmn	149-153	CD2 molecule	Homo sapiens	58-61
8472606-11	1993	The lyophilized lymphocyte analysis showed an overall frequency of outliers ranging from 3.2% to 19.7%, with a maximum for CD2 FITC (19.7%) and CD3 + HLA-DR + (12.1%).	Fluorescein-5-isothiocyanate	127-131	CD2 molecule	Homo sapiens	123-126
8418859-1	1993	An electron density map of the reactive, Cd2+ form of crystalline phosphoglucomutase from X-ray diffraction studies shows that the enzymic phosphate donates a nonbridging oxygen to the ligand sphere of the bound metal ion, which appears to be tetracoordinate.	Phosphates	139-148	CD2 molecule	Homo sapiens	41-44
8418859-1	1993	An electron density map of the reactive, Cd2+ form of crystalline phosphoglucomutase from X-ray diffraction studies shows that the enzymic phosphate donates a nonbridging oxygen to the ligand sphere of the bound metal ion, which appears to be tetracoordinate.	Oxygen	171-177	CD2 molecule	Homo sapiens	41-44
8418859-1	1993	An electron density map of the reactive, Cd2+ form of crystalline phosphoglucomutase from X-ray diffraction studies shows that the enzymic phosphate donates a nonbridging oxygen to the ligand sphere of the bound metal ion, which appears to be tetracoordinate.	Metals	212-217	CD2 molecule	Homo sapiens	41-44
8418859-2	1993	31P and 113Cd NMR spectroscopy are used to assess changes in the properties of bound Cd2+ produced by substrate/product and by substrate/product analog inhibitors.	ET bromodomain inhibitor	0-3	CD2 molecule	Homo sapiens	85-88
8418859-2	1993	31P and 113Cd NMR spectroscopy are used to assess changes in the properties of bound Cd2+ produced by substrate/product and by substrate/product analog inhibitors.	Cadmium, isotope of mass 113	8-13	CD2 molecule	Homo sapiens	85-88
8418859-5	1993	In addition, there is a loss of the 31P-113Cd J coupling that characterizes the monophosphate complexes of the Cd2+ enzyme either during or immediately after the PO3- transfer step that produces the bisphosphate complex, indicating a further change at the metal binding site.	monophosphate	80-93	CD2 molecule	Homo sapiens	111-114
8418859-5	1993	In addition, there is a loss of the 31P-113Cd J coupling that characterizes the monophosphate complexes of the Cd2+ enzyme either during or immediately after the PO3- transfer step that produces the bisphosphate complex, indicating a further change at the metal binding site.	bisphosphate	199-211	CD2 molecule	Homo sapiens	111-114
8418859-5	1993	In addition, there is a loss of the 31P-113Cd J coupling that characterizes the monophosphate complexes of the Cd2+ enzyme either during or immediately after the PO3- transfer step that produces the bisphosphate complex, indicating a further change at the metal binding site.	Metals	256-261	CD2 molecule	Homo sapiens	111-114
7902076-3	1993	It is to note that CD28 triggering led to calcium mobilization, whereas stimulation via CD2 did not.	Calcium	42-49	CD2 molecule	Homo sapiens	19-22
1359883-8	1992	Activation of T cells either with phorbol 12,13-dibutyrate or by CD2-CD3 cross-linking caused [32P]Pi incorporation into the same gamma-chain Ser residues.	Phosphorus-32	95-98	CD2 molecule	Homo sapiens	65-68
8099003-1	1993	The in vitro exposure of human lymphocytes to degradation products (Fe, Ni or Co) of metallic biomaterials causes a significant reduction of lymphocytes expressing the molecules involved in T lymphocyte activation, CD2 and CD3.	Iron	68-70	CD2 molecule	Homo sapiens	215-218
8099003-1	1993	The in vitro exposure of human lymphocytes to degradation products (Fe, Ni or Co) of metallic biomaterials causes a significant reduction of lymphocytes expressing the molecules involved in T lymphocyte activation, CD2 and CD3.	Cobalt	78-80	CD2 molecule	Homo sapiens	215-218
8431555-2	1993	CD2+, CD3+, and CD8+ lymphocyte subsets were selectively reduced by the leucyl-leucine methyl ester treatment (CD2: 84.2-67.5%; CD3: 76.1-62.3%; and CD8: 8.0-3.4%), but there was no significant reduction in the CD4+ and CD19+ subsets (CD4: 68.2-64.7%; and CD19: 22.6-33.2%).	leucyl-leucine-methyl ester	72-99	CD2 molecule	Homo sapiens	0-3
8431555-2	1993	CD2+, CD3+, and CD8+ lymphocyte subsets were selectively reduced by the leucyl-leucine methyl ester treatment (CD2: 84.2-67.5%; CD3: 76.1-62.3%; and CD8: 8.0-3.4%), but there was no significant reduction in the CD4+ and CD19+ subsets (CD4: 68.2-64.7%; and CD19: 22.6-33.2%).	leucyl-leucine-methyl ester	72-99	CD2 molecule	Homo sapiens	111-114
8324385-4	1993	Suramin suppressed the proliferation of PBMC in response to various stimuli, including OKT3, phytohemagglutinin (PHA), phorbolmyristate-acetate (PMA) and ionomycin, purified protein derivate of Mycobacterium tuberculosis (PPD) and antibodies against CD2.	Suramin	0-7	CD2 molecule	Homo sapiens	250-253
8324385-9	1993	Suramin also decreased the expression of T cell surface molecules such as CD2, CD25 and CD4 in preactivated PBMC and had pronounced effects on cytokine production.	Suramin	0-7	CD2 molecule	Homo sapiens	74-77
1385399-0	1992	N-glycosylation is required for human CD2 immunoadhesion functions.	Nitrogen	0-1	CD2 molecule	Homo sapiens	38-41
1385399-2	1992	Two domains comprise the CD2 extracellular segment, with all adhesion functions localized to the amino-terminal domain that contains a single N-glycosylation site at Asn65.	Nitrogen	142-143	CD2 molecule	Homo sapiens	25-28
1385399-3	1992	We have defined an important role for the N-linked glycans attached to Asn65 of this domain in mediating CD2-CD58 interactions and also characterize its N-glycotype structure.	n-linked glycans	42-58	CD2 molecule	Homo sapiens	105-108
1385399-5	1992	Electrospray ionization-mass spectrometry demonstrates that high mannose oligosaccharides ((Man)nGlcNAc2, n = 5-9) are the only N-glycotypes occupying Asn65 when soluble CD2 is expressed in Chinese hamster ovary cells.	mannose oligosaccharides	65-89	CD2 molecule	Homo sapiens	170-173
1385399-6	1992	Based on a model of human CD2 secondary structure, we propose that N-glycosylation is required for stabilizing domain 1 in the human receptor.	Nitrogen	67-68	CD2 molecule	Homo sapiens	26-29
1385399-7	1992	Thus, N-glycosylation is essential for human CD2 adhesion functions.	Nitrogen	6-7	CD2 molecule	Homo sapiens	45-48
8093441-5	1993	Moreover, despite the incapacity of T lymphocytes to undergo DNA synthesis in the CD3/TcR-modulated state, CD2 triggering still results in tyrosine phosphorylation of some unknown protein substrates.	Tyrosine	139-147	CD2 molecule	Homo sapiens	107-110
7678115-0	1993	Tyrosine phosphorylation of CD6 by stimulation of CD3: augmentation by the CD4 and CD2 coreceptors.	Tyrosine	0-8	CD2 molecule	Homo sapiens	83-86
7678115-4	1993	Tyr phosphorylation was observed when the T cells were activated by crosslinking CD3 or by cocrosslinking CD3 with CD2 or CD4, but not when the cells were stimulated by crosslinking CD2, CD4, or CD28 alone.	Tyrosine	0-3	CD2 molecule	Homo sapiens	115-118
7678115-5	1993	Unlike other Tyr kinase substrates, such as the phospholipase C gamma 1-associated pp35/36 protein, whose level of Tyr phosphorylation is highest when T cells are activated by cocrosslinking CD3 with CD2, the levels of CD6 Tyr phosphorylation are highest when T cells were activated by cocrosslinking CD3 with CD4.	Tyrosine	13-16	CD2 molecule	Homo sapiens	200-203
7678115-5	1993	Unlike other Tyr kinase substrates, such as the phospholipase C gamma 1-associated pp35/36 protein, whose level of Tyr phosphorylation is highest when T cells are activated by cocrosslinking CD3 with CD2, the levels of CD6 Tyr phosphorylation are highest when T cells were activated by cocrosslinking CD3 with CD4.	Tyrosine	115-118	CD2 molecule	Homo sapiens	200-203
7678845-5	1993	CD2 was shown to syn-cap (unidirectionally cocap) with CD44 and CD11a/CD18 (LFA-1), an observation potentially related to functional cooperation among these molecules in T cell activation.	cocap	43-48	CD2 molecule	Homo sapiens	0-3
8492341-6	1993	Pharmacokinetic parameters of hydroxocobalamin were best defined in the group who received both antidotes: t1/2 (alpha), 0.52 h; t1/2 (beta), 2.83 h; Vd (beta), 0.24 L/kg; and mean peak serum concentration 753 mcg/mL (560 mumol/L) at 0-50 minutes after completion of infusion.	Hydroxocobalamin	30-46	CD2 molecule	Homo sapiens	107-122
1471158-1	1992	Nanomolar concentrations of cadmium (Cd2+) produce an immediate rise in free Ca2+ in human dermal fibroblasts, which is mostly caused by the release of stored Ca2+ via inositol trisphosphate.	Cadmium	28-35	CD2 molecule	Homo sapiens	37-40
1471158-1	1992	Nanomolar concentrations of cadmium (Cd2+) produce an immediate rise in free Ca2+ in human dermal fibroblasts, which is mostly caused by the release of stored Ca2+ via inositol trisphosphate.	inositol 1,2,3-trisphosphate	168-190	CD2 molecule	Homo sapiens	37-40
1471158-3	1992	A prior incubation with wheat germ agglutinin (WGA) or certain other lectins inhibited calcium release evoked by Cd2+.	Calcium	87-94	CD2 molecule	Homo sapiens	113-116
1471158-9	1992	WGA probably inhibits Ca2+ release produced by Cd2+ by binding to N-acetylneuraminic acid in the external domain of a plasma membrane receptor.	N-Acetylneuraminic Acid	66-89	CD2 molecule	Homo sapiens	47-50
1369037-0	1992	Biomimetic metal-sorbing vesicles: Cd2+ uptake by phosphatidylcholine vesicles doped with ionophore A23187.	Metals	11-16	CD2 molecule	Homo sapiens	35-38
1369037-0	1992	Biomimetic metal-sorbing vesicles: Cd2+ uptake by phosphatidylcholine vesicles doped with ionophore A23187.	Phosphatidylcholines	50-69	CD2 molecule	Homo sapiens	35-38
1369037-0	1992	Biomimetic metal-sorbing vesicles: Cd2+ uptake by phosphatidylcholine vesicles doped with ionophore A23187.	Calcimycin	100-106	CD2 molecule	Homo sapiens	35-38
1369037-1	1992	Unilamellar phosphatidylcholine vesicles, harboring the ionophore, A23187, in the bilayer and the water-soluble chelating agent, nitrilotriacetate, in the vesicle interior, rapidly sequester and concentrate Cd2+ from dilute aqueous solution.	Phosphatidylcholines	12-31	CD2 molecule	Homo sapiens	207-210
1369037-1	1992	Unilamellar phosphatidylcholine vesicles, harboring the ionophore, A23187, in the bilayer and the water-soluble chelating agent, nitrilotriacetate, in the vesicle interior, rapidly sequester and concentrate Cd2+ from dilute aqueous solution.	Calcimycin	67-73	CD2 molecule	Homo sapiens	207-210
1369037-1	1992	Unilamellar phosphatidylcholine vesicles, harboring the ionophore, A23187, in the bilayer and the water-soluble chelating agent, nitrilotriacetate, in the vesicle interior, rapidly sequester and concentrate Cd2+ from dilute aqueous solution.	Nitrilotriacetic Acid	129-146	CD2 molecule	Homo sapiens	207-210
1359883-8	1992	Activation of T cells either with phorbol 12,13-dibutyrate or by CD2-CD3 cross-linking caused [32P]Pi incorporation into the same gamma-chain Ser residues.	Serine	142-145	CD2 molecule	Homo sapiens	65-68
1420924-2	1992	The extent of trans-gauche isomerization at the 4 and 4" positions of the acyl chains of fully hydrated 4,4,4",4"-d4 1,2-dipalmitoylphosphatidylethanolamine (4-d4 DPPE) bilayers was quantitatively evaluated from the infrared (IR) intensity of the CD2 rocking modes.	4,4,4",4"-d4 1,2-dipalmitoylphosphatidylethanolamine	104-156	CD2 molecule	Homo sapiens	247-250
9908824-0	1992	Fusion yields for carbon-cluster impact on CD2 targets.	Carbon	18-24	CD2 molecule	Homo sapiens	43-46
1492955-8	1992	The presence of other cations inhibited uranium-binding in the following order: Cu2+ > Cd2+ > Zn2+ > Mg2+ > Ca2+.	Uranium	40-47	CD2 molecule	Homo sapiens	90-93
1356634-9	1992	Ligands to three of these molecules have been identified; ICAM-1, LFA-3, and hyaluronic acid binding to LFA-1, LFA-2, and CD44, respectively.	Hyaluronic Acid	77-92	CD2 molecule	Homo sapiens	111-116
1375131-6	1992	Although T11(3)-epitope expression induced by anti-T11(2) mAb was not affected by treatment of cells with anti-HVS6B6, both Ca2+ influx and phosphatidylinositol turnover induced by anti-CD2 mAbs were markedly enhanced by the pretreatment of T cells with anti-HVS6B6 mAb.	Phosphatidylinositols	140-160	CD2 molecule	Homo sapiens	186-189
1354231-6	1992	In contrast, anti-1A4 inhibited CD2-mediated calcium mobilization and the serine esterase activity of NK cell granules.	Calcium	45-52	CD2 molecule	Homo sapiens	32-35
1354232-0	1992	CD2 triggering stimulates the formation of platelet-activating factor-acether from alkyl-arachidonoyl-glycerophosphocholine in a human CD4+ T lymphocyte clone.	alkyl-arachidonoyl-glycerophosphocholine	83-123	CD2 molecule	Homo sapiens	0-3
1354232-4	1992	i) Hydrolysis of alkyl-acyl-GPC upon CD2 stimulation was evidenced: [3H]alkyl-lyso-GPC was formed from [3H]alkyl-acyl-GPC in [3H] alkyl-labeled cells; alkyl-lyso-GPC production was also bioassayed after CD2 triggering.	Tritium	69-71	CD2 molecule	Homo sapiens	37-40
1354232-4	1992	i) Hydrolysis of alkyl-acyl-GPC upon CD2 stimulation was evidenced: [3H]alkyl-lyso-GPC was formed from [3H]alkyl-acyl-GPC in [3H] alkyl-labeled cells; alkyl-lyso-GPC production was also bioassayed after CD2 triggering.	Tritium	69-71	CD2 molecule	Homo sapiens	203-206
1354232-4	1992	i) Hydrolysis of alkyl-acyl-GPC upon CD2 stimulation was evidenced: [3H]alkyl-lyso-GPC was formed from [3H]alkyl-acyl-GPC in [3H] alkyl-labeled cells; alkyl-lyso-GPC production was also bioassayed after CD2 triggering.	Tritium	104-106	CD2 molecule	Homo sapiens	37-40
1353888-4	1992	Mutational analysis of the CD2 cytoplasmic domain demonstrates that the carboxyl-terminal asparagine is essential for T-cell receptor-induced changes in CD2 avidity but is not essential for CD2-mediated signaling, establishing that the cytoplasmic portion of CD2 consists of distinct functional domains.	Asparagine	90-100	CD2 molecule	Homo sapiens	27-30
1353888-4	1992	Mutational analysis of the CD2 cytoplasmic domain demonstrates that the carboxyl-terminal asparagine is essential for T-cell receptor-induced changes in CD2 avidity but is not essential for CD2-mediated signaling, establishing that the cytoplasmic portion of CD2 consists of distinct functional domains.	Asparagine	90-100	CD2 molecule	Homo sapiens	153-156
1353888-4	1992	Mutational analysis of the CD2 cytoplasmic domain demonstrates that the carboxyl-terminal asparagine is essential for T-cell receptor-induced changes in CD2 avidity but is not essential for CD2-mediated signaling, establishing that the cytoplasmic portion of CD2 consists of distinct functional domains.	Asparagine	90-100	CD2 molecule	Homo sapiens	153-156
1353888-4	1992	Mutational analysis of the CD2 cytoplasmic domain demonstrates that the carboxyl-terminal asparagine is essential for T-cell receptor-induced changes in CD2 avidity but is not essential for CD2-mediated signaling, establishing that the cytoplasmic portion of CD2 consists of distinct functional domains.	Asparagine	90-100	CD2 molecule	Homo sapiens	153-156
1354232-4	1992	i) Hydrolysis of alkyl-acyl-GPC upon CD2 stimulation was evidenced: [3H]alkyl-lyso-GPC was formed from [3H]alkyl-acyl-GPC in [3H] alkyl-labeled cells; alkyl-lyso-GPC production was also bioassayed after CD2 triggering.	Tritium	104-106	CD2 molecule	Homo sapiens	203-206
1354232-4	1992	i) Hydrolysis of alkyl-acyl-GPC upon CD2 stimulation was evidenced: [3H]alkyl-lyso-GPC was formed from [3H]alkyl-acyl-GPC in [3H] alkyl-labeled cells; alkyl-lyso-GPC production was also bioassayed after CD2 triggering.	Tritium	104-106	CD2 molecule	Homo sapiens	37-40
1354232-4	1992	i) Hydrolysis of alkyl-acyl-GPC upon CD2 stimulation was evidenced: [3H]alkyl-lyso-GPC was formed from [3H]alkyl-acyl-GPC in [3H] alkyl-labeled cells; alkyl-lyso-GPC production was also bioassayed after CD2 triggering.	Tritium	104-106	CD2 molecule	Homo sapiens	203-206
1354232-5	1992	ii) The rate of arachidonate transfer from diacyl-GPC to alkyl-acyl-GPC increased after CD2 stimulation of the [3H]arachidonate-labeled P28D T cells, demonstrating alkyl-lyso-GPC formation.	Arachidonic Acid	16-28	CD2 molecule	Homo sapiens	88-91
1354232-5	1992	ii) The rate of arachidonate transfer from diacyl-GPC to alkyl-acyl-GPC increased after CD2 stimulation of the [3H]arachidonate-labeled P28D T cells, demonstrating alkyl-lyso-GPC formation.	Tritium	112-114	CD2 molecule	Homo sapiens	88-91
1354232-5	1992	ii) The rate of arachidonate transfer from diacyl-GPC to alkyl-acyl-GPC increased after CD2 stimulation of the [3H]arachidonate-labeled P28D T cells, demonstrating alkyl-lyso-GPC formation.	Arachidonic Acid	115-127	CD2 molecule	Homo sapiens	88-91
1577948-4	1992	Thus, despite a great variability between individuals, 10(-13) M F8Fa was found to enhance the proliferation of T cells induced by phytohemagglutinin or anti-CD2 monoclonal antibodies, while 10(-7) M F8Fa inhibited T cell proliferation, without affecting cell viability.	f8fa	65-69	CD2 molecule	Homo sapiens	158-161
1350980-1	1992	Activated human T cells via the CD2 or the CD3 pathways exhibited a higher capacity than resting T lymphocytes to incorporate and metabolize [3H]pafacether (paf) at 37 degrees C. Resting T lymphocytes lacked specific binding capacity for paf, yet high-affinity paf receptors (paf-R) were induced on CD3- or CD2-dependent activation.	Tritium	142-144	CD2 molecule	Homo sapiens	32-35
1427430-5	1992	With these clones we studied the ability of CsA to inhibit TNF and IL-3/GM-CSF production, which was stimulated with specific monoclonal antibodies directed against the CD2 and CD3 surface antigens.	Cyclosporine	44-47	CD2 molecule	Homo sapiens	169-172
1427430-7	1992	In fact, at 400 ng/ml CsA a residual production of IL-3/GM-CSF was present in all clones tested (CD3: 21.8% and CD2: 14.4% of the maximal IL-3/GM-CSF activity), while secretion of TNF was virtually abrogated at 100 ng/ml.	Cyclosporine	22-25	CD2 molecule	Homo sapiens	112-115
1371947-1	1992	The preferential growth of CD3-CD2-CD11a/CD18- thymocytes was obtained by stimulation of CD2-CD3- thymic cells with low doses of PMA (0.5 ng/ml) and subsequent culture in the presence of recombinant interleukin-2 (100 U/ml).	Tetradecanoylphorbol Acetate	129-132	CD2 molecule	Homo sapiens	31-34
1371947-1	1992	The preferential growth of CD3-CD2-CD11a/CD18- thymocytes was obtained by stimulation of CD2-CD3- thymic cells with low doses of PMA (0.5 ng/ml) and subsequent culture in the presence of recombinant interleukin-2 (100 U/ml).	Tetradecanoylphorbol Acetate	129-132	CD2 molecule	Homo sapiens	89-92
1303963-4	1992	Exposure of DNA in vitro to Cd2+ or to Cd2+ hydrogen peroxide does not result in strand breaks or alkali-labile sites.	Hydrogen Peroxide	44-61	CD2 molecule	Homo sapiens	39-42
1346114-0	1992	Regulation of D-3 phosphoinositides during T cell activation via the T cell antigen receptor/CD3 complex and CD2 antigens.	d-3 phosphoinositides	14-35	CD2 molecule	Homo sapiens	109-112
1346114-1	1992	An immediate consequence of T cell activation via the T cell receptor (TcR)/CD3 complex and CD2 antigen is the hydrolysis of phosphatidylinositol-(4,5)-bisphosphate and the generation of inositol-(1,4,5)-trisphosphate and diacylglycerol which then regulate intracellular calcium and protein kinase C. Changes in cellular levels of phosphoinositides phosphorylated on the D-4 and D-5 position during T cell activation have been well documented.	Phosphatidylinositol 4,5-Diphosphate	125-164	CD2 molecule	Homo sapiens	92-95
1346114-1	1992	An immediate consequence of T cell activation via the T cell receptor (TcR)/CD3 complex and CD2 antigen is the hydrolysis of phosphatidylinositol-(4,5)-bisphosphate and the generation of inositol-(1,4,5)-trisphosphate and diacylglycerol which then regulate intracellular calcium and protein kinase C. Changes in cellular levels of phosphoinositides phosphorylated on the D-4 and D-5 position during T cell activation have been well documented.	-(1,4,5)-trisphosphate	195-217	CD2 molecule	Homo sapiens	92-95
1346114-1	1992	An immediate consequence of T cell activation via the T cell receptor (TcR)/CD3 complex and CD2 antigen is the hydrolysis of phosphatidylinositol-(4,5)-bisphosphate and the generation of inositol-(1,4,5)-trisphosphate and diacylglycerol which then regulate intracellular calcium and protein kinase C. Changes in cellular levels of phosphoinositides phosphorylated on the D-4 and D-5 position during T cell activation have been well documented.	Diglycerides	222-236	CD2 molecule	Homo sapiens	92-95
1346114-1	1992	An immediate consequence of T cell activation via the T cell receptor (TcR)/CD3 complex and CD2 antigen is the hydrolysis of phosphatidylinositol-(4,5)-bisphosphate and the generation of inositol-(1,4,5)-trisphosphate and diacylglycerol which then regulate intracellular calcium and protein kinase C. Changes in cellular levels of phosphoinositides phosphorylated on the D-4 and D-5 position during T cell activation have been well documented.	Phosphatidylinositols	331-348	CD2 molecule	Homo sapiens	92-95
1346114-3	1992	In the present study we have examined the levels and regulation of D-3 phosphoinositides in T cells activated by the TcR/CD3 complex and CD2 antigens.	d-3 phosphoinositides	67-88	CD2 molecule	Homo sapiens	137-140
1346114-5	1992	Activation of the TcR/CD3 complex or CD2 antigen results in modulation of PtdIns(3,4)P2 and a putative PtdIns(3,4,5)P3 in T cells but does not change levels of PtdIns(3)P.	phosphatidylinositol 3,4-diphosphate	74-87	CD2 molecule	Homo sapiens	37-40
1346114-5	1992	Activation of the TcR/CD3 complex or CD2 antigen results in modulation of PtdIns(3,4)P2 and a putative PtdIns(3,4,5)P3 in T cells but does not change levels of PtdIns(3)P.	phosphatidylinositol 3,4,5-triphosphate	103-118	CD2 molecule	Homo sapiens	37-40
1346114-5	1992	Activation of the TcR/CD3 complex or CD2 antigen results in modulation of PtdIns(3,4)P2 and a putative PtdIns(3,4,5)P3 in T cells but does not change levels of PtdIns(3)P.	phosphatidylinositol 3-phosphate	160-170	CD2 molecule	Homo sapiens	37-40
1372020-0	1992	CD2/LFA-3 ligation induces phospholipase-C gamma 1 tyrosine phosphorylation and regulates CD3 signaling.	Tyrosine	51-59	CD2 molecule	Homo sapiens	0-3
1372020-2	1992	Stimulation of the T cell surface receptor CD2 similarly propagates early signals through phosphatidylinositol-PLC activation.	Phosphatidylinositols	90-110	CD2 molecule	Homo sapiens	43-46
1372020-5	1992	We show that stimulation of CD2 receptors on T cells caused tyrosine phosphorylation of PLC gamma 1.	Tyrosine	60-68	CD2 molecule	Homo sapiens	28-31
1372020-6	1992	Cross-linking of CD2 with CD3 receptors augmented the phosphorylation of PLC gamma 1 on tyrosine, whereas ligation of the CD45 tyrosine phosphatase with CD2 receptors prevented PLC gamma 1 tyrosine phosphorylation.	Tyrosine	88-96	CD2 molecule	Homo sapiens	17-20
1372020-6	1992	Cross-linking of CD2 with CD3 receptors augmented the phosphorylation of PLC gamma 1 on tyrosine, whereas ligation of the CD45 tyrosine phosphatase with CD2 receptors prevented PLC gamma 1 tyrosine phosphorylation.	Tyrosine	127-135	CD2 molecule	Homo sapiens	153-156
1372020-10	1992	CD3 receptor modulation potently down-regulated CD2-induced PLC gamma 1 tyrosine phosphorylation and calcium mobilization.	Tyrosine	72-80	CD2 molecule	Homo sapiens	48-51
1372020-10	1992	CD3 receptor modulation potently down-regulated CD2-induced PLC gamma 1 tyrosine phosphorylation and calcium mobilization.	Calcium	101-108	CD2 molecule	Homo sapiens	48-51
1363475-0	1992	Ethanol-induced CD3 and CD2 hyporesponsiveness of peripheral blood T lymphocytes.	Ethanol	0-7	CD2 molecule	Homo sapiens	24-27
1363475-4	1992	These changes were accompanied by faulty T-cell proliferation in response to anti-CD3 and anti-CD2 mAb and inhibition of CD3- and CD2-mediated rises in intracellular calcium and, to a lesser extent, inositol 1,4,5-triphosphate levels.	Calcium	166-173	CD2 molecule	Homo sapiens	130-133
1363475-4	1992	These changes were accompanied by faulty T-cell proliferation in response to anti-CD3 and anti-CD2 mAb and inhibition of CD3- and CD2-mediated rises in intracellular calcium and, to a lesser extent, inositol 1,4,5-triphosphate levels.	Inositol 1,4,5-Trisphosphate	199-226	CD2 molecule	Homo sapiens	130-133
1303963-7	1992	Cd2+ also induces a "pro-oxidant state" by causing a depletion of cellular glutathione.	Glutathione	75-86	CD2 molecule	Homo sapiens	0-3
1285264-6	1992	Ba2+ currents were blocked more effectively by Cd2+ than by Ni2+, were suppressed by 0.5 microM omega-conotoxin, and were virtually unaffected by amiloride.	N-methyl-valyl-amiclenomycin	0-4	CD2 molecule	Homo sapiens	47-50
1724971-7	1991	Cd2+ added to a Ca(2+)-free Ringer type medium containing propranolol enhanced K+ permeability similar to that obtained with Ca2+.	Propranolol	58-69	CD2 molecule	Homo sapiens	0-3
1660061-2	1991	The mechanism of Cd2+ block of Ca2+ currents (ICa) was explored in squid neurons using whole-cell patch clamp.	isocyanic acid	46-49	CD2 molecule	Homo sapiens	17-20
1919052-9	1991	Anti-CD2 and anti-LFA-3 MoAb strongly inhibited the proliferative responses of nickel-specific peripheral blood T lymphocytes from all 42 patients.	Nickel	79-85	CD2 molecule	Homo sapiens	5-8
1919052-10	1991	These results indicated that the receptor-ligand interaction between CD2 and LFA-3 is essential for in vitro activation of nickel-specific peripheral blood T lymphocytes.	Nickel	123-129	CD2 molecule	Homo sapiens	69-72
1835757-5	1991	In addition, GT1b ganglioside could also decrease strongly the expression of the T cell antigens CD3, CD2, CD4, CD8 and the alpha/beta T cell receptor antigenic complex whereas it did not affect HLA-class I antigens.	trisialoganglioside GT1	13-29	CD2 molecule	Homo sapiens	102-105
1717576-4	1991	We found that nonmitogenic amounts of ionomycin selectively and maximally up-regulated T cell CD7 on mature (peripheral blood) T cells after 24 h. Whereas CD7 expression was increased 78 +/- 25% by 0.5 microM ionomycin, expression of CD25 (IL-2R alpha), class II MHC, 4F2, transferrin receptor, CD2, CD3, CD4, CD5, and CD8 molecules was not increased.	Ionomycin	38-47	CD2 molecule	Homo sapiens	234-237
1717576-4	1991	We found that nonmitogenic amounts of ionomycin selectively and maximally up-regulated T cell CD7 on mature (peripheral blood) T cells after 24 h. Whereas CD7 expression was increased 78 +/- 25% by 0.5 microM ionomycin, expression of CD25 (IL-2R alpha), class II MHC, 4F2, transferrin receptor, CD2, CD3, CD4, CD5, and CD8 molecules was not increased.	Ionomycin	209-218	CD2 molecule	Homo sapiens	234-237
1928767-9	1991	Mean arterial pressure decreased to 74 +/- 2 mmHg in the clonidine group (-26 +/- 2 vs. -15 +/- 2% in the placebo group at T11) despite a significant increase in the cumulative fluid volume.	Clonidine	57-66	CD2 molecule	Homo sapiens	123-126
1940902-2	1991	By use of a filter separation method, together with a permeabilizing agent (Triton X-100), two cellular Cd2+ pools have been distinguished.	Octoxynol	76-88	CD2 molecule	Homo sapiens	104-107
1685602-7	1991	Using radioiodine-labeled CD-2 MoAb, heating was found to reduce the number of cell surface E-receptors by 42% on PBL and by 27% on HD-MAR cells.	Iodine-131	6-17	CD2 molecule	Homo sapiens	26-30
1682154-6	1991	The combination of CD2 mAb GT2/OKT11 used in the present study to trigger the CD2 antigen is able to act in synergy with phorbol 12,13-dibutyrate or ionomycin to induce NF-AT expression.	Phorbol 12,13-Dibutyrate	121-145	CD2 molecule	Homo sapiens	19-22
1682154-6	1991	The combination of CD2 mAb GT2/OKT11 used in the present study to trigger the CD2 antigen is able to act in synergy with phorbol 12,13-dibutyrate or ionomycin to induce NF-AT expression.	Phorbol 12,13-Dibutyrate	121-145	CD2 molecule	Homo sapiens	78-81
1682154-6	1991	The combination of CD2 mAb GT2/OKT11 used in the present study to trigger the CD2 antigen is able to act in synergy with phorbol 12,13-dibutyrate or ionomycin to induce NF-AT expression.	Ionomycin	149-158	CD2 molecule	Homo sapiens	19-22
1682154-6	1991	The combination of CD2 mAb GT2/OKT11 used in the present study to trigger the CD2 antigen is able to act in synergy with phorbol 12,13-dibutyrate or ionomycin to induce NF-AT expression.	Ionomycin	149-158	CD2 molecule	Homo sapiens	78-81
1822524-4	1991	About 96% of Cd2+ uptake was inhibited by DIDS (4,4"-diisothiocyanatostilbene-2,2"-disulphonic acid) with IC50 (concentration giving 50% of maximal inhibition) of 0.3 microM and by furosemide with IC50 of 500 microM and was resistant to ouabain and amiloride.	4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid	42-46	CD2 molecule	Homo sapiens	13-16
1822524-4	1991	About 96% of Cd2+ uptake was inhibited by DIDS (4,4"-diisothiocyanatostilbene-2,2"-disulphonic acid) with IC50 (concentration giving 50% of maximal inhibition) of 0.3 microM and by furosemide with IC50 of 500 microM and was resistant to ouabain and amiloride.	4,4"-diisothiocyanatostilbene-2,2"-disulphonic acid	48-99	CD2 molecule	Homo sapiens	13-16
1822524-4	1991	About 96% of Cd2+ uptake was inhibited by DIDS (4,4"-diisothiocyanatostilbene-2,2"-disulphonic acid) with IC50 (concentration giving 50% of maximal inhibition) of 0.3 microM and by furosemide with IC50 of 500 microM and was resistant to ouabain and amiloride.	Furosemide	181-191	CD2 molecule	Homo sapiens	13-16
1822524-4	1991	About 96% of Cd2+ uptake was inhibited by DIDS (4,4"-diisothiocyanatostilbene-2,2"-disulphonic acid) with IC50 (concentration giving 50% of maximal inhibition) of 0.3 microM and by furosemide with IC50 of 500 microM and was resistant to ouabain and amiloride.	Ouabain	237-244	CD2 molecule	Homo sapiens	13-16
1822524-4	1991	About 96% of Cd2+ uptake was inhibited by DIDS (4,4"-diisothiocyanatostilbene-2,2"-disulphonic acid) with IC50 (concentration giving 50% of maximal inhibition) of 0.3 microM and by furosemide with IC50 of 500 microM and was resistant to ouabain and amiloride.	Amiloride	249-258	CD2 molecule	Homo sapiens	13-16
1822524-7	1991	DIDS-sensitive Cd2+ uptake required the presence of external HCO3-.	4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid	0-4	CD2 molecule	Homo sapiens	15-18
1822524-7	1991	DIDS-sensitive Cd2+ uptake required the presence of external HCO3-.	Bicarbonates	61-66	CD2 molecule	Homo sapiens	15-18
1822524-8	1991	HCO3- ions had a biphasic effect on Cd2+ uptake.	Bicarbonates	0-4	CD2 molecule	Homo sapiens	36-39
1822524-11	1991	Depending on the presence or absence of external Cl-, a maximal Cd2+ uptake of 1.7 or 0.37 mmol (l cells)-1 h-1 was observed at bicarbonate concentrations of 15.6 or 11 mM respectively.	Bicarbonates	128-139	CD2 molecule	Homo sapiens	64-67
1822524-13	1991	In the presence of bicarbonate, external Cl- ions strongly stimulated Cd2+ uptake, with linear increase between 70 and 125 mM.	Bicarbonates	19-30	CD2 molecule	Homo sapiens	70-73
1822524-16	1991	DIDS-sensitive Cd2+ uptake was modestly inhibited by physiological concentrations of external phosphate and was resistant to external K+, Mg2+ and Ca2+.	4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid	0-4	CD2 molecule	Homo sapiens	15-18
1822524-16	1991	DIDS-sensitive Cd2+ uptake was modestly inhibited by physiological concentrations of external phosphate and was resistant to external K+, Mg2+ and Ca2+.	Phosphates	94-103	CD2 molecule	Homo sapiens	15-18
1822524-16	1991	DIDS-sensitive Cd2+ uptake was modestly inhibited by physiological concentrations of external phosphate and was resistant to external K+, Mg2+ and Ca2+.	magnesium ion	138-142	CD2 molecule	Homo sapiens	15-18
1660061-4	1991	External Cd2+ up to 250 microM reduced ICa reversibly.	isocyanic acid	39-42	CD2 molecule	Homo sapiens	9-12
1917142-3	1991	The major fraction of the trypsin inhibitor (T1-1) was purified to apparent homogeneity by anion-exchange and gel-filtration high-performance liquid chromatography (HPLC) and sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) followed by transblotting to Immobilon.	Sodium Dodecyl Sulfate	175-197	CD2 molecule	Homo sapiens	45-49
1917142-3	1991	The major fraction of the trypsin inhibitor (T1-1) was purified to apparent homogeneity by anion-exchange and gel-filtration high-performance liquid chromatography (HPLC) and sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) followed by transblotting to Immobilon.	polyacrylamide	198-212	CD2 molecule	Homo sapiens	45-49
1917142-3	1991	The major fraction of the trypsin inhibitor (T1-1) was purified to apparent homogeneity by anion-exchange and gel-filtration high-performance liquid chromatography (HPLC) and sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) followed by transblotting to Immobilon.	Sodium Dodecyl Sulfate	234-237	CD2 molecule	Homo sapiens	45-49
1917142-6	1991	The activity of T1-1 was acid-stable and heat-resistant, and its molecular weight was 115 kDa by SDS-PAGE.	Sodium Dodecyl Sulfate	97-100	CD2 molecule	Homo sapiens	16-20
1715359-5	1991	In addition, pretreatment of T cells with anti-1A4 inhibited the normally sustained intracellular calcium mobilization seen after triggering of T cells via the CD2 or CD3 pathways.	Calcium	98-105	CD2 molecule	Homo sapiens	160-163
1679947-4	1991	The enhancing effect of lithium on IL-2 production showed some differences from that of tetradecanoylphorbol acetate (TPA) in the following aspects: (i) TPA could reverse the inhibitory effect of anti-CD2 monoclonal antibody on IL-2 production, whereas lithium could not; and (ii) lithium was unable to synergistically induce IL-2 production with anti-CD3 monoclonal antibody as TPA did.	Tetradecanoylphorbol Acetate	153-156	CD2 molecule	Homo sapiens	201-204
1679947-4	1991	The enhancing effect of lithium on IL-2 production showed some differences from that of tetradecanoylphorbol acetate (TPA) in the following aspects: (i) TPA could reverse the inhibitory effect of anti-CD2 monoclonal antibody on IL-2 production, whereas lithium could not; and (ii) lithium was unable to synergistically induce IL-2 production with anti-CD3 monoclonal antibody as TPA did.	Tetradecanoylphorbol Acetate	153-156	CD2 molecule	Homo sapiens	201-204
1679947-4	1991	The enhancing effect of lithium on IL-2 production showed some differences from that of tetradecanoylphorbol acetate (TPA) in the following aspects: (i) TPA could reverse the inhibitory effect of anti-CD2 monoclonal antibody on IL-2 production, whereas lithium could not; and (ii) lithium was unable to synergistically induce IL-2 production with anti-CD3 monoclonal antibody as TPA did.	Lithium	24-31	CD2 molecule	Homo sapiens	201-204
1679714-0	1991	The T cell receptor/CD3 complex and CD2 stimulate the tyrosine phosphorylation of indistinguishable patterns of polypeptides in the human T leukemic cell line Jurkat.	Tyrosine	54-62	CD2 molecule	Homo sapiens	36-39
1677813-0	1991	CD3-dependent increase in cyclic AMP in human T-cells following stimulation of the CD2 receptor.	Cyclic AMP	26-36	CD2 molecule	Homo sapiens	83-86
1678351-2	1991	We have previously shown that p56lck, a lymphocyte-specific protein tyrosine kinase, is hyperphosphorylated on serine and tyrosine residues 15 minutes after activation via CD2 with a concomitant shift to a higher molecular mass.	Serine	111-117	CD2 molecule	Homo sapiens	172-175
1678351-2	1991	We have previously shown that p56lck, a lymphocyte-specific protein tyrosine kinase, is hyperphosphorylated on serine and tyrosine residues 15 minutes after activation via CD2 with a concomitant shift to a higher molecular mass.	Tyrosine	68-76	CD2 molecule	Homo sapiens	172-175
1677813-2	1991	Anti-CD2 receptor antibodies shared with anti-CD3 antibodies the ability to potentiate dose dependently the adenosine- and forskolin-stimulated cyclic adenosine monophosphate (cAMP) accumulation, whereas stimulation of the CD45 receptor had no effect on cyclase activity.	Adenosine	108-117	CD2 molecule	Homo sapiens	5-8
1648515-1	1991	The binding of endothelin (ET) to human placenta ET receptor was strongly inhibited by cadmium ions (Cd2+) (IC50 = 2 x 10(-5) M).	Cadmium	87-94	CD2 molecule	Homo sapiens	101-104
1677813-2	1991	Anti-CD2 receptor antibodies shared with anti-CD3 antibodies the ability to potentiate dose dependently the adenosine- and forskolin-stimulated cyclic adenosine monophosphate (cAMP) accumulation, whereas stimulation of the CD45 receptor had no effect on cyclase activity.	Colforsin	123-132	CD2 molecule	Homo sapiens	5-8
1648515-4	1991	The inhibitory effect of Cd2+ on solubilized ET receptor was partially reversed by the chelating agent, ethylenediaminetetraacetic acid (EDTA), whereas the effect was irreversible for the membrane-associated receptor.	Edetic Acid	104-135	CD2 molecule	Homo sapiens	25-28
1648515-4	1991	The inhibitory effect of Cd2+ on solubilized ET receptor was partially reversed by the chelating agent, ethylenediaminetetraacetic acid (EDTA), whereas the effect was irreversible for the membrane-associated receptor.	Edetic Acid	137-141	CD2 molecule	Homo sapiens	25-28
1677813-2	1991	Anti-CD2 receptor antibodies shared with anti-CD3 antibodies the ability to potentiate dose dependently the adenosine- and forskolin-stimulated cyclic adenosine monophosphate (cAMP) accumulation, whereas stimulation of the CD45 receptor had no effect on cyclase activity.	Cyclic AMP	144-174	CD2 molecule	Homo sapiens	5-8
1677813-2	1991	Anti-CD2 receptor antibodies shared with anti-CD3 antibodies the ability to potentiate dose dependently the adenosine- and forskolin-stimulated cyclic adenosine monophosphate (cAMP) accumulation, whereas stimulation of the CD45 receptor had no effect on cyclase activity.	Cyclic AMP	176-180	CD2 molecule	Homo sapiens	5-8
1680333-2	1991	The CD2 protein mediates adhesion to SRBC.	srbc	37-41	CD2 molecule	Homo sapiens	4-7
1651978-6	1991	In addition, we find that internal Cd2+ is as effective as external Cd2+ in blocking Ba2+ currents through the channels, again suggesting identical interactions of ions with each end of the pore.	N-methyl-valyl-amiclenomycin	85-89	CD2 molecule	Homo sapiens	35-38
1651978-6	1991	In addition, we find that internal Cd2+ is as effective as external Cd2+ in blocking Ba2+ currents through the channels, again suggesting identical interactions of ions with each end of the pore.	N-methyl-valyl-amiclenomycin	85-89	CD2 molecule	Homo sapiens	68-71
1674518-0	1991	CD2 antigen mediated activation of the guanine nucleotide binding proteins p21ras in human T lymphocytes.	Guanine Nucleotides	39-57	CD2 molecule	Homo sapiens	0-3
1674518-6	1991	In the present report, we demonstrate that the TCR/CD3 complex and the CD2 Ag control the accumulation of p21ras-GTP complexes via a regulatory effect on p21ras GTPase activity.	Guanosine Triphosphate	113-116	CD2 molecule	Homo sapiens	71-74
1709660-5	1991	Cytochalasins, at low concentrations, enhanced the rise in intracellular Ca2+ and production of IP3 in CD4 cells activated by anti-CD2 or CD3 antibodies.	Inositol 1,4,5-Trisphosphate	96-99	CD2 molecule	Homo sapiens	131-134
1709660-7	1991	These results suggest that cytochalasins enhance the proliferation of CD4 cells by affecting early events in signal transduction after activation through the CD3-Ti Ag-receptor complex or CD2 molecule.	Cytochalasins	27-40	CD2 molecule	Homo sapiens	188-191
1715762-1	1991	T cell proliferation, in the presence of monocytes, triggered either by an anti-CD3 monoclonal antibody (mAb) or by a mitogenic pair of anti-CD2 mAbs was inhibited either by the calcium chelator EGTA or the calcium channel blocker nifedipin.	Egtazic Acid	195-199	CD2 molecule	Homo sapiens	141-144
1804290-1	1991	Metallothionein (MT) is a cysteine-rich protein with antioxidant and metal-chelating activities that is readily inducible by exposure to a variety of stimuli including heavy metals such as cadmium (Cd2+).	Metals	69-74	CD2 molecule	Homo sapiens	198-201
1804290-1	1991	Metallothionein (MT) is a cysteine-rich protein with antioxidant and metal-chelating activities that is readily inducible by exposure to a variety of stimuli including heavy metals such as cadmium (Cd2+).	Cadmium	189-196	CD2 molecule	Homo sapiens	198-201
1804290-6	1991	Electrophoretic-autoradiographic analysis of [35S]-cysteine-labeled protein synthesized by cultured cells after Cd2+ treatment revealed increased MT-like protein content.	Sulfur-35	46-49	CD2 molecule	Homo sapiens	112-115
1804290-6	1991	Electrophoretic-autoradiographic analysis of [35S]-cysteine-labeled protein synthesized by cultured cells after Cd2+ treatment revealed increased MT-like protein content.	Cysteine	51-59	CD2 molecule	Homo sapiens	112-115
1711070-0	1991	Interaction of CD2 with its ligand lymphocyte function-associated antigen-3 induces adenosine 3",5"-cyclic monophosphate production in T lymphocytes.	Cyclic AMP	84-120	CD2 molecule	Homo sapiens	15-18
1711070-6	1991	By using a RIA sensitive to the femtomolar range and specific for cAMP, we demonstrate that purified LFA-3, like anti-CD2 mAb, is capable of inducing marked, transient increases in the intracellular concentration of cAMP.	Cyclic AMP	216-220	CD2 molecule	Homo sapiens	118-121
1711070-7	1991	Presentation of purified LFA-3, like anti-CD2 mAb, is capable of inducing marked, transient increases in the intracellular concentration of cAMP.	Cyclic AMP	140-144	CD2 molecule	Homo sapiens	42-45
1711070-9	1991	The cytoplasmic domain of CD2 is necessary for these ligand-induced cAMP changes, demonstrating that LFA-3 binding to CD2 transduces a signal to the cell.	Cyclic AMP	68-72	CD2 molecule	Homo sapiens	26-29
1711070-9	1991	The cytoplasmic domain of CD2 is necessary for these ligand-induced cAMP changes, demonstrating that LFA-3 binding to CD2 transduces a signal to the cell.	Cyclic AMP	68-72	CD2 molecule	Homo sapiens	118-121
1711070-10	1991	Experiments using the phosphodiesterase inhibitor 3-isobutyl-1-methyl-xanthine showed that CD2-mediated regulation of cAMP levels occurs primarily by the stimulation of cAMP production rather than by the inhibition of cAMP degradation.	1-Methyl-3-isobutylxanthine	50-78	CD2 molecule	Homo sapiens	91-94
1711070-10	1991	Experiments using the phosphodiesterase inhibitor 3-isobutyl-1-methyl-xanthine showed that CD2-mediated regulation of cAMP levels occurs primarily by the stimulation of cAMP production rather than by the inhibition of cAMP degradation.	Cyclic AMP	118-122	CD2 molecule	Homo sapiens	91-94
1711070-10	1991	Experiments using the phosphodiesterase inhibitor 3-isobutyl-1-methyl-xanthine showed that CD2-mediated regulation of cAMP levels occurs primarily by the stimulation of cAMP production rather than by the inhibition of cAMP degradation.	Cyclic AMP	169-173	CD2 molecule	Homo sapiens	91-94
1711070-10	1991	Experiments using the phosphodiesterase inhibitor 3-isobutyl-1-methyl-xanthine showed that CD2-mediated regulation of cAMP levels occurs primarily by the stimulation of cAMP production rather than by the inhibition of cAMP degradation.	Cyclic AMP	169-173	CD2 molecule	Homo sapiens	91-94
1711070-11	1991	These results demonstrate that the interaction of LFA-3 with CD2, in the absence of other stimuli, is capable of initiating intracellular biochemical changes and suggest that CD2/LFA-3 interactions may regulate T cell function at least in part through the generation of intracellular cAMP.	Cyclic AMP	284-288	CD2 molecule	Homo sapiens	61-64
1711070-11	1991	These results demonstrate that the interaction of LFA-3 with CD2, in the absence of other stimuli, is capable of initiating intracellular biochemical changes and suggest that CD2/LFA-3 interactions may regulate T cell function at least in part through the generation of intracellular cAMP.	Cyclic AMP	284-288	CD2 molecule	Homo sapiens	175-178
1648375-2	1991	Cadmium2+ inhibited the erythrocyte Na+,K(+)-ATPase enzyme with a 50% inhibition at a Cd2+ concentration of 6.25 microM.	cadmium2+	0-9	CD2 molecule	Homo sapiens	86-89
1648375-3	1991	The Cd2+ inhibition in the human erythrocyte was non-competitive with respect to Na+,K+, and ATP.	Adenosine Triphosphate	93-96	CD2 molecule	Homo sapiens	4-7
1657901-3	1991	The PPi-ase activity of the enzyme can be inhibited by cadmium ions (Cd2+), perhaps by replacing Zn2+ from the active site of the enzyme molecule.	Cadmium	55-62	CD2 molecule	Homo sapiens	69-72
1657901-3	1991	The PPi-ase activity of the enzyme can be inhibited by cadmium ions (Cd2+), perhaps by replacing Zn2+ from the active site of the enzyme molecule.	Zinc	97-101	CD2 molecule	Homo sapiens	69-72
1673981-11	1991	Stimulation of T cells with ionomycin and PMA greatly increased the expression of CD2 and CD44 without increasing the number of molecules associated with the cytoskeleton.	Ionomycin	28-37	CD2 molecule	Homo sapiens	82-85
1673981-11	1991	Stimulation of T cells with ionomycin and PMA greatly increased the expression of CD2 and CD44 without increasing the number of molecules associated with the cytoskeleton.	Tetradecanoylphorbol Acetate	42-45	CD2 molecule	Homo sapiens	82-85
1685336-5	1991	The use of a CD2 mAb, D66, able to mobilize exclusively Ca2+ from intracellular stores, resulted in 51% inhibition of PS synthesis.	Phosphatidylserines	118-120	CD2 molecule	Homo sapiens	13-16
1685336-6	1991	N-Ethylmaleimide (NEM), which inhibits both the release of Ca2+ from internal stores and the influx of Ca2+, totally prevents the inhibition of PS synthesis induced by PHA, anti-CD3 or anti-CD2 mAbs.	Ethylmaleimide	0-16	CD2 molecule	Homo sapiens	190-193
1685336-6	1991	N-Ethylmaleimide (NEM), which inhibits both the release of Ca2+ from internal stores and the influx of Ca2+, totally prevents the inhibition of PS synthesis induced by PHA, anti-CD3 or anti-CD2 mAbs.	Ethylmaleimide	18-21	CD2 molecule	Homo sapiens	190-193
1685336-6	1991	N-Ethylmaleimide (NEM), which inhibits both the release of Ca2+ from internal stores and the influx of Ca2+, totally prevents the inhibition of PS synthesis induced by PHA, anti-CD3 or anti-CD2 mAbs.	Phosphatidylserines	144-146	CD2 molecule	Homo sapiens	190-193
1677314-1	1991	An increase in intracellular calcium concentration stimulated by anti-CD2 or CD3 antibodies has been measured with Fura-2 in P28 cells, a human CD4+ T cell clone.	Calcium	29-36	CD2 molecule	Homo sapiens	70-73
1651120-7	1991	For either the binary lipid or ternary lipid-protein systems reconstituted with DMPC-d54, linewidth parameters of the DMPC-d54 acyl chain CD2 symmetric stretching modes at 2,103 cm-1 provide a sensitive measure of the conformational and dynamic properties of the perdeuterated lipid component, while the 3,000 cm-1 C-H spectral region reflects the bilayer characteristics of the DMPA species in the complex.	Dimyristoylphosphatidylcholine	80-84	CD2 molecule	Homo sapiens	138-141
1651120-7	1991	For either the binary lipid or ternary lipid-protein systems reconstituted with DMPC-d54, linewidth parameters of the DMPC-d54 acyl chain CD2 symmetric stretching modes at 2,103 cm-1 provide a sensitive measure of the conformational and dynamic properties of the perdeuterated lipid component, while the 3,000 cm-1 C-H spectral region reflects the bilayer characteristics of the DMPA species in the complex.	Dimyristoylphosphatidylcholine	118-122	CD2 molecule	Homo sapiens	138-141
1707760-5	1991	This correlation held even for the CD28/CD2 pathway which was previously shown to be calcium-independent; however by employing FACS analysis of [Ca2+]i within individual cells, a subset of cells activated via CD28/CD2 was found to respond with a measurable rise in [Ca2+]i.	Calcium	85-92	CD2 molecule	Homo sapiens	35-38
1707760-5	1991	This correlation held even for the CD28/CD2 pathway which was previously shown to be calcium-independent; however by employing FACS analysis of [Ca2+]i within individual cells, a subset of cells activated via CD28/CD2 was found to respond with a measurable rise in [Ca2+]i.	Calcium	85-92	CD2 molecule	Homo sapiens	40-43
1673843-7	1991	Low responses to anti-CD2 were corrected to normal by the coaddition of a submitogenic amount of phorbol myristate acetate (1 ng/ml).	Tetradecanoylphorbol Acetate	97-122	CD2 molecule	Homo sapiens	22-25
1677314-1	1991	An increase in intracellular calcium concentration stimulated by anti-CD2 or CD3 antibodies has been measured with Fura-2 in P28 cells, a human CD4+ T cell clone.	Fura-2	115-121	CD2 molecule	Homo sapiens	70-73
1673433-6	1991	Here we show that NK cell activation induced by mAb reactive with CD2 (either anti-T11.1 alone or with anti-T11.2 in combination) also results in the tyrosine phosphorylation of zeta.	Tyrosine	150-158	CD2 molecule	Homo sapiens	66-69
1677314-6	1991	It is concluded that the effects of nitrendipine on potassium channels may account for a large part of the inhibition that nitrendipine exerts on the calcium increase elicited by CD2 or CD3 stimulation.	Nitrendipine	36-48	CD2 molecule	Homo sapiens	179-182
1677314-6	1991	It is concluded that the effects of nitrendipine on potassium channels may account for a large part of the inhibition that nitrendipine exerts on the calcium increase elicited by CD2 or CD3 stimulation.	Nitrendipine	123-135	CD2 molecule	Homo sapiens	179-182
1677314-6	1991	It is concluded that the effects of nitrendipine on potassium channels may account for a large part of the inhibition that nitrendipine exerts on the calcium increase elicited by CD2 or CD3 stimulation.	Calcium	150-157	CD2 molecule	Homo sapiens	179-182
1706751-5	1991	In the CD2 transfectant, a combination of anti-T11(2) + anti-T11(3) monoclonal antibodies (mAbs) induced a rise in intracellular free calcium [( Ca2+]i), IL-6 production, and histamine release.	Calcium	134-141	CD2 molecule	Homo sapiens	7-10
1671400-4	1991	The CD3-mediated CD2 up-regulation was suppressed by cycloheximide and actinomycin D, indicating that it requires de novo protein and RNA synthesis.	Cycloheximide	53-66	CD2 molecule	Homo sapiens	17-20
1850171-8	1991	In one separate experiment we also tested the effect of the substrates progesterone, 17 alpha-hydroxy-progesterone, and androstenedione on Cd2(+)-treated Leydig cells.	Progesterone	71-83	CD2 molecule	Homo sapiens	139-142
1850171-8	1991	In one separate experiment we also tested the effect of the substrates progesterone, 17 alpha-hydroxy-progesterone, and androstenedione on Cd2(+)-treated Leydig cells.	Androstenedione	120-135	CD2 molecule	Homo sapiens	139-142
1850171-11	1991	Dose-response depression in both hCG- and db-cAMP-stimulated T production were seen with Cd2+, Co2+, Cu2+, Hg2+, Ni2+, and Zn2+ treatment.	db-cAMP	42-49	CD2 molecule	Homo sapiens	89-92
1850171-12	1991	Surprisingly, Cd2+, Co2+, Ni2+, and Zn2+, which caused a depression in hCG- and db-cAMP-stimulated T production, caused significant increases in HCHOL- and PREG-stimulated T production over untreated and similarly stimulated cultures.	Nickel(2+)	26-30	CD2 molecule	Homo sapiens	14-17
1850171-12	1991	Surprisingly, Cd2+, Co2+, Ni2+, and Zn2+, which caused a depression in hCG- and db-cAMP-stimulated T production, caused significant increases in HCHOL- and PREG-stimulated T production over untreated and similarly stimulated cultures.	Zinc	36-40	CD2 molecule	Homo sapiens	14-17
1850171-12	1991	Surprisingly, Cd2+, Co2+, Ni2+, and Zn2+, which caused a depression in hCG- and db-cAMP-stimulated T production, caused significant increases in HCHOL- and PREG-stimulated T production over untreated and similarly stimulated cultures.	db-cAMP	80-87	CD2 molecule	Homo sapiens	14-17
1850171-12	1991	Surprisingly, Cd2+, Co2+, Ni2+, and Zn2+, which caused a depression in hCG- and db-cAMP-stimulated T production, caused significant increases in HCHOL- and PREG-stimulated T production over untreated and similarly stimulated cultures.	hchol	145-150	CD2 molecule	Homo sapiens	14-17
1671400-7	1991	Moreover, IL-2-dependent events may also help in enhancing CD2 hyper-expression because it was only partially inhibitable by cyclosporine, dexamethasone, or Mar-108 (CD25) mAb.	Dexamethasone	139-152	CD2 molecule	Homo sapiens	59-62
1671400-4	1991	The CD3-mediated CD2 up-regulation was suppressed by cycloheximide and actinomycin D, indicating that it requires de novo protein and RNA synthesis.	Dactinomycin	71-84	CD2 molecule	Homo sapiens	17-20
1671400-6	1991	CD2 up-regulation appeared to be elicited by a protein kinase C-dependent mechanism because it was abrogated by staurosporine, a potent protein kinase C inhibitor.	Staurosporine	112-125	CD2 molecule	Homo sapiens	0-3
1671400-7	1991	Moreover, IL-2-dependent events may also help in enhancing CD2 hyper-expression because it was only partially inhibitable by cyclosporine, dexamethasone, or Mar-108 (CD25) mAb.	Cyclosporine	125-137	CD2 molecule	Homo sapiens	59-62
1671400-7	1991	Moreover, IL-2-dependent events may also help in enhancing CD2 hyper-expression because it was only partially inhibitable by cyclosporine, dexamethasone, or Mar-108 (CD25) mAb.	mar-108	157-164	CD2 molecule	Homo sapiens	59-62
1671730-7	1991	RESULTS: Significant differences were seen in lymphocyte phenotype in the methadone-treated group, with elevations in the T-cell helper subset CD4+CD26+; in CD8 and CD8+I2+ cells, suppressor/cytotoxic T lymphocytes, and activated suppressor/cytotoxic T cells; and in CD2+CD26+ cells and activated total T lymphocytes.	Methadone	74-83	CD2 molecule	Homo sapiens	147-150
1705513-4	1991	We have shown that FK-506, like CsA, is able to inhibit T cell activation mediated not only by the T cell receptor-CD3 complex, but also via another surface molecule, CD2.	Tacrolimus	19-25	CD2 molecule	Homo sapiens	167-170
1671002-4	1991	Proliferation induced via the CD2 pathway was very sensitive to the presence of monocytes whose inhibitory effect was reversed by indomethacin.	Indomethacin	130-142	CD2 molecule	Homo sapiens	30-33
1671002-5	1991	While the potent inhibitory effect of PGE2 on proliferation induced via the CD2 pathway was weakly antagonized by anti-Leu-13, the combined effects of anti-Leu-13 and PGE2 on the CD3 pathway were additive and very inhibitory.	Dinoprostone	38-42	CD2 molecule	Homo sapiens	76-79
1705513-4	1991	We have shown that FK-506, like CsA, is able to inhibit T cell activation mediated not only by the T cell receptor-CD3 complex, but also via another surface molecule, CD2.	Cyclosporine	32-35	CD2 molecule	Homo sapiens	167-170
1981560-5	1990	Activation of CD3 and CD2 by monoclonal antibodies also stimulated phospholipase C activity as measured by breakdown of membrane phosphoinositides in wild-type but not in mutant Jurkat cells.	Phosphatidylinositols	129-146	CD2 molecule	Homo sapiens	22-25
1674659-0	1991	Diacylglycerol production in Jurkat T-cells: differences between CD3, CD2 and PHA activation pathways.	Diglycerides	0-14	CD2 molecule	Homo sapiens	70-73
1674659-1	1991	Diacylglycerol (DAG) production induced after stimulation with either CD3 mAb, a pair of CD2 mAbs or phytohaemagglutinin has been monitored in Jurkat T-cells prelabelled to isotopic equilibrium with seven [3H]- or [14C] fatty acids.	Diglycerides	0-14	CD2 molecule	Homo sapiens	89-92
1674659-1	1991	Diacylglycerol (DAG) production induced after stimulation with either CD3 mAb, a pair of CD2 mAbs or phytohaemagglutinin has been monitored in Jurkat T-cells prelabelled to isotopic equilibrium with seven [3H]- or [14C] fatty acids.	Diglycerides	16-19	CD2 molecule	Homo sapiens	89-92
1814859-0	1991	Hb Hoshida [beta 43(CD2)Glu----Gln] observed in a Yugoslavian family.	glu----gln	24-34	CD2 molecule	Homo sapiens	20-23
1676547-8	1991	The response via CD2 plus CD28 is IL-2-dependent, as demonstrated by the ability of mAb against the IL-2 receptor to block proliferation, and is almost completely inhibited by cyclosporine A (CsA).	Cyclosporine	192-195	CD2 molecule	Homo sapiens	17-20
1824804-7	1991	The suppression was mediated by a small population of BMC that expressed a CD2+, CD8+, CD16+, DR-, CD3-, CD38- phenotype.	S-benzyl-N-malonylcysteine	54-57	CD2 molecule	Homo sapiens	75-78
1824804-10	1991	In contrast, in recipients given CD2- DBMC or DR- CD16- DBMC infusions, the tolerance-promoting effect of DBMC was absent, and there were no long-term survivors.	4,6-Di-tert-butyl-m-cresol	38-42	CD2 molecule	Homo sapiens	33-36
2176593-3	1990	The two resonances at 168.5 and 169.9 ppm observed in the 13C-NMR spectrum of the Cd2 derivative obtained with [13C]oxalate each correspond to slowly exchanging oxalate specifically bound to a single site.	13c	58-61	CD2 molecule	Homo sapiens	82-85
2176593-3	1990	The two resonances at 168.5 and 169.9 ppm observed in the 13C-NMR spectrum of the Cd2 derivative obtained with [13C]oxalate each correspond to slowly exchanging oxalate specifically bound to a single site.	[13c]oxalate	111-123	CD2 molecule	Homo sapiens	82-85
2176593-3	1990	The two resonances at 168.5 and 169.9 ppm observed in the 13C-NMR spectrum of the Cd2 derivative obtained with [13C]oxalate each correspond to slowly exchanging oxalate specifically bound to a single site.	Oxalates	116-123	CD2 molecule	Homo sapiens	82-85
2260708-4	1990	Nickel (Ni2+, 50 microM) inhibited maximal T current (-65.6 +/- 5.9%) more than L current (-15.7 +/- 2.4%), and 10 microM cadmium (Cd2+) inhibited L current (-65.5 +/- 5.9%) without significant effect on T current (-8.7 +/- 8.1%).	Nickel	0-6	CD2 molecule	Homo sapiens	131-134
2260708-4	1990	Nickel (Ni2+, 50 microM) inhibited maximal T current (-65.6 +/- 5.9%) more than L current (-15.7 +/- 2.4%), and 10 microM cadmium (Cd2+) inhibited L current (-65.5 +/- 5.9%) without significant effect on T current (-8.7 +/- 8.1%).	Cadmium	122-129	CD2 molecule	Homo sapiens	131-134
2260708-10	1990	Finally, 4.2 mM Mg2+ and 50 microM Ni2+ elicited a similar decrease in the late diastolic slope of subsidiary pacemaker action potentials, whereas 10 microM Cd2+ markedly inhibited action potential amplitude.	magnesium ion	16-20	CD2 molecule	Homo sapiens	157-160
1984413-8	1991	Incubating the cells with Zn2+ prior to assaying efflux in the absence of Zn2+ strongly inhibited the stimulation of 45Ca2+ efflux by Cd2+, pH 6, and the removal of external Na+ without affecting the stimulation of efflux by ATP.	Zinc	26-30	CD2 molecule	Homo sapiens	134-137
1676547-8	1991	The response via CD2 plus CD28 is IL-2-dependent, as demonstrated by the ability of mAb against the IL-2 receptor to block proliferation, and is almost completely inhibited by cyclosporine A (CsA).	Cyclosporine	176-190	CD2 molecule	Homo sapiens	17-20
1977524-5	1990	In contrast, concentrations of cytochalasin expected to bind only high affinity binding sites (0.125-1 microM), represented by surface actin filaments, enhanced T4 cell proliferation and interleukin 2 production stimulated by mAb to CD2, CD3, or class I major histocompatibility complex (MHC) molecules, but not those induced by mAb to the T cell receptor, paraformaldehyde fixed, or viable antigen-bearing APC, allogeneic APC, or ionomycin and PMA.	Cytochalasins	31-43	CD2 molecule	Homo sapiens	233-236
1702899-4	1990	Isoprinosine significantly enhanced the lymphoproliferative response after stimulation with phytohaemagglutinin (PHA) and purified derivative of tuberculin (PPD), while isoprinosine had no effect on the following immune parameters: the expression of surface markers on blood mononuclear cells including CD2, CD3, CD4, CD8, CD14, CD19, CD20, CD25, leu-8, and HLA-DR.	Inosine Pranobex	0-12	CD2 molecule	Homo sapiens	303-306
1977524-5	1990	In contrast, concentrations of cytochalasin expected to bind only high affinity binding sites (0.125-1 microM), represented by surface actin filaments, enhanced T4 cell proliferation and interleukin 2 production stimulated by mAb to CD2, CD3, or class I major histocompatibility complex (MHC) molecules, but not those induced by mAb to the T cell receptor, paraformaldehyde fixed, or viable antigen-bearing APC, allogeneic APC, or ionomycin and PMA.	paraform	357-373	CD2 molecule	Homo sapiens	233-236
1977524-5	1990	In contrast, concentrations of cytochalasin expected to bind only high affinity binding sites (0.125-1 microM), represented by surface actin filaments, enhanced T4 cell proliferation and interleukin 2 production stimulated by mAb to CD2, CD3, or class I major histocompatibility complex (MHC) molecules, but not those induced by mAb to the T cell receptor, paraformaldehyde fixed, or viable antigen-bearing APC, allogeneic APC, or ionomycin and PMA.	Ionomycin	431-440	CD2 molecule	Homo sapiens	233-236
1700752-10	1990	Conversely, prestimulation of T cell clone P28 by CD3 or CD2-specific mAb inhibits the Ca2(+)-mobilizing effect of TG.	Thapsigargin	115-117	CD2 molecule	Homo sapiens	57-60
2128706-1	1990	The stability of complexes formed by Cd2+ in hemolyzed human erythrocytes was studied by spin-echo 1H NMR spectroscopy.	Hydrogen	99-101	CD2 molecule	Homo sapiens	37-40
2128706-2	1990	Changes in resonances for the carbon-bonded protons of glutathione (GSH) upon addition of the ethylenediaminetetraacetic acid complex of Cd2+ (Cd(EDTA)2-) and the appearance of resonances for Mg(EDTA)2- indicate that the Cd(EDTA)2- complex dissociates in hemolyzed erythrocytes with the formation of Cd(GSH)x and Mg(EDTA)2- complexes.	Carbon	30-36	CD2 molecule	Homo sapiens	137-140
2128706-2	1990	Changes in resonances for the carbon-bonded protons of glutathione (GSH) upon addition of the ethylenediaminetetraacetic acid complex of Cd2+ (Cd(EDTA)2-) and the appearance of resonances for Mg(EDTA)2- indicate that the Cd(EDTA)2- complex dissociates in hemolyzed erythrocytes with the formation of Cd(GSH)x and Mg(EDTA)2- complexes.	Glutathione	55-66	CD2 molecule	Homo sapiens	137-140
2128706-2	1990	Changes in resonances for the carbon-bonded protons of glutathione (GSH) upon addition of the ethylenediaminetetraacetic acid complex of Cd2+ (Cd(EDTA)2-) and the appearance of resonances for Mg(EDTA)2- indicate that the Cd(EDTA)2- complex dissociates in hemolyzed erythrocytes with the formation of Cd(GSH)x and Mg(EDTA)2- complexes.	Glutathione	68-71	CD2 molecule	Homo sapiens	137-140
2128706-2	1990	Changes in resonances for the carbon-bonded protons of glutathione (GSH) upon addition of the ethylenediaminetetraacetic acid complex of Cd2+ (Cd(EDTA)2-) and the appearance of resonances for Mg(EDTA)2- indicate that the Cd(EDTA)2- complex dissociates in hemolyzed erythrocytes with the formation of Cd(GSH)x and Mg(EDTA)2- complexes.	Edetic Acid	94-125	CD2 molecule	Homo sapiens	137-140
2128706-2	1990	Changes in resonances for the carbon-bonded protons of glutathione (GSH) upon addition of the ethylenediaminetetraacetic acid complex of Cd2+ (Cd(EDTA)2-) and the appearance of resonances for Mg(EDTA)2- indicate that the Cd(EDTA)2- complex dissociates in hemolyzed erythrocytes with the formation of Cd(GSH)x and Mg(EDTA)2- complexes.	cd(edta	143-150	CD2 molecule	Homo sapiens	137-140
2128706-2	1990	Changes in resonances for the carbon-bonded protons of glutathione (GSH) upon addition of the ethylenediaminetetraacetic acid complex of Cd2+ (Cd(EDTA)2-) and the appearance of resonances for Mg(EDTA)2- indicate that the Cd(EDTA)2- complex dissociates in hemolyzed erythrocytes with the formation of Cd(GSH)x and Mg(EDTA)2- complexes.	mg(edta)2	192-201	CD2 molecule	Homo sapiens	137-140
2128706-2	1990	Changes in resonances for the carbon-bonded protons of glutathione (GSH) upon addition of the ethylenediaminetetraacetic acid complex of Cd2+ (Cd(EDTA)2-) and the appearance of resonances for Mg(EDTA)2- indicate that the Cd(EDTA)2- complex dissociates in hemolyzed erythrocytes with the formation of Cd(GSH)x and Mg(EDTA)2- complexes.	Glutathione	303-306	CD2 molecule	Homo sapiens	137-140
2128706-2	1990	Changes in resonances for the carbon-bonded protons of glutathione (GSH) upon addition of the ethylenediaminetetraacetic acid complex of Cd2+ (Cd(EDTA)2-) and the appearance of resonances for Mg(EDTA)2- indicate that the Cd(EDTA)2- complex dissociates in hemolyzed erythrocytes with the formation of Cd(GSH)x and Mg(EDTA)2- complexes.	mg(edta)2	313-322	CD2 molecule	Homo sapiens	137-140
2128706-3	1990	A semiquantitative estimate of the overall stability constant for the complexation of Cd2+ in hemolyzed erythrocytes was obtained from spin-echo 1H NMR data.	Hydrogen	145-147	CD2 molecule	Homo sapiens	86-89
1979333-6	1990	Since defective anti-CD2-induced mitogenesis could be reversed by phorbol myristate acetate, but not calcium ionophore A23187, it is probably correlated with impaired protein kinase C activation.	Tetradecanoylphorbol Acetate	66-91	CD2 molecule	Homo sapiens	21-24
1976695-0	1990	Activation of tyrosine phosphorylation in human T cells via the CD2 pathway.	Tyrosine	14-22	CD2 molecule	Homo sapiens	64-67
1976695-3	1990	Using antiphosphotyrosine antibody to detect tyrosine phosphorylation of cellular substrates, we demonstrate that mAb stimulation of either CD3 or CD2 results in tyrosine phosphorylation of the TCR-zeta chain and 135- and 100-kDa proteins.	Tyrosine	17-25	CD2 molecule	Homo sapiens	147-150
1976695-3	1990	Using antiphosphotyrosine antibody to detect tyrosine phosphorylation of cellular substrates, we demonstrate that mAb stimulation of either CD3 or CD2 results in tyrosine phosphorylation of the TCR-zeta chain and 135- and 100-kDa proteins.	Tyrosine	45-53	CD2 molecule	Homo sapiens	147-150
1976695-4	1990	However, differences are observed between CD3 and CD2 ligation; only the former results in rapid tyrosine phosphorylation of 72-, 65-, and 40-kDa substrates.	Tyrosine	97-105	CD2 molecule	Homo sapiens	50-53
1976695-5	1990	Co-aggregation of CD2 and CD45, a tyrosine phosphatase, results in inhibition of intracellular calcium elevation and T cell proliferation.	Calcium	95-102	CD2 molecule	Homo sapiens	18-21
1976463-2	1990	Unlike resting CD4+ normal T lymphocytes that can be activated only by a two-signal stimulation, T-CLL cells proliferated and released IL-2 in response to a pair of anti-CD2 monoclonal antibodies (MoAbs) or concanavalin A (Con A) in the absence of both accessory cells (AC) and phorbol myristate acetate (PMA).	Tetradecanoylphorbol Acetate	278-303	CD2 molecule	Homo sapiens	170-173
1975259-2	1990	Interaction of the glycosyl phosphatidylinositol-linked differentiation Ag CD73 (ecto-5"-nucleotidase) with the CD73-specific mAb 1E9 generates agonistic signals that strongly synergize with T cell activation induced by CD3 and CD2 mAb.	Glycosylphosphatidylinositols	19-48	CD2 molecule	Homo sapiens	228-231
1975259-12	1990	Finally, the functional association between CD73 and integral membrane molecules like CD3 and CD2 suggests that GPI-anchored molecules may play a role in transmembrane signaling mediated by conventional second messenger systems.	Glycosylphosphatidylinositols	112-115	CD2 molecule	Homo sapiens	94-97
2379381-9	1990	A decreased mean ketanserin elimination half-life (t1/2 = 12 +/- 4 and 10 +/- 3h vs 16 +/- 3 and 18 +/- 4h in healthy controls after oral ketanserin 40mg and intravenous ketanserin 5mg, respectively) contrasted with a substantial increase in t1/2 for ketanserinol (33 +/- 13 vs 19 +/- 4h).	Ketanserin	17-27	CD2 molecule	Homo sapiens	51-99
1982981-3	1990	GF induced the lymphocyte proliferation in combination with phorbol ester (PMA) or anti-CD2 monoclonal antibodies (mAb) with PMA.	gf	0-2	CD2 molecule	Homo sapiens	88-91
1982981-3	1990	GF induced the lymphocyte proliferation in combination with phorbol ester (PMA) or anti-CD2 monoclonal antibodies (mAb) with PMA.	Tetradecanoylphorbol Acetate	125-128	CD2 molecule	Homo sapiens	88-91
2394762-4	1990	These findings suggest that Fe3+, Co2+, and Ni2+ ions may interfere with T cell activation since both CD2 and CD3 are involved in that process.	ferric sulfate	28-32	CD2 molecule	Homo sapiens	102-105
2394762-4	1990	These findings suggest that Fe3+, Co2+, and Ni2+ ions may interfere with T cell activation since both CD2 and CD3 are involved in that process.	Cobalt(2+)	34-38	CD2 molecule	Homo sapiens	102-105
2394762-4	1990	These findings suggest that Fe3+, Co2+, and Ni2+ ions may interfere with T cell activation since both CD2 and CD3 are involved in that process.	Nickel(2+)	44-48	CD2 molecule	Homo sapiens	102-105
1696526-2	1990	We found that CD1+ cells expressed high levels of CD25 antigen upon triggering with specific monoclonal antibodies (mAbs) (anti-CD3, anti-CD2, anti-CD28) in association with low doses of Phorbol-13-myristate-12-acetate (PMA).	Tetradecanoylphorbol Acetate	220-223	CD2 molecule	Homo sapiens	50-53
2266002-1	1990	Cadmium (Cd2+), an environmental contaminant, has been shown to inhibit, even if not totally, natural killer (NK) cell-mediated cytotoxicity and antibody-dependent cellular cytotoxicity (ADCC) of human peripheral blood lymphocytes in a dose- and time-dependent manner.	Cadmium	0-7	CD2 molecule	Homo sapiens	9-12
2266002-5	1990	Our results indicate that Cd2+ did not block effector-target conjugate formation, but rather interfered with the hydrolysis of phosphoinositides, as shown by the decrease of inositol trisphosphate (IP3), which is known to release stored Ca2+.	Phosphatidylinositols	127-144	CD2 molecule	Homo sapiens	26-29
2266002-5	1990	Our results indicate that Cd2+ did not block effector-target conjugate formation, but rather interfered with the hydrolysis of phosphoinositides, as shown by the decrease of inositol trisphosphate (IP3), which is known to release stored Ca2+.	inositol 1,2,3-trisphosphate	174-196	CD2 molecule	Homo sapiens	26-29
2266002-5	1990	Our results indicate that Cd2+ did not block effector-target conjugate formation, but rather interfered with the hydrolysis of phosphoinositides, as shown by the decrease of inositol trisphosphate (IP3), which is known to release stored Ca2+.	Inositol 1,4,5-Trisphosphate	198-201	CD2 molecule	Homo sapiens	26-29
2394762-3	1990	Following this preliminary analysis, lymphocytes were exposed to the metal ions found to inhibit the E-rosette reaction (Fe3+, Ni2+, and Co2+) in order to determine which of the following surface antigens were affected: CD2, CD3, CD4, CD8, CD1, CD22, CD10, and HLA-DR. Our results showed that the in vitro treatment of lymphocytes with Fe3+ or Co2+ caused inhibition of CD2 only, whereas Ni2+ caused inhibition of both CD2 and CD3 antigens.	Metals	69-74	CD2 molecule	Homo sapiens	220-223
2394762-3	1990	Following this preliminary analysis, lymphocytes were exposed to the metal ions found to inhibit the E-rosette reaction (Fe3+, Ni2+, and Co2+) in order to determine which of the following surface antigens were affected: CD2, CD3, CD4, CD8, CD1, CD22, CD10, and HLA-DR. Our results showed that the in vitro treatment of lymphocytes with Fe3+ or Co2+ caused inhibition of CD2 only, whereas Ni2+ caused inhibition of both CD2 and CD3 antigens.	Metals	69-74	CD2 molecule	Homo sapiens	245-248
2394762-3	1990	Following this preliminary analysis, lymphocytes were exposed to the metal ions found to inhibit the E-rosette reaction (Fe3+, Ni2+, and Co2+) in order to determine which of the following surface antigens were affected: CD2, CD3, CD4, CD8, CD1, CD22, CD10, and HLA-DR. Our results showed that the in vitro treatment of lymphocytes with Fe3+ or Co2+ caused inhibition of CD2 only, whereas Ni2+ caused inhibition of both CD2 and CD3 antigens.	Metals	69-74	CD2 molecule	Homo sapiens	245-248
2379381-9	1990	A decreased mean ketanserin elimination half-life (t1/2 = 12 +/- 4 and 10 +/- 3h vs 16 +/- 3 and 18 +/- 4h in healthy controls after oral ketanserin 40mg and intravenous ketanserin 5mg, respectively) contrasted with a substantial increase in t1/2 for ketanserinol (33 +/- 13 vs 19 +/- 4h).	Ketanserin	138-148	CD2 molecule	Homo sapiens	51-99
2379381-9	1990	A decreased mean ketanserin elimination half-life (t1/2 = 12 +/- 4 and 10 +/- 3h vs 16 +/- 3 and 18 +/- 4h in healthy controls after oral ketanserin 40mg and intravenous ketanserin 5mg, respectively) contrasted with a substantial increase in t1/2 for ketanserinol (33 +/- 13 vs 19 +/- 4h).	Ketanserin	138-148	CD2 molecule	Homo sapiens	51-99
1972730-4	1990	CD2 M1 (271-272), CD2 M2 (278-279), and CD2 M4 (264-265) mutants replaced the positively charged adjacent aa histidine and arginine (HR) in the wild-type CD2 sequence with aspartic and glutamic acid (DE) at positions 271-272, 278-279, and 264-265, respectively.	Arginine	123-131	CD2 molecule	Homo sapiens	0-3
1972660-0	1990	Characterization of functional GTP binding proteins in Jurkat T cell mutants lacking either CD3-Ti or CD2 surface receptors.	Guanosine Triphosphate	31-34	CD2 molecule	Homo sapiens	102-105
1972660-6	1990	In the wild type Jurkat cell line as well as in CD3- and CD2- variants, AlF4- can activate the G protein(s) presumably associated with phospholipase C to generate polyphosphoinositide turnover as well as an increase in cytoplasmic free calcium ions.	Calcium	236-243	CD2 molecule	Homo sapiens	57-60
1972730-4	1990	CD2 M1 (271-272), CD2 M2 (278-279), and CD2 M4 (264-265) mutants replaced the positively charged adjacent aa histidine and arginine (HR) in the wild-type CD2 sequence with aspartic and glutamic acid (DE) at positions 271-272, 278-279, and 264-265, respectively.	Histidine	109-118	CD2 molecule	Homo sapiens	0-3
1972730-4	1990	CD2 M1 (271-272), CD2 M2 (278-279), and CD2 M4 (264-265) mutants replaced the positively charged adjacent aa histidine and arginine (HR) in the wild-type CD2 sequence with aspartic and glutamic acid (DE) at positions 271-272, 278-279, and 264-265, respectively.	troxerutin	133-135	CD2 molecule	Homo sapiens	0-3
1972730-4	1990	CD2 M1 (271-272), CD2 M2 (278-279), and CD2 M4 (264-265) mutants replaced the positively charged adjacent aa histidine and arginine (HR) in the wild-type CD2 sequence with aspartic and glutamic acid (DE) at positions 271-272, 278-279, and 264-265, respectively.	troxerutin	133-135	CD2 molecule	Homo sapiens	18-21
1972730-4	1990	CD2 M1 (271-272), CD2 M2 (278-279), and CD2 M4 (264-265) mutants replaced the positively charged adjacent aa histidine and arginine (HR) in the wild-type CD2 sequence with aspartic and glutamic acid (DE) at positions 271-272, 278-279, and 264-265, respectively.	troxerutin	133-135	CD2 molecule	Homo sapiens	18-21
1972730-4	1990	CD2 M1 (271-272), CD2 M2 (278-279), and CD2 M4 (264-265) mutants replaced the positively charged adjacent aa histidine and arginine (HR) in the wild-type CD2 sequence with aspartic and glutamic acid (DE) at positions 271-272, 278-279, and 264-265, respectively.	troxerutin	133-135	CD2 molecule	Homo sapiens	18-21
1972730-4	1990	CD2 M1 (271-272), CD2 M2 (278-279), and CD2 M4 (264-265) mutants replaced the positively charged adjacent aa histidine and arginine (HR) in the wild-type CD2 sequence with aspartic and glutamic acid (DE) at positions 271-272, 278-279, and 264-265, respectively.	aspartic	172-180	CD2 molecule	Homo sapiens	0-3
1972730-4	1990	CD2 M1 (271-272), CD2 M2 (278-279), and CD2 M4 (264-265) mutants replaced the positively charged adjacent aa histidine and arginine (HR) in the wild-type CD2 sequence with aspartic and glutamic acid (DE) at positions 271-272, 278-279, and 264-265, respectively.	Glutamic Acid	185-198	CD2 molecule	Homo sapiens	0-3
1972730-6	1990	Stimulation of transfectants CD2 FL, CD2 M1 (271-272), and CD2 M2 (278-279) with anti-T11(2) + anti-T11(3) antibodies resulted in a rise in cytosolic-free calcium [( Ca2+]i) and subsequent interleukin 2 (IL-2) secretion.	Calcium	155-162	CD2 molecule	Homo sapiens	37-40
1972730-6	1990	Stimulation of transfectants CD2 FL, CD2 M1 (271-272), and CD2 M2 (278-279) with anti-T11(2) + anti-T11(3) antibodies resulted in a rise in cytosolic-free calcium [( Ca2+]i) and subsequent interleukin 2 (IL-2) secretion.	Calcium	155-162	CD2 molecule	Homo sapiens	37-40
1972730-8	1990	Thus, alteration of histidine 264 and/or arginine 265 within the first PPPGHR motif affects the process of signal transduction via CD2, whereas identical mutations in residues at 271-272 or 278-279 were individually without effect.	Histidine	20-29	CD2 molecule	Homo sapiens	131-134
1972730-8	1990	Thus, alteration of histidine 264 and/or arginine 265 within the first PPPGHR motif affects the process of signal transduction via CD2, whereas identical mutations in residues at 271-272 or 278-279 were individually without effect.	Arginine	41-49	CD2 molecule	Homo sapiens	131-134
1970938-10	1990	We also found that, after CD2 stimulation, calcium flux in T cells was normal immediately after engraftment.	Calcium	43-50	CD2 molecule	Homo sapiens	26-29
1970727-0	1990	Stage specific phosphoinositides turnover capacity of human intrathymic T cells following CD2-triggering.	Phosphatidylinositols	15-32	CD2 molecule	Homo sapiens	90-93
2160746-2	1990	Treatment of the cells with diamide decreased their cellular glutathione content to 51.6 +/- 7% of control and significantly decreased their cadmium accumulation both as a function of time and as a function of Cd2+ concentration.	Diamide	28-35	CD2 molecule	Homo sapiens	210-213
1691441-2	1990	Stimulation of these cells with monoclonal antibodies to CD2 induced phosphorylation of the chimeric glycoprotein on tyrosine, receptor downmodulation, and mitogenesis.	Tyrosine	117-125	CD2 molecule	Homo sapiens	57-60
2350543-4	1990	The method is based on the observation that the CD2 rocking modes from the acyl chains of specifically deuterated phospholipids occur at frequencies in the Fourier transform infrared spectrum which depend upon the local geometry (trans or gauche) of the C-C-C skeleton surrounding a central CD2 group.	Phospholipids	114-127	CD2 molecule	Homo sapiens	48-51
2350543-4	1990	The method is based on the observation that the CD2 rocking modes from the acyl chains of specifically deuterated phospholipids occur at frequencies in the Fourier transform infrared spectrum which depend upon the local geometry (trans or gauche) of the C-C-C skeleton surrounding a central CD2 group.	Phospholipids	114-127	CD2 molecule	Homo sapiens	291-294
1970635-0	1990	Glutathione regulates activation-dependent DNA synthesis in highly purified normal human T lymphocytes stimulated via the CD2 and CD3 antigens.	Glutathione	0-11	CD2 molecule	Homo sapiens	122-125
1970635-2	1990	L-Buthionine-(S,R)-sulfoximine (BSO), which inactivates gamma-glutamylcysteine synthetase and therefore inhibits GSH synthesis, inhibited proliferation elicited by monoclonal antibodies directed at cluster designation 2 (CD2) and CD3 antigens, or by sn-1,2-dioctanoylglycerol and ionomycin.	l-buthionine sulfoximine	0-30	CD2 molecule	Homo sapiens	221-224
1970635-2	1990	L-Buthionine-(S,R)-sulfoximine (BSO), which inactivates gamma-glutamylcysteine synthetase and therefore inhibits GSH synthesis, inhibited proliferation elicited by monoclonal antibodies directed at cluster designation 2 (CD2) and CD3 antigens, or by sn-1,2-dioctanoylglycerol and ionomycin.	Buthionine Sulfoximine	32-35	CD2 molecule	Homo sapiens	221-224
1970727-1	1990	Triggering of distinct CD2 epitopes on human T lymphocytes increases their phosphatidylinositol (PI) cycle-related metabolism.	Phosphatidylinositols	75-95	CD2 molecule	Homo sapiens	23-26
2321246-4	1990	MT synthesis measured by following Cd2(+)-induced [35S] incorporation into MT was found not to differ between T20 and T27.	Sulfur-35	51-54	CD2 molecule	Homo sapiens	35-38
2321246-7	1990	The two subpopulations were found to have comparable initial GSH contents, but showed different Cd2(+)-induced changes in [GSH] when the cells were exposed to 5 microM Cd2+.	Glutathione	123-126	CD2 molecule	Homo sapiens	96-99
2321246-7	1990	The two subpopulations were found to have comparable initial GSH contents, but showed different Cd2(+)-induced changes in [GSH] when the cells were exposed to 5 microM Cd2+.	Glutathione	123-126	CD2 molecule	Homo sapiens	168-171
2321246-8	1990	T27 cells maintained their GSH content following Cd2+ exposure but T20 cells showed a Cd2(+)-induced decrease in GSH content.	Glutathione	113-116	CD2 molecule	Homo sapiens	86-89
2332766-3	1990	The complexation of glutathione and related ligands by the nitrilotriacetic acid complex of Cd2+ (Cd(NTA)-) has been investigated by 1H NMR as a model for the coordination chemistry of Cd2+ and GSH in biological systems.	Glutathione	20-31	CD2 molecule	Homo sapiens	92-95
2156931-7	1990	The specificity of CD3/Ti in the Jurkat cell response is demonstrated by the fact that OKT-11(CD2) and anti-CD4 mAb did not stimulate a MAP-2K response.	okt-11	87-93	CD2 molecule	Homo sapiens	94-97
1968928-3	1990	Our results show that arachidonic acid or its derivatives are released after CD2 triggering.	Arachidonic Acid	22-38	CD2 molecule	Homo sapiens	77-80
1968928-5	1990	Extracellular calcium appears to play a critical role because the effects of CD2 mAb were inhibited in a Ca2(+)-depleted medium.	Calcium	14-21	CD2 molecule	Homo sapiens	77-80
2332766-3	1990	The complexation of glutathione and related ligands by the nitrilotriacetic acid complex of Cd2+ (Cd(NTA)-) has been investigated by 1H NMR as a model for the coordination chemistry of Cd2+ and GSH in biological systems.	Glutathione	20-31	CD2 molecule	Homo sapiens	185-188
2332766-3	1990	The complexation of glutathione and related ligands by the nitrilotriacetic acid complex of Cd2+ (Cd(NTA)-) has been investigated by 1H NMR as a model for the coordination chemistry of Cd2+ and GSH in biological systems.	Nitrilotriacetic Acid	59-80	CD2 molecule	Homo sapiens	92-95
2332766-3	1990	The complexation of glutathione and related ligands by the nitrilotriacetic acid complex of Cd2+ (Cd(NTA)-) has been investigated by 1H NMR as a model for the coordination chemistry of Cd2+ and GSH in biological systems.	Nitrilotriacetic Acid	59-80	CD2 molecule	Homo sapiens	185-188
2332766-3	1990	The complexation of glutathione and related ligands by the nitrilotriacetic acid complex of Cd2+ (Cd(NTA)-) has been investigated by 1H NMR as a model for the coordination chemistry of Cd2+ and GSH in biological systems.	cd(nta)	98-105	CD2 molecule	Homo sapiens	92-95
2332766-3	1990	The complexation of glutathione and related ligands by the nitrilotriacetic acid complex of Cd2+ (Cd(NTA)-) has been investigated by 1H NMR as a model for the coordination chemistry of Cd2+ and GSH in biological systems.	cd(nta)	98-105	CD2 molecule	Homo sapiens	185-188
2332766-3	1990	The complexation of glutathione and related ligands by the nitrilotriacetic acid complex of Cd2+ (Cd(NTA)-) has been investigated by 1H NMR as a model for the coordination chemistry of Cd2+ and GSH in biological systems.	Hydrogen	133-135	CD2 molecule	Homo sapiens	92-95
2332766-3	1990	The complexation of glutathione and related ligands by the nitrilotriacetic acid complex of Cd2+ (Cd(NTA)-) has been investigated by 1H NMR as a model for the coordination chemistry of Cd2+ and GSH in biological systems.	Glutathione	194-197	CD2 molecule	Homo sapiens	92-95
2332766-8	1990	The results indicate that formation constants for binding of a thiolate donor group by Cd2+, either as the free ion or in a coordinately unsaturated complex, are in the range 10(5)-10(6).	thiolate	63-71	CD2 molecule	Homo sapiens	87-90
1690148-0	1990	An activating combination of CD2 antibodies stimulates tyrosine phosphorylation in a T lymphocyte cell line.	Tyrosine	55-63	CD2 molecule	Homo sapiens	29-32
2354220-4	1990	Cd2+ (5 mM) causes a complete inhibition of active Ca2+ transport, whereas Mn2+ and Mg2+ inhibit this process by 85% and 35%, respectively; amiloride (500 microM) is fairly ineffective.	Amiloride	140-149	CD2 molecule	Homo sapiens	0-3
2135667-7	1990	In [3H]ethanolamine-prelabeled cells, but not in [3H]choline-prelabeled cells, PHA, CD3 and CD2 induced the breakdown of PC.	Phosphatidylcholines	121-123	CD2 molecule	Homo sapiens	92-95
2135667-1	1990	Activation of Jurkat T cells with either phytohemagglutinin (PHA), CD3 or CD2 monoclonal antibodies (mAbs) induces the production of diacylglycerol (DAG) from two different sources.	Diglycerides	133-147	CD2 molecule	Homo sapiens	74-77
2135667-1	1990	Activation of Jurkat T cells with either phytohemagglutinin (PHA), CD3 or CD2 monoclonal antibodies (mAbs) induces the production of diacylglycerol (DAG) from two different sources.	Diglycerides	149-152	CD2 molecule	Homo sapiens	74-77
1690148-1	1990	The activating combination of CD2 antibodies Leu-5b plus 9.1 stimulates tyrosine phosphorylation in the human T cell line Jurkat.	Tyrosine	72-80	CD2 molecule	Homo sapiens	30-33
1690148-3	1990	These data provide evidence that signal transduction by the CD2 receptor is coupled to an increase in tyrosine phosphorylation that is similar to that coupled to the CD3 receptor.	Tyrosine	102-110	CD2 molecule	Homo sapiens	60-63
1970158-3	1990	The current components which could be suppressed by addition of Cd2+ to the perfusate were taken as presynaptic iCa.	isocyanic acid	112-115	CD2 molecule	Homo sapiens	64-67
1970158-5	1990	If the electrode was perfused with Ringer"s solution containing the blockers for iNa and iK, the same, obviously complete block of iCa was obtained by 50 and 100 microM Cd2+, an average of 96% block by 20 microM Cd2+ and 50% block by about 5 microM Cd2+.	isocyanic acid	131-134	CD2 molecule	Homo sapiens	169-172
1970158-5	1990	If the electrode was perfused with Ringer"s solution containing the blockers for iNa and iK, the same, obviously complete block of iCa was obtained by 50 and 100 microM Cd2+, an average of 96% block by 20 microM Cd2+ and 50% block by about 5 microM Cd2+.	isocyanic acid	131-134	CD2 molecule	Homo sapiens	212-215
1970158-5	1990	If the electrode was perfused with Ringer"s solution containing the blockers for iNa and iK, the same, obviously complete block of iCa was obtained by 50 and 100 microM Cd2+, an average of 96% block by 20 microM Cd2+ and 50% block by about 5 microM Cd2+.	isocyanic acid	131-134	CD2 molecule	Homo sapiens	212-215
1970158-7	1990	When the electrode was perfused with Ringer"s solution containing TTX, 20 microM Cd2+ added to the perfusate reduced the rate of phasic release of quanta insignificantly for short depolarizing pulses and by a factor of about 10 for longer pulses.	Tetrodotoxin	66-69	CD2 molecule	Homo sapiens	81-84
2157839-20	1990	The transient and sustained Ba2+ currents in F-11 cells were reversibly blocked by brief exposure to Cd2+ or Ni2+.	N-methyl-valyl-amiclenomycin	28-32	CD2 molecule	Homo sapiens	101-104
1688586-4	1990	The phosphorylated zeta-polypeptide of CD2-activated cells was immunoprecipitated with antiphosphotyrosine antibodies and migrated to a 21- to 23-kDa position during SDS/PAGE.	Sodium Dodecyl Sulfate	166-169	CD2 molecule	Homo sapiens	39-42
1688586-5	1990	These results indicate that stimulation of human T cells via the CD2 Ag with the T11(2) and T11(3) mAb activates not only protein kinase C but also tyrosine kinase(s), resulting in the phosphorylation of the CD3 gamma-chain and the tyrosine phosphorylation of the zeta-chain, respectively.	Tyrosine	148-156	CD2 molecule	Homo sapiens	65-68
1982385-0	1990	Energy donor-dependent effect of Cd2+ on [14C]glutamate transport in Staphylococcus aureus.	Glutamic Acid	46-55	CD2 molecule	Homo sapiens	33-36
1982385-1	1990	In starved cells of Cd2(+)-sensitive Staphylococcus aureus 17810S preloaded with either glutamate or pyruvate, [14C]glutamate transport was blocked by 10 microM Cd2+, whereas in cells preloaded with lactate, [14C]glutamate transport was not affected.	Glutamic Acid	88-97	CD2 molecule	Homo sapiens	20-23
1982385-1	1990	In starved cells of Cd2(+)-sensitive Staphylococcus aureus 17810S preloaded with either glutamate or pyruvate, [14C]glutamate transport was blocked by 10 microM Cd2+, whereas in cells preloaded with lactate, [14C]glutamate transport was not affected.	Glutamic Acid	88-97	CD2 molecule	Homo sapiens	161-164
1982385-1	1990	In starved cells of Cd2(+)-sensitive Staphylococcus aureus 17810S preloaded with either glutamate or pyruvate, [14C]glutamate transport was blocked by 10 microM Cd2+, whereas in cells preloaded with lactate, [14C]glutamate transport was not affected.	Pyruvic Acid	101-109	CD2 molecule	Homo sapiens	161-164
1982385-1	1990	In starved cells of Cd2(+)-sensitive Staphylococcus aureus 17810S preloaded with either glutamate or pyruvate, [14C]glutamate transport was blocked by 10 microM Cd2+, whereas in cells preloaded with lactate, [14C]glutamate transport was not affected.	Carbon-14	112-115	CD2 molecule	Homo sapiens	20-23
1982385-1	1990	In starved cells of Cd2(+)-sensitive Staphylococcus aureus 17810S preloaded with either glutamate or pyruvate, [14C]glutamate transport was blocked by 10 microM Cd2+, whereas in cells preloaded with lactate, [14C]glutamate transport was not affected.	Carbon-14	112-115	CD2 molecule	Homo sapiens	161-164
1982385-1	1990	In starved cells of Cd2(+)-sensitive Staphylococcus aureus 17810S preloaded with either glutamate or pyruvate, [14C]glutamate transport was blocked by 10 microM Cd2+, whereas in cells preloaded with lactate, [14C]glutamate transport was not affected.	Glutamic Acid	116-125	CD2 molecule	Homo sapiens	20-23
1982385-1	1990	In starved cells of Cd2(+)-sensitive Staphylococcus aureus 17810S preloaded with either glutamate or pyruvate, [14C]glutamate transport was blocked by 10 microM Cd2+, whereas in cells preloaded with lactate, [14C]glutamate transport was not affected.	Glutamic Acid	116-125	CD2 molecule	Homo sapiens	161-164
1982385-1	1990	In starved cells of Cd2(+)-sensitive Staphylococcus aureus 17810S preloaded with either glutamate or pyruvate, [14C]glutamate transport was blocked by 10 microM Cd2+, whereas in cells preloaded with lactate, [14C]glutamate transport was not affected.	Lactic Acid	199-206	CD2 molecule	Homo sapiens	161-164
1982385-1	1990	In starved cells of Cd2(+)-sensitive Staphylococcus aureus 17810S preloaded with either glutamate or pyruvate, [14C]glutamate transport was blocked by 10 microM Cd2+, whereas in cells preloaded with lactate, [14C]glutamate transport was not affected.	Carbon-14	209-212	CD2 molecule	Homo sapiens	161-164
1982385-1	1990	In starved cells of Cd2(+)-sensitive Staphylococcus aureus 17810S preloaded with either glutamate or pyruvate, [14C]glutamate transport was blocked by 10 microM Cd2+, whereas in cells preloaded with lactate, [14C]glutamate transport was not affected.	Glutamic Acid	116-125	CD2 molecule	Homo sapiens	20-23
1982385-1	1990	In starved cells of Cd2(+)-sensitive Staphylococcus aureus 17810S preloaded with either glutamate or pyruvate, [14C]glutamate transport was blocked by 10 microM Cd2+, whereas in cells preloaded with lactate, [14C]glutamate transport was not affected.	Glutamic Acid	116-125	CD2 molecule	Homo sapiens	161-164
1982385-2	1990	This differential effect of Cd2+ could be due to the presence or absence of dithiols in the substrate oxidizing systems.	dithiol	76-84	CD2 molecule	Homo sapiens	28-31
1982385-3	1990	In starved cells of Cd2(+)-resistant strain 17810R preloaded with either of the three substrates, [14C]glutamate transport was insensitive to 10 microM Cd2+.	Carbon-14	99-102	CD2 molecule	Homo sapiens	20-23
1982385-3	1990	In starved cells of Cd2(+)-resistant strain 17810R preloaded with either of the three substrates, [14C]glutamate transport was insensitive to 10 microM Cd2+.	Glutamic Acid	103-112	CD2 molecule	Homo sapiens	20-23
2148867-1	1990	Certain heavy metal actions such as Cd2+ and Pb2+ mimic Ca2+ effectively in stimulating calmodulin (CaM).	Metals	14-19	CD2 molecule	Homo sapiens	36-39
2148867-6	1990	However, after reconstitution of CDTA-treated skeletal myofibril with TnC, the response of ATPase to Ca2+, Cd2+ or Pb2+ was restored.	CDTA	33-37	CD2 molecule	Homo sapiens	107-110
1697005-8	1990	The most frequently observed CD groups among T ALL cells were CD5 (100% and 88.9% in children and adults respectively), CD7 (93.1% and 84.6%) and CD2 (76.7% and 76.9%).	Cadmium	29-31	CD2 molecule	Homo sapiens	146-149
1688586-0	1990	Activation of human T lymphocytes via the CD2 antigen results in tyrosine phosphorylation of T cell antigen receptor zeta-chains.	Tyrosine	65-73	CD2 molecule	Homo sapiens	42-45
1982219-4	1990	Evidence was obtained that paf inhibited T cell proliferation induced by immobilized CD3 mAb (OKT3i), but potentiated that induced by a combination with the CD2 mAb, anti-(T11.1 + D66).	Platelet Activating Factor	27-30	CD2 molecule	Homo sapiens	157-160
1982219-12	1990	When considered together, these data demonstrate that paf, a phospholipid cytokine released during inflammatory reactions, play a differential regulatory role in T cell activation induced via the CD3 and CD2 (T11.1 + D66) pathways.	Platelet Activating Factor	54-57	CD2 molecule	Homo sapiens	204-207
33825448-5	2021	Y3+ attracts extra F- ions from P5+ and Cd2+ during crystallization because of its stronger ability to attract F- ions, leading to most Y3+ ions being crystallized into the NaYF4 crystals.	y3+	0-3	CD2 molecule	Homo sapiens	40-43
6893328-1	1980	Binding of Cd2+ to concanavalin A and the subsequent induction of saccharide-binding activity has been studied at pH 6.5.	Carbohydrates	66-76	CD2 molecule	Homo sapiens	11-14
6893328-2	1980	We found that Cd2+ bound to both metal sites, S1 and S2, and that Cd2+ alone would induce sugar binding in concanavalin A.	Metals	33-38	CD2 molecule	Homo sapiens	14-17
6893328-2	1980	We found that Cd2+ bound to both metal sites, S1 and S2, and that Cd2+ alone would induce sugar binding in concanavalin A.	Sugars	90-95	CD2 molecule	Homo sapiens	66-69
6893328-3	1980	Using the fluorescent sugar 4-methylumbelliferyl alpha-D-mannopyranoside we determined that full saccharide-binding activity was obtained only when the total bound Cd2+ stoichiometry reached 2 ions/concanavalin A subunit.	sugar 4-methylumbelliferyl alpha-d-mannopyranoside	22-72	CD2 molecule	Homo sapiens	164-167
6893328-3	1980	Using the fluorescent sugar 4-methylumbelliferyl alpha-D-mannopyranoside we determined that full saccharide-binding activity was obtained only when the total bound Cd2+ stoichiometry reached 2 ions/concanavalin A subunit.	Carbohydrates	97-107	CD2 molecule	Homo sapiens	164-167
6893328-4	1980	We also report evidence suggesting that the binding of Cd2+ to S2 is the crucial step in activation and that Cd2+ binding to S1 induces a form of concanavalin A similar to that induced by Zn2+, Ni2+, or Co2+ and different from that induced by Mn2+.	Manganese(2+)	243-247	CD2 molecule	Homo sapiens	109-112
33798824-5	2021	In this study, we investigated the effect of the simultaneous exposure of Cd2+ and nano Fe2O3 on conjugative transfer of plasmid RP4 from Pseudomonas putida KT2442 to water microbial community.	kt2442	157-163	CD2 molecule	Homo sapiens	74-77
33798824-5	2021	In this study, we investigated the effect of the simultaneous exposure of Cd2+ and nano Fe2O3 on conjugative transfer of plasmid RP4 from Pseudomonas putida KT2442 to water microbial community.	Water	167-172	CD2 molecule	Homo sapiens	74-77
33798824-9	2021	The mechanisms of the exacerbated conjugative transfer of ARGs were involved in the enhancement of cell membrane permeability, antioxidant enzyme activities, and mRNA expression levels of the conjugation genes by the co-effect of Cd2+ and nano Fe2O3.	args	58-62	CD2 molecule	Homo sapiens	230-233
33798824-10	2021	This study confirmed that the simultaneous exposure to Cd2+and nano Fe2O3 exerted a synergetic co-effect on plasmid-mediated conjunctive transfer of ARGs, emphasizing that the co-effect of nanomaterials and heavy metals should be prudently evaluated when combating antibiotic resistance.	args	149-153	CD2 molecule	Homo sapiens	55-58
33825448-5	2021	Y3+ attracts extra F- ions from P5+ and Cd2+ during crystallization because of its stronger ability to attract F- ions, leading to most Y3+ ions being crystallized into the NaYF4 crystals.	y3+	136-139	CD2 molecule	Homo sapiens	40-43
33813292-4	2021	Owing to the strong adsorption of Cd2+ by BMBC, the presence of BMBC in the medium led to a decrease in effluent Cd2+.	bmbc	42-46	CD2 molecule	Homo sapiens	34-37
33813292-4	2021	Owing to the strong adsorption of Cd2+ by BMBC, the presence of BMBC in the medium led to a decrease in effluent Cd2+.	bmbc	42-46	CD2 molecule	Homo sapiens	113-116
33813292-5	2021	The presence of Cd2+ in the solution slightly inhibited the transport of BMBC.	bmbc	73-77	CD2 molecule	Homo sapiens	16-19
33813292-6	2021	The transport of Cd2+ was facilitated by BMBC due to the high affinity.	bmbc	41-45	CD2 molecule	Homo sapiens	17-20
31755702-2	2019	Among the metal-dependent HDAC isozymes, HDAC6 is unique in that it contains two catalytic domains, CD1 and CD2.	Metals	10-15	CD2 molecule	Homo sapiens	108-111
33767048-4	2021	The results indicated that STB has the highest surface area (49.71 m2/g), more inorganic minerals (Kaolinite) as well as relatively stable physicochemical properties with 10% tire particles (TP) at 700  C. The adsorption results indicated that the pseudo-second-order equation and Langmuir isotherm model could better describe the adsorption of Cd2+ and TC by STB.	stb	27-30	CD2 molecule	Homo sapiens	345-348
33590399-0	2021	Adsorption mechanism of Zn2+, Ni2+, Cd2+, and Cu2+ ions by carbon-based adsorbents: interpretation of the adsorption isotherms via physical modelling.	Carbon	59-65	CD2 molecule	Homo sapiens	36-39
33590399-1	2021	A theoretical physicochemical and thermodynamic investigation of the adsorption of heavy metals Zn2+, Cd2+, Ni2+, and Cu2+on carbon-based adsorbents was performed with statistical physics fundaments.	Carbon	125-131	CD2 molecule	Homo sapiens	102-105
24520713-0	2013	Removal of Cd2+ from water by Friedel"s salt (FS: 3CaO x A12O3 x CaCI2 x 10H2O): sorption characteristics and mechanisms.	Water	21-26	CD2 molecule	Homo sapiens	11-14
32797863-6	2020	Intracellular free Cd2+ cation and Cd-MTs are identified, along with Cd2+ transformation to Cd-glutathione (GSH) adduct/complex, as further demonstrated by ESI-MS.	Glutathione	108-111	CD2 molecule	Homo sapiens	69-72
25792026-0	2015	Simultaneous spectrophotometric determination of Cu2+, Hg2+, and Cd2+ ions using 2-(3-hydroxy-1-methylbut-2-enylideneamino)pyridine-3-ol.	2-(3-hydroxy-1-methylbut-2-enylideneamino)pyridine-3-ol	81-136	CD2 molecule	Homo sapiens	65-68
25792026-1	2015	New complexes of Cu2+, Hg2+, and Cd2+ with a recently synthesized Schiff base derived from 2-(3-hydroxy-1-methylbut-2-enylideneamino)pyridine-3-ol were applied for their simultaneous determination with artificial neural networks.	Schiff Bases	66-77	CD2 molecule	Homo sapiens	33-36
25792026-1	2015	New complexes of Cu2+, Hg2+, and Cd2+ with a recently synthesized Schiff base derived from 2-(3-hydroxy-1-methylbut-2-enylideneamino)pyridine-3-ol were applied for their simultaneous determination with artificial neural networks.	2-(3-hydroxy-1-methylbut-2-enylideneamino)pyridine-3-ol	91-146	CD2 molecule	Homo sapiens	33-36
25792026-8	2015	Under the working conditions, the proposed methods were successfully applied to simultaneous determination of Hg2+, Cu2+, and Cd2+ in different water and soil samples.	Water	144-149	CD2 molecule	Homo sapiens	126-129
32797863-3	2020	The incorporation of sodium dodecyl sulfate (SDS) in running buffer significantly reduces the peak width of Cd2+from 170 s to 26 s in the electrophoretogram, causing a 5.3-fold improvement on the sensitivity.	Sodium Dodecyl Sulfate	21-43	CD2 molecule	Homo sapiens	108-111
32797863-3	2020	The incorporation of sodium dodecyl sulfate (SDS) in running buffer significantly reduces the peak width of Cd2+from 170 s to 26 s in the electrophoretogram, causing a 5.3-fold improvement on the sensitivity.	Sodium Dodecyl Sulfate	45-48	CD2 molecule	Homo sapiens	108-111
32797863-5	2020	The transformation of cadmium in HepG2 and MCF-7 cells is evaluated after their incubation with Cd2+ reinforced culture medium.	Cadmium	22-29	CD2 molecule	Homo sapiens	96-99
32797863-6	2020	Intracellular free Cd2+ cation and Cd-MTs are identified, along with Cd2+ transformation to Cd-glutathione (GSH) adduct/complex, as further demonstrated by ESI-MS.	cd-glutathione	92-106	CD2 molecule	Homo sapiens	19-22
32797863-6	2020	Intracellular free Cd2+ cation and Cd-MTs are identified, along with Cd2+ transformation to Cd-glutathione (GSH) adduct/complex, as further demonstrated by ESI-MS.	cd-glutathione	92-106	CD2 molecule	Homo sapiens	69-72
32797863-6	2020	Intracellular free Cd2+ cation and Cd-MTs are identified, along with Cd2+ transformation to Cd-glutathione (GSH) adduct/complex, as further demonstrated by ESI-MS.	Glutathione	108-111	CD2 molecule	Homo sapiens	19-22
24520713-2	2013	In this study, Friedel"s salt (FS: 3CaO x A12O3 x CaCl2 x10H2O), a hexagonal layered inorganic absorbent, was synthesized to remove Cd2+ from water.	Friedel's salt	15-29	CD2 molecule	Homo sapiens	132-135
24520713-2	2013	In this study, Friedel"s salt (FS: 3CaO x A12O3 x CaCl2 x10H2O), a hexagonal layered inorganic absorbent, was synthesized to remove Cd2+ from water.	Fluorine	31-33	CD2 molecule	Homo sapiens	132-135
24520713-2	2013	In this study, Friedel"s salt (FS: 3CaO x A12O3 x CaCl2 x10H2O), a hexagonal layered inorganic absorbent, was synthesized to remove Cd2+ from water.	cacl2 x10h2o	50-62	CD2 molecule	Homo sapiens	132-135
7843095-1	1994	Cd2+ provokes an immediate production of inositol trisphosphate and the release of Ca2+ from internal stores in human fibroblasts and some other mammalian cells.	inositol 1,2,3-trisphosphate	41-63	CD2 molecule	Homo sapiens	0-3
8530919-8	1995	The interaction between Cd2+ and maleimide spin labeled (MSL) SPT was studied by the ESR method.	maleimide	33-42	CD2 molecule	Homo sapiens	24-27
8530919-10	1995	The conjugation of maleimide with thiol group results in the decrease of Cd2+ high-affinitive binding sites from 6 to 1.	maleimide	19-28	CD2 molecule	Homo sapiens	73-76
8530919-10	1995	The conjugation of maleimide with thiol group results in the decrease of Cd2+ high-affinitive binding sites from 6 to 1.	Sulfhydryl Compounds	34-39	CD2 molecule	Homo sapiens	73-76
7843095-2	1994	Ni2+, Co2+, Fe2+, and Mn2+ evoke the release of stored Ca2+, but are less potent than Cd2+ (apparent K0.5 = 40 nM).	Manganese(2+)	22-26	CD2 molecule	Homo sapiens	86-89
7843095-3	1994	Zn2+ and Cu2+ competitively inhibit Ca2+ release evoked by Cd2+ without affecting Ca2+ release by hormones such as bradykinin.	Zinc	0-4	CD2 molecule	Homo sapiens	59-62
34920220-1	2022	A new strategy that simultaneous use of KHCO3 activated biochar and nano-MgO incorporation for Pb2+ and Cd2+ removal from water was raised.	potassium bicarbonate	40-45	CD2 molecule	Homo sapiens	104-107
34920220-1	2022	A new strategy that simultaneous use of KHCO3 activated biochar and nano-MgO incorporation for Pb2+ and Cd2+ removal from water was raised.	mgo	73-76	CD2 molecule	Homo sapiens	104-107
34920220-1	2022	A new strategy that simultaneous use of KHCO3 activated biochar and nano-MgO incorporation for Pb2+ and Cd2+ removal from water was raised.	Water	122-127	CD2 molecule	Homo sapiens	104-107
34920220-3	2022	The synthesized MgO-K-BC had a large adsorption capacity for Pb2+ (1625.5 mg/g) and Cd2+ (480.8 mg/g).	mgo-k-bc	16-24	CD2 molecule	Homo sapiens	84-87
34920220-4	2022	Multiple characterization and comparative test have been performed to demonstrate that ion-exchange, precipitation, and complexation are the main mechanisms for Pb2+ and Cd2+ removal by MgO-K-BC.	mgo-k-bc	186-194	CD2 molecule	Homo sapiens	170-173
34920220-6	2022	The O-top of MgO was the most stable adsorption site for Pb2+/Cd2+ adsorption compared with other adsorption sites (Mg-top, bridge, and hollow).	mgo	13-16	CD2 molecule	Homo sapiens	62-65
34920220-6	2022	The O-top of MgO was the most stable adsorption site for Pb2+/Cd2+ adsorption compared with other adsorption sites (Mg-top, bridge, and hollow).	Lead(2+)	57-61	CD2 molecule	Homo sapiens	62-65
34920220-7	2022	In addition, the results of charge density maps and projected density of state (PDOS) showed that the overlap of electron cloud and orbits between MgO and Pb2+ were denser than Cd2+, indicating that MgO-K-BC had a stronger affinity for Pb2+ than Cd2+, so that, MgO-K-BC had a higher adsorption capacity for Pb2+ than Cd2+.	mgo	147-150	CD2 molecule	Homo sapiens	246-249
34920220-7	2022	In addition, the results of charge density maps and projected density of state (PDOS) showed that the overlap of electron cloud and orbits between MgO and Pb2+ were denser than Cd2+, indicating that MgO-K-BC had a stronger affinity for Pb2+ than Cd2+, so that, MgO-K-BC had a higher adsorption capacity for Pb2+ than Cd2+.	mgo	147-150	CD2 molecule	Homo sapiens	317-320
34920220-7	2022	In addition, the results of charge density maps and projected density of state (PDOS) showed that the overlap of electron cloud and orbits between MgO and Pb2+ were denser than Cd2+, indicating that MgO-K-BC had a stronger affinity for Pb2+ than Cd2+, so that, MgO-K-BC had a higher adsorption capacity for Pb2+ than Cd2+.	Lead(2+)	155-159	CD2 molecule	Homo sapiens	246-249
34920220-7	2022	In addition, the results of charge density maps and projected density of state (PDOS) showed that the overlap of electron cloud and orbits between MgO and Pb2+ were denser than Cd2+, indicating that MgO-K-BC had a stronger affinity for Pb2+ than Cd2+, so that, MgO-K-BC had a higher adsorption capacity for Pb2+ than Cd2+.	Lead(2+)	155-159	CD2 molecule	Homo sapiens	317-320
34920220-7	2022	In addition, the results of charge density maps and projected density of state (PDOS) showed that the overlap of electron cloud and orbits between MgO and Pb2+ were denser than Cd2+, indicating that MgO-K-BC had a stronger affinity for Pb2+ than Cd2+, so that, MgO-K-BC had a higher adsorption capacity for Pb2+ than Cd2+.	mgo-k-bc	199-207	CD2 molecule	Homo sapiens	177-180
34920220-7	2022	In addition, the results of charge density maps and projected density of state (PDOS) showed that the overlap of electron cloud and orbits between MgO and Pb2+ were denser than Cd2+, indicating that MgO-K-BC had a stronger affinity for Pb2+ than Cd2+, so that, MgO-K-BC had a higher adsorption capacity for Pb2+ than Cd2+.	Lead(2+)	236-240	CD2 molecule	Homo sapiens	177-180
34920220-7	2022	In addition, the results of charge density maps and projected density of state (PDOS) showed that the overlap of electron cloud and orbits between MgO and Pb2+ were denser than Cd2+, indicating that MgO-K-BC had a stronger affinity for Pb2+ than Cd2+, so that, MgO-K-BC had a higher adsorption capacity for Pb2+ than Cd2+.	Lead(2+)	236-240	CD2 molecule	Homo sapiens	317-320
34920220-7	2022	In addition, the results of charge density maps and projected density of state (PDOS) showed that the overlap of electron cloud and orbits between MgO and Pb2+ were denser than Cd2+, indicating that MgO-K-BC had a stronger affinity for Pb2+ than Cd2+, so that, MgO-K-BC had a higher adsorption capacity for Pb2+ than Cd2+.	mgo-k-bc	261-269	CD2 molecule	Homo sapiens	177-180
34920220-7	2022	In addition, the results of charge density maps and projected density of state (PDOS) showed that the overlap of electron cloud and orbits between MgO and Pb2+ were denser than Cd2+, indicating that MgO-K-BC had a stronger affinity for Pb2+ than Cd2+, so that, MgO-K-BC had a higher adsorption capacity for Pb2+ than Cd2+.	mgo-k-bc	261-269	CD2 molecule	Homo sapiens	246-249
34920220-7	2022	In addition, the results of charge density maps and projected density of state (PDOS) showed that the overlap of electron cloud and orbits between MgO and Pb2+ were denser than Cd2+, indicating that MgO-K-BC had a stronger affinity for Pb2+ than Cd2+, so that, MgO-K-BC had a higher adsorption capacity for Pb2+ than Cd2+.	Lead(2+)	307-311	CD2 molecule	Homo sapiens	177-180
34920220-7	2022	In addition, the results of charge density maps and projected density of state (PDOS) showed that the overlap of electron cloud and orbits between MgO and Pb2+ were denser than Cd2+, indicating that MgO-K-BC had a stronger affinity for Pb2+ than Cd2+, so that, MgO-K-BC had a higher adsorption capacity for Pb2+ than Cd2+.	Lead(2+)	307-311	CD2 molecule	Homo sapiens	246-249
34929593-0	2022	New insights into the capture performance and mechanism of hazardous metals Cr3+ and Cd2+ onto an effective layered double hydroxide based material.	hydroxide ion	123-132	CD2 molecule	Homo sapiens	85-88
34929593-3	2022	The strong chelation of the phosphonate groups with heavy metal ions proved it an excellent adsorbent leading to a maximum adsorption capacity of 156.95 mg/g (Cr3+) and 198.34 mg/g (Cd2+) separately.	Organophosphonates	28-39	CD2 molecule	Homo sapiens	182-185
34929593-3	2022	The strong chelation of the phosphonate groups with heavy metal ions proved it an excellent adsorbent leading to a maximum adsorption capacity of 156.95 mg/g (Cr3+) and 198.34 mg/g (Cd2+) separately.	Metals	58-63	CD2 molecule	Homo sapiens	182-185
34742969-2	2022	In this study, the comparative transport behaviors of Cd2+ and CrO42- in water-saturated soil columns were investigated under a variety of hydrochemical and hydraulic conditions such as pH, ionic strength (IS), and flow rate.	Water	73-78	CD2 molecule	Homo sapiens	54-57
7843095-3	1994	Zn2+ and Cu2+ competitively inhibit Ca2+ release evoked by Cd2+ without affecting Ca2+ release by hormones such as bradykinin.	cupric ion	9-13	CD2 molecule	Homo sapiens	59-62
7843095-8	1994	Cd2+ and other stimuli that raise cytosolic-free Ca2+ induce cyclic (AMP) production, apparently by activating a calmodulin-dependent adenylyl cyclase.	cyclic (	61-69	CD2 molecule	Homo sapiens	0-3
7843095-8	1994	Cd2+ and other stimuli that raise cytosolic-free Ca2+ induce cyclic (AMP) production, apparently by activating a calmodulin-dependent adenylyl cyclase.	Adenosine Monophosphate	69-73	CD2 molecule	Homo sapiens	0-3
34762884-4	2022	Moreover, even in the presence of other potentially interfering toxic metal ions such as As3+, Cd2+ and Pb2+, Cd/Zr-UiO-66 (1:9) still presented good anti-interference abilities.	Metals	70-75	CD2 molecule	Homo sapiens	95-98
34762884-4	2022	Moreover, even in the presence of other potentially interfering toxic metal ions such as As3+, Cd2+ and Pb2+, Cd/Zr-UiO-66 (1:9) still presented good anti-interference abilities.	Cadmium	110-112	CD2 molecule	Homo sapiens	95-98
34762884-4	2022	Moreover, even in the presence of other potentially interfering toxic metal ions such as As3+, Cd2+ and Pb2+, Cd/Zr-UiO-66 (1:9) still presented good anti-interference abilities.	zr-uio-66	113-122	CD2 molecule	Homo sapiens	95-98
34968939-0	2022	Efficient removal of Cd2+ from aqueous solution with a novel composite of silicon supported nano iron/aluminum/magnesium (hydr)oxides prepared from biotite.	Silicon	74-81	CD2 molecule	Homo sapiens	21-24
34929268-2	2022	In this study, a novel modified gangue material (MGE) is synthesized from coal gangue (GE) through a low-temperature assisted with alkali roasting method, and is applied to the immobilization of cadmium (Cd2+) in contaminated soil.	Cadmium	195-202	CD2 molecule	Homo sapiens	204-207
34929268-4	2022	The results showed that a large number of active groups (Si-O, Al-O, Fe-O, -OH, -CO, and -COOH) are observed on the surface of MGE, which is conducive to the removal of Cd2+.	Silicon	57-59	CD2 molecule	Homo sapiens	169-172
34929268-4	2022	The results showed that a large number of active groups (Si-O, Al-O, Fe-O, -OH, -CO, and -COOH) are observed on the surface of MGE, which is conducive to the removal of Cd2+.	Aluminum	63-65	CD2 molecule	Homo sapiens	169-172
34929268-4	2022	The results showed that a large number of active groups (Si-O, Al-O, Fe-O, -OH, -CO, and -COOH) are observed on the surface of MGE, which is conducive to the removal of Cd2+.	Carbon Monoxide	81-83	CD2 molecule	Homo sapiens	169-172
34929268-4	2022	The results showed that a large number of active groups (Si-O, Al-O, Fe-O, -OH, -CO, and -COOH) are observed on the surface of MGE, which is conducive to the removal of Cd2+.	Carbonic Acid	90-94	CD2 molecule	Homo sapiens	169-172
34929284-3	2022	The results showed that the mobility of different metal ions followed the order of Cd2+ < Zn2+ < Ni2+ < Mn2+ < Co2+ despite of LMWOAs-free or LMWOAs-addition.	Metals	50-55	CD2 molecule	Homo sapiens	83-86
34968939-0	2022	Efficient removal of Cd2+ from aqueous solution with a novel composite of silicon supported nano iron/aluminum/magnesium (hydr)oxides prepared from biotite.	Iron	97-101	CD2 molecule	Homo sapiens	21-24
34968939-0	2022	Efficient removal of Cd2+ from aqueous solution with a novel composite of silicon supported nano iron/aluminum/magnesium (hydr)oxides prepared from biotite.	Aluminum	102-110	CD2 molecule	Homo sapiens	21-24
34968939-0	2022	Efficient removal of Cd2+ from aqueous solution with a novel composite of silicon supported nano iron/aluminum/magnesium (hydr)oxides prepared from biotite.	Magnesium Hydroxide	111-133	CD2 molecule	Homo sapiens	21-24
34968939-1	2022	Taking low cost silicate minerals to develop efficient Cd2+ adsorption materials was favorable to the comprehensive utilization of minerals and remediation of environmental pollution.	Silicates	16-24	CD2 molecule	Homo sapiens	55-58
34968939-2	2022	In this study, a composite of silicon supported nano iron/aluminum/magnesium (hydr)oxides was prepared with biotite by combining acid leaching and base precipitation process, which was used to remove Cd2+.	Silicon	30-37	CD2 molecule	Homo sapiens	200-203
34991009-3	2022	Orange-red emissive carbon dots (OR-CDs), prepared from the calcination of selected carbon sources 5-amino-1, 10-phenanthroline (Aphen) and salicylic acid (SA), were found to act as a "turn on" type fluorescence probe for Cd2+ detection.	Carbon	20-26	CD2 molecule	Homo sapiens	222-225
34991009-3	2022	Orange-red emissive carbon dots (OR-CDs), prepared from the calcination of selected carbon sources 5-amino-1, 10-phenanthroline (Aphen) and salicylic acid (SA), were found to act as a "turn on" type fluorescence probe for Cd2+ detection.	Cadmium	36-39	CD2 molecule	Homo sapiens	222-225
34991009-3	2022	Orange-red emissive carbon dots (OR-CDs), prepared from the calcination of selected carbon sources 5-amino-1, 10-phenanthroline (Aphen) and salicylic acid (SA), were found to act as a "turn on" type fluorescence probe for Cd2+ detection.	Carbon	84-90	CD2 molecule	Homo sapiens	222-225
34991009-3	2022	Orange-red emissive carbon dots (OR-CDs), prepared from the calcination of selected carbon sources 5-amino-1, 10-phenanthroline (Aphen) and salicylic acid (SA), were found to act as a "turn on" type fluorescence probe for Cd2+ detection.	5-amino-1, 10-phenanthroline	99-127	CD2 molecule	Homo sapiens	222-225
34991009-3	2022	Orange-red emissive carbon dots (OR-CDs), prepared from the calcination of selected carbon sources 5-amino-1, 10-phenanthroline (Aphen) and salicylic acid (SA), were found to act as a "turn on" type fluorescence probe for Cd2+ detection.	aphen	129-134	CD2 molecule	Homo sapiens	222-225
34991009-3	2022	Orange-red emissive carbon dots (OR-CDs), prepared from the calcination of selected carbon sources 5-amino-1, 10-phenanthroline (Aphen) and salicylic acid (SA), were found to act as a "turn on" type fluorescence probe for Cd2+ detection.	Salicylic Acid	140-154	CD2 molecule	Homo sapiens	222-225
34991009-3	2022	Orange-red emissive carbon dots (OR-CDs), prepared from the calcination of selected carbon sources 5-amino-1, 10-phenanthroline (Aphen) and salicylic acid (SA), were found to act as a "turn on" type fluorescence probe for Cd2+ detection.	Salicylic Acid	156-158	CD2 molecule	Homo sapiens	222-225
34991009-5	2022	The OR-CDs consist of a basic unit of nine aromatic rings, and the N/O binding sites on the OR-CDs can specifically bind with Cd2+, leading to aggregation induced enhanced emission (AIEE).	Cadmium	7-10	CD2 molecule	Homo sapiens	126-129
34991009-5	2022	The OR-CDs consist of a basic unit of nine aromatic rings, and the N/O binding sites on the OR-CDs can specifically bind with Cd2+, leading to aggregation induced enhanced emission (AIEE).	Cadmium	95-98	CD2 molecule	Homo sapiens	126-129
34991009-7	2022	OR-CDs can not only be used for intracellular Cd2+ imaging but also have the potential to alleviate cadmium poison in living organisms.	Cadmium	3-6	CD2 molecule	Homo sapiens	46-49
34968939-2	2022	In this study, a composite of silicon supported nano iron/aluminum/magnesium (hydr)oxides was prepared with biotite by combining acid leaching and base precipitation process, which was used to remove Cd2+.	Iron	53-57	CD2 molecule	Homo sapiens	200-203
34991009-7	2022	OR-CDs can not only be used for intracellular Cd2+ imaging but also have the potential to alleviate cadmium poison in living organisms.	Cadmium	100-107	CD2 molecule	Homo sapiens	46-49
34968939-2	2022	In this study, a composite of silicon supported nano iron/aluminum/magnesium (hydr)oxides was prepared with biotite by combining acid leaching and base precipitation process, which was used to remove Cd2+.	Aluminum	58-66	CD2 molecule	Homo sapiens	200-203
34968939-2	2022	In this study, a composite of silicon supported nano iron/aluminum/magnesium (hydr)oxides was prepared with biotite by combining acid leaching and base precipitation process, which was used to remove Cd2+.	Magnesium Hydroxide	67-89	CD2 molecule	Homo sapiens	200-203
34968939-2	2022	In this study, a composite of silicon supported nano iron/aluminum/magnesium (hydr)oxides was prepared with biotite by combining acid leaching and base precipitation process, which was used to remove Cd2+.	biotite	108-115	CD2 molecule	Homo sapiens	200-203
34564046-6	2022	As a result, the removal capacity for Cd2+ was dramatically increased to 239.7 mg/g with the equal antigorite dosage (the molar ratio of SP/MS = 1:0.5), which is also much higher than the other reported clay minerals.	serpentine (alkaloid)	137-139	CD2 molecule	Homo sapiens	38-41
34968939-7	2022	Cd2+ removal mechanisms were consisted of surface complexation and ion exchange between Cd2+ and other metal ions, and the ion exchange interaction played the major role.	Metals	103-108	CD2 molecule	Homo sapiens	0-3
34564046-9	2022	Based on these findings, this study demonstrated the effectiveness of mechanochemical incorporation of sulfate for enhancing the Cd2+ removal capacity of serpentine, as well as the high efficiency of new pathway for Cd2+ precipitation.	Sulfates	103-110	CD2 molecule	Homo sapiens	129-132
34968939-7	2022	Cd2+ removal mechanisms were consisted of surface complexation and ion exchange between Cd2+ and other metal ions, and the ion exchange interaction played the major role.	Metals	103-108	CD2 molecule	Homo sapiens	88-91
34564046-9	2022	Based on these findings, this study demonstrated the effectiveness of mechanochemical incorporation of sulfate for enhancing the Cd2+ removal capacity of serpentine, as well as the high efficiency of new pathway for Cd2+ precipitation.	Sulfates	103-110	CD2 molecule	Homo sapiens	216-219
34773780-8	2022	According to the simulation of the adsorption process by Materials Studio, the characterization of the scanning electron microscope-energy dispersive instrument and the results of the adsorption experiment, in the solution, the precipitate formed by WTF and Cd2+ has multilayer adsorption of HMs, and can further adsorb HM by -OH.	medrysone	292-295	CD2 molecule	Homo sapiens	258-261
34564046-9	2022	Based on these findings, this study demonstrated the effectiveness of mechanochemical incorporation of sulfate for enhancing the Cd2+ removal capacity of serpentine, as well as the high efficiency of new pathway for Cd2+ precipitation.	serpentine (alkaloid)	154-164	CD2 molecule	Homo sapiens	129-132
34571471-6	2022	The Langmuir model shows that the maximum adsorption capacity of Pb2+, Cu2+, Cd2+, and Zn2+ are 338.58, 51.61, 32.34, and 25.05 mg g-1, respectively.	Lead(2+)	65-69	CD2 molecule	Homo sapiens	77-80
34624764-0	2022	n-type absorber by Cd2+ doping achieves high-performance carbon-based CsPbIBr2 perovskite solar cells.	Carbon	57-63	CD2 molecule	Homo sapiens	19-22
34624764-5	2022	In this work, an appropriate amount of Cd2+ (1.0% mol of Pb2+) is added into the CsPbIBr2 precursor solution to fabricate high quality CsPbIBr2 film with improved crystallinity, reduced trap density, suppressed photo-generated carrier recombination, displayed n-type doping and optimized energy level alignment.	Lead(2+)	57-61	CD2 molecule	Homo sapiens	39-42
34624764-6	2022	The corresponding carbon-based all-inorganic Cd2+-doped CsPbIBr2 PSCs achieve a maximum PCE of 10.63% with a high open circuit voltage (VOC) of 1.324 V, which are much higher than those of the control one with a PCE of 8.48% and an VOC of 1.235 V. The unencapsulated device can still retain more than 92% of the initial PCE when stored at ambient atmosphere (25  C, relative humidity about 30%) for 40 days.	Carbon	18-24	CD2 molecule	Homo sapiens	45-48
34461549-4	2022	The removal percentage of Tl+ was over 92% even when the concentration of coexisting ions (e.g. Zn2+, Cd2+, Cu2+, and Pb2+) were 10,000 times higher than the initial concentration of Tl+.	Thallium	26-29	CD2 molecule	Homo sapiens	102-105
34610397-2	2022	In terms of removing aqueous heavy metal ions (Pb2+, Cd2+, Cu2+), the maximum adsorption capacities of UiO-66-EDTMPA reached 558.67, 271.34 and 210.89 mg/g, which were 8.77 (Pb2+), 5.63 (Cd2+) and 5.19 (Cu2+) times higher than raw UiO-66 respectively.	Metals	35-40	CD2 molecule	Homo sapiens	53-56
34610397-2	2022	In terms of removing aqueous heavy metal ions (Pb2+, Cd2+, Cu2+), the maximum adsorption capacities of UiO-66-EDTMPA reached 558.67, 271.34 and 210.89 mg/g, which were 8.77 (Pb2+), 5.63 (Cd2+) and 5.19 (Cu2+) times higher than raw UiO-66 respectively.	Lead(2+)	47-51	CD2 molecule	Homo sapiens	187-190
34610397-2	2022	In terms of removing aqueous heavy metal ions (Pb2+, Cd2+, Cu2+), the maximum adsorption capacities of UiO-66-EDTMPA reached 558.67, 271.34 and 210.89 mg/g, which were 8.77 (Pb2+), 5.63 (Cd2+) and 5.19 (Cu2+) times higher than raw UiO-66 respectively.	uio-66-edtmpa	103-116	CD2 molecule	Homo sapiens	53-56
34610397-2	2022	In terms of removing aqueous heavy metal ions (Pb2+, Cd2+, Cu2+), the maximum adsorption capacities of UiO-66-EDTMPA reached 558.67, 271.34 and 210.89 mg/g, which were 8.77 (Pb2+), 5.63 (Cd2+) and 5.19 (Cu2+) times higher than raw UiO-66 respectively.	uio-66-edtmpa	103-116	CD2 molecule	Homo sapiens	187-190
34610397-8	2022	(2) The coordination between O, N atoms of EDTMPA and heavy metal ions (Pb2+, Cd2+, Cu2+) resulted in spontaneous adsorption.	Nitrogen	32-33	CD2 molecule	Homo sapiens	78-81
34610397-8	2022	(2) The coordination between O, N atoms of EDTMPA and heavy metal ions (Pb2+, Cd2+, Cu2+) resulted in spontaneous adsorption.	(ethylenedinitrilo)-tetramethylenephosphonic acid	43-49	CD2 molecule	Homo sapiens	78-81
34610397-8	2022	(2) The coordination between O, N atoms of EDTMPA and heavy metal ions (Pb2+, Cd2+, Cu2+) resulted in spontaneous adsorption.	Metals	60-65	CD2 molecule	Homo sapiens	78-81
34818763-6	2022	We revealed the inhibition of Cd2+ absorption by CaSO4 is largely due to the competition between Ca2+ and Cd2+ for ion channels or transporter.	Calcium Sulfate	49-54	CD2 molecule	Homo sapiens	30-33
34818763-6	2022	We revealed the inhibition of Cd2+ absorption by CaSO4 is largely due to the competition between Ca2+ and Cd2+ for ion channels or transporter.	Calcium Sulfate	49-54	CD2 molecule	Homo sapiens	106-109
34798586-0	2022	Mercapto-functionalized ordered mesoporous silica-modified PVDF membrane for efficiently scavenging Cd2+ from water.	mesoporous	32-42	CD2 molecule	Homo sapiens	100-103
34798586-0	2022	Mercapto-functionalized ordered mesoporous silica-modified PVDF membrane for efficiently scavenging Cd2+ from water.	Silicon Dioxide	43-49	CD2 molecule	Homo sapiens	100-103
34798586-0	2022	Mercapto-functionalized ordered mesoporous silica-modified PVDF membrane for efficiently scavenging Cd2+ from water.	polyvinylidene fluoride	59-63	CD2 molecule	Homo sapiens	100-103
34798586-0	2022	Mercapto-functionalized ordered mesoporous silica-modified PVDF membrane for efficiently scavenging Cd2+ from water.	Water	110-115	CD2 molecule	Homo sapiens	100-103
34798586-2	2022	The OMS materials were analyzed by FT-IR spectra, N2 sorption, and small angle X-ray scattering to evaluate their potential for scavenging Cd2+ from water.	Water	149-154	CD2 molecule	Homo sapiens	139-142
34798586-5	2022	The MPTMS-OMS/PVDF exhibited a dynamic adsorption capacity for Cd2+ in water.	mptms-oms	4-13	CD2 molecule	Homo sapiens	63-66
34798586-5	2022	The MPTMS-OMS/PVDF exhibited a dynamic adsorption capacity for Cd2+ in water.	polyvinylidene fluoride	14-18	CD2 molecule	Homo sapiens	63-66
34798586-5	2022	The MPTMS-OMS/PVDF exhibited a dynamic adsorption capacity for Cd2+ in water.	Water	71-76	CD2 molecule	Homo sapiens	63-66
34798586-6	2022	At an MPTMS-OMS content of 5 wt%, the Cd2+ removal efficiency was 90%, whereas the pure PVDF showed no Cd2+ adsorption capacity.	mptms-oms	6-15	CD2 molecule	Homo sapiens	38-41
34798586-7	2022	These results highlight the potential of the MPTMS-OMS/PVDF membrane to eliminate Cd2+ during the decontamination of aqueous streams containing low-concentrations of contaminants.	mptms-oms	45-54	CD2 molecule	Homo sapiens	82-85
34798586-7	2022	These results highlight the potential of the MPTMS-OMS/PVDF membrane to eliminate Cd2+ during the decontamination of aqueous streams containing low-concentrations of contaminants.	polyvinylidene fluoride	55-59	CD2 molecule	Homo sapiens	82-85
34782267-4	2022	It was also concluded that the ratio of Raman intensities at the maximum of the peak of the symmetric CD2 stretching and at a maximum near 2168 cm-1 reflects the conformational order of the hydrocarbon chain and can be used for an evaluation of the fraction of the all-trans sequences.	Hydrocarbons	190-201	CD2 molecule	Homo sapiens	102-105
34399259-3	2022	The characteristics of XRD, FTIR, SEM, and XPS manifested that dissolution-precipitation, cation exchange, complexation, and cation-pi interaction were the main four mechanisms for the sorption of Pb2+ and Cd2+ using composite material PC1 (nHAP/BC = 1/1).	Lead(2+)	197-201	CD2 molecule	Homo sapiens	206-209
34736691-1	2022	Taking advantage of an exquisite hairpin DNA for strand displacement amplification (SDA) and the magnetic Fe3O4-graphene oxide nanosheets (MGN) as the carrier, an immobilization-free ECL biosensor was constructed for ultra-trace detection of Cd2+.	fe3o4-graphene oxide	106-126	CD2 molecule	Homo sapiens	242-245
34610424-4	2022	Mg2+ contributes to Pb2+ and Cd2+ adsorption among coexisting cations.	magnesium ion	0-4	CD2 molecule	Homo sapiens	29-32
34826898-0	2022	A novel approach for the removal of Pb2+ and Cd2+ from wastewater by sulfur-ferromagnetic nanoparticles (SFMNs).	Sulfur	69-75	CD2 molecule	Homo sapiens	45-48
34826898-5	2022	The ability of the SFMNs to remove Pb2+ and Cd2+ was studied at different temperatures and initial metal ions concentrations.	Metals	99-104	CD2 molecule	Homo sapiens	44-47
34826898-6	2022	The adsorption kinetics showed that the adsorption equilibrium time of Pb2+ and Cd2+ was 300 min consequently adsorption process of SFMNs fit well (R2 > 0.99) with pseudo-second-order model.	Lead(2+)	71-75	CD2 molecule	Homo sapiens	80-83
34826898-7	2022	The adsorption thermodynamics showed that the adsorption of Pb2+ and Cd2+ on SFMNs is spontaneous (negative value of DeltaG0) endothermic process (positive value of DeltaH0) and fit well (R2 > 0.98) with the Langmuir isothermal model.	Lead(2+)	60-64	CD2 molecule	Homo sapiens	69-72
34311401-5	2022	Adsorption of KCB for Pb2+ and Cd2+ reached 50.44 mg g-1 and 33.77 mg g-1, respectively.	kcb	14-17	CD2 molecule	Homo sapiens	31-34
34311401-6	2022	Metal ions in contaminated soil were removed by reactive barrier through electromigration, electrodialysis and electrophoresis, the removal efficiency of Pb2+ and Cd2+ in soil reached 92.87% and 86.19%.	Metals	0-5	CD2 molecule	Homo sapiens	163-166
34403904-2	2022	This study demonstrates the electrochemically assisted uptake and release of cadmium ions (Cd2+) using a redox-active Cu-based metal-organic framework (MOF) electrode.	Cadmium	77-84	CD2 molecule	Homo sapiens	91-94
34403904-2	2022	This study demonstrates the electrochemically assisted uptake and release of cadmium ions (Cd2+) using a redox-active Cu-based metal-organic framework (MOF) electrode.	Copper	118-120	CD2 molecule	Homo sapiens	91-94
34403904-2	2022	This study demonstrates the electrochemically assisted uptake and release of cadmium ions (Cd2+) using a redox-active Cu-based metal-organic framework (MOF) electrode.	Metals	127-132	CD2 molecule	Homo sapiens	91-94
34403904-4	2022	This work utilized copper within the CuGA structure as a redox center to attract Cd2+ by means of Cu2+/Cu+ reduction, exhibiting rapid uptake kinetics and a much higher capacity (>60 mg g-1) compared to the case without electrochemical assistance (~15 mg g-1).	Copper	19-25	CD2 molecule	Homo sapiens	81-84
34403904-4	2022	This work utilized copper within the CuGA structure as a redox center to attract Cd2+ by means of Cu2+/Cu+ reduction, exhibiting rapid uptake kinetics and a much higher capacity (>60 mg g-1) compared to the case without electrochemical assistance (~15 mg g-1).	cupric ion	98-102	CD2 molecule	Homo sapiens	81-84
34403904-4	2022	This work utilized copper within the CuGA structure as a redox center to attract Cd2+ by means of Cu2+/Cu+ reduction, exhibiting rapid uptake kinetics and a much higher capacity (>60 mg g-1) compared to the case without electrochemical assistance (~15 mg g-1).	Copper	103-106	CD2 molecule	Homo sapiens	81-84
34403904-5	2022	In addition, by applying an opposite overpotential to induce the re-oxidation of copper, the facile recovery of Cd2+ and the regeneration of the electrode were possible without regenerants.	Copper	81-87	CD2 molecule	Homo sapiens	112-115
34403904-7	2022	This work presents the feasibility of a Cu-based MOF electrode as a reusable platform for the efficient removal of Cd2+, supporting the continued discovery and development of new Faradaic electrodes for electrochemical wastewater treatments.	Copper	40-42	CD2 molecule	Homo sapiens	115-118
34844140-3	2022	It is known that subjects with IDA as well as smokers have elevated blood levels of toxic divalent cations, particularly cadmium (Cd2+) and lead (Pb2+).	Cadmium	121-128	CD2 molecule	Homo sapiens	130-133
34855374-0	2021	Connectivity Replication of Neutral Eu3+- and Tb3+-Based Metal-Organic Frameworks (MOFs) from Anionic Cd2+-Based MOF Crystallites.	eu3+	36-40	CD2 molecule	Homo sapiens	102-105
34959014-6	2021	Batch adsorption experiment indicated that the maximum adsorption for Cd2+ (Qm = 32.157 mg/g) and Pb2+ (Qm = 39.216 mg/g) on aged biochar surface was much larger than that of Cd2+ (Qm = 7.573 mg/g) and Pb2+ (Qm = 8.134 mg/g) on fresh biochar.	Lead(2+)	98-102	CD2 molecule	Homo sapiens	175-178
34959014-6	2021	Batch adsorption experiment indicated that the maximum adsorption for Cd2+ (Qm = 32.157 mg/g) and Pb2+ (Qm = 39.216 mg/g) on aged biochar surface was much larger than that of Cd2+ (Qm = 7.573 mg/g) and Pb2+ (Qm = 8.134 mg/g) on fresh biochar.	Lead(2+)	202-206	CD2 molecule	Homo sapiens	70-73
34959014-7	2021	The underlying adsorption mechanisms for Cd2+ and Pb2+ on fresh biochar were dominated by coprecipitation, cation exchange and cation-pi interaction, whereas surface complexation and cation exchange appeared to be more vital for aged biochar, as more active adsorption sites and Oxygen-containing functional groups were formed on its surface during aging, which was well explained by BET, XPS, FTIR and Elemental Analysis.	Oxygen	279-285	CD2 molecule	Homo sapiens	41-44
34510599-7	2021	Supported by quantum chemical calculations, this new mode is assigned to a second n as (CD 2 ) band in alkyl-chain fragments embedded in a polar environment of the anions/solvent present in the vicinity of the imidazolium cation and electrode.	imidazolium	210-221	CD2 molecule	Homo sapiens	88-92
34855374-0	2021	Connectivity Replication of Neutral Eu3+- and Tb3+-Based Metal-Organic Frameworks (MOFs) from Anionic Cd2+-Based MOF Crystallites.	tb3+	46-50	CD2 molecule	Homo sapiens	102-105
34877783-0	2022	A chalcone-based fluorescent chemosensor for detecting Mg2+ and Cd2.	Chalcone	2-10	CD2 molecule	Homo sapiens	64-67
34426326-2	2021	In this study, different types of spectroscopy including ultraviolet-visible absorption, Fourier transform infrared, and fluorescence spectroscopy was used to investigate the binding characteristics of Fe3+, Cu2+, Cr3+, Cd2+, and Zn2+ with DOM from wetland water.	Water	257-262	CD2 molecule	Homo sapiens	220-223
34792522-2	2021	Herein, the rational design and synthesis of two mesoporous anionic MOFs, (Zn3(ITTC)3)(Me2 NH2)3 3DMF H2O (1) and (Cd2(ITTC)3)(Me2NH2)5 2DMF (2), where H3ITTC = 4,4",4""-(1H-imidazole-2,4,5-triyl) tribenzoic acid, is reported.	mesoporous	49-59	CD2 molecule	Homo sapiens	115-125
34873260-2	2021	In this article, by employing full atomistic molecular dynamics (MD) simulations and density functional theory dispersion corrected (DFT-D3) calculations, the effects of 6-mercaptonicotinic acid (MNA) and L-cysteine (CYS) on the stability of gold nanoparticles (AuNPs) and their sensitivity against Cd2+ were investigated.	6-Mercaptonicotinic acid	170-194	CD2 molecule	Homo sapiens	299-302
34873260-2	2021	In this article, by employing full atomistic molecular dynamics (MD) simulations and density functional theory dispersion corrected (DFT-D3) calculations, the effects of 6-mercaptonicotinic acid (MNA) and L-cysteine (CYS) on the stability of gold nanoparticles (AuNPs) and their sensitivity against Cd2+ were investigated.	mna	196-199	CD2 molecule	Homo sapiens	299-302
34873260-2	2021	In this article, by employing full atomistic molecular dynamics (MD) simulations and density functional theory dispersion corrected (DFT-D3) calculations, the effects of 6-mercaptonicotinic acid (MNA) and L-cysteine (CYS) on the stability of gold nanoparticles (AuNPs) and their sensitivity against Cd2+ were investigated.	Cysteine	205-215	CD2 molecule	Homo sapiens	299-302
34873260-2	2021	In this article, by employing full atomistic molecular dynamics (MD) simulations and density functional theory dispersion corrected (DFT-D3) calculations, the effects of 6-mercaptonicotinic acid (MNA) and L-cysteine (CYS) on the stability of gold nanoparticles (AuNPs) and their sensitivity against Cd2+ were investigated.	Cysteine	217-220	CD2 molecule	Homo sapiens	299-302
34873260-5	2021	Moreover, functionalized AuNPs have considerable ability for selective detection of Cd2+ in the presence of different metal ions.	Metals	118-123	CD2 molecule	Homo sapiens	84-87
34873260-6	2021	Based on the MD simulation results, MNA-CYS-AuNPs (functionalized AuNPs with both functional groups) have the maximum sensitivity against Cd2+ in comparison with MNA-AuNPs and CYS-AuNPs due to the strong electrostatic interactions.	mna	36-39	CD2 molecule	Homo sapiens	138-141
34873260-6	2021	Based on the MD simulation results, MNA-CYS-AuNPs (functionalized AuNPs with both functional groups) have the maximum sensitivity against Cd2+ in comparison with MNA-AuNPs and CYS-AuNPs due to the strong electrostatic interactions.	Cysteine	40-43	CD2 molecule	Homo sapiens	138-141
34873260-7	2021	DFT-D3 calculations reveal that the most probable interactions between the metal ions and functional groups are electrostatic, and Cd2+ can aggregate functionalized AuNPs due to strong electrostatic interactions with MNA and CYS groups.	Metals	75-80	CD2 molecule	Homo sapiens	131-134
34873260-7	2021	DFT-D3 calculations reveal that the most probable interactions between the metal ions and functional groups are electrostatic, and Cd2+ can aggregate functionalized AuNPs due to strong electrostatic interactions with MNA and CYS groups.	mna	217-220	CD2 molecule	Homo sapiens	131-134
34873260-7	2021	DFT-D3 calculations reveal that the most probable interactions between the metal ions and functional groups are electrostatic, and Cd2+ can aggregate functionalized AuNPs due to strong electrostatic interactions with MNA and CYS groups.	Cysteine	225-228	CD2 molecule	Homo sapiens	131-134
34946761-1	2021	Thermodynamic Investigation of the Binary and Ternary Interactions with Cd2+, Cu2+ and UO22+ in NaCl at Different Ionic Strengths and Temperatures.	uo22+	87-92	CD2 molecule	Homo sapiens	72-75
34946761-1	2021	Thermodynamic Investigation of the Binary and Ternary Interactions with Cd2+, Cu2+ and UO22+ in NaCl at Different Ionic Strengths and Temperatures.	Sodium Chloride	96-100	CD2 molecule	Homo sapiens	72-75
34946761-4	2021	In particular for cadmium, the formation of only MLH, ML and ML2 (M = Cd2+; L = dopamine) species was obtained.	Cadmium	18-25	CD2 molecule	Homo sapiens	70-73
34946761-8	2021	As a further contribution to this kind of investigation, the ternary interactions of dopamine with UO22+/Cd2+ and UO22+/Cu2+ were investigated at I = 0.15 mol dm-3 and T = 298.15K.	Dopamine	85-93	CD2 molecule	Homo sapiens	105-108
34860227-6	2021	In all four coordination polymers pairs of CH3-bpeb molecules were bound or encapsulated by the Cd2 secondary building units at an appropriate distance and orientation for solid-state (2 + 2) photodimerization of one pair of C C bonds.	ch3-bpeb	43-51	CD2 molecule	Homo sapiens	96-99
34797044-1	2021	A sodalite Cd66-cage-based metal-organic framework (MOF), namely, CPM-9S, has been constructed based on Cd9 and Cd5 metal-organic clusters (MOCs), which, to the best our knowledge, represents the first Cd-cage-based MOF that contains the highest-nuclear Cd-based MOC and the largest number of Cd2+ ions in a cage.	Cadmium	202-204	CD2 molecule	Homo sapiens	293-296
34877783-1	2022	As a chalcone-based fluorescent turn-on chemosensor to Mg2+ and Cd2+ , SBOD (sodium (E)-2-(3-(5-bromothiophen-2-yl)-3-oxoprop-1-en-1-yl)-4,6-dichlorophenolate) was designed and synthesized.	Chalcone	5-13	CD2 molecule	Homo sapiens	64-67
34877783-1	2022	As a chalcone-based fluorescent turn-on chemosensor to Mg2+ and Cd2+ , SBOD (sodium (E)-2-(3-(5-bromothiophen-2-yl)-3-oxoprop-1-en-1-yl)-4,6-dichlorophenolate) was designed and synthesized.	magnesium ion	55-59	CD2 molecule	Homo sapiens	64-67
34877783-1	2022	As a chalcone-based fluorescent turn-on chemosensor to Mg2+ and Cd2+ , SBOD (sodium (E)-2-(3-(5-bromothiophen-2-yl)-3-oxoprop-1-en-1-yl)-4,6-dichlorophenolate) was designed and synthesized.	sbod (	71-77	CD2 molecule	Homo sapiens	64-67
34877783-1	2022	As a chalcone-based fluorescent turn-on chemosensor to Mg2+ and Cd2+ , SBOD (sodium (E)-2-(3-(5-bromothiophen-2-yl)-3-oxoprop-1-en-1-yl)-4,6-dichlorophenolate) was designed and synthesized.	sodium (e)-2-(3-(5-bromothiophen-2-yl)-3-oxoprop-1-en-1-yl)-4,6-dichlorophenolate	77-158	CD2 molecule	Homo sapiens	64-67
34877783-2	2022	SBOD detected selectively Mg2+ and Cd2+ through effective fluorescence increase.	magnesium ion	26-30	CD2 molecule	Homo sapiens	35-38
34877783-4	2022	The binding modes of SBOD for Mg2+ and Cd2+ were determined to be 1:1 by ESI-MS and Job plot.	magnesium ion	30-34	CD2 molecule	Homo sapiens	39-42
34877783-5	2022	Association mechanisms of SBOD to Mg2+ and Cd2+ were illustrated by ESI-MS, UV-vis and fluorescent spectroscopy and calculations.	magnesium ion	34-38	CD2 molecule	Homo sapiens	43-46
34217937-1	2021	In this study, we investigated the feasibility on the utilization of coffee husk as biosorbents for the removal of heavy metal ions such as Pb2+ and Cd2+ from wastewater.	coffee husk	69-80	CD2 molecule	Homo sapiens	149-152
34753585-2	2021	Herein, the dht ligand containing hydroxy group (-OH) is used to design and synthesize a 2D luminescent (Cd2(idc)(dht)(H2O)4) (1); H2idc = 4,5-imidazoledicarboxylic acid and H2dht = 2,5-dihydroxyterephthalic acid for sensing amino acids.	Water	119-122	CD2 molecule	Homo sapiens	105-108
34753585-2	2021	Herein, the dht ligand containing hydroxy group (-OH) is used to design and synthesize a 2D luminescent (Cd2(idc)(dht)(H2O)4) (1); H2idc = 4,5-imidazoledicarboxylic acid and H2dht = 2,5-dihydroxyterephthalic acid for sensing amino acids.	h2idc	131-136	CD2 molecule	Homo sapiens	105-108
34753585-2	2021	Herein, the dht ligand containing hydroxy group (-OH) is used to design and synthesize a 2D luminescent (Cd2(idc)(dht)(H2O)4) (1); H2idc = 4,5-imidazoledicarboxylic acid and H2dht = 2,5-dihydroxyterephthalic acid for sensing amino acids.	1H-Imidazole-4,5-dicarboxylic acid	139-169	CD2 molecule	Homo sapiens	105-108
34753585-2	2021	Herein, the dht ligand containing hydroxy group (-OH) is used to design and synthesize a 2D luminescent (Cd2(idc)(dht)(H2O)4) (1); H2idc = 4,5-imidazoledicarboxylic acid and H2dht = 2,5-dihydroxyterephthalic acid for sensing amino acids.	2,5-dihydroxyterephthalic acid	182-212	CD2 molecule	Homo sapiens	105-108
34399167-2	2021	Herein, we developed a novel kind of electrochemical microRNA biosensor based on two-dimensional nanomaterial of antimonene nano-flakes (AMNFs) and carbon quantum dots (CQDs) which were used as substrating to cadmium ion (Cd2+) for specific detection of breast cancer-relevant biomarker-microRNA-21.	antimonene	113-123	CD2 molecule	Homo sapiens	222-225
34399167-2	2021	Herein, we developed a novel kind of electrochemical microRNA biosensor based on two-dimensional nanomaterial of antimonene nano-flakes (AMNFs) and carbon quantum dots (CQDs) which were used as substrating to cadmium ion (Cd2+) for specific detection of breast cancer-relevant biomarker-microRNA-21.	Carbon	148-154	CD2 molecule	Homo sapiens	222-225
34399167-2	2021	Herein, we developed a novel kind of electrochemical microRNA biosensor based on two-dimensional nanomaterial of antimonene nano-flakes (AMNFs) and carbon quantum dots (CQDs) which were used as substrating to cadmium ion (Cd2+) for specific detection of breast cancer-relevant biomarker-microRNA-21.	Cadmium	209-216	CD2 molecule	Homo sapiens	222-225
34217937-6	2021	Kinetic studies showed that the sorption of Pb2+ and Cd2+ on biosorbents can be described by the Freundlich isotherm and second-order kinetic model.	Lead(2+)	44-48	CD2 molecule	Homo sapiens	53-56
34217937-7	2021	The coffee husk-derived biosorbent was capable of removing 89.6% of Pb2+ and 81.5% Cd2+ ions from wastewater, and therefore can be considered as low-cost and efficient adsorbent to remove heavy metal ions from wastewater.	Metals	194-199	CD2 molecule	Homo sapiens	83-86
34885669-0	2021	Thermodynamic Solution Properties of a Biodegradable Chelant (L-glutamic-N,N-diacetic Acid, L-GLDA) and Its Sequestering Ability toward Cd2.	l-glutamic-n,n-diacetic acid	62-90	CD2 molecule	Homo sapiens	136-139
34517645-6	2021	Under the optimal conditions of 30 mM K3(Fe(CN)6), OD600 = 1 cell concentration, and 50 mM phosphate-buffered solution (PBS), the half-maximal inhibitory concentration (IC50) values measured for Cd2+, Cu2+ and Ni2+ were 3.99 mg/L, 1.16 mg/L and 2.37 mg/L, respectively.	KS 3	38-40	CD2 molecule	Homo sapiens	195-198
34517645-6	2021	Under the optimal conditions of 30 mM K3(Fe(CN)6), OD600 = 1 cell concentration, and 50 mM phosphate-buffered solution (PBS), the half-maximal inhibitory concentration (IC50) values measured for Cd2+, Cu2+ and Ni2+ were 3.99 mg/L, 1.16 mg/L and 2.37 mg/L, respectively.	fe(cn)6	41-48	CD2 molecule	Homo sapiens	195-198
34517645-6	2021	Under the optimal conditions of 30 mM K3(Fe(CN)6), OD600 = 1 cell concentration, and 50 mM phosphate-buffered solution (PBS), the half-maximal inhibitory concentration (IC50) values measured for Cd2+, Cu2+ and Ni2+ were 3.99 mg/L, 1.16 mg/L and 2.37 mg/L, respectively.	phosphate-buffered solution	91-118	CD2 molecule	Homo sapiens	195-198
34517645-6	2021	Under the optimal conditions of 30 mM K3(Fe(CN)6), OD600 = 1 cell concentration, and 50 mM phosphate-buffered solution (PBS), the half-maximal inhibitory concentration (IC50) values measured for Cd2+, Cu2+ and Ni2+ were 3.99 mg/L, 1.16 mg/L and 2.37 mg/L, respectively.	pbs	120-123	CD2 molecule	Homo sapiens	195-198
34699192-6	2021	Quantitation of Pb2+ in both lab and natural water samples was rapid (2-3 min), accurate, precise, and highly linear in the 25-1000 ppb range and was shown to be sufficiently selective in the presence of other common heavy metal ions such as Cu2+, Cd2+, and Zn2+.	Lead(2+)	16-20	CD2 molecule	Homo sapiens	248-251
34311356-5	2021	The adsorption capacities of Cu2+ and Cd2+ followed the order of BB > MB > HB.	cupric ion	29-33	CD2 molecule	Homo sapiens	38-41
34311356-6	2021	DW and FT aging both increased the adsorption capacity of Cu2+, but decreased that of Cd2+ in the three biochars, resulting in a reduction in Cu bioavailability and increase in Cd bioavailability in the biochars after the saturated adsorption of Cu2+ and Cd2+.	cupric ion	58-62	CD2 molecule	Homo sapiens	255-258
34311356-6	2021	DW and FT aging both increased the adsorption capacity of Cu2+, but decreased that of Cd2+ in the three biochars, resulting in a reduction in Cu bioavailability and increase in Cd bioavailability in the biochars after the saturated adsorption of Cu2+ and Cd2+.	Copper	142-144	CD2 molecule	Homo sapiens	86-89
34311356-6	2021	DW and FT aging both increased the adsorption capacity of Cu2+, but decreased that of Cd2+ in the three biochars, resulting in a reduction in Cu bioavailability and increase in Cd bioavailability in the biochars after the saturated adsorption of Cu2+ and Cd2+.	Cadmium	177-179	CD2 molecule	Homo sapiens	86-89
34311356-6	2021	DW and FT aging both increased the adsorption capacity of Cu2+, but decreased that of Cd2+ in the three biochars, resulting in a reduction in Cu bioavailability and increase in Cd bioavailability in the biochars after the saturated adsorption of Cu2+ and Cd2+.	Cadmium	177-179	CD2 molecule	Homo sapiens	255-258
34311356-6	2021	DW and FT aging both increased the adsorption capacity of Cu2+, but decreased that of Cd2+ in the three biochars, resulting in a reduction in Cu bioavailability and increase in Cd bioavailability in the biochars after the saturated adsorption of Cu2+ and Cd2+.	cupric ion	246-250	CD2 molecule	Homo sapiens	86-89
34928852-1	2021	The objective of this work was to study the treatment of wastewater containing cadmium ions (Cd2+).	Cadmium	79-86	CD2 molecule	Homo sapiens	93-96
34816449-5	2022	The unique selectivity of CTEA was examined by measuring the binding affinity of NiCast and the CTEA receptor for Ni2+ , Zn2+ , Cd2+ , and Cu2+ under different conditions.	ctea	26-30	CD2 molecule	Homo sapiens	128-131
34885669-0	2021	Thermodynamic Solution Properties of a Biodegradable Chelant (L-glutamic-N,N-diacetic Acid, L-GLDA) and Its Sequestering Ability toward Cd2.	l-glda	92-98	CD2 molecule	Homo sapiens	136-139
34885669-4	2021	Formation constants of GLDA with Cd2+ were determined in NaCl(aq) at different ionic strength values.	nacl(aq)	57-65	CD2 molecule	Homo sapiens	33-36
34885669-7	2021	The sequestering ability of GLDA toward Cd2+, evaluated by means of pL0.5, was maximum at pH~10, whereas the presence of a chloride containing a supporting electrolyte exerted a negative effect.	Chlorides	123-131	CD2 molecule	Homo sapiens	40-43
34827713-3	2021	In this study, EPS extracted from soil with a steam method were used to study the adsorption behaviors of Cu2+ and Cd2+, employing quartz sand as a subsurface porous medium.	cupric ion	106-110	CD2 molecule	Homo sapiens	115-118
34827713-9	2021	This also demonstrated that EPS can promote the co-migration of Cu2+ and Cd2+ in saturated porous media.	cupric ion	64-68	CD2 molecule	Homo sapiens	73-76
34773451-7	2021	The high concentrations of TME-loaded nanocrystals will induce the inhibition of cells activity and proliferation, particularly for Pb2+ and Cd2+ -loaded nanocrystals.	1,1,1-TRIS(HYDROXYMETHYL)ETHANE	27-30	CD2 molecule	Homo sapiens	141-144
34702451-0	2021	Adsorption of Pb2+, Cu2+ and Cd2+ by sulfhydryl modified chitosan beads.	Chitosan	57-65	CD2 molecule	Homo sapiens	29-32
34702451-1	2021	A chitosan-based bead was synthesized by crosslinking as well as sulfhydryl modification reaction and its removal ability of Pb2+, Cu2+ and Cd2+ was investigated.	Chitosan	2-10	CD2 molecule	Homo sapiens	140-143
34702451-3	2021	The adsorption of Pb2+, Cu2+ and Cd2+ by the beads was carried out at different pH, ionic strength, contact time and initial concentration and the maximum adsorption capacities were 273.7 mg/g, 163.3 mg/g and 183.1 mg/g, respectively.	Lead(2+)	18-22	CD2 molecule	Homo sapiens	33-36
34702451-5	2021	Finally, the adsorption processes of Pb2+, Cu2+ and Cd2+ were well fitted by the Langmuir isotherm model and the pseudo second-order kinetics model, respectively.	Lead(2+)	37-41	CD2 molecule	Homo sapiens	52-55
34869207-2	2021	The recognition behaviors of 1 in dichloromethane/acetonitrile solution to alkali metal ions (Na+ and K+), alkaline earth metal ions (Mg2+ and Ca2+), and transition metal ions (Co2+, Ni2+, Zn2+, Cd2+, Cu2+, Mn2+, and Ag+) have been investigated by UV-Vis and fluorescence spectra.	Methylene Chloride	34-49	CD2 molecule	Homo sapiens	195-198
34869207-2	2021	The recognition behaviors of 1 in dichloromethane/acetonitrile solution to alkali metal ions (Na+ and K+), alkaline earth metal ions (Mg2+ and Ca2+), and transition metal ions (Co2+, Ni2+, Zn2+, Cd2+, Cu2+, Mn2+, and Ag+) have been investigated by UV-Vis and fluorescence spectra.	acetonitrile	50-62	CD2 molecule	Homo sapiens	195-198
34869207-2	2021	The recognition behaviors of 1 in dichloromethane/acetonitrile solution to alkali metal ions (Na+ and K+), alkaline earth metal ions (Mg2+ and Ca2+), and transition metal ions (Co2+, Ni2+, Zn2+, Cd2+, Cu2+, Mn2+, and Ag+) have been investigated by UV-Vis and fluorescence spectra.	Metals	165-170	CD2 molecule	Homo sapiens	195-198
34118630-1	2021	The efforts of this study aimed to evaluate the feasibility of the nanotubular halloysites in weathered pegmatites (NaHWP) for removing heavy metals (i.e., Cd2+, Pb2+) from water.	Lead(2+)	162-166	CD2 molecule	Homo sapiens	156-159
34118630-1	2021	The efforts of this study aimed to evaluate the feasibility of the nanotubular halloysites in weathered pegmatites (NaHWP) for removing heavy metals (i.e., Cd2+, Pb2+) from water.	Water	173-178	CD2 molecule	Homo sapiens	156-159
34182633-7	2021	The desorption kinetics showed a lower rate constant (k) and higher initial desorption constant (h) for Mn2+ than Cd2+ and Ag+, suggesting both high- and low-affinity interaction sites for Mn2+.	Manganese(2+)	189-193	CD2 molecule	Homo sapiens	114-117
34118630-2	2021	Furthermore, two novel intelligent models, such as teaching-learning-based optimization (TLBO)-artificial neural network (ANN), and TLBO-support vector regression (SVR), named as TLBO-ANN and TLBO-SVR models, respectively, were proposed to predict the Cd2+ and Pb2+ absorption efficiencies from water using the NaHWP absorbent.	Water	295-300	CD2 molecule	Homo sapiens	252-255
34118630-2	2021	Furthermore, two novel intelligent models, such as teaching-learning-based optimization (TLBO)-artificial neural network (ANN), and TLBO-support vector regression (SVR), named as TLBO-ANN and TLBO-SVR models, respectively, were proposed to predict the Cd2+ and Pb2+ absorption efficiencies from water using the NaHWP absorbent.	nahwp	311-316	CD2 molecule	Homo sapiens	252-255
34118630-3	2021	Databases used, including 53 experiments for Pb2+ absorption and 56 experiments for Cd2+ absorption from water, under the catalysis of different conditions, such as initial concentration of Pb2+ and Cd2+, solution pH, adsorbent weight, and contact time.	Water	105-110	CD2 molecule	Homo sapiens	84-87
34118630-4	2021	Subsequently, the TLBO-ANN and TLBO-SVR models were developed and applied to predict the efficiencies of Cd2+ and Pb2+ absorption from water, aiming to evaluate the role as well as the effects of different conditions on the absorption efficiencies using the NaHWP absorbent.	Water	135-140	CD2 molecule	Homo sapiens	105-108
34118630-7	2021	The two novel hybrid models proposed, i.e., TLBO-ANN and TLBO-SVR, also yielded the dominant performances and accuracies in predicting the Cd2+ and Pb2+ absorption efficiencies from water, i.e., RMSE = 1.190 and 1.102, R2 = 0.951 and 0.957, VAF = 94.436 and 95.028 for the TLBO-ANN and TLBO-SVR models, respectively, in predicting the Pb2+ absorption efficiency from water; RMSE = 3.084 and 3.442, R2 = 0.971 and 0.965, VAF = 96.499 and 96.415 for the TLBO-ANN and TLBO-SVR models, respectively, in predicting the Cd2+ absorption efficiency from water.	Water	182-187	CD2 molecule	Homo sapiens	139-142
34118630-8	2021	Furthermore, the validation results also demonstrated these findings in practice through 23 experiments with the accuracies of 98.3% and 98.37% for the TLBO-ANN and TLBO-SVR models, respectively, in predicting the Pb2+ absorption efficiency from water; the accuracies of 98.3% and 97.46% for the TLBO-ANN and TLBO-SVR models, respectively, in predicting the Cd2+ absorption efficiency from water.	Water	390-395	CD2 molecule	Homo sapiens	358-361
34716519-1	2022	In this study, chitosan/sodium alginate/nano cellulose (CSA-N) nanocomposite hydrogels were prepared using a completely green route and used as sorbents to adsorb Cd2+ ions from water and soil systems of an environmental aspect.	Chitosan	15-23	CD2 molecule	Homo sapiens	163-166
34097214-1	2021	This paper presents an experimental study on continuous adsorptive removal of Cd2+ from the water body using a bio-nanocomposite hydrogel within a fixed-bed column (FBC) system.	Water	92-97	CD2 molecule	Homo sapiens	78-81
34644054-1	2021	A new type of metal-organic framework, (Cd2(pdc)(H2O)(DMA)2)n (pdc = 3,5-pyrazoledicarboxylic acid; DMA = dimethylamine), named Cd-MOF, was synthesized and characterized.	Metals	14-19	CD2 molecule	Homo sapiens	40-43
34644054-1	2021	A new type of metal-organic framework, (Cd2(pdc)(H2O)(DMA)2)n (pdc = 3,5-pyrazoledicarboxylic acid; DMA = dimethylamine), named Cd-MOF, was synthesized and characterized.	Water	49-52	CD2 molecule	Homo sapiens	40-43
34644054-1	2021	A new type of metal-organic framework, (Cd2(pdc)(H2O)(DMA)2)n (pdc = 3,5-pyrazoledicarboxylic acid; DMA = dimethylamine), named Cd-MOF, was synthesized and characterized.	3,5-pyrazoledicarboxylic acid	69-98	CD2 molecule	Homo sapiens	40-43
34644054-1	2021	A new type of metal-organic framework, (Cd2(pdc)(H2O)(DMA)2)n (pdc = 3,5-pyrazoledicarboxylic acid; DMA = dimethylamine), named Cd-MOF, was synthesized and characterized.	N-myristoyl-alaninol	100-103	CD2 molecule	Homo sapiens	40-43
34644054-1	2021	A new type of metal-organic framework, (Cd2(pdc)(H2O)(DMA)2)n (pdc = 3,5-pyrazoledicarboxylic acid; DMA = dimethylamine), named Cd-MOF, was synthesized and characterized.	dimethylamine	106-119	CD2 molecule	Homo sapiens	40-43
34644054-1	2021	A new type of metal-organic framework, (Cd2(pdc)(H2O)(DMA)2)n (pdc = 3,5-pyrazoledicarboxylic acid; DMA = dimethylamine), named Cd-MOF, was synthesized and characterized.	cd-mof	128-134	CD2 molecule	Homo sapiens	40-43
34769930-2	2021	The objective of this study was to investigate the characteristics and mechanisms of Cd2+ adsorption on biochars produced by co-pyrolysis of HS-PP with various mixing ratios.	hs-pp	141-146	CD2 molecule	Homo sapiens	85-88
34182442-12	2021	The LMCT produced by EDTA-Fe under natural light promotes the replacement process, and finally, the released Cd2+ is captured by S-NZVI and removed as CdS and Fe-O-Cd.	edta-fe	21-28	CD2 molecule	Homo sapiens	109-112
34182442-12	2021	The LMCT produced by EDTA-Fe under natural light promotes the replacement process, and finally, the released Cd2+ is captured by S-NZVI and removed as CdS and Fe-O-Cd.	Cadmium	151-154	CD2 molecule	Homo sapiens	109-112
34182442-12	2021	The LMCT produced by EDTA-Fe under natural light promotes the replacement process, and finally, the released Cd2+ is captured by S-NZVI and removed as CdS and Fe-O-Cd.	fe-o-cd	159-166	CD2 molecule	Homo sapiens	109-112
34810312-2	2021	We conducted the adsorption studies of potentially toxic metal ions (Cu2+, Co2+ and Cd2+) using the composite of Fe3O4 and zeolitic imidazole framework-8 (Fe3O4@ZIF-8) for the first time.	Metals	57-62	CD2 molecule	Homo sapiens	84-87
34810312-2	2021	We conducted the adsorption studies of potentially toxic metal ions (Cu2+, Co2+ and Cd2+) using the composite of Fe3O4 and zeolitic imidazole framework-8 (Fe3O4@ZIF-8) for the first time.	ferryl iron	113-118	CD2 molecule	Homo sapiens	84-87
34810312-2	2021	We conducted the adsorption studies of potentially toxic metal ions (Cu2+, Co2+ and Cd2+) using the composite of Fe3O4 and zeolitic imidazole framework-8 (Fe3O4@ZIF-8) for the first time.	imidazole	132-141	CD2 molecule	Homo sapiens	84-87
34810312-2	2021	We conducted the adsorption studies of potentially toxic metal ions (Cu2+, Co2+ and Cd2+) using the composite of Fe3O4 and zeolitic imidazole framework-8 (Fe3O4@ZIF-8) for the first time.	ferryl iron	155-160	CD2 molecule	Homo sapiens	84-87
34810312-7	2021	To remove potentially toxic metals (Cu2+, Co2+ and Cd2+), the influence of adsorbent dosage, contact time, pH, and adsorbate concentration on the adsorption performance of Fe3O4@ZIF-8 was investigated.	ferryl iron	172-177	CD2 molecule	Homo sapiens	51-54
34810312-8	2021	The Langmuir isotherm accurately represented the adsorption processes, with absorption magnitudes of Fe3O4@ZIF-8 determined to be 46.82 mg g-1, 71.29 mg g-1 and 54.49 mg g-1 for Cu2+, Co2+ and Cd2+, respectively.	ferryl iron	101-106	CD2 molecule	Homo sapiens	193-196
34810312-9	2021	According to the adsorption mechanism analysis, the primary Cu2+, Co2+ and Cd2+ removal methods of Fe3O4@ZIF-8 were ion exchange and coordination bonds.	ferryl iron	99-104	CD2 molecule	Homo sapiens	75-78
34810312-10	2021	The uptake capacity of Cu2+, Co2+ and Cd2+ solution by Fe3O4@ZIF-8 were not significantly affected by the presence of counter ions.	ferryl iron	55-60	CD2 molecule	Homo sapiens	38-41
34810312-11	2021	The material exhibited superior regenerative properties for Cu2+, Co2+ and Cd2+ ions from water for up to three cycles.	Water	90-95	CD2 molecule	Homo sapiens	75-78
34810312-12	2021	This study concluded that the Fe3O4@ZIF-8 could be a viable candidate for eliminating potentially toxic metals (Cu2+, Co2+ and Cd2+).	ferryl iron	30-35	CD2 molecule	Homo sapiens	127-130
34716519-1	2022	In this study, chitosan/sodium alginate/nano cellulose (CSA-N) nanocomposite hydrogels were prepared using a completely green route and used as sorbents to adsorb Cd2+ ions from water and soil systems of an environmental aspect.	Alginates	24-39	CD2 molecule	Homo sapiens	163-166
34716519-1	2022	In this study, chitosan/sodium alginate/nano cellulose (CSA-N) nanocomposite hydrogels were prepared using a completely green route and used as sorbents to adsorb Cd2+ ions from water and soil systems of an environmental aspect.	nano cellulose	40-54	CD2 molecule	Homo sapiens	163-166
34716519-1	2022	In this study, chitosan/sodium alginate/nano cellulose (CSA-N) nanocomposite hydrogels were prepared using a completely green route and used as sorbents to adsorb Cd2+ ions from water and soil systems of an environmental aspect.	csa-n	56-61	CD2 molecule	Homo sapiens	163-166
34716519-1	2022	In this study, chitosan/sodium alginate/nano cellulose (CSA-N) nanocomposite hydrogels were prepared using a completely green route and used as sorbents to adsorb Cd2+ ions from water and soil systems of an environmental aspect.	Water	178-183	CD2 molecule	Homo sapiens	163-166
34746574-0	2021	Novel Silanized Graphene Oxide/TiO2 Multifunctional Nanocomposite Photocatalysts: Simultaneous Removal of Cd2+ and Photodegradation of Phenols under Visible Light Irradiation.	graphene oxide	16-30	CD2 molecule	Homo sapiens	106-109
34746574-0	2021	Novel Silanized Graphene Oxide/TiO2 Multifunctional Nanocomposite Photocatalysts: Simultaneous Removal of Cd2+ and Photodegradation of Phenols under Visible Light Irradiation.	titanium dioxide	31-35	CD2 molecule	Homo sapiens	106-109
34426395-3	2021	In this study, four chemical aging hydrochars (CAHCs) were obtained by using nitric acid (HNO3) with mass fractions of 5% (N5-HC), 10% (N10-HC), and 15% (N15-HC) to age the pristine HC (N0-HC) and remove the Cd2+ from the aqueous solution.	Nitric Acid	77-88	CD2 molecule	Homo sapiens	208-211
34426395-3	2021	In this study, four chemical aging hydrochars (CAHCs) were obtained by using nitric acid (HNO3) with mass fractions of 5% (N5-HC), 10% (N10-HC), and 15% (N15-HC) to age the pristine HC (N0-HC) and remove the Cd2+ from the aqueous solution.	Nitric Acid	90-94	CD2 molecule	Homo sapiens	208-211
34426395-4	2021	The results displayed that the N15-HC adsorption capacity was 19.99 mg g-1 (initial Cd2+ concentration was 50 mg L-1), which increased by 7.4 folds compared to N0-HC.	n15-hc	31-37	CD2 molecule	Homo sapiens	84-87
34426395-5	2021	After chemical aging, the specific surface area and oxygen-containing functional groups of CAHCs were increased, which contributed to combination with Cd2+ by physical adsorption and surface complexation.	Oxygen	52-58	CD2 molecule	Homo sapiens	151-154
34426395-7	2021	These findings have important implications for wastewater treatment to transform the forestry waste into a valuable adsorbent for Cd2+ removal from water.	Water	148-153	CD2 molecule	Homo sapiens	130-133
34722960-0	2021	Removal of Cd2+ and Pb2+ from Wastewater through Sequent Addition of KR-Slag, Ca(OH)2 Derived from Eggshells and CO2 Gas.	Calcium Hydroxide	78-85	CD2 molecule	Homo sapiens	11-14
34329121-7	2021	Moreover, biogenic CMC-FeS complex with CMC-to-FeS molar ratio of 0.0005 performed well in the presence of bicarbonate (5 mM), humic acid (10 mg/L), or co-existing cations such as Pb2+, Ni2+, Cd2+, Mn2+, and Cu2+ (200 ug/L) at pH 7.0, and displayed relatively high oxidation resistance and stability ability.	Carboxymethylcellulose Sodium	19-22	CD2 molecule	Homo sapiens	192-195
34329121-7	2021	Moreover, biogenic CMC-FeS complex with CMC-to-FeS molar ratio of 0.0005 performed well in the presence of bicarbonate (5 mM), humic acid (10 mg/L), or co-existing cations such as Pb2+, Ni2+, Cd2+, Mn2+, and Cu2+ (200 ug/L) at pH 7.0, and displayed relatively high oxidation resistance and stability ability.	Carboxymethylcellulose Sodium	40-43	CD2 molecule	Homo sapiens	192-195
34271357-7	2021	In the verification test of toxic metals remediation in a real landfill leachate (RLL), all of the Pb2+ and Cd2+ (initial concentrations: Pb2+ = 25 mg/L; Cd2+ = 5.6205 mg/L) was mineralized simultaneously, which further confirmed the feasibility of MICP for toxic metal remediation in landfill leachate.	Lead(2+)	99-103	CD2 molecule	Homo sapiens	154-157
34271357-7	2021	In the verification test of toxic metals remediation in a real landfill leachate (RLL), all of the Pb2+ and Cd2+ (initial concentrations: Pb2+ = 25 mg/L; Cd2+ = 5.6205 mg/L) was mineralized simultaneously, which further confirmed the feasibility of MICP for toxic metal remediation in landfill leachate.	Lead(2+)	138-142	CD2 molecule	Homo sapiens	108-111
34271357-7	2021	In the verification test of toxic metals remediation in a real landfill leachate (RLL), all of the Pb2+ and Cd2+ (initial concentrations: Pb2+ = 25 mg/L; Cd2+ = 5.6205 mg/L) was mineralized simultaneously, which further confirmed the feasibility of MICP for toxic metal remediation in landfill leachate.	micp	249-253	CD2 molecule	Homo sapiens	108-111
34271357-7	2021	In the verification test of toxic metals remediation in a real landfill leachate (RLL), all of the Pb2+ and Cd2+ (initial concentrations: Pb2+ = 25 mg/L; Cd2+ = 5.6205 mg/L) was mineralized simultaneously, which further confirmed the feasibility of MICP for toxic metal remediation in landfill leachate.	micp	249-253	CD2 molecule	Homo sapiens	154-157
34271357-7	2021	In the verification test of toxic metals remediation in a real landfill leachate (RLL), all of the Pb2+ and Cd2+ (initial concentrations: Pb2+ = 25 mg/L; Cd2+ = 5.6205 mg/L) was mineralized simultaneously, which further confirmed the feasibility of MICP for toxic metal remediation in landfill leachate.	Metals	264-269	CD2 molecule	Homo sapiens	108-111
34722960-6	2021	More than 99% of Cd2+ and Pb2+ was removed with 1 g/L of KR-slag, 0.5 g/L of Ca(OH)2, and CO2 injection at a rate of 1 L/min.	Krypton	57-59	CD2 molecule	Homo sapiens	17-20
34722960-6	2021	More than 99% of Cd2+ and Pb2+ was removed with 1 g/L of KR-slag, 0.5 g/L of Ca(OH)2, and CO2 injection at a rate of 1 L/min.	Carbon Dioxide	90-93	CD2 molecule	Homo sapiens	17-20
34722960-8	2021	Following the injection of CO2, removal efficiency has increased from 58.7 to 99.8 and 71.2 to 99.3% for Cd2+ and Pb2+, respectively.	Carbon Dioxide	27-30	CD2 molecule	Homo sapiens	105-108
34722960-12	2021	Contrarily, it was observed that a relatively higher concentration of metals was released in acidic solutions due to the substitution of metal ions (Cd2+ and Pb2+) with H+ ions.	Metals	70-76	CD2 molecule	Homo sapiens	149-152
34722960-12	2021	Contrarily, it was observed that a relatively higher concentration of metals was released in acidic solutions due to the substitution of metal ions (Cd2+ and Pb2+) with H+ ions.	Metals	137-142	CD2 molecule	Homo sapiens	149-152
34722993-1	2021	A novel triazole-bridged coumarin-benzimidazole-conjugated fluorescence sensor (4) has been developed for selective detection of Cd2+ over other competitive metal ions.	Triazoles	8-16	CD2 molecule	Homo sapiens	129-132
34722993-1	2021	A novel triazole-bridged coumarin-benzimidazole-conjugated fluorescence sensor (4) has been developed for selective detection of Cd2+ over other competitive metal ions.	coumarin	25-33	CD2 molecule	Homo sapiens	129-132
34722993-1	2021	A novel triazole-bridged coumarin-benzimidazole-conjugated fluorescence sensor (4) has been developed for selective detection of Cd2+ over other competitive metal ions.	benzimidazole	34-47	CD2 molecule	Homo sapiens	129-132
34722993-1	2021	A novel triazole-bridged coumarin-benzimidazole-conjugated fluorescence sensor (4) has been developed for selective detection of Cd2+ over other competitive metal ions.	Metals	157-162	CD2 molecule	Homo sapiens	129-132
34722993-4	2021	The involvement of benzimidazole and triazole moieties in Cd2+ binding was confirmed by different spectroscopic techniques such as UV-vis, Fourier transform infrared, nuclear magnetic resonance, and ESI mass.	benzimidazole	19-32	CD2 molecule	Homo sapiens	58-61
34633693-0	2022	Simultaneous determination of mitotane, its metabolite and 5 steroid hormones in urine samples by capillary electrophoresis using beta-CD2 SDS1 complexes as hydrophobic compounds solubilizers.	sds1	139-143	CD2 molecule	Homo sapiens	135-138
34722993-4	2021	The involvement of benzimidazole and triazole moieties in Cd2+ binding was confirmed by different spectroscopic techniques such as UV-vis, Fourier transform infrared, nuclear magnetic resonance, and ESI mass.	Triazoles	37-45	CD2 molecule	Homo sapiens	58-61
34289637-6	2021	Among the nanocomposite products, both graphene- and graphene oxide-MPM samples showed a significantly improved adsorption capacity towards Cd2+.	Graphite	39-47	CD2 molecule	Homo sapiens	140-143
34216960-0	2021	Biologically produced sulfur as a novel adsorbent to remove Cd2+ from aqueous solutions.	Sulfur	22-28	CD2 molecule	Homo sapiens	60-63
34216960-2	2021	Capability of BPS to remove Cd2+ from aqueous solutions was tested and its removal efficiency was compared to that of granular activated carbon (GAC).	bps	14-17	CD2 molecule	Homo sapiens	28-31
34216960-3	2021	Kinetics of Cd2+ removal by BPS was a two-stage process with an initial rapid adsorption showing 45% of initial Cd2+ was removed within 5 min, followed by a slower adsorption.	bps	28-31	CD2 molecule	Homo sapiens	12-15
34216960-3	2021	Kinetics of Cd2+ removal by BPS was a two-stage process with an initial rapid adsorption showing 45% of initial Cd2+ was removed within 5 min, followed by a slower adsorption.	bps	28-31	CD2 molecule	Homo sapiens	112-115
34216960-5	2021	Thermodynamic parameters showed that Cd2+ adsorption by BPS was favorable and endothermic.	bps	56-59	CD2 molecule	Homo sapiens	37-40
34216960-6	2021	Data from XPS proved the main adsorption mechanism to be complexation of Cd2+ with sulfides in the BPS.	Sulfides	83-91	CD2 molecule	Homo sapiens	73-76
34216960-6	2021	Data from XPS proved the main adsorption mechanism to be complexation of Cd2+ with sulfides in the BPS.	bps	99-102	CD2 molecule	Homo sapiens	73-76
34216960-7	2021	Results demonstrated that BPS can be recycled as a novel adsorbent for Cd2+ removal from wastewater.	bps	26-29	CD2 molecule	Homo sapiens	71-74
34289637-6	2021	Among the nanocomposite products, both graphene- and graphene oxide-MPM samples showed a significantly improved adsorption capacity towards Cd2+.	graphene oxide	53-67	CD2 molecule	Homo sapiens	140-143
34927952-1	2021	The imbalance of Zn2+ /Cd2+ in the human body can lead to many serious diseases due to the overuse of antibiotics and deposition in animal products.	Zinc	17-21	CD2 molecule	Homo sapiens	23-26
34927952-3	2021	Herein, silicon quantum dots (SiQDs) are designed as a functional platform for the detection of tetracycline and Zn2+ /Cd2+ .	Silicon	8-15	CD2 molecule	Homo sapiens	119-122
34927952-3	2021	Herein, silicon quantum dots (SiQDs) are designed as a functional platform for the detection of tetracycline and Zn2+ /Cd2+ .	Tetracycline	96-108	CD2 molecule	Homo sapiens	119-122
34927952-3	2021	Herein, silicon quantum dots (SiQDs) are designed as a functional platform for the detection of tetracycline and Zn2+ /Cd2+ .	Zinc	113-117	CD2 molecule	Homo sapiens	119-122
34927952-4	2021	The  COOH functionalized SiQDs with the emission wavelength of 450 nm are chelated with Eu(NO3 )3 to form SiQDs-Eu3+ ratio fluorescent probes, which can be used to detect tetracycline (TCs) and Zn2+ /Cd2+ by fluorescence resonance energy transfer (FRET) principle sequentially.	Carbonic Acid	5-9	CD2 molecule	Homo sapiens	200-203
34927952-4	2021	The  COOH functionalized SiQDs with the emission wavelength of 450 nm are chelated with Eu(NO3 )3 to form SiQDs-Eu3+ ratio fluorescent probes, which can be used to detect tetracycline (TCs) and Zn2+ /Cd2+ by fluorescence resonance energy transfer (FRET) principle sequentially.	eu3+	112-116	CD2 molecule	Homo sapiens	200-203
34927952-4	2021	The  COOH functionalized SiQDs with the emission wavelength of 450 nm are chelated with Eu(NO3 )3 to form SiQDs-Eu3+ ratio fluorescent probes, which can be used to detect tetracycline (TCs) and Zn2+ /Cd2+ by fluorescence resonance energy transfer (FRET) principle sequentially.	Zinc	194-198	CD2 molecule	Homo sapiens	200-203
34927952-6	2021	The detection limit of TCs and Zn2+ /Cd2+ are 0.2 x 10-6  m and 3 x 10-6  m, respectively, when the pH of the solution is 7.4.	Technetium	23-26	CD2 molecule	Homo sapiens	37-40
34927952-6	2021	The detection limit of TCs and Zn2+ /Cd2+ are 0.2 x 10-6  m and 3 x 10-6  m, respectively, when the pH of the solution is 7.4.	Zinc	31-35	CD2 molecule	Homo sapiens	37-40
34499067-2	2021	Here, we determined the Cd2+-induced membrane permeability of human MCF-7 cells using ferrocene methanol molecular probes based on scanning electrochemical microscopy (SECM).	ferrocenemethanol	86-104	CD2 molecule	Homo sapiens	24-27
34166940-0	2021	Efficient performance of magnesium oxide loaded biochar for the significant removal of Pb2+ and Cd2+ from aqueous solution.	Magnesium Oxide	25-40	CD2 molecule	Homo sapiens	96-99
34499835-4	2021	The adsorption capacities of HA-Ca/Fe3O4 for Pb2+, Cu2+, and Cd2+ were 208.33, 98.33, and 99.01 mg g-1, respectively.	ferryl iron	35-40	CD2 molecule	Homo sapiens	61-64
34499835-5	2021	The 0.02-0.1 times concentrations in alkali and alkaline-earth metals promoted Pb2+ and Cd2+ adsorption; however, any concentration of alkali and alkaline-earth metals inhibited Cu2+-ion adsorption, probably owing to the differences in ionic radii between the interfering and heavy-metal ions.	Metals	282-287	CD2 molecule	Homo sapiens	88-91
34499835-6	2021	Pb2+, Cu2+, and Cd2+ removal using HA-Ca/Fe3O4 occurred via ion exchange, complexation of O-containing functional groups, mineral precipitation, and pi-electron coordination.	ferryl iron	41-46	CD2 molecule	Homo sapiens	16-19
34499835-8	2021	In practice, HA-Ca/Fe3O4 can remove 99% Pb2+ and 91% Cu2+ and Cd2+ from real wastewater samples.	ferryl iron	19-24	CD2 molecule	Homo sapiens	62-65
34552089-6	2021	These findings help explain sexual dimorphism in human autoimmunity, as we find that CD2 polymorphisms are associated with rheumatoid arthritis and 17-beta-estradiol-regulation of CD2 is conserved in human T cells.	Estradiol	148-165	CD2 molecule	Homo sapiens	180-183
34576301-4	2021	Moreover, adverse effects induced by HPTE or DES were worsened by concurrent TCR and CD2 differentiation signaling, compared with EDC exposure post-signaling.	Diethylstilbestrol	45-48	CD2 molecule	Homo sapiens	85-88
34380211-5	2021	The P speciation shows a significant effect on the P-enriched biochars" passivation performance, especially orthophosphate, which is essential for the immobilization of Cd2+ by forming phosphate precipitation.	Phosphates	108-122	CD2 molecule	Homo sapiens	169-172
34380211-5	2021	The P speciation shows a significant effect on the P-enriched biochars" passivation performance, especially orthophosphate, which is essential for the immobilization of Cd2+ by forming phosphate precipitation.	Phosphates	185-194	CD2 molecule	Homo sapiens	169-172
34380211-6	2021	Pyrophosphate and orthophosphate monoester in AP-BC and PC-BC can promote Cd2+ passivation via the formation of P-Cd complexes or organometallic chelates.	diphosphoric acid	0-13	CD2 molecule	Homo sapiens	74-77
34380211-6	2021	Pyrophosphate and orthophosphate monoester in AP-BC and PC-BC can promote Cd2+ passivation via the formation of P-Cd complexes or organometallic chelates.	Phosphates	18-32	CD2 molecule	Homo sapiens	74-77
34111746-9	2021	The fabricated PM/g-C3N4/ASPE sensor exhibits superior stability, repeatability, good anti-interference, and applicability for recognition of Pb2+ and Cd2+ ions in real water samples.	Promethium	15-17	CD2 molecule	Homo sapiens	151-154
34380211-6	2021	Pyrophosphate and orthophosphate monoester in AP-BC and PC-BC can promote Cd2+ passivation via the formation of P-Cd complexes or organometallic chelates.	p-cd	112-116	CD2 molecule	Homo sapiens	74-77
34111746-9	2021	The fabricated PM/g-C3N4/ASPE sensor exhibits superior stability, repeatability, good anti-interference, and applicability for recognition of Pb2+ and Cd2+ ions in real water samples.	aspe	25-29	CD2 molecule	Homo sapiens	151-154
34111746-9	2021	The fabricated PM/g-C3N4/ASPE sensor exhibits superior stability, repeatability, good anti-interference, and applicability for recognition of Pb2+ and Cd2+ ions in real water samples.	Water	169-174	CD2 molecule	Homo sapiens	151-154
34134416-0	2021	2D-layered Mg(OH)2 material adsorbing cellobiose via interfacial chemical coupling and its applications in handling toxic Cd2+ and UO22+ ions.	Milk of magnesia	11-18	CD2 molecule	Homo sapiens	122-125
34374276-5	2021	In the two-step reaction (route III), an endocyclic Cd2+ complex, (Cd(L)I2) (3), obtained in the first step was utilized in the following reaction with Cu(CH3CN)4PF6, giving rise to an endo/exocyclic tetranuclear Cu+ complex, (Cu4(L)2(CH3CN)6)(PF6)4 (4), via Cd2+   2Cu+ substitution, which is not accessible by conventional procedures.	(cd(l)i2) (3	66-78	CD2 molecule	Homo sapiens	52-55
34374276-5	2021	In the two-step reaction (route III), an endocyclic Cd2+ complex, (Cd(L)I2) (3), obtained in the first step was utilized in the following reaction with Cu(CH3CN)4PF6, giving rise to an endo/exocyclic tetranuclear Cu+ complex, (Cu4(L)2(CH3CN)6)(PF6)4 (4), via Cd2+   2Cu+ substitution, which is not accessible by conventional procedures.	(cd(l)i2) (3	66-78	CD2 molecule	Homo sapiens	259-262
34374276-5	2021	In the two-step reaction (route III), an endocyclic Cd2+ complex, (Cd(L)I2) (3), obtained in the first step was utilized in the following reaction with Cu(CH3CN)4PF6, giving rise to an endo/exocyclic tetranuclear Cu+ complex, (Cu4(L)2(CH3CN)6)(PF6)4 (4), via Cd2+   2Cu+ substitution, which is not accessible by conventional procedures.	cu(ch3cn)4pf6	152-165	CD2 molecule	Homo sapiens	52-55
34374276-5	2021	In the two-step reaction (route III), an endocyclic Cd2+ complex, (Cd(L)I2) (3), obtained in the first step was utilized in the following reaction with Cu(CH3CN)4PF6, giving rise to an endo/exocyclic tetranuclear Cu+ complex, (Cu4(L)2(CH3CN)6)(PF6)4 (4), via Cd2+   2Cu+ substitution, which is not accessible by conventional procedures.	cu(ch3cn)4pf6	152-165	CD2 molecule	Homo sapiens	259-262
34374276-5	2021	In the two-step reaction (route III), an endocyclic Cd2+ complex, (Cd(L)I2) (3), obtained in the first step was utilized in the following reaction with Cu(CH3CN)4PF6, giving rise to an endo/exocyclic tetranuclear Cu+ complex, (Cu4(L)2(CH3CN)6)(PF6)4 (4), via Cd2+   2Cu+ substitution, which is not accessible by conventional procedures.	Copper	213-216	CD2 molecule	Homo sapiens	52-55
34374276-5	2021	In the two-step reaction (route III), an endocyclic Cd2+ complex, (Cd(L)I2) (3), obtained in the first step was utilized in the following reaction with Cu(CH3CN)4PF6, giving rise to an endo/exocyclic tetranuclear Cu+ complex, (Cu4(L)2(CH3CN)6)(PF6)4 (4), via Cd2+   2Cu+ substitution, which is not accessible by conventional procedures.	Copper	213-216	CD2 molecule	Homo sapiens	259-262
34374276-6	2021	Solution studies by comparative NMR and electrospray ionization mass spectroscopy also support metal substitution by showing the stronger binding affinity of Cu+ over Cd2+.	Metals	95-100	CD2 molecule	Homo sapiens	167-170
34374276-6	2021	Solution studies by comparative NMR and electrospray ionization mass spectroscopy also support metal substitution by showing the stronger binding affinity of Cu+ over Cd2+.	Copper	158-161	CD2 molecule	Homo sapiens	167-170
34134416-6	2021	On the basis of calculated structural/interfacial properties and experimental findings, the 2D Mg(OH)2 in terms of three-layer model was unraveled to substitute toxic Cd2+ ion and sorb radioactive UO22+ that is coordinated by water and hydroxyl groups.	2d mg(oh)2	92-102	CD2 molecule	Homo sapiens	167-170
34134416-6	2021	On the basis of calculated structural/interfacial properties and experimental findings, the 2D Mg(OH)2 in terms of three-layer model was unraveled to substitute toxic Cd2+ ion and sorb radioactive UO22+ that is coordinated by water and hydroxyl groups.	Water	226-231	CD2 molecule	Homo sapiens	167-170
34134416-6	2021	On the basis of calculated structural/interfacial properties and experimental findings, the 2D Mg(OH)2 in terms of three-layer model was unraveled to substitute toxic Cd2+ ion and sorb radioactive UO22+ that is coordinated by water and hydroxyl groups.	Hydroxyl Radical	236-244	CD2 molecule	Homo sapiens	167-170
34101337-3	2021	The fluorescent behavior of C-1 upon the addition of Zn2+ or Cd2+ showed a "turn-on" response accompanied with fluorescence enhancement at 510 nm by 6 times for Cd2+ and by 13 times for Zn2+ .	Zinc	53-57	CD2 molecule	Homo sapiens	161-164
34101337-3	2021	The fluorescent behavior of C-1 upon the addition of Zn2+ or Cd2+ showed a "turn-on" response accompanied with fluorescence enhancement at 510 nm by 6 times for Cd2+ and by 13 times for Zn2+ .	Zinc	186-190	CD2 molecule	Homo sapiens	61-64
34101337-3	2021	The fluorescent behavior of C-1 upon the addition of Zn2+ or Cd2+ showed a "turn-on" response accompanied with fluorescence enhancement at 510 nm by 6 times for Cd2+ and by 13 times for Zn2+ .	Carbon	28-29	CD2 molecule	Homo sapiens	61-64
34101337-3	2021	The fluorescent behavior of C-1 upon the addition of Zn2+ or Cd2+ showed a "turn-on" response accompanied with fluorescence enhancement at 510 nm by 6 times for Cd2+ and by 13 times for Zn2+ .	Carbon	28-29	CD2 molecule	Homo sapiens	161-164
34559076-1	2021	An excellent magnetic multi-walled carbon nanotubes (MMWCNT) containing carboxyl material modified with ferroferric oxide (Fe3O4) nanoparticles was synthesized as the adsorbent for magnetic solid-phase extraction (MSPE) of five heavy metal ions (Pb2+, Cu2+, Co2+, Cd2+, Cr4+) in water samples followed by on-line inductively coupled plasma mass spectrometry (ICP-MS) detection.	Carbon	35-41	CD2 molecule	Homo sapiens	264-267
34074399-3	2021	In this scheme, initially the phosphorescence of Cd2+-binding aptamer conjugated long afterglow nanoparticles (Zn2GeO4:Mn) was quenched by black hole quencher 1 (BHQ1) modified complementary DNA.	zinc germanate	111-118	CD2 molecule	Homo sapiens	49-52
34074399-6	2021	This method was successfully demonstrated for Cd2+ detection in drinking water and yesso scallop samples.	Water	73-78	CD2 molecule	Homo sapiens	46-49
34559076-1	2021	An excellent magnetic multi-walled carbon nanotubes (MMWCNT) containing carboxyl material modified with ferroferric oxide (Fe3O4) nanoparticles was synthesized as the adsorbent for magnetic solid-phase extraction (MSPE) of five heavy metal ions (Pb2+, Cu2+, Co2+, Cd2+, Cr4+) in water samples followed by on-line inductively coupled plasma mass spectrometry (ICP-MS) detection.	ferryl iron	123-128	CD2 molecule	Homo sapiens	264-267
34449598-3	2021	In Cd2+ and Cu2+ ion sorption tests, the synthesized dihydrazide-based PAMH hydrogel particles exhibited sorption capacities of 85 mg/g for copper and 47 mg/g for cadmium.	dihydrazide	53-64	CD2 molecule	Homo sapiens	3-6
34443225-5	2021	The review comprehensively discusses the progress made by various adsorbents such as natural materials, synthetic, agricultural, biopolymers, and commercial for extraction of the metal ions such as Ni2+, Cu2+, Pb2+, Cd2+, As2+ and Zn2+ along with their adsorption mechanisms.	Metals	179-184	CD2 molecule	Homo sapiens	216-219
34492822-0	2021	A novel remediation method of cadmium (Cd) contaminated soil: Dynamic equilibrium of Cd2+ rapid release from soil to water and selective adsorption by PP-g-AA fibers-ball at low concentration.	Cadmium	30-37	CD2 molecule	Homo sapiens	85-88
34492822-0	2021	A novel remediation method of cadmium (Cd) contaminated soil: Dynamic equilibrium of Cd2+ rapid release from soil to water and selective adsorption by PP-g-AA fibers-ball at low concentration.	Cadmium	39-41	CD2 molecule	Homo sapiens	85-88
34492822-0	2021	A novel remediation method of cadmium (Cd) contaminated soil: Dynamic equilibrium of Cd2+ rapid release from soil to water and selective adsorption by PP-g-AA fibers-ball at low concentration.	Water	117-122	CD2 molecule	Homo sapiens	85-88
34492822-2	2021	This study found that the acid-extractable fraction Cd(II) in soil could be released rapidly into water at very low Cd2+ concentration.	cd(ii)	52-58	CD2 molecule	Homo sapiens	116-119
34492822-4	2021	It could remove promptly trace Cd2+ from water even in the presence of interfering metal ions.	Water	41-46	CD2 molecule	Homo sapiens	31-34
34492822-4	2021	It could remove promptly trace Cd2+ from water even in the presence of interfering metal ions.	Metals	83-88	CD2 molecule	Homo sapiens	31-34
34492822-5	2021	Moreover, Cd(II) desorbed from soil to water could be continuously adsorbed by PP-g-AA fibers-ball, which kept the Cd2+ concentration always at a low level.	cd(ii)	10-16	CD2 molecule	Homo sapiens	115-118
34492822-5	2021	Moreover, Cd(II) desorbed from soil to water could be continuously adsorbed by PP-g-AA fibers-ball, which kept the Cd2+ concentration always at a low level.	Water	39-44	CD2 molecule	Homo sapiens	115-118
34449598-0	2021	Poly (Amidehydrazide) Hydrogel Particles for Removal of Cu2+ and Cd2+ Ions from Water.	poly (amidehydrazide)	0-21	CD2 molecule	Homo sapiens	65-68
34449598-0	2021	Poly (Amidehydrazide) Hydrogel Particles for Removal of Cu2+ and Cd2+ Ions from Water.	Water	80-85	CD2 molecule	Homo sapiens	65-68
34579312-5	2021	The presence of isosteviol and gibberellic acid (GA) significantly alleviated the inhibitory effect on the growth of wheat seedling under 10 microM Cd2+ stress.	isosteviol	16-26	CD2 molecule	Homo sapiens	148-151
34579312-5	2021	The presence of isosteviol and gibberellic acid (GA) significantly alleviated the inhibitory effect on the growth of wheat seedling under 10 microM Cd2+ stress.	gibberellic acid	31-47	CD2 molecule	Homo sapiens	148-151
34579312-5	2021	The presence of isosteviol and gibberellic acid (GA) significantly alleviated the inhibitory effect on the growth of wheat seedling under 10 microM Cd2+ stress.	gibberellic acid	49-51	CD2 molecule	Homo sapiens	148-151
34492884-3	2021	The results showed that Cd2+ and Pb2+ can form both inner- and outer-sphere complexes on Wyoming MMT, while Zn2+ only formed outer-sphere complex due to the stronger hydration interaction of Zn2+ than Cd2+ and Pb2+.	Lead(2+)	33-37	CD2 molecule	Homo sapiens	201-204
34492884-3	2021	The results showed that Cd2+ and Pb2+ can form both inner- and outer-sphere complexes on Wyoming MMT, while Zn2+ only formed outer-sphere complex due to the stronger hydration interaction of Zn2+ than Cd2+ and Pb2+.	Zinc	191-195	CD2 molecule	Homo sapiens	24-27
34492884-3	2021	The results showed that Cd2+ and Pb2+ can form both inner- and outer-sphere complexes on Wyoming MMT, while Zn2+ only formed outer-sphere complex due to the stronger hydration interaction of Zn2+ than Cd2+ and Pb2+.	Lead(2+)	210-214	CD2 molecule	Homo sapiens	24-27
34492884-3	2021	The results showed that Cd2+ and Pb2+ can form both inner- and outer-sphere complexes on Wyoming MMT, while Zn2+ only formed outer-sphere complex due to the stronger hydration interaction of Zn2+ than Cd2+ and Pb2+.	Lead(2+)	210-214	CD2 molecule	Homo sapiens	201-204
34449598-3	2021	In Cd2+ and Cu2+ ion sorption tests, the synthesized dihydrazide-based PAMH hydrogel particles exhibited sorption capacities of 85 mg/g for copper and 47 mg/g for cadmium.	3-methyl-2-phenyl-5,6,7,8-tetrahydro[1]benzothieno[2,3-b]pyridin-4-amine	71-75	CD2 molecule	Homo sapiens	3-6
34449598-3	2021	In Cd2+ and Cu2+ ion sorption tests, the synthesized dihydrazide-based PAMH hydrogel particles exhibited sorption capacities of 85 mg/g for copper and 47 mg/g for cadmium.	Copper	140-146	CD2 molecule	Homo sapiens	3-6
34361261-1	2021	The adsorption capacity of synthetic NaX zeolite for Pb2+, Cd2+, Cu2+ and Zn2+ in single and multi-component systems were investigated.	nax zeolite	37-48	CD2 molecule	Homo sapiens	59-62
34447788-4	2021	Using solution NMR and UV-vis spectroscopy, we found that Cd2+ spontaneously replaced Zn2+ in both structural sites of the C1B domain, with the formation of all-Cd and mixed Zn/Cd protein species.	Zinc	86-90	CD2 molecule	Homo sapiens	58-61
34447788-4	2021	Using solution NMR and UV-vis spectroscopy, we found that Cd2+ spontaneously replaced Zn2+ in both structural sites of the C1B domain, with the formation of all-Cd and mixed Zn/Cd protein species.	Cadmium	161-163	CD2 molecule	Homo sapiens	58-61
34447788-6	2021	Both Cys3His metal-ion sites of C1B have higher affinity to Cd2+ than Zn2+, but are thermodynamically and kinetically inequivalent with respect to the metal ion replacement, despite the identical coordination spheres.	Metals	13-18	CD2 molecule	Homo sapiens	60-63
34447788-7	2021	We find that even in the presence of the oxygen-rich sites presented by the neighboring peripheral membrane-binding C2 domain, the thiol-rich sites can successfully compete for the available Cd2+.	Oxygen	41-47	CD2 molecule	Homo sapiens	191-194
34447788-7	2021	We find that even in the presence of the oxygen-rich sites presented by the neighboring peripheral membrane-binding C2 domain, the thiol-rich sites can successfully compete for the available Cd2+.	Sulfhydryl Compounds	131-136	CD2 molecule	Homo sapiens	191-194
34447788-8	2021	Our results indicate that Cd2+ can target the entire membrane-binding regulatory region of PKCs, and that the competition between the thiol- and oxygen-rich sites will likely determine the activation pattern of PKCs.	Sulfhydryl Compounds	134-139	CD2 molecule	Homo sapiens	26-29
34447788-8	2021	Our results indicate that Cd2+ can target the entire membrane-binding regulatory region of PKCs, and that the competition between the thiol- and oxygen-rich sites will likely determine the activation pattern of PKCs.	Oxygen	145-151	CD2 molecule	Homo sapiens	26-29
34190309-0	2021	Bi-metallic zeolite imidazole framework nanofibers for the selective determination of Cd2+ ions.	metallic zeolite	3-19	CD2 molecule	Homo sapiens	86-89
34190309-0	2021	Bi-metallic zeolite imidazole framework nanofibers for the selective determination of Cd2+ ions.	imidazole	20-29	CD2 molecule	Homo sapiens	86-89
34190309-6	2021	The established heavy metal ion detector shows excellent anti-interference abilities toward the observed electroactive species, and it was successfully employed using a tap water sample for Cd2+ ion detection, where good results were observed.	Metals	22-27	CD2 molecule	Homo sapiens	190-193
34190309-6	2021	The established heavy metal ion detector shows excellent anti-interference abilities toward the observed electroactive species, and it was successfully employed using a tap water sample for Cd2+ ion detection, where good results were observed.	Water	173-178	CD2 molecule	Homo sapiens	190-193
34286718-6	2021	The specificity of the developed platform was cross-validated against various metallic pollutants and cations commonly found in water bodies (i.e., Cd2+, Pb2+, Cr3+, Fe3+, Mg2+, Ca2+, Zn2+, K+ and Al3+).	Water	128-133	CD2 molecule	Homo sapiens	148-151
34268544-2	2021	Herein, a novel methodology using self-reduction instead of electrodeposition was developed for the ASV sensing of HMIs (selecting Cd2+ as a representative analyte) by introducing Ti3C2Tx MXene nanoribbons (Ti3C2Tx NR) as a sensing element that can exhibit direct adsorption and reduction capabilities towards HMIs.	ASV	100-103	CD2 molecule	Homo sapiens	131-134
34283578-4	2021	The theoretical calculation and experimental results confirm that Ag+ replaces Cd2+ in CdSe and retains the crystal structure of MoSe2.	cdse	87-91	CD2 molecule	Homo sapiens	79-82
34361261-2	2021	The effects of electronegativity and hydration energy on the selective adsorption, as well as potential selective adsorption mechanism of the NaX zeolite for Pb2+, Cd2+, Cu2+ and Zn2+ were also discussed.	nax zeolite	142-153	CD2 molecule	Homo sapiens	164-167
34361261-3	2021	The maximum adsorption capacity order of the heavy metals in the single system was Pb2+ > Cd2+ > Cu2+ > Zn2+, and this could be related to their hydration energy and electronegativity.	Lead(2+)	83-87	CD2 molecule	Homo sapiens	90-93
34361261-3	2021	The maximum adsorption capacity order of the heavy metals in the single system was Pb2+ > Cd2+ > Cu2+ > Zn2+, and this could be related to their hydration energy and electronegativity.	cupric ion	97-101	CD2 molecule	Homo sapiens	90-93
34361261-3	2021	The maximum adsorption capacity order of the heavy metals in the single system was Pb2+ > Cd2+ > Cu2+ > Zn2+, and this could be related to their hydration energy and electronegativity.	Zinc	104-108	CD2 molecule	Homo sapiens	90-93
34361261-5	2021	The selective adsorption capacities of the metals were in the order, Pb2+ > Cd2+   Cu2+ > Zn2+.	cupric ion	83-87	CD2 molecule	Homo sapiens	76-79
34361261-5	2021	The selective adsorption capacities of the metals were in the order, Pb2+ > Cd2+   Cu2+ > Zn2+.	Zinc	90-94	CD2 molecule	Homo sapiens	76-79
34224011-6	2021	The metal ionic radii were acting on calculated sorption capacity and that sorption efficiency related to ionic radii of metal was as follows: R(Ni2+) <= R(Cd2+) < R(Cu2+) < R(Pb2+).	Metals	4-9	CD2 molecule	Homo sapiens	156-159
34148513-6	2021	Besides, consortium TC showed tolerances to high concentrations of pyrene (up to 1000 mg/L) and different heavy metal stresses (including Zn2+, Cd2+, and Pb2+).	Technetium	20-22	CD2 molecule	Homo sapiens	144-147
34148513-6	2021	Besides, consortium TC showed tolerances to high concentrations of pyrene (up to 1000 mg/L) and different heavy metal stresses (including Zn2+, Cd2+, and Pb2+).	pyrene	67-73	CD2 molecule	Homo sapiens	144-147
34148513-6	2021	Besides, consortium TC showed tolerances to high concentrations of pyrene (up to 1000 mg/L) and different heavy metal stresses (including Zn2+, Cd2+, and Pb2+).	Metals	112-117	CD2 molecule	Homo sapiens	144-147
34224011-0	2021	Removal of metallic trace elements (Pb2+, Cd2+, Cu2+, and Ni2+) from aqueous solution by adsorption onto cerium oxide modified activated carbon.	Carbon	137-143	CD2 molecule	Homo sapiens	42-45
34241721-7	2022	According to calculations, Cd2+ ion in soil solution was mostly bounded to associates CdOH+, partly to associates CdCO30 and CdHCO3+.	cdoh+	86-91	CD2 molecule	Homo sapiens	27-30
34241721-7	2022	According to calculations, Cd2+ ion in soil solution was mostly bounded to associates CdOH+, partly to associates CdCO30 and CdHCO3+.	cdco30	114-120	CD2 molecule	Homo sapiens	27-30
34241721-7	2022	According to calculations, Cd2+ ion in soil solution was mostly bounded to associates CdOH+, partly to associates CdCO30 and CdHCO3+.	cdhco3+	125-132	CD2 molecule	Homo sapiens	27-30
34241721-9	2022	The ratio of "active (Cd2+) to total Cd" reduced from 33.5% in control option to 28.0% in the option of phosphogypsum dose 40 t ha-1.	phosphogypsum	104-117	CD2 molecule	Homo sapiens	22-25
34224011-1	2021	The equilibrium and kinetic studies of removal of Pb2+, Cd2+, Ni2+, and Cu2+ metal ions were carried out using activated carbon prepared from palm kernel shell and doped with CeO2 (Ce/AC).	Carbon	121-127	CD2 molecule	Homo sapiens	56-59
34224011-6	2021	The metal ionic radii were acting on calculated sorption capacity and that sorption efficiency related to ionic radii of metal was as follows: R(Ni2+) <= R(Cd2+) < R(Cu2+) < R(Pb2+).	Metals	121-126	CD2 molecule	Homo sapiens	156-159
34224011-6	2021	The metal ionic radii were acting on calculated sorption capacity and that sorption efficiency related to ionic radii of metal was as follows: R(Ni2+) <= R(Cd2+) < R(Cu2+) < R(Pb2+).	Arginine	154-155	CD2 molecule	Homo sapiens	156-159
34279263-0	2021	Amorphous-Crystalline Calcium Phosphate Coating Promotes In Vitro Growth of Tumor-Derived Jurkat T Cells Activated by Anti-CD2/CD3/CD28 Antibodies.	calcium phosphate	22-39	CD2 molecule	Homo sapiens	123-126
34298880-1	2021	BACKGROUND: The proximal tubule (PT) is the major target of cadmium (Cd2+) nephrotoxicity.	Cadmium	60-67	CD2 molecule	Homo sapiens	69-72
34279263-7	2021	A decrease in the ZP magnitudes of CaP coatings deposited at 200-250 V was strongly associated with elevated hTERT expression in tumor-derived Jurkat T cells preliminarily activated with anti-CD2/CD3/CD28 antibodies and then contacted in vitro with CaP-coated samples for 14 days.	calcium phosphate	35-38	CD2 molecule	Homo sapiens	192-195
34132526-1	2021	Herein, we propose the topotactic and self-templated fabrication of Zn1-xCdxSe porous nanobelt-ZnO nanorod (termed as ZnCdSe/ZnO) photoelectrode via the cadmium (Cd2+) ion-exchange process on zinc (Zn) foil.	Zinc Oxide	95-98	CD2 molecule	Homo sapiens	162-165
34206233-1	2021	This contribution deals with the mechanochemical synthesis, characterization, and thermoelectric properties of tetrahedrite-based materials, Cu12-xMxSb4S13 (M = Fe2+, Zn2+, Cd2+; x = 0, 1.5, 2).	tetrahedrite	111-123	CD2 molecule	Homo sapiens	173-176
34207326-1	2021	The objective of this work was to fabricate modified cellulose nanofibers (CNFs) for the removal of heavy metal ions (Cd2+ and Pb2+) from wastewater.	Metals	106-111	CD2 molecule	Homo sapiens	118-121
34203125-4	2021	More impressively, the as-prepared ZnO-Ag/PPy displayed enhanced adsorption of Cd2+ and PO43- ions in the mixed solution.	zno-ag	35-41	CD2 molecule	Homo sapiens	79-82
34203125-4	2021	More impressively, the as-prepared ZnO-Ag/PPy displayed enhanced adsorption of Cd2+ and PO43- ions in the mixed solution.	phenylpyruvic acid	42-45	CD2 molecule	Homo sapiens	79-82
34132526-1	2021	Herein, we propose the topotactic and self-templated fabrication of Zn1-xCdxSe porous nanobelt-ZnO nanorod (termed as ZnCdSe/ZnO) photoelectrode via the cadmium (Cd2+) ion-exchange process on zinc (Zn) foil.	zncdse	118-124	CD2 molecule	Homo sapiens	162-165
34132526-1	2021	Herein, we propose the topotactic and self-templated fabrication of Zn1-xCdxSe porous nanobelt-ZnO nanorod (termed as ZnCdSe/ZnO) photoelectrode via the cadmium (Cd2+) ion-exchange process on zinc (Zn) foil.	Zinc Oxide	125-128	CD2 molecule	Homo sapiens	162-165
34132526-1	2021	Herein, we propose the topotactic and self-templated fabrication of Zn1-xCdxSe porous nanobelt-ZnO nanorod (termed as ZnCdSe/ZnO) photoelectrode via the cadmium (Cd2+) ion-exchange process on zinc (Zn) foil.	Cadmium	153-160	CD2 molecule	Homo sapiens	162-165
34132526-1	2021	Herein, we propose the topotactic and self-templated fabrication of Zn1-xCdxSe porous nanobelt-ZnO nanorod (termed as ZnCdSe/ZnO) photoelectrode via the cadmium (Cd2+) ion-exchange process on zinc (Zn) foil.	Zinc	198-200	CD2 molecule	Homo sapiens	162-165
34132526-4	2021	In particular Cd2+ ion temperature (140  C/18 h), the optimized ZnCdSe/ZnO-(F) photoelectrode shows an excellent photocurrent density of 14 mA cm-2 at 0 V vs Ag/AgCl with 219 mumol cm-2 hydrogen gas evolution for 3 h under 1 sun illumination.	zncdse	64-70	CD2 molecule	Homo sapiens	14-17
34132526-4	2021	In particular Cd2+ ion temperature (140  C/18 h), the optimized ZnCdSe/ZnO-(F) photoelectrode shows an excellent photocurrent density of 14 mA cm-2 at 0 V vs Ag/AgCl with 219 mumol cm-2 hydrogen gas evolution for 3 h under 1 sun illumination.	Zinc Oxide	71-74	CD2 molecule	Homo sapiens	14-17
34032091-2	2021	Here, a superparamagnetic nano-Fe3O4@SiO2 functionalized material (MFS) was prepared via a co-precipitation method, and the adsorption thermodynamic and kinetic characteristics of Cd2+ were studied by isothermal adsorption tests and kinetic experiments.	ferryl iron	31-36	CD2 molecule	Homo sapiens	180-183
34032091-2	2021	Here, a superparamagnetic nano-Fe3O4@SiO2 functionalized material (MFS) was prepared via a co-precipitation method, and the adsorption thermodynamic and kinetic characteristics of Cd2+ were studied by isothermal adsorption tests and kinetic experiments.	Silicon Dioxide	37-41	CD2 molecule	Homo sapiens	180-183
35417724-0	2022	Inhibitory effects of zinc chloride (ZnCl2), n-acetyl-L-cysteine (NAC), and calcium/calmodulin dependent protein kinase II inhibitor (KN93) on Cd2+-induced abnormal cell morphology and membrane permeability.	zinc chloride	22-35	CD2 molecule	Homo sapiens	143-146
34085125-8	2021	The amount of Cd sorption among treatments decreased in the order of A40 > A30 > A20 > A10 > A0, and the Langmuir model was more suitable to study the Cd2+ adsorption on biochar-amended soil than Freundlich model.	Cadmium	14-16	CD2 molecule	Homo sapiens	151-154
34720350-3	2021	In this study, the dehydration mechanism of a natural levyne previously exchanged with Cd2+ has been monitored in situ by single crystal X-ray diffraction.	levyne	54-60	CD2 molecule	Homo sapiens	87-90
34200211-3	2021	Adsorption performances of the hydrogel toward Pb2+, Cu2+ and Cd2+ in water under different condition as well as multi-ion competitive sorption were investigated.	Lead(2+)	47-51	CD2 molecule	Homo sapiens	62-65
34200211-3	2021	Adsorption performances of the hydrogel toward Pb2+, Cu2+ and Cd2+ in water under different condition as well as multi-ion competitive sorption were investigated.	Water	70-75	CD2 molecule	Homo sapiens	62-65
35417724-0	2022	Inhibitory effects of zinc chloride (ZnCl2), n-acetyl-L-cysteine (NAC), and calcium/calmodulin dependent protein kinase II inhibitor (KN93) on Cd2+-induced abnormal cell morphology and membrane permeability.	zinc chloride	37-42	CD2 molecule	Homo sapiens	143-146
35429859-3	2022	A water-soluble histidine-modified perylene diimide fluorescent probe was synthesized by a one-step method, and the probe can form supramolecular aggregates in the presence of Cd2+.	Water	2-7	CD2 molecule	Homo sapiens	176-179
35429859-3	2022	A water-soluble histidine-modified perylene diimide fluorescent probe was synthesized by a one-step method, and the probe can form supramolecular aggregates in the presence of Cd2+.	Histidine	16-25	CD2 molecule	Homo sapiens	176-179
35417724-0	2022	Inhibitory effects of zinc chloride (ZnCl2), n-acetyl-L-cysteine (NAC), and calcium/calmodulin dependent protein kinase II inhibitor (KN93) on Cd2+-induced abnormal cell morphology and membrane permeability.	Acetylcysteine	45-64	CD2 molecule	Homo sapiens	143-146
35417724-0	2022	Inhibitory effects of zinc chloride (ZnCl2), n-acetyl-L-cysteine (NAC), and calcium/calmodulin dependent protein kinase II inhibitor (KN93) on Cd2+-induced abnormal cell morphology and membrane permeability.	Acetylcysteine	66-69	CD2 molecule	Homo sapiens	143-146
35429859-3	2022	A water-soluble histidine-modified perylene diimide fluorescent probe was synthesized by a one-step method, and the probe can form supramolecular aggregates in the presence of Cd2+.	perylenediimide	35-51	CD2 molecule	Homo sapiens	176-179
35417724-4	2022	0.5 mmol L-1 NAC and 5 mumol L-1 KN93 could significantly inhibit the effects of Cd2+ on the morphology and membrane permeability of MCF-7 cells (p < 0.01).	Acetylcysteine	13-16	CD2 molecule	Homo sapiens	81-84
35417724-4	2022	0.5 mmol L-1 NAC and 5 mumol L-1 KN93 could significantly inhibit the effects of Cd2+ on the morphology and membrane permeability of MCF-7 cells (p < 0.01).	KN 93	33-37	CD2 molecule	Homo sapiens	81-84
35417724-6	2022	The results of cell activity experiment showed that 10 mumol L-1 ZnCl2, 0.5 mmol L-1 NAC and 5 mumol L-1 KN93 could inhibit the effect of Cd2+ on the activity of MCF-7 cells.	zinc chloride	65-70	CD2 molecule	Homo sapiens	138-141
35417724-6	2022	The results of cell activity experiment showed that 10 mumol L-1 ZnCl2, 0.5 mmol L-1 NAC and 5 mumol L-1 KN93 could inhibit the effect of Cd2+ on the activity of MCF-7 cells.	Acetylcysteine	85-88	CD2 molecule	Homo sapiens	138-141
35417724-6	2022	The results of cell activity experiment showed that 10 mumol L-1 ZnCl2, 0.5 mmol L-1 NAC and 5 mumol L-1 KN93 could inhibit the effect of Cd2+ on the activity of MCF-7 cells.	KN 93	105-109	CD2 molecule	Homo sapiens	138-141
35417724-7	2022	By comparing the inhibitory effects of ZnCl2, NAC and KN93 on Cd2+- induced cytotoxicity, 5 mumol L-1 KN93 had the robust effect on the maintenance of MCF-7 cell morphology and cell membrane integrity.	zinc chloride	39-44	CD2 molecule	Homo sapiens	62-65
35417724-7	2022	By comparing the inhibitory effects of ZnCl2, NAC and KN93 on Cd2+- induced cytotoxicity, 5 mumol L-1 KN93 had the robust effect on the maintenance of MCF-7 cell morphology and cell membrane integrity.	Acetylcysteine	46-49	CD2 molecule	Homo sapiens	62-65
35417724-7	2022	By comparing the inhibitory effects of ZnCl2, NAC and KN93 on Cd2+- induced cytotoxicity, 5 mumol L-1 KN93 had the robust effect on the maintenance of MCF-7 cell morphology and cell membrane integrity.	KN 93	54-58	CD2 molecule	Homo sapiens	62-65
35417724-8	2022	Our research provided evidence on Zn supplement, NAC as antioxidant drugs, and KN93 as special inhibitor for the detoxification of Cd2+-reduced abnormal cell morphology and membrane permeability.	KN 93	79-83	CD2 molecule	Homo sapiens	131-134
35526481-2	2022	Cadmium ion (Cd2+) as a hazardous water pollutant is seriously detrimental to human health, food safety, and ecological areas.	Cadmium	0-7	CD2 molecule	Homo sapiens	13-16
35526481-2	2022	Cadmium ion (Cd2+) as a hazardous water pollutant is seriously detrimental to human health, food safety, and ecological areas.	Water	34-39	CD2 molecule	Homo sapiens	13-16
35526481-3	2022	Hence, we successfully designed a simple detection array for monitoring of ultra-low levels of Cd2+ ion by combining the advantages of aptamer as a high sensitive and selective sensing probe and zeolitic imidazolate framework-8 (ZIF-8) as a superior fluorescence quenching inducer.	imidazolate	204-215	CD2 molecule	Homo sapiens	95-98
35526481-7	2022	The aptasensor could detect Cd2+ in the diverse real sample, including tap water, milk, coffee, and human blood serum.	Water	75-80	CD2 molecule	Homo sapiens	28-31
35439494-4	2022	Thus, to tackle this challenge, TX-100 SnO2 nanoparticles based chemically modified sensor is introduced to assess the quantity of Cd+2 in the water system.	Tin(IV) oxide	39-43	CD2 molecule	Homo sapiens	131-135
35439494-4	2022	Thus, to tackle this challenge, TX-100 SnO2 nanoparticles based chemically modified sensor is introduced to assess the quantity of Cd+2 in the water system.	Water	143-148	CD2 molecule	Homo sapiens	131-135
35550748-6	2022	This review also discuss the methods used in the synthesis of the SDAs, their affinity for the removal of Pb2+ and Cd2+, and the mechanisms involved in the processes.	sdas	66-70	CD2 molecule	Homo sapiens	115-118
35439494-9	2022	Moreover, the excellent stability and anti-interference behavior of the sensor highlights its dynamic profile to be commercially utilized for the determination of Cd+2 ions in water bodies.	Water	176-181	CD2 molecule	Homo sapiens	163-167
35550924-2	2022	Here, fungal-sponge composite carriers (FSC) were assembled and immobilized with strain WZ39 in a bioreactor to remove NO3--N, Ca2+, and Cd2+.	wz39	88-92	CD2 molecule	Homo sapiens	137-140
35358804-6	2022	The adsorption isotherms of heavy metals coincided with Langmuir model or Freundlich model, and the adsorption capacities for Pb2+, Cu2+, Ni2+, Cd2+ could reach up to 661.5 mg/g, 116.3 mg/g, 117.3 mg/g, 235.2 mg/g respectively.	Lead(2+)	126-130	CD2 molecule	Homo sapiens	144-147
35500345-4	2022	It was found that the pure water permeability (11.6 Lm-2h-1bar-1) of the THPC modified membrane was three times larger than that of the original PEI-TMC membrane (3.4 Lm-2h-1bar-1) while maintaining a high level of ion rejections (around 95% for Zn2+, Cd2+, Ni2+, Cu2+ and about 90% for Pb2+).	tetramethylolphosphonium chloride	73-77	CD2 molecule	Homo sapiens	252-255
35500345-4	2022	It was found that the pure water permeability (11.6 Lm-2h-1bar-1) of the THPC modified membrane was three times larger than that of the original PEI-TMC membrane (3.4 Lm-2h-1bar-1) while maintaining a high level of ion rejections (around 95% for Zn2+, Cd2+, Ni2+, Cu2+ and about 90% for Pb2+).	pei	145-148	CD2 molecule	Homo sapiens	252-255
35149468-4	2022	Under the optimal conditions, the electrochemical aptasensor showed linear response to Cd2+ and Pb2+ in the range of 0.1 to 1000 nmol/L, and the detection limits of Cd2+ and Pb2+ achieved 89.31 and 16.44 pmol/L (3sigma), respectively.	Lead(2+)	96-100	CD2 molecule	Homo sapiens	165-168
35149468-4	2022	Under the optimal conditions, the electrochemical aptasensor showed linear response to Cd2+ and Pb2+ in the range of 0.1 to 1000 nmol/L, and the detection limits of Cd2+ and Pb2+ achieved 89.31 and 16.44 pmol/L (3sigma), respectively.	Lead(2+)	174-178	CD2 molecule	Homo sapiens	87-90
35358811-2	2022	The findings revealed that the SDBS/ABsep had a rougher surface and higher porosity, and the maximum adsorption capacity of Cd2+ onto SDBS/ABsep was 241.39 mg g-1, which was 5.32 times higher than that on Sep.	absep	36-41	CD2 molecule	Homo sapiens	124-127
35358811-2	2022	The findings revealed that the SDBS/ABsep had a rougher surface and higher porosity, and the maximum adsorption capacity of Cd2+ onto SDBS/ABsep was 241.39 mg g-1, which was 5.32 times higher than that on Sep.	absep	139-144	CD2 molecule	Homo sapiens	124-127
35182527-6	2022	This research elaborates a simplistic, and reliable preconcentration column method highly developed for the determination of Cd2+, Fe3+, Co2+, Cr3+, Cu2+, Mn2+, Pb2+ and Ni2+ ions in model solutions and real water samples by flame atomic absorption spectrometry (FAAS).	Water	208-213	CD2 molecule	Homo sapiens	125-128
35248619-0	2022	Hierarchically porous biochar templated by in situ formed ZnO for rapid Pb2+ and Cd2+ adsorption in wastewater: Experiment and molecular dynamics study.	Zinc Oxide	58-61	CD2 molecule	Homo sapiens	81-84
35216977-5	2022	The EDS and FTIR results suggested that ion-exchange and complexation between CGB/Aged-CGB with Cd2+/Zn2+ played a dominant role in adsorption processes.	Zinc	101-105	CD2 molecule	Homo sapiens	96-99
35129745-5	2022	The results indicated that at pH 6, a pseudo-second-order kinetic model was applicable to describe adsorption of studied heavy metals by sulfonated polystyrene with adsorption capacities of 7.48 mg Cu2+/g, 7.23 mg Zn2+/g, and 6.50 mg Cd2+/g, respectively.	sulfonated polystyrene	137-159	CD2 molecule	Homo sapiens	234-237
35129745-6	2022	Moreover, the ion exchange process between sulfonated polystyrene resin and Cu2+, Zn2+, Cd2+ ions followed the Langmuir isotherm adsorption model with R2 higher than 96%.	sulfonated polystyrene	43-65	CD2 molecule	Homo sapiens	88-91
35129745-6	2022	Moreover, the ion exchange process between sulfonated polystyrene resin and Cu2+, Zn2+, Cd2+ ions followed the Langmuir isotherm adsorption model with R2 higher than 96%.	cupric ion	76-80	CD2 molecule	Homo sapiens	88-91
35248619-7	2022	When applied to treat desulfurization wastewater from power plants, HPBC yielded 100% removal of Pb2+ and Cd2+, much higher than that by using commercial activated carbon (28%).	hpbc	68-72	CD2 molecule	Homo sapiens	106-109
35248619-9	2022	The adsorption of Pb2+ and Cd2+ on HPBC was mainly achieved by diffusion, oxygen functional group complexation, and precipitation.	hpbc	35-39	CD2 molecule	Homo sapiens	27-30
35248619-9	2022	The adsorption of Pb2+ and Cd2+ on HPBC was mainly achieved by diffusion, oxygen functional group complexation, and precipitation.	Oxygen	74-80	CD2 molecule	Homo sapiens	27-30
35093378-7	2022	The open literature reports that spent adsorbents based on polysaccharides with iron oxides may adsorb up to 1 g g-1 of organic pollutants and up to near 100% of metallic ions from wastewater (Cu2+, Cd2+, Zn2+, Pb2+).	Polysaccharides	59-74	CD2 molecule	Homo sapiens	199-202
35584535-4	2022	A fine-tuning of the Mn2+ concentration from 1 to 50 mol % Cd2+ induces a substantial red shift of emission spectra from 570 to 630 nm due to the shrinkage of the crystalline host lattice, and the maximum intensity of emission is achieved at 20 mol % Mn2+ doping.	Manganese(2+)	21-25	CD2 molecule	Homo sapiens	59-62
35584535-4	2022	A fine-tuning of the Mn2+ concentration from 1 to 50 mol % Cd2+ induces a substantial red shift of emission spectra from 570 to 630 nm due to the shrinkage of the crystalline host lattice, and the maximum intensity of emission is achieved at 20 mol % Mn2+ doping.	Manganese(2+)	251-255	CD2 molecule	Homo sapiens	59-62
35093378-7	2022	The open literature reports that spent adsorbents based on polysaccharides with iron oxides may adsorb up to 1 g g-1 of organic pollutants and up to near 100% of metallic ions from wastewater (Cu2+, Cd2+, Zn2+, Pb2+).	ferric oxide	80-91	CD2 molecule	Homo sapiens	199-202
35093378-7	2022	The open literature reports that spent adsorbents based on polysaccharides with iron oxides may adsorb up to 1 g g-1 of organic pollutants and up to near 100% of metallic ions from wastewater (Cu2+, Cd2+, Zn2+, Pb2+).	metallic	162-170	CD2 molecule	Homo sapiens	199-202
35093378-7	2022	The open literature reports that spent adsorbents based on polysaccharides with iron oxides may adsorb up to 1 g g-1 of organic pollutants and up to near 100% of metallic ions from wastewater (Cu2+, Cd2+, Zn2+, Pb2+).	Zinc	205-209	CD2 molecule	Homo sapiens	199-202
35093378-7	2022	The open literature reports that spent adsorbents based on polysaccharides with iron oxides may adsorb up to 1 g g-1 of organic pollutants and up to near 100% of metallic ions from wastewater (Cu2+, Cd2+, Zn2+, Pb2+).	Lead(2+)	211-215	CD2 molecule	Homo sapiens	199-202
35623439-5	2022	According to the theoretical calculations and experimental results, Fe-ions could be readily recovered from wastewater because it has the best adsorption efficiency among all other co-existing metals (Ni2+, Cd2+, Co2+, Cu2+, and Cr6+).	Iron	68-70	CD2 molecule	Homo sapiens	207-210
35537082-1	2022	To design nonlinear optical (NLO) materials, we focused on combinations of d10 metal cation (Cd2+)-based chloride and morpholine molecules to form organic-inorganic hybrids.	d10 metal cation	75-91	CD2 molecule	Homo sapiens	93-96
35619002-4	2022	The ability of P(AA-AN)-talc to capture (Pb2+, Cd2+, Co2+, Zn2+, and Sr2+) as multi-component aqueous solutions was performed by a batch method.	p(aa-an)	15-23	CD2 molecule	Homo sapiens	47-50
35537082-1	2022	To design nonlinear optical (NLO) materials, we focused on combinations of d10 metal cation (Cd2+)-based chloride and morpholine molecules to form organic-inorganic hybrids.	Chlorides	105-113	CD2 molecule	Homo sapiens	93-96
35537082-2	2022	The O of morpholine containing lone-pair electrons can be integrated with Cd2+ by a ligand-to-metal charge transfer (LMCT) strategy to build acentric structures benefiting from the second-order Jahn-Teller effect.	morpholine	9-19	CD2 molecule	Homo sapiens	74-77
35537082-2	2022	The O of morpholine containing lone-pair electrons can be integrated with Cd2+ by a ligand-to-metal charge transfer (LMCT) strategy to build acentric structures benefiting from the second-order Jahn-Teller effect.	Metals	94-99	CD2 molecule	Homo sapiens	74-77
35624611-1	2022	Cadmium ions (Cd2+) are extremely toxic heavy metal pollutants found in the environment, and which endanger human health.	Cadmium	0-7	CD2 molecule	Homo sapiens	14-17
35007541-7	2022	Moreover, UiO-66 incorporated membranes were highly-effective in the removal of contaminants like heavy metal ions (Sr2+, Pb2+, Cd2+, and Cr6+) and HA at the same time.	uio-66	10-16	CD2 molecule	Homo sapiens	128-131
35007541-7	2022	Moreover, UiO-66 incorporated membranes were highly-effective in the removal of contaminants like heavy metal ions (Sr2+, Pb2+, Cd2+, and Cr6+) and HA at the same time.	Metals	104-109	CD2 molecule	Homo sapiens	128-131
35567805-4	2022	Employing the diversity of colorimetric responses of metal ions to the two sensing channels, nine metal ions including Cr3+, Fe3+, Cu2+, Co2+, Ni2+, Pb2+, Mg2+, K+, and Cd2+ were well distinguished with a discrimination accuracy of 100% at a concentration as low as 50 nM.	Metals	53-58	CD2 molecule	Homo sapiens	169-172
35567805-4	2022	Employing the diversity of colorimetric responses of metal ions to the two sensing channels, nine metal ions including Cr3+, Fe3+, Cu2+, Co2+, Ni2+, Pb2+, Mg2+, K+, and Cd2+ were well distinguished with a discrimination accuracy of 100% at a concentration as low as 50 nM.	Metals	98-103	CD2 molecule	Homo sapiens	169-172
35228083-2	2022	The results suggested that both protein-like molecules and marine humic acids could react with trace metals (Cu2+ and Cd2+).	Humic Substances	66-77	CD2 molecule	Homo sapiens	118-121
35065113-1	2022	In this study, the nano-scale spatial distribution of natural organic matter (NOM) on the surface of iron (hydr)oxides and its relevance to oxyanion (PO43-) and metal cation (Cd2+ and Cu2+) adsorption to the assemblage of oxide (goethite) and NOM (humic acids (HA) or fulvic acids (FA)) was investigated with experiments and advanced surface complexation modeling.	iron (hydr)oxides	101-118	CD2 molecule	Homo sapiens	175-178
35065113-1	2022	In this study, the nano-scale spatial distribution of natural organic matter (NOM) on the surface of iron (hydr)oxides and its relevance to oxyanion (PO43-) and metal cation (Cd2+ and Cu2+) adsorption to the assemblage of oxide (goethite) and NOM (humic acids (HA) or fulvic acids (FA)) was investigated with experiments and advanced surface complexation modeling.	Metals	161-166	CD2 molecule	Homo sapiens	175-178
35065113-4	2022	The results showed that with the increase of NOM loading on oxides, deviation between the MSM and NOM-CD model became bigger for PO43-, but smaller for Cd2+ and Cu2+.	Oxides	60-66	CD2 molecule	Homo sapiens	152-155
35065113-4	2022	The results showed that with the increase of NOM loading on oxides, deviation between the MSM and NOM-CD model became bigger for PO43-, but smaller for Cd2+ and Cu2+.	Cadmium	102-104	CD2 molecule	Homo sapiens	152-155
35624611-1	2022	Cadmium ions (Cd2+) are extremely toxic heavy metal pollutants found in the environment, and which endanger human health.	Metals	46-51	CD2 molecule	Homo sapiens	14-17
35624611-2	2022	Therefore, it is critical to develop a sensitive and simple method for rapidly detecting Cd2+ in water samples.	Water	97-102	CD2 molecule	Homo sapiens	89-92
35624611-3	2022	Herein, an enzymic membrane was developed based on an easy and rapid immobilization method of horseradish peroxidase (HRP), for determination of Cd2+ in drinking water.	Water	162-167	CD2 molecule	Homo sapiens	145-148
35624611-8	2022	The use of this enzymic membrane proved to be advantageous when reversible inhibitors such as the copper ion (Cu2+) were present in water samples, as Cu2+ can interfere with Cd2+ and cause erroneous results.	Copper	98-104	CD2 molecule	Homo sapiens	174-177
35624611-8	2022	The use of this enzymic membrane proved to be advantageous when reversible inhibitors such as the copper ion (Cu2+) were present in water samples, as Cu2+ can interfere with Cd2+ and cause erroneous results.	cupric ion	110-114	CD2 molecule	Homo sapiens	174-177
35624611-8	2022	The use of this enzymic membrane proved to be advantageous when reversible inhibitors such as the copper ion (Cu2+) were present in water samples, as Cu2+ can interfere with Cd2+ and cause erroneous results.	Water	132-137	CD2 molecule	Homo sapiens	174-177
35624611-8	2022	The use of this enzymic membrane proved to be advantageous when reversible inhibitors such as the copper ion (Cu2+) were present in water samples, as Cu2+ can interfere with Cd2+ and cause erroneous results.	cupric ion	150-154	CD2 molecule	Homo sapiens	174-177
35074749-5	2022	Moreover, the percentages of Cd2+ and Zn2+ in soil pore water showed a dynamic increase in smithsonite-spiked treatments but a decrease in sphalerite-spiked treatments.	Water	56-61	CD2 molecule	Homo sapiens	29-32
35510764-4	2022	After being anchored with a photocatalysis center (eosin-5-isothiocyanate, EY), the constructed LHS could sequentially transfer energy between two kinds of chromophores (CD1 and CD2), and further transfer to EY center with a high efficiency of 84%.	alpha-glutamyltyrosine	75-77	CD2 molecule	Homo sapiens	178-181
35074749-5	2022	Moreover, the percentages of Cd2+ and Zn2+ in soil pore water showed a dynamic increase in smithsonite-spiked treatments but a decrease in sphalerite-spiked treatments.	Smithsonite	91-102	CD2 molecule	Homo sapiens	29-32
35074749-5	2022	Moreover, the percentages of Cd2+ and Zn2+ in soil pore water showed a dynamic increase in smithsonite-spiked treatments but a decrease in sphalerite-spiked treatments.	zinc sulfide	139-149	CD2 molecule	Homo sapiens	29-32
35085618-0	2022	MgO-loaded nitrogen and phosphorus self-doped biochar: High-efficient adsorption of aquatic Cu2+, Cd2+, and Pb2+ and its remediation efficiency on heavy metal contaminated soil.	Nitrogen	11-19	CD2 molecule	Homo sapiens	98-101
35411895-2	2022	A novel water-stable metal organic framework material (Cd2(Hdpb)(H2O)3) (Cd-MOF) was synthesized based on H5dpb (H5dpb = 3,5-diphosphonobenzoic acid) and Cd2+ ions.	Water	8-13	CD2 molecule	Homo sapiens	55-58
35411895-2	2022	A novel water-stable metal organic framework material (Cd2(Hdpb)(H2O)3) (Cd-MOF) was synthesized based on H5dpb (H5dpb = 3,5-diphosphonobenzoic acid) and Cd2+ ions.	Water	8-13	CD2 molecule	Homo sapiens	154-157
35411895-2	2022	A novel water-stable metal organic framework material (Cd2(Hdpb)(H2O)3) (Cd-MOF) was synthesized based on H5dpb (H5dpb = 3,5-diphosphonobenzoic acid) and Cd2+ ions.	Metals	21-26	CD2 molecule	Homo sapiens	55-58
35411895-2	2022	A novel water-stable metal organic framework material (Cd2(Hdpb)(H2O)3) (Cd-MOF) was synthesized based on H5dpb (H5dpb = 3,5-diphosphonobenzoic acid) and Cd2+ ions.	Metals	21-26	CD2 molecule	Homo sapiens	154-157
35411895-2	2022	A novel water-stable metal organic framework material (Cd2(Hdpb)(H2O)3) (Cd-MOF) was synthesized based on H5dpb (H5dpb = 3,5-diphosphonobenzoic acid) and Cd2+ ions.	Water	65-68	CD2 molecule	Homo sapiens	55-58
35411895-2	2022	A novel water-stable metal organic framework material (Cd2(Hdpb)(H2O)3) (Cd-MOF) was synthesized based on H5dpb (H5dpb = 3,5-diphosphonobenzoic acid) and Cd2+ ions.	Water	65-68	CD2 molecule	Homo sapiens	154-157
35411895-2	2022	A novel water-stable metal organic framework material (Cd2(Hdpb)(H2O)3) (Cd-MOF) was synthesized based on H5dpb (H5dpb = 3,5-diphosphonobenzoic acid) and Cd2+ ions.	cd-mof	73-79	CD2 molecule	Homo sapiens	55-58
35411895-2	2022	A novel water-stable metal organic framework material (Cd2(Hdpb)(H2O)3) (Cd-MOF) was synthesized based on H5dpb (H5dpb = 3,5-diphosphonobenzoic acid) and Cd2+ ions.	cd-mof	73-79	CD2 molecule	Homo sapiens	154-157
35411895-2	2022	A novel water-stable metal organic framework material (Cd2(Hdpb)(H2O)3) (Cd-MOF) was synthesized based on H5dpb (H5dpb = 3,5-diphosphonobenzoic acid) and Cd2+ ions.	h5dpb	106-111	CD2 molecule	Homo sapiens	55-58
35411895-2	2022	A novel water-stable metal organic framework material (Cd2(Hdpb)(H2O)3) (Cd-MOF) was synthesized based on H5dpb (H5dpb = 3,5-diphosphonobenzoic acid) and Cd2+ ions.	h5dpb	106-111	CD2 molecule	Homo sapiens	154-157
35411895-2	2022	A novel water-stable metal organic framework material (Cd2(Hdpb)(H2O)3) (Cd-MOF) was synthesized based on H5dpb (H5dpb = 3,5-diphosphonobenzoic acid) and Cd2+ ions.	h5dpb	113-118	CD2 molecule	Homo sapiens	55-58
35411895-2	2022	A novel water-stable metal organic framework material (Cd2(Hdpb)(H2O)3) (Cd-MOF) was synthesized based on H5dpb (H5dpb = 3,5-diphosphonobenzoic acid) and Cd2+ ions.	h5dpb	113-118	CD2 molecule	Homo sapiens	154-157
35411895-2	2022	A novel water-stable metal organic framework material (Cd2(Hdpb)(H2O)3) (Cd-MOF) was synthesized based on H5dpb (H5dpb = 3,5-diphosphonobenzoic acid) and Cd2+ ions.	3,5-DIPHOSPHONOBENZOIC ACID	121-148	CD2 molecule	Homo sapiens	55-58
35411895-3	2022	Cd2+ ions are connected with phosphonates and carboxyl groups of H5dpb to form an infinitely extended 1D chain, which is further connected by the Hdpb4- ligand and coordinated water to form a three-dimensional network structure.	Organophosphonates	29-41	CD2 molecule	Homo sapiens	0-3
35411895-3	2022	Cd2+ ions are connected with phosphonates and carboxyl groups of H5dpb to form an infinitely extended 1D chain, which is further connected by the Hdpb4- ligand and coordinated water to form a three-dimensional network structure.	h5dpb	65-70	CD2 molecule	Homo sapiens	0-3
35411895-3	2022	Cd2+ ions are connected with phosphonates and carboxyl groups of H5dpb to form an infinitely extended 1D chain, which is further connected by the Hdpb4- ligand and coordinated water to form a three-dimensional network structure.	Water	176-181	CD2 molecule	Homo sapiens	0-3
35436089-4	2022	Based on their crystal structures, the origin of the chirality in Au24Cd2 was found to be the twist of the kernel and the chiral arrangement of the metal-ligand surface.	Metals	148-153	CD2 molecule	Homo sapiens	70-73
35085618-1	2022	In this study, the MgO-loaded fish scale biochar (MgO-FB) was synthesized by impregnation of MgCl2 using fish scales as precursor, and the modified biochar was applied for the adsorption of aquatic Cu2+, Cd2+, and Pb2+, and the immobilization of heavy metals in soils.	mgo	19-22	CD2 molecule	Homo sapiens	204-207
35085618-2	2022	The maximum adsorption capacities of MgO-FB for Cu2+, Cd2+, and Pb2+ were 505.8, 327.2, and 661.2 mg/g, respectively.	mgo-fb	37-43	CD2 molecule	Homo sapiens	54-57
35085618-4	2022	Multiple characterizations and comparative experiments have demonstrated that the hydroxyapatite components and the MgO micro-nanoparticles on MgO-FB enhanced the adsorption capacity for Cu2+, Cd2+, and Pb2+ through ion-exchange and precipitation process.	Durapatite	82-96	CD2 molecule	Homo sapiens	193-196
35085618-4	2022	Multiple characterizations and comparative experiments have demonstrated that the hydroxyapatite components and the MgO micro-nanoparticles on MgO-FB enhanced the adsorption capacity for Cu2+, Cd2+, and Pb2+ through ion-exchange and precipitation process.	mgo	116-119	CD2 molecule	Homo sapiens	193-196
35085618-4	2022	Multiple characterizations and comparative experiments have demonstrated that the hydroxyapatite components and the MgO micro-nanoparticles on MgO-FB enhanced the adsorption capacity for Cu2+, Cd2+, and Pb2+ through ion-exchange and precipitation process.	mgo-fb	143-149	CD2 molecule	Homo sapiens	193-196
35348554-1	2022	A novel CdII-based two-fold interpenetrated metal-organic framework (MOF), namely {(Cd2(BTDB)2(4,4-bpy)) DMF}n (JXUST-14), (H2BTDB = 4,4"-(benzo(c)(1,2,5)thiadiazole-4,7-diyl)dibenzoic acid and 4,4-bpy = 4,4-bipyridine), has been prepared and characterized.	Cadmium ion	8-12	CD2 molecule	Homo sapiens	84-87
35066234-5	2022	It has been found that the Cd2+ ions accept photoelectrons from MnO2-xunder irradiation for the in-situ growth of CdS nanocrystals, which enables a close contact between the two components, providing high-speed electron-transport channels for photocatalysis.	manganese dioxide	64-68	CD2 molecule	Homo sapiens	27-30
35571766-2	2022	In this report, powder- and paper-based optical nanosensors using mesoporous silica nanospheres as carriers were designed for determination of Co2+ and Cd2+ in commonly used cosmetics.	mesoporous silica	66-83	CD2 molecule	Homo sapiens	152-155
35571766-5	2022	POCs and PBCs were constructed with thick decoration of optical probes, leading to the formation of active surface centers for monitoring of Co2+ and Cd2+ in cosmetic products.	pbcs	9-13	CD2 molecule	Homo sapiens	150-153
35571766-7	2022	Digital image colorimetric analysis (DICA) was used to quantify the color of PBCs and deduce the corresponding concentrations of Co2+ and Cd2+ using calibration curves.	pbcs	77-81	CD2 molecule	Homo sapiens	138-141
35571766-11	2022	To the best of our knowledge, this is the first time simple PBCs have been designed for monitoring Co2+ and Cd2+ with detection limits of 2.2 x 10-7 and 1.3 x 10-7 M. A limited amount of manufactured POCs (about 20 mg) were used for all measurements, and commercial filter paper treated with mesoporous nanosphere silica was used for sensing Co2+ and Cd2+ ions.	pbcs	60-64	CD2 molecule	Homo sapiens	108-111
35219138-0	2022	Spectroscopic characterization of Mn2+ and Cd2+ coordination to phosphorothioates in the conserved A9 metal site of the hammerhead ribozyme.	phosphorothioates	64-81	CD2 molecule	Homo sapiens	43-46
35219138-0	2022	Spectroscopic characterization of Mn2+ and Cd2+ coordination to phosphorothioates in the conserved A9 metal site of the hammerhead ribozyme.	Metals	102-107	CD2 molecule	Homo sapiens	43-46
35219138-6	2022	Here, we use EPR, electron spin-echo envelope modulation (ESEEM), and X-ray absorption spectroscopic methods to directly probe the structural consequences of Mn2+ and Cd2+ coordination to Rp and Sp phosphorothioate modifications at the A9/G10.1 site in the truncated hammerhead ribozyme (tHHRz).	sp phosphorothioate	195-214	CD2 molecule	Homo sapiens	167-170
35219138-7	2022	The results demonstrate that while Cd2+ does indeed bind to S in the thio-substituted ligand, Mn2+ coordinates to the non-sulfur oxo group of this phosphorothioate, regardless of isomer.	Sulfur	60-61	CD2 molecule	Homo sapiens	35-38
35357176-3	2022	Using the anion-induced outer surface interaction of Q(n)s derived from (CdxCly)n- anions formed by Cd2+ cations in a HCl medium, four different TMeQ(6)-(CdxCly)n--based supramolecular frameworks are constructed.	Anions	10-15	CD2 molecule	Homo sapiens	100-103
35357176-3	2022	Using the anion-induced outer surface interaction of Q(n)s derived from (CdxCly)n- anions formed by Cd2+ cations in a HCl medium, four different TMeQ(6)-(CdxCly)n--based supramolecular frameworks are constructed.	Glutamine	53-54	CD2 molecule	Homo sapiens	100-103
35357176-3	2022	Using the anion-induced outer surface interaction of Q(n)s derived from (CdxCly)n- anions formed by Cd2+ cations in a HCl medium, four different TMeQ(6)-(CdxCly)n--based supramolecular frameworks are constructed.	Nitrogen	55-58	CD2 molecule	Homo sapiens	100-103
35357176-3	2022	Using the anion-induced outer surface interaction of Q(n)s derived from (CdxCly)n- anions formed by Cd2+ cations in a HCl medium, four different TMeQ(6)-(CdxCly)n--based supramolecular frameworks are constructed.	(cdxcly)n- anions	72-89	CD2 molecule	Homo sapiens	100-103
35357176-3	2022	Using the anion-induced outer surface interaction of Q(n)s derived from (CdxCly)n- anions formed by Cd2+ cations in a HCl medium, four different TMeQ(6)-(CdxCly)n--based supramolecular frameworks are constructed.	Hydrochloric Acid	118-121	CD2 molecule	Homo sapiens	100-103
35357176-3	2022	Using the anion-induced outer surface interaction of Q(n)s derived from (CdxCly)n- anions formed by Cd2+ cations in a HCl medium, four different TMeQ(6)-(CdxCly)n--based supramolecular frameworks are constructed.	tmeq(6)-(cdxcly)n	145-162	CD2 molecule	Homo sapiens	100-103
35404034-1	2022	The work reports a modeling analysis of single-compound and binary adsorption of Pb2+ and Cd2+ ions from polluted water onto the activated carbon at room temperature.	Water	114-119	CD2 molecule	Homo sapiens	90-93
35404034-1	2022	The work reports a modeling analysis of single-compound and binary adsorption of Pb2+ and Cd2+ ions from polluted water onto the activated carbon at room temperature.	Carbon	139-145	CD2 molecule	Homo sapiens	90-93
35348554-1	2022	A novel CdII-based two-fold interpenetrated metal-organic framework (MOF), namely {(Cd2(BTDB)2(4,4-bpy)) DMF}n (JXUST-14), (H2BTDB = 4,4"-(benzo(c)(1,2,5)thiadiazole-4,7-diyl)dibenzoic acid and 4,4-bpy = 4,4-bipyridine), has been prepared and characterized.	4,4"-(benzo(c)(1,2,5)thiadiazole-4,7-diyl)dibenzoic acid	133-189	CD2 molecule	Homo sapiens	84-87
35348554-1	2022	A novel CdII-based two-fold interpenetrated metal-organic framework (MOF), namely {(Cd2(BTDB)2(4,4-bpy)) DMF}n (JXUST-14), (H2BTDB = 4,4"-(benzo(c)(1,2,5)thiadiazole-4,7-diyl)dibenzoic acid and 4,4-bpy = 4,4-bipyridine), has been prepared and characterized.	4,4-bpy	194-201	CD2 molecule	Homo sapiens	84-87
35348554-1	2022	A novel CdII-based two-fold interpenetrated metal-organic framework (MOF), namely {(Cd2(BTDB)2(4,4-bpy)) DMF}n (JXUST-14), (H2BTDB = 4,4"-(benzo(c)(1,2,5)thiadiazole-4,7-diyl)dibenzoic acid and 4,4-bpy = 4,4-bipyridine), has been prepared and characterized.	4,4'-bipyridyl	204-218	CD2 molecule	Homo sapiens	84-87
35065379-0	2022	Functionalized Cu-based metal oxide nanoparticles with enhanced Cd+2 adsorption capacity and their ecotoxicity assessment by molecular docking.	Copper	15-17	CD2 molecule	Homo sapiens	64-68
35464208-6	2022	Complexes 1-6 all exhibited efficient fluorescence quenching response to Fe3+ ions in water, and were not interfered by the following metal ions: Cu2+, Cd2+, Mg2+, Ni2+, Co2+, Ca2+, Ba2+, Sr2+, Li+, Na+, K+, Al3+, Fe2+, Pb2+, Cr3+, Mn2+ and Zn2+.	ferric sulfate	73-77	CD2 molecule	Homo sapiens	152-155
35319883-0	2022	Controlled Modulation of the Structure and Luminescence Properties of Zero-Dimensional Manganese Halide Hybrids through Structure-Directing Metal-Ion (Cd2+ and Zn2+) Centers.	manganese halide	87-103	CD2 molecule	Homo sapiens	151-154
35319883-0	2022	Controlled Modulation of the Structure and Luminescence Properties of Zero-Dimensional Manganese Halide Hybrids through Structure-Directing Metal-Ion (Cd2+ and Zn2+) Centers.	Metals	140-145	CD2 molecule	Homo sapiens	151-154
35319883-5	2022	Herein, we demonstrate a rational synthetic strategy to modulate the structure and luminescence properties of 0D Mn(II) halide hybrids utilizing the structure-directing d10 metal ions (Cd2+/Zn2+).	Manganese(2+)	113-119	CD2 molecule	Homo sapiens	185-188
35319883-5	2022	Herein, we demonstrate a rational synthetic strategy to modulate the structure and luminescence properties of 0D Mn(II) halide hybrids utilizing the structure-directing d10 metal ions (Cd2+/Zn2+).	decane	169-172	CD2 molecule	Homo sapiens	185-188
35319883-5	2022	Herein, we demonstrate a rational synthetic strategy to modulate the structure and luminescence properties of 0D Mn(II) halide hybrids utilizing the structure-directing d10 metal ions (Cd2+/Zn2+).	Metals	173-178	CD2 molecule	Homo sapiens	185-188
35319883-6	2022	0D metal halide hybrids of Cd2+/Zn2+, which act as hosts with tunable structures, accept Mn2+ ions as substitutional dopants.	Metals	3-8	CD2 molecule	Homo sapiens	27-30
35319883-6	2022	0D metal halide hybrids of Cd2+/Zn2+, which act as hosts with tunable structures, accept Mn2+ ions as substitutional dopants.	Manganese(2+)	89-93	CD2 molecule	Homo sapiens	27-30
35319883-10	2022	Optical and single-crystal X-ray diffraction structural analysis of the host and the doped system supports our experimental data and confirms the structure-directing role played by Cd2+/Zn2+ centers.	Zinc	186-190	CD2 molecule	Homo sapiens	181-184
35458309-4	2022	The effectiveness of this composite as a water purification fixed-bed filter was optimized in a batch system for the removal of cadmium (Cd+2) and lead (Pb+2) ions, and additionally characterized for its antimicrobial and antifungal properties and cytotoxicity effect.	Water	41-46	CD2 molecule	Homo sapiens	137-141
35458309-4	2022	The effectiveness of this composite as a water purification fixed-bed filter was optimized in a batch system for the removal of cadmium (Cd+2) and lead (Pb+2) ions, and additionally characterized for its antimicrobial and antifungal properties and cytotoxicity effect.	Cadmium	128-135	CD2 molecule	Homo sapiens	137-141
35448122-3	2022	The overall sorption tendency of the APCA-functionalized composite sorbents followed the sequence Co2+ < Zn2+ < Cd2+ <= Pb2+ < Ni2+, meaning that Co2+ ions had the lowest affinity for the sorbent"s functional groups, whereas the Ni2+ ions were strongly and preferentially adsorbed.	Nickel(2+)	127-131	CD2 molecule	Homo sapiens	112-115
35448122-3	2022	The overall sorption tendency of the APCA-functionalized composite sorbents followed the sequence Co2+ < Zn2+ < Cd2+ <= Pb2+ < Ni2+, meaning that Co2+ ions had the lowest affinity for the sorbent"s functional groups, whereas the Ni2+ ions were strongly and preferentially adsorbed.	Carbon Dioxide	146-150	CD2 molecule	Homo sapiens	112-115
35000179-9	2022	The metal ions adsorbed onto MMPSS were able to desorb effectively in the presence of HCl and retained 83.01%, 84.66%, and 81.83% of the initial adsorption capacity for Cu2+, Cd2+, and Pb2+ respectively after 5 consecutive cycles.	Metals	4-9	CD2 molecule	Homo sapiens	175-178
35000179-9	2022	The metal ions adsorbed onto MMPSS were able to desorb effectively in the presence of HCl and retained 83.01%, 84.66%, and 81.83% of the initial adsorption capacity for Cu2+, Cd2+, and Pb2+ respectively after 5 consecutive cycles.	Hydrochloric Acid	86-89	CD2 molecule	Homo sapiens	175-178
35065379-0	2022	Functionalized Cu-based metal oxide nanoparticles with enhanced Cd+2 adsorption capacity and their ecotoxicity assessment by molecular docking.	metal oxide	24-35	CD2 molecule	Homo sapiens	64-68
35065379-3	2022	Based on the maximum Cadmium (Cd+2) ion adsorption capacity, functionalized Cu2O (fCu2O) NPs were selected for the detailed characterization and batch studies.	cuprous oxide	76-80	CD2 molecule	Homo sapiens	30-34
35065379-7	2022	The maximum Cd+2 adsorption on fCu2O NPs was observed at initial solution pH 7.	fcu2o	31-36	CD2 molecule	Homo sapiens	12-16
35353224-4	2022	The magnetized bauxite residue exhibited excellent removal efficiencies for Cu2+, Cd2+ and Pb2+ with maximum adsorption capacities of 219.0 mg g-1, 275.4 mg g-1, and 100.4 mg g-1, which could be quickly separated through a magnet.	Aluminum Oxide	15-22	CD2 molecule	Homo sapiens	82-85
35108751-2	2022	Here, taking advantage of the feature that cadmium ion (Cd2+ ) has an overwhelming preference for phosphates, we developed a robust and simple Cd2+ co-precipitation strategy for the selective isolation of intact phosphoproteins.	Cadmium	43-50	CD2 molecule	Homo sapiens	56-59
35108751-2	2022	Here, taking advantage of the feature that cadmium ion (Cd2+ ) has an overwhelming preference for phosphates, we developed a robust and simple Cd2+ co-precipitation strategy for the selective isolation of intact phosphoproteins.	Cadmium	43-50	CD2 molecule	Homo sapiens	143-146
35108751-2	2022	Here, taking advantage of the feature that cadmium ion (Cd2+ ) has an overwhelming preference for phosphates, we developed a robust and simple Cd2+ co-precipitation strategy for the selective isolation of intact phosphoproteins.	Phosphates	98-108	CD2 molecule	Homo sapiens	56-59
35108751-2	2022	Here, taking advantage of the feature that cadmium ion (Cd2+ ) has an overwhelming preference for phosphates, we developed a robust and simple Cd2+ co-precipitation strategy for the selective isolation of intact phosphoproteins.	Phosphates	98-108	CD2 molecule	Homo sapiens	143-146
35146864-1	2022	In this work, a highly sensitive biosensor for detecting cadmium ions (Cd2+ ) was developed based on Cd2+ -specific DNA aptamer and hybridization chain reaction (HCR).	Cadmium	57-64	CD2 molecule	Homo sapiens	71-74
35146864-1	2022	In this work, a highly sensitive biosensor for detecting cadmium ions (Cd2+ ) was developed based on Cd2+ -specific DNA aptamer and hybridization chain reaction (HCR).	Cadmium	57-64	CD2 molecule	Homo sapiens	101-104
35234782-6	2022	Cadmium ions (Cd2+) were employed as the specific ion chelation probe for cysteine detection, and the formed Cd2+/cysteine chelate complex served as the electron acceptor for sensitive PEC sensing under low-power LED illumination.	Cadmium	0-7	CD2 molecule	Homo sapiens	14-17
35234782-6	2022	Cadmium ions (Cd2+) were employed as the specific ion chelation probe for cysteine detection, and the formed Cd2+/cysteine chelate complex served as the electron acceptor for sensitive PEC sensing under low-power LED illumination.	Cadmium	0-7	CD2 molecule	Homo sapiens	109-112
35234782-6	2022	Cadmium ions (Cd2+) were employed as the specific ion chelation probe for cysteine detection, and the formed Cd2+/cysteine chelate complex served as the electron acceptor for sensitive PEC sensing under low-power LED illumination.	Cysteine	74-82	CD2 molecule	Homo sapiens	14-17
35234782-6	2022	Cadmium ions (Cd2+) were employed as the specific ion chelation probe for cysteine detection, and the formed Cd2+/cysteine chelate complex served as the electron acceptor for sensitive PEC sensing under low-power LED illumination.	Cysteine	74-82	CD2 molecule	Homo sapiens	109-112
35234782-6	2022	Cadmium ions (Cd2+) were employed as the specific ion chelation probe for cysteine detection, and the formed Cd2+/cysteine chelate complex served as the electron acceptor for sensitive PEC sensing under low-power LED illumination.	Cysteine	114-122	CD2 molecule	Homo sapiens	14-17
35234782-6	2022	Cadmium ions (Cd2+) were employed as the specific ion chelation probe for cysteine detection, and the formed Cd2+/cysteine chelate complex served as the electron acceptor for sensitive PEC sensing under low-power LED illumination.	Cysteine	114-122	CD2 molecule	Homo sapiens	109-112
35424768-1	2022	Cadmium ions (Cd2+) have caused relatively serious pollution, threatening human health and ecosystems.	Cadmium	0-7	CD2 molecule	Homo sapiens	14-17
35424768-5	2022	Simultaneously, N,B-CQDs can be used to detect l-cysteine because significant fluorescence quenching was observed when l-Cys was added into the N,B-CQDs/Cd2+ system.	Cysteine	47-57	CD2 molecule	Homo sapiens	153-156
35424768-5	2022	Simultaneously, N,B-CQDs can be used to detect l-cysteine because significant fluorescence quenching was observed when l-Cys was added into the N,B-CQDs/Cd2+ system.	Cysteine	119-124	CD2 molecule	Homo sapiens	153-156
35424768-6	2022	In the two fluorescence "turn-on" and "turn-off" processes, this fluorescent probe obtained a good linear relationship over Cd2+ concentration ranging from 2.5 microM to 22.5 microM with a detection limit of 0.45 microM, while the concentration of l-cysteine showed a linear relationship in the range of 2.5-17.5 microM with a detection limit of 0.28 microM.	Cysteine	248-258	CD2 molecule	Homo sapiens	124-127
35224594-4	2022	In the case of djurleite Cu1.94S NDs, the Cu+ was immediately substituted by Cd2+ and solid wurtzite CdS NDs were produced.	Copper	42-45	CD2 molecule	Homo sapiens	77-80
35299369-8	2022	Compared with the detection limits of heavy metal solution obtained by using a single characteristic light wavelength, the detection limits of Cd2+, Cu2+ and Cr6+ achieved through using multi-channel detection system can be reduced by 42.64%, 38.12%, and 20.62%, respectively, and these detection limits are found as 0.0041mg/L, 0.0091mg/L, and 0.0112mg/L, respectively.	Metals	44-49	CD2 molecule	Homo sapiens	143-146
35101736-6	2022	The NetWAS analysis found that genes associated with natural killer (NK) cells (PTPRCAP, BLNK, HCK, ARHGEF11, GPR183, TRPV2, SHKBP1, CD2) showed significant differences between rapid and slow responders of nilotinib.	nilotinib	206-215	CD2 molecule	Homo sapiens	133-136
35230635-8	2022	The SIP signals differentiated the interactions between loess and Pb2+/Cd2+ by displaying a peak shift to a higher frequency on the imaginary conductivity spectra during Pb2+ flow-through, which was attributed to calcite dissolution and proved by the high correlation (R2 = 0.9366) between the estimated dissolved calcite mass and the peak of imaginary conductivity.	Lead(2+)	66-70	CD2 molecule	Homo sapiens	71-74
35230635-8	2022	The SIP signals differentiated the interactions between loess and Pb2+/Cd2+ by displaying a peak shift to a higher frequency on the imaginary conductivity spectra during Pb2+ flow-through, which was attributed to calcite dissolution and proved by the high correlation (R2 = 0.9366) between the estimated dissolved calcite mass and the peak of imaginary conductivity.	Lead(2+)	170-174	CD2 molecule	Homo sapiens	71-74
35196016-5	2022	The chelation behavior of the Pb2+-DNA and the Cd2+-DNA complex solutions after adding EDTA were compared.	Edetic Acid	87-91	CD2 molecule	Homo sapiens	47-50
35196016-7	2022	The fast binding dynamics and the slower chelation dynamics of the Pb2+ scenario compared to that of Cd2+ suggested that Pb2+ was more capable to induce DNA conformational change and that the Pb2+-DNA complex was more stable than the Cd2+-DNA complex.	Lead(2+)	67-71	CD2 molecule	Homo sapiens	234-237
35196016-7	2022	The fast binding dynamics and the slower chelation dynamics of the Pb2+ scenario compared to that of Cd2+ suggested that Pb2+ was more capable to induce DNA conformational change and that the Pb2+-DNA complex was more stable than the Cd2+-DNA complex.	Lead(2+)	121-125	CD2 molecule	Homo sapiens	101-104
35269490-9	2022	Only the Cd2+ current was able to cause the decay of channel activity, presumably as a result of Zn2+ to Cd2+ replacement.	Zinc	97-101	CD2 molecule	Homo sapiens	9-12
35212781-0	2022	Monitoring the Cd2+ release from Cd-containing quantum dots in simulated body fluids by size exclusion chromatography coupled with ICP-MS. Quantification of Cd2+ release from Cd-containing quantum dots (QDs) is of fundamental importance to elucidate its toxicity to organisms, but remains a great challenge due to the lack of appropriate analytical method.	Cadmium	175-177	CD2 molecule	Homo sapiens	157-160
35296559-6	2022	Notably, loss of CD58 (the ligand of the CD2 T-cell costimulatory receptor), a gene frequently altered in cancer, led to decreased TCE-mediated cytotoxicity, T-cell activation and antitumor efficacy in vitro and in vivo.	Trichloroethylene	131-134	CD2 molecule	Homo sapiens	41-44
35220392-10	2022	This study provides explanation for the high gammaH2AX level in unperturbed ES cells and early embryos, and suggests Nanog-C/CD2 as a promising drug candidate applied to Rad51-related basic research and therapeutic application studies.	gammah2ax	45-54	CD2 molecule	Homo sapiens	125-128
35212781-4	2022	Selecting CdSe@ZnS as the typical QDs, the Cd2+ release process in four typical simulated body fluids, namely, simulated gastric fluid, simulated sweat, Gamble"s solution, and artificial lysosomal fluid, was monitored using the developed SEC-ICP-MS method.	cdse	10-14	CD2 molecule	Homo sapiens	43-46
35212781-5	2022	The media pH is identified as the decisive factor which controls the dissolution of ZnS shells and also the Cd2+ release kinetics and final concentration.	Zinc	84-87	CD2 molecule	Homo sapiens	108-111
34935834-1	2022	A solvothermal reaction of Cd(II) with the dicarboxyl-functionalized arylhydrazone pro-ligands, 5-(2-(2,4,6-trioxotetrahydro-pyrimidin-5(2H)-ylidene)hydrazineyl)isophthalic acid (H5L1) and 5-(2-(2,4-dioxopentan-3-ylidene)hydrazineyl)isophthalic acid (H3L2), or their halogen bond donor centre(s) decorated analogs 2,4,6-triiodo-5-(2-(2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)hydrazineyl)isophthalic acid (H5L3) and 5-(2-(2,4-dioxopentan-3-ylidene)hydrazineyl)-2,4,6-triiodoisophthalic acid (H3L4), leads to the formation of known (Cd(H3L1)(H2O)2)n (1) and new {(Cd(HL2)(H2O)2(DMF)) H2O}n (2), (Cd(H3L3))n (3) and {(Cd2(mu-H2O)2(mu-H2L4)2(H2L4)2) 2H2O}n (4) coordination compounds, respectively.	Water	545-548	CD2 molecule	Homo sapiens	620-623
35080892-6	2022	The GaMD US/dual-water approach is tested on the 1D Potential of Mean Force (PMF) of the solvated CD2-CD58 system (168 000 atoms), allowing the AMOEBA PMF to converge within 1 kcal/mol of the experimental value.	Water	17-22	CD2 molecule	Homo sapiens	98-101
35115613-5	2022	In turbidity measurements, AADAAC-(FPGVG)4 revealed strong self-assembling ability in the presence of metal ions such as Cd2+ and Zn2+.	aadaac	27-33	CD2 molecule	Homo sapiens	121-124
35115613-5	2022	In turbidity measurements, AADAAC-(FPGVG)4 revealed strong self-assembling ability in the presence of metal ions such as Cd2+ and Zn2+.	Metals	102-107	CD2 molecule	Homo sapiens	121-124
35115613-6	2022	The results from colorimetric analysis indicated that AADAAC-(FPGVG)4 could capture Cd2+ and Zn2+.	aadaac	54-60	CD2 molecule	Homo sapiens	84-87
35005894-2	2022	Here, we present the synthesis and structural characterization of three hybrid metal (Zn2+ and Cd2+)-DOC compounds.	Metals	79-84	CD2 molecule	Homo sapiens	95-98
35096433-1	2022	Calcinated and acidified clay modified carbon graphite electrode was deployed in the simultaneous evaluation of traces of Pb2+ and Cd2+ in solution.	carbon graphite	39-54	CD2 molecule	Homo sapiens	131-134
34931211-0	2022	Dual-wavelength electrochemiluminescence ratiometry for hydrogen sulfide detection based on Cd2+-doped g-C3N4 nanosheets.	Hydrogen Sulfide	56-72	CD2 molecule	Homo sapiens	92-95
34931211-0	2022	Dual-wavelength electrochemiluminescence ratiometry for hydrogen sulfide detection based on Cd2+-doped g-C3N4 nanosheets.	c3n4	105-109	CD2 molecule	Homo sapiens	92-95
34931211-1	2022	Herein, a novel and facile dual-wavelength ratiometric electrochemiluminescence-resonance energy transfer (ECL-RET) sensor for hydrogen sulfide (H2S) detection was constructed based on the interaction between S2- and Cd2+-doped g-C3N4 nanosheets (NSs).	Hydrogen Sulfide	127-143	CD2 molecule	Homo sapiens	217-220
34931211-1	2022	Herein, a novel and facile dual-wavelength ratiometric electrochemiluminescence-resonance energy transfer (ECL-RET) sensor for hydrogen sulfide (H2S) detection was constructed based on the interaction between S2- and Cd2+-doped g-C3N4 nanosheets (NSs).	Deuterium	145-148	CD2 molecule	Homo sapiens	217-220
34931211-3	2022	In the presence of H2S, CdS was formed in situ on g-C3N4 NSs by the adsorption of S2- and Cd2+, generating another ECL emission at 515 nm.	Deuterium	19-22	CD2 molecule	Homo sapiens	90-93
34931211-3	2022	In the presence of H2S, CdS was formed in situ on g-C3N4 NSs by the adsorption of S2- and Cd2+, generating another ECL emission at 515 nm.	Cadmium	24-27	CD2 molecule	Homo sapiens	90-93
34931211-3	2022	In the presence of H2S, CdS was formed in situ on g-C3N4 NSs by the adsorption of S2- and Cd2+, generating another ECL emission at 515 nm.	g-c3n4 nss	50-60	CD2 molecule	Homo sapiens	90-93
35138533-0	2022	Removal of Cd2+ from water containing Ca2+ and Mg2+ using titanate nanotubes modified by carbon.	Water	21-26	CD2 molecule	Homo sapiens	11-14
35138533-0	2022	Removal of Cd2+ from water containing Ca2+ and Mg2+ using titanate nanotubes modified by carbon.	magnesium ion	47-51	CD2 molecule	Homo sapiens	11-14
35138533-0	2022	Removal of Cd2+ from water containing Ca2+ and Mg2+ using titanate nanotubes modified by carbon.	Carbon	89-95	CD2 molecule	Homo sapiens	11-14
35138533-2	2022	When Cd2+ is removed from water by adsorption, it will be inhibited by these two ions.	Water	26-31	CD2 molecule	Homo sapiens	5-8
35138533-7	2022	The experimental results show the order of adsorption amount to Cd2+ is TNT (171.56 mg/g) > TNT/C (166 mg/g) > TNT/HC (159.88 mg/g) when there is no Ca2+ or Mg2+.	Trinitrotoluene	72-75	CD2 molecule	Homo sapiens	64-67
35138533-7	2022	The experimental results show the order of adsorption amount to Cd2+ is TNT (171.56 mg/g) > TNT/C (166 mg/g) > TNT/HC (159.88 mg/g) when there is no Ca2+ or Mg2+.	Trinitrotoluene	111-114	CD2 molecule	Homo sapiens	64-67
35138533-7	2022	The experimental results show the order of adsorption amount to Cd2+ is TNT (171.56 mg/g) > TNT/C (166 mg/g) > TNT/HC (159.88 mg/g) when there is no Ca2+ or Mg2+.	magnesium ion	157-161	CD2 molecule	Homo sapiens	64-67
35138533-8	2022	But when there is 0.1 M Ca2+ or Mg2+ in the water, the order of Cd2+ adsorption capacity becomes TNT/HC (44.28, 49.04 mg/g) > TNT/C (58.84, 69.32 mg/g) > TNT (65.52, 70.6 mg/g).	magnesium ion	32-36	CD2 molecule	Homo sapiens	64-67
35138533-8	2022	But when there is 0.1 M Ca2+ or Mg2+ in the water, the order of Cd2+ adsorption capacity becomes TNT/HC (44.28, 49.04 mg/g) > TNT/C (58.84, 69.32 mg/g) > TNT (65.52, 70.6 mg/g).	Water	44-49	CD2 molecule	Homo sapiens	64-67
35138533-9	2022	It indicates that the surface carbon modification can alleviate the hindrance of Ca2+ or Mg2+ to Cd2+ removal.	Carbon	30-36	CD2 molecule	Homo sapiens	97-100
35138533-9	2022	It indicates that the surface carbon modification can alleviate the hindrance of Ca2+ or Mg2+ to Cd2+ removal.	magnesium ion	89-93	CD2 molecule	Homo sapiens	97-100
35138533-10	2022	This is because the carbon on the surface of TNT captured part of Ca2+ or Mg2+; it made more Cd2+ be successfully absorbed by TNT through ion exchange.	Carbon	20-26	CD2 molecule	Homo sapiens	93-96
35138533-10	2022	This is because the carbon on the surface of TNT captured part of Ca2+ or Mg2+; it made more Cd2+ be successfully absorbed by TNT through ion exchange.	magnesium ion	74-78	CD2 molecule	Homo sapiens	93-96
35138533-12	2022	The results of this paper can provide ideas for the adsorption and removal of Cd2+ in water in the presence of Ca2+ or Mg2+.	Water	86-91	CD2 molecule	Homo sapiens	78-81
35138533-12	2022	The results of this paper can provide ideas for the adsorption and removal of Cd2+ in water in the presence of Ca2+ or Mg2+.	magnesium ion	119-123	CD2 molecule	Homo sapiens	78-81
34935834-1	2022	A solvothermal reaction of Cd(II) with the dicarboxyl-functionalized arylhydrazone pro-ligands, 5-(2-(2,4,6-trioxotetrahydro-pyrimidin-5(2H)-ylidene)hydrazineyl)isophthalic acid (H5L1) and 5-(2-(2,4-dioxopentan-3-ylidene)hydrazineyl)isophthalic acid (H3L2), or their halogen bond donor centre(s) decorated analogs 2,4,6-triiodo-5-(2-(2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)hydrazineyl)isophthalic acid (H5L3) and 5-(2-(2,4-dioxopentan-3-ylidene)hydrazineyl)-2,4,6-triiodoisophthalic acid (H3L4), leads to the formation of known (Cd(H3L1)(H2O)2)n (1) and new {(Cd(HL2)(H2O)2(DMF)) H2O}n (2), (Cd(H3L3))n (3) and {(Cd2(mu-H2O)2(mu-H2L4)2(H2L4)2) 2H2O}n (4) coordination compounds, respectively.	Water	575-578	CD2 molecule	Homo sapiens	620-623
34935834-1	2022	A solvothermal reaction of Cd(II) with the dicarboxyl-functionalized arylhydrazone pro-ligands, 5-(2-(2,4,6-trioxotetrahydro-pyrimidin-5(2H)-ylidene)hydrazineyl)isophthalic acid (H5L1) and 5-(2-(2,4-dioxopentan-3-ylidene)hydrazineyl)isophthalic acid (H3L2), or their halogen bond donor centre(s) decorated analogs 2,4,6-triiodo-5-(2-(2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)hydrazineyl)isophthalic acid (H5L3) and 5-(2-(2,4-dioxopentan-3-ylidene)hydrazineyl)-2,4,6-triiodoisophthalic acid (H3L4), leads to the formation of known (Cd(H3L1)(H2O)2)n (1) and new {(Cd(HL2)(H2O)2(DMF)) H2O}n (2), (Cd(H3L3))n (3) and {(Cd2(mu-H2O)2(mu-H2L4)2(H2L4)2) 2H2O}n (4) coordination compounds, respectively.	Water	587-590	CD2 molecule	Homo sapiens	620-623
34935834-1	2022	A solvothermal reaction of Cd(II) with the dicarboxyl-functionalized arylhydrazone pro-ligands, 5-(2-(2,4,6-trioxotetrahydro-pyrimidin-5(2H)-ylidene)hydrazineyl)isophthalic acid (H5L1) and 5-(2-(2,4-dioxopentan-3-ylidene)hydrazineyl)isophthalic acid (H3L2), or their halogen bond donor centre(s) decorated analogs 2,4,6-triiodo-5-(2-(2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)hydrazineyl)isophthalic acid (H5L3) and 5-(2-(2,4-dioxopentan-3-ylidene)hydrazineyl)-2,4,6-triiodoisophthalic acid (H3L4), leads to the formation of known (Cd(H3L1)(H2O)2)n (1) and new {(Cd(HL2)(H2O)2(DMF)) H2O}n (2), (Cd(H3L3))n (3) and {(Cd2(mu-H2O)2(mu-H2L4)2(H2L4)2) 2H2O}n (4) coordination compounds, respectively.	Water	627-630	CD2 molecule	Homo sapiens	620-623
35010101-0	2022	Improved One- and Multiple-Photon Excited Photoluminescence from Cd2+-Doped CsPbBr3 Perovskite NCs.	perovskite	84-94	CD2 molecule	Homo sapiens	65-68
35051078-4	2022	The purpose of our study was to evaluate the mitigative role of excess Zn2+ supply to Cd2+ uptake/translocation and toxicity in clary sage.	Zinc	71-75	CD2 molecule	Homo sapiens	86-89
35051078-10	2022	Excess Zn2+ ameliorated the adverse effects of Cd2+ on PSII photochemistry, increasing the fraction of energy used for photochemistry (PhiPSII) and restoring PSII redox state and maximum PSII efficiency (Fv/Fm), while decreasing excess excitation energy at PSII (EXC).	Zinc	7-11	CD2 molecule	Homo sapiens	47-50
35051078-11	2022	We conclude that excess Zn2+ application eliminated the adverse effects of Cd2+ toxicity, reducing Cd2+ uptake and translocation and restoring chloroplast ultrastructure and PSII photochemical efficiency.	Zinc	24-28	CD2 molecule	Homo sapiens	75-78
35051078-11	2022	We conclude that excess Zn2+ application eliminated the adverse effects of Cd2+ toxicity, reducing Cd2+ uptake and translocation and restoring chloroplast ultrastructure and PSII photochemical efficiency.	Zinc	24-28	CD2 molecule	Homo sapiens	99-102
35051078-12	2022	Thus, excess Zn2+ application can be used as an important method for low Cd2+-accumulating crops, limiting Cd2+ entry into the food chain.	Zinc	13-17	CD2 molecule	Homo sapiens	73-76
35051078-12	2022	Thus, excess Zn2+ application can be used as an important method for low Cd2+-accumulating crops, limiting Cd2+ entry into the food chain.	Zinc	13-17	CD2 molecule	Homo sapiens	107-110
35071864-3	2022	More specifically, the end-of-waste from the thermal inertization of cement-asbestos and glass powder from domestic glass containers have been employed as sources for the hydrothermal synthesis of a tobermorite-rich material (TRM) successfully tested for the selective removal of Pb2+, Zn2+, Cd2+, and Ni2+ from aqueous solutions.	tobermorite	199-210	CD2 molecule	Homo sapiens	292-295
35071864-3	2022	More specifically, the end-of-waste from the thermal inertization of cement-asbestos and glass powder from domestic glass containers have been employed as sources for the hydrothermal synthesis of a tobermorite-rich material (TRM) successfully tested for the selective removal of Pb2+, Zn2+, Cd2+, and Ni2+ from aqueous solutions.	Lead(2+)	280-284	CD2 molecule	Homo sapiens	292-295
35071864-3	2022	More specifically, the end-of-waste from the thermal inertization of cement-asbestos and glass powder from domestic glass containers have been employed as sources for the hydrothermal synthesis of a tobermorite-rich material (TRM) successfully tested for the selective removal of Pb2+, Zn2+, Cd2+, and Ni2+ from aqueous solutions.	Zinc	286-290	CD2 molecule	Homo sapiens	292-295
35071864-3	2022	More specifically, the end-of-waste from the thermal inertization of cement-asbestos and glass powder from domestic glass containers have been employed as sources for the hydrothermal synthesis of a tobermorite-rich material (TRM) successfully tested for the selective removal of Pb2+, Zn2+, Cd2+, and Ni2+ from aqueous solutions.	Nickel(2+)	302-306	CD2 molecule	Homo sapiens	292-295
35010101-7	2022	Cd2+ doping results in a two-photon absorption cross-section, reaching 2.6 x 106 Goeppert-Mayer (GM), which is among the highest reported for CsPbBr3 NCs.	gm	97-99	CD2 molecule	Homo sapiens	0-3
2556060-9	1989	Results show that epidural anesthesia with sensory blockade above T-10 to T-11 blocks spontaneous peroneal MSA as well as the marked sympathetic activation induced by apnea.	t-10	66-70	CD2 molecule	Homo sapiens	74-78
2575034-2	1989	Stimulation of cells via the TcR/CD3-complex or via the CD2 molecule increases inositol phosphates and cytoplasmic free calcium.	Inositol Phosphates	79-98	CD2 molecule	Homo sapiens	56-59
2575034-2	1989	Stimulation of cells via the TcR/CD3-complex or via the CD2 molecule increases inositol phosphates and cytoplasmic free calcium.	Calcium	120-127	CD2 molecule	Homo sapiens	56-59
2483716-1	1989	Nanomolar concentrations of the novel immunosuppressive drug FK-506 inhibit the proliferation of human T lymphocytes in vitro induced by mitogenic lectins or by monoclonal antibodies directed against the CD3 or CD2 surface antigens.	Tacrolimus	61-67	CD2 molecule	Homo sapiens	211-214
2573952-2	1989	The addition of phorbol ester PMA, which activates Ca2+/phospholipid-dependent enzyme protein kinase C, or calcium ionophore A23187, which increases intracytosolic free Ca2+ concentration, enhanced, but did not normalize, the defective anti-CD2-mediated T-cell mitogenesis.	Phorbol Esters	16-29	CD2 molecule	Homo sapiens	241-244
2573636-0	1989	Phorbol esters regulate CD2- and CD3-mediated calcium responses in peripheral blood-derived human T cells.	Phorbol Esters	0-14	CD2 molecule	Homo sapiens	24-27
2573636-0	1989	Phorbol esters regulate CD2- and CD3-mediated calcium responses in peripheral blood-derived human T cells.	Calcium	46-53	CD2 molecule	Homo sapiens	24-27
2573636-1	1989	The purpose of the present study was to examine the effect of protein kinase C (pkC) activation on calcium responses generated through the CD3 and CD2 Ag in both normal peripheral blood-derived T lymphocytes and the leukemic T cell line Jurkat.	Calcium	99-106	CD2 molecule	Homo sapiens	147-150
2573636-3	1989	Thus, the pkC activator phorbol-12,13-dibutyrate (Pdbu) enhances calcium responses induced via CD3 and CD2 molecules in normal T cells by accelerating the rate of elevation of intracellular calcium levels and increasing the maximum change in calcium concentration achieved.	Phorbol 12,13-Dibutyrate	24-48	CD2 molecule	Homo sapiens	103-106
2573636-3	1989	Thus, the pkC activator phorbol-12,13-dibutyrate (Pdbu) enhances calcium responses induced via CD3 and CD2 molecules in normal T cells by accelerating the rate of elevation of intracellular calcium levels and increasing the maximum change in calcium concentration achieved.	Phorbol 12,13-Dibutyrate	50-54	CD2 molecule	Homo sapiens	103-106
2573636-3	1989	Thus, the pkC activator phorbol-12,13-dibutyrate (Pdbu) enhances calcium responses induced via CD3 and CD2 molecules in normal T cells by accelerating the rate of elevation of intracellular calcium levels and increasing the maximum change in calcium concentration achieved.	Calcium	65-72	CD2 molecule	Homo sapiens	103-106
2573636-4	1989	In contrast, Pdbu inhibits both CD3- and CD2-induced calcium responses in Jurkat cells.	Calcium	53-60	CD2 molecule	Homo sapiens	41-44
2481585-0	1989	The lymphocyte-specific protein tyrosine kinase p56lck is hyperphosphorylated on serine and tyrosine residues within minutes after activation via T cell receptor or CD2.	Serine	81-87	CD2 molecule	Homo sapiens	165-168
2481585-0	1989	The lymphocyte-specific protein tyrosine kinase p56lck is hyperphosphorylated on serine and tyrosine residues within minutes after activation via T cell receptor or CD2.	Tyrosine	32-40	CD2 molecule	Homo sapiens	165-168
2574677-5	1989	Anti-CD2 and PHA, but not IL 2, induced intracytoplasmic Ca2+ influx phosphatidyl inositol turnover as well as IL 2 receptor expression.	Phosphatidylinositols	69-90	CD2 molecule	Homo sapiens	5-8
2573952-2	1989	The addition of phorbol ester PMA, which activates Ca2+/phospholipid-dependent enzyme protein kinase C, or calcium ionophore A23187, which increases intracytosolic free Ca2+ concentration, enhanced, but did not normalize, the defective anti-CD2-mediated T-cell mitogenesis.	Calcimycin	125-131	CD2 molecule	Homo sapiens	241-244
2788303-2	1989	The binding of mitogenic lectins phytohaemagglutinin (PHA), concanavalin A (Con A) and/or of monoclonal antibodies to different receptors such as antigen receptor complex or CD2 on human T cells generates increases in the concentrations of inositol triphosphate (IP3) and cytoplasmic free calcium.	Inositol triphosphate	240-261	CD2 molecule	Homo sapiens	174-177
2506442-0	1989	Calcium phosphate-mediated transfection alters metallothionein gene expression in response to Cd2+ and Zn2+.	calcium phosphate	0-17	CD2 molecule	Homo sapiens	94-97
2473913-2	1989	Sequential studies show that preincubation of CD2-, CD3-, CD4-, CD6-, and CD8- BM cells with PTDA, but not with recombinant (r) IL2 or PHA increased their capacity to proliferate in liquid culture and to form agar T-cell colonies provided both PHA and rIL2 were added to the cultures.	ptda	93-97	CD2 molecule	Homo sapiens	46-49
2473913-4	1989	The selective effect of PTDA on CD2-, CD3-, CD4-, CD6-, CD8- BM cells was abolished by adding a CD7 monoclonal antibody to the T-cell-purging coctail.	ptda	24-28	CD2 molecule	Homo sapiens	32-35
2473913-5	1989	Cell marker studies performed on T-cell-depleted BM-derived liquid or agar cultures have shown that they contain up to 70%-85% CD2+, CD3+, CD4+, CD8- cells.	Agar	70-74	CD2 molecule	Homo sapiens	127-130
2672132-1	1989	Intravenous cyclophosphamide therapy of severe systemic lupus is associated with reduction in the numbers of circulating T and B lymphocytes, suppression of T11 (CD2) receptor-mediated responses, and suppression of autoantibody production.	Cyclophosphamide	12-28	CD2 molecule	Homo sapiens	157-160
2672132-1	1989	Intravenous cyclophosphamide therapy of severe systemic lupus is associated with reduction in the numbers of circulating T and B lymphocytes, suppression of T11 (CD2) receptor-mediated responses, and suppression of autoantibody production.	Cyclophosphamide	12-28	CD2 molecule	Homo sapiens	162-165
2608070-0	1989	Inhibition of phosphatidylserine synthesis induced by triggering CD2 or the CD3-TCR complex in a human T cell line.	Phosphatidylserines	14-32	CD2 molecule	Homo sapiens	65-68
2608070-2	1989	Activation of Jurkat T cells with phytohemagglutinin, CD3 or CD2 mAbs results in a marked inhibition of phosphatidylserine (PS) synthesis.	Phosphatidylserines	104-122	CD2 molecule	Homo sapiens	61-64
2608070-2	1989	Activation of Jurkat T cells with phytohemagglutinin, CD3 or CD2 mAbs results in a marked inhibition of phosphatidylserine (PS) synthesis.	Phosphatidylserines	124-126	CD2 molecule	Homo sapiens	61-64
2608070-3	1989	Monitoring PS synthesis in T cells shows that: (i) after modulation of CD3 molecules the cells become refractory to further treatment with CD3 mAbs as well as to a further challenge with CD2 mAbs; and (ii) treatment of T cells with fluoride ions and cholera toxin, two known effectors of guanosine triphosphate-binding proteins, also resulted in a strong inhibition of the synthesis of this phospholipid.	Phosphatidylserines	11-13	CD2 molecule	Homo sapiens	187-190
2478163-1	1989	The addition of monosialoganglioside GM1 to serum-free culture medium efficiently and specifically inhibited CD4 antigen expression on normal T lymphocytes from peripheral blood or thymus as well as on cells from H9 and Molt-3 lines; other molecules such as CD3, CD2 and CD8 were not affected.	G(M1) Ganglioside	16-40	CD2 molecule	Homo sapiens	263-266
2788303-2	1989	The binding of mitogenic lectins phytohaemagglutinin (PHA), concanavalin A (Con A) and/or of monoclonal antibodies to different receptors such as antigen receptor complex or CD2 on human T cells generates increases in the concentrations of inositol triphosphate (IP3) and cytoplasmic free calcium.	Inositol 1,4,5-Trisphosphate	263-266	CD2 molecule	Homo sapiens	174-177
2788303-2	1989	The binding of mitogenic lectins phytohaemagglutinin (PHA), concanavalin A (Con A) and/or of monoclonal antibodies to different receptors such as antigen receptor complex or CD2 on human T cells generates increases in the concentrations of inositol triphosphate (IP3) and cytoplasmic free calcium.	Calcium	289-296	CD2 molecule	Homo sapiens	174-177
2567337-4	1989	Anti-T11(2) plus anti-T11(3) antibody stimulation of cells expressing a full-length CD2 cDNA results in a characteristic rise in cytosolic-free calcium [( Ca2+]i), and subsequent IL-2 secretion that accompany CD2 stimulation in human T lymphocytes.	Calcium	144-151	CD2 molecule	Homo sapiens	84-87
2473910-1	1989	The modulatory activity of dextran sulfate with a relative molecular mass of 8 and 500 kDa and pentosan polysulfate with a relative molecular mass of 6 kDa on human T cell surface molecules CD2, CD3, CD4, CD8 and HLA-DR was investigated by analytical flow cytometry.	Pentosan Sulfuric Polyester	95-115	CD2 molecule	Homo sapiens	190-193
2473910-2	1989	The 500-kDa dextran sulfate induces a complete disappearance of the CD4 and a 50% diminution of CD2 immune reactivity on peripheral blood lymphocytes after a 4-h incubation while the low molecular mass polyanions do not.	Dextran Sulfate	12-27	CD2 molecule	Homo sapiens	96-99
2574494-2	1989	In this paper we show that the stimulation of the human cloned leukemic T cell line Jurkat by anti-CD2 as well as anti-CD3 monoclonal antibodies induces translocation from cytosol to cell membrane of protein kinase-C (PKC), which is dependent on the formation of 1,2-diacylglycerol from inositol 4,5-diphosphate.	1,2-diacylglycerol	263-281	CD2 molecule	Homo sapiens	99-102
2574494-2	1989	In this paper we show that the stimulation of the human cloned leukemic T cell line Jurkat by anti-CD2 as well as anti-CD3 monoclonal antibodies induces translocation from cytosol to cell membrane of protein kinase-C (PKC), which is dependent on the formation of 1,2-diacylglycerol from inositol 4,5-diphosphate.	inositol 4,5-diphosphate	287-311	CD2 molecule	Homo sapiens	99-102
2567497-6	1989	Several recent studies have indicated a requirement for the Ti-CD3 complex in CD2 signalling.	ti-cd3	60-66	CD2 molecule	Homo sapiens	78-81
2567497-9	1989	Here we use a digitonin-based solubilization procedure to explore this possibility and show that 40% of the cell-surface CD2 molecules can be specifically co-precipitated in association with the Ti-CD3 complex.	Digitonin	14-23	CD2 molecule	Homo sapiens	121-124
2567497-9	1989	Here we use a digitonin-based solubilization procedure to explore this possibility and show that 40% of the cell-surface CD2 molecules can be specifically co-precipitated in association with the Ti-CD3 complex.	ti-cd3	195-201	CD2 molecule	Homo sapiens	121-124
2925617-13	1989	(v) All beta chain residues at the alpha 1 beta 2 interface are identical with those in the human chain except two: Glu(G3)----Val and Glu(CD2)----Thr; these differences in charged residues may explain the dissociation to dimers.	Glutamic Acid	135-138	CD2 molecule	Homo sapiens	139-142
2566120-5	1989	We show here that an antibody which recognizes the beta-subunit of VLA-4 (CD29) on T cells can inhibit CD4+ cell proliferation triggered by CD2 or CD3, and that binding of this antibody to activated T cells leads to an increase in cyclic AMP levels which is comparable to that elicited by forskolin.	Cyclic AMP	231-241	CD2 molecule	Homo sapiens	74-77
2566120-5	1989	We show here that an antibody which recognizes the beta-subunit of VLA-4 (CD29) on T cells can inhibit CD4+ cell proliferation triggered by CD2 or CD3, and that binding of this antibody to activated T cells leads to an increase in cyclic AMP levels which is comparable to that elicited by forskolin.	Colforsin	289-298	CD2 molecule	Homo sapiens	74-77
2540174-6	1989	Cd2+ probably acts at an extracellular site because loading the cells with a heavy metal chelator only slightly inhibited Cd2+-evoked 45Ca2+ efflux.	Metals	83-88	CD2 molecule	Homo sapiens	0-3
2540174-6	1989	Cd2+ probably acts at an extracellular site because loading the cells with a heavy metal chelator only slightly inhibited Cd2+-evoked 45Ca2+ efflux.	Metals	83-88	CD2 molecule	Homo sapiens	122-125
2540174-7	1989	Cd2+ increased [3H]inositol polyphosphates; [3H]inositol trisphosphate increased 4-fold in 15 s. Zn2+ reversibly blocked 45Ca2+ efflux evoked by Cd2+ but not that produced by bradykinin.	3h]inositol polyphosphates	16-42	CD2 molecule	Homo sapiens	0-3
2540174-7	1989	Cd2+ increased [3H]inositol polyphosphates; [3H]inositol trisphosphate increased 4-fold in 15 s. Zn2+ reversibly blocked 45Ca2+ efflux evoked by Cd2+ but not that produced by bradykinin.	Zinc	97-101	CD2 molecule	Homo sapiens	0-3
2540174-7	1989	Cd2+ increased [3H]inositol polyphosphates; [3H]inositol trisphosphate increased 4-fold in 15 s. Zn2+ reversibly blocked 45Ca2+ efflux evoked by Cd2+ but not that produced by bradykinin.	Zinc	97-101	CD2 molecule	Homo sapiens	145-148
2540174-8	1989	Zn2+ competitively (Ki = approximately 0.4 microM) inhibited net Ca2+ efflux produced by Cd2+.	Zinc	0-4	CD2 molecule	Homo sapiens	89-92
2567674-2	1989	Here we demonstrate that the triggering of subclones of the human T leukemia Jurkat cell line by anti-CD2 as well as anti-CD3 monoclonal antibodies is able to induce activation (i.e. translocation from cytosol to cell membrane) of protein kinase C (PKC), which is dependent on the formation of 1,2-diacylglycerol from inositol 4-5-bisphosphate.	1,2-diacylglycerol	294-312	CD2 molecule	Homo sapiens	102-105
2567674-2	1989	Here we demonstrate that the triggering of subclones of the human T leukemia Jurkat cell line by anti-CD2 as well as anti-CD3 monoclonal antibodies is able to induce activation (i.e. translocation from cytosol to cell membrane) of protein kinase C (PKC), which is dependent on the formation of 1,2-diacylglycerol from inositol 4-5-bisphosphate.	inositol 4,5-bisphosphate	318-343	CD2 molecule	Homo sapiens	102-105
2567674-3	1989	The kinetics of PKC translocation parallels the rise in intracellular calcium following both CD2 and CD3 stimulations.	Calcium	70-77	CD2 molecule	Homo sapiens	93-96
2567675-5	1989	CyA-induced inhibition of both anti-CD3- and anti-CD2-mediated proliferation could not be reversed by addition of either PMA (1 ng/ml) or anti-CD28.	Cyclosporine	0-3	CD2 molecule	Homo sapiens	50-53
2564856-9	1989	Our findings provide evidence for an intrinsic functional defect in cord CD2-mediated T cell activation, which is linked to an impaired increase of free cytoplasmic calcium, as confirmed by the effectiveness of calcium ionophore A23187 in restoring a good CD2-induced cord T cell proliferation and by measurement of cellular calcium uptake after activation via the CD2 molecule.	Calcium	165-172	CD2 molecule	Homo sapiens	73-76
2564856-9	1989	Our findings provide evidence for an intrinsic functional defect in cord CD2-mediated T cell activation, which is linked to an impaired increase of free cytoplasmic calcium, as confirmed by the effectiveness of calcium ionophore A23187 in restoring a good CD2-induced cord T cell proliferation and by measurement of cellular calcium uptake after activation via the CD2 molecule.	Calcium	211-218	CD2 molecule	Homo sapiens	73-76
2564856-9	1989	Our findings provide evidence for an intrinsic functional defect in cord CD2-mediated T cell activation, which is linked to an impaired increase of free cytoplasmic calcium, as confirmed by the effectiveness of calcium ionophore A23187 in restoring a good CD2-induced cord T cell proliferation and by measurement of cellular calcium uptake after activation via the CD2 molecule.	Calcium	211-218	CD2 molecule	Homo sapiens	256-259
2564856-9	1989	Our findings provide evidence for an intrinsic functional defect in cord CD2-mediated T cell activation, which is linked to an impaired increase of free cytoplasmic calcium, as confirmed by the effectiveness of calcium ionophore A23187 in restoring a good CD2-induced cord T cell proliferation and by measurement of cellular calcium uptake after activation via the CD2 molecule.	Calcium	211-218	CD2 molecule	Homo sapiens	256-259
2564856-9	1989	Our findings provide evidence for an intrinsic functional defect in cord CD2-mediated T cell activation, which is linked to an impaired increase of free cytoplasmic calcium, as confirmed by the effectiveness of calcium ionophore A23187 in restoring a good CD2-induced cord T cell proliferation and by measurement of cellular calcium uptake after activation via the CD2 molecule.	Calcimycin	229-235	CD2 molecule	Homo sapiens	73-76
2564856-9	1989	Our findings provide evidence for an intrinsic functional defect in cord CD2-mediated T cell activation, which is linked to an impaired increase of free cytoplasmic calcium, as confirmed by the effectiveness of calcium ionophore A23187 in restoring a good CD2-induced cord T cell proliferation and by measurement of cellular calcium uptake after activation via the CD2 molecule.	Calcimycin	229-235	CD2 molecule	Homo sapiens	256-259
2564856-9	1989	Our findings provide evidence for an intrinsic functional defect in cord CD2-mediated T cell activation, which is linked to an impaired increase of free cytoplasmic calcium, as confirmed by the effectiveness of calcium ionophore A23187 in restoring a good CD2-induced cord T cell proliferation and by measurement of cellular calcium uptake after activation via the CD2 molecule.	Calcimycin	229-235	CD2 molecule	Homo sapiens	256-259
2564856-9	1989	Our findings provide evidence for an intrinsic functional defect in cord CD2-mediated T cell activation, which is linked to an impaired increase of free cytoplasmic calcium, as confirmed by the effectiveness of calcium ionophore A23187 in restoring a good CD2-induced cord T cell proliferation and by measurement of cellular calcium uptake after activation via the CD2 molecule.	Calcium	211-218	CD2 molecule	Homo sapiens	73-76
2564856-9	1989	Our findings provide evidence for an intrinsic functional defect in cord CD2-mediated T cell activation, which is linked to an impaired increase of free cytoplasmic calcium, as confirmed by the effectiveness of calcium ionophore A23187 in restoring a good CD2-induced cord T cell proliferation and by measurement of cellular calcium uptake after activation via the CD2 molecule.	Calcium	211-218	CD2 molecule	Homo sapiens	256-259
2564856-9	1989	Our findings provide evidence for an intrinsic functional defect in cord CD2-mediated T cell activation, which is linked to an impaired increase of free cytoplasmic calcium, as confirmed by the effectiveness of calcium ionophore A23187 in restoring a good CD2-induced cord T cell proliferation and by measurement of cellular calcium uptake after activation via the CD2 molecule.	Calcium	211-218	CD2 molecule	Homo sapiens	256-259
2542344-0	1989	Cholera toxin inhibits the increase in cytoplasmic free calcium induced via the CD2 pathway of human T-lymphocyte activation.	Calcium	56-63	CD2 molecule	Homo sapiens	80-83
2542344-1	1989	We investigated the action of cholera toxin on the intracellular ionized calcium [Ca2+]i increase induced by anti-CD2 and anti-CD3 monoclonal antibodies in the leukemic human T-cell line Jurkat.	Calcium	73-80	CD2 molecule	Homo sapiens	114-117
2542344-8	1989	In addition, the present study demonstrated that the rise in cellular cAMP partially inhibits the [Ca2+]i increase induced by anti-CD2 and anti-CD3 mAbs.	Cyclic AMP	70-74	CD2 molecule	Homo sapiens	131-134
2564029-13	1989	In contrast, addition of PHA plus SRBC, which bind to the CD2 receptors caused IL-2R expression, IL-2 production, and proliferation.	srbc	34-38	CD2 molecule	Homo sapiens	58-61
2729929-1	1989	Cadmium accumulation and transport were studied in two strains of Mycobacterium scrofulaceum differing in their susceptibility to Cd2+ toxicity.	Cadmium	0-7	CD2 molecule	Homo sapiens	130-133
2729929-2	1989	A 10-fold excess of either Zn2+ or Mn2+ partially antagonized inhibition of growth by Cd2+.	Zinc	27-31	CD2 molecule	Homo sapiens	86-89
2729929-2	1989	A 10-fold excess of either Zn2+ or Mn2+ partially antagonized inhibition of growth by Cd2+.	Manganese(2+)	35-39	CD2 molecule	Homo sapiens	86-89
2729929-8	1989	Increased Cd2+ in culture medium resulted in decreased Mn2+ and Zn2+ in cells of the susceptible strain but did not reduce the Mn2+ and Zn2+ content of cells of the tolerant strain.	Manganese(2+)	55-59	CD2 molecule	Homo sapiens	10-13
2729929-8	1989	Increased Cd2+ in culture medium resulted in decreased Mn2+ and Zn2+ in cells of the susceptible strain but did not reduce the Mn2+ and Zn2+ content of cells of the tolerant strain.	Zinc	64-68	CD2 molecule	Homo sapiens	10-13
2784064-5	1989	In the presence of the phorbol ester TPA, leukemic blasts from two cases differentiated along the B precursor pathway to the [CD2-CD10+CD19+CD20+C mu+slg-] pre-B cell stage.	Tetradecanoylphorbol Acetate	37-40	CD2 molecule	Homo sapiens	126-129
2784064-15	1989	Cross-linking of CD2 as well as CD19 antigens on FL 8.2 CD2+ cells caused an increase of intracellular ionized calcium.	Calcium	111-118	CD2 molecule	Homo sapiens	17-20
2784064-15	1989	Cross-linking of CD2 as well as CD19 antigens on FL 8.2 CD2+ cells caused an increase of intracellular ionized calcium.	Calcium	111-118	CD2 molecule	Homo sapiens	56-59
2564843-4	1989	Calcium mobilization in CD3- LGL induced by CLB/FcR gran I is associated with inhibition of natural killer cell (NK) killing, and inhibition of the enhanced NK killing induced by the anti-CD2 low-density monoclonal antibody, 9.1.	Calcium	0-7	CD2 molecule	Homo sapiens	188-191
2918858-5	1989	The CD3-CD2, CD3-CD4, CD3-CD6 and CD3-CD8 heteroconjugates each gained two to three orders of magnitude in titer in calcium mobilization compared to unconjugated CD3 or the CD3-CD3 conjugate.	Calcium	116-123	CD2 molecule	Homo sapiens	8-11
2536766-5	1989	Before culture, the intracellular calcium mobilization in newborn NK cells induced by mAb to CD2 and CD16 did not differ from that of adult NK cells.	Calcium	34-41	CD2 molecule	Homo sapiens	93-96
2469486-1	1989	Thermodynamic parameters, enthalpy and entropy, for the binding of the divalent cations, Mg+2, Ca+2, Sr+2, Ba+2, and Cd+2, to gramicidin A, incorporated into lysophosphatidylcholine, have been determined using a combination of Tl-205 nuclear magnetic resonance spectroscopy and competition binding.	Lysophosphatidylcholines	158-181	CD2 molecule	Homo sapiens	117-121
2914945-0	1989	113Cd NMR of Cd2+-substituted carboxypeptidase.	Cadmium, isotope of mass 113	0-5	CD2 molecule	Homo sapiens	13-16
2918858-2	1989	In addition to the CD3-T cell receptor complex, the CD2, CD4, CD5, CD7, CD8 and CD28 receptors mobilize cytoplasmic calcium within minutes of binding with monoclonal antibodies and additional crosslinking occurs on the cell surface.	Calcium	116-123	CD2 molecule	Homo sapiens	52-55
2563972-2	1989	The results show that the appropriate stimulation of both CD2 or CD3 antigens results in phosphorylation of a 80-kDa putative PKC substrate and that this phosphorylation event is sensitive to a PKC inhibitor, sphinganine.	safingol	209-220	CD2 molecule	Homo sapiens	58-61
2523728-2	1989	Time-dependent 31P saturation-transfer studies were conducted with the Cd2+-activated form of muscle phosphoglucomutase to probe the origin of the 100-fold difference between its catalytic efficiency (in terms of kcat) and that of the more efficient Mg2+-activated enzyme.	ET bromodomain inhibitor	15-18	CD2 molecule	Homo sapiens	71-74
2523728-2	1989	Time-dependent 31P saturation-transfer studies were conducted with the Cd2+-activated form of muscle phosphoglucomutase to probe the origin of the 100-fold difference between its catalytic efficiency (in terms of kcat) and that of the more efficient Mg2+-activated enzyme.	magnesium ion	250-254	CD2 molecule	Homo sapiens	71-74
2523728-3	1989	The present paper describes the equilibrium mixture of phosphoglucomutase and its substrate/product pair when the concentration of the Cd2+ enzyme approaches that of the substrate and how the nine-spin 31P NMR system provided by this mixture was treated.	ET bromodomain inhibitor	202-205	CD2 molecule	Homo sapiens	135-138
2523728-4	1989	It shows that the presence of abortive complexes is not a significant factor in the reduced activity of the Cd2+ enzyme since the complex of the dephosphoenzyme and glucose 1,6-bisphosphate, which accounts for a large majority of the enzyme present at equilibrium, is catalytically competent.	glucose-1,6-bisphosphate	165-189	CD2 molecule	Homo sapiens	108-111
2523728-9	1989	They also provide minimal estimates of 350 and 150 s-1 for the rate constants describing (PO3-) transfer from the Cd2+ phosphoenzyme to the 6-position of bound glucose 1-phosphate and to the 1-position of bound glucose 6-phosphate, respectively.	glucose-1-phosphate	160-179	CD2 molecule	Homo sapiens	114-117
2523728-9	1989	They also provide minimal estimates of 350 and 150 s-1 for the rate constants describing (PO3-) transfer from the Cd2+ phosphoenzyme to the 6-position of bound glucose 1-phosphate and to the 1-position of bound glucose 6-phosphate, respectively.	Glucose-6-Phosphate	211-230	CD2 molecule	Homo sapiens	114-117
2523729-3	1989	Before this comparison was made, net rate constants for the Cd2+ enzyme, obtained at high enzyme concentration via 31P NMR saturation-transfer studies [Post, C. B., Ray, W. J., Jr., &amp; Gorenstein, D. G. (1989) Biochemistry (preceding paper in this issue)], were appropriately scaled by using the observed constants to calculate both the expected isotope-transfer rate at equilibrium and the steady-state rate under initial velocity conditions and comparing the calculated values with those measured in dilute solution.	ET bromodomain inhibitor	115-118	CD2 molecule	Homo sapiens	60-63
2523729-6	1989	In fact, it is unlikely that the efficiency of (PO3-) transfer to the 6-hydroxyl group of bound Glc-1-P (thermodynamically favorable direction) is reduced by more than an order of magnitude in the Cd2+ enzyme.	glucose-1-phosphate	96-103	CD2 molecule	Homo sapiens	197-200
2467893-0	1989	Hb F-Fukuyama or A gamma T43(CD2)Asp----Asn.	asp----asn	33-43	CD2 molecule	Homo sapiens	29-32
2521616-8	1989	These observations suggest that CD2- but not LFA-1-mediated interactions, as well as TCR and stimulating antigen binding, are absolutely necessary to activate Th-TCC.	th-tcc	159-165	CD2 molecule	Homo sapiens	32-35
2538540-8	1989	In Na+-free medium containing tetraethylammonium (TEA+), and in the presence of 4-aminopyridine (4-AP), inward Ca2+ currents were revealed that inactivated slowly and were blocked by Cd2+ and Mn2+.	Tetraethylammonium	30-48	CD2 molecule	Homo sapiens	183-186
2538540-8	1989	In Na+-free medium containing tetraethylammonium (TEA+), and in the presence of 4-aminopyridine (4-AP), inward Ca2+ currents were revealed that inactivated slowly and were blocked by Cd2+ and Mn2+.	4-Aminopyridine	80-95	CD2 molecule	Homo sapiens	183-186
2538540-8	1989	In Na+-free medium containing tetraethylammonium (TEA+), and in the presence of 4-aminopyridine (4-AP), inward Ca2+ currents were revealed that inactivated slowly and were blocked by Cd2+ and Mn2+.	4-Aminopyridine	97-101	CD2 molecule	Homo sapiens	183-186
2609769-3	1989	Besides sufficient therapeutic efficacy, leakadin has shown a manifest immunocorrective effect, increasing the counts of CD2+ and CD3+ cells, i. e. of the total T-lymphocyte pool (including the "young" cells) and, consequently, of its mature fraction, CD4+ and theophyllin-resistant T-lymphocytes, CD8+ cells; this fact recommends the drug for the treatment of patients with Kaposi"s sarcoma.	Leakadine	41-49	CD2 molecule	Homo sapiens	121-124
2849938-0	1988	PGE2-induced cyclic AMP accumulation in human CD4+ T cells is strongly enhanced during the CD2-mediated activatory process.	Dinoprostone	0-4	CD2 molecule	Homo sapiens	91-94
2849938-0	1988	PGE2-induced cyclic AMP accumulation in human CD4+ T cells is strongly enhanced during the CD2-mediated activatory process.	Cyclic AMP	13-23	CD2 molecule	Homo sapiens	91-94
2849938-2	1988	The anti-CD2 stimulation strongly potentiates the PGE2-induced cAMP production while both PMA and A23187 produced a less potent effect.	Dinoprostone	50-54	CD2 molecule	Homo sapiens	9-12
2849938-2	1988	The anti-CD2 stimulation strongly potentiates the PGE2-induced cAMP production while both PMA and A23187 produced a less potent effect.	Cyclic AMP	63-67	CD2 molecule	Homo sapiens	9-12
2849938-3	1988	On the opposite the anti-CD2 treatment is without any effect on the basal cAMP level contrasting with a marked increase of intracellular cAMP concentrations with A23187 or the combination of A23187 and PMA.	Cyclic AMP	137-141	CD2 molecule	Homo sapiens	25-28
2849938-3	1988	On the opposite the anti-CD2 treatment is without any effect on the basal cAMP level contrasting with a marked increase of intracellular cAMP concentrations with A23187 or the combination of A23187 and PMA.	Calcimycin	162-168	CD2 molecule	Homo sapiens	25-28
2849938-3	1988	On the opposite the anti-CD2 treatment is without any effect on the basal cAMP level contrasting with a marked increase of intracellular cAMP concentrations with A23187 or the combination of A23187 and PMA.	Calcimycin	191-197	CD2 molecule	Homo sapiens	25-28
2849938-4	1988	These results suggest that activation of CD4+ human T cells via the CD2 molecule significantly influences the cAMP-related transduction pathway.	Cyclic AMP	110-114	CD2 molecule	Homo sapiens	68-71
2973067-2	1988	Formation of homoaggregates of CD3, CD2, or CD28 on the surface of T cells induced by crosslinking with monoclonal antibodies (mAbs) results in an increase in cytoplasmic free calcium concentration ([Ca2+]i).	Calcium	176-183	CD2 molecule	Homo sapiens	36-39
2460537-0	1988	Is a natural ligand of the T lymphocyte CD2 molecule a sulfated carbohydrate?	Carbohydrates	64-76	CD2 molecule	Homo sapiens	40-43
2460537-2	1988	Inasmuch as the CD2 (E rosette receptor, T11, LFA-2) molecule of human T lymphocytes is a cell surface glycoprotein involved in the adhesion of T cells to various target cells the possibility that CD2 binds SP was investigated.	sp	207-209	CD2 molecule	Homo sapiens	16-19
2460537-2	1988	Inasmuch as the CD2 (E rosette receptor, T11, LFA-2) molecule of human T lymphocytes is a cell surface glycoprotein involved in the adhesion of T cells to various target cells the possibility that CD2 binds SP was investigated.	sp	207-209	CD2 molecule	Homo sapiens	41-44
2460537-2	1988	Inasmuch as the CD2 (E rosette receptor, T11, LFA-2) molecule of human T lymphocytes is a cell surface glycoprotein involved in the adhesion of T cells to various target cells the possibility that CD2 binds SP was investigated.	sp	207-209	CD2 molecule	Homo sapiens	46-51
2460537-2	1988	Inasmuch as the CD2 (E rosette receptor, T11, LFA-2) molecule of human T lymphocytes is a cell surface glycoprotein involved in the adhesion of T cells to various target cells the possibility that CD2 binds SP was investigated.	sp	207-209	CD2 molecule	Homo sapiens	197-200
2460537-3	1988	It was found that E rosetting of human T lymphocytes, a phenomenon involving CD2, was readily inhibited by the SP dextran sulfate (DxS) and, to a lesser extent, by the sulfated polymer polyvinyl sulfate whereas 11 other SP had no effect on E rosetting, this effect occurring at the T cell level.	Dextran Sulfate	114-129	CD2 molecule	Homo sapiens	77-80
2460537-3	1988	It was found that E rosetting of human T lymphocytes, a phenomenon involving CD2, was readily inhibited by the SP dextran sulfate (DxS) and, to a lesser extent, by the sulfated polymer polyvinyl sulfate whereas 11 other SP had no effect on E rosetting, this effect occurring at the T cell level.	Dextran Sulfate	131-134	CD2 molecule	Homo sapiens	77-80
2460537-3	1988	It was found that E rosetting of human T lymphocytes, a phenomenon involving CD2, was readily inhibited by the SP dextran sulfate (DxS) and, to a lesser extent, by the sulfated polymer polyvinyl sulfate whereas 11 other SP had no effect on E rosetting, this effect occurring at the T cell level.	polyvinyl sulfate	185-202	CD2 molecule	Homo sapiens	77-80
2460537-3	1988	It was found that E rosetting of human T lymphocytes, a phenomenon involving CD2, was readily inhibited by the SP dextran sulfate (DxS) and, to a lesser extent, by the sulfated polymer polyvinyl sulfate whereas 11 other SP had no effect on E rosetting, this effect occurring at the T cell level.	sp	111-113	CD2 molecule	Homo sapiens	77-80
2460537-4	1988	mAb binding studies revealed that DxS and polyvinyl sulfate, but none of the other SP tested, inhibited the binding to T cells of the anti-CD2 mAb OKT11 and anti-T112 but augmented expression of the T113 epitope of the CD2 molecule.	Dextran Sulfate	34-37	CD2 molecule	Homo sapiens	139-142
2460537-4	1988	mAb binding studies revealed that DxS and polyvinyl sulfate, but none of the other SP tested, inhibited the binding to T cells of the anti-CD2 mAb OKT11 and anti-T112 but augmented expression of the T113 epitope of the CD2 molecule.	Dextran Sulfate	34-37	CD2 molecule	Homo sapiens	219-222
2460537-4	1988	mAb binding studies revealed that DxS and polyvinyl sulfate, but none of the other SP tested, inhibited the binding to T cells of the anti-CD2 mAb OKT11 and anti-T112 but augmented expression of the T113 epitope of the CD2 molecule.	polyvinyl sulfate	42-59	CD2 molecule	Homo sapiens	139-142
2460537-4	1988	mAb binding studies revealed that DxS and polyvinyl sulfate, but none of the other SP tested, inhibited the binding to T cells of the anti-CD2 mAb OKT11 and anti-T112 but augmented expression of the T113 epitope of the CD2 molecule.	polyvinyl sulfate	42-59	CD2 molecule	Homo sapiens	219-222
2460537-6	1988	Direct evidence that CD2 binds DxS was demonstrated by the ability of DxS-coupled fibers to totally deplete the CD2 Ag from lysates of radiolabeled human T lymphocytes and by the quantitative recovery of the CD2 Ag in fiber eluates.	Dextran Sulfate	31-34	CD2 molecule	Homo sapiens	21-24
2460537-6	1988	Direct evidence that CD2 binds DxS was demonstrated by the ability of DxS-coupled fibers to totally deplete the CD2 Ag from lysates of radiolabeled human T lymphocytes and by the quantitative recovery of the CD2 Ag in fiber eluates.	Dextran Sulfate	31-34	CD2 molecule	Homo sapiens	112-115
2460537-6	1988	Direct evidence that CD2 binds DxS was demonstrated by the ability of DxS-coupled fibers to totally deplete the CD2 Ag from lysates of radiolabeled human T lymphocytes and by the quantitative recovery of the CD2 Ag in fiber eluates.	Dextran Sulfate	31-34	CD2 molecule	Homo sapiens	112-115
2460537-8	1988	Collectively, the data indicate that the CD2 molecule specifically binds DxS and suggest that a potential target cell ligand for CD2 is a sulfated carbohydrate structure.	Carbohydrates	147-159	CD2 molecule	Homo sapiens	41-44
2460537-8	1988	Collectively, the data indicate that the CD2 molecule specifically binds DxS and suggest that a potential target cell ligand for CD2 is a sulfated carbohydrate structure.	Carbohydrates	147-159	CD2 molecule	Homo sapiens	129-132
3264092-1	1988	We have synthesized 3 immunotoxins (ITs) by covalently coupling the saporin-6 hemitoxin (SAP) to OKT11, SOT3, and SOT1a murine monoclonal antibodies that recognize human T lymphocyte CD2, CD3, and CD5 surface antigens, respectively.	saporin-6 hemitoxin	68-87	CD2 molecule	Homo sapiens	183-186
3264092-1	1988	We have synthesized 3 immunotoxins (ITs) by covalently coupling the saporin-6 hemitoxin (SAP) to OKT11, SOT3, and SOT1a murine monoclonal antibodies that recognize human T lymphocyte CD2, CD3, and CD5 surface antigens, respectively.	BENSULIDE	89-92	CD2 molecule	Homo sapiens	183-186
2972629-7	1988	The depressed proliferative response of CD2+ TIL could not be reversed in vitro when phorbol-esters were used in combination with ionomycin, which bypass the TCR.	Phorbol Esters	85-99	CD2 molecule	Homo sapiens	40-43
3147981-5	1988	In the presence or absence of the monocytes, CD3, as well as certain combinations of CD2 monoclonal antibodies including the D66 monoclonal antibody, were able to increase the intracellular calcium concentration as measured by Quin 2 fluorescence.	Calcium	190-197	CD2 molecule	Homo sapiens	85-88
3147981-5	1988	In the presence or absence of the monocytes, CD3, as well as certain combinations of CD2 monoclonal antibodies including the D66 monoclonal antibody, were able to increase the intracellular calcium concentration as measured by Quin 2 fluorescence.	Quin2	227-233	CD2 molecule	Homo sapiens	85-88
3147981-6	1988	EGTA, a Ca++ chelator, completely inhibited CD2- and CD3- mediated T-cell proliferation, indicating that calcium uptake is necessary during the T-cell proliferation.	Egtazic Acid	0-4	CD2 molecule	Homo sapiens	44-47
3147981-6	1988	EGTA, a Ca++ chelator, completely inhibited CD2- and CD3- mediated T-cell proliferation, indicating that calcium uptake is necessary during the T-cell proliferation.	Calcium	105-112	CD2 molecule	Homo sapiens	44-47
3147981-8	1988	In the CD2 pathway, EGTA-inhibited proliferation of T cells could be completely restored by addition of exogenous interleukin 2 as well as exogenous recombinant interleukin 1.	Egtazic Acid	20-24	CD2 molecule	Homo sapiens	7-10
2906908-0	1988	Iron exerts a specific inhibitory effect on CD2 expression of human PBL.	Iron	0-4	CD2 molecule	Homo sapiens	44-47
2906908-4	1988	Competition experiments further indicated that iron interacts specifically with CD2 on T lymphocytes.	Iron	47-51	CD2 molecule	Homo sapiens	80-83
2461305-4	1988	However, combinations of CD2 monoclonal antibodies, that stimulated an increase in the cytoplasmic calcium concentration of the human T cell line Jurkat, failed to induce a similar signal in the transfectants.	Calcium	99-106	CD2 molecule	Homo sapiens	25-28
2900689-0	1988	Crosslinking CD3 with CD2 using sepharose-immobilized antibodies enhances T lymphocyte proliferation.	Sepharose	32-41	CD2 molecule	Homo sapiens	22-25
2904172-4	1988	Ciclosporin A (CyA) inhibited T-cell DNA synthesis after activation via CD2 and CD3.	Cyclosporine	0-13	CD2 molecule	Homo sapiens	72-75
2901445-0	1988	All CD2-positive human lymphocytes rosette with sheep erythrocytes in the presence of polyethylene glycol.	Polyethylene Glycols	86-105	CD2 molecule	Homo sapiens	4-7
2459194-4	1988	We show here that although purified multimeric LFA-3 is not capable of initiating transmembrane signaling events on its own, the combination of LFA-3 and the anti-CD2 mAb CD2.1 induces intracellular calcium increases, phosphatidylinositol second messenger generation and lymphokine secretion in the T cell leukemic line Jurkat.	Calcium	199-206	CD2 molecule	Homo sapiens	163-166
2459194-4	1988	We show here that although purified multimeric LFA-3 is not capable of initiating transmembrane signaling events on its own, the combination of LFA-3 and the anti-CD2 mAb CD2.1 induces intracellular calcium increases, phosphatidylinositol second messenger generation and lymphokine secretion in the T cell leukemic line Jurkat.	Calcium	199-206	CD2 molecule	Homo sapiens	171-174
2459194-4	1988	We show here that although purified multimeric LFA-3 is not capable of initiating transmembrane signaling events on its own, the combination of LFA-3 and the anti-CD2 mAb CD2.1 induces intracellular calcium increases, phosphatidylinositol second messenger generation and lymphokine secretion in the T cell leukemic line Jurkat.	Phosphatidylinositols	218-238	CD2 molecule	Homo sapiens	163-166
2459194-4	1988	We show here that although purified multimeric LFA-3 is not capable of initiating transmembrane signaling events on its own, the combination of LFA-3 and the anti-CD2 mAb CD2.1 induces intracellular calcium increases, phosphatidylinositol second messenger generation and lymphokine secretion in the T cell leukemic line Jurkat.	Phosphatidylinositols	218-238	CD2 molecule	Homo sapiens	171-174
2900689-3	1988	When CD3 was simultaneously crosslinked with CD2 using Sepharose beads coupled to antibodies directed at both determinants, T cell proliferation was markedly enhanced (stimulation index = 8- to 11-fold).	Sepharose	55-64	CD2 molecule	Homo sapiens	45-48
2900689-8	1988	Human thymocytes, the majority of which express both CD3 and CD2, were similarly activated by Sepharose-immobilized antibodies.	Sepharose	94-103	CD2 molecule	Homo sapiens	61-64
2899908-3	1988	The HIV-1--infected T cells were unable to mobilize Ca2+ after stimulation with anti-CD3, whereas CD2-induced calcium mobilization remained intact.	Calcium	110-117	CD2 molecule	Homo sapiens	98-101
2901964-2	1988	Activation of human T lymphocytes via the CD2 molecule produces an enhanced turnover of phosphatidylinositol (PI) cycle-related phospholipids accompanied by the increased production of diacylglycerol (DG) and phosphorylated derivatives of inositol (IP).	Phosphatidylinositols	88-108	CD2 molecule	Homo sapiens	42-45
2901964-2	1988	Activation of human T lymphocytes via the CD2 molecule produces an enhanced turnover of phosphatidylinositol (PI) cycle-related phospholipids accompanied by the increased production of diacylglycerol (DG) and phosphorylated derivatives of inositol (IP).	Phospholipids	128-141	CD2 molecule	Homo sapiens	42-45
2901964-2	1988	Activation of human T lymphocytes via the CD2 molecule produces an enhanced turnover of phosphatidylinositol (PI) cycle-related phospholipids accompanied by the increased production of diacylglycerol (DG) and phosphorylated derivatives of inositol (IP).	Diglycerides	185-199	CD2 molecule	Homo sapiens	42-45
2901964-2	1988	Activation of human T lymphocytes via the CD2 molecule produces an enhanced turnover of phosphatidylinositol (PI) cycle-related phospholipids accompanied by the increased production of diacylglycerol (DG) and phosphorylated derivatives of inositol (IP).	Inositol	100-108	CD2 molecule	Homo sapiens	42-45
2901964-2	1988	Activation of human T lymphocytes via the CD2 molecule produces an enhanced turnover of phosphatidylinositol (PI) cycle-related phospholipids accompanied by the increased production of diacylglycerol (DG) and phosphorylated derivatives of inositol (IP).	ip	249-251	CD2 molecule	Homo sapiens	42-45
2901964-3	1988	In this report we demonstrate that increased levels of intracellular cyclic AMP induced in human T lymphocytes by prostaglandin E2 or dibutyryl cAMP antagonize these early biochemical events of the CD2 activation process.	Cyclic AMP	69-79	CD2 molecule	Homo sapiens	198-201
2901964-3	1988	In this report we demonstrate that increased levels of intracellular cyclic AMP induced in human T lymphocytes by prostaglandin E2 or dibutyryl cAMP antagonize these early biochemical events of the CD2 activation process.	Dinoprostone	114-130	CD2 molecule	Homo sapiens	198-201
2901964-3	1988	In this report we demonstrate that increased levels of intracellular cyclic AMP induced in human T lymphocytes by prostaglandin E2 or dibutyryl cAMP antagonize these early biochemical events of the CD2 activation process.	Cyclic AMP	144-148	CD2 molecule	Homo sapiens	198-201
2901964-4	1988	Thus, a substantial inhibition of the CD2-induced increase in 32P-phosphatidic acid and 32P-PI values is observed.	32p-phosphatidic acid	62-83	CD2 molecule	Homo sapiens	38-41
2901964-4	1988	Thus, a substantial inhibition of the CD2-induced increase in 32P-phosphatidic acid and 32P-PI values is observed.	Phosphorus-32	62-65	CD2 molecule	Homo sapiens	38-41
2901964-6	1988	We also report here that cAMP does inhibit the CD2-induced proliferation in a dose-dependent manner while the proliferation generated independently of DG and IP production by a combination of Ca2+ ionophore A23187 and 12-O-tetradecanoylphorbol 13-acetate is not affected.	Cyclic AMP	25-29	CD2 molecule	Homo sapiens	47-50
2901964-6	1988	We also report here that cAMP does inhibit the CD2-induced proliferation in a dose-dependent manner while the proliferation generated independently of DG and IP production by a combination of Ca2+ ionophore A23187 and 12-O-tetradecanoylphorbol 13-acetate is not affected.	Tetradecanoylphorbol Acetate	218-254	CD2 molecule	Homo sapiens	47-50
2901964-0	1988	Cyclic AMP-mediated alteration of the CD2 activation process in human T lymphocytes.	Cyclic AMP	0-10	CD2 molecule	Homo sapiens	38-41
2901355-2	1988	Previously, we have shown that paraformaldehyde-fixed monocytes are able to fully complement, in terms of [3H]dThd incorporation, a primary stimulus delivered to purified T cells by monoclonal antibodies (mAb) reacting with CD3 or CD2 molecules.	paraform	31-47	CD2 molecule	Homo sapiens	231-234
3260936-11	1988	Similarly, in CD3- CD2- CD7+ clones [Ca2+]i increments and inositol phosphate formation occurred after stimulation with PHA.	Inositol Phosphates	59-77	CD2 molecule	Homo sapiens	19-22
3260251-8	1988	In medium lacking sodium bicarbonate the intracellular alkalinization via the CD2 structure could be blocked by the amiloride analogue 5-(N-methyl-N-isobutyl)amiloride (MIA), which indicates that this increase in pH is mediated by the amiloride-sensitive Na+/H+ antiporter.	Sodium Bicarbonate	18-36	CD2 molecule	Homo sapiens	78-81
3260251-8	1988	In medium lacking sodium bicarbonate the intracellular alkalinization via the CD2 structure could be blocked by the amiloride analogue 5-(N-methyl-N-isobutyl)amiloride (MIA), which indicates that this increase in pH is mediated by the amiloride-sensitive Na+/H+ antiporter.	Amiloride	116-125	CD2 molecule	Homo sapiens	78-81
3260251-8	1988	In medium lacking sodium bicarbonate the intracellular alkalinization via the CD2 structure could be blocked by the amiloride analogue 5-(N-methyl-N-isobutyl)amiloride (MIA), which indicates that this increase in pH is mediated by the amiloride-sensitive Na+/H+ antiporter.	5-(N-methyl-N-isobutyl)amiloride	135-167	CD2 molecule	Homo sapiens	78-81
2900149-6	1988	Moreover, analysis of phosphatidylinositol and phosphatidic acid metabolic changes mediated by each signal separately or together suggests that, in this model, IL2 increases the phosphoinositide turnover induced by anti-CD2 antibodies up to a level required for helper function acquisition.	Phosphatidylinositols	178-194	CD2 molecule	Homo sapiens	220-223
2898370-0	1988	CD2 is involved in regulating cyclic AMP levels in T cells.	Cyclic AMP	30-40	CD2 molecule	Homo sapiens	0-3
2897246-3	1988	Soluble phase anti-CD2 also inhibited accessory cell-dependent increases in intracellular free calcium concentration and cell-to-cell contact among oxidizing mitogen-treated T cells and accessory cells.	Calcium	95-102	CD2 molecule	Homo sapiens	19-22
2898370-1	1988	The human T lymphocyte-specific CD2 (T11) molecule, that regulates T cell activation, is capable of mediating increases of intracellular cAMP.	Cyclic AMP	137-141	CD2 molecule	Homo sapiens	32-35
2898370-2	1988	Monoclonal antibodies directed to different epitopes of the CD2 molecule which either induce or inhibit T cell proliferation are capable of triggering an increase of cAMP comparable to that induced by reagents which activate adenylate cyclase.	Cyclic AMP	166-170	CD2 molecule	Homo sapiens	60-63
2896216-9	1988	The protein synthesis inhibitor, cycloheximide, increased its half-time by fourfold to 3.5 h. The data imply the existence of a labile factor, dependent on protein synthesis that is important in the regulation of CD2 mRNA.	Cycloheximide	33-46	CD2 molecule	Homo sapiens	213-216
2454190-1	1988	Pairs of monoclonal antibodies (mAb) defining epitopes T 11.1 and T 11.2 on the CD 2 molecule are mitogenic for purified human T cells in the presence of a submitogenic dose of 12-O-tetradecanoylphorbol 13-acetate (TPA).	Tetradecanoylphorbol Acetate	177-213	CD2 molecule	Homo sapiens	80-84
2454190-1	1988	Pairs of monoclonal antibodies (mAb) defining epitopes T 11.1 and T 11.2 on the CD 2 molecule are mitogenic for purified human T cells in the presence of a submitogenic dose of 12-O-tetradecanoylphorbol 13-acetate (TPA).	Tetradecanoylphorbol Acetate	215-218	CD2 molecule	Homo sapiens	80-84
2899354-7	1988	Antibody L180/1, specific for the T11 (CD2) target structure (T11TS) on SE, homologous to the human CD2 ligand LFA-3, abolished the response to SENAGO alone or when combined with PEG or TPA.	Polyethylene Glycols	179-182	CD2 molecule	Homo sapiens	39-42
2899354-7	1988	Antibody L180/1, specific for the T11 (CD2) target structure (T11TS) on SE, homologous to the human CD2 ligand LFA-3, abolished the response to SENAGO alone or when combined with PEG or TPA.	Tetradecanoylphorbol Acetate	186-189	CD2 molecule	Homo sapiens	34-37
2899354-7	1988	Antibody L180/1, specific for the T11 (CD2) target structure (T11TS) on SE, homologous to the human CD2 ligand LFA-3, abolished the response to SENAGO alone or when combined with PEG or TPA.	Tetradecanoylphorbol Acetate	186-189	CD2 molecule	Homo sapiens	39-42
3257905-3	1988	Soluble-phase anti-CD2 also inhibited anti-CD3 and accessory cell-dependent increases in intracellular free calcium concentration.	Calcium	108-115	CD2 molecule	Homo sapiens	19-22
3257905-4	1988	Crosslinked anti-CD2, on the other hand, mediated an increase in the concentration of intracellular free calcium in T cells.	Calcium	105-112	CD2 molecule	Homo sapiens	17-20
2964474-7	1988	Down-regulation of CD2 by anti-CD4 mAb also occurred with the transformed T cell line, KE-37, which demonstrates that such effects can occur without mononuclear phagocytic accessory cells.	ke-37	87-92	CD2 molecule	Homo sapiens	19-22
3383288-2	1988	We separated a family of Cd2+-binding proteins from Cd2+-exposed human peripheral blood lymphocytes by gel filtration chromatography, and characterized them by SDS-gel electrophoresis.	Sodium Dodecyl Sulfate	160-163	CD2 molecule	Homo sapiens	25-28
2896111-0	1988	Cyclosporin A does not inhibit the PHA-stimulated increase in intracellular Ca2+ concentration but inhibits the increase in E-rosette receptor (CD2) expression and appearance of interleukin-2 receptors (CD25).	Cyclosporine	0-13	CD2 molecule	Homo sapiens	144-147
3126073-9	1988	Taken together, these data show that IL2-dependent proliferation can be induced through the simultaneous binding of anti-CD28 and anti-CD2 antibodies, possibly through phosphatidyl inositol-independent pathways.	Phosphatidylinositols	168-189	CD2 molecule	Homo sapiens	121-124
2895712-5	1988	The effect of paf-acether on the expression of CD2 and CD3, two human T cell surface glycoproteins, was investigated by indirect immunofluorescence and flow cytometry.	Platelet Activating Factor	14-25	CD2 molecule	Homo sapiens	47-50
2467491-2	1988	Exposure to colour developing agents that are derivatives of p-phenylenediamine, e.g. CD-2 and CD-3, are known to cause lichenoid lesions and allergic contact dermatitis.	4-phenylenediamine	61-79	CD2 molecule	Homo sapiens	86-90
3313052-0	1987	An LFA-3 cDNA encodes a phospholipid-linked membrane protein homologous to its receptor CD2.	Phospholipids	24-36	CD2 molecule	Homo sapiens	88-91
3343706-2	1988	Morphine effects on T11, Leu2a, and Leu3a antigenic markers on leukocytes from rhesus monkeys and humans were assessed by using single- and two-color cytofluorometric analyses.	Morphine	0-8	CD2 molecule	Homo sapiens	20-23
3343706-7	1988	Furthermore, in the single-color analyses, the effects of morphine on kinetics of T11 expression were quite similar for both human and monkey cells.	Morphine	58-66	CD2 molecule	Homo sapiens	82-85
3343706-12	1988	The effects of morphine on kinetics of Leu2a and T11 expression were at obvious variance between species.	Morphine	15-23	CD2 molecule	Homo sapiens	49-52
2856574-2	1987	Sperm chromatin, depleted of zinc with EDTA, regained stability in the detergent SDS after exposure to Cd2+ in vitro.	Sodium Dodecyl Sulfate	81-84	CD2 molecule	Homo sapiens	103-106
3314610-8	1987	Within the smokers, the mean 99mTc-DTPA clearance (T1/2 25 +/- 4 min) was faster than the mean 113mIn-DTPA clearance (34 +/- 6 min), (p less than 0.05).	Pentetic Acid	35-39	CD2 molecule	Homo sapiens	51-68
3683440-2	1987	Cd2+ was the most active followed by Cu2+, Hg2+, Zn2+ and Ag2.	cupric ion	37-41	CD2 molecule	Homo sapiens	0-3
3683440-2	1987	Cd2+ was the most active followed by Cu2+, Hg2+, Zn2+ and Ag2.	Mercuric cation	43-47	CD2 molecule	Homo sapiens	0-3
3683440-2	1987	Cd2+ was the most active followed by Cu2+, Hg2+, Zn2+ and Ag2.	Zinc	49-53	CD2 molecule	Homo sapiens	0-3
2451212-9	1988	In presence of 13.5mM Cao, the inorganic Ca-channel blockers La3+ and Cd2+ diminished the duration and rate of bursts of channel openings in a similar manner as low Cao.	lime	22-25	CD2 molecule	Homo sapiens	70-73
2451212-9	1988	In presence of 13.5mM Cao, the inorganic Ca-channel blockers La3+ and Cd2+ diminished the duration and rate of bursts of channel openings in a similar manner as low Cao.	lime	165-168	CD2 molecule	Homo sapiens	70-73
3125819-1	1987	Human platelets incubated with Cd2+ took up the cation slowly, and the uptake was speeded up by ionophore A23187.	Calcimycin	106-112	CD2 molecule	Homo sapiens	31-34
3125819-4	1987	Washed platelets incubated with Cd2+ showed a general increase in protein phosphorylation concurrent with a slow release of serotonin.	Serotonin	124-133	CD2 molecule	Homo sapiens	32-35
3125819-5	1987	In the presence of ionophore A23187, however, Cd2+ had a biphasic effect on protein phosphorylation: stimulatory at low and inhibitory at high Cd2+ concentrations.	Calcimycin	29-35	CD2 molecule	Homo sapiens	46-49
3125819-6	1987	The phosphorylation of two proteins with molecular masses close to 43 and 20 kDa was more sensitive to the inhibitory effect of Cd2+, and under similar conditions, the primary effect of Cd2+ on serotonin release was inhibitory, although at lower Cd2+ concentrations a slight stimulation was noted.	Serotonin	194-203	CD2 molecule	Homo sapiens	128-131
3125819-6	1987	The phosphorylation of two proteins with molecular masses close to 43 and 20 kDa was more sensitive to the inhibitory effect of Cd2+, and under similar conditions, the primary effect of Cd2+ on serotonin release was inhibitory, although at lower Cd2+ concentrations a slight stimulation was noted.	Serotonin	194-203	CD2 molecule	Homo sapiens	186-189
3125819-6	1987	The phosphorylation of two proteins with molecular masses close to 43 and 20 kDa was more sensitive to the inhibitory effect of Cd2+, and under similar conditions, the primary effect of Cd2+ on serotonin release was inhibitory, although at lower Cd2+ concentrations a slight stimulation was noted.	Serotonin	194-203	CD2 molecule	Homo sapiens	186-189
2444644-7	1987	Thus, when peripheral blood T cells were deprived of cell surface T3/Ti by anti-T3 modulation, anti-T11(2) plus anti-T11(3)-induced mitogenesis and transmembrane signal generation in the form of calcium mobilization were inhibited.	Calcium	195-202	CD2 molecule	Homo sapiens	100-103
3309123-14	1987	The results show that LFA-3 is attached to the cell membrane by a phosphatidylinositol glycolipid moiety, and confirm previous findings (37-41) that LFA-3 is a cell adhesion molecule that mediates adhesion by interacting with CD2 antigen.	phosphatidylinositol glycolipid	66-97	CD2 molecule	Homo sapiens	226-229
2444644-7	1987	Thus, when peripheral blood T cells were deprived of cell surface T3/Ti by anti-T3 modulation, anti-T11(2) plus anti-T11(3)-induced mitogenesis and transmembrane signal generation in the form of calcium mobilization were inhibited.	Calcium	195-202	CD2 molecule	Homo sapiens	117-120
2826103-8	1987	The activating effects of the metal ions tested were in the order of Ca2+ greater than Cd2+ greater than Zn2+ greater than Co2+ greater than Sr2+ for Ca2+-sensitive myosin ATPase and Ca2+ greater than Cd2+ greater than Sr2+ greater than Zn2+ greater than Hg2+ greater than Co2+ for cAMP phosphodiesterase.	Metals	30-35	CD2 molecule	Homo sapiens	87-90
2826103-8	1987	The activating effects of the metal ions tested were in the order of Ca2+ greater than Cd2+ greater than Zn2+ greater than Co2+ greater than Sr2+ for Ca2+-sensitive myosin ATPase and Ca2+ greater than Cd2+ greater than Sr2+ greater than Zn2+ greater than Hg2+ greater than Co2+ for cAMP phosphodiesterase.	Metals	30-35	CD2 molecule	Homo sapiens	201-204
2826103-8	1987	The activating effects of the metal ions tested were in the order of Ca2+ greater than Cd2+ greater than Zn2+ greater than Co2+ greater than Sr2+ for Ca2+-sensitive myosin ATPase and Ca2+ greater than Cd2+ greater than Sr2+ greater than Zn2+ greater than Hg2+ greater than Co2+ for cAMP phosphodiesterase.	Cobalt(2+)	123-127	CD2 molecule	Homo sapiens	201-204
2826103-9	1987	Cd2+ activated both enzyme activities most efficiently among the metal ions tested except Ca2+.	Metals	65-70	CD2 molecule	Homo sapiens	0-3
3103134-1	1987	Antibodies binding to a large subset of T-cell differentiation antigens, including CD2, CD4, CD5, CD6, CD7, CD8, Tp44, and CDw18, cause an increase in the cytoplasmic calcium concentration [( Ca2+]i) after the antigens are crosslinked on the cell surface.	Calcium	167-174	CD2 molecule	Homo sapiens	83-86
2820751-4	1987	The cytoplasmic region of T11 is a lengthy, proline-rich segment; secondary structural analysis predicts it to have a nonglobular conformation.	Proline	44-51	CD2 molecule	Homo sapiens	26-29
3037009-0	1987	Analysis of the bond between encephalomyocarditis virus and its human erythrocyte receptor by affinity chromatography on virus-sepharose columns.	Sepharose	127-136	CD2 molecule	Homo sapiens	70-90
3036123-4	1987	The results suggest that activation of CD2/CD3 receptors by lectins could potentiate the endogenous cyclic AMP stimulator adenosine via activation of protein kinase C.	Cyclic AMP	100-110	CD2 molecule	Homo sapiens	39-42
3036123-4	1987	The results suggest that activation of CD2/CD3 receptors by lectins could potentiate the endogenous cyclic AMP stimulator adenosine via activation of protein kinase C.	Adenosine	122-131	CD2 molecule	Homo sapiens	39-42
3107949-4	1987	The increased expression of CD2 and the initial expression of Tac were totally inhibited by cycloheximide, but were not affected by sufficient actinomycin-D to block the T cell proliferative response.	Cycloheximide	92-105	CD2 molecule	Homo sapiens	28-31
2822468-2	1987	Previous studies have shown that kidney uptake of cadmium in vivo results from proximal tubule absorption of the circulating cadmium metallothionein complex (CdMT), and intracellular release of the Cd2+ ion prior to induction of renal metallothionein.	Cadmium	50-57	CD2 molecule	Homo sapiens	198-201
2434339-4	1987	We show that this activation is initiated by a T11-mediated increase in the concentration of free cytoplasmic calcium ions ([Ca2+]i).	Calcium	110-117	CD2 molecule	Homo sapiens	47-50
2434339-7	1987	In addition antibodies to either the T11 molecules or T3-Ti antigen receptor complex induce marked elevations in IP3, other inositol phosphate compounds and DAG.	Inositol 1,4,5-Trisphosphate	113-116	CD2 molecule	Homo sapiens	37-40
2434339-7	1987	In addition antibodies to either the T11 molecules or T3-Ti antigen receptor complex induce marked elevations in IP3, other inositol phosphate compounds and DAG.	Inositol Phosphates	124-142	CD2 molecule	Homo sapiens	37-40
2434339-7	1987	In addition antibodies to either the T11 molecules or T3-Ti antigen receptor complex induce marked elevations in IP3, other inositol phosphate compounds and DAG.	1,2-diacylglycerol	157-160	CD2 molecule	Homo sapiens	37-40
2434339-8	1987	Taken together, these data indicate that, during T cell activation, due to the perturbation of T11 molecules or T3-Ti antigen receptor complex, membrane phosphoinositides are specifically hydrolyzed.	Phosphatidylinositols	153-170	CD2 molecule	Homo sapiens	95-98
2880725-4	1987	This communication demonstrates that CD2 contains N-linked carbohydrate as endo-beta-N-acetylglucosaminidase F digestion reduced its apparent mol.	n-linked carbohydrate	50-71	CD2 molecule	Homo sapiens	37-40
2880725-6	1987	CD2 was purified from the T leukemia cell line J6 by immunoaffinity chromatography and preparative SDS-polyacrylamide gel electrophoresis (PAGE).	Sodium Dodecyl Sulfate	99-102	CD2 molecule	Homo sapiens	0-3
2880725-6	1987	CD2 was purified from the T leukemia cell line J6 by immunoaffinity chromatography and preparative SDS-polyacrylamide gel electrophoresis (PAGE).	polyacrylamide	103-117	CD2 molecule	Homo sapiens	0-3
2959502-2	1987	113Cd NMR studies have unambiguously shown that the 7 g-atoms of Cd2+ bound per mole of the mammalian MT are located in two separate metal clusters, one containing 4 metal ions and the other, 3 metal ions.	Cadmium, isotope of mass 113	0-5	CD2 molecule	Homo sapiens	65-68
2959502-2	1987	113Cd NMR studies have unambiguously shown that the 7 g-atoms of Cd2+ bound per mole of the mammalian MT are located in two separate metal clusters, one containing 4 metal ions and the other, 3 metal ions.	Metals	133-138	CD2 molecule	Homo sapiens	65-68
2959502-2	1987	113Cd NMR studies have unambiguously shown that the 7 g-atoms of Cd2+ bound per mole of the mammalian MT are located in two separate metal clusters, one containing 4 metal ions and the other, 3 metal ions.	Metals	166-171	CD2 molecule	Homo sapiens	65-68
2959502-2	1987	113Cd NMR studies have unambiguously shown that the 7 g-atoms of Cd2+ bound per mole of the mammalian MT are located in two separate metal clusters, one containing 4 metal ions and the other, 3 metal ions.	Metals	166-171	CD2 molecule	Homo sapiens	65-68
2959502-4	1987	With the exception of one of the Cd2+ sites in this latter cluster, all the Cd2+ ions are tetrahedrally coordinated to four cysteine thiolate ligands with single cysteinyl sulfurs bridging adjacent metals.	cysteine thiolate	124-141	CD2 molecule	Homo sapiens	76-79
2959502-4	1987	With the exception of one of the Cd2+ sites in this latter cluster, all the Cd2+ ions are tetrahedrally coordinated to four cysteine thiolate ligands with single cysteinyl sulfurs bridging adjacent metals.	cysteinyl sulfurs	162-179	CD2 molecule	Homo sapiens	76-79
2959502-7	1987	For the 3-metal cluster, the affinity is found to decrease in the order Cu+ greater than Cd2+ greater than Zn2+ with Cd2+ greater than Zn2+ for the 4 metal cluster and Cd2+ (4-metal cluster) greater than Cd2+ (3-metal cluster).	Copper	72-75	CD2 molecule	Homo sapiens	89-92
2959502-7	1987	For the 3-metal cluster, the affinity is found to decrease in the order Cu+ greater than Cd2+ greater than Zn2+ with Cd2+ greater than Zn2+ for the 4 metal cluster and Cd2+ (4-metal cluster) greater than Cd2+ (3-metal cluster).	Copper	72-75	CD2 molecule	Homo sapiens	117-120
2959502-7	1987	For the 3-metal cluster, the affinity is found to decrease in the order Cu+ greater than Cd2+ greater than Zn2+ with Cd2+ greater than Zn2+ for the 4 metal cluster and Cd2+ (4-metal cluster) greater than Cd2+ (3-metal cluster).	Copper	72-75	CD2 molecule	Homo sapiens	117-120
2959502-7	1987	For the 3-metal cluster, the affinity is found to decrease in the order Cu+ greater than Cd2+ greater than Zn2+ with Cd2+ greater than Zn2+ for the 4 metal cluster and Cd2+ (4-metal cluster) greater than Cd2+ (3-metal cluster).	Copper	72-75	CD2 molecule	Homo sapiens	117-120
2959502-7	1987	For the 3-metal cluster, the affinity is found to decrease in the order Cu+ greater than Cd2+ greater than Zn2+ with Cd2+ greater than Zn2+ for the 4 metal cluster and Cd2+ (4-metal cluster) greater than Cd2+ (3-metal cluster).	Zinc	107-111	CD2 molecule	Homo sapiens	89-92
2959502-7	1987	For the 3-metal cluster, the affinity is found to decrease in the order Cu+ greater than Cd2+ greater than Zn2+ with Cd2+ greater than Zn2+ for the 4 metal cluster and Cd2+ (4-metal cluster) greater than Cd2+ (3-metal cluster).	Zinc	107-111	CD2 molecule	Homo sapiens	117-120
2959502-7	1987	For the 3-metal cluster, the affinity is found to decrease in the order Cu+ greater than Cd2+ greater than Zn2+ with Cd2+ greater than Zn2+ for the 4 metal cluster and Cd2+ (4-metal cluster) greater than Cd2+ (3-metal cluster).	Zinc	107-111	CD2 molecule	Homo sapiens	117-120
2959502-7	1987	For the 3-metal cluster, the affinity is found to decrease in the order Cu+ greater than Cd2+ greater than Zn2+ with Cd2+ greater than Zn2+ for the 4 metal cluster and Cd2+ (4-metal cluster) greater than Cd2+ (3-metal cluster).	Zinc	107-111	CD2 molecule	Homo sapiens	117-120
2959502-7	1987	For the 3-metal cluster, the affinity is found to decrease in the order Cu+ greater than Cd2+ greater than Zn2+ with Cd2+ greater than Zn2+ for the 4 metal cluster and Cd2+ (4-metal cluster) greater than Cd2+ (3-metal cluster).	Zinc	135-139	CD2 molecule	Homo sapiens	89-92
2959502-7	1987	For the 3-metal cluster, the affinity is found to decrease in the order Cu+ greater than Cd2+ greater than Zn2+ with Cd2+ greater than Zn2+ for the 4 metal cluster and Cd2+ (4-metal cluster) greater than Cd2+ (3-metal cluster).	Zinc	135-139	CD2 molecule	Homo sapiens	117-120
2959502-7	1987	For the 3-metal cluster, the affinity is found to decrease in the order Cu+ greater than Cd2+ greater than Zn2+ with Cd2+ greater than Zn2+ for the 4 metal cluster and Cd2+ (4-metal cluster) greater than Cd2+ (3-metal cluster).	Zinc	135-139	CD2 molecule	Homo sapiens	117-120
2959502-7	1987	For the 3-metal cluster, the affinity is found to decrease in the order Cu+ greater than Cd2+ greater than Zn2+ with Cd2+ greater than Zn2+ for the 4 metal cluster and Cd2+ (4-metal cluster) greater than Cd2+ (3-metal cluster).	Zinc	135-139	CD2 molecule	Homo sapiens	117-120
2822468-9	1987	The studies also suggest that zinc status and maintenance of the renal ZnMT pool may play an important role in regulating cadmium-induced renal proteinuria and calcuria by preventing Cd2+ perturbation of the proximal tubule cell lysosome system.	znmt	71-75	CD2 molecule	Homo sapiens	183-186
2822468-9	1987	The studies also suggest that zinc status and maintenance of the renal ZnMT pool may play an important role in regulating cadmium-induced renal proteinuria and calcuria by preventing Cd2+ perturbation of the proximal tubule cell lysosome system.	Cadmium	122-129	CD2 molecule	Homo sapiens	183-186
2425294-3	1986	This conductance persisted when Ca2+-flux into neurones was blocked with Cd2+ and it was suppressed by muscarine (20 microM).	Muscarine	103-112	CD2 molecule	Homo sapiens	73-76
3730278-1	1986	Lichen planus-like eruptions are known to be caused by occupational exposure to colour film developing agents that are derivatives of p-phenylenediamine (PPDA), e.g. CD-2 and CD-3.	4-phenylenediamine	134-152	CD2 molecule	Homo sapiens	166-170
3730278-1	1986	Lichen planus-like eruptions are known to be caused by occupational exposure to colour film developing agents that are derivatives of p-phenylenediamine (PPDA), e.g. CD-2 and CD-3.	4-phenylenediamine	154-158	CD2 molecule	Homo sapiens	166-170
3025193-2	1986	Divalent metal ion-induced membrane aggregation showed a dependence on the ionic radius, being optimal for Cd2+.	Metals	9-14	CD2 molecule	Homo sapiens	107-110
2427570-5	1986	When purified T-PBL preparation is used, the level of [3H]TdR incorporation observed with anti-(GT2 + 9.6/T11(1)) Ab was not significant; however, it did prove significant, although greatly reduced, with the other anti-CD2 pairs tested.	t-pbl	14-19	CD2 molecule	Homo sapiens	219-222
2427570-8	1986	To induce IL 2 synthesis, the necessity to cross-link anti-CD2 Ab was demonstrated by coupling one Ab on Sepharose beads and adding the second Ab in the soluble phase: under these circumstances, anti-CD2 pairs were mitogenic solely in the presence of AC.	Sepharose	105-114	CD2 molecule	Homo sapiens	59-62
2427570-8	1986	To induce IL 2 synthesis, the necessity to cross-link anti-CD2 Ab was demonstrated by coupling one Ab on Sepharose beads and adding the second Ab in the soluble phase: under these circumstances, anti-CD2 pairs were mitogenic solely in the presence of AC.	Sepharose	105-114	CD2 molecule	Homo sapiens	200-203
2424873-5	1986	In functional assays, anti-CD2, anti-DR VI-15C, and anti-CD25 MoAbs blocked the proliferative response to DT and anti-CD3, anti-CD4, anti-D44 MoAbs had intermediate inhibition effects.	Thymidine	106-108	CD2 molecule	Homo sapiens	27-30
2424873-7	1986	Surface marker analysis revealed that the expression of CD2 to CD7 antigens (and also CD25) may be modified following incubation of the TLC with TPA or sodium butyrate but not with 5-azacytidine.	Tetradecanoylphorbol Acetate	145-148	CD2 molecule	Homo sapiens	56-59
2424873-7	1986	Surface marker analysis revealed that the expression of CD2 to CD7 antigens (and also CD25) may be modified following incubation of the TLC with TPA or sodium butyrate but not with 5-azacytidine.	Butyric Acid	152-167	CD2 molecule	Homo sapiens	56-59
2424873-7	1986	Surface marker analysis revealed that the expression of CD2 to CD7 antigens (and also CD25) may be modified following incubation of the TLC with TPA or sodium butyrate but not with 5-azacytidine.	Azacitidine	181-194	CD2 molecule	Homo sapiens	56-59
2423344-0	1986	Tetrodotoxin-sensitive and tetrodotoxin-resistant Na+ channels differ in their sensitivity to Cd2+ and Zn2+.	Tetrodotoxin	0-12	CD2 molecule	Homo sapiens	94-97
2944489-3	1986	By the same token Cd2+ inhibits the ADP and ATP exchange-reaction and also inhibits succinate oxidation.	Adenosine Diphosphate	36-39	CD2 molecule	Homo sapiens	18-21
2944489-3	1986	By the same token Cd2+ inhibits the ADP and ATP exchange-reaction and also inhibits succinate oxidation.	Adenosine Triphosphate	44-47	CD2 molecule	Homo sapiens	18-21
2944489-3	1986	By the same token Cd2+ inhibits the ADP and ATP exchange-reaction and also inhibits succinate oxidation.	Succinic Acid	84-93	CD2 molecule	Homo sapiens	18-21
3084290-5	1986	It is shown that calcium mobilization can be induced in these cells by mAb to CD2 and purified PHA but not by anti-CD3 mAb.	Calcium	17-24	CD2 molecule	Homo sapiens	78-81
3084290-6	1986	This indicates that calcium mobilization can be induced via the CD2 molecule in NK cells not expressing CD3 and that activation through CD2 is separate from the antigen receptor CD3 pathway.	Calcium	20-27	CD2 molecule	Homo sapiens	64-67
2423344-6	1986	The results suggest that Cd2+ acts competitively with veratridine or batrachotoxin and that the difference in the effects of Cd2+ and Zn2+ on 22Na+ fluxes in TTX-sensitive and TTX-resistant cells is related to differences at the site of action of alkaloid neurotoxins.	Tetrodotoxin	158-161	CD2 molecule	Homo sapiens	25-28
2423344-6	1986	The results suggest that Cd2+ acts competitively with veratridine or batrachotoxin and that the difference in the effects of Cd2+ and Zn2+ on 22Na+ fluxes in TTX-sensitive and TTX-resistant cells is related to differences at the site of action of alkaloid neurotoxins.	Tetrodotoxin	158-161	CD2 molecule	Homo sapiens	125-128
2423344-6	1986	The results suggest that Cd2+ acts competitively with veratridine or batrachotoxin and that the difference in the effects of Cd2+ and Zn2+ on 22Na+ fluxes in TTX-sensitive and TTX-resistant cells is related to differences at the site of action of alkaloid neurotoxins.	Tetrodotoxin	176-179	CD2 molecule	Homo sapiens	25-28
3517166-9	1986	The LFA-2 deoxycholate complex had an apparent Mr of 68,000 by gel filtration, suggesting it was monomeric.	Deoxycholic Acid	10-22	CD2 molecule	Homo sapiens	4-9
3019305-5	1986	All exchange processes were first-order, and two categories of metal were found: Ca2+ and Cd2+ in one, the lanthanides comprising the other.	Metals	63-68	CD2 molecule	Homo sapiens	90-93
2420827-7	1986	Both the CD2 and CD3 responses were diminished in magnitude and duration by EGTA.	Egtazic Acid	76-80	CD2 molecule	Homo sapiens	9-12
2421850-8	1986	The sulfhydryl inhibitor, N-ethylmaleimide increased, but the sulfhydryl donor, dimercaptosuccinate, abolished the effect of Cd2+ on transport.	dimercaptosuccinate	80-99	CD2 molecule	Homo sapiens	125-128
2421850-9	1986	N-ethylmaleimide also amplified the Cd2+ effect on decreasing SH group content of sciatic nerve homogenate.	Ethylmaleimide	0-16	CD2 molecule	Homo sapiens	36-39
2423344-0	1986	Tetrodotoxin-sensitive and tetrodotoxin-resistant Na+ channels differ in their sensitivity to Cd2+ and Zn2+.	Tetrodotoxin	27-39	CD2 molecule	Homo sapiens	94-97
2423344-4	1986	The 22Na+ uptake experiments using veratridine or batrachotoxin to activate Na+ channels indicated that TTX-resistant Na+ channels are more sensitive to the inhibitory action of Cd2+ (IC50(Cd2+) = 0.2 mM) and of Zn2+ (IC50(Zn2+) = 50 microM) than TTX-sensitive Na+ channels (IC50(Cd2+) = 5 mM, IC50(Zn2+) = 2 mM).	Sodium-22	4-9	CD2 molecule	Homo sapiens	178-181
2423344-4	1986	The 22Na+ uptake experiments using veratridine or batrachotoxin to activate Na+ channels indicated that TTX-resistant Na+ channels are more sensitive to the inhibitory action of Cd2+ (IC50(Cd2+) = 0.2 mM) and of Zn2+ (IC50(Zn2+) = 50 microM) than TTX-sensitive Na+ channels (IC50(Cd2+) = 5 mM, IC50(Zn2+) = 2 mM).	Veratridine	35-46	CD2 molecule	Homo sapiens	178-181
2423344-4	1986	The 22Na+ uptake experiments using veratridine or batrachotoxin to activate Na+ channels indicated that TTX-resistant Na+ channels are more sensitive to the inhibitory action of Cd2+ (IC50(Cd2+) = 0.2 mM) and of Zn2+ (IC50(Zn2+) = 50 microM) than TTX-sensitive Na+ channels (IC50(Cd2+) = 5 mM, IC50(Zn2+) = 2 mM).	Tetrodotoxin	104-107	CD2 molecule	Homo sapiens	178-181
2423344-4	1986	The 22Na+ uptake experiments using veratridine or batrachotoxin to activate Na+ channels indicated that TTX-resistant Na+ channels are more sensitive to the inhibitory action of Cd2+ (IC50(Cd2+) = 0.2 mM) and of Zn2+ (IC50(Zn2+) = 50 microM) than TTX-sensitive Na+ channels (IC50(Cd2+) = 5 mM, IC50(Zn2+) = 2 mM).	Tetrodotoxin	104-107	CD2 molecule	Homo sapiens	189-192
2423344-4	1986	The 22Na+ uptake experiments using veratridine or batrachotoxin to activate Na+ channels indicated that TTX-resistant Na+ channels are more sensitive to the inhibitory action of Cd2+ (IC50(Cd2+) = 0.2 mM) and of Zn2+ (IC50(Zn2+) = 50 microM) than TTX-sensitive Na+ channels (IC50(Cd2+) = 5 mM, IC50(Zn2+) = 2 mM).	Tetrodotoxin	104-107	CD2 molecule	Homo sapiens	189-192
2423344-4	1986	The 22Na+ uptake experiments using veratridine or batrachotoxin to activate Na+ channels indicated that TTX-resistant Na+ channels are more sensitive to the inhibitory action of Cd2+ (IC50(Cd2+) = 0.2 mM) and of Zn2+ (IC50(Zn2+) = 50 microM) than TTX-sensitive Na+ channels (IC50(Cd2+) = 5 mM, IC50(Zn2+) = 2 mM).	Zinc	212-216	CD2 molecule	Homo sapiens	178-181
2423344-4	1986	The 22Na+ uptake experiments using veratridine or batrachotoxin to activate Na+ channels indicated that TTX-resistant Na+ channels are more sensitive to the inhibitory action of Cd2+ (IC50(Cd2+) = 0.2 mM) and of Zn2+ (IC50(Zn2+) = 50 microM) than TTX-sensitive Na+ channels (IC50(Cd2+) = 5 mM, IC50(Zn2+) = 2 mM).	Zinc	223-227	CD2 molecule	Homo sapiens	178-181
2423344-4	1986	The 22Na+ uptake experiments using veratridine or batrachotoxin to activate Na+ channels indicated that TTX-resistant Na+ channels are more sensitive to the inhibitory action of Cd2+ (IC50(Cd2+) = 0.2 mM) and of Zn2+ (IC50(Zn2+) = 50 microM) than TTX-sensitive Na+ channels (IC50(Cd2+) = 5 mM, IC50(Zn2+) = 2 mM).	Tetrodotoxin	247-250	CD2 molecule	Homo sapiens	178-181
2423344-4	1986	The 22Na+ uptake experiments using veratridine or batrachotoxin to activate Na+ channels indicated that TTX-resistant Na+ channels are more sensitive to the inhibitory action of Cd2+ (IC50(Cd2+) = 0.2 mM) and of Zn2+ (IC50(Zn2+) = 50 microM) than TTX-sensitive Na+ channels (IC50(Cd2+) = 5 mM, IC50(Zn2+) = 2 mM).	Zinc	223-227	CD2 molecule	Homo sapiens	178-181
2423344-5	1986	Electrophysiological experiments showed that high concentrations of Cd2+ (IC50 = 2 mM) are necessary to inhibit both TTX-sensitive and TTX-insensitive Na+ channels when the channels are activated by voltage steps.	Tetrodotoxin	117-120	CD2 molecule	Homo sapiens	68-71
2423344-5	1986	Electrophysiological experiments showed that high concentrations of Cd2+ (IC50 = 2 mM) are necessary to inhibit both TTX-sensitive and TTX-insensitive Na+ channels when the channels are activated by voltage steps.	Tetrodotoxin	135-138	CD2 molecule	Homo sapiens	68-71
2417941-2	1986	The rise in calcium mobilization induced by purified PHA (PHA-P) does not occur in a cell line which lacks CD2 expression, and can be blocked in other T cells by anti-CD2 antibodies.	Calcium	12-19	CD2 molecule	Homo sapiens	107-110
3081579-3	1986	The immunotoxins studied were T cell-specific monoclonal anti-T11 antibodies conjugated by disulfide linkage to ribosome-inactivating toxins.	Disulfides	91-100	CD2 molecule	Homo sapiens	62-65
3510919-2	1986	To better understand the molecular nature of this defect, we have investigated insulin binding to circulating monocytes, erythrocytes, and the Triton X-100-solubilized erythrocyte receptor, and insulin-stimulated receptor autophosphorylation using cells and receptor from three type A patients.	Octoxynol	143-155	CD2 molecule	Homo sapiens	168-188
2417941-2	1986	The rise in calcium mobilization induced by purified PHA (PHA-P) does not occur in a cell line which lacks CD2 expression, and can be blocked in other T cells by anti-CD2 antibodies.	Calcium	12-19	CD2 molecule	Homo sapiens	167-170
2417941-3	1986	A combination of monoclonal antibodies to different epitopes of CD2 causes calcium mobilization and mitogenesis.	Calcium	75-82	CD2 molecule	Homo sapiens	64-67
2998298-4	1985	Binding of Cd2+ allowed CaM to bind 2 moles chlorpromazine, or to form a complex with skeletal muscle troponin-I, troponin-T, or phosphodiesterase.	Chlorpromazine	44-58	CD2 molecule	Homo sapiens	11-14
11539091-7	1986	It is concluded that Cd2+ can act like certain other stresses (K+ and Mg2+ deficiency, excess NH4+, low pH, salinity, osmotic stress, wilting) to induce substantial increases in Put in plant cells.	magnesium ion	70-74	CD2 molecule	Homo sapiens	21-24
11539091-7	1986	It is concluded that Cd2+ can act like certain other stresses (K+ and Mg2+ deficiency, excess NH4+, low pH, salinity, osmotic stress, wilting) to induce substantial increases in Put in plant cells.	Ammonium Compounds	94-98	CD2 molecule	Homo sapiens	21-24
2992964-2	1985	In the presence of Cd2+ selectivity to ADP[alpha S] and to ATP[beta S] isomers is reversed; in the presence of Co2+, selectivity is lost.	Adenosine Diphosphate	39-42	CD2 molecule	Homo sapiens	19-22
2992964-2	1985	In the presence of Cd2+ selectivity to ADP[alpha S] and to ATP[beta S] isomers is reversed; in the presence of Co2+, selectivity is lost.	Adenosine Triphosphate	59-62	CD2 molecule	Homo sapiens	19-22
2992964-2	1985	In the presence of Cd2+ selectivity to ADP[alpha S] and to ATP[beta S] isomers is reversed; in the presence of Co2+, selectivity is lost.	Cobalt(2+)	111-115	CD2 molecule	Homo sapiens	19-22
2420972-7	1986	They practically disappeared on replacing external Ca2+ with Mg2+ and were blocked by millimolar additions of Cd2+ to the bath.	magnesium ion	61-65	CD2 molecule	Homo sapiens	110-113
2998298-5	1985	Complex formation with phosphodiesterase led to its activation, which was observed even in the presence of glutathione or cysteine, agents known to chelate Cd2+.	Glutathione	107-118	CD2 molecule	Homo sapiens	156-159
2998298-5	1985	Complex formation with phosphodiesterase led to its activation, which was observed even in the presence of glutathione or cysteine, agents known to chelate Cd2+.	Cysteine	122-130	CD2 molecule	Homo sapiens	156-159
6089914-3	1984	The cells pretreated with Cd2+ showed slight activity of the release, but no recovery was observed with other divalent cations such as Mg2+, Sr2+, Co2+, Ba2+ and Zn2+.	N-methyl-valyl-amiclenomycin	153-157	CD2 molecule	Homo sapiens	26-29
4012806-3	1985	While intravenously administered Cd2+ salts result in Cd2+ binding loosely to plasma proteins, and subsequently being deposited in the liver, Cd complexed with metallothionein remains tightly bound during glomerular filtration, and most of the dose of Cd is deposited in the kidney.	Cadmium	33-35	CD2 molecule	Homo sapiens	54-57
4012806-3	1985	While intravenously administered Cd2+ salts result in Cd2+ binding loosely to plasma proteins, and subsequently being deposited in the liver, Cd complexed with metallothionein remains tightly bound during glomerular filtration, and most of the dose of Cd is deposited in the kidney.	Cadmium	54-56	CD2 molecule	Homo sapiens	33-36
3838251-1	1985	The interaction of Al3+, Cd2+ and Mn2+ with phosphatidylserine-containing lipid vesicles was studied.	Phosphatidylserines	44-62	CD2 molecule	Homo sapiens	25-28
6151183-1	1984	A small and very slow inward calcium current has been identified in isolated single ventricular cells using TTX and Cd2+ to block the sodium and fast calcium currents.	Calcium	29-36	CD2 molecule	Homo sapiens	116-119
6151183-1	1984	A small and very slow inward calcium current has been identified in isolated single ventricular cells using TTX and Cd2+ to block the sodium and fast calcium currents.	Sodium	134-140	CD2 molecule	Homo sapiens	116-119
6151183-1	1984	A small and very slow inward calcium current has been identified in isolated single ventricular cells using TTX and Cd2+ to block the sodium and fast calcium currents.	Calcium	150-157	CD2 molecule	Homo sapiens	116-119
3888954-3	1985	The addition of 20 microM Cd2+ or Zn2+ (but not Mn2+) to the cell suspensions preloaded with 109Cd2+ caused the exchange of Cd2+.	Zinc	34-38	CD2 molecule	Homo sapiens	96-99
3888954-3	1985	The addition of 20 microM Cd2+ or Zn2+ (but not Mn2+) to the cell suspensions preloaded with 109Cd2+ caused the exchange of Cd2+.	109cd2+	93-100	CD2 molecule	Homo sapiens	26-29
2860921-1	1985	Substitution of Cd2+ for Zn2+ yields a hexameric insulin species containing 3 mol of metal ion per hexamer.	Metals	85-90	CD2 molecule	Homo sapiens	16-19
2860921-2	1985	The Cd2+ binding loci consist of the two His(B10) sites and a new site involving the Glu(B13) residues located at the center of the hexamer [Sudmeier, J. L., Bell, S. J., Storm, M. C., &amp; Dunn, M. F. (1981) Science (Washington, D.C.) 212, 560-562].	Histidine	41-44	CD2 molecule	Homo sapiens	4-7
2860921-2	1985	The Cd2+ binding loci consist of the two His(B10) sites and a new site involving the Glu(B13) residues located at the center of the hexamer [Sudmeier, J. L., Bell, S. J., Storm, M. C., &amp; Dunn, M. F. (1981) Science (Washington, D.C.) 212, 560-562].	Glutamic Acid	85-88	CD2 molecule	Homo sapiens	4-7
2860921-2	1985	The Cd2+ binding loci consist of the two His(B10) sites and a new site involving the Glu(B13) residues located at the center of the hexamer [Sudmeier, J. L., Bell, S. J., Storm, M. C., &amp; Dunn, M. F. (1981) Science (Washington, D.C.) 212, 560-562].	Adenosine Monophosphate	186-189	CD2 molecule	Homo sapiens	4-7
2860921-5	1985	The kinetics of the reaction of 2,2",2"-terpyridine (terpy) with the exchange-labile (In)6(Cd2+)2 and (In)6(Co2+)2 derivatives are biphasic and involve the rapid formation of an intermediate with coordination of one terpy molecule to each protein-bound metal ion; then, in a rate-limiting step the terpy-coordinated metal ion dissociates from the protein, and a second molecule of terpy binds to the metal ion to form a bis complex.	2,2',2''-terpyridine	32-51	CD2 molecule	Homo sapiens	91-94
2860921-5	1985	The kinetics of the reaction of 2,2",2"-terpyridine (terpy) with the exchange-labile (In)6(Cd2+)2 and (In)6(Co2+)2 derivatives are biphasic and involve the rapid formation of an intermediate with coordination of one terpy molecule to each protein-bound metal ion; then, in a rate-limiting step the terpy-coordinated metal ion dissociates from the protein, and a second molecule of terpy binds to the metal ion to form a bis complex.	2,2',2''-terpyridine	40-45	CD2 molecule	Homo sapiens	91-94
2860921-7	1985	In contrast to the kinetic behavior of (In)6(Co2+)2 and (In)6(Cd2+)2, the Cd2+ ions bound to the hybrid (In)6(Co3+)2Cd2+ react quite slowly with terpy (t1/2 = 1 h at pH 8.0).	(co3+)2cd2+	109-120	CD2 molecule	Homo sapiens	74-77
6489346-3	1984	The swelling is inhibited by ruthenium red, suggesting that this effect of Cd2+ requires its entry into mitochondria.	Ruthenium Red	29-42	CD2 molecule	Homo sapiens	75-78
6489346-5	1984	In the presence of K+, Rb+ or Li+, but not of Na+, addition of Cd2+ produces first efflux of H+ into the medium followed by discharge of the pH gradient or uncoupling.	Rubidium	23-26	CD2 molecule	Homo sapiens	63-66
6489346-8	1984	Its activation by Cd2+ is similar to the known effect of p-chloromercuriphenyl sulfonate.	4-Chloromercuribenzenesulfonate	57-88	CD2 molecule	Homo sapiens	18-21
6334536-0	1984	Stability constants of Mg2+ and Cd2+ complexes of adenine nucleotides and thionucleotides and rate constants for formation and dissociation of MgATP and MgADP.	Adenine Nucleotides	50-69	CD2 molecule	Homo sapiens	32-35
6334536-0	1984	Stability constants of Mg2+ and Cd2+ complexes of adenine nucleotides and thionucleotides and rate constants for formation and dissociation of MgATP and MgADP.	Thionucleotides	74-89	CD2 molecule	Homo sapiens	32-35
6334536-1	1984	Stability constants for the Mg2+ and Cd2+ complexes of ATP, ADP, ATP alpha S, ATP beta S, and ADP alpha S have been determined at 30 degrees C and mu = 0.1 M by 31P NMR.	Adenosine Triphosphate	55-58	CD2 molecule	Homo sapiens	37-40
6334536-1	1984	Stability constants for the Mg2+ and Cd2+ complexes of ATP, ADP, ATP alpha S, ATP beta S, and ADP alpha S have been determined at 30 degrees C and mu = 0.1 M by 31P NMR.	Adenosine Diphosphate	60-63	CD2 molecule	Homo sapiens	37-40
6334536-1	1984	Stability constants for the Mg2+ and Cd2+ complexes of ATP, ADP, ATP alpha S, ATP beta S, and ADP alpha S have been determined at 30 degrees C and mu = 0.1 M by 31P NMR.	Adenosine Triphosphate	65-68	CD2 molecule	Homo sapiens	37-40
6334536-1	1984	Stability constants for the Mg2+ and Cd2+ complexes of ATP, ADP, ATP alpha S, ATP beta S, and ADP alpha S have been determined at 30 degrees C and mu = 0.1 M by 31P NMR.	Sulfur	0-1	CD2 molecule	Homo sapiens	37-40
6334536-1	1984	Stability constants for the Mg2+ and Cd2+ complexes of ATP, ADP, ATP alpha S, ATP beta S, and ADP alpha S have been determined at 30 degrees C and mu = 0.1 M by 31P NMR.	adenosine 5'-O-(2-thiotriphosphate)	78-88	CD2 molecule	Homo sapiens	37-40
6334536-1	1984	Stability constants for the Mg2+ and Cd2+ complexes of ATP, ADP, ATP alpha S, ATP beta S, and ADP alpha S have been determined at 30 degrees C and mu = 0.1 M by 31P NMR.	Adenosine Diphosphate	94-97	CD2 molecule	Homo sapiens	37-40
6334536-1	1984	Stability constants for the Mg2+ and Cd2+ complexes of ATP, ADP, ATP alpha S, ATP beta S, and ADP alpha S have been determined at 30 degrees C and mu = 0.1 M by 31P NMR.	ET bromodomain inhibitor	161-164	CD2 molecule	Homo sapiens	37-40
6334536-2	1984	Besides being of the utmost importance for determining species distributions for enzymatic studies, these constants allow an estimation of the preference of Cd2+ for sulfur vs. oxygen coordination in phosphorothioate complexes.	Sulfur	166-172	CD2 molecule	Homo sapiens	157-160
6334536-2	1984	Besides being of the utmost importance for determining species distributions for enzymatic studies, these constants allow an estimation of the preference of Cd2+ for sulfur vs. oxygen coordination in phosphorothioate complexes.	Oxygen	177-183	CD2 molecule	Homo sapiens	157-160
6334536-2	1984	Besides being of the utmost importance for determining species distributions for enzymatic studies, these constants allow an estimation of the preference of Cd2+ for sulfur vs. oxygen coordination in phosphorothioate complexes.	Parathion	200-216	CD2 molecule	Homo sapiens	157-160
6334536-7	1984	Proton NMR demonstrates that bidentate Cd2+ complexes form intramolecular chelates with the N-7 of adenine while Mg2+ nucleotides and the tridenate CdATP alpha S do not.	n-7 of adenine	92-106	CD2 molecule	Homo sapiens	39-42
6334536-7	1984	Proton NMR demonstrates that bidentate Cd2+ complexes form intramolecular chelates with the N-7 of adenine while Mg2+ nucleotides and the tridenate CdATP alpha S do not.	mg2+ nucleotides	113-129	CD2 molecule	Homo sapiens	39-42
6334536-7	1984	Proton NMR demonstrates that bidentate Cd2+ complexes form intramolecular chelates with the N-7 of adenine while Mg2+ nucleotides and the tridenate CdATP alpha S do not.	cdatp	148-153	CD2 molecule	Homo sapiens	39-42
6089914-3	1984	The cells pretreated with Cd2+ showed slight activity of the release, but no recovery was observed with other divalent cations such as Mg2+, Sr2+, Co2+, Ba2+ and Zn2+.	Zinc	162-166	CD2 molecule	Homo sapiens	26-29
6147346-10	1984	The results indicate that the major effect of these inhibitors is on FB dithiol and leave little doubt that Cd2+ is indeed bound to a vicinal dithiol group.	vicinal dithiol	134-149	CD2 molecule	Homo sapiens	108-111
6329303-3	1984	Calculation of Vmax/Km values confirmed reversal of the Rp/Sp ratios for ATP[beta S] with Mg2+ [16] and Cd2+ [2], providing evidence that the metal is coordinated to the beta-phosphate at the active site.	Metals	142-147	CD2 molecule	Homo sapiens	104-107
6611200-6	1984	During blastic transformation, the erythrocyte rosette receptor was induced by TPA on sheep erythrocyte-rosette-negative Sezary cells from one patient.	Tetradecanoylphorbol Acetate	79-82	CD2 molecule	Homo sapiens	47-63
6611200-9	1984	Blastic transformation of CTCL cells was observed with both TPA and phytohemagglutinin, but helper T-cell antigen Leu 3a (T4) and erythrocyte rosette receptor changes occurred only with TPA.	Tetradecanoylphorbol Acetate	186-189	CD2 molecule	Homo sapiens	142-158
6430343-8	1984	Acetazolamide (5-acetylamido-1,3,4-thiadiazole 2-sulfonamide) is also a strong inhibitor although its affinity for the Cd2+ enzyme is less than its affinity for the native enzyme.	Acetazolamide	0-13	CD2 molecule	Homo sapiens	119-122
6469967-2	1984	The equilibrium binding experiments have shown that there are two cadmium binding sites on STnC with a high affinity for Cd2+ (KCd congruent to 10(7) M-1) and two with a lower affinity for Cd2+ (KCd congruent to 10(3) M-1).	Cadmium	66-73	CD2 molecule	Homo sapiens	121-124
6469967-4	1984	In the presence of Mg2+ the affinity of Cd2+ for the higher affinity sites was lowered, yielding a KMg of approximately 10(3) M-1.	magnesium ion	19-23	CD2 molecule	Homo sapiens	40-43
6469967-18	1984	Since the direct binding experiments clearly demonstrate that the high affinity Cd2+ sites are the Ca2+-Mg2+ sites, we can only conclude that Cd2+ binding to the protein (probably to the lower affinity Ca2+-specific sites) dramatically alters the affinity of the Ca2+-Mg2+ sites for Ca2+.	magnesium ion	104-108	CD2 molecule	Homo sapiens	80-83
6469967-18	1984	Since the direct binding experiments clearly demonstrate that the high affinity Cd2+ sites are the Ca2+-Mg2+ sites, we can only conclude that Cd2+ binding to the protein (probably to the lower affinity Ca2+-specific sites) dramatically alters the affinity of the Ca2+-Mg2+ sites for Ca2+.	magnesium ion	104-108	CD2 molecule	Homo sapiens	142-145
6469967-18	1984	Since the direct binding experiments clearly demonstrate that the high affinity Cd2+ sites are the Ca2+-Mg2+ sites, we can only conclude that Cd2+ binding to the protein (probably to the lower affinity Ca2+-specific sites) dramatically alters the affinity of the Ca2+-Mg2+ sites for Ca2+.	magnesium ion	268-272	CD2 molecule	Homo sapiens	142-145
6430343-5	1984	The Cd2+-carbonic anhydrases also have significant CO2 hydration activities.	N2,N6-bis(4-(2-aminoethoxy)quinolin-2-yl)-4-((4-fluorobenzyl)oxy)pyridine-2,6-dicarboxamide	51-54	CD2 molecule	Homo sapiens	4-7
6430343-8	1984	Acetazolamide (5-acetylamido-1,3,4-thiadiazole 2-sulfonamide) is also a strong inhibitor although its affinity for the Cd2+ enzyme is less than its affinity for the native enzyme.	5-acetylamido-1,3,4-thiadiazole 2-sulfonamide	15-60	CD2 molecule	Homo sapiens	119-122
6329303-2	1984	In the presence of Mg2+ the Rp diastereomers of both ATP[alpha S] and ATP[beta S] were the preferred substrates, whereas in the presence of Cd2+ the Sp diastereomers were the more active.	Adenosine Triphosphate	70-73	CD2 molecule	Homo sapiens	140-143
6329303-2	1984	In the presence of Mg2+ the Rp diastereomers of both ATP[alpha S] and ATP[beta S] were the preferred substrates, whereas in the presence of Cd2+ the Sp diastereomers were the more active.	TFF2 protein, human	149-151	CD2 molecule	Homo sapiens	140-143
6329303-3	1984	Calculation of Vmax/Km values confirmed reversal of the Rp/Sp ratios for ATP[beta S] with Mg2+ [16] and Cd2+ [2], providing evidence that the metal is coordinated to the beta-phosphate at the active site.	beta-phosphate	170-184	CD2 molecule	Homo sapiens	104-107
6329303-3	1984	Calculation of Vmax/Km values confirmed reversal of the Rp/Sp ratios for ATP[beta S] with Mg2+ [16] and Cd2+ [2], providing evidence that the metal is coordinated to the beta-phosphate at the active site.	TFF2 protein, human	59-61	CD2 molecule	Homo sapiens	104-107
6329303-3	1984	Calculation of Vmax/Km values confirmed reversal of the Rp/Sp ratios for ATP[beta S] with Mg2+ [16] and Cd2+ [2], providing evidence that the metal is coordinated to the beta-phosphate at the active site.	Adenosine Triphosphate	73-76	CD2 molecule	Homo sapiens	104-107
6329303-5	1984	The Vmax for CdATP [gamma S] was some 90-fold less than that for MgATP[gamma S], suggesting that Cd2+ is bound to S from the gamma-P and that the breaking of the Cd-S bond is the rate determining step of the reaction.	cdatp	13-18	CD2 molecule	Homo sapiens	97-100
6329303-5	1984	The Vmax for CdATP [gamma S] was some 90-fold less than that for MgATP[gamma S], suggesting that Cd2+ is bound to S from the gamma-P and that the breaking of the Cd-S bond is the rate determining step of the reaction.	Adenosine Triphosphate	65-70	CD2 molecule	Homo sapiens	97-100
6145600-1	1984	Cd2+ competitively antagonizes Ca2+ in the evoked release of acetylcholine from nerve terminals in the frog sciatic-sartorius neuromuscular junction.	Acetylcholine	61-74	CD2 molecule	Homo sapiens	0-3
6742841-4	1984	A similar incidence of tolerance to Cd2+ was demonstrated by isolates of both water types and was not associated with multiple antibiotic resistance.	Water	78-83	CD2 molecule	Homo sapiens	36-39
6145600-6	1984	At higher concentrations, Cd2+ is either relatively impermeable to the presynaptic nerve membrane or, if it does enter the nerve terminal, it is less effective than such metals as Pb2+, La3+ or Hg2+ in increasing the rate of spontaneous transmitter release.	Lead	180-184	CD2 molecule	Homo sapiens	26-29
6145600-6	1984	At higher concentrations, Cd2+ is either relatively impermeable to the presynaptic nerve membrane or, if it does enter the nerve terminal, it is less effective than such metals as Pb2+, La3+ or Hg2+ in increasing the rate of spontaneous transmitter release.	lanthanum(3+)	186-190	CD2 molecule	Homo sapiens	26-29
6145600-6	1984	At higher concentrations, Cd2+ is either relatively impermeable to the presynaptic nerve membrane or, if it does enter the nerve terminal, it is less effective than such metals as Pb2+, La3+ or Hg2+ in increasing the rate of spontaneous transmitter release.	Mercuric cation	194-198	CD2 molecule	Homo sapiens	26-29
6734560-14	1984	The toxicity of parenterally administered Cd2+ is strongly enhanced when administered as complexes with NTA or STPP , but it is much decreased when administered as a complex with EDTA.	Edetic Acid	179-183	CD2 molecule	Homo sapiens	42-45
6734560-16	1984	The uptake of Cd2+ from ligated intestine in vivo was not affected by administration of Cd2+ as complexes with CYS or GSH, but significantly reduced by complexation with EDTA or BAL.	Edetic Acid	170-174	CD2 molecule	Homo sapiens	14-17
6734560-1	1984	The toxicity of cadmium is determined by chelation reactions: in vivo, Cd2+ exists exclusively in coordination complexes with biological ligands, or with administered chelating agents.	Cadmium	16-23	CD2 molecule	Homo sapiens	71-74
6734560-16	1984	The uptake of Cd2+ from ligated intestine in vivo was not affected by administration of Cd2+ as complexes with CYS or GSH, but significantly reduced by complexation with EDTA or BAL.	Dimercaprol	178-181	CD2 molecule	Homo sapiens	14-17
6734560-8	1984	Cd2+ in metallothionein (MT) is coordinated with 4 thiolate groups, and the log stability constant is estimated to 25.5.	thiolate	51-59	CD2 molecule	Homo sapiens	0-3
6734560-17	1984	The acute toxicity of orally administered Cd2+ is reduced when Cd2+ is administered as a complex with EDTA.	Edetic Acid	102-106	CD2 molecule	Homo sapiens	42-45
6734560-9	1984	Complexes between Cd2+ and low molecular weight monodentate or bidentate ligands, e.g., free amino acids (LMW-Cd), seem to exist very briefly, and Cd2+ is rapidly bound to high molecular weight proteins, mainly serum albumin.	lmw-cd	106-112	CD2 molecule	Homo sapiens	18-21
6734560-17	1984	The acute toxicity of orally administered Cd2+ is reduced when Cd2+ is administered as a complex with EDTA.	Edetic Acid	102-106	CD2 molecule	Homo sapiens	63-66
6734560-9	1984	Complexes between Cd2+ and low molecular weight monodentate or bidentate ligands, e.g., free amino acids (LMW-Cd), seem to exist very briefly, and Cd2+ is rapidly bound to high molecular weight proteins, mainly serum albumin.	lmw-cd	106-112	CD2 molecule	Homo sapiens	147-150
6320866-6	1984	With as little as 5 mol % egg PA in egg PC, Cd2+ induces phase separation up to about 25 degrees C. The phase behavior of egg PA/spin-labeled PC in the presence of Cd2+ was very similar to that of egg PA/egg PC in the 10-35 degrees C temperature range.	Protactinium	30-32	CD2 molecule	Homo sapiens	44-47
6734560-11	1984	After about 1 day the Cd-MT complex (MT-Cd) almost exclusively accounts for the total retained dose of Cd2+, independent of the route of exposure.	cd-mt	22-27	CD2 molecule	Homo sapiens	103-106
6734560-11	1984	After about 1 day the Cd-MT complex (MT-Cd) almost exclusively accounts for the total retained dose of Cd2+, independent of the route of exposure.	mt-cd	37-42	CD2 molecule	Homo sapiens	103-106
6734560-14	1984	The toxicity of parenterally administered Cd2+ is strongly enhanced when administered as complexes with NTA or STPP , but it is much decreased when administered as a complex with EDTA.	Nitrilotriacetic Acid	104-107	CD2 molecule	Homo sapiens	42-45
6734560-14	1984	The toxicity of parenterally administered Cd2+ is strongly enhanced when administered as complexes with NTA or STPP , but it is much decreased when administered as a complex with EDTA.	triphosphoric acid	111-115	CD2 molecule	Homo sapiens	42-45
6320979-13	1984	Pb2+ is about 3 X 10(3) times more potent than is Mg2+, about 150 times more potent than is either Mn2+ or Co2+, and about 3 times more potent than Cd2+ is in blocking evoked release of ACh.	Lead	0-4	CD2 molecule	Homo sapiens	148-151
6320979-13	1984	Pb2+ is about 3 X 10(3) times more potent than is Mg2+, about 150 times more potent than is either Mn2+ or Co2+, and about 3 times more potent than Cd2+ is in blocking evoked release of ACh.	Acetylcholine	186-189	CD2 molecule	Homo sapiens	148-151
6320866-6	1984	With as little as 5 mol % egg PA in egg PC, Cd2+ induces phase separation up to about 25 degrees C. The phase behavior of egg PA/spin-labeled PC in the presence of Cd2+ was very similar to that of egg PA/egg PC in the 10-35 degrees C temperature range.	pc	40-42	CD2 molecule	Homo sapiens	44-47
6140015-0	1983	The effects of Al3+, Cd2+ and Mn2+ on human erythrocyte choline transport.	Choline	56-63	CD2 molecule	Homo sapiens	21-24
6235431-0	1984	Effects of Cd2+ on ATP-driven membrane potential in beef heart mitochondrial H+-ATPase: a study using the voltage-sensitive probe oxonol VI.	Adenosine Triphosphate	19-22	CD2 molecule	Homo sapiens	11-14
6235431-3	1984	The steady-state potential was discharged by oligomycin and/or Cd2+ (a dithiol reagent).	dithiol	71-78	CD2 molecule	Homo sapiens	63-66
6235431-6	1984	Both effects of Cd2+ were inhibited by dithiothreitol.	Dithiothreitol	39-53	CD2 molecule	Homo sapiens	16-19
6140015-4	1983	The effects of Cd2+ and Mn2+ (but not Al3+) on choline accumulation were reversed by removing the cations from the extracellular medium by washing.	Choline	47-54	CD2 molecule	Homo sapiens	15-18
6140015-8	1983	These results suggest that inhibition of choline accumulation and efflux in erythrocytes by Al3+, Cd2+ and Mn2+ is not explicable solely in terms of either inhibition of Ca-Mg-ATPase, or inhibition of Na-K-ATPase causing reduced intracellular K+.	Choline	41-48	CD2 molecule	Homo sapiens	98-101
6314931-3	1983	Calmodulin dependent phosphodiesterase was activated with Pb2+, Ca2+, Sr2+, Ba2+, and Cd2+ (EC50 about 0.8 microM).	strontium cation	70-74	CD2 molecule	Homo sapiens	86-89
6626547-5	1983	The low permeabilities to both Cd2+ and CdCl2 are consistent with biological studies which suggest that Cd transport and toxicity are protein mediated and correlated with Cd2+, not CdCl2, concentration.	Cadmium Chloride	40-45	CD2 molecule	Homo sapiens	171-174
6652354-1	1983	The relationship between inhibition of tension by Cd2+ in aorta and the kinetics of cadmium uptake and efflux was studied.	Cadmium	84-91	CD2 molecule	Homo sapiens	50-53
6409155-1	1983	The binding of Cd2+ by molecules in the intracellular region of human erythrocytes has been studied by 1H-NMR spectroscopy.	Hydrogen	103-105	CD2 molecule	Homo sapiens	15-18
6409155-2	1983	From changes in spin-echo Fourier transform NMR spectra for both intact and hemolyzed erythrocytes to which CdCl2 was added, direct evidence was obtained for the binding of Cd2+ by intracellular glutathione and hemoglobin.	Cadmium Chloride	108-113	CD2 molecule	Homo sapiens	173-176
6409155-2	1983	From changes in spin-echo Fourier transform NMR spectra for both intact and hemolyzed erythrocytes to which CdCl2 was added, direct evidence was obtained for the binding of Cd2+ by intracellular glutathione and hemoglobin.	Glutathione	195-206	CD2 molecule	Homo sapiens	173-176
6409155-3	1983	Time-courses were measured by 1H-NMR for the uptake of Cd2+ by intact erythrocytes in saline/glucose solution and in whole blood.	Hydrogen	30-32	CD2 molecule	Homo sapiens	55-58
6409155-3	1983	Time-courses were measured by 1H-NMR for the uptake of Cd2+ by intact erythrocytes in saline/glucose solution and in whole blood.	Sodium Chloride	86-92	CD2 molecule	Homo sapiens	55-58
6409155-3	1983	Time-courses were measured by 1H-NMR for the uptake of Cd2+ by intact erythrocytes in saline/glucose solution and in whole blood.	Glucose	93-100	CD2 molecule	Homo sapiens	55-58
6409155-5	1983	The effectiveness of the disodium salt of EDTA and of various thiol-chelating agents for releasing glutathione from its Cd2 + complexes in hemolyzed erythrocytes was also studied.	disodium salt	25-38	CD2 molecule	Homo sapiens	120-123
6409155-5	1983	The effectiveness of the disodium salt of EDTA and of various thiol-chelating agents for releasing glutathione from its Cd2 + complexes in hemolyzed erythrocytes was also studied.	Glutathione	99-110	CD2 molecule	Homo sapiens	120-123
6652354-4	1983	Cadmium uptake increased with an increase of the Cd2+ concentration (0.01-0.5 mM).	Cadmium	0-7	CD2 molecule	Homo sapiens	49-52
6868086-1	1983	Cd2+ cytotoxicity, uptake, and partitioning, and Cd2+-induced metallothioneine synthesis were studied in cultured peripheral human blood cells.	metallothioneine	62-78	CD2 molecule	Homo sapiens	49-52
6868086-10	1983	Instead Cd2+ appeared in a Sephadex G-75 peak of approximately 60,000 Da, as well as in the void peak.	sephadex	27-40	CD2 molecule	Homo sapiens	8-11
6825199-2	1983	Studies with Cd-Mt labelled with [3H]cystine showed that both Cd2+ and tritium uptake in the kidneys were complete 4 h after injection.	[3h]cystine	33-44	CD2 molecule	Homo sapiens	62-65
6612697-1	1983	Subcutaneously administered dihydroergotamine (DHE) becomes rapidly and completely available to the human systemic circulation, with peak plasma levels of 1.4-3.5 ng/mL/mg achieved in less than 1 h. The elimination of DHE from plasma is biphasic, t 1/2 alpha = 1h, t 1/2 beta = 4-5 h. DHE exhibits linear dose proportionality.	Dihydroergotamine	28-45	CD2 molecule	Homo sapiens	247-281
6612697-1	1983	Subcutaneously administered dihydroergotamine (DHE) becomes rapidly and completely available to the human systemic circulation, with peak plasma levels of 1.4-3.5 ng/mL/mg achieved in less than 1 h. The elimination of DHE from plasma is biphasic, t 1/2 alpha = 1h, t 1/2 beta = 4-5 h. DHE exhibits linear dose proportionality.	Dihydroergotamine	47-50	CD2 molecule	Homo sapiens	247-281
6825199-3	1983	During this period, renal copper content doubles due to the replacement of thionein-bound Cd2+ with Cu2+.	Copper	26-32	CD2 molecule	Homo sapiens	90-93
6825199-3	1983	During this period, renal copper content doubles due to the replacement of thionein-bound Cd2+ with Cu2+.	Lys-Cys-Thr-Cys-Cys-Ala	75-83	CD2 molecule	Homo sapiens	90-93
6825199-6	1983	Consequently, at 4 h virtually all of the Cd-Mt was degraded, resulting in a high concentration of non-thionein bound Cd2+.	Cadmium	42-44	CD2 molecule	Homo sapiens	118-121
6825199-10	1983	By 4 days, 80% of the renal Cd2+ is bound to endogenous thionein.	Lys-Cys-Thr-Cys-Cys-Ala	56-64	CD2 molecule	Homo sapiens	28-31
6825199-11	1983	These studies demonstrate that even small amounts of non-thionein bound Cd2+ are toxic to the kidney.	Lys-Cys-Thr-Cys-Cys-Ala	57-65	CD2 molecule	Homo sapiens	72-75
7055571-1	1982	In this study amphotericin B released the divalent trace metals Zn2+, Co2+, Cu2+, Ni2+, Mn2+, Fe2+, Cd2+ and Pb2+ from multilamellar liposomes containing cholesterol.	Amphotericin B	14-28	CD2 molecule	Homo sapiens	100-103
6618290-3	1983	When Cu2+, Zn2+, Mg2+, Co2+, Fe2+, Ba2+, or Cd2+ were introduced into the transport medium to the final concentrations of 2.5 and 5.0 mM, they inhibited significantly the L-leucine uptake into platelets.	Leucine	171-180	CD2 molecule	Homo sapiens	44-47
7079574-0	1982	Effect of hydrogen ions on influx and efflux of Ba2+ and Cd2+ in adrenal medulla.	Hydrogen	10-18	CD2 molecule	Homo sapiens	57-60
7225357-3	1981	Divalent cations bind to dipalmitoylphosphatidylcholine in the sequence Ca2+ approximately equal to Cd2+ approximately equal to Mn2+ greater than Ca2+ approximately equal to Mg2+ greater than Ba2+.	1,2-Dipalmitoylphosphatidylcholine	25-55	CD2 molecule	Homo sapiens	100-103
7079574-7	1982	Barium in the tissue is proportional to secretion, but it appears that only part of the Cd2+ entering the cells is involved in initiating adrenal catecholamine release.	Catecholamines	146-159	CD2 molecule	Homo sapiens	88-91
7315181-6	1981	Elimination of dopamine from plasma after termination of infusion had a biphasic course with t 1/2 alpha around 1 min and t 1/2 beta about 9 min in both groups.	Dopamine	15-23	CD2 molecule	Homo sapiens	93-140
7260081-1	1981	The structures of Ca2+ and Cd2+ complexes with dipalmitoyl- and dimyristoylphosphatidic acids have been investigated by differential scanning calorimetry and small angle X-ray diffraction.	dipalmitoyl- and dimyristoylphosphatidic acids	47-93	CD2 molecule	Homo sapiens	27-30
6274056-2	1981	EBV-infected cells were cultured in microtest plates for three weeks and specific antibody activities for sheep red blood cell (SRBC) were detected in the culture supernatants by hemolysis and those for phosphorylcholine (PC) and for hepatitis B surface antigen (HBsAg) by passive hemagglutination.	Phosphorylcholine	203-220	CD2 molecule	Homo sapiens	128-132
7225357-3	1981	Divalent cations bind to dipalmitoylphosphatidylcholine in the sequence Ca2+ approximately equal to Cd2+ approximately equal to Mn2+ greater than Ca2+ approximately equal to Mg2+ greater than Ba2+.	Manganese(2+)	128-132	CD2 molecule	Homo sapiens	100-103
206286-6	1978	The inhibiting effect of Cd2+ is removed in the presence of exogenous Mn2+ or hydroxylamine.	Manganese(2+)	70-74	CD2 molecule	Homo sapiens	25-28
7213661-0	1980	Hemoglobin Milledgeville (alpha 44 (CD2) Pro leads to Leu): a new variant with increased oxygen affinity.	Proline	41-44	CD2 molecule	Homo sapiens	36-39
7213661-0	1980	Hemoglobin Milledgeville (alpha 44 (CD2) Pro leads to Leu): a new variant with increased oxygen affinity.	Leucine	54-57	CD2 molecule	Homo sapiens	36-39
7213661-0	1980	Hemoglobin Milledgeville (alpha 44 (CD2) Pro leads to Leu): a new variant with increased oxygen affinity.	Oxygen	89-95	CD2 molecule	Homo sapiens	36-39
7213661-5	1980	Fractionation of trypsin and chymotrypsin digests of isolated alpha chains demonstrated a single abnormal peptide representing a Pro leads to Leu substitution at alpha 44 (CD2).	Leucine	142-145	CD2 molecule	Homo sapiens	172-175
7213661-7	1980	The alpha CD2 proline residue normally participates in the formation of the alpha 1 beta 2 subunit interface in the deoxy quaternary conformation, but not in oxyhemoglobin; the leucine substitution may produce destabilization of the deoxy conformation with a resulting shift in equilibrium toward the oxy conformation.	Proline	14-21	CD2 molecule	Homo sapiens	10-13
6256747-6	1980	When the temperature or the hemoglobin concentration was increased (i) several additional histidine resonances in sickle hemoglobin solutions had larger T1-1 values than the corresponding ones in normal hemoglobin and (ii) the differences between the T1-1 values (sickle versus normal hemoglobin) of these histidine resonances as well as that of the beta 2 histidine resonance gradually increased.	Histidine	90-99	CD2 molecule	Homo sapiens	153-157
6256747-6	1980	When the temperature or the hemoglobin concentration was increased (i) several additional histidine resonances in sickle hemoglobin solutions had larger T1-1 values than the corresponding ones in normal hemoglobin and (ii) the differences between the T1-1 values (sickle versus normal hemoglobin) of these histidine resonances as well as that of the beta 2 histidine resonance gradually increased.	Histidine	90-99	CD2 molecule	Homo sapiens	251-255
7378385-4	1980	In both gel and liquid-crystal phases, the Raman line widths depend on the position of the CD2 group, being minimum at position 6 and increasing toward both ends of the hydrocarbon chain.	Hydrocarbons	169-180	CD2 molecule	Homo sapiens	91-94
6966303-3	1980	Treatment of sheep red blood cells (SRBC) with 2-aminoethylisothiouronium bromide (AET) accelerates and enhances E-rosette formation providing an effective and time saving method which takes less than 2 h to perform.	2-aminoethylisothiouronium bromide	47-81	CD2 molecule	Homo sapiens	36-40
6966303-3	1980	Treatment of sheep red blood cells (SRBC) with 2-aminoethylisothiouronium bromide (AET) accelerates and enhances E-rosette formation providing an effective and time saving method which takes less than 2 h to perform.	2-(2-Aminoethyl)isothiourea dihydrobromide	83-86	CD2 molecule	Homo sapiens	36-40
570415-4	1979	The most probable order parameter for the (-CD2)n portion of the homogeneous fraction of cholesteryl palmitate-d31 was determined from the quadrupolar splittings to be S = 0.1 which is less than one-half that of the order parameter found for the lecithin chains.	cholesteryl palmitate	89-110	CD2 molecule	Homo sapiens	44-47
570415-4	1979	The most probable order parameter for the (-CD2)n portion of the homogeneous fraction of cholesteryl palmitate-d31 was determined from the quadrupolar splittings to be S = 0.1 which is less than one-half that of the order parameter found for the lecithin chains.	Lecithins	246-254	CD2 molecule	Homo sapiens	44-47
206286-6	1978	The inhibiting effect of Cd2+ is removed in the presence of exogenous Mn2+ or hydroxylamine.	Hydroxylamine	78-91	CD2 molecule	Homo sapiens	25-28
857425-0	1977	Identification of sialosylparagloboside as the erythrocyte receptor for an "anti-p" antibody.	sialosylparagloboside	18-39	CD2 molecule	Homo sapiens	47-67
563749-2	1978	Separation of the tryptic peptides of her beta chains disclosed two half-sized peaks in the regions of beta T-11.	Peptides	26-34	CD2 molecule	Homo sapiens	108-112
410009-0	1977	Studes of calcium absorption in man using a CD-2 whole-body counter.	Calcium	10-17	CD2 molecule	Homo sapiens	44-48
186278-8	1976	It appears that Cd2+ interferes with the release of acetylcholine from motor nerve terminals by reducing the transmembrane influxes of Ca2+, the influx possibly relating to SH groups of membrane constituents.	Acetylcholine	52-65	CD2 molecule	Homo sapiens	16-19
977944-1	1976	Some of the lymphoid cells selectively incorporating radioactive thymidine 3 days after primary immunization with SRBC which are capable of specifically localizing in the lymph nodes of adoptively immunized syngeneic recipients challenged with SRBC (SLC-SRBC)2 are also capable of specifically localizing in lymph nodes challenged with the red blood cells of a varieth of other mammalian species.	radioactive thymidine	53-74	CD2 molecule	Homo sapiens	114-118
62007-9	1976	In contrast, the DHT levels in the hypertrophied and malignant tissue were proportional to the Cd2+ concentrations.	Dihydrotestosterone	17-20	CD2 molecule	Homo sapiens	95-98
977944-1	1976	Some of the lymphoid cells selectively incorporating radioactive thymidine 3 days after primary immunization with SRBC which are capable of specifically localizing in the lymph nodes of adoptively immunized syngeneic recipients challenged with SRBC (SLC-SRBC)2 are also capable of specifically localizing in lymph nodes challenged with the red blood cells of a varieth of other mammalian species.	radioactive thymidine	53-74	CD2 molecule	Homo sapiens	244-248
977944-1	1976	Some of the lymphoid cells selectively incorporating radioactive thymidine 3 days after primary immunization with SRBC which are capable of specifically localizing in the lymph nodes of adoptively immunized syngeneic recipients challenged with SRBC (SLC-SRBC)2 are also capable of specifically localizing in lymph nodes challenged with the red blood cells of a varieth of other mammalian species.	radioactive thymidine	53-74	CD2 molecule	Homo sapiens	244-248
14096350-1	1964	THE TOPICAL ACTION OF 3-METHYL-4-AMINO-N-DIETHYL-ANILINE MONOHYDROCHLORIDE (CD-2) ON THE SKIN.	3-methyl-4-amino-n-diethyl-aniline monohydrochloride	22-74	CD2 molecule	Homo sapiens	76-80
56201-1	1976	Results with modified human red cell membrane sialoglycoproteins indicate that alkali-labile sialic acid and amino groups are parts of the erythrocyte receptor sites recognized by common rabbit and human anti-M and -N sera.	N-Acetylneuraminic Acid	93-104	CD2 molecule	Homo sapiens	139-159
1191655-1	1975	The inhibitory effect of the Cd2+ in the electron transport of the isolated chloroplasts has been observed by measuring the oxygen uptake from the solution and the fluorescence induction.	Oxygen	124-130	CD2 molecule	Homo sapiens	29-32
1191655-2	1975	Cd2+ is found to be an inhibitor on the donor side of Photosystem II and its action site, as determined by experiments using hydroxylamine and exogenous Mn, is supposed to be on the water-splitting enzyme itself.	Hydroxylamine	125-138	CD2 molecule	Homo sapiens	0-3
1191655-2	1975	Cd2+ is found to be an inhibitor on the donor side of Photosystem II and its action site, as determined by experiments using hydroxylamine and exogenous Mn, is supposed to be on the water-splitting enzyme itself.	Water	182-187	CD2 molecule	Homo sapiens	0-3
4850239-0	1974	A new delta chain variant, haemoglobin-A2-Melbourne or alpha2 delta2 43Glu-Lys(CD2).	Lysine	75-78	CD2 molecule	Homo sapiens	79-82
18961944-0	1976	Extraction and photometric determination of microamounts of Zn2+, Cd2+ and Hg2+ with 1-(2-quinolylazo)-2-acenaphthylenol.	1-(2-quinolylazo)-2-acenaphthylenol	85-120	CD2 molecule	Homo sapiens	66-69
1277730-5	1976	The higher serum concentrations of dicloxacillin, as compared with cloxacillin, are also attributable to slower (renal) elimination (T 1/2: 42 and 33 min, respectively).	Dicloxacillin	35-48	CD2 molecule	Homo sapiens	133-149
1277730-5	1976	The higher serum concentrations of dicloxacillin, as compared with cloxacillin, are also attributable to slower (renal) elimination (T 1/2: 42 and 33 min, respectively).	Cloxacillin	37-48	CD2 molecule	Homo sapiens	133-149
170355-4	1975	The hydro-osmotic response to cyclic AMP was also reduced by the Cd2+, but the response due to hypertonicity of the serosal bathing solution was unaffected.	Cyclic AMP	30-40	CD2 molecule	Homo sapiens	65-68
33524729-3	2021	This article studies the adsorption behavior of heavy metal cations (Pb2+, Cd2+, Cu2+, and Zn2+) on charged montmorillonite surfaces from a new theoretical foundation based on the quantum mechanics analysis of surface O atoms in this electric field, which reveals that polarization-induced covalent bonding is a strong adsorption force.	Metals	54-59	CD2 molecule	Homo sapiens	75-78
33831833-2	2021	Herein, we report an electrochemical sensing platform based on binary assembly of silica nanochannels and polydimethylsiloxane that is able to detect Pb2+ and Cd2+ in real food samples without complex pretreatments.	Silicon Dioxide	82-88	CD2 molecule	Homo sapiens	159-162
33831833-2	2021	Herein, we report an electrochemical sensing platform based on binary assembly of silica nanochannels and polydimethylsiloxane that is able to detect Pb2+ and Cd2+ in real food samples without complex pretreatments.	baysilon	106-126	CD2 molecule	Homo sapiens	159-162
33581542-3	2021	The presence of Cd2+/Cu2+ increased the adsorption capacity of DEHP (>23%) in a nonlinear manner.	cupric ion	21-25	CD2 molecule	Homo sapiens	16-19
33581542-3	2021	The presence of Cd2+/Cu2+ increased the adsorption capacity of DEHP (>23%) in a nonlinear manner.	Diethylhexyl Phthalate	63-67	CD2 molecule	Homo sapiens	16-19
33581542-4	2021	Fourier transform infrared spectroscopy revealed that the stretching vibration of soil functional groups changed under different pollution combinations, while quantum chemical simulation, including an independent gradient model and localized orbital locator, proved that outer-orbital complexes could be formed by electrostatic interaction between Cd2+/Cu2+ and DEHP.	cupric ion	353-357	CD2 molecule	Homo sapiens	348-351
33581542-4	2021	Fourier transform infrared spectroscopy revealed that the stretching vibration of soil functional groups changed under different pollution combinations, while quantum chemical simulation, including an independent gradient model and localized orbital locator, proved that outer-orbital complexes could be formed by electrostatic interaction between Cd2+/Cu2+ and DEHP.	Diethylhexyl Phthalate	362-366	CD2 molecule	Homo sapiens	348-351
34047563-7	2021	The analysis of data reveals that photoinduced electron transfer is responsible for fluorescence quenching of QDs in the presence of first-row TM ions and destruction/removal of trap/defect states in the case of Cd2+ causes the FE.	Iron	228-230	CD2 molecule	Homo sapiens	212-215
33507501-0	2021	Amino-modified hollow alumina spheres: effective adsorbent for Cd2+, Pb2+, As(V), and diclofenac removal.	Aluminum Oxide	22-29	CD2 molecule	Homo sapiens	63-66
33507501-4	2021	Introduction of a large number of the amino group, 6.9 mmol g-1, contributes to achieving high adsorption capacities, qm, of 95.6, 124.9, 61.3, and 125.9 mg g-1 for Cd2+, Pb2+, As(V), and DCF, respectively, which is obtained by using the Langmuir model.	asunaprevir	177-182	CD2 molecule	Homo sapiens	165-168
33507501-4	2021	Introduction of a large number of the amino group, 6.9 mmol g-1, contributes to achieving high adsorption capacities, qm, of 95.6, 124.9, 61.3, and 125.9 mg g-1 for Cd2+, Pb2+, As(V), and DCF, respectively, which is obtained by using the Langmuir model.	Pentostatin	188-191	CD2 molecule	Homo sapiens	165-168
33512727-2	2021	Herein, we present evidence that pre-and post- intraperitoneal administration of tacrolimus (FK506) is very effective in reducing CCR3/SigleF+ eosinophils in Aspergillus-challenged asthma and EoE, CD2-IL-5 induced global eosinophilia and DOX regulated IL-13 induced asthma.	Tacrolimus	81-91	CD2 molecule	Homo sapiens	197-200
33512727-2	2021	Herein, we present evidence that pre-and post- intraperitoneal administration of tacrolimus (FK506) is very effective in reducing CCR3/SigleF+ eosinophils in Aspergillus-challenged asthma and EoE, CD2-IL-5 induced global eosinophilia and DOX regulated IL-13 induced asthma.	Tacrolimus	93-98	CD2 molecule	Homo sapiens	197-200
33545470-5	2021	DON+Cd2+, DON, and Cd2+ induced dose-dependent fluorescence signal in the biosensors (at environmental exposure levels).	deoxynivalenol	0-4	CD2 molecule	Homo sapiens	19-22
33545470-5	2021	DON+Cd2+, DON, and Cd2+ induced dose-dependent fluorescence signal in the biosensors (at environmental exposure levels).	deoxynivalenol	0-3	CD2 molecule	Homo sapiens	4-7
34047563-8	2021	In FT-IR experiments, a prominent peak at 670 cm-1, corresponding to Cd-S stretching vibrations, indicates strong ground-state interactions between the -SH of GSH and Cd2+ ions.	Glutathione	159-162	CD2 molecule	Homo sapiens	167-170
34047563-9	2021	Moreover, a decrease in the diffusion coefficient of QDs in the presence of Cd2+ ions during fluorescence correlation spectroscopy (FCS) studies further substantiates the removal of GSH by Cd2+ from the surface of QDs.	Glutathione	182-185	CD2 molecule	Homo sapiens	76-79
34047563-9	2021	Moreover, a decrease in the diffusion coefficient of QDs in the presence of Cd2+ ions during fluorescence correlation spectroscopy (FCS) studies further substantiates the removal of GSH by Cd2+ from the surface of QDs.	Glutathione	182-185	CD2 molecule	Homo sapiens	189-192
34047563-11	2021	More importantly, these results also suggest that Cd2+ can effectively be used for enhancing the fluorescence quantum yield of thiol-capped QDs such as GSH@ZAIS.	Sulfhydryl Compounds	127-132	CD2 molecule	Homo sapiens	50-53
34047563-11	2021	More importantly, these results also suggest that Cd2+ can effectively be used for enhancing the fluorescence quantum yield of thiol-capped QDs such as GSH@ZAIS.	Glutathione	152-155	CD2 molecule	Homo sapiens	50-53
33894969-1	2021	Cadmium (Cd2+) is a toxic metal ion widely existing in water, soil and food.	Cadmium	0-7	CD2 molecule	Homo sapiens	9-12
34038101-2	2021	The balance of water coordination and the multitude of bonding of the weakly coordinated nitrate lead to a progressive change in the coordination number of the Cd2+ ions from eight to seven to six without great perturbation to the 4-fold interpenetration three-dimensional framework.	Water	15-20	CD2 molecule	Homo sapiens	160-163
34038101-2	2021	The balance of water coordination and the multitude of bonding of the weakly coordinated nitrate lead to a progressive change in the coordination number of the Cd2+ ions from eight to seven to six without great perturbation to the 4-fold interpenetration three-dimensional framework.	Nitrates	89-96	CD2 molecule	Homo sapiens	160-163
33742515-4	2021	The switching process was preferentially activated by metal ions of intermediate base over phosphate complexation preference ( i.e. Pb 2+ , Cd 2+ ) and operated with diversely structured DNA molecules.	Metals	54-59	CD2 molecule	Homo sapiens	140-144
33742515-4	2021	The switching process was preferentially activated by metal ions of intermediate base over phosphate complexation preference ( i.e. Pb 2+ , Cd 2+ ) and operated with diversely structured DNA molecules.	Phosphates	91-100	CD2 molecule	Homo sapiens	140-144
33894969-1	2021	Cadmium (Cd2+) is a toxic metal ion widely existing in water, soil and food.	Metals	26-31	CD2 molecule	Homo sapiens	9-12
33894969-1	2021	Cadmium (Cd2+) is a toxic metal ion widely existing in water, soil and food.	Water	55-60	CD2 molecule	Homo sapiens	9-12
33894969-5	2021	Plenty of H1H2 complex, the product after the Cd2+-mediated CHA, are generated, which can connect magnetic microparticles (MMPs) and polystyrene microparticles (PMPs), forming "MMPs-H1H2-PMPs" sandwich structure.	h1h2	10-14	CD2 molecule	Homo sapiens	46-49
33894969-5	2021	Plenty of H1H2 complex, the product after the Cd2+-mediated CHA, are generated, which can connect magnetic microparticles (MMPs) and polystyrene microparticles (PMPs), forming "MMPs-H1H2-PMPs" sandwich structure.	Polystyrenes	133-144	CD2 molecule	Homo sapiens	46-49
33894969-9	2021	The proposed device exhibits a limit of detection of 11.3 nM of Cd2+, selectivity >200-fold against other metal ions, high tolerance to the interferents present in drinking water and high recovery rate in tap water.	Metals	106-111	CD2 molecule	Homo sapiens	64-67
33894969-9	2021	The proposed device exhibits a limit of detection of 11.3 nM of Cd2+, selectivity >200-fold against other metal ions, high tolerance to the interferents present in drinking water and high recovery rate in tap water.	Water	173-178	CD2 molecule	Homo sapiens	64-67
33894969-9	2021	The proposed device exhibits a limit of detection of 11.3 nM of Cd2+, selectivity >200-fold against other metal ions, high tolerance to the interferents present in drinking water and high recovery rate in tap water.	Water	209-214	CD2 molecule	Homo sapiens	64-67
33581577-0	2021	Porous 3,4-di(3,5-dicarboxyphenyl)phthalate-based Cd2+ coordination polymer and its potential applications.	3,4-di(3,5-dicarboxyphenyl)phthalate	7-43	CD2 molecule	Homo sapiens	50-53
33890594-1	2021	We report herein the synthesis, structural characterization and electrocatalytic properties of three new coordination polymers, resulting from the combination of divalent metal (Ca2+, Cd2+ or Co2+) salts with (2-carboxyethyl)(phenyl)phosphinic acid.	Metals	171-176	CD2 molecule	Homo sapiens	184-187
33890594-1	2021	We report herein the synthesis, structural characterization and electrocatalytic properties of three new coordination polymers, resulting from the combination of divalent metal (Ca2+, Cd2+ or Co2+) salts with (2-carboxyethyl)(phenyl)phosphinic acid.	(2-carboxyethyl)(phenyl)phosphinic acid	209-248	CD2 molecule	Homo sapiens	184-187
33929182-1	2021	By the reaction of inorganic-ligand CdS/Cd2+ quantum dots (QDs) with inorganic-ligand CdSe/CdS/S2- nanoplatelets (NPLs), semiconductor CdS QDs were fused with CdSe/CdS NPLs to yield all-inorganic assemblies, accompanied by great photoluminescence-enhancement.	cdse	86-90	CD2 molecule	Homo sapiens	40-43
33929182-1	2021	By the reaction of inorganic-ligand CdS/Cd2+ quantum dots (QDs) with inorganic-ligand CdSe/CdS/S2- nanoplatelets (NPLs), semiconductor CdS QDs were fused with CdSe/CdS NPLs to yield all-inorganic assemblies, accompanied by great photoluminescence-enhancement.	Cadmium	86-89	CD2 molecule	Homo sapiens	40-43
33929182-1	2021	By the reaction of inorganic-ligand CdS/Cd2+ quantum dots (QDs) with inorganic-ligand CdSe/CdS/S2- nanoplatelets (NPLs), semiconductor CdS QDs were fused with CdSe/CdS NPLs to yield all-inorganic assemblies, accompanied by great photoluminescence-enhancement.	cdse	159-163	CD2 molecule	Homo sapiens	40-43
33929182-1	2021	By the reaction of inorganic-ligand CdS/Cd2+ quantum dots (QDs) with inorganic-ligand CdSe/CdS/S2- nanoplatelets (NPLs), semiconductor CdS QDs were fused with CdSe/CdS NPLs to yield all-inorganic assemblies, accompanied by great photoluminescence-enhancement.	Cadmium	86-89	CD2 molecule	Homo sapiens	40-43
33978882-2	2021	Moreover, the cation-binding property of the calix [4] arene derivative (Quin-Calix) has been investigated towards Cu2+, Ba2+, Cd2+, Co2+, Ni2+, Zn2+ and Fe3+ ions, and the recognition event monitored by UV-Vis absorption and fluorescence studies.	arene	55-60	CD2 molecule	Homo sapiens	127-130
33997932-6	2021	The maximum removal amounts were found to be 55.7 mg/g for Pb2+, 33.9 mg/g for Cd2+, and 10.2 mg/g for Ni2+ in the sulfonated trityl-bearing polymer 5a while those found for the sulfonated triphenyl-bearing polymer 5b were 31.5 mg/g for Pb2+, 26.6 mg/g for Cd2+, and 7.0 mg/g for Ni2+, respectively.	Nickel(2+)	103-107	CD2 molecule	Homo sapiens	257-260
33983566-1	2021	Fluorescence probes that selectively image cadmium are useful for detecting and tracking the amount of Cd2+ in cells and tissues.	Cadmium	43-50	CD2 molecule	Homo sapiens	103-106
33983566-2	2021	In this study, we designed and synthesized a novel Cd2+ fluorescence probe based on the pyridine-pyrimidine structure, 4-(methylsulfanyl)-6-(pyridin-2-yl)pyrimidin-2-amine (3), as a low-molecular-weight fluorescence probe for Cd2+.	pyridine-pyrimidine	88-107	CD2 molecule	Homo sapiens	51-54
33983566-2	2021	In this study, we designed and synthesized a novel Cd2+ fluorescence probe based on the pyridine-pyrimidine structure, 4-(methylsulfanyl)-6-(pyridin-2-yl)pyrimidin-2-amine (3), as a low-molecular-weight fluorescence probe for Cd2+.	pyridine-pyrimidine	88-107	CD2 molecule	Homo sapiens	226-229
33983566-2	2021	In this study, we designed and synthesized a novel Cd2+ fluorescence probe based on the pyridine-pyrimidine structure, 4-(methylsulfanyl)-6-(pyridin-2-yl)pyrimidin-2-amine (3), as a low-molecular-weight fluorescence probe for Cd2+.	SCHEMBL7142629	119-171	CD2 molecule	Homo sapiens	51-54
33983566-2	2021	In this study, we designed and synthesized a novel Cd2+ fluorescence probe based on the pyridine-pyrimidine structure, 4-(methylsulfanyl)-6-(pyridin-2-yl)pyrimidin-2-amine (3), as a low-molecular-weight fluorescence probe for Cd2+.	SCHEMBL7142629	119-171	CD2 molecule	Homo sapiens	226-229
33686735-5	2021	We further perform pseudomorphic cation exchanges of Cu1.94S tetradecahedra with Zn2+ and Cd2+ to produce polyhedral zinc sulfide (ZnS) and cadmium sulfide (CdS) NPs.	zinc sulfide	117-129	CD2 molecule	Homo sapiens	90-93
33686735-5	2021	We further perform pseudomorphic cation exchanges of Cu1.94S tetradecahedra with Zn2+ and Cd2+ to produce polyhedral zinc sulfide (ZnS) and cadmium sulfide (CdS) NPs.	zinc sulfide	131-134	CD2 molecule	Homo sapiens	90-93
33686735-5	2021	We further perform pseudomorphic cation exchanges of Cu1.94S tetradecahedra with Zn2+ and Cd2+ to produce polyhedral zinc sulfide (ZnS) and cadmium sulfide (CdS) NPs.	cadmium sulfide	140-155	CD2 molecule	Homo sapiens	90-93
33581577-3	2021	Here the solvothermal self-assembly between Cd2+ and a hexacarboxylic acid creates such a porous material [(CH3)2NH2]6[Cd3(L)2] 5DMF 3H2O (H6L = 3,4-di(3,5-dicarboxyphenyl)phthalic acid) 1.	3,4-di(3,5-dicarboxyphenyl)phthalic acid	145-185	CD2 molecule	Homo sapiens	44-47
33581577-3	2021	Here the solvothermal self-assembly between Cd2+ and a hexacarboxylic acid creates such a porous material [(CH3)2NH2]6[Cd3(L)2] 5DMF 3H2O (H6L = 3,4-di(3,5-dicarboxyphenyl)phthalic acid) 1.	hexacarboxylic acid	55-74	CD2 molecule	Homo sapiens	44-47
33581577-3	2021	Here the solvothermal self-assembly between Cd2+ and a hexacarboxylic acid creates such a porous material [(CH3)2NH2]6[Cd3(L)2] 5DMF 3H2O (H6L = 3,4-di(3,5-dicarboxyphenyl)phthalic acid) 1.	[(ch3)2nh2]6[cd3(l)2] 5dmf 3h2o	106-137	CD2 molecule	Homo sapiens	44-47
33581577-3	2021	Here the solvothermal self-assembly between Cd2+ and a hexacarboxylic acid creates such a porous material [(CH3)2NH2]6[Cd3(L)2] 5DMF 3H2O (H6L = 3,4-di(3,5-dicarboxyphenyl)phthalic acid) 1.	H6L	139-142	CD2 molecule	Homo sapiens	44-47
33975099-4	2021	High-dose of ZnO or ZIF-8 NPs co-exposure with Cd2+ would reduce the cell viability while low-dose of ZnO or ZIF-8 NPs co-exposure with Cd2+showed antagonism and the particle size has no remarkable effect on the combined toxicity.	Zinc Oxide	13-16	CD2 molecule	Homo sapiens	47-50
32212074-0	2021	Zn2+ and Cd2+ removal from wastewater using clinoptilolite as adsorbent.	clinoptilolite	44-58	CD2 molecule	Homo sapiens	9-12
32212074-9	2021	In particular, clinoptilolite permitted high Cd2+ abatement, probably due to its greater affinity with adsorbent in the single system.	clinoptilolite	15-29	CD2 molecule	Homo sapiens	45-48
33975099-4	2021	High-dose of ZnO or ZIF-8 NPs co-exposure with Cd2+ would reduce the cell viability while low-dose of ZnO or ZIF-8 NPs co-exposure with Cd2+showed antagonism and the particle size has no remarkable effect on the combined toxicity.	Zinc Oxide	13-16	CD2 molecule	Homo sapiens	136-139
33975099-4	2021	High-dose of ZnO or ZIF-8 NPs co-exposure with Cd2+ would reduce the cell viability while low-dose of ZnO or ZIF-8 NPs co-exposure with Cd2+showed antagonism and the particle size has no remarkable effect on the combined toxicity.	Zinc Oxide	102-105	CD2 molecule	Homo sapiens	136-139
33884551-4	2021	It was found heavy metals like Cd2+ and Pb2+ will inhibit the degradation of alpha-cypermethrin, especially at high concentrations.	cypermethrin	77-95	CD2 molecule	Homo sapiens	31-34
33876935-3	2021	Herein, we carefully control the kinetics of reverse cation exchange between CuxS 2D nanosheets and ligand-coordinated Cd2+ cations to control the Cu doping sites in CdS nanosheets (NSs).	Cadmium	166-169	CD2 molecule	Homo sapiens	119-122
33922514-1	2021	Analytical performance and efficiency are two pivotal issues for developing an on-site and real-time aptasensor for cadmium (Cd2+) determination.	Cadmium	116-123	CD2 molecule	Homo sapiens	125-128
33922514-3	2021	In this work, we found that fluorescence intensity of 6-carboxyfluorescein(FAM)-labeled aptamer (FAM-aptamer) could be remarkably amplified by 3-(N-morpholino)propane sulfonic acid (MOPS), then fell proportionally as Cd2+ concentration introduced.	6-carboxyfluorescein	54-74	CD2 molecule	Homo sapiens	217-220
33922514-3	2021	In this work, we found that fluorescence intensity of 6-carboxyfluorescein(FAM)-labeled aptamer (FAM-aptamer) could be remarkably amplified by 3-(N-morpholino)propane sulfonic acid (MOPS), then fell proportionally as Cd2+ concentration introduced.	morpholinopropane sulfonic acid	143-180	CD2 molecule	Homo sapiens	217-220
33922514-3	2021	In this work, we found that fluorescence intensity of 6-carboxyfluorescein(FAM)-labeled aptamer (FAM-aptamer) could be remarkably amplified by 3-(N-morpholino)propane sulfonic acid (MOPS), then fell proportionally as Cd2+ concentration introduced.	morpholinopropane sulfonic acid	182-186	CD2 molecule	Homo sapiens	217-220
33884551-0	2021	Effects of Cd2+ and Pb2+ on enantioselective degradation behavior of alpha-cypermethrin in soils and their combined effect on activities of soil enzymes.	cypermethrin	69-87	CD2 molecule	Homo sapiens	11-14
33884551-3	2021	In this study, the influence of Cd2+ and Pb2+ on the degradation of alpha-cypermethrin and its metabolites, 3-phenoxphenoxybenzoic acid (3-PBA) and 3-(2",2"-dichlorovinyl)-2,2-dimethylcyclopropane carboxylic acid (DCCA), were investigated through soil incubation experiment.	cypermethrin	68-86	CD2 molecule	Homo sapiens	32-35
33880707-0	2021	The C2-Symmetry Colorimetric Dye Based on a Thiosemicarbazone Derivative and its Cadmium Complex for Detecting Heavy Metal Cations (Ni2+, Co2+, Cd2+, and Cu2+) Collectively, in DMF.	Thiosemicarbazones	44-61	CD2 molecule	Homo sapiens	144-147
33884551-3	2021	In this study, the influence of Cd2+ and Pb2+ on the degradation of alpha-cypermethrin and its metabolites, 3-phenoxphenoxybenzoic acid (3-PBA) and 3-(2",2"-dichlorovinyl)-2,2-dimethylcyclopropane carboxylic acid (DCCA), were investigated through soil incubation experiment.	3-pba	137-142	CD2 molecule	Homo sapiens	32-35
33884551-3	2021	In this study, the influence of Cd2+ and Pb2+ on the degradation of alpha-cypermethrin and its metabolites, 3-phenoxphenoxybenzoic acid (3-PBA) and 3-(2",2"-dichlorovinyl)-2,2-dimethylcyclopropane carboxylic acid (DCCA), were investigated through soil incubation experiment.	3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane carboxylic acid	148-212	CD2 molecule	Homo sapiens	32-35
33884551-3	2021	In this study, the influence of Cd2+ and Pb2+ on the degradation of alpha-cypermethrin and its metabolites, 3-phenoxphenoxybenzoic acid (3-PBA) and 3-(2",2"-dichlorovinyl)-2,2-dimethylcyclopropane carboxylic acid (DCCA), were investigated through soil incubation experiment.	3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane carboxylic acid	214-218	CD2 molecule	Homo sapiens	32-35
33880707-0	2021	The C2-Symmetry Colorimetric Dye Based on a Thiosemicarbazone Derivative and its Cadmium Complex for Detecting Heavy Metal Cations (Ni2+, Co2+, Cd2+, and Cu2+) Collectively, in DMF.	Cadmium	81-88	CD2 molecule	Homo sapiens	144-147
33880707-0	2021	The C2-Symmetry Colorimetric Dye Based on a Thiosemicarbazone Derivative and its Cadmium Complex for Detecting Heavy Metal Cations (Ni2+, Co2+, Cd2+, and Cu2+) Collectively, in DMF.	Metals	117-122	CD2 molecule	Homo sapiens	144-147
33880707-0	2021	The C2-Symmetry Colorimetric Dye Based on a Thiosemicarbazone Derivative and its Cadmium Complex for Detecting Heavy Metal Cations (Ni2+, Co2+, Cd2+, and Cu2+) Collectively, in DMF.	Dimethylformamide	177-180	CD2 molecule	Homo sapiens	144-147
33880707-5	2021	Explicitly, the two probes (H and P) were able to collectively discriminate heavy metal cations such as Cd2+, Co2+, Zn2+, Cu2+, Ni2+, and Ag+, both in DMF, among all other heavy metal cations tested.	Phosphorus	34-35	CD2 molecule	Homo sapiens	104-107
33880707-5	2021	Explicitly, the two probes (H and P) were able to collectively discriminate heavy metal cations such as Cd2+, Co2+, Zn2+, Cu2+, Ni2+, and Ag+, both in DMF, among all other heavy metal cations tested.	Metals	82-87	CD2 molecule	Homo sapiens	104-107
33880707-5	2021	Explicitly, the two probes (H and P) were able to collectively discriminate heavy metal cations such as Cd2+, Co2+, Zn2+, Cu2+, Ni2+, and Ag+, both in DMF, among all other heavy metal cations tested.	Dimethylformamide	151-154	CD2 molecule	Homo sapiens	104-107
33880707-5	2021	Explicitly, the two probes (H and P) were able to collectively discriminate heavy metal cations such as Cd2+, Co2+, Zn2+, Cu2+, Ni2+, and Ag+, both in DMF, among all other heavy metal cations tested.	Metals	178-183	CD2 molecule	Homo sapiens	104-107
33924306-3	2021	It has been reported that cadmium (Cd2+) increase the activities of OCTs while being a substrate of MATEs.	Cadmium	26-33	CD2 molecule	Homo sapiens	35-38
33872616-5	2021	We focused on the adsorption of Pb2+, Cu2+ and Cd2+ from acidic solutions onto cellulose-TiO2/REC composite nanofibrous mats in multiple systems because the magnitudes of heavy metal concentrations in wastewater typically varied.	titanium dioxide	89-93	CD2 molecule	Homo sapiens	47-50
33872616-5	2021	We focused on the adsorption of Pb2+, Cu2+ and Cd2+ from acidic solutions onto cellulose-TiO2/REC composite nanofibrous mats in multiple systems because the magnitudes of heavy metal concentrations in wastewater typically varied.	rectorite	94-97	CD2 molecule	Homo sapiens	47-50
34056232-6	2021	Colorimetric data showed linearity of response in a physiologically relevant range (0-20 muM Cu2+) with high selectivity for Cu2+ ions over biologically and environmentally relevant metals such as Na+, K+, Mn2+, Ca2+, Zn2+, Co2+, Mg2+, Ni2+, Fe3+, Cd2+, and Pb2+.	cupric ion	125-129	CD2 molecule	Homo sapiens	248-251
33924306-3	2021	It has been reported that cadmium (Cd2+) increase the activities of OCTs while being a substrate of MATEs.	octs	68-72	CD2 molecule	Homo sapiens	35-38
33872870-1	2021	This work presents an electrochemical device based on a composite modification of amine functionalized Zr(IV) metal-organic framework (UiO-66-NH2) and multi-walled carbon nanotubes (MWCNTs) for voltammetry determination of cadmium ions (Cd2+).	Amines	82-87	CD2 molecule	Homo sapiens	237-240
33872870-1	2021	This work presents an electrochemical device based on a composite modification of amine functionalized Zr(IV) metal-organic framework (UiO-66-NH2) and multi-walled carbon nanotubes (MWCNTs) for voltammetry determination of cadmium ions (Cd2+).	Cadmium	223-230	CD2 molecule	Homo sapiens	237-240
33500026-0	2021	Fabrication of NiS2 Nanomaterials for Cd2+ Sensing.	nis2	15-19	CD2 molecule	Homo sapiens	38-41
32241840-4	2021	We found that, in addition to CD56 expression (97%), BPDCN showed a number of aberrancies, including decreased/negative CD38 (82%), positive CD7 (64%), negative CD2 (81%), negative CD303 (56%), increased HLA-DR (69%) and decreased CD123 (78%).	bpdcn	53-58	CD2 molecule	Homo sapiens	161-164
33247401-2	2021	It was found that Cd2+ caused a significant decrease in ATZ degradation and increased its half-life from 17-34 days to 30-57 days (p < 0.0001).	Atrazine	56-59	CD2 molecule	Homo sapiens	18-21
33247401-5	2021	In the presence of Cd2+, the DIA content was significantly lower and the HYA content was significantly higher.	dia	29-32	CD2 molecule	Homo sapiens	19-22
33500026-2	2021	It has been designated as a first-class pollutant in sewage by China, therefore there is an urgent need to find new, more effective, and low-cost method to accurately detect Cadmium ion (Cd2+) concentration.	Cadmium	174-181	CD2 molecule	Homo sapiens	187-190
33500026-3	2021	We experimentally prepared a new Cd2+ sensor based on NiS2 nanomaterials capable of measuring Cd2+ concentration.	nis2	54-58	CD2 molecule	Homo sapiens	33-36
33500026-3	2021	We experimentally prepared a new Cd2+ sensor based on NiS2 nanomaterials capable of measuring Cd2+ concentration.	nis2	54-58	CD2 molecule	Homo sapiens	94-97
33500026-4	2021	The corresponding relationship between over potential of NiS2 nanomaterials in H2SO4 electrolyte solutions with different Cd2+ concentration and reduction peak with change of Cd2+ concentration was obtained by electrochemical method.	nis2	57-61	CD2 molecule	Homo sapiens	122-125
33500026-4	2021	The corresponding relationship between over potential of NiS2 nanomaterials in H2SO4 electrolyte solutions with different Cd2+ concentration and reduction peak with change of Cd2+ concentration was obtained by electrochemical method.	nis2	57-61	CD2 molecule	Homo sapiens	175-178
33500026-4	2021	The corresponding relationship between over potential of NiS2 nanomaterials in H2SO4 electrolyte solutions with different Cd2+ concentration and reduction peak with change of Cd2+ concentration was obtained by electrochemical method.	sulfuric acid	79-84	CD2 molecule	Homo sapiens	122-125
33500026-4	2021	The corresponding relationship between over potential of NiS2 nanomaterials in H2SO4 electrolyte solutions with different Cd2+ concentration and reduction peak with change of Cd2+ concentration was obtained by electrochemical method.	sulfuric acid	79-84	CD2 molecule	Homo sapiens	175-178
33905367-1	2021	In this experiment, three kinds of hydrous manganese dioxide (HMO) with different Zeta potentials were synthesized, and combined with KMnO4 for deep removal of Pb2+, Cd2+ and Ni2+.	hydrous manganese dioxide	35-60	CD2 molecule	Homo sapiens	166-169
33905367-1	2021	In this experiment, three kinds of hydrous manganese dioxide (HMO) with different Zeta potentials were synthesized, and combined with KMnO4 for deep removal of Pb2+, Cd2+ and Ni2+.	hmo	62-65	CD2 molecule	Homo sapiens	166-169
33905367-1	2021	In this experiment, three kinds of hydrous manganese dioxide (HMO) with different Zeta potentials were synthesized, and combined with KMnO4 for deep removal of Pb2+, Cd2+ and Ni2+.	Potassium Permanganate	134-139	CD2 molecule	Homo sapiens	166-169
33905367-4	2021	After regenerating HMO with acidic KMnO4 as eluent, the removal rates of Pb2+, Cd2+ and Ni2+ could still reach 79.25%, 80.13% and 60.43% after five cycles of adsorption.	hmo	19-22	CD2 molecule	Homo sapiens	79-82
33905367-4	2021	After regenerating HMO with acidic KMnO4 as eluent, the removal rates of Pb2+, Cd2+ and Ni2+ could still reach 79.25%, 80.13% and 60.43% after five cycles of adsorption.	Potassium Permanganate	35-40	CD2 molecule	Homo sapiens	79-82
33898275-0	2021	Carbohydrate biopolymers, lignin based adsorbents for removal of heavy metals (Cd2+, Pb2+, Zn2+) from wastewater, regeneration and reuse for spent adsorbents including latent fingerprint detection: A review.	carbohydrate biopolymers	0-24	CD2 molecule	Homo sapiens	79-82
33831704-8	2021	Chemical characterization and density functional theory (DFT) calculation reveal that the Cd2+ recognition sites of functional groups are C-S and C S. Cd2+ mass transport in IIM suggest that the imprint effects provide a binding force that would delay Cd2+ to permeate through IIM, so as to selectively separate Cd2+ with other ions.	Carbon	0-1	CD2 molecule	Homo sapiens	90-93
33831704-8	2021	Chemical characterization and density functional theory (DFT) calculation reveal that the Cd2+ recognition sites of functional groups are C-S and C S. Cd2+ mass transport in IIM suggest that the imprint effects provide a binding force that would delay Cd2+ to permeate through IIM, so as to selectively separate Cd2+ with other ions.	Carbon	0-1	CD2 molecule	Homo sapiens	151-154
33831704-8	2021	Chemical characterization and density functional theory (DFT) calculation reveal that the Cd2+ recognition sites of functional groups are C-S and C S. Cd2+ mass transport in IIM suggest that the imprint effects provide a binding force that would delay Cd2+ to permeate through IIM, so as to selectively separate Cd2+ with other ions.	Carbon	0-1	CD2 molecule	Homo sapiens	151-154
33831704-8	2021	Chemical characterization and density functional theory (DFT) calculation reveal that the Cd2+ recognition sites of functional groups are C-S and C S. Cd2+ mass transport in IIM suggest that the imprint effects provide a binding force that would delay Cd2+ to permeate through IIM, so as to selectively separate Cd2+ with other ions.	Carbon	0-1	CD2 molecule	Homo sapiens	151-154
33898275-0	2021	Carbohydrate biopolymers, lignin based adsorbents for removal of heavy metals (Cd2+, Pb2+, Zn2+) from wastewater, regeneration and reuse for spent adsorbents including latent fingerprint detection: A review.	Lignin	26-32	CD2 molecule	Homo sapiens	79-82
33898275-7	2021	These nanocomposites were used for the adsorption of highly toxic metals such as Cd2+, Pb2+ and Zn2+ in water.	Water	104-109	CD2 molecule	Homo sapiens	81-84
33898275-12	2021	Chitosan, carboxymethyl cellulose, alginate and lignin based nanocomposites have demonstrated better adsorption activities due to great physical and chemical properties for the chelation of heavy metals such as Cd2+, Pb2+ and Zn2+ from water and also higher regeneration with various eluents after several desorption-adsorption cycles.	Chitosan	0-8	CD2 molecule	Homo sapiens	211-214
33898275-12	2021	Chitosan, carboxymethyl cellulose, alginate and lignin based nanocomposites have demonstrated better adsorption activities due to great physical and chemical properties for the chelation of heavy metals such as Cd2+, Pb2+ and Zn2+ from water and also higher regeneration with various eluents after several desorption-adsorption cycles.	Carboxymethylcellulose Sodium	10-33	CD2 molecule	Homo sapiens	211-214
33898275-12	2021	Chitosan, carboxymethyl cellulose, alginate and lignin based nanocomposites have demonstrated better adsorption activities due to great physical and chemical properties for the chelation of heavy metals such as Cd2+, Pb2+ and Zn2+ from water and also higher regeneration with various eluents after several desorption-adsorption cycles.	Alginates	35-43	CD2 molecule	Homo sapiens	211-214
33898275-12	2021	Chitosan, carboxymethyl cellulose, alginate and lignin based nanocomposites have demonstrated better adsorption activities due to great physical and chemical properties for the chelation of heavy metals such as Cd2+, Pb2+ and Zn2+ from water and also higher regeneration with various eluents after several desorption-adsorption cycles.	Lignin	48-54	CD2 molecule	Homo sapiens	211-214
33898275-12	2021	Chitosan, carboxymethyl cellulose, alginate and lignin based nanocomposites have demonstrated better adsorption activities due to great physical and chemical properties for the chelation of heavy metals such as Cd2+, Pb2+ and Zn2+ from water and also higher regeneration with various eluents after several desorption-adsorption cycles.	Zinc	226-230	CD2 molecule	Homo sapiens	211-214
33898275-12	2021	Chitosan, carboxymethyl cellulose, alginate and lignin based nanocomposites have demonstrated better adsorption activities due to great physical and chemical properties for the chelation of heavy metals such as Cd2+, Pb2+ and Zn2+ from water and also higher regeneration with various eluents after several desorption-adsorption cycles.	Water	236-241	CD2 molecule	Homo sapiens	211-214
33183753-4	2021	Applying a voltage of 2 V in successive ionic layer adsorption reaction (VASILAR) to create an electric field, which assists Cd2+ and SeSO32- ions rapidly diffuse into the TiO2/ZnS mesoporous film to react forming CdSe QDs at room temperature.	titanium dioxide	172-176	CD2 molecule	Homo sapiens	125-128
33183753-4	2021	Applying a voltage of 2 V in successive ionic layer adsorption reaction (VASILAR) to create an electric field, which assists Cd2+ and SeSO32- ions rapidly diffuse into the TiO2/ZnS mesoporous film to react forming CdSe QDs at room temperature.	zns mesoporous	177-191	CD2 molecule	Homo sapiens	125-128
33183753-4	2021	Applying a voltage of 2 V in successive ionic layer adsorption reaction (VASILAR) to create an electric field, which assists Cd2+ and SeSO32- ions rapidly diffuse into the TiO2/ZnS mesoporous film to react forming CdSe QDs at room temperature.	cdse qds	214-222	CD2 molecule	Homo sapiens	125-128
33559717-1	2021	Pollution with the heavy metal cadmium (Cd2+) is a global problem.	Cadmium	31-38	CD2 molecule	Homo sapiens	40-43
33665691-6	2021	The results showed that sub-chronical Cd2+ exposure induced lower MT content and higher MDA level in the gills than in the acute exposure.	Malondialdehyde	88-91	CD2 molecule	Homo sapiens	38-41
33665691-7	2021	In the hepatopancreas, acute Cd2+ exposure decreased the pentose phosphate pathway activity and NADPH content; however, an increased G6PDH activity and NADPH content were detected in sub-chronic Cd2+ exposure (2.86 mg/L).	Pentosephosphates	57-74	CD2 molecule	Homo sapiens	29-32
33221003-10	2021	The TBBPA debromination rate by S-nZVI@alginate is initially enhanced followed by a decrease with an increase in TBBPA concentration, while it can increase 3.3-, 8.9- and 5.6-fold by increasing S-nZVI@alginate dosage, decreasing pH and adding co-contaminant Cd2+, respectively.	tetrabromobisphenol A	4-9	CD2 molecule	Homo sapiens	258-261
33221003-10	2021	The TBBPA debromination rate by S-nZVI@alginate is initially enhanced followed by a decrease with an increase in TBBPA concentration, while it can increase 3.3-, 8.9- and 5.6-fold by increasing S-nZVI@alginate dosage, decreasing pH and adding co-contaminant Cd2+, respectively.	Alginates	39-47	CD2 molecule	Homo sapiens	258-261
33221003-10	2021	The TBBPA debromination rate by S-nZVI@alginate is initially enhanced followed by a decrease with an increase in TBBPA concentration, while it can increase 3.3-, 8.9- and 5.6-fold by increasing S-nZVI@alginate dosage, decreasing pH and adding co-contaminant Cd2+, respectively.	tetrabromobisphenol A	113-118	CD2 molecule	Homo sapiens	258-261
33221003-10	2021	The TBBPA debromination rate by S-nZVI@alginate is initially enhanced followed by a decrease with an increase in TBBPA concentration, while it can increase 3.3-, 8.9- and 5.6-fold by increasing S-nZVI@alginate dosage, decreasing pH and adding co-contaminant Cd2+, respectively.	Alginates	201-209	CD2 molecule	Homo sapiens	258-261
33595278-3	2021	In this strategy, terminal deoxynucleotidyl transferase (TdT) and polynucleotide kinase (PNK), H2O2, and mucin 1 can be sensitively detected using Cu2+, Ag+, and Cd2+ as the signal probe, respectively.	cupric ion	147-151	CD2 molecule	Homo sapiens	162-165
33559717-3	2021	In this study, we used a novel biomaterial based on calcium-crosslinked alginate-encapsulated bacteria to precipitate Cd2+ in polluted water.	Calcium	52-59	CD2 molecule	Homo sapiens	118-121
33559717-3	2021	In this study, we used a novel biomaterial based on calcium-crosslinked alginate-encapsulated bacteria to precipitate Cd2+ in polluted water.	Alginates	72-80	CD2 molecule	Homo sapiens	118-121
33559717-3	2021	In this study, we used a novel biomaterial based on calcium-crosslinked alginate-encapsulated bacteria to precipitate Cd2+ in polluted water.	Water	135-140	CD2 molecule	Homo sapiens	118-121
33559717-4	2021	Our results show that calcium-crosslinked alginate-encapsulated bacteria effectively removed Cd2+ ions from cadmium-polluted water.	Calcium	22-29	CD2 molecule	Homo sapiens	93-96
33559717-4	2021	Our results show that calcium-crosslinked alginate-encapsulated bacteria effectively removed Cd2+ ions from cadmium-polluted water.	Alginates	42-50	CD2 molecule	Homo sapiens	93-96
33559717-4	2021	Our results show that calcium-crosslinked alginate-encapsulated bacteria effectively removed Cd2+ ions from cadmium-polluted water.	Cadmium	108-115	CD2 molecule	Homo sapiens	93-96
33559717-4	2021	Our results show that calcium-crosslinked alginate-encapsulated bacteria effectively removed Cd2+ ions from cadmium-polluted water.	Water	125-130	CD2 molecule	Homo sapiens	93-96
33559717-5	2021	Approximately 100% of Cd2+ ions were removed by 10 g (wet weight) of this biomaterial when the loading concentration of Cd2+ reached 1 mM in a volume of 50 ml water.	Water	159-164	CD2 molecule	Homo sapiens	22-25
33559717-5	2021	Approximately 100% of Cd2+ ions were removed by 10 g (wet weight) of this biomaterial when the loading concentration of Cd2+ reached 1 mM in a volume of 50 ml water.	Water	159-164	CD2 molecule	Homo sapiens	120-123
33559717-10	2021	Our results indicated that calcium-crosslinked alginate-encapsulated bacteria are suitable for depletion of Cd2+ in polluted water and for production of CdS nanoparticles.	Calcium	27-34	CD2 molecule	Homo sapiens	108-111
33564927-1	2021	A colorimetric paper-based enzyme-coupled antimony tin oxide nanoparticle (ATONP) nanobiosensor for selective detection of Cd2+ ions in clams and mussels is presented.	Antimony tin oxide	42-60	CD2 molecule	Homo sapiens	123-126
33559717-10	2021	Our results indicated that calcium-crosslinked alginate-encapsulated bacteria are suitable for depletion of Cd2+ in polluted water and for production of CdS nanoparticles.	Alginates	47-55	CD2 molecule	Homo sapiens	108-111
33559717-10	2021	Our results indicated that calcium-crosslinked alginate-encapsulated bacteria are suitable for depletion of Cd2+ in polluted water and for production of CdS nanoparticles.	Water	125-130	CD2 molecule	Homo sapiens	108-111
33559717-11	2021	These calcium-crosslinked alginate-encapsulated bacteria are safe for biological manipulation and can be widely used to produce CdS nanoparticles during bioremediation of Cd2+-polluted water.	Calcium	6-13	CD2 molecule	Homo sapiens	171-174
33559717-11	2021	These calcium-crosslinked alginate-encapsulated bacteria are safe for biological manipulation and can be widely used to produce CdS nanoparticles during bioremediation of Cd2+-polluted water.	Alginates	26-34	CD2 molecule	Homo sapiens	171-174
33559717-11	2021	These calcium-crosslinked alginate-encapsulated bacteria are safe for biological manipulation and can be widely used to produce CdS nanoparticles during bioremediation of Cd2+-polluted water.	Cadmium	128-131	CD2 molecule	Homo sapiens	171-174
33559717-11	2021	These calcium-crosslinked alginate-encapsulated bacteria are safe for biological manipulation and can be widely used to produce CdS nanoparticles during bioremediation of Cd2+-polluted water.	Water	185-190	CD2 molecule	Homo sapiens	171-174
33559717-12	2021	KEY POINTS:   Calcium-crosslinked alginate-encapsulated bacteria can effectively precipitate Cd2+ in water coupled with production of CdS quantum dots.	Calcium	14-21	CD2 molecule	Homo sapiens	93-96
33559717-12	2021	KEY POINTS:   Calcium-crosslinked alginate-encapsulated bacteria can effectively precipitate Cd2+ in water coupled with production of CdS quantum dots.	Alginates	34-42	CD2 molecule	Homo sapiens	93-96
33559717-12	2021	KEY POINTS:   Calcium-crosslinked alginate-encapsulated bacteria can effectively precipitate Cd2+ in water coupled with production of CdS quantum dots.	Water	101-106	CD2 molecule	Homo sapiens	93-96
33559717-12	2021	KEY POINTS:   Calcium-crosslinked alginate-encapsulated bacteria can effectively precipitate Cd2+ in water coupled with production of CdS quantum dots.	Cadmium	134-137	CD2 molecule	Homo sapiens	93-96
33316620-0	2021	Simultaneous adsorption of Cd2+ and photocatalytic degradation of tris-(2-chloroisopropyl) phosphate (TCPP) by mesoporous TiO2.	mesoporous tio2	111-126	CD2 molecule	Homo sapiens	27-30
33310517-2	2021	Sorption and incubation experiments were conducted to compare the effectiveness of dolomite phosphate rock (DPR), humic acid activated dolomite phosphate rock (ADPR) and biochar (BC) in immobilizing Cd2+ and Pb2+ in two representative agricultural soils in south Florida (Alfisol-Riviera and Spodosol -Ankona series).	Humic Substances	114-124	CD2 molecule	Homo sapiens	199-202
33316620-1	2021	In this work, the prepared mesoporous TiO2 was employed to eliminate the environmental risk induced by the combined pollution (tris-(2-chloroisopropyl) phosphate (TCPP) and Cd2+).	mesoporous tio2	27-42	CD2 molecule	Homo sapiens	173-176
33316620-3	2021	In the combined pollution system, the prepared TiO2 simultaneously exhibited a higher adsorption and photocatalytic activity for Cd2+ and TCPP at neutral condition, respectively.	titanium dioxide	47-51	CD2 molecule	Homo sapiens	129-132
33316620-4	2021	The adsorption of Cd2+ and photo-degradation of TCPP by mesoporous TiO2 followed pseudo-second-order and pseudo-first-order kinetics model, respectively.	tri-(2-chloroisopropyl)phosphate	48-52	CD2 molecule	Homo sapiens	18-21
33316620-4	2021	The adsorption of Cd2+ and photo-degradation of TCPP by mesoporous TiO2 followed pseudo-second-order and pseudo-first-order kinetics model, respectively.	mesoporous tio2	56-71	CD2 molecule	Homo sapiens	18-21
33316620-5	2021	The removal efficiency of TCPP was improved from 67% to 100% when the concentration of co-existed Cd2+ increased from 0.5 mg L-1 to 2 mg L-1, due to the fact that the adsorbed Cd2+ on the surface of TiO2 scavenged electron and thus inhibited the photo-generated electron-hole pairs recombination.	tri-(2-chloroisopropyl)phosphate	26-30	CD2 molecule	Homo sapiens	98-101
33316620-5	2021	The removal efficiency of TCPP was improved from 67% to 100% when the concentration of co-existed Cd2+ increased from 0.5 mg L-1 to 2 mg L-1, due to the fact that the adsorbed Cd2+ on the surface of TiO2 scavenged electron and thus inhibited the photo-generated electron-hole pairs recombination.	tri-(2-chloroisopropyl)phosphate	26-30	CD2 molecule	Homo sapiens	176-179
33316620-5	2021	The removal efficiency of TCPP was improved from 67% to 100% when the concentration of co-existed Cd2+ increased from 0.5 mg L-1 to 2 mg L-1, due to the fact that the adsorbed Cd2+ on the surface of TiO2 scavenged electron and thus inhibited the photo-generated electron-hole pairs recombination.	titanium dioxide	199-203	CD2 molecule	Homo sapiens	98-101
33316620-5	2021	The removal efficiency of TCPP was improved from 67% to 100% when the concentration of co-existed Cd2+ increased from 0.5 mg L-1 to 2 mg L-1, due to the fact that the adsorbed Cd2+ on the surface of TiO2 scavenged electron and thus inhibited the photo-generated electron-hole pairs recombination.	titanium dioxide	199-203	CD2 molecule	Homo sapiens	176-179
33316620-6	2021	In addition, six degradation intermediates were determined by high resolution mass spectrum (HRMS) and potential transformation pathways of TCPP under the co-existence of Cd2+ were proposed.	tri-(2-chloroisopropyl)phosphate	140-144	CD2 molecule	Homo sapiens	171-174
33218815-6	2021	It favors the transport of Cd2+ due to the electrostatic repulsion between positively charged iron oxide and Cd2+.	ferric oxide	94-104	CD2 molecule	Homo sapiens	27-30
33218815-8	2021	The increase in the concentration of Cd2+ favors the transport of SDZ in cleaned sand.	Sulfadiazine	66-69	CD2 molecule	Homo sapiens	37-40
33218815-9	2021	However, in iron oxide coated sand, the influence of Cd2+ on the transport of SDZ was dependent on the concentration of Cd2+.	ferric oxide	12-22	CD2 molecule	Homo sapiens	53-56
33218815-9	2021	However, in iron oxide coated sand, the influence of Cd2+ on the transport of SDZ was dependent on the concentration of Cd2+.	ferric oxide	12-22	CD2 molecule	Homo sapiens	120-123
33218815-9	2021	However, in iron oxide coated sand, the influence of Cd2+ on the transport of SDZ was dependent on the concentration of Cd2+.	Sulfadiazine	78-81	CD2 molecule	Homo sapiens	53-56
33218815-9	2021	However, in iron oxide coated sand, the influence of Cd2+ on the transport of SDZ was dependent on the concentration of Cd2+.	Sulfadiazine	78-81	CD2 molecule	Homo sapiens	120-123
33464824-5	2021	GA revealed excellent efficiency for removal of highly toxic metals, such as Cd2+ and Pb2+.	Gallium	0-2	CD2 molecule	Homo sapiens	77-80
33497206-0	2021	Hierarchical Construction and Magnetic Difference of {Co12M12} (M = Co2+/Cd2+) Aggregates from {Co14} Cluster-Based Precursors in the Presence of Homo/Heterometal Salts.	co12m12	54-61	CD2 molecule	Homo sapiens	73-76
33189980-2	2021	The sensing phenomenon with different metal ions (Cr3+, Mn2+, Fe2+, Fe3+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+) was investigated by employing absorption and fluorescence titrations, which demonstrated that probe 1 exhibited selective fluorescent sensing behavior towards Fe2+ ion among various other metal ions.	Metals	38-43	CD2 molecule	Homo sapiens	98-101
33189980-2	2021	The sensing phenomenon with different metal ions (Cr3+, Mn2+, Fe2+, Fe3+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+) was investigated by employing absorption and fluorescence titrations, which demonstrated that probe 1 exhibited selective fluorescent sensing behavior towards Fe2+ ion among various other metal ions.	ammonium ferrous sulfate	263-267	CD2 molecule	Homo sapiens	98-101
33189980-2	2021	The sensing phenomenon with different metal ions (Cr3+, Mn2+, Fe2+, Fe3+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+) was investigated by employing absorption and fluorescence titrations, which demonstrated that probe 1 exhibited selective fluorescent sensing behavior towards Fe2+ ion among various other metal ions.	Metals	292-297	CD2 molecule	Homo sapiens	98-101
33497206-0	2021	Hierarchical Construction and Magnetic Difference of {Co12M12} (M = Co2+/Cd2+) Aggregates from {Co14} Cluster-Based Precursors in the Presence of Homo/Heterometal Salts.	Carbon Dioxide	68-72	CD2 molecule	Homo sapiens	73-76
33497206-0	2021	Hierarchical Construction and Magnetic Difference of {Co12M12} (M = Co2+/Cd2+) Aggregates from {Co14} Cluster-Based Precursors in the Presence of Homo/Heterometal Salts.	co14	96-100	CD2 molecule	Homo sapiens	73-76
33497206-4	2021	Compared to the {Co14} precursor, magnetic difference revealed that spin-canting and magnetic ordering had been enhanced in {Co24} and suppressed in {Co12Cd12} when dotted with diamagnetic Cd2+ ions.	co14	17-21	CD2 molecule	Homo sapiens	189-192
33572333-0	2021	Tuned Cd2+ Selectivity: Showcase of Electronic and Regio-Effect of pi-Extended Di-2-Picolylamine-Substituted Quinoline-Based Tolans.	di-2-picolylamine	79-96	CD2 molecule	Homo sapiens	6-9
33572333-0	2021	Tuned Cd2+ Selectivity: Showcase of Electronic and Regio-Effect of pi-Extended Di-2-Picolylamine-Substituted Quinoline-Based Tolans.	quinoline	109-118	CD2 molecule	Homo sapiens	6-9
33572333-2	2021	The electron-poor CN-tolan (2b) showed clear selectivity for Cd2+ (>>Zn2+) over other metal ions via turn-on fluorescence, while the electron-rich MeO-tolan (2a) displayed no clear metal selectivity.	meo-tolan	147-156	CD2 molecule	Homo sapiens	61-64
33572333-6	2021	The fluorescence titration of 2b (10 mM) with Cd2+ showed that the limit of detection (LOD) of the Cd2+-selective 2b was 158 nM in PBS (phosphate-buffered saline) (10 mM, pH 7.2) containing 50% MeOH.	pbs	131-134	CD2 molecule	Homo sapiens	99-102
33572333-6	2021	The fluorescence titration of 2b (10 mM) with Cd2+ showed that the limit of detection (LOD) of the Cd2+-selective 2b was 158 nM in PBS (phosphate-buffered saline) (10 mM, pH 7.2) containing 50% MeOH.	Phosphate-Buffered Saline	136-161	CD2 molecule	Homo sapiens	46-49
33572333-6	2021	The fluorescence titration of 2b (10 mM) with Cd2+ showed that the limit of detection (LOD) of the Cd2+-selective 2b was 158 nM in PBS (phosphate-buffered saline) (10 mM, pH 7.2) containing 50% MeOH.	Phosphate-Buffered Saline	136-161	CD2 molecule	Homo sapiens	99-102
33572333-6	2021	The fluorescence titration of 2b (10 mM) with Cd2+ showed that the limit of detection (LOD) of the Cd2+-selective 2b was 158 nM in PBS (phosphate-buffered saline) (10 mM, pH 7.2) containing 50% MeOH.	Methanol	194-198	CD2 molecule	Homo sapiens	99-102
33562318-0	2021	New Insights into Cd2+/Fe3+ Co-Doped BiOBr for Enhancing the Photocatalysis Efficiency of Dye Decomposition under Visible-Light.	ferric sulfate	23-27	CD2 molecule	Homo sapiens	18-21
33443271-2	2021	It possesses no aggregation-induced emission (AIE) characteristics but can detect Cd2+ and Zn2+ ions selectively in the "off-on" mode based on the AIE of their complexes in the media of THF/HEPES and THF/H2O, respectively, which will provide a new strategy for target detection based on AIE.	tetrahydrofuran	186-189	CD2 molecule	Homo sapiens	82-85
33443271-2	2021	It possesses no aggregation-induced emission (AIE) characteristics but can detect Cd2+ and Zn2+ ions selectively in the "off-on" mode based on the AIE of their complexes in the media of THF/HEPES and THF/H2O, respectively, which will provide a new strategy for target detection based on AIE.	HEPES	190-195	CD2 molecule	Homo sapiens	82-85
33742882-7	2021	The Pb2+ and Cd2+ adsorbed by the biochar was stably bound in the form of heavy metal sulfide and a chelated amino group.	metal sulfide	80-93	CD2 molecule	Homo sapiens	13-16
33562318-0	2021	New Insights into Cd2+/Fe3+ Co-Doped BiOBr for Enhancing the Photocatalysis Efficiency of Dye Decomposition under Visible-Light.	bismuth oxybromide	37-42	CD2 molecule	Homo sapiens	18-21
33443271-2	2021	It possesses no aggregation-induced emission (AIE) characteristics but can detect Cd2+ and Zn2+ ions selectively in the "off-on" mode based on the AIE of their complexes in the media of THF/HEPES and THF/H2O, respectively, which will provide a new strategy for target detection based on AIE.	tetrahydrofuran	200-203	CD2 molecule	Homo sapiens	82-85
33443271-2	2021	It possesses no aggregation-induced emission (AIE) characteristics but can detect Cd2+ and Zn2+ ions selectively in the "off-on" mode based on the AIE of their complexes in the media of THF/HEPES and THF/H2O, respectively, which will provide a new strategy for target detection based on AIE.	Water	204-207	CD2 molecule	Homo sapiens	82-85
33562318-3	2021	Moreover, the novel Cd2+/Fe3+ co-doped BiOBr photocatalysts with ~0.42 eV impurity bands presented remarkably enhanced photocatalytic activities with being 3.10 times that of pure BiOBr, by achieving e-/h+ efficient separation and narrowed bandgap with the ions synergistic effect of Cd2+ and Fe3+.	ferric sulfate	25-29	CD2 molecule	Homo sapiens	20-23
33443271-7	2021	The chemosensor coordinates with the Cd2+ and Zn2+ ions in different formation and coordination modes, leading to the emission position of the aggregates at 560 and 645 nm, respectively, based on which Cd2+ ions were successfully differentiated from Zn2+ ions.	Zinc	46-50	CD2 molecule	Homo sapiens	202-205
33562318-3	2021	Moreover, the novel Cd2+/Fe3+ co-doped BiOBr photocatalysts with ~0.42 eV impurity bands presented remarkably enhanced photocatalytic activities with being 3.10 times that of pure BiOBr, by achieving e-/h+ efficient separation and narrowed bandgap with the ions synergistic effect of Cd2+ and Fe3+.	ferric sulfate	25-29	CD2 molecule	Homo sapiens	284-287
33443271-7	2021	The chemosensor coordinates with the Cd2+ and Zn2+ ions in different formation and coordination modes, leading to the emission position of the aggregates at 560 and 645 nm, respectively, based on which Cd2+ ions were successfully differentiated from Zn2+ ions.	Zinc	250-254	CD2 molecule	Homo sapiens	37-40
33443271-7	2021	The chemosensor coordinates with the Cd2+ and Zn2+ ions in different formation and coordination modes, leading to the emission position of the aggregates at 560 and 645 nm, respectively, based on which Cd2+ ions were successfully differentiated from Zn2+ ions.	Zinc	250-254	CD2 molecule	Homo sapiens	202-205
33562318-3	2021	Moreover, the novel Cd2+/Fe3+ co-doped BiOBr photocatalysts with ~0.42 eV impurity bands presented remarkably enhanced photocatalytic activities with being 3.10 times that of pure BiOBr, by achieving e-/h+ efficient separation and narrowed bandgap with the ions synergistic effect of Cd2+ and Fe3+.	ferric sulfate	293-297	CD2 molecule	Homo sapiens	20-23
33443271-8	2021	Moreover, the detection of Cd2+ and Zn2+ ions was realized qualitatively via test paper and quantitatively in water.	Water	110-115	CD2 molecule	Homo sapiens	27-30
33562318-3	2021	Moreover, the novel Cd2+/Fe3+ co-doped BiOBr photocatalysts with ~0.42 eV impurity bands presented remarkably enhanced photocatalytic activities with being 3.10 times that of pure BiOBr, by achieving e-/h+ efficient separation and narrowed bandgap with the ions synergistic effect of Cd2+ and Fe3+.	ferric sulfate	293-297	CD2 molecule	Homo sapiens	284-287
33562318-4	2021	Based on DFT insights, the photodegradation mechanism was systematically studied that the conversion of multivalent Fe3+ ions promoted the production of  O2-, and Cd2+ ions worked as electron transfer mediators, which elucidated that the  O2- and h+VB mainly participated in the catalytic reaction.	ferric sulfate	116-120	CD2 molecule	Homo sapiens	163-166
33080510-1	2021	The paper explains the relationship between the energy of hydrogen bonds and the distance between associated carboxyl groups of malonic acid (MA) molecules by means of infrared spectroscopic studies of crystals of its four isotopic varieties [CH2(COOH)2, h4-MA; CH2(COOD)2, d2c-MA; CD2(COOH)2, d2m-MA; CD2(COOD)2, d4-MA].	malonic acid	128-140	CD2 molecule	Homo sapiens	282-285
33080510-1	2021	The paper explains the relationship between the energy of hydrogen bonds and the distance between associated carboxyl groups of malonic acid (MA) molecules by means of infrared spectroscopic studies of crystals of its four isotopic varieties [CH2(COOH)2, h4-MA; CH2(COOD)2, d2c-MA; CD2(COOH)2, d2m-MA; CD2(COOD)2, d4-MA].	malonic acid	128-140	CD2 molecule	Homo sapiens	302-305
33285503-0	2021	Hydroxyapatite modified sludge-based biochar for the adsorption of Cu2+ and Cd2+: Adsorption behavior and mechanisms.	Durapatite	0-14	CD2 molecule	Homo sapiens	76-79
33690385-1	2021	A novel fiber-optic Mach-Zehnder interferometer based on SnO2, MoS2, SnO2/MoS2, and SnO2-MoS2 sensing film for cadmium-ion (Cd2+) detection is proposed and fabricated.	Cadmium	111-118	CD2 molecule	Homo sapiens	124-127
33285503-1	2021	This study prepared sewage sludge, a municipal solid waste, into a biochar modified by hydroxyapatite (HAP) as a new and efficient absorbent (HAP-SSBC) for removal of Cu2+ and Cd2+ from aqueous solution.	Durapatite	87-101	CD2 molecule	Homo sapiens	176-179
32822946-4	2021	By comparing the changes in physicochemical properties of anaerobic fermentative hydrochars (AFHCs), adsorption behaviors of Cadmium (Cd2+) on AFHCs were evaluated.	Cadmium	125-132	CD2 molecule	Homo sapiens	134-137
33387773-4	2021	As a result, the adsorption capacity of Cd2+ on MFB (17.4 mg g-1) was more than two times higher than that on FB (7.2 mg g-1), and the adsorption of Cd2+ on MFB was controlled by physisorption and chemisorption.	BETA-L-FUCOSE	48-51	CD2 molecule	Homo sapiens	40-43
33387773-4	2021	As a result, the adsorption capacity of Cd2+ on MFB (17.4 mg g-1) was more than two times higher than that on FB (7.2 mg g-1), and the adsorption of Cd2+ on MFB was controlled by physisorption and chemisorption.	BETA-L-FUCOSE	48-51	CD2 molecule	Homo sapiens	149-152
33387773-4	2021	As a result, the adsorption capacity of Cd2+ on MFB (17.4 mg g-1) was more than two times higher than that on FB (7.2 mg g-1), and the adsorption of Cd2+ on MFB was controlled by physisorption and chemisorption.	BETA-L-FUCOSE	157-160	CD2 molecule	Homo sapiens	40-43
33387773-4	2021	As a result, the adsorption capacity of Cd2+ on MFB (17.4 mg g-1) was more than two times higher than that on FB (7.2 mg g-1), and the adsorption of Cd2+ on MFB was controlled by physisorption and chemisorption.	BETA-L-FUCOSE	157-160	CD2 molecule	Homo sapiens	149-152
33210665-2	2021	In this paper, a novel flexible, disposable sensor for Cd2+ and Pb2+ with ultrahigh sensitivity and a fast response, based on acid-etched Fe/Fe2O3 encapsulated into a disposable carbon cloth electrode, has been successfully fabricated.	Carbon	178-184	CD2 molecule	Homo sapiens	55-58
33210665-3	2021	Differential pulse anode stripping voltammetry (DPASV) was used to investigate the stripping behavior of Cd2+ and Pb2+, achieving high sensitivity for Cd2+ and Pb2+ (338.7 and 408.0 muA mM-1 cm-2) with limits of detection (LODs) of 0.42 ppb and 0.50 ppb, respectively.	Lead(2+)	114-118	CD2 molecule	Homo sapiens	151-154
33210665-3	2021	Differential pulse anode stripping voltammetry (DPASV) was used to investigate the stripping behavior of Cd2+ and Pb2+, achieving high sensitivity for Cd2+ and Pb2+ (338.7 and 408.0 muA mM-1 cm-2) with limits of detection (LODs) of 0.42 ppb and 0.50 ppb, respectively.	Lead(2+)	160-164	CD2 molecule	Homo sapiens	105-108
33210665-5	2021	Such an electrode can detect Cd2+ and Pb2+ in actual water samples so this is a good candidate to act as a simple and convenient sensor for general applications.	Water	53-58	CD2 molecule	Homo sapiens	29-32
33406172-1	2021	Herein, combined with a pervasive smartphone installed with a color recognition app, dual-responsive CDs@Eu/GMP ICPs were designed as a red-to-blue paper-based colorimetric sensor for the point-of-use analysis of cerebral acetylcholinesterase (AChE) upon Cd2+ exposure.	Cadmium	101-104	CD2 molecule	Homo sapiens	255-258
33406172-5	2021	This obvious red-to-blue fluorescent color changes of CDs@Eu/GMP ICPs on test paper could then be integrated with the smartphone for point-of-use analysis of cerebral AChE upon Cd2+ exposure, which not only offers a new analytical platform for a better understanding of the environmental risk of Alzheimer"s Dementia (AD), but also holds great potential in the early diagnosis of AD even at the asymptomatic stage with the decrease in CSF AChE as an early biomarker.	Cadmium	54-57	CD2 molecule	Homo sapiens	177-180
33498433-5	2021	In this work, the coordination capacity of harzianic acid was studied to evaluate the formation and stability of complexes formed with toxic heavy metals (i.e., Cd2+, Co2+, Ni2+, and Pb2+), which might have a crucial role in the tolerance of plants growing in metal-contaminated soils and in abiotic stress.	harzianic acid	43-57	CD2 molecule	Homo sapiens	161-164
32931970-1	2021	Cadmium (Cd2+), as the primary contaminant in Chinese soils, is dangerous to human health and ecological security.	Cadmium	0-7	CD2 molecule	Homo sapiens	9-12
33498039-6	2021	The maximum adsorption capacity of 2D alpha-MnO2 nanosheets reached 1.604 mmol g-1 (Pb2+) and 0.813 mmol g-1 (Cd2+), respectively and can maintain stable after five cycles.	2d alpha-mno2	35-48	CD2 molecule	Homo sapiens	110-113
33179667-6	2021	In addition, in the presence of other metal ions, such as Pb2+, Mn2+, Ni2+, Co2+, Cu2+, Zn2+, Na+, Ca2+, and Cd2+, at the same concentration, the current signal remained almost unchanged, manifesting high selectivity for Ag+.	Metals	38-43	CD2 molecule	Homo sapiens	109-112
33210665-0	2021	Acid-etched Fe/Fe2O3 nanoparticles encapsulated into carbon cloth as a novel voltammetric sensor for the simultaneous detection of Cd2+ and Pb2.	Iron	12-14	CD2 molecule	Homo sapiens	131-134
33210665-0	2021	Acid-etched Fe/Fe2O3 nanoparticles encapsulated into carbon cloth as a novel voltammetric sensor for the simultaneous detection of Cd2+ and Pb2.	Iron(III) oxide	15-20	CD2 molecule	Homo sapiens	131-134
33210665-0	2021	Acid-etched Fe/Fe2O3 nanoparticles encapsulated into carbon cloth as a novel voltammetric sensor for the simultaneous detection of Cd2+ and Pb2.	Carbon	53-59	CD2 molecule	Homo sapiens	131-134
33210665-2	2021	In this paper, a novel flexible, disposable sensor for Cd2+ and Pb2+ with ultrahigh sensitivity and a fast response, based on acid-etched Fe/Fe2O3 encapsulated into a disposable carbon cloth electrode, has been successfully fabricated.	Iron	138-140	CD2 molecule	Homo sapiens	55-58
33210665-2	2021	In this paper, a novel flexible, disposable sensor for Cd2+ and Pb2+ with ultrahigh sensitivity and a fast response, based on acid-etched Fe/Fe2O3 encapsulated into a disposable carbon cloth electrode, has been successfully fabricated.	Iron(III) oxide	141-146	CD2 molecule	Homo sapiens	55-58
33297055-1	2021	Zinc (Zn2+) and cadmium (Cd2+) in water pose serious threats to human health and the environment.	Cadmium	16-23	CD2 molecule	Homo sapiens	25-28
33297055-1	2021	Zinc (Zn2+) and cadmium (Cd2+) in water pose serious threats to human health and the environment.	Water	34-39	CD2 molecule	Homo sapiens	25-28
33297055-2	2021	In search for a more effective treatment technology, we prepared a type of carboxymethyl cellulose (CMC) bridged chlorapatite (CMC-CAP) nanoparticles and tested the material for removal of Zn2+ and Cd2+ from water.	Carboxymethylcellulose Sodium	75-98	CD2 molecule	Homo sapiens	198-201
33297055-2	2021	In search for a more effective treatment technology, we prepared a type of carboxymethyl cellulose (CMC) bridged chlorapatite (CMC-CAP) nanoparticles and tested the material for removal of Zn2+ and Cd2+ from water.	Carboxymethylcellulose Sodium	100-103	CD2 molecule	Homo sapiens	198-201
33297055-4	2021	CMC-CAP showed rapid adsorption kinetics and 22.8% and 11.2% higher equilibrium uptake for Zn2+ and Cd2+, respectively, than pristine CAP.	Carboxymethylcellulose Sodium	0-3	CD2 molecule	Homo sapiens	100-103
33297055-5	2021	An extended dual-mode isotherm model, which takes into account both sorption and chemical precipitation, provided the best fits to the sorption isotherms, giving a maximum Langmuir sorption capacity of 141.1 mg g-1 for Zn2+ and 150.2 mg g-1 for Cd2+ by CMC-CAP.	Zinc	219-223	CD2 molecule	Homo sapiens	245-248
33297063-7	2021	The combination of operating variables (BRT- 3 min, CD- 2.14 Adm-2SC- 3 gL-1and SOT- 1.9 min) giving minimum operating cost (0.65 US$/kg COD removed) achieving oil removal (88%) meeting discharge standards was found out by optimizing the RSM models for cost and oil removal.	Oils	160-163	CD2 molecule	Homo sapiens	52-57
32822946-8	2021	WHCs treated with AF own higher adsorption capacity of Cd2+, which was attributed to the higher negative charge, more exchangeable cations, and more oxygen-containing functional groups.	Oxygen	149-155	CD2 molecule	Homo sapiens	55-58
33188635-7	2021	The fluorescence of HL2 with other metal ions (Fe3+, Mg2+, Na+, Cd2+, Cu2+, Co2+, Ni2+, Ca2+, and K+) was also investigated.	Metals	35-40	CD2 molecule	Homo sapiens	64-67
33504700-4	2021	As a consequence, an excellent performance on removal of Cd2+, Zn2+ and Cu2+ ions was found for this solid.	cupric ion	72-76	CD2 molecule	Homo sapiens	57-60
33221600-2	2021	In this paper, we report the preparation of two blue light-emitting silver-doped CDs, CD-1 and CD-2, through one- and two-step routes, respectively, by using polyethyleneimine, citric acid, and AgNO3 as raw materials.	silver-doped	68-80	CD2 molecule	Homo sapiens	95-99
33221600-2	2021	In this paper, we report the preparation of two blue light-emitting silver-doped CDs, CD-1 and CD-2, through one- and two-step routes, respectively, by using polyethyleneimine, citric acid, and AgNO3 as raw materials.	cds	81-84	CD2 molecule	Homo sapiens	95-99
33221600-2	2021	In this paper, we report the preparation of two blue light-emitting silver-doped CDs, CD-1 and CD-2, through one- and two-step routes, respectively, by using polyethyleneimine, citric acid, and AgNO3 as raw materials.	aziridine	158-175	CD2 molecule	Homo sapiens	95-99
33221600-2	2021	In this paper, we report the preparation of two blue light-emitting silver-doped CDs, CD-1 and CD-2, through one- and two-step routes, respectively, by using polyethyleneimine, citric acid, and AgNO3 as raw materials.	Silver Nitrate	194-199	CD2 molecule	Homo sapiens	95-99
33221600-5	2021	CD-2 exhibiting longer emission wavelength, larger particle size, and higher silver content displayed higher antibacterial activity against microorganisms than CD-1.	Silver	77-83	CD2 molecule	Homo sapiens	0-4
33504707-0	2021	Selective adsorption behavior of Cd2+ imprinted acrylamide-crosslinked-poly(alginic acid) magnetic polymers: fabrication, characterization, adsorption performance and mechanism.	poly(alginic acid) magnetic polymers	71-107	CD2 molecule	Homo sapiens	33-36
33063809-2	2020	Utilization of methoxy-substituted quinoline and isoquinoline chromophores, conformational restriction and multidentate coordination structure allow discrimination between Zn2+ and Cd2+.	methoxy-substituted quinoline	15-44	CD2 molecule	Homo sapiens	181-184
33504707-1	2021	Poly(acrylamide) grafted and glutaraldehyde-crosslinked alginic acid nano-magnetic adsorbent (AAMA) was prepared by selecting Cd2+ as a template ion.	polyacrylamide	0-15	CD2 molecule	Homo sapiens	126-129
33504707-1	2021	Poly(acrylamide) grafted and glutaraldehyde-crosslinked alginic acid nano-magnetic adsorbent (AAMA) was prepared by selecting Cd2+ as a template ion.	Glutaral	29-43	CD2 molecule	Homo sapiens	126-129
33504707-1	2021	Poly(acrylamide) grafted and glutaraldehyde-crosslinked alginic acid nano-magnetic adsorbent (AAMA) was prepared by selecting Cd2+ as a template ion.	Alginic Acid	56-68	CD2 molecule	Homo sapiens	126-129
33504707-4	2021	These results suggested that the AAMA was the aggregates of Fe3O4 nanoparticles with a diameter of about 50-100 nm and had selectivity for Cd2+ adsorption.	aama	33-37	CD2 molecule	Homo sapiens	139-142
33504707-4	2021	These results suggested that the AAMA was the aggregates of Fe3O4 nanoparticles with a diameter of about 50-100 nm and had selectivity for Cd2+ adsorption.	ferryl iron	60-65	CD2 molecule	Homo sapiens	139-142
33504707-9	2021	Therefore, AAMA would be useful as a selective and high adsorption capacity nano-magnetic adsorbent in the removal of Cd2+ from wastewater.	aama	11-15	CD2 molecule	Homo sapiens	118-121
33384476-6	2020	When NCs are treated with Cs-carboxylates (including Cs-oleate), most of the Cd2+ ions are expelled from NCs upon aging, and the NCs phase evolves from cubic to orthorhombic and their emission color changes from blue to green.	cs-carboxylates	26-41	CD2 molecule	Homo sapiens	77-80
33384476-6	2020	When NCs are treated with Cs-carboxylates (including Cs-oleate), most of the Cd2+ ions are expelled from NCs upon aging, and the NCs phase evolves from cubic to orthorhombic and their emission color changes from blue to green.	cs-oleate	53-62	CD2 molecule	Homo sapiens	77-80
33063809-2	2020	Utilization of methoxy-substituted quinoline and isoquinoline chromophores, conformational restriction and multidentate coordination structure allow discrimination between Zn2+ and Cd2+.	isoquinoline	49-61	CD2 molecule	Homo sapiens	181-184
33384476-7	2020	Instead, when NCs are coated with ammonium bromides, the loss of Cd2+ ions is suppressed and the NCs tend to retain their blue emission (both in colloidal dispersions and in electroluminescent devices), as well as their cubic phase, over time.	ammonium bromide	34-51	CD2 molecule	Homo sapiens	65-68
33301596-3	2021	Especially, Tb-complex is a bifunctional sensor for acac and Cd2+ , through luminescence "turn on" and "turn off", respectively.	Terbium	12-14	CD2 molecule	Homo sapiens	61-64
33301596-0	2021	Luminescent Lanthanide Complex Sensor for Acac and Cd2.	Lanthanoid Series Elements	12-22	CD2 molecule	Homo sapiens	51-54
33196166-0	2020	Naked Eye Cd2+ Ion Detection and Reversible Iodine Uptake by a Three-Dimensional Pillared-Layered Zn-MOF.	zn-mof	98-104	CD2 molecule	Homo sapiens	10-13
33315892-4	2020	Indeed, treatment with 4-Aminopyridine (4-AP), a partial blocker of delayed rectifier and A-type K+ channels, at low doses induces a bursting profile in CSCs significantly different than that produced at high doses or when it is applied at low doses but with cadmium (Cd2+), a blocker of high voltage-activated (HVA) Ca2+ channels.	4-Aminopyridine	23-38	CD2 molecule	Homo sapiens	268-271
33315892-4	2020	Indeed, treatment with 4-Aminopyridine (4-AP), a partial blocker of delayed rectifier and A-type K+ channels, at low doses induces a bursting profile in CSCs significantly different than that produced at high doses or when it is applied at low doses but with cadmium (Cd2+), a blocker of high voltage-activated (HVA) Ca2+ channels.	4-Aminopyridine	40-44	CD2 molecule	Homo sapiens	268-271
33315892-7	2020	Model investigation reveals that 4-AP is potentiating HVA, inducing square-wave bursting at low doses and pseudo-plateau bursting at high doses, whereas Cd2+ is potentiating K(Ca), inducing pseudo-plateau bursting when applied in combination with low doses of 4-AP.	4-Aminopyridine	260-264	CD2 molecule	Homo sapiens	153-156
32574881-5	2020	Batch experiments showed that the ZnS-cells exhibited high adsorption efficiency for Pb2+and Cd2+, the removal rate of Pb2+ and Cd2+ by ZnS-cells was 140 % and 160 % higher than that of pure P. chrysosporium, respectively.	Lead(2+)	119-123	CD2 molecule	Homo sapiens	93-96
32585527-0	2020	A new alendronate doped HAP nanomaterial for Pb2+, Cu2+ and Cd2+ effect absorption.	Alendronate	6-17	CD2 molecule	Homo sapiens	60-63
33190490-8	2020	Cd2+ has the highest affinity for Delta231-ZntA, in contrast to ZntA, which has the highest affinity for Pb2+.	Lead(2+)	105-109	CD2 molecule	Homo sapiens	0-3
32585527-3	2020	When the doping amount of AL was 10 %, the maximum adsorption capacity of AL-HAP for Pb2+, Cd2+ and Cu2+ can reach 1431.8, 469 and 226.6 mg/g, respectively, which was much higher than that reported in other literature.	Alendronate	26-28	CD2 molecule	Homo sapiens	91-94
32585527-3	2020	When the doping amount of AL was 10 %, the maximum adsorption capacity of AL-HAP for Pb2+, Cd2+ and Cu2+ can reach 1431.8, 469 and 226.6 mg/g, respectively, which was much higher than that reported in other literature.	Alendronate	74-76	CD2 molecule	Homo sapiens	91-94
32717505-2	2020	The rate of complex formation depended on the ratio of Cd2+ ions to chlorophyll concentration in the solution.	Chlorophyll	68-79	CD2 molecule	Homo sapiens	55-58
32798528-6	2020	It is shown that during the initial stage (first 20 minutes for Cd2+ ions and 30 minutes for Pb2+ ions) the kinetics of the process of sorption of metal ions by suspended HA preparations is better described by pseudo-second order equation.	Metals	147-152	CD2 molecule	Homo sapiens	64-67
32798528-11	2020	It was found that the limiting specific sorption of Pb2+ ions is almost an order of magnitude higher than that of Cd2+ ions and amounts to 0.16-0.29 mmol/dm3 and 0.0078-0.034 mmol/dm3, respectively.	Lead(2+)	52-56	CD2 molecule	Homo sapiens	114-117
32798528-11	2020	It was found that the limiting specific sorption of Pb2+ ions is almost an order of magnitude higher than that of Cd2+ ions and amounts to 0.16-0.29 mmol/dm3 and 0.0078-0.034 mmol/dm3, respectively.	DM3	180-183	CD2 molecule	Homo sapiens	114-117
32748352-1	2020	In this paper, folic acid-coated graphene oxide nanocomposite (FA-GO) is used as an adsorbent for the treatment of heavy metals including cadmium (Cd2+) and copper (Cu2+) ions.	Folic Acid	15-25	CD2 molecule	Homo sapiens	147-150
32748352-1	2020	In this paper, folic acid-coated graphene oxide nanocomposite (FA-GO) is used as an adsorbent for the treatment of heavy metals including cadmium (Cd2+) and copper (Cu2+) ions.	graphene oxide	33-47	CD2 molecule	Homo sapiens	147-150
32748352-1	2020	In this paper, folic acid-coated graphene oxide nanocomposite (FA-GO) is used as an adsorbent for the treatment of heavy metals including cadmium (Cd2+) and copper (Cu2+) ions.	Cadmium	138-145	CD2 molecule	Homo sapiens	147-150
32748352-9	2020	Also, isotherm calculations express maximum computational adsorption capacities of 103.1 and 116.3 mg g-1 for Cd2+ and Cu2+ ions, correspondingly.	cupric ion	119-123	CD2 molecule	Homo sapiens	110-113
32748352-12	2020	Finally, thermodynamic studies show that the adsorption of Cu2+ and Cd2+ onto the FA-GO nanocomposite is an endothermic and spontaneous process.	graphene oxide	85-87	CD2 molecule	Homo sapiens	68-71
32763407-5	2020	Under competitive conditions (Cu2+, Ni2+, Fe2+ and Cd2+ ions), the change of pH value from 4 to 6 resulted in a remarkable quenching of Co2+ selectivity generated by the zeolite shift from the H-form to the Na-form.	cupric ion	30-34	CD2 molecule	Homo sapiens	51-54
33160013-4	2020	In this work, novel pyrene modified nanocrystalline cellulose (NP-1) was designed as a fluorescence sensor for selective determination of Cd2+ in food and soil samples.	pyrene	20-26	CD2 molecule	Homo sapiens	138-141
32763407-5	2020	Under competitive conditions (Cu2+, Ni2+, Fe2+ and Cd2+ ions), the change of pH value from 4 to 6 resulted in a remarkable quenching of Co2+ selectivity generated by the zeolite shift from the H-form to the Na-form.	Carbon Dioxide	136-140	CD2 molecule	Homo sapiens	51-54
33341791-9	2020	The selectivity of heavy metal ions resulted in the magnitude order of Pb2+ > Cu2+ > Cd2+ > Ni2+ > Co2+.	Metals	25-30	CD2 molecule	Homo sapiens	85-88
32808354-9	2020	Assessment of target cell death using the CD2-based FCC shows a significantly higher percent specific lysis of the target cells compared to the standard CRA and the FCC assay using CFSE and 7-AAD.	7-aminoactinomycin D	190-195	CD2 molecule	Homo sapiens	42-45
33262427-7	2020	Biological analysis indicates that microorganism activity of the manganese-oxidizing bacteria in the SLB provided an opportunity for delta-MnO2 formation, after which cadmium was removed by surface complexation with MnO2 (  MnOH0 + Cd2+       MnOCd+  +  H+).	Cadmium	167-174	CD2 molecule	Homo sapiens	232-235
33324835-1	2020	We prepared the monomer PCDA-HP composed of 5-hydroxy-N 1,N 3-bis(pyridin-2-ylmethyl)isophthalamide (HP) as a cadmium ion tweezer and then polymerized them to form a polydiacetylene (PDA)-based sensor (PDA-HP), which displayed selective and sensitive colorimetric and fluorometric change upon addition of a cadmium ion (Cd2+) at both pH 7.4 and 6.8.	pcda-hp	24-31	CD2 molecule	Homo sapiens	320-323
33266040-1	2020	The current work demonstrates an electrochemical aptasensor for sensitive determination of Cd2+ based on the Ti-modified Co3O4 nanoparticles.	co3o4	121-126	CD2 molecule	Homo sapiens	91-94
33266040-3	2020	In addition, the sensing is based on the increase in electrochemical probe thionine current signal due to the binding of aptamer to Cd2+ via specific recognition.	thionine	75-83	CD2 molecule	Homo sapiens	132-135
33324835-1	2020	We prepared the monomer PCDA-HP composed of 5-hydroxy-N 1,N 3-bis(pyridin-2-ylmethyl)isophthalamide (HP) as a cadmium ion tweezer and then polymerized them to form a polydiacetylene (PDA)-based sensor (PDA-HP), which displayed selective and sensitive colorimetric and fluorometric change upon addition of a cadmium ion (Cd2+) at both pH 7.4 and 6.8.	Hematoporphyrins	29-31	CD2 molecule	Homo sapiens	320-323
33324835-2	2020	The PDA-HP polymer was highly selective for Cd2+ over other metal ions with colorimetric change.	Metals	60-65	CD2 molecule	Homo sapiens	44-47
33324835-4	2020	Naked-eye detection of Cd2+ was accomplished in an aqueous solution through a PDA-based sensor system.	polydiacetylene	78-81	CD2 molecule	Homo sapiens	23-26
33078952-4	2020	Moreover, the hydrogel has been used to remove toxic heavy metal ions Pb2+ and Cd2+ from wastewater.	Metals	59-64	CD2 molecule	Homo sapiens	79-82
33198230-3	2020	In the present work, a bismuth modified porous graphene (Bi@PG) electrode as an electrochemical sensor was adopted for the detection of heavy metal Cd2+ in an aqueous solution.	bismuth modified porous graphene	23-55	CD2 molecule	Homo sapiens	148-151
33198230-3	2020	In the present work, a bismuth modified porous graphene (Bi@PG) electrode as an electrochemical sensor was adopted for the detection of heavy metal Cd2+ in an aqueous solution.	Bismuth	57-60	CD2 molecule	Homo sapiens	148-151
33198230-3	2020	In the present work, a bismuth modified porous graphene (Bi@PG) electrode as an electrochemical sensor was adopted for the detection of heavy metal Cd2+ in an aqueous solution.	pg	60-62	CD2 molecule	Homo sapiens	148-151
33198230-7	2020	Meanwhile, the Bi@PG electrode showed tremendous potential in composite detection of multifold heavy metals (such as Pb2+ and Cd2+) and wider linear range.	Bismuth	15-17	CD2 molecule	Homo sapiens	126-129
33198230-7	2020	Meanwhile, the Bi@PG electrode showed tremendous potential in composite detection of multifold heavy metals (such as Pb2+ and Cd2+) and wider linear range.	pg	18-20	CD2 molecule	Homo sapiens	126-129
32721736-4	2020	The removal efficiency of Pb2+/Cd2+ by SA/S2- gel were both increased compared with pure SA gel.	Lead(2+)	26-30	CD2 molecule	Homo sapiens	31-34
32721736-4	2020	The removal efficiency of Pb2+/Cd2+ by SA/S2- gel were both increased compared with pure SA gel.	Alginates	39-41	CD2 molecule	Homo sapiens	31-34
32721736-4	2020	The removal efficiency of Pb2+/Cd2+ by SA/S2- gel were both increased compared with pure SA gel.	Alginates	89-91	CD2 molecule	Homo sapiens	31-34
32721736-5	2020	The adsorbed Pb2+/Cd2+ was in-situ transformed into PbS/CdS quantum dots (QDs) possessing photo-catalytic activity, which induced the degradation of dyes under UV irradiation.	Lead(2+)	13-17	CD2 molecule	Homo sapiens	18-21
32721736-5	2020	The adsorbed Pb2+/Cd2+ was in-situ transformed into PbS/CdS quantum dots (QDs) possessing photo-catalytic activity, which induced the degradation of dyes under UV irradiation.	Lead	52-55	CD2 molecule	Homo sapiens	18-21
32721736-5	2020	The adsorbed Pb2+/Cd2+ was in-situ transformed into PbS/CdS quantum dots (QDs) possessing photo-catalytic activity, which induced the degradation of dyes under UV irradiation.	Cadmium	56-59	CD2 molecule	Homo sapiens	18-21
33025958-0	2020	Cucurbiturils regulating Fe3O4-Au nanoparticles as a multi-functional platform for Cd2+ sensing and nitrocompound catalysis.	fe3o4-au	25-33	CD2 molecule	Homo sapiens	83-86
33025958-1	2020	Herein, through the interfacial regulation of cucurbiturils (CBs) on Fe3O4-Au nanoparticles, a novel multifunctional platform is constructed for the sensitive detection of Cd2+ and the selective catalytic reduction (SCR) of nitrocompounds.	cucurbit(n)uril	46-59	CD2 molecule	Homo sapiens	172-175
33025958-1	2020	Herein, through the interfacial regulation of cucurbiturils (CBs) on Fe3O4-Au nanoparticles, a novel multifunctional platform is constructed for the sensitive detection of Cd2+ and the selective catalytic reduction (SCR) of nitrocompounds.	fe3o4-au	69-77	CD2 molecule	Homo sapiens	172-175
33312651-4	2020	Highly purified chitosan prepared from HCl treated chitin only showed effective for Pb2+, however, those prepared from CH3COOH treated chitin showed effective for Pb2+, Cd2+ and Cu2+ adsorption due to a little amount of CBC.	Acetic Acid	119-126	CD2 molecule	Homo sapiens	169-172
33312651-4	2020	Highly purified chitosan prepared from HCl treated chitin only showed effective for Pb2+, however, those prepared from CH3COOH treated chitin showed effective for Pb2+, Cd2+ and Cu2+ adsorption due to a little amount of CBC.	Chitin	135-141	CD2 molecule	Homo sapiens	169-172
33312651-7	2020	High Ca(OH)2-bearing chitosan prepared from HCl and H2SO4 treated chtin showed the optimum Cd2+ (978 mg/g) and Cu2+ (852 mg/g) adsorption at an initial pH value of 2.10.	ca(oh)	5-11	CD2 molecule	Homo sapiens	91-94
33312651-7	2020	High Ca(OH)2-bearing chitosan prepared from HCl and H2SO4 treated chtin showed the optimum Cd2+ (978 mg/g) and Cu2+ (852 mg/g) adsorption at an initial pH value of 2.10.	Hydrochloric Acid	44-47	CD2 molecule	Homo sapiens	91-94
33312651-7	2020	High Ca(OH)2-bearing chitosan prepared from HCl and H2SO4 treated chtin showed the optimum Cd2+ (978 mg/g) and Cu2+ (852 mg/g) adsorption at an initial pH value of 2.10.	sulfuric acid	52-57	CD2 molecule	Homo sapiens	91-94
33294387-1	2020	Cadmium (Cd2+) is considered a human carcinogen as it causes oxidative stress and alters DNA repair responses.	Cadmium	0-7	CD2 molecule	Homo sapiens	9-12
33294387-3	2020	We hypothesized that Cd2+ could be transported into cells via a membrane copper (Cu) transporter, CTR1.	Copper	73-79	CD2 molecule	Homo sapiens	21-24
33294387-3	2020	We hypothesized that Cd2+ could be transported into cells via a membrane copper (Cu) transporter, CTR1.	Copper	81-83	CD2 molecule	Homo sapiens	21-24
33078952-0	2020	Peptide-Based Gel in Environmental Remediation: Removal of Toxic Organic Dyes and Hazardous Pb2+ and Cd2+ Ions from Wastewater and Oil Spill Recovery.	Peptides	0-7	CD2 molecule	Homo sapiens	101-104
31813121-9	2020	The trioctahedral smectite (saponite) showed a good efficiency for the adsorption of Cd2+ from the real sample (up to 100%) which at least partly can be explained by cation exchange.	saponite	28-36	CD2 molecule	Homo sapiens	85-88
32659425-3	2020	Low concentrations of Cd2+ and montmorillonite or their combinations enhanced biofilm formation by increasing polysaccharides proportion in the biofilm matrix, and the maximum adsorption capacity of Cd2+ by biofilm was increased by 1.5 times.	Polysaccharides	110-125	CD2 molecule	Homo sapiens	22-25
32659425-3	2020	Low concentrations of Cd2+ and montmorillonite or their combinations enhanced biofilm formation by increasing polysaccharides proportion in the biofilm matrix, and the maximum adsorption capacity of Cd2+ by biofilm was increased by 1.5 times.	Polysaccharides	110-125	CD2 molecule	Homo sapiens	199-202
32763304-2	2020	In short, biotinylated Cd2+ aptamers are immobilized by biotin-avidin binding on the bottoms of the microplate, the complementary strands of Cd2+ aptamers are connected to the Au-MoS2 nanocomposites which have the function of enhanced peroxidase-like activity.	Biotin	10-16	CD2 molecule	Homo sapiens	23-26
32763304-2	2020	In short, biotinylated Cd2+ aptamers are immobilized by biotin-avidin binding on the bottoms of the microplate, the complementary strands of Cd2+ aptamers are connected to the Au-MoS2 nanocomposites which have the function of enhanced peroxidase-like activity.	Biotin	10-16	CD2 molecule	Homo sapiens	141-144
32736182-0	2020	Enhanced Cd2+ and Zn2+ removal from heavy metal wastewater in constructed wetlands with resistant microorganisms.	Metals	42-47	CD2 molecule	Homo sapiens	9-12
32593826-2	2020	We found that PRGO contained a large amount of oxygen-containing groups (hydroxyl and carboxyl groups) and exhibited high Cd2+ adsorption efficiency at pH values above 4, achieving a maximum adsorption capacity of 434.78 mg/g for Cd.	prgo	14-18	CD2 molecule	Homo sapiens	122-125
32593826-4	2020	The electrokinetic remediation experiment showed that the PRGO auxiliary electrode promoted the migration of Cd and effectively controlled the increase in soil pH near the cathode, possibly due to ion exchange between the surface functional groups on the auxiliary electrode and Cd2+.	prgo	58-62	CD2 molecule	Homo sapiens	279-282
32593826-4	2020	The electrokinetic remediation experiment showed that the PRGO auxiliary electrode promoted the migration of Cd and effectively controlled the increase in soil pH near the cathode, possibly due to ion exchange between the surface functional groups on the auxiliary electrode and Cd2+.	Cadmium	109-111	CD2 molecule	Homo sapiens	279-282
32604509-2	2020	The synthesized flower-like, alpha-Fe2O3 were separated cadmium (Cd2+) chromium (Cr6+) and lead ions (Pb2+) from wastewater.	alpha-fe2o3	29-40	CD2 molecule	Homo sapiens	65-68
32798797-3	2020	In this study, the soil was collected from a mid-latitude agricultural site in Liaoning Province, China, which was spiked with cadmium (Cd2+) and lead (Pb2+).	Cadmium	127-134	CD2 molecule	Homo sapiens	136-139
32741761-0	2020	Promoting the decontamination of different types of water pollutants (Cd2+, safranin dye, and phosphate) using a novel structure of exfoliated bentonite admixed with cellulose nanofiber.	Bentonite	143-152	CD2 molecule	Homo sapiens	70-73
32741761-1	2020	Exfoliated bentonite sheets admixed with nano-cellulose fibers (EXB/CF) were prepared as advanced bio-composite of enhanced decontamination properties for different species of water pollutants (Cd2+, safranin dye, and phosphate).	Bentonite	11-20	CD2 molecule	Homo sapiens	194-197
32623678-4	2020	The sorption isotherms and kinetics of Cd2+ sorption on WP-MMT-H2O2 and WP-MMT-NaOH were investigated.	Hydrogen Peroxide	63-67	CD2 molecule	Homo sapiens	39-42
32623678-4	2020	The sorption isotherms and kinetics of Cd2+ sorption on WP-MMT-H2O2 and WP-MMT-NaOH were investigated.	Sodium Hydroxide	79-83	CD2 molecule	Homo sapiens	39-42
32604509-2	2020	The synthesized flower-like, alpha-Fe2O3 were separated cadmium (Cd2+) chromium (Cr6+) and lead ions (Pb2+) from wastewater.	CR 6	81-85	CD2 molecule	Homo sapiens	65-68
32604509-2	2020	The synthesized flower-like, alpha-Fe2O3 were separated cadmium (Cd2+) chromium (Cr6+) and lead ions (Pb2+) from wastewater.	Cadmium	56-63	CD2 molecule	Homo sapiens	65-68
32604509-2	2020	The synthesized flower-like, alpha-Fe2O3 were separated cadmium (Cd2+) chromium (Cr6+) and lead ions (Pb2+) from wastewater.	Chromium	71-79	CD2 molecule	Homo sapiens	65-68
32964285-9	2020	We investigated whether the cytotoxicity of TRPM7 permeant metal ions Ni2+, Zn2+, Cd2+, Co2+, Mn2+, Sr2+, and Ba2+ requires TRPM7 channel activity.	strontium cation	100-104	CD2 molecule	Homo sapiens	82-85
32964285-2	2020	It has been proposed to constitute a cellular entry pathway for Mg2+ and divalent metal cations such as Ca2+, Zn2+, Cd2+, Mn2+, and Ni2+.	magnesium ion	64-68	CD2 molecule	Homo sapiens	116-119
32974629-1	2020	In this paper, a CO2-effervescence assisted dispersive micro solid-phase extraction procedure (CO2-EA-DmuSPE) using a magnetic layered double hydroxide modified with polyaniline and a surfactant (Zn-Al-LDH-PA-DBSNa-Fe3O4) was applied for the pre-concentration of heavy metals (Ni2+, Pb2+, Co2+, and Cd2+).	Carbon Dioxide	17-20	CD2 molecule	Homo sapiens	299-302
32964285-2	2020	It has been proposed to constitute a cellular entry pathway for Mg2+ and divalent metal cations such as Ca2+, Zn2+, Cd2+, Mn2+, and Ni2+.	Metals	82-87	CD2 molecule	Homo sapiens	116-119
32964285-9	2020	We investigated whether the cytotoxicity of TRPM7 permeant metal ions Ni2+, Zn2+, Cd2+, Co2+, Mn2+, Sr2+, and Ba2+ requires TRPM7 channel activity.	Metals	59-64	CD2 molecule	Homo sapiens	82-85
32916618-3	2020	This was accomplished by translational fusion of Cd-binding peptides to the N- or C-terminus of a PHB synthase that catalyzes PHB synthesis and mediates assembly of Cd2 or Cd1 coated PHB beads, respectively.	Cadmium	49-51	CD2 molecule	Homo sapiens	165-168
33204474-0	2020	Shell biomass material supported nano-zero valent iron to remove Pb2+ and Cd2+ in water.	Iron	50-54	CD2 molecule	Homo sapiens	74-77
33204474-0	2020	Shell biomass material supported nano-zero valent iron to remove Pb2+ and Cd2+ in water.	Water	82-87	CD2 molecule	Homo sapiens	74-77
33204474-7	2020	For the mixed solution of Pb2+ and Cd2+, only the adsorption of Pb2+ by UVS-NZVI conforms to the Langmuir model.	Lead(2+)	64-68	CD2 molecule	Homo sapiens	35-38
33070855-0	2020	Pyridine-2-sulfonic (or carboxylic) acid modified glassy carbon electrode for anodic stripping voltammetry analysis of Cd2+ and Pb2.	pyridine-2-sulfonic (or carboxylic) acid	0-40	CD2 molecule	Homo sapiens	119-122
33070855-0	2020	Pyridine-2-sulfonic (or carboxylic) acid modified glassy carbon electrode for anodic stripping voltammetry analysis of Cd2+ and Pb2.	Carbon	57-63	CD2 molecule	Homo sapiens	119-122
33070855-1	2020	Monolayer-scale pyridine-2-sulfonic acid (PySA) or pyridine-2-carboxylic acid (PyCA) modified glassy carbon electrode (GCE) was prepared for anodic stripping voltammetry (ASV) analysis of Cd2+ and Pb2+.	pyridine-2-sulfonic acid	16-40	CD2 molecule	Homo sapiens	188-191
33070855-4	2020	In combination with the in-situ bismuth film method, both PySA/GCE and PyCA/GCE offered very high analytical performance for ASV analysis of Cd2+ and Pb2+, including the very low values of limit of detection (LOD, S/N = 3) and high stability.	ASV	125-128	CD2 molecule	Homo sapiens	141-144
33070855-7	2020	The Cu2+ and Ni2+ interferences, which still appear as a challenge for ASV analysis of Cd2+ and Pb2+, were found to be well inhibited by the additions of K4Fe(CN)6 and Ga(III) into the detection solution.	cupric ion	4-8	CD2 molecule	Homo sapiens	87-90
33070855-7	2020	The Cu2+ and Ni2+ interferences, which still appear as a challenge for ASV analysis of Cd2+ and Pb2+, were found to be well inhibited by the additions of K4Fe(CN)6 and Ga(III) into the detection solution.	Nickel(2+)	13-17	CD2 molecule	Homo sapiens	87-90
33070855-7	2020	The Cu2+ and Ni2+ interferences, which still appear as a challenge for ASV analysis of Cd2+ and Pb2+, were found to be well inhibited by the additions of K4Fe(CN)6 and Ga(III) into the detection solution.	k4fe(cn)6	154-163	CD2 molecule	Homo sapiens	87-90
33070855-8	2020	The modified electrode was used for Cd2+ and Pb2+ analysis in real water samples with satisfactory results.	Water	67-72	CD2 molecule	Homo sapiens	36-39
32974629-1	2020	In this paper, a CO2-effervescence assisted dispersive micro solid-phase extraction procedure (CO2-EA-DmuSPE) using a magnetic layered double hydroxide modified with polyaniline and a surfactant (Zn-Al-LDH-PA-DBSNa-Fe3O4) was applied for the pre-concentration of heavy metals (Ni2+, Pb2+, Co2+, and Cd2+).	co2-ea-dmuspe	95-108	CD2 molecule	Homo sapiens	299-302
32974629-1	2020	In this paper, a CO2-effervescence assisted dispersive micro solid-phase extraction procedure (CO2-EA-DmuSPE) using a magnetic layered double hydroxide modified with polyaniline and a surfactant (Zn-Al-LDH-PA-DBSNa-Fe3O4) was applied for the pre-concentration of heavy metals (Ni2+, Pb2+, Co2+, and Cd2+).	zn-al-ldh-pa-dbsna-fe3o4	196-220	CD2 molecule	Homo sapiens	299-302
32784022-4	2020	Here, we report on the activity of Bst exo- in the presence of Mg2+, Mn2+, Ca2+, Cd2+, Co2+, Cu2+, Ni2+ and Zn2+ in the model molecular systems which included amplification of circular and linear DNA templates; conditions providing effective and highly specific isothermal amplification were determined.	Zinc	108-112	CD2 molecule	Homo sapiens	81-84
33086639-0	2020	Removal of Cd2+ from Water by Use of Super-Macroporous Cryogels and Comparison to Commercial Adsorbents.	Water	21-26	CD2 molecule	Homo sapiens	11-14
33086639-7	2020	The cryogels were compared to commercially available adsorbents (zeolite Y and cation exchange resin) for the removal of Cd2+ from various water matrices (ultrapure water, tap water and river water) and the results showed that, under the experimental conditions used, the cryogels can be more effective adsorbents.	Water	139-144	CD2 molecule	Homo sapiens	121-124
32702805-7	2020	According to Langmuir model, the maximum adsorption efficiency of the SiO2@TW nanocomposites was 153 mg/g for Pb2+ and 222 mg/g for Cd2+ but maximum adsorption efficiency of residual tea waste for Pb2+ was 125 mg/g and for Cd2+ was 142.9 mg/g.	Silicon Dioxide	70-74	CD2 molecule	Homo sapiens	223-226
32965095-7	2020	Ion exchange with Ca2+ and Mg2+ is shown to be the main mechanism of Cd2+ elimination.	magnesium ion	27-31	CD2 molecule	Homo sapiens	69-72
32512310-5	2020	We found that most of the divalent metal ions (Mn2+, Zn2+, Co2+, Ni2+, and Cd2+), except Mg2+ and Ca2+, could cause monomolecular DNA condensation.	Metals	35-40	CD2 molecule	Homo sapiens	75-78
32702805-0	2020	Pb2+ and Cd2+ recovery from water using residual tea waste and SiO2@TW nanocomposites.	Water	28-33	CD2 molecule	Homo sapiens	9-12
32702805-0	2020	Pb2+ and Cd2+ recovery from water using residual tea waste and SiO2@TW nanocomposites.	Silicon Dioxide	63-67	CD2 molecule	Homo sapiens	9-12
32702805-1	2020	This work reports the fabrication of SiO2@TW nanocomposites and their application for Pb2+ and Cd2+ ions sequestration from simulated water.	Silicon Dioxide	37-41	CD2 molecule	Homo sapiens	95-98
32702805-1	2020	This work reports the fabrication of SiO2@TW nanocomposites and their application for Pb2+ and Cd2+ ions sequestration from simulated water.	Water	134-139	CD2 molecule	Homo sapiens	95-98
32702805-5	2020	The experiments were carried out in batch mode to explore the effect of various operating parameters on the sequestration of Pb2+ and Cd2+ ions from water.	Water	149-154	CD2 molecule	Homo sapiens	134-137
32702805-7	2020	According to Langmuir model, the maximum adsorption efficiency of the SiO2@TW nanocomposites was 153 mg/g for Pb2+ and 222 mg/g for Cd2+ but maximum adsorption efficiency of residual tea waste for Pb2+ was 125 mg/g and for Cd2+ was 142.9 mg/g.	Silicon Dioxide	70-74	CD2 molecule	Homo sapiens	132-135
32599331-2	2020	Silicon (Si) may reduce the mobility of the contaminants in the environment so that we studied the extent and the mechanisms of the interactions between Pb2+, Cd2+ and Cu2+ and silicic acid during its polymerization.	Silicon	0-7	CD2 molecule	Homo sapiens	159-162
32599331-8	2020	Polymerized silica bound relative to the initial concentrations (10 mmol L-1) up to 2.1% Cd2+, 2% Cu2+ and 1.4% Pb2+.	Silicon Dioxide	12-18	CD2 molecule	Homo sapiens	89-92
33062196-1	2020	Cadmium (Cd2+) is an environmental toxicant and a human carcinogen.	Cadmium	0-7	CD2 molecule	Homo sapiens	9-12
32929275-5	2020	CD2-CD58 interactions in the corolla boosted signaling by 77% as compared with central CD2-CD58 interactions.	corolla	29-36	CD2 molecule	Homo sapiens	0-3
32929275-7	2020	CD2 numbers and motifs in its cytoplasmic tail controlled corolla formation.	corolla	58-65	CD2 molecule	Homo sapiens	0-3
32942553-5	2020	This result suggests that the interaction of the Cd2+ ion with TDMPzP will produce a stable complex.	tdmpzp	63-69	CD2 molecule	Homo sapiens	49-52
32880425-2	2020	Herein, the excited-state proton transfer (ESPT) concept-based luminescent sensor [Cd2(2,5-tpt)(4,5-idc)(H2O)4] (1) (2,5-tpt = 2,5-dihydroxyterephthalic acid and 4,5-idc = 4,5-imidazoledicarboxylic acid) has been designed for discriminative detection via enol-keto tautomerism.	Water	105-108	CD2 molecule	Homo sapiens	83-86
32880425-2	2020	Herein, the excited-state proton transfer (ESPT) concept-based luminescent sensor [Cd2(2,5-tpt)(4,5-idc)(H2O)4] (1) (2,5-tpt = 2,5-dihydroxyterephthalic acid and 4,5-idc = 4,5-imidazoledicarboxylic acid) has been designed for discriminative detection via enol-keto tautomerism.	2,5-tpt	87-94	CD2 molecule	Homo sapiens	83-86
32880425-2	2020	Herein, the excited-state proton transfer (ESPT) concept-based luminescent sensor [Cd2(2,5-tpt)(4,5-idc)(H2O)4] (1) (2,5-tpt = 2,5-dihydroxyterephthalic acid and 4,5-idc = 4,5-imidazoledicarboxylic acid) has been designed for discriminative detection via enol-keto tautomerism.	2,5-dihydroxyterephthalic acid	127-157	CD2 molecule	Homo sapiens	83-86
32880425-2	2020	Herein, the excited-state proton transfer (ESPT) concept-based luminescent sensor [Cd2(2,5-tpt)(4,5-idc)(H2O)4] (1) (2,5-tpt = 2,5-dihydroxyterephthalic acid and 4,5-idc = 4,5-imidazoledicarboxylic acid) has been designed for discriminative detection via enol-keto tautomerism.	4,5-idc	96-103	CD2 molecule	Homo sapiens	83-86
32880425-2	2020	Herein, the excited-state proton transfer (ESPT) concept-based luminescent sensor [Cd2(2,5-tpt)(4,5-idc)(H2O)4] (1) (2,5-tpt = 2,5-dihydroxyterephthalic acid and 4,5-idc = 4,5-imidazoledicarboxylic acid) has been designed for discriminative detection via enol-keto tautomerism.	1H-Imidazole-4,5-dicarboxylic acid	172-202	CD2 molecule	Homo sapiens	83-86
32928473-1	2020	Cadmium ions (Cd2+) greatly threat human health and the environment due to its extremely severe toxicity.	Cadmium	0-7	CD2 molecule	Homo sapiens	14-17
32928473-3	2020	In this work, a novel microfluidic-based fluorescent electronic eye (E-eye) combined with tetrasodium iminodisuccinate (IDS)-etched CdTe/CdS quantum dots (QDs) was developed for portable and sensitive detection of trace Cd2+ in water environment.	Tetrasodium iminodisuccinate	90-118	CD2 molecule	Homo sapiens	220-223
32928473-3	2020	In this work, a novel microfluidic-based fluorescent electronic eye (E-eye) combined with tetrasodium iminodisuccinate (IDS)-etched CdTe/CdS quantum dots (QDs) was developed for portable and sensitive detection of trace Cd2+ in water environment.	iminodisuccinic acid	120-123	CD2 molecule	Homo sapiens	220-223
32928473-3	2020	In this work, a novel microfluidic-based fluorescent electronic eye (E-eye) combined with tetrasodium iminodisuccinate (IDS)-etched CdTe/CdS quantum dots (QDs) was developed for portable and sensitive detection of trace Cd2+ in water environment.	cadmium telluride	132-136	CD2 molecule	Homo sapiens	220-223
32928473-3	2020	In this work, a novel microfluidic-based fluorescent electronic eye (E-eye) combined with tetrasodium iminodisuccinate (IDS)-etched CdTe/CdS quantum dots (QDs) was developed for portable and sensitive detection of trace Cd2+ in water environment.	Cadmium	137-140	CD2 molecule	Homo sapiens	220-223
32772649-0	2022	Adsorption of Cu2+, Cd2+ and Pb2+ in wastewater by modified chitosan hydrogel.	Chitosan	60-68	CD2 molecule	Homo sapiens	20-23
33005188-0	2020	Evaluation of Geophagy Clay Capacity in Adsorbing Cd2+ and Pb2+ for Water Treatment in Southeast Nigeria.	Water	68-73	CD2 molecule	Homo sapiens	50-53
33005188-2	2020	This study determines elemental concentration of geophagy clay and evaluates its adsorptive capacity in removing Cd2+ and Pb2+ in water.	Water	130-135	CD2 molecule	Homo sapiens	113-116
33005188-5	2020	The adsorptive capacity of Cd2+ and Pb2+ on the clay samples was evaluated using standard solutions of the metal ions.	Metals	107-112	CD2 molecule	Homo sapiens	27-30
33005188-9	2020	The study, therefore, concluded that geophagy clay possesses the capacity to adsorb Cd2+ and Pb2+ for water treatment.	Water	102-107	CD2 molecule	Homo sapiens	84-87
32804500-4	2020	Further, 1 was postsynthetically modified using light by exploiting the parallel arrangement of the olefinic double bondsof the bpee pillars based on a [2 + 2] cycloaddition reaction to produce {[Cd2(pzdc)2(rctt-tpcb)] 3H2O}n, (1IR) (rctt-tpcb = regio cis,trans,trans-tetrakis(4-pyridyl)cyclobutane) in a single-crystal-to-single-crystal transformation (SCSC) manner.	(1ir) (rctt-tpcb	227-243	CD2 molecule	Homo sapiens	196-199
32804500-4	2020	Further, 1 was postsynthetically modified using light by exploiting the parallel arrangement of the olefinic double bondsof the bpee pillars based on a [2 + 2] cycloaddition reaction to produce {[Cd2(pzdc)2(rctt-tpcb)] 3H2O}n, (1IR) (rctt-tpcb = regio cis,trans,trans-tetrakis(4-pyridyl)cyclobutane) in a single-crystal-to-single-crystal transformation (SCSC) manner.	cis,trans,trans-tetrakis(4-pyridyl)cyclobutane	252-298	CD2 molecule	Homo sapiens	196-199
32623602-10	2020	The treatment of Cd2+, and Si in a 2.5 mM concentration was the most efficient variant for Cd2+ removal from medium.	Silicon	27-29	CD2 molecule	Homo sapiens	91-94
32339875-0	2020	Urea formaldehyde modified alginate beads with improved stability and enhanced removal of Pb2+, Cd2+, and Cu2.	Urea	0-4	CD2 molecule	Homo sapiens	96-99
32339875-0	2020	Urea formaldehyde modified alginate beads with improved stability and enhanced removal of Pb2+, Cd2+, and Cu2.	Alginates	27-35	CD2 molecule	Homo sapiens	96-99
32623602-3	2020	Silicon is a beneficial element that seems to change the plant"s response to the Cd2+ presence.	Silicon	0-7	CD2 molecule	Homo sapiens	81-84
32623602-4	2020	The aim of the present study was to investigate the Cd2+ tolerance patterns of poplar callus cells exposed to Cd+2 and/or Si over short and long cultivation periods.	Silicon	122-124	CD2 molecule	Homo sapiens	52-55
32339875-6	2020	For example, the adsorption capacities of Pb2+, Cd2+, and Cu2+ on air-dried alginate-UF (1: 2.5) beads were 1.66, 0.61, and 0.80 mmol/g, which were 39.88%, 9.29%, and 9.52% higher than those of the corresponding unmodified alginate beads, respectively.	Alginates	76-84	CD2 molecule	Homo sapiens	48-51
32339875-6	2020	For example, the adsorption capacities of Pb2+, Cd2+, and Cu2+ on air-dried alginate-UF (1: 2.5) beads were 1.66, 0.61, and 0.80 mmol/g, which were 39.88%, 9.29%, and 9.52% higher than those of the corresponding unmodified alginate beads, respectively.	UD	85-87	CD2 molecule	Homo sapiens	48-51
32434113-5	2020	The lignin-based hydrogels inherited lignin"s natural mechanical and environmental stability and the FeS nanoparticles efficiently adsorbed Cd2+ and enhanced Cd2+ desorption from soils by producing H+.	Lignin	4-10	CD2 molecule	Homo sapiens	158-161
32434113-7	2020	In addition, Fe2+ displaced from the composite was gradually oxidized to form solid iron oxide hydroxide, which increased Cd2+ sorption.	ammonium ferrous sulfate	13-17	CD2 molecule	Homo sapiens	122-125
32434113-7	2020	In addition, Fe2+ displaced from the composite was gradually oxidized to form solid iron oxide hydroxide, which increased Cd2+ sorption.	Ferric oxyhydroxide	84-104	CD2 molecule	Homo sapiens	122-125
32615534-9	2020	Both the mobile phases contained ammonium acetate and formic acid that promote the formation of ammoniated precursor ions that can be easily fragmented ([M + NH4]+, TAC m/z 821.3; 13CD2-TAC m/z 824.3).	ammonium acetate	33-49	CD2 molecule	Homo sapiens	182-185
32615534-9	2020	Both the mobile phases contained ammonium acetate and formic acid that promote the formation of ammoniated precursor ions that can be easily fragmented ([M + NH4]+, TAC m/z 821.3; 13CD2-TAC m/z 824.3).	formic acid	54-65	CD2 molecule	Homo sapiens	182-185
32445865-6	2020	Cd2+ markedly increased levels of mitochondrial reactive oxygen species (ROS) in both the distal and proximal compartments of the nerve terminal, which was associated with lipid peroxidation mainly in the distal region.	Reactive Oxygen Species	48-71	CD2 molecule	Homo sapiens	0-3
32331121-4	2020	The clusters were formed by the reaction of Cd2+ and S2- ions generated via the decomposition of thioglycolic acid.	2-mercaptoacetate	97-114	CD2 molecule	Homo sapiens	44-47
32736725-0	2020	Morphology-controlled electrochemical sensing of environmental Cd2+ and Pb2+ ions on expanded graphite supported CeO2 nanomaterials.	Graphite	94-102	CD2 molecule	Homo sapiens	63-66
32736725-1	2020	Heavy metal ions (e.g., Cd2+ and Pb2+) are widely existed in environment and highly toxic.	Metals	6-11	CD2 molecule	Homo sapiens	24-27
32736725-6	2020	The interface using nanorod-shape CeO2 nanomaterials supported on expanded graphite exhibits superior electrochemical activity, namely remarkable signal enhancement for the monitoring of Cd2+ and Pb2+ ions.	ceric oxide	34-38	CD2 molecule	Homo sapiens	187-190
32736725-6	2020	The interface using nanorod-shape CeO2 nanomaterials supported on expanded graphite exhibits superior electrochemical activity, namely remarkable signal enhancement for the monitoring of Cd2+ and Pb2+ ions.	Graphite	75-83	CD2 molecule	Homo sapiens	187-190
32662780-5	2020	2.0 mug L-1 Cd2+ was selectively captured by the derived UiO66-NH2@phage composite with an adsorption efficiency of 100%.	uio66-nh2	57-66	CD2 molecule	Homo sapiens	12-15
32808469-3	2020	A selective chelation enhancement of fluorescence (CHEF) effect was observed in the presence of Zn2+ in the case of L1, and in the presence of Cd2+ in the case of L2, following the formation of a 1 : 1 and a 1 : 2 metal/ligand complex, respectively, which was also confirmed by potentiometric measurements.	Metals	214-219	CD2 molecule	Homo sapiens	143-146
32808469-4	2020	1 H and 13 C NMR measurements in CD3 CN/CDCl3 in combination with molecular mechanics calculations show that for both complexes of L1 and L2 with Zn2+ and Cd2+ , respectively, the coordination of the carbonyl group from the pendant arm could be the origin of the observed optical selectivity.	Chloroform-D	40-45	CD2 molecule	Homo sapiens	155-158
32627793-0	2020	Surface precipitation of Mn2+ on clay minerals enhances Cd2+ sorption under anoxic conditions.	Manganese(2+)	25-29	CD2 molecule	Homo sapiens	56-59
32627793-2	2020	In this study, the effects of Mn2+ on Cd2+ sorption to two types of clay minerals, a well-crystalline natural kaolinite (KGa-1b) and a synthetic montmorillonite (Syn-1), were investigated.	Manganese(2+)	30-34	CD2 molecule	Homo sapiens	38-41
32627793-4	2020	At low Mn2+ and Cd2+ concentrations (1 and 5 muM), both metals exhibited similar affinity for sorption to the clays, suggesting that elevated Mn2+ concentrations might effectively decrease Cd2+ sorption as predicted using a three-plane surface complexation model.	Manganese(2+)	142-146	CD2 molecule	Homo sapiens	189-192
32627793-5	2020	However, competitive Mn-Cd experiments at higher concentrations (>=50 muM) revealed that for both clay minerals, the presence of Mn2+ increased Cd2+ sorption to the solid phases.	Manganese(2+)	129-133	CD2 molecule	Homo sapiens	144-147
32627793-6	2020	Although solutions were undersaturated with respect to known Mn(ii) solid phases, analysis using X-ray absorption spectroscopy (XAS) evidenced the formation of Mn(ii)-containing solid phases which can specifically adsorb or incorporate Cd2+.	Manganese(2+)	160-166	CD2 molecule	Homo sapiens	236-239
32627793-7	2020	This process, which was mediated by the presence of clay minerals, overcompensated the decrease in Cd2+ adsorption to clay surfaces due to competition with Mn2+.	Manganese(2+)	156-160	CD2 molecule	Homo sapiens	99-102
32627793-8	2020	We conclude that, contrary to predictions based on a competitive surface complexation model, elevated Mn2+ concentrations can contribute to decrease dissolved Cd2+ concentrations in anoxic clay-containing environments, such as contaminated sediments or flooded paddy soils.	Manganese(2+)	102-106	CD2 molecule	Homo sapiens	159-162
32558275-3	2020	In this respect, we showed that limiting iron (Fe) uptake makes bacteria much more susceptible to Cu2 + or Cd2+ poisoning.	Iron	41-45	CD2 molecule	Homo sapiens	107-110
32558275-3	2020	In this respect, we showed that limiting iron (Fe) uptake makes bacteria much more susceptible to Cu2 + or Cd2+ poisoning.	Iron	47-49	CD2 molecule	Homo sapiens	107-110
32585429-1	2020	The application of graphene oxide (GO) in the environment can have a positive or negative effect on the toxicity of pollutants, but the effect of GO on cadmium (Cd2+)-stressed lettuce has not yet been thoroughly studied.	graphene oxide	146-148	CD2 molecule	Homo sapiens	161-164
32585429-1	2020	The application of graphene oxide (GO) in the environment can have a positive or negative effect on the toxicity of pollutants, but the effect of GO on cadmium (Cd2+)-stressed lettuce has not yet been thoroughly studied.	Cadmium	152-159	CD2 molecule	Homo sapiens	161-164
32585429-3	2020	We found that the foliar application of 30 mg L-1 of GO could significantly reduce signs of Cd2+ toxicity in lettuce.	graphene oxide	53-55	CD2 molecule	Homo sapiens	92-95
32446077-6	2020	In addition, the aromatic structure C=Cpi can also adsorb Cd2+ to generate C=Cpi-Cd.	cpi-cd	77-83	CD2 molecule	Homo sapiens	58-61
32512147-3	2020	Cd+2 exposures induced decreased cell viability, reactive oxygen species (ROS) generation, altered Akt/ERK signaling pathway activation, PGE2 and COX-2 expression in a human primary gallbladder epithelial cell model.	Reactive Oxygen Species	49-72	CD2 molecule	Homo sapiens	0-4
32512147-3	2020	Cd+2 exposures induced decreased cell viability, reactive oxygen species (ROS) generation, altered Akt/ERK signaling pathway activation, PGE2 and COX-2 expression in a human primary gallbladder epithelial cell model.	Reactive Oxygen Species	74-77	CD2 molecule	Homo sapiens	0-4
32512147-3	2020	Cd+2 exposures induced decreased cell viability, reactive oxygen species (ROS) generation, altered Akt/ERK signaling pathway activation, PGE2 and COX-2 expression in a human primary gallbladder epithelial cell model.	Dinoprostone	137-141	CD2 molecule	Homo sapiens	0-4
32512147-8	2020	Importantly, we observed Cd+2 also caused a dose dependent change in the COX-2 and PGE2 expression levels.	Dinoprostone	83-87	CD2 molecule	Homo sapiens	25-29
32854399-4	2020	More importantly, we used it as a SERS substrate to detect cadmium ions and found that its limit of detection (LOD) reaches up to 2.6 x 10-8 M, which is lower than the highest allowable Cd2+ concentration in drinking water set by the World Health Organization (WHO) and Environmental Protection Agency (EPA).	sers	34-38	CD2 molecule	Homo sapiens	186-189
32854399-4	2020	More importantly, we used it as a SERS substrate to detect cadmium ions and found that its limit of detection (LOD) reaches up to 2.6 x 10-8 M, which is lower than the highest allowable Cd2+ concentration in drinking water set by the World Health Organization (WHO) and Environmental Protection Agency (EPA).	Cadmium	59-66	CD2 molecule	Homo sapiens	186-189
32854399-4	2020	More importantly, we used it as a SERS substrate to detect cadmium ions and found that its limit of detection (LOD) reaches up to 2.6 x 10-8 M, which is lower than the highest allowable Cd2+ concentration in drinking water set by the World Health Organization (WHO) and Environmental Protection Agency (EPA).	Water	217-222	CD2 molecule	Homo sapiens	186-189
32854399-5	2020	Therefore, the proposed composite can be applicable to the detection of Cd2+ in drinking water and in soil.	Water	89-94	CD2 molecule	Homo sapiens	72-75
32787258-1	2020	A photochemically crushable and regenerative metal-organic framework (DTEMOF) was developed by complexation of photochromic ligand PyDTEopen and 5-nitroisophthalate (nip2-) with Cd2+ in DMF/MeOH.	Metals	45-50	CD2 molecule	Homo sapiens	178-181
32787258-1	2020	A photochemically crushable and regenerative metal-organic framework (DTEMOF) was developed by complexation of photochromic ligand PyDTEopen and 5-nitroisophthalate (nip2-) with Cd2+ in DMF/MeOH.	pydteopen	131-140	CD2 molecule	Homo sapiens	178-181
32787258-1	2020	A photochemically crushable and regenerative metal-organic framework (DTEMOF) was developed by complexation of photochromic ligand PyDTEopen and 5-nitroisophthalate (nip2-) with Cd2+ in DMF/MeOH.	5-nitroisophthalic acid	145-164	CD2 molecule	Homo sapiens	178-181
32787258-1	2020	A photochemically crushable and regenerative metal-organic framework (DTEMOF) was developed by complexation of photochromic ligand PyDTEopen and 5-nitroisophthalate (nip2-) with Cd2+ in DMF/MeOH.	Dimethylformamide	186-189	CD2 molecule	Homo sapiens	178-181
32787258-1	2020	A photochemically crushable and regenerative metal-organic framework (DTEMOF) was developed by complexation of photochromic ligand PyDTEopen and 5-nitroisophthalate (nip2-) with Cd2+ in DMF/MeOH.	Methanol	190-194	CD2 molecule	Homo sapiens	178-181
32783891-1	2021	Exposure to toxic metal contaminants, such as cadmium complexes (Cd2+), has been shown to induce adverse effects on various organs and tissues.	Metals	18-23	CD2 molecule	Homo sapiens	65-68
32783891-1	2021	Exposure to toxic metal contaminants, such as cadmium complexes (Cd2+), has been shown to induce adverse effects on various organs and tissues.	cadmium complexes	46-63	CD2 molecule	Homo sapiens	65-68
32268232-2	2020	Little is known about the leaching of hazardous Cd2+ from colored microplastics containing cadmium pigment in aquatic systems.	Cadmium	91-98	CD2 molecule	Homo sapiens	48-51
32268232-3	2020	Here, we reported the release of Cd2+ from different sized microplastics containing cadmium pigment in aqueous phase under simulated sunlight.	Cadmium	84-91	CD2 molecule	Homo sapiens	33-36
32268232-4	2020	The release of Cd2+ was caused by the photo-dissolution of cadmium pigment.	Cadmium	59-66	CD2 molecule	Homo sapiens	15-18
32268232-8	2020	Part of the polymer matrix was degraded into soluble organic carbon under simulated sunlight, resulting in continuous Cd2+ release from the pigment particles embedded in the polymer.	Polymers	12-19	CD2 molecule	Homo sapiens	118-121
32268232-8	2020	Part of the polymer matrix was degraded into soluble organic carbon under simulated sunlight, resulting in continuous Cd2+ release from the pigment particles embedded in the polymer.	Carbon	61-67	CD2 molecule	Homo sapiens	118-121
32268232-8	2020	Part of the polymer matrix was degraded into soluble organic carbon under simulated sunlight, resulting in continuous Cd2+ release from the pigment particles embedded in the polymer.	Polymers	174-181	CD2 molecule	Homo sapiens	118-121
32268232-10	2020	The degradation of the polymer matrix and the release of Cd2+ were intertwined.	Polymers	23-30	CD2 molecule	Homo sapiens	57-60
32445865-6	2020	Cd2+ markedly increased levels of mitochondrial reactive oxygen species (ROS) in both the distal and proximal compartments of the nerve terminal, which was associated with lipid peroxidation mainly in the distal region.	Reactive Oxygen Species	73-76	CD2 molecule	Homo sapiens	0-3
32445865-7	2020	Zn2+, whose transport systems translocate Cd2+, markedly enhanced the effects of Cd2+ on both the mitochondrial ROS levels and timing of neurotransmitter release.	Zinc	0-4	CD2 molecule	Homo sapiens	42-45
32445865-7	2020	Zn2+, whose transport systems translocate Cd2+, markedly enhanced the effects of Cd2+ on both the mitochondrial ROS levels and timing of neurotransmitter release.	Zinc	0-4	CD2 molecule	Homo sapiens	81-84
32445865-7	2020	Zn2+, whose transport systems translocate Cd2+, markedly enhanced the effects of Cd2+ on both the mitochondrial ROS levels and timing of neurotransmitter release.	Reactive Oxygen Species	112-115	CD2 molecule	Homo sapiens	42-45
32445865-7	2020	Zn2+, whose transport systems translocate Cd2+, markedly enhanced the effects of Cd2+ on both the mitochondrial ROS levels and timing of neurotransmitter release.	Reactive Oxygen Species	112-115	CD2 molecule	Homo sapiens	81-84
32445865-8	2020	Furthermore, in the presence of Zn2+ ions, Cd2+ also desynchronized the neurotransmitter release in the proximal region.	Zinc	32-36	CD2 molecule	Homo sapiens	43-46
32445865-9	2020	Thus, in synapses Cd2+ at very low concentrations can increase mitochondrial ROS, lipid peroxidation and disturb the timing of neurotransmitter release via a ROS/TRPV-dependent mechanism.	Reactive Oxygen Species	77-80	CD2 molecule	Homo sapiens	18-21
32445865-9	2020	Thus, in synapses Cd2+ at very low concentrations can increase mitochondrial ROS, lipid peroxidation and disturb the timing of neurotransmitter release via a ROS/TRPV-dependent mechanism.	Reactive Oxygen Species	158-161	CD2 molecule	Homo sapiens	18-21
32445865-9	2020	Thus, in synapses Cd2+ at very low concentrations can increase mitochondrial ROS, lipid peroxidation and disturb the timing of neurotransmitter release via a ROS/TRPV-dependent mechanism.	trpv	162-166	CD2 molecule	Homo sapiens	18-21
32584539-2	2020	Herein, a linear alternating supramolecular polymer is constructed via host-guest inclusion interaction between cyclodextrin-dimer (CD2) and bifunctional adamantane-conjugated porphyrin (TPP-Ad2).	Cyclodextrins	112-124	CD2 molecule	Homo sapiens	132-135
32584539-4	2020	The nanoplatform obtained by this linear alternating su-pramolecular polymer (TPP-Ad2/CD2) presents significantly enhanced PDT efficacy, providing a promising path for PDT.	su-pramolecular polymer	53-76	CD2 molecule	Homo sapiens	86-89
32335452-2	2020	The single and combined Ni2+ and Cd2+ had no adverse impacts on the COD removal, whereas the NH4+-N removal efficiency declined sharply from about 99% to 34.42% and 42.67% under the single Ni2+ and combined Ni2+ and Cd2+.	nh4+-n	93-99	CD2 molecule	Homo sapiens	216-219
32335452-5	2020	The combined Ni2+ and Cd2+ declined the microbial diversity and richness less than the sum of those under single Ni2+ and Cd2+.	Nickel(2+)	13-17	CD2 molecule	Homo sapiens	122-125
32618180-7	2020	At low Cd2+ concentration, Cd2+ mainly interacted with phosphate groups on aptamer, resulting in the stretched ssDNA and a few vertical hairpin structures.	Phosphates	55-64	CD2 molecule	Homo sapiens	7-10
32618180-7	2020	At low Cd2+ concentration, Cd2+ mainly interacted with phosphate groups on aptamer, resulting in the stretched ssDNA and a few vertical hairpin structures.	Phosphates	55-64	CD2 molecule	Homo sapiens	27-30
32335452-5	2020	The combined Ni2+ and Cd2+ declined the microbial diversity and richness less than the sum of those under single Ni2+ and Cd2+.	Nickel(2+)	113-117	CD2 molecule	Homo sapiens	22-25
32488932-0	2020	Unraveling the Origin of Differentiable "Turn-On" Fluorescence Sensing of Zn2+ and Cd2+ ions with Squaramides.	squaramide	98-109	CD2 molecule	Homo sapiens	83-86
32304944-4	2020	The maximum capacities of Pb2+, Cd2+, Cu2+, and Zn2+ were 649, 210, 90 and 88 mg/g, and the distribution coefficients (Kd) was ~108 mL/g for Pb2+ which emphasized the superior effectiveness of Na6Al6Si10O32 12H2O contrasted with other zeolites.	Lead(2+)	141-145	CD2 molecule	Homo sapiens	32-35
32296905-5	2020	The low charge transfer resistance and high electroactive surface area contributed to the high sensitivity for Cd2+ (0.0767 muA (0.225 mug L-1)-1), As3+ (0.2213 muA (mug L-1)-1), and Se4+ (muA (mug L-1)-1).	se4+	183-187	CD2 molecule	Homo sapiens	111-114
32304944-3	2020	Herein, we sought out and firstly synthesized the uniform octahedral zeolite Na6Al6Si10O32 12H2O for heavy metal ions trap, proven extraordinarily effective decontamination of M2+ (Pb2+, Cd2+, Cu2+, and Zn2+).	na6al6si10o32 12h2o	77-96	CD2 molecule	Homo sapiens	187-190
32296905-9	2020	Surface water analysis resulted in average percent recoveries of 109% for Cd2+, 93% for As3+, and 92% for Se4+, indicating the proposed method is accurate and reliable for the simultaneous detection of Cd2+, As3+, and Se4+ in real water samples.	Water	8-13	CD2 molecule	Homo sapiens	74-77
32296905-9	2020	Surface water analysis resulted in average percent recoveries of 109% for Cd2+, 93% for As3+, and 92% for Se4+, indicating the proposed method is accurate and reliable for the simultaneous detection of Cd2+, As3+, and Se4+ in real water samples.	Water	8-13	CD2 molecule	Homo sapiens	202-205
32296905-9	2020	Surface water analysis resulted in average percent recoveries of 109% for Cd2+, 93% for As3+, and 92% for Se4+, indicating the proposed method is accurate and reliable for the simultaneous detection of Cd2+, As3+, and Se4+ in real water samples.	se4+	106-110	CD2 molecule	Homo sapiens	202-205
32296905-9	2020	Surface water analysis resulted in average percent recoveries of 109% for Cd2+, 93% for As3+, and 92% for Se4+, indicating the proposed method is accurate and reliable for the simultaneous detection of Cd2+, As3+, and Se4+ in real water samples.	Water	231-236	CD2 molecule	Homo sapiens	202-205
32500261-10	2020	The surface activity of the product was also investigated and it was found it can adsorb Pb2+ and Cd2+ from the water with 100% efficiency.	Water	112-117	CD2 molecule	Homo sapiens	98-101
32601866-2	2021	In this research, biosorption technique was employed to remove cadmium (Cd2+) from an aqueous system using a novel biosorbent developed from okara waste (OW), a residue from soya bean-based food and beverage processing.	Cadmium	63-70	CD2 molecule	Homo sapiens	72-75
32629753-0	2020	Experimental and Theoretical Analysis of Lead Pb2+ and Cd2+ Retention from a Single Salt Using a Hollow Fiber PES Membrane.	Salts	84-88	CD2 molecule	Homo sapiens	55-58
32629753-0	2020	Experimental and Theoretical Analysis of Lead Pb2+ and Cd2+ Retention from a Single Salt Using a Hollow Fiber PES Membrane.	polyether sulfone	110-113	CD2 molecule	Homo sapiens	55-58
32629753-1	2020	The present work reports the performance of three types of polyethersulfone (PES) membrane in the removal of highly polluting and toxic lead Pb2+ and cadmium Cd2+ ions from a single salt.	polyether sulfone	59-75	CD2 molecule	Homo sapiens	158-161
32629753-1	2020	The present work reports the performance of three types of polyethersulfone (PES) membrane in the removal of highly polluting and toxic lead Pb2+ and cadmium Cd2+ ions from a single salt.	polyether sulfone	77-80	CD2 molecule	Homo sapiens	158-161
32601866-9	2021	The Cd2+ loaded OW biosorbent could be regenerated using 0.4 M of HCl solution and regeneration was studied for 4 adsorption-desorption cycles.	Hydrochloric Acid	66-69	CD2 molecule	Homo sapiens	4-7
32601866-10	2021	The present investigation supported that OW can be reused as a value-added biosorbent product for the removal of Cd2+ from the contaminated water.	Water	140-145	CD2 molecule	Homo sapiens	113-116
32276162-1	2020	The relationship between the chemical forms of Cu2+ and Cd2+ adsorbed on the roots of different wheat cultivars and their phytotoxic effects on the plants were investigated.	cupric ion	47-51	CD2 molecule	Homo sapiens	56-59
32247238-4	2020	Cadmium stress decreased the plant growth related attributes, water relations as well as the activities of monodehydroascorbate reductase (MDHAR) and dehydroascorbate reductase (DHAR), but enhanced proline content, leaf Cd2+ content, oxidative stress-related traits, activities of ascorbate peroxidase (APX) and glutathione reductase (GR), and the activities of antioxidant defence system-related enzymes as well as NR activity and endogenous nitric oxide content.	Cadmium	0-7	CD2 molecule	Homo sapiens	220-223
32276162-6	2020	Coexisting cations, such as Ca2+, Mg2+, K+, and NH4+, alleviated Cu2+ and Cd2+ toxicity to wheat roots through competition for adsorption sites on the roots, which decreased exchangeable and complexed Cu2+ and Cd2+ on wheat roots.	cupric ion	201-205	CD2 molecule	Homo sapiens	74-77
32276162-5	2020	The negative charge and functional groups on ZM895 and AK68 roots were greater than on DMW and TK6 roots, which led to more exchangeable and complexed Cu2+ and Cd2+ on ZM895 and AK68 roots and increased Cu2+ and Cd2+ toxicity compared to DMW and TK6.	cupric ion	151-155	CD2 molecule	Homo sapiens	212-215
32276162-7	2020	The Ca2+ and Mg2+ were most effective in alleviating heavy metal toxicity and they decreased exchangeable Cu2+ on AK68 roots by 39.14% and 47.82%, and exchangeable Cd2+ by 8.51% and 28.23%, respectively.	magnesium ion	13-17	CD2 molecule	Homo sapiens	164-167
32276162-5	2020	The negative charge and functional groups on ZM895 and AK68 roots were greater than on DMW and TK6 roots, which led to more exchangeable and complexed Cu2+ and Cd2+ on ZM895 and AK68 roots and increased Cu2+ and Cd2+ toxicity compared to DMW and TK6.	cupric ion	203-207	CD2 molecule	Homo sapiens	160-163
32276162-5	2020	The negative charge and functional groups on ZM895 and AK68 roots were greater than on DMW and TK6 roots, which led to more exchangeable and complexed Cu2+ and Cd2+ on ZM895 and AK68 roots and increased Cu2+ and Cd2+ toxicity compared to DMW and TK6.	SCHEMBL3244018	87-90	CD2 molecule	Homo sapiens	160-163
32278141-0	2020	New insights into the release mechanism of Cd2+ from CdTe quantum dots within single cells in situ.	cadmium telluride	53-57	CD2 molecule	Homo sapiens	43-46
32276162-5	2020	The negative charge and functional groups on ZM895 and AK68 roots were greater than on DMW and TK6 roots, which led to more exchangeable and complexed Cu2+ and Cd2+ on ZM895 and AK68 roots and increased Cu2+ and Cd2+ toxicity compared to DMW and TK6.	SCHEMBL3244018	87-90	CD2 molecule	Homo sapiens	212-215
32278141-2	2020	However, the toxic effects of Cd-QDs to single cells is still controversial, due to the release mechanism of QDs to Cd2+in situ and the cytotoxic effects of QDs and Cd2+ respectively are still unclear.	cd-qds	30-36	CD2 molecule	Homo sapiens	116-119
32276162-6	2020	Coexisting cations, such as Ca2+, Mg2+, K+, and NH4+, alleviated Cu2+ and Cd2+ toxicity to wheat roots through competition for adsorption sites on the roots, which decreased exchangeable and complexed Cu2+ and Cd2+ on wheat roots.	magnesium ion	34-38	CD2 molecule	Homo sapiens	74-77
32276162-6	2020	Coexisting cations, such as Ca2+, Mg2+, K+, and NH4+, alleviated Cu2+ and Cd2+ toxicity to wheat roots through competition for adsorption sites on the roots, which decreased exchangeable and complexed Cu2+ and Cd2+ on wheat roots.	Ammonium Compounds	48-52	CD2 molecule	Homo sapiens	74-77
32276162-6	2020	Coexisting cations, such as Ca2+, Mg2+, K+, and NH4+, alleviated Cu2+ and Cd2+ toxicity to wheat roots through competition for adsorption sites on the roots, which decreased exchangeable and complexed Cu2+ and Cd2+ on wheat roots.	Ammonium Compounds	48-52	CD2 molecule	Homo sapiens	210-213
32535720-8	2020	An efficient, regenerable, and stable sensor device was fabricated for sensitive and selective detection of Cd2+ in contaminated water samples.	Water	129-134	CD2 molecule	Homo sapiens	108-111
32088540-0	2020	Simultaneous removal of Pb2+, Cu2+ and Cd2+ ions from wastewater using hierarchical porous polyacrylic acid grafted with lignin.	carbopol 940	91-107	CD2 molecule	Homo sapiens	39-42
32088540-0	2020	Simultaneous removal of Pb2+, Cu2+ and Cd2+ ions from wastewater using hierarchical porous polyacrylic acid grafted with lignin.	Lignin	121-127	CD2 molecule	Homo sapiens	39-42
32088540-3	2020	Acid-pretreated alkali lignin acts as a hierarchical pore-forming agent that enhances the simultaneous adsorption capacities for Pb2+, Cu2+ and Cd2+ ions from wastewater.	Lignin	23-29	CD2 molecule	Homo sapiens	144-147
32458904-2	2020	In these complexes the L and L1 ligands are shown to coordinate Zn2+ and Cd2+ ions through the 2,2"-bipyridine moiety.	2,2'-Dipyridyl	95-110	CD2 molecule	Homo sapiens	73-76
32143042-5	2020	While in binary-metal systems, the Pb2+ adsorption was slightly influenced by the coexisting Cd2+, but the Cd2+ adsorption capacities were decreased by over 5 times.	Metals	16-21	CD2 molecule	Homo sapiens	93-96
32143042-5	2020	While in binary-metal systems, the Pb2+ adsorption was slightly influenced by the coexisting Cd2+, but the Cd2+ adsorption capacities were decreased by over 5 times.	Metals	16-21	CD2 molecule	Homo sapiens	107-110
32143042-5	2020	While in binary-metal systems, the Pb2+ adsorption was slightly influenced by the coexisting Cd2+, but the Cd2+ adsorption capacities were decreased by over 5 times.	Lead	35-39	CD2 molecule	Homo sapiens	93-96
32608795-3	2020	Heavy metal ions (Ni2+, Cd2+, Cu2+, and Zn2+) can reduce the removal efficiency of urea by mixed strains, and the degree of influence was Cd2+ > Cu2+ > Ni2+ > Zn2+.	Metals	6-11	CD2 molecule	Homo sapiens	24-27
32608795-3	2020	Heavy metal ions (Ni2+, Cd2+, Cu2+, and Zn2+) can reduce the removal efficiency of urea by mixed strains, and the degree of influence was Cd2+ > Cu2+ > Ni2+ > Zn2+.	Metals	6-11	CD2 molecule	Homo sapiens	138-141
32608795-3	2020	Heavy metal ions (Ni2+, Cd2+, Cu2+, and Zn2+) can reduce the removal efficiency of urea by mixed strains, and the degree of influence was Cd2+ > Cu2+ > Ni2+ > Zn2+.	Nickel(2+)	18-22	CD2 molecule	Homo sapiens	138-141
32608795-3	2020	Heavy metal ions (Ni2+, Cd2+, Cu2+, and Zn2+) can reduce the removal efficiency of urea by mixed strains, and the degree of influence was Cd2+ > Cu2+ > Ni2+ > Zn2+.	cupric ion	30-34	CD2 molecule	Homo sapiens	138-141
32608795-3	2020	Heavy metal ions (Ni2+, Cd2+, Cu2+, and Zn2+) can reduce the removal efficiency of urea by mixed strains, and the degree of influence was Cd2+ > Cu2+ > Ni2+ > Zn2+.	Zinc	40-44	CD2 molecule	Homo sapiens	138-141
32608795-3	2020	Heavy metal ions (Ni2+, Cd2+, Cu2+, and Zn2+) can reduce the removal efficiency of urea by mixed strains, and the degree of influence was Cd2+ > Cu2+ > Ni2+ > Zn2+.	Urea	83-87	CD2 molecule	Homo sapiens	24-27
32608795-3	2020	Heavy metal ions (Ni2+, Cd2+, Cu2+, and Zn2+) can reduce the removal efficiency of urea by mixed strains, and the degree of influence was Cd2+ > Cu2+ > Ni2+ > Zn2+.	Urea	83-87	CD2 molecule	Homo sapiens	138-141
32608795-3	2020	Heavy metal ions (Ni2+, Cd2+, Cu2+, and Zn2+) can reduce the removal efficiency of urea by mixed strains, and the degree of influence was Cd2+ > Cu2+ > Ni2+ > Zn2+.	cupric ion	145-149	CD2 molecule	Homo sapiens	24-27
32608795-3	2020	Heavy metal ions (Ni2+, Cd2+, Cu2+, and Zn2+) can reduce the removal efficiency of urea by mixed strains, and the degree of influence was Cd2+ > Cu2+ > Ni2+ > Zn2+.	Nickel(2+)	152-156	CD2 molecule	Homo sapiens	24-27
32608795-3	2020	Heavy metal ions (Ni2+, Cd2+, Cu2+, and Zn2+) can reduce the removal efficiency of urea by mixed strains, and the degree of influence was Cd2+ > Cu2+ > Ni2+ > Zn2+.	Zinc	159-163	CD2 molecule	Homo sapiens	24-27
32608795-3	2020	Heavy metal ions (Ni2+, Cd2+, Cu2+, and Zn2+) can reduce the removal efficiency of urea by mixed strains, and the degree of influence was Cd2+ > Cu2+ > Ni2+ > Zn2+.	Zinc	159-163	CD2 molecule	Homo sapiens	138-141
32463227-3	2020	The distorted octahedral coordination of the d0 metal cations (Nb5+) coupled with the increased covalency in the lattice by the introduction of d10 metal cations (Cd2+) is responsible for the acentric structures.	Metals	48-53	CD2 molecule	Homo sapiens	163-166
32463227-3	2020	The distorted octahedral coordination of the d0 metal cations (Nb5+) coupled with the increased covalency in the lattice by the introduction of d10 metal cations (Cd2+) is responsible for the acentric structures.	d10 metal	144-153	CD2 molecule	Homo sapiens	163-166
32219259-2	2020	The twenty-cysteinyl mammalian metallothioneins protect the proteome by sequestering heavy metals into thermodynamically stable metal thiolate structures when metalated with seven Cd2+.	metal thiolate	128-142	CD2 molecule	Homo sapiens	180-183
32062548-7	2020	Moreover, both Cd2+ and Zn2+ removal efficiency are less than 2 % in Pb-Cd or Pb-Zn coexisted solution, indicating the composite possessed high selectivity for Pb2+ removal.	Lead	69-74	CD2 molecule	Homo sapiens	15-18
32062548-7	2020	Moreover, both Cd2+ and Zn2+ removal efficiency are less than 2 % in Pb-Cd or Pb-Zn coexisted solution, indicating the composite possessed high selectivity for Pb2+ removal.	Lead	69-71	CD2 molecule	Homo sapiens	15-18
32062548-7	2020	Moreover, both Cd2+ and Zn2+ removal efficiency are less than 2 % in Pb-Cd or Pb-Zn coexisted solution, indicating the composite possessed high selectivity for Pb2+ removal.	Lead	160-164	CD2 molecule	Homo sapiens	15-18
32041068-7	2020	For the three metals, Pb2+ exhibited significantly stronger sorption than did Cu2+ and Cd2+ due to the strong electrostatic interaction.	Metals	14-20	CD2 molecule	Homo sapiens	87-90
31377930-0	2020	Synthesis and characterization of GO/FeSO4 composites for the effective removal of Hg2+ and Cd2+ ions from the synthetic effluent.	ferrous sulfate	37-42	CD2 molecule	Homo sapiens	92-95
32677757-1	2020	Methionine (Met) cationized with Zn2+ , forming Zn (Met-H)+ (ACN) where ACN = acetonitrile, Zn (Met-H)+ , and ZnCl+ (Met), as well as Cd2+ , forming CdCl+ (Met), were examined by infrared multiple photon dissociation (IRMPD) action spectroscopy using light generated from the FELIX free electron laser.	Methionine	0-10	CD2 molecule	Homo sapiens	134-137
32677757-1	2020	Methionine (Met) cationized with Zn2+ , forming Zn (Met-H)+ (ACN) where ACN = acetonitrile, Zn (Met-H)+ , and ZnCl+ (Met), as well as Cd2+ , forming CdCl+ (Met), were examined by infrared multiple photon dissociation (IRMPD) action spectroscopy using light generated from the FELIX free electron laser.	Methionine	0-3	CD2 molecule	Homo sapiens	134-137
32677757-1	2020	Methionine (Met) cationized with Zn2+ , forming Zn (Met-H)+ (ACN) where ACN = acetonitrile, Zn (Met-H)+ , and ZnCl+ (Met), as well as Cd2+ , forming CdCl+ (Met), were examined by infrared multiple photon dissociation (IRMPD) action spectroscopy using light generated from the FELIX free electron laser.	Zinc	33-37	CD2 molecule	Homo sapiens	134-137
32677757-1	2020	Methionine (Met) cationized with Zn2+ , forming Zn (Met-H)+ (ACN) where ACN = acetonitrile, Zn (Met-H)+ , and ZnCl+ (Met), as well as Cd2+ , forming CdCl+ (Met), were examined by infrared multiple photon dissociation (IRMPD) action spectroscopy using light generated from the FELIX free electron laser.	met-h	52-57	CD2 molecule	Homo sapiens	134-137
32677757-1	2020	Methionine (Met) cationized with Zn2+ , forming Zn (Met-H)+ (ACN) where ACN = acetonitrile, Zn (Met-H)+ , and ZnCl+ (Met), as well as Cd2+ , forming CdCl+ (Met), were examined by infrared multiple photon dissociation (IRMPD) action spectroscopy using light generated from the FELIX free electron laser.	3-hydroxy-5-estrane-17-carbonitrile	61-64	CD2 molecule	Homo sapiens	134-137
33488194-1	2020	Two newly synthesized Schiff bases DMCA and DMBA were used for selective detection of Cd2+ over a wide range of other metal ions in acetonitrile (ACN)/ Tris-HCl buffer (10 mM, pH 7.32, v/v 2:1).	Schiff Bases	22-34	CD2 molecule	Homo sapiens	86-89
33488194-1	2020	Two newly synthesized Schiff bases DMCA and DMBA were used for selective detection of Cd2+ over a wide range of other metal ions in acetonitrile (ACN)/ Tris-HCl buffer (10 mM, pH 7.32, v/v 2:1).	dmca	35-39	CD2 molecule	Homo sapiens	86-89
33488194-1	2020	Two newly synthesized Schiff bases DMCA and DMBA were used for selective detection of Cd2+ over a wide range of other metal ions in acetonitrile (ACN)/ Tris-HCl buffer (10 mM, pH 7.32, v/v 2:1).	6,11-dimethylbenzo(b)naphtho(2,3-d)thiophene	44-48	CD2 molecule	Homo sapiens	86-89
33488194-2	2020	The sensors can detect Cd2+ ions by colour changes from colourless to orange for DMBA and yellow to reddish for DMCA.	6,11-dimethylbenzo(b)naphtho(2,3-d)thiophene	81-85	CD2 molecule	Homo sapiens	23-26
33488194-2	2020	The sensors can detect Cd2+ ions by colour changes from colourless to orange for DMBA and yellow to reddish for DMCA.	dmca	112-116	CD2 molecule	Homo sapiens	23-26
33488194-4	2020	The complex stoichiometry between the sensors, DMBA and DMCA, and Cd2+ was found to be 2:1 and the binding constants were calculated to be 2.65 x1012 M-2 and 4.95 x1012 M-2, respectively.	6,11-dimethylbenzo(b)naphtho(2,3-d)thiophene	47-51	CD2 molecule	Homo sapiens	66-69
33488194-4	2020	The complex stoichiometry between the sensors, DMBA and DMCA, and Cd2+ was found to be 2:1 and the binding constants were calculated to be 2.65 x1012 M-2 and 4.95 x1012 M-2, respectively.	dmca	56-60	CD2 molecule	Homo sapiens	66-69
32677757-1	2020	Methionine (Met) cationized with Zn2+ , forming Zn (Met-H)+ (ACN) where ACN = acetonitrile, Zn (Met-H)+ , and ZnCl+ (Met), as well as Cd2+ , forming CdCl+ (Met), were examined by infrared multiple photon dissociation (IRMPD) action spectroscopy using light generated from the FELIX free electron laser.	Zinc	48-50	CD2 molecule	Homo sapiens	134-137
32677757-6	2020	Further, the comparison between the current work and previous analyses involving alkali metal cationized Met as well as cysteine (the other sulfur containing amino acid) cationized with Zn2+ and Cd2+ allows for the elucidation of important metal dependent trends associated with physiologically important metal-sulfur binding.	Cysteine	120-128	CD2 molecule	Homo sapiens	195-198
32677757-6	2020	Further, the comparison between the current work and previous analyses involving alkali metal cationized Met as well as cysteine (the other sulfur containing amino acid) cationized with Zn2+ and Cd2+ allows for the elucidation of important metal dependent trends associated with physiologically important metal-sulfur binding.	Sulfur	140-146	CD2 molecule	Homo sapiens	195-198
32677757-6	2020	Further, the comparison between the current work and previous analyses involving alkali metal cationized Met as well as cysteine (the other sulfur containing amino acid) cationized with Zn2+ and Cd2+ allows for the elucidation of important metal dependent trends associated with physiologically important metal-sulfur binding.	Metals	240-245	CD2 molecule	Homo sapiens	195-198
32677757-6	2020	Further, the comparison between the current work and previous analyses involving alkali metal cationized Met as well as cysteine (the other sulfur containing amino acid) cationized with Zn2+ and Cd2+ allows for the elucidation of important metal dependent trends associated with physiologically important metal-sulfur binding.	Metals	240-245	CD2 molecule	Homo sapiens	195-198
32443800-8	2020	By increasing the HMF grafting from 130% (CS-HMF1) to 310% (CS-HMF3), an increase of 24% (26 m/g) was observed for Cu2+ adsorption and 19% (20 mg/g) for Cd2+.	Chitosan	60-62	CD2 molecule	Homo sapiens	153-156
32233376-7	2020	The system was used for real-time exploration of intracellular antagonism of Cu2+ against Cd2+.	cupric ion	77-81	CD2 molecule	Homo sapiens	90-93
32494740-7	2020	Intermedilysin binds to the sialyl-TF O-glycan on its erythrocyte receptor, CD59.	o-glycan	38-46	CD2 molecule	Homo sapiens	54-74
32429042-5	2020	The adsorbent had great selectivity for Pb2+ from the aqueous solution containing coexisting ions including Cd2+, Co2+, Cr3+, Cu2+, Ni2+ and Zn2+.	Lead(2+)	40-44	CD2 molecule	Homo sapiens	108-111
32106032-1	2020	Pb2+ and Cd2+ are the most ubiquitous heavy metal ion pollutants, and they have aroused much attention due to their irreversible and significant damage to human organ.	Metals	44-49	CD2 molecule	Homo sapiens	9-12
32106032-5	2020	However, adding fluoride ion to the FP solution containing Pb2+ or Cd2+ resulted in a distinct phenomenon in which the pale purple color fades out to colorless for a Pb2+-containing solution and deepen to dark purple for a Cd2+-containing solution, which is attributable to the different coordination mechanisms.	Fluorides	16-24	CD2 molecule	Homo sapiens	67-70
32106032-5	2020	However, adding fluoride ion to the FP solution containing Pb2+ or Cd2+ resulted in a distinct phenomenon in which the pale purple color fades out to colorless for a Pb2+-containing solution and deepen to dark purple for a Cd2+-containing solution, which is attributable to the different coordination mechanisms.	Fluorides	16-24	CD2 molecule	Homo sapiens	223-226
32106032-5	2020	However, adding fluoride ion to the FP solution containing Pb2+ or Cd2+ resulted in a distinct phenomenon in which the pale purple color fades out to colorless for a Pb2+-containing solution and deepen to dark purple for a Cd2+-containing solution, which is attributable to the different coordination mechanisms.	Lead	59-63	CD2 molecule	Homo sapiens	223-226
32106032-5	2020	However, adding fluoride ion to the FP solution containing Pb2+ or Cd2+ resulted in a distinct phenomenon in which the pale purple color fades out to colorless for a Pb2+-containing solution and deepen to dark purple for a Cd2+-containing solution, which is attributable to the different coordination mechanisms.	Lead	166-170	CD2 molecule	Homo sapiens	67-70
32106032-8	2020	Moreover, FP was successfully used to rapidly detect trace amounts of hazardous Pb2+ and Cd2+ in tap water with good relative recovery and the relative standard deviations (RSD) were 1.8% for Pb2+ and 0.3% for Cd2+, providing a novel approach for detecting Pb2+ and Cd2+ in practical application.	Water	101-106	CD2 molecule	Homo sapiens	89-92
32286799-1	2020	A metal-organic supramolecular nanobelt was synthesized by quantitative self-assembling terpyridine-functionized tetraphenylethylene (TPE) and Cd2+, which only showed a weak emission both in solution or aggregated state.	Metals	2-7	CD2 molecule	Homo sapiens	143-146
31918077-4	2020	The ITC analyses of exchange reactions demonstrated that Zn-ShMT exhibited up to 6, 6, and 7 binding sites for Cd2+, Pb2+ and Cu2+.	Zinc	57-59	CD2 molecule	Homo sapiens	111-114
32455220-7	2020	In addition, the adsorption capacity of different metal ions follows the order Ag+ < Cd2+ < Cu2+ < Pb2+ < Fe3+, indicating that the PPy/GO composite electrode has stronger adsorption capacity for the added state, and the adsorption capacity for ions with the same valence state decreases with the increase in ion hydration radius.	Metals	50-55	CD2 molecule	Homo sapiens	85-88
31918077-2	2020	In this study, we analysed the stoichiometry of ShMT yielded in vivo and exchange reactions of the Zn-ShMT with Cd2+, Pb2+ and Cu2+in vitro via electrospray ionization time-of-flight mass spectrometry (ESI-TOF-MS), circular dichroism (CD) spectroscopy, inductively coupled plasma mass spectrometry (ICP-MS), and isothermal titration calorimetry (ITC).	Zinc	99-101	CD2 molecule	Homo sapiens	112-115
31958647-1	2020	The partial nitrification efficiency response to the presence of cadmium (Cd2+) and microplastics was investigated.	Cadmium	65-72	CD2 molecule	Homo sapiens	74-77
31958647-5	2020	The ammonia oxidation rate was improved with the co-existence of PVC and Cd2+ at the conditions PVC1000 and PVC5000, which could be attributed to the PVC.	Ammonia	4-11	CD2 molecule	Homo sapiens	73-76
31918077-5	2020	By the analyses of the UV and CD spectra in the substitution experiments showed that the geometric structural stability of metal-ShMT could be influenced when excess of over 6, 6, or 7 equivalents of Cd2+, Pb2+, or Cu2+ were added into Zn-ShMT.	Zinc	236-238	CD2 molecule	Homo sapiens	200-203
32238299-2	2020	METHODS: We delineate expansion methods using interleukin (IL)-2, IL-7 and allogeneic feeder cells and anti-CD2/CD3/CD28 stimulation by which to dependably augment Th2 polarization and direct cytotoxicity of human peripheral blood CD3+Valpha24+Vbeta11+ iNKT cells.	th2	164-167	CD2 molecule	Homo sapiens	108-111
32238299-6	2020	Moreover, CD2/CD3/CD28 stimulation of expanded iNKT cells augmented their (alpha-GalCer-independent) killing of Jurkat cells.	alpha-galactosylceramide	75-87	CD2 molecule	Homo sapiens	10-13
32349316-4	2020	Energy-dispersive X-ray spectroscopy (EDS) results indicate the partial replacement of Cd2+ by Ag+ when AgNO3 concentration is increased.	Silver Nitrate	104-109	CD2 molecule	Homo sapiens	87-90
32365912-3	2020	The obtained BiNPs/Ti3C2Tx nano-composite was applied for sensors construction of electrochemical detecting of Pb2+ and Cd2+ heavy metal ions.	Metals	131-136	CD2 molecule	Homo sapiens	120-123
32365912-6	2020	After conditions optimization, the BiNPs@Ti3C2Tx nano-sensor could detect Pb2+ and Cd2+ simultaneously and the detection limits were 10.8 nM for Pb2+ and 12.4 nM for Cd2+.	Lead(2+)	74-78	CD2 molecule	Homo sapiens	166-169
32365912-6	2020	After conditions optimization, the BiNPs@Ti3C2Tx nano-sensor could detect Pb2+ and Cd2+ simultaneously and the detection limits were 10.8 nM for Pb2+ and 12.4 nM for Cd2+.	Lead(2+)	145-149	CD2 molecule	Homo sapiens	83-86
32391500-0	2020	Tripeptide Derivative-Modified Glassy Carbon Electrode: A Novel Electrochemical Sensor for Sensitive and Selective Detection of Cd2+ Ions.	tripeptide K-26	0-10	CD2 molecule	Homo sapiens	128-131
32391500-0	2020	Tripeptide Derivative-Modified Glassy Carbon Electrode: A Novel Electrochemical Sensor for Sensitive and Selective Detection of Cd2+ Ions.	Carbon	38-44	CD2 molecule	Homo sapiens	128-131
32391500-4	2020	A sharp electrochemical signal of oxidized Cd at -0.84 V versus Ag/AgCl provides evidence for the higher sensing ability of Cbz-APL/GCE than bare GCE at -0.79 V. Moreover, on Cbz-APL/GCE, extraordinary low detection limits of 4.34 fM and linearity range of 15 nM to 0.1 pM with coefficients of correlation higher than 0.99 for Cd2+ were achieved.	Cadmium	43-45	CD2 molecule	Homo sapiens	327-330
32391500-4	2020	A sharp electrochemical signal of oxidized Cd at -0.84 V versus Ag/AgCl provides evidence for the higher sensing ability of Cbz-APL/GCE than bare GCE at -0.79 V. Moreover, on Cbz-APL/GCE, extraordinary low detection limits of 4.34 fM and linearity range of 15 nM to 0.1 pM with coefficients of correlation higher than 0.99 for Cd2+ were achieved.	GCE	132-135	CD2 molecule	Homo sapiens	327-330
32391500-5	2020	Besides, the influence of inorganic and organic interferents on the targeted analyte signals was examined, and high selectivity of Cbz-APL/GCE for Cd2+ ions was observed.	GCE	139-142	CD2 molecule	Homo sapiens	147-150
32391500-6	2020	Lastly, the validity and applicability of the developed electrochemical sensor for the detection of Cd2+ ions were checked in real water samples, and 100% recovery was obtained.	Water	131-136	CD2 molecule	Homo sapiens	100-103
32101795-0	2020	Fluorescence turn off-on probe (beta-cyclodextrin-hydroxyquinoline) for monitoring of Cd2+ ions and tetracycline.	beta-cyclodextrin-hydroxyquinoline	32-66	CD2 molecule	Homo sapiens	86-89
32053282-2	2020	The binding affinities obtained for the encapsulation of the planar PAHs guests in CD2 Cl2 are found to exponentially increase with the number of pi-electrons of the guest (1.3 > logK >6.6).	Polycyclic Aromatic Hydrocarbons	68-72	CD2 molecule	Homo sapiens	83-86
32237220-2	2020	Their protonation and binding ability for Cu2+ , Zn2+ , Cd2+ and Pb2+ have been studied by coupling potentiometric titrations with UV-vis absorption and fluorescence emission measurements in water.	Water	191-196	CD2 molecule	Homo sapiens	56-59
32101795-1	2020	In this paper, a photoluminescent turn off-on switch probe beta-cyclodextrin-hydroxyquinoline (beta-CD-HQ) was efficiently applied for detection and measurement of Cd2+ ions and detection of tetracycline.	beta-cyclodextrin-hydroxyquinoline	59-93	CD2 molecule	Homo sapiens	164-167
32101795-1	2020	In this paper, a photoluminescent turn off-on switch probe beta-cyclodextrin-hydroxyquinoline (beta-CD-HQ) was efficiently applied for detection and measurement of Cd2+ ions and detection of tetracycline.	beta-cd-hq	95-105	CD2 molecule	Homo sapiens	164-167
32101795-2	2020	The proposed assay has shown an excellent selective fluorescence response toward Cd2+ ions over other ions like Al3+, Pb2+, Zn2+, Co2+, K+, Na+ and Sr2+.	ALUMINUM ION	112-116	CD2 molecule	Homo sapiens	81-84
32101795-2	2020	The proposed assay has shown an excellent selective fluorescence response toward Cd2+ ions over other ions like Al3+, Pb2+, Zn2+, Co2+, K+, Na+ and Sr2+.	Lead(2+)	118-122	CD2 molecule	Homo sapiens	81-84
32101795-2	2020	The proposed assay has shown an excellent selective fluorescence response toward Cd2+ ions over other ions like Al3+, Pb2+, Zn2+, Co2+, K+, Na+ and Sr2+.	Zinc	124-128	CD2 molecule	Homo sapiens	81-84
32101795-2	2020	The proposed assay has shown an excellent selective fluorescence response toward Cd2+ ions over other ions like Al3+, Pb2+, Zn2+, Co2+, K+, Na+ and Sr2+.	Carbon Dioxide	130-134	CD2 molecule	Homo sapiens	81-84
32101795-2	2020	The proposed assay has shown an excellent selective fluorescence response toward Cd2+ ions over other ions like Al3+, Pb2+, Zn2+, Co2+, K+, Na+ and Sr2+.	strontium cation	148-152	CD2 molecule	Homo sapiens	81-84
32062486-6	2020	Cu2+ showed an antagonistic effect on the adsorption of Cd2+ and Ni2+, while Cd2+ and Ni2+ produced a synergistic effect on Cu2+.	cupric ion	124-128	CD2 molecule	Homo sapiens	77-80
32062486-8	2020	An increase in Ni2+ or Cd2+ concentrations plays a synergistic effect on the adsorption of Cu2+, while an antagonistic adsorption for Ni2+ occurred with increasing Cu2+ or Cd2+ concentrations.	cupric ion	91-95	CD2 molecule	Homo sapiens	23-26
32062486-1	2020	In this work, the interactions and adsorption mechanisms of Cu2+, Cd2+, and Ni2+ on boron nitride (BN) were tested by the simultaneous removal of metal ions from synthetic wastewater.	boron nitride	84-97	CD2 molecule	Homo sapiens	66-69
32062486-1	2020	In this work, the interactions and adsorption mechanisms of Cu2+, Cd2+, and Ni2+ on boron nitride (BN) were tested by the simultaneous removal of metal ions from synthetic wastewater.	boron nitride	99-101	CD2 molecule	Homo sapiens	66-69
32062486-8	2020	An increase in Ni2+ or Cd2+ concentrations plays a synergistic effect on the adsorption of Cu2+, while an antagonistic adsorption for Ni2+ occurred with increasing Cu2+ or Cd2+ concentrations.	Nickel(2+)	134-138	CD2 molecule	Homo sapiens	172-175
32062486-6	2020	Cu2+ showed an antagonistic effect on the adsorption of Cd2+ and Ni2+, while Cd2+ and Ni2+ produced a synergistic effect on Cu2+.	cupric ion	0-4	CD2 molecule	Homo sapiens	56-59
31732340-5	2020	Upon incorporating with ZnO NPs, the electrosorption efficiency was enhanced from 17% to 33% for Pb2+, from 21% to 29% for Cd2+ and from 21% to 35% for mixed Pb2+ and Cd2+ ions.	Zinc Oxide	24-27	CD2 molecule	Homo sapiens	123-126
32170528-5	2020	Three-dimensional surface analysis indicated increasing Cd2+ equilibrium concentration (Ceq) with Hg2+ and Pb2+ initial concentration (Ci), showing synergistic effect and low Cd2+ affinity to the solid phase.	2-(Trimethylsilyl)ethanol	88-91	CD2 molecule	Homo sapiens	56-59
32170528-5	2020	Three-dimensional surface analysis indicated increasing Cd2+ equilibrium concentration (Ceq) with Hg2+ and Pb2+ initial concentration (Ci), showing synergistic effect and low Cd2+ affinity to the solid phase.	2-(Trimethylsilyl)ethanol	88-91	CD2 molecule	Homo sapiens	175-178
32170528-5	2020	Three-dimensional surface analysis indicated increasing Cd2+ equilibrium concentration (Ceq) with Hg2+ and Pb2+ initial concentration (Ci), showing synergistic effect and low Cd2+ affinity to the solid phase.	Mercuric cation	98-102	CD2 molecule	Homo sapiens	56-59
32170528-5	2020	Three-dimensional surface analysis indicated increasing Cd2+ equilibrium concentration (Ceq) with Hg2+ and Pb2+ initial concentration (Ci), showing synergistic effect and low Cd2+ affinity to the solid phase.	Lead	107-111	CD2 molecule	Homo sapiens	56-59
32170528-7	2020	After integrating the sorption and desorption fluorescence peaks, the MF for Cd2+, Pb2+, and Hg2+ was around 0.2, 0.5, and 0.1 in riverbank sediment, and 0.3, 0.9, and 0.1 in sediment, respectively.	Lead	83-87	CD2 molecule	Homo sapiens	77-80
31732340-5	2020	Upon incorporating with ZnO NPs, the electrosorption efficiency was enhanced from 17% to 33% for Pb2+, from 21% to 29% for Cd2+ and from 21% to 35% for mixed Pb2+ and Cd2+ ions.	Zinc Oxide	24-27	CD2 molecule	Homo sapiens	167-170
31753647-0	2020	Rapid ratiometric detection of Cd2+ based on the formation of ZnSe/CdS quantum dots.	Zinc	62-66	CD2 molecule	Homo sapiens	31-34
31753647-0	2020	Rapid ratiometric detection of Cd2+ based on the formation of ZnSe/CdS quantum dots.	Cadmium	67-70	CD2 molecule	Homo sapiens	31-34
31753647-2	2020	Here, we establish a simple, rapid and ratiometric strategy for the recognition of Cd2+ based on the formation of core-shell ZnSe/CdS structure using ZnSe quantum dots (QDs).	Zinc	125-129	CD2 molecule	Homo sapiens	83-86
31753647-2	2020	Here, we establish a simple, rapid and ratiometric strategy for the recognition of Cd2+ based on the formation of core-shell ZnSe/CdS structure using ZnSe quantum dots (QDs).	Cadmium	130-133	CD2 molecule	Homo sapiens	83-86
31753647-2	2020	Here, we establish a simple, rapid and ratiometric strategy for the recognition of Cd2+ based on the formation of core-shell ZnSe/CdS structure using ZnSe quantum dots (QDs).	Zinc	150-154	CD2 molecule	Homo sapiens	83-86
31753647-4	2020	In the detection process, ZnSe QDs only possess absorption peak at 343 nm, the formation of ZnSe/CdS after the addition of Cd2+ leads to the appearance of the new peak at 397 nm, while other heavy metal ions could not cause the appearance of new absorption peak.	Zinc	26-30	CD2 molecule	Homo sapiens	123-126
31753647-4	2020	In the detection process, ZnSe QDs only possess absorption peak at 343 nm, the formation of ZnSe/CdS after the addition of Cd2+ leads to the appearance of the new peak at 397 nm, while other heavy metal ions could not cause the appearance of new absorption peak.	Zinc	92-96	CD2 molecule	Homo sapiens	123-126
31753647-4	2020	In the detection process, ZnSe QDs only possess absorption peak at 343 nm, the formation of ZnSe/CdS after the addition of Cd2+ leads to the appearance of the new peak at 397 nm, while other heavy metal ions could not cause the appearance of new absorption peak.	Cadmium	97-100	CD2 molecule	Homo sapiens	123-126
30102121-0	2020	Fixed-bed column system for Cd2+ uptake from aqueous solution by sodium- and thiourea-modified clinoptilolite-rich tuff.	Sodium	65-71	CD2 molecule	Homo sapiens	28-31
33558934-1	2020	Theoretical studies on conformational analysis, geometry optimizations and frequencies for citrate at the MP2/LANL2DZ level portrait it as a promising candidate for a complexing agent for cadmium (II) ion (Cd2+) and cadmium sulfide (CdS).	Citric Acid	91-98	CD2 molecule	Homo sapiens	206-209
33558934-1	2020	Theoretical studies on conformational analysis, geometry optimizations and frequencies for citrate at the MP2/LANL2DZ level portrait it as a promising candidate for a complexing agent for cadmium (II) ion (Cd2+) and cadmium sulfide (CdS).	cadmium (ii)	188-200	CD2 molecule	Homo sapiens	206-209
33558934-3	2020	The most stable structures involved the interaction between the LUMO of Cd2+/CdS and the most dense region of the HOMO of the citrate ion.	cadmium sulfide	77-80	CD2 molecule	Homo sapiens	72-75
33558934-3	2020	The most stable structures involved the interaction between the LUMO of Cd2+/CdS and the most dense region of the HOMO of the citrate ion.	Citric Acid	126-133	CD2 molecule	Homo sapiens	72-75
30102121-0	2020	Fixed-bed column system for Cd2+ uptake from aqueous solution by sodium- and thiourea-modified clinoptilolite-rich tuff.	Thiourea	77-85	CD2 molecule	Homo sapiens	28-31
30102121-0	2020	Fixed-bed column system for Cd2+ uptake from aqueous solution by sodium- and thiourea-modified clinoptilolite-rich tuff.	clinoptilolite	95-109	CD2 molecule	Homo sapiens	28-31
30102121-0	2020	Fixed-bed column system for Cd2+ uptake from aqueous solution by sodium- and thiourea-modified clinoptilolite-rich tuff.	tuff	115-119	CD2 molecule	Homo sapiens	28-31
30102121-8	2020	The zeolite modified with thiourea exhibited higher capacity in Cd2+ removal than the one modified with NaCl, in the column with 6 cm of bed height.	Zeolites	4-11	CD2 molecule	Homo sapiens	64-67
30102121-8	2020	The zeolite modified with thiourea exhibited higher capacity in Cd2+ removal than the one modified with NaCl, in the column with 6 cm of bed height.	Thiourea	26-34	CD2 molecule	Homo sapiens	64-67
32073022-8	2020	Due to the presence of various side-chain functional groups (e.g., amino, carboxyl, and sulfhydryl) on the surface of the poly(amino acid)s, these micromotors can be used as effective scavengers for the removal of heavy metals (i.e., Cd2+, Pb2+ and methylmercury).	poly(amino acid)	122-138	CD2 molecule	Homo sapiens	234-237
32187841-3	2020	Additionally, more electron-deficient pyridyls preferentially coordinated to the flanking Cd2+ of the Cd5 SBU, as exemplified by [Et2 NH2 ]2 [Cd5 (BTB)4 (DEF)2 (PyCHO)2 ]   xSol (2 a, PyCHO=4-pyridinealdehyde) and [Et2 NH2 ]2 [Cd5 (BTB)4 (DEF)2 (PyAc)2 ]   xSol (2 b, PyAc=4-acetylpyridine).	4-Pyridinecarboxaldehyde	190-208	CD2 molecule	Homo sapiens	90-93
32187841-3	2020	Additionally, more electron-deficient pyridyls preferentially coordinated to the flanking Cd2+ of the Cd5 SBU, as exemplified by [Et2 NH2 ]2 [Cd5 (BTB)4 (DEF)2 (PyCHO)2 ]   xSol (2 a, PyCHO=4-pyridinealdehyde) and [Et2 NH2 ]2 [Cd5 (BTB)4 (DEF)2 (PyAc)2 ]   xSol (2 b, PyAc=4-acetylpyridine).	pyac	246-250	CD2 molecule	Homo sapiens	90-93
32187841-3	2020	Additionally, more electron-deficient pyridyls preferentially coordinated to the flanking Cd2+ of the Cd5 SBU, as exemplified by [Et2 NH2 ]2 [Cd5 (BTB)4 (DEF)2 (PyCHO)2 ]   xSol (2 a, PyCHO=4-pyridinealdehyde) and [Et2 NH2 ]2 [Cd5 (BTB)4 (DEF)2 (PyAc)2 ]   xSol (2 b, PyAc=4-acetylpyridine).	4-acetylpyridine	273-289	CD2 molecule	Homo sapiens	90-93
32187841-3	2020	Additionally, more electron-deficient pyridyls preferentially coordinated to the flanking Cd2+ of the Cd5 SBU, as exemplified by [Et2 NH2 ]2 [Cd5 (BTB)4 (DEF)2 (PyCHO)2 ]   xSol (2 a, PyCHO=4-pyridinealdehyde) and [Et2 NH2 ]2 [Cd5 (BTB)4 (DEF)2 (PyAc)2 ]   xSol (2 b, PyAc=4-acetylpyridine).	pyridyls	38-46	CD2 molecule	Homo sapiens	90-93
32187841-3	2020	Additionally, more electron-deficient pyridyls preferentially coordinated to the flanking Cd2+ of the Cd5 SBU, as exemplified by [Et2 NH2 ]2 [Cd5 (BTB)4 (DEF)2 (PyCHO)2 ]   xSol (2 a, PyCHO=4-pyridinealdehyde) and [Et2 NH2 ]2 [Cd5 (BTB)4 (DEF)2 (PyAc)2 ]   xSol (2 b, PyAc=4-acetylpyridine).	sbu	106-109	CD2 molecule	Homo sapiens	90-93
31892044-4	2020	Cadmium ions (Cd2+) were used as signal units and also signal amplification substance which labeled before on miR-21 target.	Cadmium	0-7	CD2 molecule	Homo sapiens	14-17
32073022-8	2020	Due to the presence of various side-chain functional groups (e.g., amino, carboxyl, and sulfhydryl) on the surface of the poly(amino acid)s, these micromotors can be used as effective scavengers for the removal of heavy metals (i.e., Cd2+, Pb2+ and methylmercury).	Sulfur	14-15	CD2 molecule	Homo sapiens	234-237
31989982-6	2020	The results showed that the KMnO4-modification resulted in a successful loading of the vermicompost biochar with MnO2, which greatly improved its adsorption capacity for Cd2+.	Superoxides	28-33	CD2 molecule	Homo sapiens	170-173
31685320-2	2020	However, the effective and irreversible removal of Cd2+, coupled with a high uptake efficiency, remains a great challenge due to the relatively low bond dissociation energy of CdS.	Cadmium	176-179	CD2 molecule	Homo sapiens	51-54
31989982-6	2020	The results showed that the KMnO4-modification resulted in a successful loading of the vermicompost biochar with MnO2, which greatly improved its adsorption capacity for Cd2+.	Manganese	113-117	CD2 molecule	Homo sapiens	170-173
31989982-10	2020	Hence, KMnO4 modification has a significant effect on the Cd2+ adsorption behavior of vermicompost biochar.	Superoxides	7-12	CD2 molecule	Homo sapiens	58-61
31685320-3	2020	Herein, we propose a new strategy to overcome this challenge, by the incorporation of Cd2+ into a stable ZnxCd1-xS solid solution, rather than into CdS.	znxcd1-xs	105-114	CD2 molecule	Homo sapiens	86-89
31550667-3	2020	The novel mesoporous zeolite Beta (mBeta) can be used as adsorbent to remove the heavy metal ions (i.e., Cd2+ and/or Zn2+) from wastewater due to its excellent adsorptive performance from the electrostatic affinity, ion-exchange ability and structural channels in zeolite.	Zeolites	21-33	CD2 molecule	Homo sapiens	105-108
31685320-4	2020	This can be realised through the adsorption of Cd2+ by ZnS nanoparticles, which have exhibited a Cd2+ uptake capacity of approximate 400 mg g-1.	Zinc	55-58	CD2 molecule	Homo sapiens	47-50
31685320-4	2020	This can be realised through the adsorption of Cd2+ by ZnS nanoparticles, which have exhibited a Cd2+ uptake capacity of approximate 400 mg g-1.	Zinc	55-58	CD2 molecule	Homo sapiens	97-100
31685320-5	2020	Through this adsorption mechanism, the Cd2+ concentration in a contaminated solution could effectively be reduced from 50 ppb to <3 ppb, a WHO limit acceptable for drinking water.	Water	173-178	CD2 molecule	Homo sapiens	39-42
31685320-9	2020	This work reveals a new mechanism for Cd2+ removal with ZnS and establishes a valuable starting point for further studies into the formation of solid solutions for hazardous heavy metal removal applications.	Zinc	56-59	CD2 molecule	Homo sapiens	38-41
31670044-0	2020	A highly sensitive fluorescent sensor for Cd2+ and Zn2+ based on diarylethene with a pyrene unit.	diarylethene	65-77	CD2 molecule	Homo sapiens	42-45
31670044-0	2020	A highly sensitive fluorescent sensor for Cd2+ and Zn2+ based on diarylethene with a pyrene unit.	pyrene	85-91	CD2 molecule	Homo sapiens	42-45
31670044-3	2020	Diarylethene fluorescence sensor 1O has high selectivity and sensitivity for the detections of Cd2+ and Zn2+.	diarylethene	0-12	CD2 molecule	Homo sapiens	95-98
31670044-5	2020	The binding constants (Ka) of 1O with Cd2+ and Zn2+ in acetonitrile solution were calculated to be 5.8 x 104 mol-1 L and 6.0 x 104 mol-1 L, respectively.	acetonitrile	55-67	CD2 molecule	Homo sapiens	38-41
31670044-6	2020	The compound 1O responded to the metal ions (Cd2+/Zn2+) to form complexations with 1 : 1 stoichiometry which were verified by Job"s plot and MS analysis, respectively.	Zinc	50-54	CD2 molecule	Homo sapiens	45-48
31550667-3	2020	The novel mesoporous zeolite Beta (mBeta) can be used as adsorbent to remove the heavy metal ions (i.e., Cd2+ and/or Zn2+) from wastewater due to its excellent adsorptive performance from the electrostatic affinity, ion-exchange ability and structural channels in zeolite.	Zeolites	21-28	CD2 molecule	Homo sapiens	105-108
31594563-2	2020	Herein, glutathione (GSH) calibrated dual-functional system for GSH and cadmium ions (Cd2+) detection based on fluorescence resonance energy transfer (FRET) between NH2-NaYF4:Yb,Er/NaYF4@SiO2 upconversion nanoparticles (UCNPs) and gold nanoparticles (AuNPs) is designed.	Glutathione	8-19	CD2 molecule	Homo sapiens	86-89
31883592-8	2020	The fluorescence detection was implemented since free Cd2+ could trigger the weak fluorescence metal-sensitive dyes (Rhod-5N) to generate extremely high fluorescence signal.	Metals	95-100	CD2 molecule	Homo sapiens	54-57
31594563-2	2020	Herein, glutathione (GSH) calibrated dual-functional system for GSH and cadmium ions (Cd2+) detection based on fluorescence resonance energy transfer (FRET) between NH2-NaYF4:Yb,Er/NaYF4@SiO2 upconversion nanoparticles (UCNPs) and gold nanoparticles (AuNPs) is designed.	Glutathione	21-24	CD2 molecule	Homo sapiens	86-89
31594563-2	2020	Herein, glutathione (GSH) calibrated dual-functional system for GSH and cadmium ions (Cd2+) detection based on fluorescence resonance energy transfer (FRET) between NH2-NaYF4:Yb,Er/NaYF4@SiO2 upconversion nanoparticles (UCNPs) and gold nanoparticles (AuNPs) is designed.	Glutathione	64-67	CD2 molecule	Homo sapiens	86-89
31594563-2	2020	Herein, glutathione (GSH) calibrated dual-functional system for GSH and cadmium ions (Cd2+) detection based on fluorescence resonance energy transfer (FRET) between NH2-NaYF4:Yb,Er/NaYF4@SiO2 upconversion nanoparticles (UCNPs) and gold nanoparticles (AuNPs) is designed.	Cadmium	72-79	CD2 molecule	Homo sapiens	86-89
31594563-2	2020	Herein, glutathione (GSH) calibrated dual-functional system for GSH and cadmium ions (Cd2+) detection based on fluorescence resonance energy transfer (FRET) between NH2-NaYF4:Yb,Er/NaYF4@SiO2 upconversion nanoparticles (UCNPs) and gold nanoparticles (AuNPs) is designed.	Sodium	165-177	CD2 molecule	Homo sapiens	86-89
31594563-2	2020	Herein, glutathione (GSH) calibrated dual-functional system for GSH and cadmium ions (Cd2+) detection based on fluorescence resonance energy transfer (FRET) between NH2-NaYF4:Yb,Er/NaYF4@SiO2 upconversion nanoparticles (UCNPs) and gold nanoparticles (AuNPs) is designed.	Silicon	187-191	CD2 molecule	Homo sapiens	86-89
31594563-5	2020	However, Cd2+ can interact with GSH, which makes AuNPs easy to aggregate, resulting in a gradual decrease in red emission of UCNPs.	Glutathione	32-35	CD2 molecule	Homo sapiens	9-12
31594563-7	2020	Furthermore, the nanosensor demonstrates high selectivity for GSH and Cd2+ detection and can be applied for the detection of GSH in human plasma and Cd2+ in drinking water.	Glutathione	62-65	CD2 molecule	Homo sapiens	149-152
31594563-7	2020	Furthermore, the nanosensor demonstrates high selectivity for GSH and Cd2+ detection and can be applied for the detection of GSH in human plasma and Cd2+ in drinking water.	Glutathione	125-128	CD2 molecule	Homo sapiens	70-73
31829357-3	2020	By controlling the concentration of Cd2+ to control the reaction environment (pH value) and reaction rate, the CdSe nanocrystal is overgrown on the side or tip of the Au nanorods, which leads to a strong interaction between the excitons of CdSe nanocrystals and the plasmons of Au nanorods.	cadmium selenide	111-115	CD2 molecule	Homo sapiens	36-39
31829357-3	2020	By controlling the concentration of Cd2+ to control the reaction environment (pH value) and reaction rate, the CdSe nanocrystal is overgrown on the side or tip of the Au nanorods, which leads to a strong interaction between the excitons of CdSe nanocrystals and the plasmons of Au nanorods.	Gold	167-169	CD2 molecule	Homo sapiens	36-39
31829357-3	2020	By controlling the concentration of Cd2+ to control the reaction environment (pH value) and reaction rate, the CdSe nanocrystal is overgrown on the side or tip of the Au nanorods, which leads to a strong interaction between the excitons of CdSe nanocrystals and the plasmons of Au nanorods.	cadmium selenide	240-244	CD2 molecule	Homo sapiens	36-39
31829357-3	2020	By controlling the concentration of Cd2+ to control the reaction environment (pH value) and reaction rate, the CdSe nanocrystal is overgrown on the side or tip of the Au nanorods, which leads to a strong interaction between the excitons of CdSe nanocrystals and the plasmons of Au nanorods.	Gold	278-280	CD2 molecule	Homo sapiens	36-39
31956813-0	2020	Solid-State Chemiresistors from Two-Dimensional MoS2 Nanosheets Functionalized with l-Cysteine for In-Line Sensing of Part-Per-Billion Cd2+ Ions in Drinking Water.	Cysteine	84-94	CD2 molecule	Homo sapiens	135-138
31935902-2	2020	The APDC etchant combines with the cadmium ions (Cd2+) on the surface of the QDs, resulting in the formation of surface holes.	pyrrolidine dithiocarbamic acid	4-8	CD2 molecule	Homo sapiens	49-52
31935902-2	2020	The APDC etchant combines with the cadmium ions (Cd2+) on the surface of the QDs, resulting in the formation of surface holes.	Cadmium	35-42	CD2 molecule	Homo sapiens	49-52
31526996-10	2020	The amidocyanogen group of BS-CT-MBt inhibited adsorption of Cd2+ due to electrostatic repulsion, while Cd2+ was adsorbed on BS-SDS-MBt through electrostatic attraction induced by the sulfo group.	Sodium Dodecyl Sulfate	128-131	CD2 molecule	Homo sapiens	104-107
31526996-10	2020	The amidocyanogen group of BS-CT-MBt inhibited adsorption of Cd2+ due to electrostatic repulsion, while Cd2+ was adsorbed on BS-SDS-MBt through electrostatic attraction induced by the sulfo group.	sulfo	184-189	CD2 molecule	Homo sapiens	104-107
31634706-0	2020	Transport of Cd2+ through saturated porous media: Insight into the effects of low-molecular-weight organic acids.	organic acids	99-112	CD2 molecule	Homo sapiens	13-16
31634706-5	2020	Under acidic conditions (pH 5.0), the results indicated that LMWOAs inhibited the transport of Cd2+ even at the low concentrations of organic acids (i.e., 0.05 and 0.1 mM).	organic acids	134-147	CD2 molecule	Homo sapiens	95-98
31829381-2	2020	The compositional and structural studies revealed that the cationic substitution of Cd2+ by Ni2+ ions leads to a monotonic shift in the (220) diffraction peak, indicating the suppression of lattice distortion, while the evolution of local strain with an increase in Ni concentration is mainly associated with the mismatch in the electronegativity of the Cd2+ and Ni2+ ions.	Nickel	92-96	CD2 molecule	Homo sapiens	84-87
31829381-2	2020	The compositional and structural studies revealed that the cationic substitution of Cd2+ by Ni2+ ions leads to a monotonic shift in the (220) diffraction peak, indicating the suppression of lattice distortion, while the evolution of local strain with an increase in Ni concentration is mainly associated with the mismatch in the electronegativity of the Cd2+ and Ni2+ ions.	Nickel	92-96	CD2 molecule	Homo sapiens	354-357
31829381-2	2020	The compositional and structural studies revealed that the cationic substitution of Cd2+ by Ni2+ ions leads to a monotonic shift in the (220) diffraction peak, indicating the suppression of lattice distortion, while the evolution of local strain with an increase in Ni concentration is mainly associated with the mismatch in the electronegativity of the Cd2+ and Ni2+ ions.	Nickel	363-367	CD2 molecule	Homo sapiens	84-87
32500809-4	2020	Especially, with the presence of laccase, the removal rate of phenanthrene on Cu2+-contaminated soil was higher than that of Cd2+-contaminated soil due to the significant effect of heavy metals on the enzymatic activity of laccase.	phenanthrene	62-74	CD2 molecule	Homo sapiens	125-128
32500809-4	2020	Especially, with the presence of laccase, the removal rate of phenanthrene on Cu2+-contaminated soil was higher than that of Cd2+-contaminated soil due to the significant effect of heavy metals on the enzymatic activity of laccase.	cupric ion	78-82	CD2 molecule	Homo sapiens	125-128
31785447-3	2020	The probe is showing a strong change in color from yellow to red on treatment of Cd(II) ions, interestingly its shows bright "Switch-ON" fluorescence state upon binding of Cd2+ ions in buffer solution whereas other cations did not showed any color change as well as fluorescent change.	Cadmium	81-87	CD2 molecule	Homo sapiens	172-175
31634706-7	2020	Meanwhile, the inhibition effects of LMWOAs on Cd2+ transport in the following order of citric acid > tartaric acid > acetic acid, which was also in agreement with the decreasing complex stability constants between Cd2+ and LMWOAs.	Citric Acid	88-99	CD2 molecule	Homo sapiens	47-50
31634706-7	2020	Meanwhile, the inhibition effects of LMWOAs on Cd2+ transport in the following order of citric acid > tartaric acid > acetic acid, which was also in agreement with the decreasing complex stability constants between Cd2+ and LMWOAs.	Citric Acid	88-99	CD2 molecule	Homo sapiens	215-218
31634706-7	2020	Meanwhile, the inhibition effects of LMWOAs on Cd2+ transport in the following order of citric acid > tartaric acid > acetic acid, which was also in agreement with the decreasing complex stability constants between Cd2+ and LMWOAs.	tartaric acid	102-115	CD2 molecule	Homo sapiens	47-50
31634706-7	2020	Meanwhile, the inhibition effects of LMWOAs on Cd2+ transport in the following order of citric acid > tartaric acid > acetic acid, which was also in agreement with the decreasing complex stability constants between Cd2+ and LMWOAs.	Acetic Acid	118-129	CD2 molecule	Homo sapiens	47-50
31634706-7	2020	Meanwhile, the inhibition effects of LMWOAs on Cd2+ transport in the following order of citric acid > tartaric acid > acetic acid, which was also in agreement with the decreasing complex stability constants between Cd2+ and LMWOAs.	Acetic Acid	118-129	CD2 molecule	Homo sapiens	215-218
31634706-9	2020	Interestingly, when the LMWOA concentrations 0.5 mM, tartaric acid and citric acid still inhibited Cd2+ transport, while acetic acid slightly enhanced the Cd2+ mobility due to its weaker complexing strength.	tartaric acid	53-66	CD2 molecule	Homo sapiens	99-102
31956813-6	2020	Two-terminal chemiresistors incorporating MoS2-Cys films are demonstrated to be preferentially sensitive to Cd2+ ions at neutral pH, irrespective of other metal ions present in water flowing through the device.	Cysteine	47-50	CD2 molecule	Homo sapiens	108-111
31634706-9	2020	Interestingly, when the LMWOA concentrations 0.5 mM, tartaric acid and citric acid still inhibited Cd2+ transport, while acetic acid slightly enhanced the Cd2+ mobility due to its weaker complexing strength.	Citric Acid	71-82	CD2 molecule	Homo sapiens	99-102
31956813-9	2020	Cd2+ is selectively detected because of preferential, size-driven adsorption at the interstitials between l-cysteine functional groups, combined with pH-controlled charge transfer that removes electronic gap states from MoS2.	Cysteine	106-116	CD2 molecule	Homo sapiens	0-3
31634706-9	2020	Interestingly, when the LMWOA concentrations 0.5 mM, tartaric acid and citric acid still inhibited Cd2+ transport, while acetic acid slightly enhanced the Cd2+ mobility due to its weaker complexing strength.	Acetic Acid	121-132	CD2 molecule	Homo sapiens	155-158
31768591-0	2019	Simultaneous analysis of Pb2+ and Cd2+ at graphene/bismuth nanocomposite film-modified pencil graphite electrode using square wave anodic stripping voltammetry.	Graphite	42-50	CD2 molecule	Homo sapiens	34-37
31634706-12	2020	In addition, citric acid could obviously inhibit the transport of Cd2+ under competitive transport conditions (i.e., with competing cations), which is mainly due to different complex affinities of citric acid to Pb2+ and Cd2+.	Citric Acid	13-24	CD2 molecule	Homo sapiens	66-69
31634706-12	2020	In addition, citric acid could obviously inhibit the transport of Cd2+ under competitive transport conditions (i.e., with competing cations), which is mainly due to different complex affinities of citric acid to Pb2+ and Cd2+.	Citric Acid	13-24	CD2 molecule	Homo sapiens	221-224
31634706-12	2020	In addition, citric acid could obviously inhibit the transport of Cd2+ under competitive transport conditions (i.e., with competing cations), which is mainly due to different complex affinities of citric acid to Pb2+ and Cd2+.	Citric Acid	197-208	CD2 molecule	Homo sapiens	66-69
31634706-12	2020	In addition, citric acid could obviously inhibit the transport of Cd2+ under competitive transport conditions (i.e., with competing cations), which is mainly due to different complex affinities of citric acid to Pb2+ and Cd2+.	Citric Acid	197-208	CD2 molecule	Homo sapiens	221-224
31634706-12	2020	In addition, citric acid could obviously inhibit the transport of Cd2+ under competitive transport conditions (i.e., with competing cations), which is mainly due to different complex affinities of citric acid to Pb2+ and Cd2+.	Lead	212-216	CD2 molecule	Homo sapiens	66-69
31811219-3	2019	The bare and modified graphite electrodes were used as the working electrode in anodic stripping voltammetry for the determination of trace amounts of cadmium (Cd2+) and lead (Pb2+).	Graphite	22-30	CD2 molecule	Homo sapiens	160-163
31811219-3	2019	The bare and modified graphite electrodes were used as the working electrode in anodic stripping voltammetry for the determination of trace amounts of cadmium (Cd2+) and lead (Pb2+).	Cadmium	151-158	CD2 molecule	Homo sapiens	160-163
31768591-3	2019	A linear relationship between peak current and concentration was obtained in the range between 5-100 mug L-1 for both Cd2+ and Pb2+, with detection limits of 0.12 mug L-1 for Cd2+ and 0.29 mug L-1 for Pb2+.	Lead	201-205	CD2 molecule	Homo sapiens	118-121
31768591-0	2019	Simultaneous analysis of Pb2+ and Cd2+ at graphene/bismuth nanocomposite film-modified pencil graphite electrode using square wave anodic stripping voltammetry.	Bismuth	51-58	CD2 molecule	Homo sapiens	34-37
31768591-0	2019	Simultaneous analysis of Pb2+ and Cd2+ at graphene/bismuth nanocomposite film-modified pencil graphite electrode using square wave anodic stripping voltammetry.	Graphite	94-102	CD2 molecule	Homo sapiens	34-37
31499115-0	2019	A novel and biocompatible Fe3O4 loaded chitosan polyelectrolyte nanoparticles for the removal of Cd2+ ion.	ferryl iron	26-31	CD2 molecule	Homo sapiens	97-100
31545187-1	2019	We successfully absorbed the copper ion (Cu2+) and cadmium ion (Cd2+) from alkaline aqueous solutions using the prepared chitosan-tannin (CTS/TA) functional paper as absorbent materials.	Cadmium	51-58	CD2 molecule	Homo sapiens	64-67
31545187-3	2019	The adsorption data were described well by Langmuir isotherms, with maximum copper (Cu2+) and cadmium (Cd2+) adsorption capacities of 684.93 and 813.01 mg/m2, respectively.	Cadmium	94-101	CD2 molecule	Homo sapiens	103-106
31545187-4	2019	The experimental results also showed that the adsorption of these heavy metals was selective in the order of Cu2+ > Cd2+, as Cu2+ competed with Cd2+ for bonding sites at solution concentrations greater than or equal to 200 mg/L.	cupric ion	109-113	CD2 molecule	Homo sapiens	144-147
31545187-4	2019	The experimental results also showed that the adsorption of these heavy metals was selective in the order of Cu2+ > Cd2+, as Cu2+ competed with Cd2+ for bonding sites at solution concentrations greater than or equal to 200 mg/L.	cupric ion	125-129	CD2 molecule	Homo sapiens	116-119
31714762-3	2019	Cs2Cd(C2H)2(C2) is composed of Cd2+ cations tetrahedrally coordinated end-on by four acetylide groups.	propadienylidene	0-15	CD2 molecule	Homo sapiens	31-34
31499115-1	2019	In this work, Fe3O4 loaded chitosan (CS) nanoparticles (NPs) and microparticles (MPs) were synthesized based on ionic gelation technology for the removal of Cd2+ ion.	ferryl iron	14-19	CD2 molecule	Homo sapiens	157-160
31499115-1	2019	In this work, Fe3O4 loaded chitosan (CS) nanoparticles (NPs) and microparticles (MPs) were synthesized based on ionic gelation technology for the removal of Cd2+ ion.	Chitosan	37-39	CD2 molecule	Homo sapiens	157-160
31499115-3	2019	The results showed that particle size of Fe3O4 loaded CS NPs and MPs was in the range of 164.05-768.69 nm, and the former showed relatively higher adsorption capacities (97.86 mg/g) on Cd2+ ion than the latter after 90 min at pH 5.0 for the solutions with initial Cd2+ ion of 100 mg/L, respectively.	ferryl iron	41-46	CD2 molecule	Homo sapiens	185-188
31499115-3	2019	The results showed that particle size of Fe3O4 loaded CS NPs and MPs was in the range of 164.05-768.69 nm, and the former showed relatively higher adsorption capacities (97.86 mg/g) on Cd2+ ion than the latter after 90 min at pH 5.0 for the solutions with initial Cd2+ ion of 100 mg/L, respectively.	ferryl iron	41-46	CD2 molecule	Homo sapiens	264-267
31844778-0	2019	Fabrication of nanofibers using sodium alginate and Poly(Vinyl alcohol) for the removal of Cd2+ ions from aqueous solutions: adsorption mechanism, kinetics and thermodynamics.	sodium alginate	32-47	CD2 molecule	Homo sapiens	91-94
31732211-10	2019	Further, ATG decreases CD2, CD3, CD4, and naive (CD45RA) and stimulates T cells as translated by CD3CD69 and DR. As it should be expected from an IL-2alphaRAb agent, CD25 cells were virtually eliminated.	Antilymphocyte Serum	9-12	CD2 molecule	Homo sapiens	23-26
31781982-5	2019	The adsorption isotherm of Cd2+ on Fe3O4@PDA was in agreement with the Freundlich model, with the maximum adsorption capacity of 21.58 mg/g.	ferryl iron	35-40	CD2 molecule	Homo sapiens	27-30
31844778-0	2019	Fabrication of nanofibers using sodium alginate and Poly(Vinyl alcohol) for the removal of Cd2+ ions from aqueous solutions: adsorption mechanism, kinetics and thermodynamics.	ethylene-vinyl alcohol copolymer	52-71	CD2 molecule	Homo sapiens	91-94
31739390-2	2019	In this study, Brassia campestris L. was used as the experimental material and polluted soil with cadmium was used as the experimental soil sample, to explore the competition inhibition of calcium polypeptide application on the absorption of Cd2+ by Brassia campestris L. in the growth process, as well as the effect of calcium application on the growth.	Calcium	189-196	CD2 molecule	Homo sapiens	242-245
31634999-6	2019	After beta-CD loading, the adsorption saturation of zeolite for Cd2+ and Pb2+ are 93.06 and 175.25 mg/g, respectively.	beta-Cyclodextrins	6-13	CD2 molecule	Homo sapiens	64-67
31634999-6	2019	After beta-CD loading, the adsorption saturation of zeolite for Cd2+ and Pb2+ are 93.06 and 175.25 mg/g, respectively.	Zeolites	52-59	CD2 molecule	Homo sapiens	64-67
31634999-7	2019	The adsorption saturation of Cd2+ and Pd2+ by beta-CD-loaded vermiculite is 68.65 and 126.35 mg/g, respectively.	beta-Cyclodextrins	46-53	CD2 molecule	Homo sapiens	29-32
31493760-2	2019	In this study, molybdenum (Mo) and sulphur (S) were simultaneously introduced onto the surface of oxygen-doped graphitic carbon nitride (OCN) for the enhancement of Cd2+ adsorption.	Oxygen	98-104	CD2 molecule	Homo sapiens	165-168
31493760-2	2019	In this study, molybdenum (Mo) and sulphur (S) were simultaneously introduced onto the surface of oxygen-doped graphitic carbon nitride (OCN) for the enhancement of Cd2+ adsorption.	graphitic carbon nitride	111-135	CD2 molecule	Homo sapiens	165-168
31493760-2	2019	In this study, molybdenum (Mo) and sulphur (S) were simultaneously introduced onto the surface of oxygen-doped graphitic carbon nitride (OCN) for the enhancement of Cd2+ adsorption.	ocn	137-140	CD2 molecule	Homo sapiens	165-168
31493760-5	2019	MoO3 and MoS2 on the surface of OCN were proven to interact with Cd2+ by forming CdMoO4 and CdS species.	molybdenum trioxide	0-4	CD2 molecule	Homo sapiens	65-68
31493760-5	2019	MoO3 and MoS2 on the surface of OCN were proven to interact with Cd2+ by forming CdMoO4 and CdS species.	molybdenum disulfide	9-13	CD2 molecule	Homo sapiens	65-68
31493760-5	2019	MoO3 and MoS2 on the surface of OCN were proven to interact with Cd2+ by forming CdMoO4 and CdS species.	ocn	32-35	CD2 molecule	Homo sapiens	65-68
31493760-5	2019	MoO3 and MoS2 on the surface of OCN were proven to interact with Cd2+ by forming CdMoO4 and CdS species.	cdmoo4	81-87	CD2 molecule	Homo sapiens	65-68
31493760-5	2019	MoO3 and MoS2 on the surface of OCN were proven to interact with Cd2+ by forming CdMoO4 and CdS species.	Cadmium	92-95	CD2 molecule	Homo sapiens	65-68
31739390-4	2019	There was a significantly negative correlation between Cd concentration in Brassia campestris L. and calcium application (r = -0.99, p < 0.01) when calcium polypeptide was over-applied, which indicates that the inhibition effect of Cd2+ absorption on Brassia campestris L. is mainly through competitive inhibition rather than passivation.	Cadmium	55-57	CD2 molecule	Homo sapiens	232-235
31739390-4	2019	There was a significantly negative correlation between Cd concentration in Brassia campestris L. and calcium application (r = -0.99, p < 0.01) when calcium polypeptide was over-applied, which indicates that the inhibition effect of Cd2+ absorption on Brassia campestris L. is mainly through competitive inhibition rather than passivation.	Calcium	101-108	CD2 molecule	Homo sapiens	232-235
31739390-4	2019	There was a significantly negative correlation between Cd concentration in Brassia campestris L. and calcium application (r = -0.99, p < 0.01) when calcium polypeptide was over-applied, which indicates that the inhibition effect of Cd2+ absorption on Brassia campestris L. is mainly through competitive inhibition rather than passivation.	Calcium	148-155	CD2 molecule	Homo sapiens	232-235
31717598-1	2019	Enrichment of cadmium ion (Cd2+) from the environment may lead to kidney disease and weakened immunity in the body.	Cadmium	14-21	CD2 molecule	Homo sapiens	27-30
31409471-4	2019	Interfacial cation exchange amplification was triggered in hydrogel upon the introduction of Ag+ and Rhod-5N, and abundant Cd2+ was released from CdS to bind with Rhod-5N for substantial fluorescence enhancement.	Cadmium	146-149	CD2 molecule	Homo sapiens	123-126
31409471-4	2019	Interfacial cation exchange amplification was triggered in hydrogel upon the introduction of Ag+ and Rhod-5N, and abundant Cd2+ was released from CdS to bind with Rhod-5N for substantial fluorescence enhancement.	Rhod-5N	163-170	CD2 molecule	Homo sapiens	123-126
31788599-0	2019	Mesoporous Layered Graphene Oxide/Fe3O4/C3N3S3 Polymer Hybrids for Rapid Removal of Pb2+ and Cd2+ from Water.	graphene oxide	19-33	CD2 molecule	Homo sapiens	93-96
31788599-0	2019	Mesoporous Layered Graphene Oxide/Fe3O4/C3N3S3 Polymer Hybrids for Rapid Removal of Pb2+ and Cd2+ from Water.	ferryl iron	34-39	CD2 molecule	Homo sapiens	93-96
31788599-0	2019	Mesoporous Layered Graphene Oxide/Fe3O4/C3N3S3 Polymer Hybrids for Rapid Removal of Pb2+ and Cd2+ from Water.	c3n3s3 polymer	40-54	CD2 molecule	Homo sapiens	93-96
31788599-0	2019	Mesoporous Layered Graphene Oxide/Fe3O4/C3N3S3 Polymer Hybrids for Rapid Removal of Pb2+ and Cd2+ from Water.	Water	103-108	CD2 molecule	Homo sapiens	93-96
31788599-1	2019	Mesoporous layered magnetic hybrid GFP2 composed of C3N3S3 polymers, Fe3O4 nanoparticles (Fe3O4 NPs), and graphene oxide with a mesoporous layered "sandwich"-like structure was successfully explored by in situ simple polymerization tactic for rapid removal of Pb2+ and Cd2+ from water.	mesoporous	0-10	CD2 molecule	Homo sapiens	269-272
31717598-4	2019	Nano-copper was deposited onto the surface of carbon fiber to enhance the current concentration and mass transfer rate of Cd2+ during measurement, which improved the electrochemical detection sensitivity significantly (by up to 3.7 x 108 nA/nM) and broadened the linear range to 10~105 nM.	Copper	5-11	CD2 molecule	Homo sapiens	122-125
31717598-4	2019	Nano-copper was deposited onto the surface of carbon fiber to enhance the current concentration and mass transfer rate of Cd2+ during measurement, which improved the electrochemical detection sensitivity significantly (by up to 3.7 x 108 nA/nM) and broadened the linear range to 10~105 nM.	Carbon	46-52	CD2 molecule	Homo sapiens	122-125
31586316-0	2019	Efficient adsorption of Cd2+ from aqueous solution using metakaolin geopolymers.	KAOLIN	57-67	CD2 molecule	Homo sapiens	24-27
31229709-11	2019	Acidic surface functional groups were found to act as the key property that governs the adsorption capacity of Pb2+, Cu2+ and Cd2+.	Lead	111-115	CD2 molecule	Homo sapiens	126-129
31394422-2	2019	A three-dimensional network structure (...Au-SNH2 Mn+ H2NS-Au...) was formed after the Mn+ (Pb2+, Cd2+, Zn2+ and Ag+) coordinated the gold nanoparticles through the amino group in the thiol ligand, which promoted aurophilicity (...Au...Au...)	Gold	42-44	CD2 molecule	Homo sapiens	98-101
31394422-2	2019	A three-dimensional network structure (...Au-SNH2 Mn+ H2NS-Au...) was formed after the Mn+ (Pb2+, Cd2+, Zn2+ and Ag+) coordinated the gold nanoparticles through the amino group in the thiol ligand, which promoted aurophilicity (...Au...Au...)	dihydridotin	45-49	CD2 molecule	Homo sapiens	98-101
31394422-2	2019	A three-dimensional network structure (...Au-SNH2 Mn+ H2NS-Au...) was formed after the Mn+ (Pb2+, Cd2+, Zn2+ and Ag+) coordinated the gold nanoparticles through the amino group in the thiol ligand, which promoted aurophilicity (...Au...Au...)	h2ns	54-58	CD2 molecule	Homo sapiens	98-101
31394422-2	2019	A three-dimensional network structure (...Au-SNH2 Mn+ H2NS-Au...) was formed after the Mn+ (Pb2+, Cd2+, Zn2+ and Ag+) coordinated the gold nanoparticles through the amino group in the thiol ligand, which promoted aurophilicity (...Au...Au...)	Lead(2+)	92-96	CD2 molecule	Homo sapiens	98-101
31394422-2	2019	A three-dimensional network structure (...Au-SNH2 Mn+ H2NS-Au...) was formed after the Mn+ (Pb2+, Cd2+, Zn2+ and Ag+) coordinated the gold nanoparticles through the amino group in the thiol ligand, which promoted aurophilicity (...Au...Au...)	Zinc	104-108	CD2 molecule	Homo sapiens	98-101
31394422-2	2019	A three-dimensional network structure (...Au-SNH2 Mn+ H2NS-Au...) was formed after the Mn+ (Pb2+, Cd2+, Zn2+ and Ag+) coordinated the gold nanoparticles through the amino group in the thiol ligand, which promoted aurophilicity (...Au...Au...)	Sulfhydryl Compounds	184-189	CD2 molecule	Homo sapiens	98-101
31394422-4	2019	The differences in coordination between the amino group and metal ions resulted in different emission wavelengths (Pb2+, Cd2+, Zn2+ and Ag+: lambdaex = 365 nm~370 nm, lambdaem = 580, 645, 630 and 565 nm).	Metals	60-65	CD2 molecule	Homo sapiens	121-124
31394422-5	2019	Aggregation induced emission of amino thiol capped GNPs via coordination of Pb2+ or Cd2+ can be used as a fluorescent sensor of the both metal ions (lambdaex = 365 nm, lambdaem = 580/645 nm) and were used for living bioimaging in vivo and in vitro.	amino thiol	32-43	CD2 molecule	Homo sapiens	84-87
31394422-5	2019	Aggregation induced emission of amino thiol capped GNPs via coordination of Pb2+ or Cd2+ can be used as a fluorescent sensor of the both metal ions (lambdaex = 365 nm, lambdaem = 580/645 nm) and were used for living bioimaging in vivo and in vitro.	Metals	137-142	CD2 molecule	Homo sapiens	84-87
31299476-7	2019	Reversely, inhibition of NHX1 by amiloride treatment, enhanced Cd2+ influx in NHX1 duckweed, subsequently delayed Cd2+ efflux in both genotypes of duckweed under Cd2+ shock.	Amiloride	33-42	CD2 molecule	Homo sapiens	63-66
31404731-4	2019	The three-dimensional simulation and FTIR analysis revealed that the presence of Cu2+ suppressed Pb2+ and Cd2+ adsorptions, while the effect of Cd2+ on Cu2+ and Pb2+ adsorptions was insignificant.	cupric ion	152-156	CD2 molecule	Homo sapiens	144-147
31404731-6	2019	The preferential adsorptions of Pb2+ &gt; Cu2+ &gt; Cd2+ were likely due to the different affinities of the metals to the lone pair of electrons on the N atom from the amide groups and/or the O atoms from the -OH and -COO- groups on C-AL.	cupric ion	42-46	CD2 molecule	Homo sapiens	52-55
31404731-6	2019	The preferential adsorptions of Pb2+ &gt; Cu2+ &gt; Cd2+ were likely due to the different affinities of the metals to the lone pair of electrons on the N atom from the amide groups and/or the O atoms from the -OH and -COO- groups on C-AL.	Nitrogen	152-153	CD2 molecule	Homo sapiens	52-55
31404731-6	2019	The preferential adsorptions of Pb2+ &gt; Cu2+ &gt; Cd2+ were likely due to the different affinities of the metals to the lone pair of electrons on the N atom from the amide groups and/or the O atoms from the -OH and -COO- groups on C-AL.	Amides	168-173	CD2 molecule	Homo sapiens	52-55
31404731-3	2019	Antagonism was found to be the predominant competitive effect for Cu2+, Pb2+ and Cd2+ adsorptions by C-AL in the multi-metal adsorption system.	palmatine	101-105	CD2 molecule	Homo sapiens	81-84
31404731-3	2019	Antagonism was found to be the predominant competitive effect for Cu2+, Pb2+ and Cd2+ adsorptions by C-AL in the multi-metal adsorption system.	Metals	119-124	CD2 molecule	Homo sapiens	81-84
31404731-4	2019	The three-dimensional simulation and FTIR analysis revealed that the presence of Cu2+ suppressed Pb2+ and Cd2+ adsorptions, while the effect of Cd2+ on Cu2+ and Pb2+ adsorptions was insignificant.	cupric ion	81-85	CD2 molecule	Homo sapiens	106-109
31299476-7	2019	Reversely, inhibition of NHX1 by amiloride treatment, enhanced Cd2+ influx in NHX1 duckweed, subsequently delayed Cd2+ efflux in both genotypes of duckweed under Cd2+ shock.	Amiloride	33-42	CD2 molecule	Homo sapiens	114-117
31299476-7	2019	Reversely, inhibition of NHX1 by amiloride treatment, enhanced Cd2+ influx in NHX1 duckweed, subsequently delayed Cd2+ efflux in both genotypes of duckweed under Cd2+ shock.	Amiloride	33-42	CD2 molecule	Homo sapiens	114-117
31684470-4	2019	The thiourea group of the sensing membrane has an effective combination effect on Cd2+.	Thiourea	4-12	CD2 molecule	Homo sapiens	82-85
31669825-0	2019	Higher CD56+ or CD2+ lymphocyte percentage predicts poor steroid response in patients with immune thrombocytopenia.	Steroids	57-64	CD2 molecule	Homo sapiens	16-19
31669825-13	2019	CONCLUSIONS: This study found that newly diagnosed ITP patients with increased percentages of CD56+ or CD2+ lymphocytes in peripheral blood associated with a poorer response to steroid treatment.	Steroids	177-184	CD2 molecule	Homo sapiens	103-106
31532182-6	2019	Finally, the cation-exchange reaction between CdTe QDs and Ag+ was utilized to quench the fluorescence (FL) of the CdTe QDs, releasing free Cd2+.	cadmium telluride	46-50	CD2 molecule	Homo sapiens	140-143
31566959-8	2019	The Kx[Bi4-xMnxS6] (x = 1.28) exhibits efficient capture of Cd2+ and Pb2+ ions with high distribution coefficient, Kd (107 mL/g), and exchange capacities of 221.2 and 342.4 mg/g, respectively.	Bismuth	7-10	CD2 molecule	Homo sapiens	60-63
31532182-6	2019	Finally, the cation-exchange reaction between CdTe QDs and Ag+ was utilized to quench the fluorescence (FL) of the CdTe QDs, releasing free Cd2+.	cadmium telluride	115-119	CD2 molecule	Homo sapiens	140-143
31170603-0	2019	Synthesis of novel 1,10-phenanthroline derivatives and it used as probes for sensitive detection of Zn2+ and Cd2+ metal ions - Spectroscopic and theoretical approach.	1,10-phenanthroline	19-38	CD2 molecule	Homo sapiens	109-112
31170603-0	2019	Synthesis of novel 1,10-phenanthroline derivatives and it used as probes for sensitive detection of Zn2+ and Cd2+ metal ions - Spectroscopic and theoretical approach.	Metals	114-119	CD2 molecule	Homo sapiens	109-112
31170603-1	2019	A novel class of unexpected 1,10-phenanthrolinederivatives were synthesized from 2,3-dihydroacridin-4(1H)-ones with 3-aminonaphthalen-2-carboxylic acid in presence of phosphorus oxychloride at 130 C and simple perceptive emission intensity increasing assay was developed effectively to detect the very low concentrations of Zn2+ and Cd2+ ions.	1,10-phenanthrolinederivatives	28-58	CD2 molecule	Homo sapiens	333-336
31170603-1	2019	A novel class of unexpected 1,10-phenanthrolinederivatives were synthesized from 2,3-dihydroacridin-4(1H)-ones with 3-aminonaphthalen-2-carboxylic acid in presence of phosphorus oxychloride at 130 C and simple perceptive emission intensity increasing assay was developed effectively to detect the very low concentrations of Zn2+ and Cd2+ ions.	phosphoryl chloride	167-189	CD2 molecule	Homo sapiens	333-336
31170603-2	2019	Emission intensity of compounds 3(a-c) directly related to the concentrations of Zn2+ and Cd2+ ions was due to metal chelating enhanced fluorescence (CHEF) effect and also its further validated by fluorescence lifetime measurement.	Metals	111-116	CD2 molecule	Homo sapiens	90-93
31170603-5	2019	In addition, this proposed detection analysis has the direct application for monitoring Zn2+ and Cd2+ concentrations in tap and drinking water samples.	Water	137-142	CD2 molecule	Homo sapiens	97-100
34055309-4	2019	The results showed that the synergistic toxic mechanisms of GO and Cd2+, initiated from the adhesion of GO on HeLa cells, and followed by the recruitment of Cd2+ ions around the cell membrane, impaired the membrane integrity, morphology and adhesion capability, and triggered cell toxicity.	graphene oxide	60-62	CD2 molecule	Homo sapiens	157-160
31288199-1	2019	Although cadmium (Cd2+) is unable to form reactive oxygen species (ROS) directly, many of its adverse effects are connected to increased ROS generation resulting in cell death.	Cadmium	9-16	CD2 molecule	Homo sapiens	18-21
31288199-1	2019	Although cadmium (Cd2+) is unable to form reactive oxygen species (ROS) directly, many of its adverse effects are connected to increased ROS generation resulting in cell death.	Reactive Oxygen Species	137-140	CD2 molecule	Homo sapiens	18-21
31288199-7	2019	In conclusion, NAC exhibits dual and antagonistic effects on Cd2+ cytotoxicity in human leukemia cells.	Acetylcysteine	15-18	CD2 molecule	Homo sapiens	61-64
31129538-0	2019	Synthesis of amino-functionalized bentonite/CoFe2O4@MnO2 magnetic recoverable nanoparticles for aqueous Cd2+ removal.	Bentonite	34-43	CD2 molecule	Homo sapiens	104-107
31552221-0	2019	Preparation of Carboxymethyl Cellulose-Based Macroporous Adsorbent by Eco-Friendly Pickering-MIPEs Template for Fast Removal of Pb2+ and Cd2.	carboxymethyl-coenzyme A	15-28	CD2 molecule	Homo sapiens	137-140
31129538-0	2019	Synthesis of amino-functionalized bentonite/CoFe2O4@MnO2 magnetic recoverable nanoparticles for aqueous Cd2+ removal.	cobalt ferrite	44-51	CD2 molecule	Homo sapiens	104-107
31129538-0	2019	Synthesis of amino-functionalized bentonite/CoFe2O4@MnO2 magnetic recoverable nanoparticles for aqueous Cd2+ removal.	manganese dioxide	52-56	CD2 molecule	Homo sapiens	104-107
31171181-4	2019	The Nafion/BiSn@C/GCE was successfully applied for determination for trace Cd2+ in river samples with satisfying recoveries using the standard addition method.	GCE	18-21	CD2 molecule	Homo sapiens	75-78
31125881-0	2019	Fe-based ceramic nanocomposite membranes fabricated via e-spinning and vacuum filtration for Cd2+ ions removal.	Iron	0-2	CD2 molecule	Homo sapiens	93-96
31125881-1	2019	In this work, vacuum filtered and polymer mixed e-spinning membranes (ESPMs) made from or doped with Fe-based nanomaterials were successfully fabricated to remove Cd2+ ions from a neutral aqueous solution.	Polymers	34-41	CD2 molecule	Homo sapiens	163-166
31125881-1	2019	In this work, vacuum filtered and polymer mixed e-spinning membranes (ESPMs) made from or doped with Fe-based nanomaterials were successfully fabricated to remove Cd2+ ions from a neutral aqueous solution.	Iron	101-103	CD2 molecule	Homo sapiens	163-166
31125881-4	2019	Among them, VFM made from Fe3O4 NPs has the highest adsorption capacity (qt) with the adsorption amount of Cd2+ ions reaching about 29.3 mg/g within only 2 min due to the high specific surface area of NPs.	ferryl iron	26-31	CD2 molecule	Homo sapiens	107-110
31125881-6	2019	It was calculated that the equilibrium rate constant of VFM made from Fe3O4 NPs has reached about 0.28 g mg-1 min-1, much smaller than those of other membranes, which indicated a high Cd2+ ions removal efficiency.	ferryl iron	70-75	CD2 molecule	Homo sapiens	184-187
31517451-3	2019	The protocols include sample preparation of a 1:1 mixture of light (-CH3 )2 and heavy (-13 CD2 H)2 dimethylated intact N-glycopeptides from LO2 and HepG2 cells, RPLC-pentaHILIC 2DLC separation of the mixture, intact N-glycopeptide database search and identification using GPSeeker, and quantitation of differentially expressed intact N-glycopeptides using the quantitation module GPSeekerQuan.	n-glycopeptides	119-134	CD2 molecule	Homo sapiens	91-94
31517451-3	2019	The protocols include sample preparation of a 1:1 mixture of light (-CH3 )2 and heavy (-13 CD2 H)2 dimethylated intact N-glycopeptides from LO2 and HepG2 cells, RPLC-pentaHILIC 2DLC separation of the mixture, intact N-glycopeptide database search and identification using GPSeeker, and quantitation of differentially expressed intact N-glycopeptides using the quantitation module GPSeekerQuan.	n-glycopeptide	119-133	CD2 molecule	Homo sapiens	91-94
31267405-1	2019	Heavy metal ion contamination, in particular that associated with Pb2+, Cd2+, and Cu2+, poses a considerable threat to aquatic environments and human health.	Metals	6-11	CD2 molecule	Homo sapiens	72-75
31267405-2	2019	To obtain a highly efficient adsorbent, in this work, a facile hydrothermal method was applied to prepare acrylic acid grafted onto cellulose nanocrystal (AA-g-CNC) hydro/aerogel as an adsorbent for Pb2+, Cd2+, and Cu2+ removal.	acrylic acid	106-118	CD2 molecule	Homo sapiens	205-208
31171181-1	2019	A novel sensor based on carbon supported BiSn alloy nanoparticles (BiSn@C) was prepared for the sensitive detection of Cd2+.	Carbon	24-30	CD2 molecule	Homo sapiens	119-122
32280158-11	2019	In aqueous solutions, Cd generally occurs as the divalent Cd2+ and it is mobilized mainly in oxic, acidic conditions.	Cadmium	22-24	CD2 molecule	Homo sapiens	58-61
31286369-5	2019	The present nanocomposite was applied to remove and immobilize Cd2+ from water and soil systems.	Water	73-78	CD2 molecule	Homo sapiens	63-66
31444573-0	2019	A DFT-based analysis of adsorption of Cd2+, Cr3+, Cu2+, Hg2+, Pb2+, and Zn2+, on vanillin monomer: a study of the removal of metal ions from effluents.	vanillin	81-89	CD2 molecule	Homo sapiens	38-41
31171181-1	2019	A novel sensor based on carbon supported BiSn alloy nanoparticles (BiSn@C) was prepared for the sensitive detection of Cd2+.	bisn alloy	41-51	CD2 molecule	Homo sapiens	119-122
31171181-1	2019	A novel sensor based on carbon supported BiSn alloy nanoparticles (BiSn@C) was prepared for the sensitive detection of Cd2+.	bisn	41-45	CD2 molecule	Homo sapiens	119-122
31171181-2	2019	The BiSn@C and Nafion modified glassy carbon electrode (GCE) exhibited improved electrochemical performance in Cd2+ detection, because of its large specific surface area, abundance of active sites, good electrical conductivity, and strong cation exchange ability.	bisn	4-8	CD2 molecule	Homo sapiens	111-114
31171181-2	2019	The BiSn@C and Nafion modified glassy carbon electrode (GCE) exhibited improved electrochemical performance in Cd2+ detection, because of its large specific surface area, abundance of active sites, good electrical conductivity, and strong cation exchange ability.	perfluorosulfonic acid	15-21	CD2 molecule	Homo sapiens	111-114
31171181-2	2019	The BiSn@C and Nafion modified glassy carbon electrode (GCE) exhibited improved electrochemical performance in Cd2+ detection, because of its large specific surface area, abundance of active sites, good electrical conductivity, and strong cation exchange ability.	Carbon	38-44	CD2 molecule	Homo sapiens	111-114
31171181-3	2019	Under the optimum conditions, the fabricated sensor showed good linearity of its response from 0.01 mumol/L to 30 mumol/L for the detection of Cd2+ and a limit of detection (LOD) of 3 nmol/L, which is considerably lower than the limit specified for safe drinking water as guided by the World Health Organization.	Drinking Water	254-268	CD2 molecule	Homo sapiens	143-146
31171181-4	2019	The Nafion/BiSn@C/GCE was successfully applied for determination for trace Cd2+ in river samples with satisfying recoveries using the standard addition method.	perfluorosulfonic acid	4-10	CD2 molecule	Homo sapiens	75-78
31171181-4	2019	The Nafion/BiSn@C/GCE was successfully applied for determination for trace Cd2+ in river samples with satisfying recoveries using the standard addition method.	bisn	11-15	CD2 molecule	Homo sapiens	75-78
31171181-4	2019	The Nafion/BiSn@C/GCE was successfully applied for determination for trace Cd2+ in river samples with satisfying recoveries using the standard addition method.	Carbon	16-17	CD2 molecule	Homo sapiens	75-78
31036167-4	2019	To this aim, we report the reactivity of solutions made of Mn(II) and Mn(III) bound to Tiron and DFOB with our optimized porphyrin reagent which includes adding excess Cd2+, and compare these results with data from representative natural seawater samples.	manganese(III) acetate dihydrate	70-77	CD2 molecule	Homo sapiens	168-171
31036167-4	2019	To this aim, we report the reactivity of solutions made of Mn(II) and Mn(III) bound to Tiron and DFOB with our optimized porphyrin reagent which includes adding excess Cd2+, and compare these results with data from representative natural seawater samples.	Manganese(2+)	59-65	CD2 molecule	Homo sapiens	168-171
31036167-4	2019	To this aim, we report the reactivity of solutions made of Mn(II) and Mn(III) bound to Tiron and DFOB with our optimized porphyrin reagent which includes adding excess Cd2+, and compare these results with data from representative natural seawater samples.	Porphyrins	121-130	CD2 molecule	Homo sapiens	168-171
31265249-8	2019	Relying on the enhancement of PL intensity via cation exchange, the Cys- and Thr-capped CIS/ZnS QDs can sense Cd2+ sensitively.	pl	30-32	CD2 molecule	Homo sapiens	110-113
31251626-1	2019	Due to the potential toxicity of cadmium (Cd2+) and its presence in various waste products found in the environment, it is necessary to develop methods to attenuate and remediate Cd2+ waste.	Cadmium	33-40	CD2 molecule	Homo sapiens	42-45
31251626-1	2019	Due to the potential toxicity of cadmium (Cd2+) and its presence in various waste products found in the environment, it is necessary to develop methods to attenuate and remediate Cd2+ waste.	Cadmium	33-40	CD2 molecule	Homo sapiens	179-182
31251626-3	2019	This work focused on improving our molecular-scale understanding of the chemistry of Cd2+ interactions with gibbsite and kaolinite mineral surfaces.	Kaolin	121-130	CD2 molecule	Homo sapiens	85-88
30947989-0	2019	One-step fabrication of dopamine-inspired Au for SERS sensing of Cd2+ and polycyclic aromatic hydrocarbons.	Dopamine	24-32	CD2 molecule	Homo sapiens	65-68
30947989-0	2019	One-step fabrication of dopamine-inspired Au for SERS sensing of Cd2+ and polycyclic aromatic hydrocarbons.	Gold	42-44	CD2 molecule	Homo sapiens	65-68
30947989-0	2019	One-step fabrication of dopamine-inspired Au for SERS sensing of Cd2+ and polycyclic aromatic hydrocarbons.	sers	49-53	CD2 molecule	Homo sapiens	65-68
30947989-7	2019	More interestingly, the two-dimensional correlation spectroscopy showed that DQ modified Au exhibited a strong binding ability towards Cd2+, yielding SERS vibrational profiles that allowed the qualitative determination of Cd2+ with a detection limit of 10-8 mol L-1.	sers	150-154	CD2 molecule	Homo sapiens	135-138
30947989-7	2019	More interestingly, the two-dimensional correlation spectroscopy showed that DQ modified Au exhibited a strong binding ability towards Cd2+, yielding SERS vibrational profiles that allowed the qualitative determination of Cd2+ with a detection limit of 10-8 mol L-1.	sers	150-154	CD2 molecule	Homo sapiens	222-225
31265249-8	2019	Relying on the enhancement of PL intensity via cation exchange, the Cys- and Thr-capped CIS/ZnS QDs can sense Cd2+ sensitively.	Cysteine	68-71	CD2 molecule	Homo sapiens	110-113
31265249-8	2019	Relying on the enhancement of PL intensity via cation exchange, the Cys- and Thr-capped CIS/ZnS QDs can sense Cd2+ sensitively.	Threonine	77-80	CD2 molecule	Homo sapiens	110-113
31265249-10	2019	Moreover, intercellular Cd2+ can also be evaluated by the bright PL from the QDs, and the QDs can achieve multicolor imaging.	pl	65-67	CD2 molecule	Homo sapiens	24-27
30910674-2	2019	In this paper, a novel salecan polysaccharide-based biosorbent was designed for removal of Cd2+ ions from aqueous solutions.	salecan polysaccharide	23-45	CD2 molecule	Homo sapiens	91-94
31276422-0	2019	Correction to Adsorption of Cd2+ and Ni2+ from Aqueous Single-Metal Solutions on Graphene Oxide-Chitosan-Poly(vinyl alcohol) Hydrogels.	graphene oxide	81-95	CD2 molecule	Homo sapiens	28-31
31276422-0	2019	Correction to Adsorption of Cd2+ and Ni2+ from Aqueous Single-Metal Solutions on Graphene Oxide-Chitosan-Poly(vinyl alcohol) Hydrogels.	Chitosan	96-104	CD2 molecule	Homo sapiens	28-31
31276422-0	2019	Correction to Adsorption of Cd2+ and Ni2+ from Aqueous Single-Metal Solutions on Graphene Oxide-Chitosan-Poly(vinyl alcohol) Hydrogels.	Polyvinyl Alcohol	105-124	CD2 molecule	Homo sapiens	28-31
31140476-2	2019	The chemosensor HL exhibits rapid visual turn-on fluorescence enhancing recognition toward Mg2+/Zn2+, which is not interfered by other cations, especially for respective congeners Ca2+/Cd2+.	magnesium ion	91-95	CD2 molecule	Homo sapiens	185-188
31140476-2	2019	The chemosensor HL exhibits rapid visual turn-on fluorescence enhancing recognition toward Mg2+/Zn2+, which is not interfered by other cations, especially for respective congeners Ca2+/Cd2+.	Zinc	96-100	CD2 molecule	Homo sapiens	185-188
31029021-0	2019	A coumarin derivative as a "turn-on" fluorescence probe toward Cd2+ in live cells.	coumarin	2-10	CD2 molecule	Homo sapiens	63-66
31029021-1	2019	A novel coumarin-derived Schiff base fluorescence probe (CTB) has been successfully designed and synthesized through exploiting tris-(2-aminothyl)-amine moiety as a recognition unit for the highly selective and sensitive detection of Cd2+.	coumarin	8-16	CD2 molecule	Homo sapiens	234-237
31029021-1	2019	A novel coumarin-derived Schiff base fluorescence probe (CTB) has been successfully designed and synthesized through exploiting tris-(2-aminothyl)-amine moiety as a recognition unit for the highly selective and sensitive detection of Cd2+.	Schiff Bases	25-36	CD2 molecule	Homo sapiens	234-237
31029021-1	2019	A novel coumarin-derived Schiff base fluorescence probe (CTB) has been successfully designed and synthesized through exploiting tris-(2-aminothyl)-amine moiety as a recognition unit for the highly selective and sensitive detection of Cd2+.	tris-(2-aminothyl)-amine	128-152	CD2 molecule	Homo sapiens	234-237
31029021-5	2019	The experiments including Job"s plot, UV-Vis titration, 1H NMR titration and ESI-MS spectrum established that the probe CTB binds to Cd2+ in a 1:2 ratio.	Hydrogen	56-58	CD2 molecule	Homo sapiens	133-136
31046050-3	2019	Analogous to Ca2+ binding, Cd2+ binding triggers changes in the protein secondary and tertiary structure, including increased exposure of the hydrophobic cavities, as determined using a fluorescent probe, 1-anilinonaphthalene-8-sulfonic acid.	1-anilino-8-naphthalenesulfonate	205-241	CD2 molecule	Homo sapiens	27-30
31327088-2	2019	The optical properties of the sensor probe were investigated by employing absorption and fluorescence titrations which showed specific recognition behaviour being highly selective towards Cd2+ over the other 3d transition metal ions.	Metals	222-227	CD2 molecule	Homo sapiens	188-191
31327088-3	2019	The strong fluorometric response of probe 1 towards Cd2+ ion is attributed to inhibition of C=N isomerization effect upon coordination of the metal ion.	Metals	142-147	CD2 molecule	Homo sapiens	52-55
31327088-4	2019	The binding stoichiometry was determined by Job"s plot and the probable sensing mechanism of the probe towards Cd2+ was investigated by employing FTIR spectra analysis and 1H NMR titration experiments.	Hydrogen	172-174	CD2 molecule	Homo sapiens	111-114
30952319-0	2019	Acid Environment-improved fluorescence sensing performance: A quinoline Schiff base-containing sensor for Cd2+ with high sensitivity and selectivity.	quinoline schiff base	62-83	CD2 molecule	Homo sapiens	106-109
30952319-2	2019	In this work, a quinoline-containing Schiff base, AMQD, was utilized as fluorescence probe for Cd2+.	quinoline	16-25	CD2 molecule	Homo sapiens	95-98
30952319-2	2019	In this work, a quinoline-containing Schiff base, AMQD, was utilized as fluorescence probe for Cd2+.	Schiff Bases	37-48	CD2 molecule	Homo sapiens	95-98
30952319-3	2019	Interestingly, the obtained chemosensor exhibited much better fluorescence detection sensitivity and selectivity toward Cd2+ in acidic 10% methanol aqueous solution (pH 4) comparing to those in neutral environment.	Methanol	139-147	CD2 molecule	Homo sapiens	120-123
31120730-2	2019	In this study, a new organic-cadmium (Cd) complex formed through Cd2+ coordination with p-phenylenediamine (PPD) was used to synthesize highly active Fe-embedded N-doped carbon catalysts for the first time.	Cadmium	29-36	CD2 molecule	Homo sapiens	65-68
31120730-2	2019	In this study, a new organic-cadmium (Cd) complex formed through Cd2+ coordination with p-phenylenediamine (PPD) was used to synthesize highly active Fe-embedded N-doped carbon catalysts for the first time.	Cadmium	38-40	CD2 molecule	Homo sapiens	65-68
31120730-2	2019	In this study, a new organic-cadmium (Cd) complex formed through Cd2+ coordination with p-phenylenediamine (PPD) was used to synthesize highly active Fe-embedded N-doped carbon catalysts for the first time.	4-phenylenediamine	88-106	CD2 molecule	Homo sapiens	65-68
31120730-2	2019	In this study, a new organic-cadmium (Cd) complex formed through Cd2+ coordination with p-phenylenediamine (PPD) was used to synthesize highly active Fe-embedded N-doped carbon catalysts for the first time.	4-phenylenediamine	108-111	CD2 molecule	Homo sapiens	65-68
31120730-2	2019	In this study, a new organic-cadmium (Cd) complex formed through Cd2+ coordination with p-phenylenediamine (PPD) was used to synthesize highly active Fe-embedded N-doped carbon catalysts for the first time.	Iron	150-152	CD2 molecule	Homo sapiens	65-68
31120730-2	2019	In this study, a new organic-cadmium (Cd) complex formed through Cd2+ coordination with p-phenylenediamine (PPD) was used to synthesize highly active Fe-embedded N-doped carbon catalysts for the first time.	Carbon	170-176	CD2 molecule	Homo sapiens	65-68
31046050-4	2019	In addition, we demonstrate that Cd2+ binding modulates DREAM interactions with FITC-labeled peptides that mimic binding sites of DREAM effector proteins; helix-9 of presenilin-1, and site-1 and site 2 of potassium voltage channel 4.3 (residues 2-22 and 70-90, respectively).	Fluorescein-5-isothiocyanate	80-84	CD2 molecule	Homo sapiens	33-36
31046050-5	2019	Cd2+ association with DREAM increases its affinity for helix 9 of presenilin roughly 30-times compared to metal-free DREAM.	Metals	106-111	CD2 molecule	Homo sapiens	0-3
31046050-7	2019	The above results suggest that DREAM and probably other members of the neuronal calcium sensor family bind Cd2+ with an affinity that is superior to that for Ca2+ and the interactions between toxic Cd2+ and DREAM and other neuronal calcium sensors provide novel insight into the molecular mechanism of Cd2+ neurotoxicity.	Calcium	80-87	CD2 molecule	Homo sapiens	107-110
31046050-7	2019	The above results suggest that DREAM and probably other members of the neuronal calcium sensor family bind Cd2+ with an affinity that is superior to that for Ca2+ and the interactions between toxic Cd2+ and DREAM and other neuronal calcium sensors provide novel insight into the molecular mechanism of Cd2+ neurotoxicity.	Calcium	80-87	CD2 molecule	Homo sapiens	198-201
31046050-7	2019	The above results suggest that DREAM and probably other members of the neuronal calcium sensor family bind Cd2+ with an affinity that is superior to that for Ca2+ and the interactions between toxic Cd2+ and DREAM and other neuronal calcium sensors provide novel insight into the molecular mechanism of Cd2+ neurotoxicity.	Calcium	80-87	CD2 molecule	Homo sapiens	198-201
31046050-7	2019	The above results suggest that DREAM and probably other members of the neuronal calcium sensor family bind Cd2+ with an affinity that is superior to that for Ca2+ and the interactions between toxic Cd2+ and DREAM and other neuronal calcium sensors provide novel insight into the molecular mechanism of Cd2+ neurotoxicity.	Calcium	232-239	CD2 molecule	Homo sapiens	107-110
31046050-7	2019	The above results suggest that DREAM and probably other members of the neuronal calcium sensor family bind Cd2+ with an affinity that is superior to that for Ca2+ and the interactions between toxic Cd2+ and DREAM and other neuronal calcium sensors provide novel insight into the molecular mechanism of Cd2+ neurotoxicity.	Calcium	232-239	CD2 molecule	Homo sapiens	198-201
31046050-7	2019	The above results suggest that DREAM and probably other members of the neuronal calcium sensor family bind Cd2+ with an affinity that is superior to that for Ca2+ and the interactions between toxic Cd2+ and DREAM and other neuronal calcium sensors provide novel insight into the molecular mechanism of Cd2+ neurotoxicity.	Calcium	232-239	CD2 molecule	Homo sapiens	198-201
30878939-4	2019	However, Cd2+ removal efficiency was reduced to 12% and 80% at sixth cycle by Fe0 and Bi/Fe0, respectively.	Bismuth	86-88	CD2 molecule	Homo sapiens	9-12
31111849-0	2019	Hg2+ and Cd2+ binding of a bioinspired hexapeptide with two cysteine units constructed as a minimalistic metal ion sensing fluorescent probe.	Cysteine	60-68	CD2 molecule	Homo sapiens	9-12
31111849-0	2019	Hg2+ and Cd2+ binding of a bioinspired hexapeptide with two cysteine units constructed as a minimalistic metal ion sensing fluorescent probe.	Metals	105-110	CD2 molecule	Homo sapiens	9-12
31111849-3	2019	Both metal ions form bis-ligand complexes by the coordination of four Cys-thiolates at ligand excess above pH ~ 5.5 (Cd2+) and 7.0 (Hg2+).	Metals	5-10	CD2 molecule	Homo sapiens	117-120
31111849-6	2019	The fact that this occurs even in the presence of 1.0 eq. of Cd2+ per ligand reflects a complete displacement of the latter metal ion by Hg2+ from its peptide-bound form.	Metals	124-129	CD2 molecule	Homo sapiens	61-64
30926012-5	2019	The concentration effect of Cd2+ and chitosan on the particle size of CdS QDs was investigated.	cadmium sulfide	70-73	CD2 molecule	Homo sapiens	28-31
30878939-1	2019	Removal of cadmium (Cd2+), a highly toxic heavy metal, from aqueous solutions was investigated using nano zerovalent iron (Fe0).	Cadmium	11-18	CD2 molecule	Homo sapiens	20-23
30878939-4	2019	However, Cd2+ removal efficiency was reduced to 12% and 80% at sixth cycle by Fe0 and Bi/Fe0, respectively.	Iron	89-92	CD2 molecule	Homo sapiens	9-12
30878939-1	2019	Removal of cadmium (Cd2+), a highly toxic heavy metal, from aqueous solutions was investigated using nano zerovalent iron (Fe0).	Metals	48-53	CD2 molecule	Homo sapiens	20-23
31135144-6	2019	As a demonstration, we evaluate the nanowire as a sequestrating material capable of collecting toxic cations, like Cd2+, from water and photoreducing them (immobilizing them tightly).	Water	126-131	CD2 molecule	Homo sapiens	115-118
30878939-1	2019	Removal of cadmium (Cd2+), a highly toxic heavy metal, from aqueous solutions was investigated using nano zerovalent iron (Fe0).	Iron	117-121	CD2 molecule	Homo sapiens	20-23
30878939-6	2019	The oxidation of Fe0 and Bi/Fe0 yielded electron that played significant role in the conversion of toxic Cd2+ into non-toxic Cd0.	Iron	17-20	CD2 molecule	Homo sapiens	105-108
30878939-1	2019	Removal of cadmium (Cd2+), a highly toxic heavy metal, from aqueous solutions was investigated using nano zerovalent iron (Fe0).	Iron	123-126	CD2 molecule	Homo sapiens	20-23
30878939-6	2019	The oxidation of Fe0 and Bi/Fe0 yielded electron that played significant role in the conversion of toxic Cd2+ into non-toxic Cd0.	Bismuth	25-27	CD2 molecule	Homo sapiens	105-108
30878939-3	2019	At a reaction time of 20 min, 85% and 96% Cd2+ was removed by Fe0 and Bi/Fe0, respectively, at first cycle using [Cd2+]0 = 10 mg/L and [Fe0]0 = [Bi/Fe0]0 = 1.0 g/L.	Iron	62-65	CD2 molecule	Homo sapiens	42-45
30878939-6	2019	The oxidation of Fe0 and Bi/Fe0 yielded electron that played significant role in the conversion of toxic Cd2+ into non-toxic Cd0.	Iron	28-31	CD2 molecule	Homo sapiens	105-108
30878939-3	2019	At a reaction time of 20 min, 85% and 96% Cd2+ was removed by Fe0 and Bi/Fe0, respectively, at first cycle using [Cd2+]0 = 10 mg/L and [Fe0]0 = [Bi/Fe0]0 = 1.0 g/L.	Bismuth	70-72	CD2 molecule	Homo sapiens	42-45
30878939-3	2019	At a reaction time of 20 min, 85% and 96% Cd2+ was removed by Fe0 and Bi/Fe0, respectively, at first cycle using [Cd2+]0 = 10 mg/L and [Fe0]0 = [Bi/Fe0]0 = 1.0 g/L.	Bismuth	70-72	CD2 molecule	Homo sapiens	114-117
30878939-3	2019	At a reaction time of 20 min, 85% and 96% Cd2+ was removed by Fe0 and Bi/Fe0, respectively, at first cycle using [Cd2+]0 = 10 mg/L and [Fe0]0 = [Bi/Fe0]0 = 1.0 g/L.	Iron	73-76	CD2 molecule	Homo sapiens	42-45
30878939-3	2019	At a reaction time of 20 min, 85% and 96% Cd2+ was removed by Fe0 and Bi/Fe0, respectively, at first cycle using [Cd2+]0 = 10 mg/L and [Fe0]0 = [Bi/Fe0]0 = 1.0 g/L.	Iron	73-76	CD2 molecule	Homo sapiens	42-45
30878939-3	2019	At a reaction time of 20 min, 85% and 96% Cd2+ was removed by Fe0 and Bi/Fe0, respectively, at first cycle using [Cd2+]0 = 10 mg/L and [Fe0]0 = [Bi/Fe0]0 = 1.0 g/L.	Iron	73-76	CD2 molecule	Homo sapiens	42-45
30878939-4	2019	However, Cd2+ removal efficiency was reduced to 12% and 80% at sixth cycle by Fe0 and Bi/Fe0, respectively.	Iron	78-81	CD2 molecule	Homo sapiens	9-12
30878939-6	2019	The oxidation of Fe0 and Bi/Fe0 yielded electron that played significant role in the conversion of toxic Cd2+ into non-toxic Cd0.	(+)-Cannabidiol	125-128	CD2 molecule	Homo sapiens	105-108
30878939-10	2019	The conversion of Cd2+ into non-toxic Cd0 proved Fe0 and Bi/Fe0 to be highly efficient and rewarding in detoxification of Cd2+ and other toxic metals in aqueous environments.	(+)-Cannabidiol	38-41	CD2 molecule	Homo sapiens	122-125
30959244-0	2019	Potential use of ZnO@activated carbon nanocomposites for the adsorptive removal of Cd2+ ions in aqueous solutions.	Zinc Oxide	17-20	CD2 molecule	Homo sapiens	83-86
31018456-0	2019	Adsorption of Cd2+ on GO/PAA hydrogel and preliminary recycle to GO/PAA-CdS as efficient photocatalyst.	paa	25-28	CD2 molecule	Homo sapiens	14-17
31018456-0	2019	Adsorption of Cd2+ on GO/PAA hydrogel and preliminary recycle to GO/PAA-CdS as efficient photocatalyst.	paa-cds	68-75	CD2 molecule	Homo sapiens	14-17
31018456-3	2019	The GO/PAA-Cd2+ composite after the adsorption process was recycled through in-situ precipitation to obtain GO/PAA-CdS composites.	graphene oxide	4-6	CD2 molecule	Homo sapiens	11-14
31018456-3	2019	The GO/PAA-Cd2+ composite after the adsorption process was recycled through in-situ precipitation to obtain GO/PAA-CdS composites.	paa-cds	111-118	CD2 molecule	Homo sapiens	11-14
31018456-8	2019	The roles of GO and PAA in the successive adsorption-photocatalyst process were proved to be complementary: PAA improved the adsorption of Cd2+ while GO enhanced the photocatalyst efficiency.	paa	20-23	CD2 molecule	Homo sapiens	139-142
30831503-2	2019	In this work, a novel carboxyl, amide, carbonyl sulfide and secondary amino group grafted cellulose derivative adsorbent (modified-cellulose) was prepared in an attempt to remove heavy metal Cd2+.	carboxyl,	22-31	CD2 molecule	Homo sapiens	191-194
30831503-2	2019	In this work, a novel carboxyl, amide, carbonyl sulfide and secondary amino group grafted cellulose derivative adsorbent (modified-cellulose) was prepared in an attempt to remove heavy metal Cd2+.	Cellulose	90-99	CD2 molecule	Homo sapiens	191-194
30831503-2	2019	In this work, a novel carboxyl, amide, carbonyl sulfide and secondary amino group grafted cellulose derivative adsorbent (modified-cellulose) was prepared in an attempt to remove heavy metal Cd2+.	Cellulose	131-140	CD2 molecule	Homo sapiens	191-194
30831503-2	2019	In this work, a novel carboxyl, amide, carbonyl sulfide and secondary amino group grafted cellulose derivative adsorbent (modified-cellulose) was prepared in an attempt to remove heavy metal Cd2+.	Metals	185-190	CD2 molecule	Homo sapiens	191-194
30831503-5	2019	The Cd2+ adsorption capacity of modified-cellulose was pretty good, up to 401.1 mg/g and with 3 times enhancement.	Cellulose	40-50	CD2 molecule	Homo sapiens	4-7
30831503-7	2019	The density functional theory (DFT) calculations indicating that the Cd2+ binding ability of multi-functional groups modified cellulose was stronger than that of single-functional group modified cellulose.	Cellulose	126-135	CD2 molecule	Homo sapiens	69-72
30831503-7	2019	The density functional theory (DFT) calculations indicating that the Cd2+ binding ability of multi-functional groups modified cellulose was stronger than that of single-functional group modified cellulose.	Cellulose	195-204	CD2 molecule	Homo sapiens	69-72
31285764-5	2019	In gain-of-function studies, we adoptively transferred hCD2+ Treg from NOD.Foxp3 hCD2 to NOD/SCID that contain Treg as the only T-cell population.	treg	61-65	CD2 molecule	Homo sapiens	55-59
31285764-5	2019	In gain-of-function studies, we adoptively transferred hCD2+ Treg from NOD.Foxp3 hCD2 to NOD/SCID that contain Treg as the only T-cell population.	treg	61-65	CD2 molecule	Homo sapiens	81-85
30959244-0	2019	Potential use of ZnO@activated carbon nanocomposites for the adsorptive removal of Cd2+ ions in aqueous solutions.	Carbon	31-37	CD2 molecule	Homo sapiens	83-86
30959244-6	2019	The ratio of ZnO nanoparticles and activated carbon was optimized to achieve enhanced electrostatic interactions for the effective adsorption of cadmium ions (Cd2+).	Zinc Oxide	13-16	CD2 molecule	Homo sapiens	159-162
30959244-6	2019	The ratio of ZnO nanoparticles and activated carbon was optimized to achieve enhanced electrostatic interactions for the effective adsorption of cadmium ions (Cd2+).	Carbon	45-51	CD2 molecule	Homo sapiens	159-162
30959244-6	2019	The ratio of ZnO nanoparticles and activated carbon was optimized to achieve enhanced electrostatic interactions for the effective adsorption of cadmium ions (Cd2+).	Cadmium	145-152	CD2 molecule	Homo sapiens	159-162
30959244-9	2019	The favourable adsorption capacity of the synthesized ZnO/activated carbon (9:1) nanocomposites supported their use as an efficient sorbent material in practical performance metrics (e.g., partition coefficient of 0.54 mg g-1muM-1) for the adsorption of Cd2+ ions.	Zinc Oxide	54-57	CD2 molecule	Homo sapiens	254-257
31055909-5	2019	Heavy metal ion adsorption of the synthesized nanostructures was assessed in batch tests based on Cd2+ ion sequestration; the maximum adsorption capacity for Cd2+ was 325.89 mg/g, which is among the highest values reported for similar materials such as graphene oxide and its derivatives.	Metals	6-11	CD2 molecule	Homo sapiens	98-101
30989604-5	2019	In addition, as the Cd2+ concentration in feedwater increased, the Cd removal rate decreased, while the Cd concentration in the permeate increased.	Cadmium	67-69	CD2 molecule	Homo sapiens	20-23
30989604-9	2019	This phenomenon was the result of Cd2+ reacting with OH- and forming a Cd (OH)2 precipitate.	cd (oh)2	71-79	CD2 molecule	Homo sapiens	34-37
31020528-1	2019	Adsorption plays an important role in removing cadmium (Cd2+) from water, and magnetic adsorbents are increasingly being used due to their ease of separation and recovery.	Cadmium	47-54	CD2 molecule	Homo sapiens	56-59
31020528-1	2019	Adsorption plays an important role in removing cadmium (Cd2+) from water, and magnetic adsorbents are increasingly being used due to their ease of separation and recovery.	Water	67-72	CD2 molecule	Homo sapiens	56-59
31020528-2	2019	Magnetic Fe3O4-coated hydroxyapatite (HAP) nanoparticles (nHAP-Fe3O4) were developed by co-precipitation and then used for the removal of Cd2+ from water.	ferryl iron	9-14	CD2 molecule	Homo sapiens	138-141
31020528-2	2019	Magnetic Fe3O4-coated hydroxyapatite (HAP) nanoparticles (nHAP-Fe3O4) were developed by co-precipitation and then used for the removal of Cd2+ from water.	Durapatite	22-36	CD2 molecule	Homo sapiens	138-141
31020528-2	2019	Magnetic Fe3O4-coated hydroxyapatite (HAP) nanoparticles (nHAP-Fe3O4) were developed by co-precipitation and then used for the removal of Cd2+ from water.	nhap-fe3o4	58-68	CD2 molecule	Homo sapiens	138-141
31020528-7	2019	The mechanisms for the adsorption of Cd2+ on nHAP-Fe3O4 included rapid surface adsorption, intraparticle diffusion, and internal particle bonding, with the ion exchange with Ca2+ and chemical complexation being the most dominant.	N-hydroxy-2-aminopyrene	45-49	CD2 molecule	Homo sapiens	37-40
31020528-7	2019	The mechanisms for the adsorption of Cd2+ on nHAP-Fe3O4 included rapid surface adsorption, intraparticle diffusion, and internal particle bonding, with the ion exchange with Ca2+ and chemical complexation being the most dominant.	ferryl iron	50-55	CD2 molecule	Homo sapiens	37-40
31020528-9	2019	Results revealed that the feasibility of nHAP-Fe3O4 as an adsorbent of Cd2+ and its environmental friendliness make it an ideal focus for future research.	nhap-fe3o4	41-51	CD2 molecule	Homo sapiens	71-74
31055909-5	2019	Heavy metal ion adsorption of the synthesized nanostructures was assessed in batch tests based on Cd2+ ion sequestration; the maximum adsorption capacity for Cd2+ was 325.89 mg/g, which is among the highest values reported for similar materials such as graphene oxide and its derivatives.	Metals	6-11	CD2 molecule	Homo sapiens	158-161
31055909-5	2019	Heavy metal ion adsorption of the synthesized nanostructures was assessed in batch tests based on Cd2+ ion sequestration; the maximum adsorption capacity for Cd2+ was 325.89 mg/g, which is among the highest values reported for similar materials such as graphene oxide and its derivatives.	graphene oxide	253-267	CD2 molecule	Homo sapiens	158-161
31055909-8	2019	Moreover, Alk-Ti2Cfibr and Alk-Ti2Csheet nanostructures were tested for simulated groundwater, showing that synthesized nanostructures were capable for removing Cd2+ ions at the ppb level.	Polybrominated Biphenyls	178-181	CD2 molecule	Homo sapiens	161-164
30708152-1	2019	Adsorption behaviors and mechanisms of metal endocrine disruptors (Pb2+, Cd2+, and Hg2+) by pyrogenic carbonaceous materials including engineered carbons (biochar and activated carbon) and carbon nanomaterials (multi-walled carbon nanotubes and graphene oxide) have been investigated by experimental and density functional theory (DFT) studies.	Metals	39-44	CD2 molecule	Homo sapiens	73-76
30747203-10	2019	Moreover, compound 1 could be established as a selective and efficient sensor of Zn2+ in aqueous solution even in the presence of Cd2+ and other metal ions.	Zinc	81-85	CD2 molecule	Homo sapiens	130-133
30876580-1	2019	As an ubiquitous heavy metal pollutant, cadmium ion (Cd2+) is detrimental to food and human health even at low concentrations.	Metals	23-28	CD2 molecule	Homo sapiens	53-56
30876580-1	2019	As an ubiquitous heavy metal pollutant, cadmium ion (Cd2+) is detrimental to food and human health even at low concentrations.	Cadmium	40-47	CD2 molecule	Homo sapiens	53-56
30876580-3	2019	Here we report the use of a personal glucose meter (PGM) as the point-of-use (POU) device for portable and quantitative detection of Cd2+.	Glucose	37-44	CD2 molecule	Homo sapiens	133-136
30876580-7	2019	After magnetic separation, the invertase conjugates hydrolyze sucrose into glucose, thus establishing direct conversion of Cd2+ concentration to glucose amount, which can be directly quantified by a PGM.	Sucrose	62-69	CD2 molecule	Homo sapiens	123-126
30876580-7	2019	After magnetic separation, the invertase conjugates hydrolyze sucrose into glucose, thus establishing direct conversion of Cd2+ concentration to glucose amount, which can be directly quantified by a PGM.	Glucose	75-82	CD2 molecule	Homo sapiens	123-126
30876580-7	2019	After magnetic separation, the invertase conjugates hydrolyze sucrose into glucose, thus establishing direct conversion of Cd2+ concentration to glucose amount, which can be directly quantified by a PGM.	Glucose	145-152	CD2 molecule	Homo sapiens	123-126
31193297-0	2019	Zn2+ and Cd2+ assisted photo-catalytic degradation of chlorpyrifos in soil.	Chlorpyrifos	54-66	CD2 molecule	Homo sapiens	9-12
31193297-1	2019	The Cd2+ and Zn2+ assisted photo-catalytic degradation of soil incorporated chlorpyrifos (CLP) was reported in current study.	Chlorpyrifos	76-88	CD2 molecule	Homo sapiens	4-7
31193134-3	2019	The adsorption capacity of the magnetite was highly dependent on pH value, for Cd+2, Zn+2, Ni+2 and Cu+2 the removal performance was higher that 80% at pH = 8.	Ferrosoferric Oxide	31-40	CD2 molecule	Homo sapiens	79-83
30732763-0	2019	Removal of Cu2+, Cd2+ and Ni2+ ions from aqueous solution using a novel chitosan/polyvinyl alcohol adsorptive membrane.	Chitosan	72-80	CD2 molecule	Homo sapiens	17-20
30860246-0	2019	Acidity and Cd2+ fluorescent sensing and selective CO2 adsorption by a water-stable Eu-MOF.	Water	71-76	CD2 molecule	Homo sapiens	12-15
30682647-0	2019	A selective fluorescent chemosensor for Cd2+ based on 8-hydroxylquinoline-benzothiazole conjugate and imaging application.	8-hydroxylquinoline-benzothiazole	54-87	CD2 molecule	Homo sapiens	40-43
30682647-2	2019	The HQ-BT showed a weak fluorescence that could be strongly enhanced by coordination with various metal ions such as Al3+, Cd2+, Zn2+ in methanol containing 1% water.	Methanol	137-145	CD2 molecule	Homo sapiens	123-126
30682647-2	2019	The HQ-BT showed a weak fluorescence that could be strongly enhanced by coordination with various metal ions such as Al3+, Cd2+, Zn2+ in methanol containing 1% water.	Water	160-165	CD2 molecule	Homo sapiens	123-126
30860246-2	2019	It is a highly porous, water-stable, and luminescent material, exhibiting pH sensing in the acidic range of pH = 7-3 with selective detection for Cd2+ by an enhanced fluorescence of ~23-fold against a series of metal ions.	Water	23-28	CD2 molecule	Homo sapiens	146-149
30682647-3	2019	Interestingly, the selectivity toward Cd2+ was achieved by increasing water fraction to 30% aqueous methanol solution.	Methanol	100-108	CD2 molecule	Homo sapiens	38-41
30860246-2	2019	It is a highly porous, water-stable, and luminescent material, exhibiting pH sensing in the acidic range of pH = 7-3 with selective detection for Cd2+ by an enhanced fluorescence of ~23-fold against a series of metal ions.	Metals	211-216	CD2 molecule	Homo sapiens	146-149
30332552-3	2019	In fact, Cd2+ produces this injury through the stimulation of oxygen-derived radical generation, inducing oxidative stress.	oxygen-derived radical	62-84	CD2 molecule	Homo sapiens	9-12
31087927-6	2019	When the initial Cd2+ concentration was increased from 0 mg L-1 to approximately 200 mg L-1, the Cd2+ adsorption capacity of the Fe-modified biochar declined from 43.17 mg g-1 to 27.88 mg g-1, which was still higher than that of the unmodified biochar by at least 10 mg g-1.	Iron	129-131	CD2 molecule	Homo sapiens	17-20
31087927-6	2019	When the initial Cd2+ concentration was increased from 0 mg L-1 to approximately 200 mg L-1, the Cd2+ adsorption capacity of the Fe-modified biochar declined from 43.17 mg g-1 to 27.88 mg g-1, which was still higher than that of the unmodified biochar by at least 10 mg g-1.	Iron	129-131	CD2 molecule	Homo sapiens	97-100
31087927-7	2019	In aqueous media with a high concentration of Ca2+, the Fe-modified biochar showed better Cd2+ adsorption performance; thus, compared to MnO2 and ZnO, Fe2O3 was the best choice to enhance the heavy metal adsorption performance of the sewage sludge-derived biochar.	Iron	56-58	CD2 molecule	Homo sapiens	90-93
31087928-1	2019	In order to improve the adsorption-separation of Cd2+ in water treatment, magnetic Fe3O4 coated Ca(H2PO4)2 nanoparticles (NMCDP) were developed by coprecipitation.	Water	57-62	CD2 molecule	Homo sapiens	49-52
31087928-1	2019	In order to improve the adsorption-separation of Cd2+ in water treatment, magnetic Fe3O4 coated Ca(H2PO4)2 nanoparticles (NMCDP) were developed by coprecipitation.	ferryl iron	83-88	CD2 molecule	Homo sapiens	49-52
31087928-1	2019	In order to improve the adsorption-separation of Cd2+ in water treatment, magnetic Fe3O4 coated Ca(H2PO4)2 nanoparticles (NMCDP) were developed by coprecipitation.	nmcdp	122-127	CD2 molecule	Homo sapiens	49-52
31087928-5	2019	The adsorption rate of Cd2+ by NMCDP was fast, and adsorption equilibrium could be achieved within 1 hour.	nmcdp	31-36	CD2 molecule	Homo sapiens	23-26
31087928-8	2019	The coexisting ions in the solution had an effect on the adsorption of Cd2+, especially the divalent cation Cu2+.	cupric ion	108-112	CD2 molecule	Homo sapiens	71-74
31001697-0	2019	Simultaneous extraction of Cu2+ and Cd2+ ions in water, wastewater, and food samples using solvent-terminated dispersive liquid-liquid microextraction: optimization by multiobjective evolutionary algorithm based on decomposition.	Water	49-54	CD2 molecule	Homo sapiens	36-39
31001697-6	2019	Under optimal conditions obtained by ANN-MOEAD, the detection limit (S/N = 3), the quantitation limit(S/N = 10), and the linear range for Cu2+ were 0.05, 0.15, and 0.15-1000 mug L-1, respectively, and for Cd2+ were 0.07, 0.21, and 0.21-750 mug L-1, respectively.	cupric ion	138-142	CD2 molecule	Homo sapiens	205-208
30836753-0	2019	Adsorption of Cd2+ and Ni2+ from Aqueous Single-Metal Solutions on Graphene Oxide-Chitosan-Poly(vinyl alcohol) Hydrogels.	graphene oxide	67-81	CD2 molecule	Homo sapiens	14-17
30836753-0	2019	Adsorption of Cd2+ and Ni2+ from Aqueous Single-Metal Solutions on Graphene Oxide-Chitosan-Poly(vinyl alcohol) Hydrogels.	Chitosan	82-90	CD2 molecule	Homo sapiens	14-17
30836753-0	2019	Adsorption of Cd2+ and Ni2+ from Aqueous Single-Metal Solutions on Graphene Oxide-Chitosan-Poly(vinyl alcohol) Hydrogels.	Polyvinyl Alcohol	91-110	CD2 molecule	Homo sapiens	14-17
30836753-5	2019	Moreover, the adsorption property with respect to Cd2+ and Ni2+ in wastewater has been largely effected by the pH and was less influenced by the ionic strength and humic acid, and the GCP1:2:4 hydrogel possessed excellent adsorptive and recyclable properties.	Humic Substances	164-174	CD2 molecule	Homo sapiens	50-53
30332552-4	2019	Several molecules have been used to avoid or even reverse Cd2+-induced mitochondrial injury, for instance, cyclosporin A, resveratrol, dithiocarbamates, and even EDTA.	Cyclosporine	107-120	CD2 molecule	Homo sapiens	58-61
30332552-4	2019	Several molecules have been used to avoid or even reverse Cd2+-induced mitochondrial injury, for instance, cyclosporin A, resveratrol, dithiocarbamates, and even EDTA.	Resveratrol	122-133	CD2 molecule	Homo sapiens	58-61
30332552-4	2019	Several molecules have been used to avoid or even reverse Cd2+-induced mitochondrial injury, for instance, cyclosporin A, resveratrol, dithiocarbamates, and even EDTA.	dithiocarbamates	135-151	CD2 molecule	Homo sapiens	58-61
30332552-4	2019	Several molecules have been used to avoid or even reverse Cd2+-induced mitochondrial injury, for instance, cyclosporin A, resveratrol, dithiocarbamates, and even EDTA.	Edetic Acid	162-166	CD2 molecule	Homo sapiens	58-61
30332552-5	2019	The aim of this study was to explore the possibility that the antioxidant tamoxifen could protect mitochondria from the deleterious effects of Cd2+.	Tamoxifen	74-83	CD2 molecule	Homo sapiens	143-146
30332552-6	2019	Our results indicate that the addition of 1 mumol/L Cd2+ to mitochondria collapsed the transmembrane electrical gradient, induced the release of cytochrome c, and increased both the generation of H2O2 and the oxidative damage to mitochondrial DNA (among other measured parameters).	Hydrogen Peroxide	196-200	CD2 molecule	Homo sapiens	52-55
30328389-0	2019	Modified oil shale ash and oil shale ash zeolite for the removal of Cd2+ ion from aqueous solutions.	oil shale ash	9-22	CD2 molecule	Homo sapiens	68-71
30707884-2	2019	In the presence of divalent metal ions (e.g. Cd2+) or in some ("proton transfer") mutants (L210DN/M17DN or L213DN), the proton delivery to QB- is made rate limiting and the properties of the proton pathway can be directly examined.	Metals	28-33	CD2 molecule	Homo sapiens	45-48
30328389-0	2019	Modified oil shale ash and oil shale ash zeolite for the removal of Cd2+ ion from aqueous solutions.	oil shale ash zeolite	27-48	CD2 molecule	Homo sapiens	68-71
30328389-7	2019	And the maximum monolayer adsorption capacity determined by the Langmuir adsorption isotherm was found to be 108.70 and 169.49 mg/g for Cd2+ adsorption onto modified oil shale ash and oil shale ash zeolite, respectively.	ash zeolite	194-205	CD2 molecule	Homo sapiens	136-139
30328389-8	2019	It was concluded that Cd2+ in aqueous solutions was more efficiently removed by oil shale ash zeolite, which could be employed as a low-cost and effective alternative adsorbent for wastewater treatment than modified oil shale ash.	Zeolites	94-101	CD2 molecule	Homo sapiens	22-25
30698189-4	2019	Introduction of three methoxy substituents at the 5,6,7-positions of each quinoline moiety in BAPTQ specifically enhanced the fluorescence intensity of the Cd2+ complex, establishing the Cd2+-specific probe TriMeOBAPTQ (N,N,N",N"-tetrakis(5,6,7-trimethoxy-2-quinolylmethyl)-1,2-bis(2-aminophenoxy)ethane).	baptq	94-99	CD2 molecule	Homo sapiens	187-190
30698189-0	2019	Methoxy-substituted tetrakisquinoline analogs of EGTA and BAPTA for fluorescence detection of Cd2+ .	methoxy-substituted tetrakisquinoline	0-37	CD2 molecule	Homo sapiens	94-97
30698189-5	2019	In contrast, TriMeOEGTQ (N,N,N",N"-tetrakis(5,6,7-trimethoxy-2-quinolylmethyl)-1,2-bis(2-aminoethoxy)ethane) maintains a poor Cd2+/Zn2+ selectivity in its fluorescence response.	trimeoegtq	13-23	CD2 molecule	Homo sapiens	126-129
30698189-0	2019	Methoxy-substituted tetrakisquinoline analogs of EGTA and BAPTA for fluorescence detection of Cd2+ .	Egtazic Acid	49-53	CD2 molecule	Homo sapiens	94-97
30698189-0	2019	Methoxy-substituted tetrakisquinoline analogs of EGTA and BAPTA for fluorescence detection of Cd2+ .	1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid	58-63	CD2 molecule	Homo sapiens	94-97
30698189-6	2019	Although the crystal structures of Cd2+/Zn2+ complexes with EGTQ and BAPTQ derivatives reveal the formation of multiple components including mononuclear and dinuclear complexes, the dinuclear Cd2+ and Zn2+ complexes with a linearly extended structure are regarded as possible fluorescent species in the solution.	Zinc	40-44	CD2 molecule	Homo sapiens	35-38
30698189-3	2019	In methanol-HEPES buffer solution (9 : 1, 50 mM HEPES, 0.1 M KCl, pH = 7.5), EGTQ exhibits fluorescence enhancement induced by Zn2+ and Cd2+ with poor selectivity, but BAPTQ did not exhibit a fluorescence response to either metal ion.	Methanol	3-11	CD2 molecule	Homo sapiens	136-139
30698189-6	2019	Although the crystal structures of Cd2+/Zn2+ complexes with EGTQ and BAPTQ derivatives reveal the formation of multiple components including mononuclear and dinuclear complexes, the dinuclear Cd2+ and Zn2+ complexes with a linearly extended structure are regarded as possible fluorescent species in the solution.	Zinc	40-44	CD2 molecule	Homo sapiens	192-195
30698189-3	2019	In methanol-HEPES buffer solution (9 : 1, 50 mM HEPES, 0.1 M KCl, pH = 7.5), EGTQ exhibits fluorescence enhancement induced by Zn2+ and Cd2+ with poor selectivity, but BAPTQ did not exhibit a fluorescence response to either metal ion.	HEPES	12-17	CD2 molecule	Homo sapiens	136-139
30698189-6	2019	Although the crystal structures of Cd2+/Zn2+ complexes with EGTQ and BAPTQ derivatives reveal the formation of multiple components including mononuclear and dinuclear complexes, the dinuclear Cd2+ and Zn2+ complexes with a linearly extended structure are regarded as possible fluorescent species in the solution.	egtq	60-64	CD2 molecule	Homo sapiens	35-38
30698189-3	2019	In methanol-HEPES buffer solution (9 : 1, 50 mM HEPES, 0.1 M KCl, pH = 7.5), EGTQ exhibits fluorescence enhancement induced by Zn2+ and Cd2+ with poor selectivity, but BAPTQ did not exhibit a fluorescence response to either metal ion.	egtq	77-81	CD2 molecule	Homo sapiens	136-139
30698189-6	2019	Although the crystal structures of Cd2+/Zn2+ complexes with EGTQ and BAPTQ derivatives reveal the formation of multiple components including mononuclear and dinuclear complexes, the dinuclear Cd2+ and Zn2+ complexes with a linearly extended structure are regarded as possible fluorescent species in the solution.	egtq	60-64	CD2 molecule	Homo sapiens	192-195
30698189-4	2019	Introduction of three methoxy substituents at the 5,6,7-positions of each quinoline moiety in BAPTQ specifically enhanced the fluorescence intensity of the Cd2+ complex, establishing the Cd2+-specific probe TriMeOBAPTQ (N,N,N",N"-tetrakis(5,6,7-trimethoxy-2-quinolylmethyl)-1,2-bis(2-aminophenoxy)ethane).	quinoline	74-83	CD2 molecule	Homo sapiens	156-159
30698189-4	2019	Introduction of three methoxy substituents at the 5,6,7-positions of each quinoline moiety in BAPTQ specifically enhanced the fluorescence intensity of the Cd2+ complex, establishing the Cd2+-specific probe TriMeOBAPTQ (N,N,N",N"-tetrakis(5,6,7-trimethoxy-2-quinolylmethyl)-1,2-bis(2-aminophenoxy)ethane).	quinoline	74-83	CD2 molecule	Homo sapiens	187-190
30698189-4	2019	Introduction of three methoxy substituents at the 5,6,7-positions of each quinoline moiety in BAPTQ specifically enhanced the fluorescence intensity of the Cd2+ complex, establishing the Cd2+-specific probe TriMeOBAPTQ (N,N,N",N"-tetrakis(5,6,7-trimethoxy-2-quinolylmethyl)-1,2-bis(2-aminophenoxy)ethane).	baptq	94-99	CD2 molecule	Homo sapiens	156-159
30698189-6	2019	Although the crystal structures of Cd2+/Zn2+ complexes with EGTQ and BAPTQ derivatives reveal the formation of multiple components including mononuclear and dinuclear complexes, the dinuclear Cd2+ and Zn2+ complexes with a linearly extended structure are regarded as possible fluorescent species in the solution.	baptq	69-74	CD2 molecule	Homo sapiens	35-38
30698189-6	2019	Although the crystal structures of Cd2+/Zn2+ complexes with EGTQ and BAPTQ derivatives reveal the formation of multiple components including mononuclear and dinuclear complexes, the dinuclear Cd2+ and Zn2+ complexes with a linearly extended structure are regarded as possible fluorescent species in the solution.	baptq	69-74	CD2 molecule	Homo sapiens	192-195
30698189-6	2019	Although the crystal structures of Cd2+/Zn2+ complexes with EGTQ and BAPTQ derivatives reveal the formation of multiple components including mononuclear and dinuclear complexes, the dinuclear Cd2+ and Zn2+ complexes with a linearly extended structure are regarded as possible fluorescent species in the solution.	Zinc	201-205	CD2 molecule	Homo sapiens	35-38
30698189-7	2019	The conformational restriction of BAPTQ due to the orthophenylene moieties in the molecular skeleton is responsible for the formation of the weakly fluorescent, OH-bridged dizinc complex, which is critical to the strict Cd2+-specificity in the fluorescence response of TriMeOBAPTQ.	baptq	34-39	CD2 molecule	Homo sapiens	220-223
30698189-7	2019	The conformational restriction of BAPTQ due to the orthophenylene moieties in the molecular skeleton is responsible for the formation of the weakly fluorescent, OH-bridged dizinc complex, which is critical to the strict Cd2+-specificity in the fluorescence response of TriMeOBAPTQ.	orthophenylene	51-65	CD2 molecule	Homo sapiens	220-223
30698189-7	2019	The conformational restriction of BAPTQ due to the orthophenylene moieties in the molecular skeleton is responsible for the formation of the weakly fluorescent, OH-bridged dizinc complex, which is critical to the strict Cd2+-specificity in the fluorescence response of TriMeOBAPTQ.	dizinc	172-178	CD2 molecule	Homo sapiens	220-223
30698189-7	2019	The conformational restriction of BAPTQ due to the orthophenylene moieties in the molecular skeleton is responsible for the formation of the weakly fluorescent, OH-bridged dizinc complex, which is critical to the strict Cd2+-specificity in the fluorescence response of TriMeOBAPTQ.	trimeobaptq	269-280	CD2 molecule	Homo sapiens	220-223
30580174-0	2019	Efficient and fast removal of Pb2+ and Cd2+ from an aqueous solution using a chitosan/Mg-Al-layered double hydroxide nanocomposite.	Chitosan	77-85	CD2 molecule	Homo sapiens	39-42
30938563-17	2019	Hearing aid outcomes from this follow-up CD (CD2) cohort were positive and generally the same as for the original CD cohort.	Cadmium	41-43	CD2 molecule	Homo sapiens	45-48
30580174-0	2019	Efficient and fast removal of Pb2+ and Cd2+ from an aqueous solution using a chitosan/Mg-Al-layered double hydroxide nanocomposite.	mg-al	86-91	CD2 molecule	Homo sapiens	39-42
30580174-0	2019	Efficient and fast removal of Pb2+ and Cd2+ from an aqueous solution using a chitosan/Mg-Al-layered double hydroxide nanocomposite.	double hydroxide	100-116	CD2 molecule	Homo sapiens	39-42
30580174-4	2019	The adsorption capacity of the CS-LDH was evaluated by adsorbing Pb2+ and Cd2+ as representative heavy metals.	Chitosan	31-33	CD2 molecule	Homo sapiens	74-77
30580174-7	2019	The capacity of the CS-LDH for Pb2+ and Cd2+ adsorption was higher than that of CS and the Mg-Al-LDH, and the isothermal data followed the Langmuir isotherm model.	Chitosan	20-22	CD2 molecule	Homo sapiens	40-43
30634120-0	2019	Encapsulated green magnetic nanoparticles for the removal of toxic Pb2+ and Cd2+ from water: Development, characterization and application.	Water	86-91	CD2 molecule	Homo sapiens	76-79
30681872-6	2019	Deuterium labeling has been used to demonstrate that scrambling of H(D) occurs during the decomposition to acetonitrile of the CD(NH2)CD2 intermediate formed by decarboxylation of l-Asp-2,3,3- d3 and l-Asp-15N-2,3,3- d3.	Deuterium	0-9	CD2 molecule	Homo sapiens	134-137
30393236-5	2019	Upon addition of Cd2+, GCDSA could probably be induced to fold into a G-quadruplex structure.	gcdsa	23-28	CD2 molecule	Homo sapiens	17-20
30684805-4	2019	The Langmuir isotherms showed that the maximum sorption capacities of HBC300, HBC450, and HBC600 were 173, 138, and 130 mmol kg-1 for Cd2+, and 359, 172, and 197 mmol kg-1 for Cu2+, respectively.	cupric ion	176-180	CD2 molecule	Homo sapiens	134-137
30684805-7	2019	In a binary system, Cd2+ sorption was depressed by over four times in presence of Cu2+.	cupric ion	82-86	CD2 molecule	Homo sapiens	20-23
31070589-0	2019	Efficient removal of Hg2+, Cd2+ and Pb2+ from aqueous solution and mixed industrial wastewater using a designed chelating ligand, 2-pyridyl-N-(2"-methylthiophenyl) methyleneimine (PMTPM).	2-pyridyl-n-(2"-methylthiophenyl) methyleneimine	130-178	CD2 molecule	Homo sapiens	27-30
31070589-0	2019	Efficient removal of Hg2+, Cd2+ and Pb2+ from aqueous solution and mixed industrial wastewater using a designed chelating ligand, 2-pyridyl-N-(2"-methylthiophenyl) methyleneimine (PMTPM).	pmtpm	180-185	CD2 molecule	Homo sapiens	27-30
31070589-1	2019	The present study is focused on the removal of Hg2+, Cd2+ and Pb2+ ions from aqueous solution using a tridentate chelating agent, 2-pyridyl-N-(2"-methylthiophenyl) methyleneimine (PMTPM); and applicability of such removal from industrial wastewater using PMTPM is also investigated.	2-pyridyl-n-(2"-methylthiophenyl) methyleneimine	130-178	CD2 molecule	Homo sapiens	53-56
31070589-1	2019	The present study is focused on the removal of Hg2+, Cd2+ and Pb2+ ions from aqueous solution using a tridentate chelating agent, 2-pyridyl-N-(2"-methylthiophenyl) methyleneimine (PMTPM); and applicability of such removal from industrial wastewater using PMTPM is also investigated.	pmtpm	180-185	CD2 molecule	Homo sapiens	53-56
31070589-1	2019	The present study is focused on the removal of Hg2+, Cd2+ and Pb2+ ions from aqueous solution using a tridentate chelating agent, 2-pyridyl-N-(2"-methylthiophenyl) methyleneimine (PMTPM); and applicability of such removal from industrial wastewater using PMTPM is also investigated.	pmtpm	255-260	CD2 molecule	Homo sapiens	53-56
31070589-2	2019	The results showed that the metal ions removal efficiency using PMTPM was in the order of Hg2+(99.46%) &gt; Cd2+(95.42%) &gt; Pb2+(94.54%) under optimum reaction conditions (L:M2+ = 3:1, pH = 9, time = 24 h, temp.	Metals	28-33	CD2 molecule	Homo sapiens	108-111
30681872-6	2019	Deuterium labeling has been used to demonstrate that scrambling of H(D) occurs during the decomposition to acetonitrile of the CD(NH2)CD2 intermediate formed by decarboxylation of l-Asp-2,3,3- d3 and l-Asp-15N-2,3,3- d3.	acetonitrile	107-119	CD2 molecule	Homo sapiens	134-137
30681872-6	2019	Deuterium labeling has been used to demonstrate that scrambling of H(D) occurs during the decomposition to acetonitrile of the CD(NH2)CD2 intermediate formed by decarboxylation of l-Asp-2,3,3- d3 and l-Asp-15N-2,3,3- d3.	l-asp-2,3,3- d3	180-195	CD2 molecule	Homo sapiens	134-137
30681872-6	2019	Deuterium labeling has been used to demonstrate that scrambling of H(D) occurs during the decomposition to acetonitrile of the CD(NH2)CD2 intermediate formed by decarboxylation of l-Asp-2,3,3- d3 and l-Asp-15N-2,3,3- d3.	l-asp-15n-2,3,3- d3	200-219	CD2 molecule	Homo sapiens	134-137
30675618-4	2019	In the present study, we used magnetic tweezers to explore the interactions between lambda-DNA and two metal ions, Hg2+ and Cd2+, at the single-molecule level.	Metals	103-108	CD2 molecule	Homo sapiens	124-127
30584764-0	2019	Cd(II)- and Pb(II)-Induced Self-Assembly of Peripheral Membrane Domains from Protein Kinase C. Cd2+ and Pb2+ are xenobiotic heavy metal ions that use ionic mimicry to interfere with the cellular function of biomacromolecules.	cd(ii)	0-6	CD2 molecule	Homo sapiens	95-98
30667002-0	2019	A water-soluble BODIPY based "OFF/ON" fluorescent probe for the detection of Cd2+ ions with high selectivity and sensitivity.	Water	2-7	CD2 molecule	Homo sapiens	77-80
30584764-0	2019	Cd(II)- and Pb(II)-Induced Self-Assembly of Peripheral Membrane Domains from Protein Kinase C. Cd2+ and Pb2+ are xenobiotic heavy metal ions that use ionic mimicry to interfere with the cellular function of biomacromolecules.	pb(ii)	12-18	CD2 molecule	Homo sapiens	95-98
30584764-0	2019	Cd(II)- and Pb(II)-Induced Self-Assembly of Peripheral Membrane Domains from Protein Kinase C. Cd2+ and Pb2+ are xenobiotic heavy metal ions that use ionic mimicry to interfere with the cellular function of biomacromolecules.	Metals	130-135	CD2 molecule	Homo sapiens	95-98
30667002-1	2019	A water-soluble dilithium salt BODIPY derivative (LiBDP) with appended dicarboxylate pseudo-crown ether [NO4] coordinating sites has been designed, synthesized and characterized successfully for the selective and sensitive recognition of Cd2+ in aqueous media.	Water	2-7	CD2 molecule	Homo sapiens	238-241
30667002-1	2019	A water-soluble dilithium salt BODIPY derivative (LiBDP) with appended dicarboxylate pseudo-crown ether [NO4] coordinating sites has been designed, synthesized and characterized successfully for the selective and sensitive recognition of Cd2+ in aqueous media.	dilithium salt bodipy	16-37	CD2 molecule	Homo sapiens	238-241
30667002-1	2019	A water-soluble dilithium salt BODIPY derivative (LiBDP) with appended dicarboxylate pseudo-crown ether [NO4] coordinating sites has been designed, synthesized and characterized successfully for the selective and sensitive recognition of Cd2+ in aqueous media.	libdp	50-55	CD2 molecule	Homo sapiens	238-241
30667002-1	2019	A water-soluble dilithium salt BODIPY derivative (LiBDP) with appended dicarboxylate pseudo-crown ether [NO4] coordinating sites has been designed, synthesized and characterized successfully for the selective and sensitive recognition of Cd2+ in aqueous media.	dicarboxylate pseudo-crown ether	71-103	CD2 molecule	Homo sapiens	238-241
30667002-1	2019	A water-soluble dilithium salt BODIPY derivative (LiBDP) with appended dicarboxylate pseudo-crown ether [NO4] coordinating sites has been designed, synthesized and characterized successfully for the selective and sensitive recognition of Cd2+ in aqueous media.	N-benzyl-2-(cyclohexen-1-yl)ethanamine	105-108	CD2 molecule	Homo sapiens	238-241
30667002-2	2019	The chemosensor exhibits a remarkable increase in fluorescence intensity as well as a distinct color change upon the addition of Cd2+ over other environmentally and biologically relevant metal ions in H2O.	Metals	187-192	CD2 molecule	Homo sapiens	129-132
30667002-2	2019	The chemosensor exhibits a remarkable increase in fluorescence intensity as well as a distinct color change upon the addition of Cd2+ over other environmentally and biologically relevant metal ions in H2O.	Water	201-204	CD2 molecule	Homo sapiens	129-132
30667002-3	2019	The fluorometric response of LiBDP is attributed to the metal chelation-enhanced fluorescence (MCHEF) effect which has been confirmed by a strong association constant of 2.57 +- 1.06 x 105 M-1 and Job"s plot, indicating 1 : 1 binding stoichiometry between LiBDP and Cd2+.	Metals	56-61	CD2 molecule	Homo sapiens	266-269
30667002-3	2019	The fluorometric response of LiBDP is attributed to the metal chelation-enhanced fluorescence (MCHEF) effect which has been confirmed by a strong association constant of 2.57 +- 1.06 x 105 M-1 and Job"s plot, indicating 1 : 1 binding stoichiometry between LiBDP and Cd2+.	libdp	29-34	CD2 molecule	Homo sapiens	266-269
30681094-0	2019	Cation sensing by luminescent high-nuclearity Zn-Eu Schiff base nanoscale complexes: high sensitivity to Ag+ and Cd2+ ions at the ppm level.	zn-eu schiff base	46-63	CD2 molecule	Homo sapiens	113-116
30414954-0	2019	Modulation of luminal L-alanine transport in proximal tubular cells of frog kidney induced by low micromolar Cd2+ concentration.	Alanine	22-31	CD2 molecule	Homo sapiens	109-112
30340204-3	2019	The results showed that the sensor had high selectivity towards Cd2+ over the other metal ions in aqueous media.	Metals	84-89	CD2 molecule	Homo sapiens	64-67
30340204-7	2019	The following DFT calculation fully supported that the detailed coordination mode of Cd2+ and SQ went through six-membered carbonyl oxygen and the CO group in the amide chain.	Oxygen	132-138	CD2 molecule	Homo sapiens	85-88
30340204-7	2019	The following DFT calculation fully supported that the detailed coordination mode of Cd2+ and SQ went through six-membered carbonyl oxygen and the CO group in the amide chain.	Amides	163-168	CD2 molecule	Homo sapiens	85-88
30414954-3	2019	Therefore, the aim of this study was to investigate the effects of peritubular acute exposure to micromolar Cd2+ concentration (2.3 mumol/L) on the rapid depolarization and the rate of slow repolarization of peritubular membrane potential difference (PD), induced by luminal application of L-alanine in proximal tubular cells of frog kidney.	Alanine	290-299	CD2 molecule	Homo sapiens	108-111
30414954-5	2019	Additionally, peritubular acute exposure to Cd2+ induced change in rapid depolarization of peritubular membrane PD of -53.33 +- 13.01 mV by 18.78 +- 3.31 mV (P &lt; 0.01) after luminal application of L-alanine.	Alanine	200-209	CD2 molecule	Homo sapiens	44-47
30414954-7	2019	In conclusion, these results suggest that peritubular acute exposure to low micromolar Cd2+ concentration decreased the rapid depolarization and the rate of slow repolarization of peritubular membrane PD induced by luminal application of L-alanine.	Alanine	238-247	CD2 molecule	Homo sapiens	87-90
30414954-8	2019	This is followed by reduced luminal sodium-coupled transport of L-alanine and this change may be one of the possible mechanisms involved in the early stages of Cd2+-induced nephrotoxicity.	Sodium	36-42	CD2 molecule	Homo sapiens	160-163
30414954-8	2019	This is followed by reduced luminal sodium-coupled transport of L-alanine and this change may be one of the possible mechanisms involved in the early stages of Cd2+-induced nephrotoxicity.	Alanine	64-73	CD2 molecule	Homo sapiens	160-163
30101296-6	2019	In contrast, Cd in the xylem sap was present either as free Cd2+ or complexes with carboxyl groups (Cd-OH).	Cadmium	13-15	CD2 molecule	Homo sapiens	60-63
30567642-9	2019	The added Cd2+ would facilitate the formation of CdS on the surface of QDs, which not only can alleviate the surface defects but also can transfer energy to emissive CuInS2, thus thinning the thickness of inert shell greatly boost the detection sensitivity.	Cadmium	49-52	CD2 molecule	Homo sapiens	10-13
30121035-11	2019	The major fractions of retained Cd2+ were exchangeable Cd2+ and Fe-oxide-bound Cd2+.	fe-oxide	64-72	CD2 molecule	Homo sapiens	32-35
30261431-2	2019	The probe L exhibited highly sensitive fluorescent recognition to Cd2+ ions in HEPES buffer solutions (10.0 mM, pH 7.4).	HEPES	79-84	CD2 molecule	Homo sapiens	66-69
30261431-4	2019	The competitive experiments were found to be highly selective for the Cd2+ ions even in the existence of excess competing metal ions including Zn2+, Pb2+, Hg2+ and Cu2+ ions.	Metals	122-127	CD2 molecule	Homo sapiens	70-73
30261431-4	2019	The competitive experiments were found to be highly selective for the Cd2+ ions even in the existence of excess competing metal ions including Zn2+, Pb2+, Hg2+ and Cu2+ ions.	Zinc	143-147	CD2 molecule	Homo sapiens	70-73
30261431-4	2019	The competitive experiments were found to be highly selective for the Cd2+ ions even in the existence of excess competing metal ions including Zn2+, Pb2+, Hg2+ and Cu2+ ions.	cupric ion	164-168	CD2 molecule	Homo sapiens	70-73
30526028-0	2019	Experimental and theoretical investigations of infrared multiple photon dissociation spectra of lysine complexes with Zn2+ and Cd2.	Lysine	96-102	CD2 molecule	Homo sapiens	127-130
30602243-6	2019	The selectivity study in bimetal aqueous systems using copper, lead and zinc metals showed the adsorption order of Cu2+ &gt; Cd2+ &gt; Zn2+ &gt; Pb2+.	Copper	55-61	CD2 molecule	Homo sapiens	125-128
30602243-6	2019	The selectivity study in bimetal aqueous systems using copper, lead and zinc metals showed the adsorption order of Cu2+ &gt; Cd2+ &gt; Zn2+ &gt; Pb2+.	cupric ion	115-119	CD2 molecule	Homo sapiens	125-128
30602243-6	2019	The selectivity study in bimetal aqueous systems using copper, lead and zinc metals showed the adsorption order of Cu2+ &gt; Cd2+ &gt; Zn2+ &gt; Pb2+.	Zinc	135-139	CD2 molecule	Homo sapiens	125-128
30602243-6	2019	The selectivity study in bimetal aqueous systems using copper, lead and zinc metals showed the adsorption order of Cu2+ &gt; Cd2+ &gt; Zn2+ &gt; Pb2+.	Lead	145-149	CD2 molecule	Homo sapiens	125-128
30015025-3	2018	The coordination between the Cd2+ ion and bi-carboxylic acid linker was investigated by Fourier transform infrared (FT-IR) spectroscopy.	bi-carboxylic acid	42-60	CD2 molecule	Homo sapiens	29-32
30388682-0	2019	Cd2+ adsorption performance of tunnel-structured manganese oxides driven by electrochemically controlled redox.	manganese oxide	49-65	CD2 molecule	Homo sapiens	0-3
30388682-5	2019	The adsorption capacity of tunnel-structured manganese oxides for Cd2+ was remarkably enhanced by electrochemical redox reactions.	manganese oxide	45-61	CD2 molecule	Homo sapiens	66-69
30388682-9	2019	Due to the differences in their tunnel size and supporting ion species, the tunnel-structured manganese oxides follow the order of cryptomelane (192.0 mg g-1) &gt; todorokite (44.8 mg g-1) &gt; pyrolusite (13.5 mg g-1) in their electrochemical adsorption capacities for Cd2+.	manganese oxide	94-110	CD2 molecule	Homo sapiens	270-273
31474742-5	2019	As the expression of ZIP8, a zinc transporter having affinities for Cd2+ and Mn2+, was the highest in S3 cells, ZIP8 may contribute largely to the apical uptakes of these metals.	Manganese(2+)	77-81	CD2 molecule	Homo sapiens	68-71
31198086-7	2019	In conclusion, our work discovered a new Cd resistant gene for utilizing in transgenic crops for preventing Cd2+ influx.	Cadmium	41-43	CD2 molecule	Homo sapiens	108-111
30407104-6	2019	Furthermore, the uranyl cation was also removed preferentially in the presence of Pb2+ and Cd2+ heavy metal cations, hydronium ions, and more importantly the naturally occurring cations, Na1+, Ca2+, and Mg2+ that occur in abundant concentrations.	uranyl	17-23	CD2 molecule	Homo sapiens	91-94
30407104-6	2019	Furthermore, the uranyl cation was also removed preferentially in the presence of Pb2+ and Cd2+ heavy metal cations, hydronium ions, and more importantly the naturally occurring cations, Na1+, Ca2+, and Mg2+ that occur in abundant concentrations.	Metals	102-107	CD2 molecule	Homo sapiens	91-94
30075436-0	2018	A new multifunctional benzimidazole tagged coumarin as ratiometric fluorophore for the detection of Cd2+/F- ions and imaging in live cells.	benzimidazole	22-35	CD2 molecule	Homo sapiens	100-103
30075436-0	2018	A new multifunctional benzimidazole tagged coumarin as ratiometric fluorophore for the detection of Cd2+/F- ions and imaging in live cells.	coumarin	43-51	CD2 molecule	Homo sapiens	100-103
30075436-2	2018	The probe (3)-((2)-(1H-benzoimidazole-2-yl)-phenylimino) methyl-4-chloro-methyl-2H-chromen-2-ene (BIMC) displays excellent ratiometric responses towards Cd2+/F- ions over the tested cations/anions.	(3)-((2)-(1h-benzoimidazole-2-yl)-phenylimino) methyl-4-chloro-methyl-2h-chromen-2-ene	10-96	CD2 molecule	Homo sapiens	153-156
30075436-2	2018	The probe (3)-((2)-(1H-benzoimidazole-2-yl)-phenylimino) methyl-4-chloro-methyl-2H-chromen-2-ene (BIMC) displays excellent ratiometric responses towards Cd2+/F- ions over the tested cations/anions.	bimc	98-102	CD2 molecule	Homo sapiens	153-156
30075436-4	2018	Job"s plot and Electro spray Ionization mass spectral (ESI-MS) studies confirms 1:1 binding stoichiometry of BIMC with Cd2+/F- ions, which is further evidenced by 1H NMR titration studies.	bimc	109-113	CD2 molecule	Homo sapiens	119-122
30075436-5	2018	The reversibility studies of BIMC with Cd2+ have been investigated using ethylenediaminetetraacetic acid (EDTA).	bimc	29-33	CD2 molecule	Homo sapiens	39-42
30442667-5	2018	Furthermore, CD8+ MAIT cells have higher levels of receptors for IL-12 and IL-18, as well as of the activating receptors CD2, CD9, and NKG2D, and display superior functionality following stimulation with riboflavin-autotrophic as well as riboflavin-auxotrophic bacterial strains.	Riboflavin	204-214	CD2 molecule	Homo sapiens	121-124
28866961-2	2018	In this work, the application potential of chitosan derivative for the uptake of Pb2+, Cu2+, Ni2+, Zn2+, Cr6+, and Cd2+ ions from aqueous solution in a packed bed adsorption column was investigated.	Chitosan	43-51	CD2 molecule	Homo sapiens	115-118
30315535-3	2018	It showed that the adsorption of RhB on the tested soil was affected by Cd2+ and could be better fitted by the Freundlich model and dominantly identified as chemical adsorption according to the threshold of DeltaG0 (40 kJ/mol).	rhodamine B	33-36	CD2 molecule	Homo sapiens	72-75
30315535-4	2018	There is a positive hysteresis on the desorption of RhB, which was generally strengthened with the increasing concentration of RhB but generally weakened in the presence of Cd2+.	rhodamine B	52-55	CD2 molecule	Homo sapiens	173-176
30333154-8	2018	The larger number of CD2-CD2 lipid chain interactions in the LPP than in a symmetrical bilayer structure implied that the ceramide had primarily adopted an extended conformation.	Ceramides	122-130	CD2 molecule	Homo sapiens	21-24
30333154-8	2018	The larger number of CD2-CD2 lipid chain interactions in the LPP than in a symmetrical bilayer structure implied that the ceramide had primarily adopted an extended conformation.	Ceramides	122-130	CD2 molecule	Homo sapiens	25-28
30268883-1	2018	This study investigated the impact of pH on the migration of cadmium(II) ions (Cd2+) in relation to montmorillonite KSF colloids through a water-saturated sand column (WSSC).	Cadmium ion	61-72	CD2 molecule	Homo sapiens	79-82
30268883-7	2018	The increasing level of Cd2+ sorbed on colloids as the pH increased resulted in a long tailing of the breakthrough curve (BTC) of the total Cd, indicating that the total Cd was controlled by rate-limited reactions.	Cadmium	140-142	CD2 molecule	Homo sapiens	24-27
30533410-0	2018	Adsorption Properties and Mechanism of Cd2+ in Water by Zr-containing Silica Residue Purification.	Water	47-52	CD2 molecule	Homo sapiens	39-42
30487525-4	2018	It was found that the electrode modified with 1 mg AgNPs and 2 mg MWCNTs exhibited the best analytical response towards the determination of Pb2+ and Cd2+.	agnps	51-56	CD2 molecule	Homo sapiens	150-153
30533410-3	2018	The results showed that ZSR-P had a good effect on the adsorption and removal of Cd2+ in water.	zsr-p	24-29	CD2 molecule	Homo sapiens	81-84
30533410-0	2018	Adsorption Properties and Mechanism of Cd2+ in Water by Zr-containing Silica Residue Purification.	Zirconium	56-58	CD2 molecule	Homo sapiens	39-42
30533410-3	2018	The results showed that ZSR-P had a good effect on the adsorption and removal of Cd2+ in water.	Water	89-94	CD2 molecule	Homo sapiens	81-84
30533410-0	2018	Adsorption Properties and Mechanism of Cd2+ in Water by Zr-containing Silica Residue Purification.	Silicon Dioxide	70-76	CD2 molecule	Homo sapiens	39-42
30533410-5	2018	Under optimal conditions, the amount of Cd2+ adsorbed by ZSR-P was 43.1 mg/g.	zsr-p	57-62	CD2 molecule	Homo sapiens	40-43
30533410-1	2018	Zirconium (Zr)-containing silica residue purification (ZSR-P) discharged from industrial production of ZrOCl2 was used as an adsorbent, and CdCl2 solution was used as the simulated wastewater containing cadmium ions (Cd2+).	Zirconium	0-9	CD2 molecule	Homo sapiens	217-220
30533410-7	2018	In ZSR-P-Cd, Cd2+ was uniformly distributed on the surface of SiO2 particles and in the pores formed by the accumulation of particles.	zsr-p-cd	3-11	CD2 molecule	Homo sapiens	13-16
30533410-7	2018	In ZSR-P-Cd, Cd2+ was uniformly distributed on the surface of SiO2 particles and in the pores formed by the accumulation of particles.	Silicon Dioxide	62-66	CD2 molecule	Homo sapiens	13-16
30533410-8	2018	Adsorption of Cd2+ by ZSR-P was achieved through the reaction between Si-OH on the surface of SiO2 and Cd2+ hydroxyl compounds.	zsr-p	22-27	CD2 molecule	Homo sapiens	14-17
30533410-8	2018	Adsorption of Cd2+ by ZSR-P was achieved through the reaction between Si-OH on the surface of SiO2 and Cd2+ hydroxyl compounds.	zsr-p	22-27	CD2 molecule	Homo sapiens	103-106
30533410-8	2018	Adsorption of Cd2+ by ZSR-P was achieved through the reaction between Si-OH on the surface of SiO2 and Cd2+ hydroxyl compounds.	si-oh	70-75	CD2 molecule	Homo sapiens	14-17
30533410-8	2018	Adsorption of Cd2+ by ZSR-P was achieved through the reaction between Si-OH on the surface of SiO2 and Cd2+ hydroxyl compounds.	Silicon Dioxide	94-98	CD2 molecule	Homo sapiens	14-17
30533410-1	2018	Zirconium (Zr)-containing silica residue purification (ZSR-P) discharged from industrial production of ZrOCl2 was used as an adsorbent, and CdCl2 solution was used as the simulated wastewater containing cadmium ions (Cd2+).	Zirconium	11-13	CD2 molecule	Homo sapiens	217-220
30351074-2	2018	Compound 1 was postmodified by a photodimerization reaction between 5-F-1,3-bpeb ligands to yield [{Cd2( syn-dftpmcp)(1,3-BDC)2} 0.5DMF H2O] n ( syn-dftpmcp = syn-3,4,12,13-tetrakis(4-pyridyl)-8,17-bisfluoro-1,2,9,10-diethano[2.2]metacyclophane) (2).	5-f-1,3-bpeb	68-80	CD2 molecule	Homo sapiens	100-103
29906119-4	2018	Using well-calibrated methods, we have determined the preferred hydrogen-bonding partners of Cys- bound to native Zn2+ or xenobiotic Cd2+ in Zn-fingers of varying net charge and solvent accessibility as well as the key factors underlying the observed preference.	Hydrogen	64-72	CD2 molecule	Homo sapiens	133-136
29906119-4	2018	Using well-calibrated methods, we have determined the preferred hydrogen-bonding partners of Cys- bound to native Zn2+ or xenobiotic Cd2+ in Zn-fingers of varying net charge and solvent accessibility as well as the key factors underlying the observed preference.	Cysteine	93-96	CD2 molecule	Homo sapiens	133-136
29906119-5	2018	We show how secondary hydrogen-bonding interactions with metal-bound thiolates might exert a significant impact on Zn2+ Cd2+ substitution and thus protein function.	Hydrogen	22-30	CD2 molecule	Homo sapiens	120-123
29906119-5	2018	We show how secondary hydrogen-bonding interactions with metal-bound thiolates might exert a significant impact on Zn2+ Cd2+ substitution and thus protein function.	Metals	57-62	CD2 molecule	Homo sapiens	120-123
29906119-5	2018	We show how secondary hydrogen-bonding interactions with metal-bound thiolates might exert a significant impact on Zn2+ Cd2+ substitution and thus protein function.	thiolates	69-78	CD2 molecule	Homo sapiens	120-123
30351074-2	2018	Compound 1 was postmodified by a photodimerization reaction between 5-F-1,3-bpeb ligands to yield [{Cd2( syn-dftpmcp)(1,3-BDC)2} 0.5DMF H2O] n ( syn-dftpmcp = syn-3,4,12,13-tetrakis(4-pyridyl)-8,17-bisfluoro-1,2,9,10-diethano[2.2]metacyclophane) (2).	5dmf h2o] n	131-142	CD2 molecule	Homo sapiens	100-103
30351074-3	2018	Compounds 1 and 2 have 2D networks built from linking one-dimensional [Cd2(1,3-BDC)2] n chains via 5-F-1,3-bpeb or syn-dftpmcp bridges.	dftpmcp	119-126	CD2 molecule	Homo sapiens	71-74
30081381-8	2018	Selectivity measurements reveal that the sensor is specific for Cd2+ even in the presence of high concentrations of other metal ions.	Metals	122-127	CD2 molecule	Homo sapiens	64-67
30143155-0	2018	Preparation of polyethylene glycol diglycidyl ether (PEDGE) crosslinked chitosan/activated carbon composite film for Cd2+ removal.	Quetol 651	15-51	CD2 molecule	Homo sapiens	117-120
30143155-0	2018	Preparation of polyethylene glycol diglycidyl ether (PEDGE) crosslinked chitosan/activated carbon composite film for Cd2+ removal.	Chitosan	72-80	CD2 molecule	Homo sapiens	117-120
30143155-0	2018	Preparation of polyethylene glycol diglycidyl ether (PEDGE) crosslinked chitosan/activated carbon composite film for Cd2+ removal.	Carbon	91-97	CD2 molecule	Homo sapiens	117-120
30143155-8	2018	The obtained PEDGE crosslinked chitosan/activated carbon composite film was used for adsorption of Cd2+.	Carbon	50-56	CD2 molecule	Homo sapiens	99-102
30143155-10	2018	Based on Langmuir adsorption isotherm model, the maximum adsorption capacity (Q) of Cd2+ by PEDGE crosslinked chitosan/activated carbon composite film was 357.14 mg/g.	Carbon	129-135	CD2 molecule	Homo sapiens	84-87
30071432-1	2018	Cadmium(II) ion can affect the anode performance of bioelectrochemical systems (BES); however, how the presence of Cd2+ affect the extracellular electron transfer of anodic electrochemically active biofilms (EABs), the microbial viability and species composition of microorganism on the anode remain poorly understood.	Cadmium ion	0-11	CD2 molecule	Homo sapiens	115-118
30071432-1	2018	Cadmium(II) ion can affect the anode performance of bioelectrochemical systems (BES); however, how the presence of Cd2+ affect the extracellular electron transfer of anodic electrochemically active biofilms (EABs), the microbial viability and species composition of microorganism on the anode remain poorly understood.	eabs	208-212	CD2 molecule	Homo sapiens	115-118
30071432-2	2018	Here, we investigated the inhibitory effect of Cd2+ at different concentrations on the electrochemical performance and the biofilm community in mixed-culture enriched BES.	BES	167-170	CD2 molecule	Homo sapiens	47-50
30071432-6	2018	Cyclic voltammogram and electrochemical impedance spectroscopy revealed that high concentration of Cd2+ exceeding 5 mg L-1 can inhibit the secretion of outer membrane cytochromes, thus reducing the electron transfer between the EABs and the anode surface.	eabs	228-232	CD2 molecule	Homo sapiens	99-102
30071432-7	2018	Analysis of bacterial structures showed a decrease in Geobacter accompanied by an increase in Stenotrophomonas and Azospira in response to Cd2+ at 10 and 20 mg L-1.	azospira	115-123	CD2 molecule	Homo sapiens	139-142
30071432-8	2018	This study added to the in-depth analysis of the inhibition of Cd2+ on EABs, and provided new insights into the removing Cd2+ and organics simultaneously in BES.	eabs	71-75	CD2 molecule	Homo sapiens	63-66
30220062-0	2018	Adsorption of heavy metal tolerance strains to Pb2+ and Cd2+ in wastewater.	Metals	20-25	CD2 molecule	Homo sapiens	56-59
30220062-1	2018	The functional strains with high tolerance to heavy metal Pb2+ and Cd2+ were screened from soil obtained in a heavy metal waste accumulation area.	Metals	116-121	CD2 molecule	Homo sapiens	67-70
30220062-5	2018	Langmuir and Freundlich equation showed that the adsorption of Pb2+ and Cd2+ was mainly on the surface of monolayer.	Lead	63-67	CD2 molecule	Homo sapiens	72-75
30220062-6	2018	And the pseudo-second-order kinetic equation indicates that Cd2+ has a relatively greater adsorption rate than Pb2+ does.	Lead	111-115	CD2 molecule	Homo sapiens	60-63
29363693-2	2018	The unique metal-ligand binding properties of the Cd2+ analogue of this construct give rise to a concentration-dependent dynamic equilibrium between cube, prism, and tetrahedron-shaped architectures.	Metals	11-16	CD2 molecule	Homo sapiens	50-53
30261723-0	2018	Analysis of the Five Unimolecular Reaction Pathways of CD2ClCHFCl with Emphasis on CD2Cl(F)C: and CD2Cl(Cl)C: Formed by 1,1-HCl and 1,1-HF Elimination.	1,1-hcl	120-127	CD2 molecule	Homo sapiens	55-58
30261723-1	2018	The five unimolecular HX and DX (X = F, Cl) elimination pathways of CD2ClCHFCl* were examined using a chemical activation technique; the molecules were generated with 92 kcal mol-1 of vibrational energy in a room-temperature bath gas by a combination of CD2Cl and CHFCl radicals.	chfcl radicals	264-278	CD2 molecule	Homo sapiens	68-71
30261723-4	2018	The 1,1-HCl and 1,1-HF reactions gave carbenes, CD2Cl(F)C: and CD2Cl(Cl)C:, respectively, as products, which have hydrogen-bonded complexes with HCl or HF in the exit channel of the potential energy surface.	,1-hcl	5-11	CD2 molecule	Homo sapiens	48-51
30261723-4	2018	The 1,1-HCl and 1,1-HF reactions gave carbenes, CD2Cl(F)C: and CD2Cl(Cl)C:, respectively, as products, which have hydrogen-bonded complexes with HCl or HF in the exit channel of the potential energy surface.	Hydrogen	114-122	CD2 molecule	Homo sapiens	48-51
30261723-4	2018	The 1,1-HCl and 1,1-HF reactions gave carbenes, CD2Cl(F)C: and CD2Cl(Cl)C:, respectively, as products, which have hydrogen-bonded complexes with HCl or HF in the exit channel of the potential energy surface.	Hydrochloric Acid	8-11	CD2 molecule	Homo sapiens	48-51
30261723-4	2018	The 1,1-HCl and 1,1-HF reactions gave carbenes, CD2Cl(F)C: and CD2Cl(Cl)C:, respectively, as products, which have hydrogen-bonded complexes with HCl or HF in the exit channel of the potential energy surface.	Hafnium	20-22	CD2 molecule	Homo sapiens	48-51
30261723-6	2018	Electronic structure calculations provide information for transition states of CD2ClCHFCl and hydrogen-bonded complexes of carbenes with HF and HCl.	carbene	123-131	CD2 molecule	Homo sapiens	79-82
30261723-6	2018	Electronic structure calculations provide information for transition states of CD2ClCHFCl and hydrogen-bonded complexes of carbenes with HF and HCl.	Hafnium	85-87	CD2 molecule	Homo sapiens	79-82
30261723-6	2018	Electronic structure calculations provide information for transition states of CD2ClCHFCl and hydrogen-bonded complexes of carbenes with HF and HCl.	Hydrochloric Acid	144-147	CD2 molecule	Homo sapiens	79-82
30209882-1	2018	The double- or triple-decker 3D metallo-hexagons were obtained by self-assembly of multitopic tris-terpyridines with Cd2+ ions in near-quantitative yield.	tris-terpyridines	94-111	CD2 molecule	Homo sapiens	117-120
30007624-1	2018	The present work describes the electrochemical detection of Cd2+ using reduced graphene oxide (rGO), carboxymethyl cellulose (CMC) and glutathione (GSH) modified glassy carbon electrode (GCE) by Square Wave Anodic Stripping Voltammetry (SWASV).	graphene oxide	79-93	CD2 molecule	Homo sapiens	60-63
30229598-2	2018	The experiment revealed that the biomass and chlorophyll content of ryegrass significantly declined at high concentrations of Cd2+(10 mg L-1), while POD and PPO activities significantly increased.	Chlorophyll	45-56	CD2 molecule	Homo sapiens	126-129
30007624-1	2018	The present work describes the electrochemical detection of Cd2+ using reduced graphene oxide (rGO), carboxymethyl cellulose (CMC) and glutathione (GSH) modified glassy carbon electrode (GCE) by Square Wave Anodic Stripping Voltammetry (SWASV).	Carboxymethylcellulose Sodium	101-124	CD2 molecule	Homo sapiens	60-63
30007624-1	2018	The present work describes the electrochemical detection of Cd2+ using reduced graphene oxide (rGO), carboxymethyl cellulose (CMC) and glutathione (GSH) modified glassy carbon electrode (GCE) by Square Wave Anodic Stripping Voltammetry (SWASV).	Carboxymethylcellulose Sodium	126-129	CD2 molecule	Homo sapiens	60-63
30007624-1	2018	The present work describes the electrochemical detection of Cd2+ using reduced graphene oxide (rGO), carboxymethyl cellulose (CMC) and glutathione (GSH) modified glassy carbon electrode (GCE) by Square Wave Anodic Stripping Voltammetry (SWASV).	Glutathione	135-146	CD2 molecule	Homo sapiens	60-63
30007624-1	2018	The present work describes the electrochemical detection of Cd2+ using reduced graphene oxide (rGO), carboxymethyl cellulose (CMC) and glutathione (GSH) modified glassy carbon electrode (GCE) by Square Wave Anodic Stripping Voltammetry (SWASV).	Glutathione	148-151	CD2 molecule	Homo sapiens	60-63
30007624-1	2018	The present work describes the electrochemical detection of Cd2+ using reduced graphene oxide (rGO), carboxymethyl cellulose (CMC) and glutathione (GSH) modified glassy carbon electrode (GCE) by Square Wave Anodic Stripping Voltammetry (SWASV).	Carbon	169-175	CD2 molecule	Homo sapiens	60-63
30007624-6	2018	Finally, rGO/CMC/GSH/GCE was successfully demonstrated for the detection of Cd2+ in real samples, and the results were compared with AAS analysis.	Glutathione	17-20	CD2 molecule	Homo sapiens	76-79
30029374-0	2018	A highly sensitive colorimetric probe for Cd2+, Hg2+ and ascorbic acid determination based on trithiocyanuric acid-AuNPs.	trithiocyanuric acid	94-114	CD2 molecule	Homo sapiens	42-45
29742476-0	2018	Competitive adsorption of Cd2+, Pb2+ and Ni2+ onto Fe3+-modified argillaceous limestone: Influence of pH, ionic strength and natural organic matters.	ferric sulfate	51-55	CD2 molecule	Homo sapiens	26-29
29742476-1	2018	In present study, the feasibility of applying a natural adsorbent with Fe3+ modification (Fe3+-modified argillaceous limestone, FAL) on the competitive adsorption of heavy metals (i.e., Cd2+, Pb2+ and Ni2+) was evaluated.	ferric sulfate	71-75	CD2 molecule	Homo sapiens	186-189
29742476-1	2018	In present study, the feasibility of applying a natural adsorbent with Fe3+ modification (Fe3+-modified argillaceous limestone, FAL) on the competitive adsorption of heavy metals (i.e., Cd2+, Pb2+ and Ni2+) was evaluated.	ferric sulfate	90-94	CD2 molecule	Homo sapiens	186-189
29742476-2	2018	The current results revealed an efficient adsorption on Cd2+, Pb2+ and Ni2+ in mono-metal system.	Nickel(2+)	71-75	CD2 molecule	Homo sapiens	56-59
29742476-2	2018	The current results revealed an efficient adsorption on Cd2+, Pb2+ and Ni2+ in mono-metal system.	Mono-S	79-84	CD2 molecule	Homo sapiens	56-59
29742476-2	2018	The current results revealed an efficient adsorption on Cd2+, Pb2+ and Ni2+ in mono-metal system.	Metals	84-89	CD2 molecule	Homo sapiens	56-59
29742476-3	2018	Further experiments demonstrated a high selectivity of Pb2+ during the competitive adsorption of Cd2+, Pb2+ and Ni2+.	Lead	55-59	CD2 molecule	Homo sapiens	97-100
29742476-3	2018	Further experiments demonstrated a high selectivity of Pb2+ during the competitive adsorption of Cd2+, Pb2+ and Ni2+.	Nickel(2+)	112-116	CD2 molecule	Homo sapiens	97-100
30029374-1	2018	A highly sensitive and selective colorimetric assay is proposed for the detection of mercury ions (Hg2+), cadmium ions (Cd2+) and ascorbic acid (AA) using trithiocyanuric acid (TMT) functionalized gold nanoparticles (TMT-AuNPs).	Cadmium	106-113	CD2 molecule	Homo sapiens	120-123
29742476-6	2018	It is interestingly that various NOMs (i.e., humic acid (HA) and glycine (Gly)) exerted different effects on the adsorption behaviors, probably due to the different affinities for Pb2+, Cd2+ and Ni2+ and the redistribution of newly-formed metal-DOM complexes.	Humic Substances	45-55	CD2 molecule	Homo sapiens	186-189
30029374-1	2018	A highly sensitive and selective colorimetric assay is proposed for the detection of mercury ions (Hg2+), cadmium ions (Cd2+) and ascorbic acid (AA) using trithiocyanuric acid (TMT) functionalized gold nanoparticles (TMT-AuNPs).	trithiocyanuric acid	155-175	CD2 molecule	Homo sapiens	120-123
29742476-6	2018	It is interestingly that various NOMs (i.e., humic acid (HA) and glycine (Gly)) exerted different effects on the adsorption behaviors, probably due to the different affinities for Pb2+, Cd2+ and Ni2+ and the redistribution of newly-formed metal-DOM complexes.	Humic Substances	57-59	CD2 molecule	Homo sapiens	186-189
29742476-6	2018	It is interestingly that various NOMs (i.e., humic acid (HA) and glycine (Gly)) exerted different effects on the adsorption behaviors, probably due to the different affinities for Pb2+, Cd2+ and Ni2+ and the redistribution of newly-formed metal-DOM complexes.	Glycine	65-72	CD2 molecule	Homo sapiens	186-189
30029374-2	2018	TMT-AuNPs are dispersed in 40 mM NaCl solution, while the presence of Hg2+ and Cd2+ can induce TMT-AuNPs aggregate due to the strong interaction of Hg2+ and Cd2+ with TMT.	nacl solution	33-46	CD2 molecule	Homo sapiens	79-82
29742476-6	2018	It is interestingly that various NOMs (i.e., humic acid (HA) and glycine (Gly)) exerted different effects on the adsorption behaviors, probably due to the different affinities for Pb2+, Cd2+ and Ni2+ and the redistribution of newly-formed metal-DOM complexes.	Glycine	74-77	CD2 molecule	Homo sapiens	186-189
30029374-2	2018	TMT-AuNPs are dispersed in 40 mM NaCl solution, while the presence of Hg2+ and Cd2+ can induce TMT-AuNPs aggregate due to the strong interaction of Hg2+ and Cd2+ with TMT.	Mercuric cation	70-74	CD2 molecule	Homo sapiens	157-160
30029374-3	2018	Then the quantitative detection of Hg2+ and Cd2+can be realized in the linear range from 5 x 10-9 to 1 x 10-6 M and 1 x 10-8 to 3 x 10-7 M, with a lower detection limit of 2.8 nM for Hg2+ and 3.5 nM for Cd2+ (S/N = 3), respectively.	Mercuric cation	35-39	CD2 molecule	Homo sapiens	203-206
30029374-3	2018	Then the quantitative detection of Hg2+ and Cd2+can be realized in the linear range from 5 x 10-9 to 1 x 10-6 M and 1 x 10-8 to 3 x 10-7 M, with a lower detection limit of 2.8 nM for Hg2+ and 3.5 nM for Cd2+ (S/N = 3), respectively.	Mercuric cation	183-187	CD2 molecule	Homo sapiens	44-47
30029374-4	2018	To distinguish Hg2+ from Cd2+, a reductive biological small molecule ascorbic acid (AA) was used based on the different redox interaction of AA with Hg2+ and Cd2+.	Ascorbic Acid	69-82	CD2 molecule	Homo sapiens	25-28
30029374-4	2018	To distinguish Hg2+ from Cd2+, a reductive biological small molecule ascorbic acid (AA) was used based on the different redox interaction of AA with Hg2+ and Cd2+.	Ascorbic Acid	69-82	CD2 molecule	Homo sapiens	158-161
29904983-4	2018	In this context, we evaluated the formation of cation-pi complexes derived from [6]- and [7]helicene, involving Sn2+ , Cd2+ , and In+ in addition of Ag+ , which appears as a plausible modification of such helicoidal structure.	[6]- and	80-88	CD2 molecule	Homo sapiens	119-122
30236153-5	2018	RESULTS: We show that Treg are indispensable for tolerance induced by coreceptor and costimulation blockade as depletion of which with an anti-hCD2 antibody resulted in rejection of hESC-derived pancreatic islets in NOD.Foxp3hCD2 mice.	treg	22-26	CD2 molecule	Homo sapiens	143-147
29904983-4	2018	In this context, we evaluated the formation of cation-pi complexes derived from [6]- and [7]helicene, involving Sn2+ , Cd2+ , and In+ in addition of Ag+ , which appears as a plausible modification of such helicoidal structure.	heptahelicene	89-100	CD2 molecule	Homo sapiens	119-122
29959734-0	2018	Equilibrium adsorption study of the adsorptive removal of Cd2+ and Cr6+ using activated carbon.	Carbon	88-94	CD2 molecule	Homo sapiens	58-61
30043269-5	2018	With only sucrose as substrate, GtfZ-CD2 was found to mainly catalyze sucrose hydrolysis and leucrose synthesis.	Sucrose	10-17	CD2 molecule	Homo sapiens	37-40
30043269-5	2018	With only sucrose as substrate, GtfZ-CD2 was found to mainly catalyze sucrose hydrolysis and leucrose synthesis.	Sucrose	70-77	CD2 molecule	Homo sapiens	37-40
30043269-5	2018	With only sucrose as substrate, GtfZ-CD2 was found to mainly catalyze sucrose hydrolysis and leucrose synthesis.	leucrose	93-101	CD2 molecule	Homo sapiens	37-40
30043269-6	2018	When dextran was available as acceptor substrate, GtfZ-CD2 displayed an efficient transglycosidase activity with sucrose as donor substrate.	Dextrans	5-12	CD2 molecule	Homo sapiens	55-58
30043269-6	2018	When dextran was available as acceptor substrate, GtfZ-CD2 displayed an efficient transglycosidase activity with sucrose as donor substrate.	Sucrose	113-120	CD2 molecule	Homo sapiens	55-58
30043269-8	2018	Structural characterization of the products revealed that GtfZ-CD2 catalyzes the synthesis of single glucosyl (alpha1   3) linked branches onto dextran, resulting in the production of highly branched comb-like alpha-glucan products.	Dextrans	144-151	CD2 molecule	Homo sapiens	63-66
30043269-8	2018	Structural characterization of the products revealed that GtfZ-CD2 catalyzes the synthesis of single glucosyl (alpha1   3) linked branches onto dextran, resulting in the production of highly branched comb-like alpha-glucan products.	alpha-glucan	210-222	CD2 molecule	Homo sapiens	63-66
29959734-3	2018	The adsorption isotherms of Cd2+ and Cr6+ on activated carbon can fit the Langmuir model well, and correlation coefficients were above 0.99, all higher than the Freundlich and Temkin models.	Carbon	55-61	CD2 molecule	Homo sapiens	28-31
29959734-8	2018	The speciation on activated carbon was mainly residual Cd2+ and Cr6+, and the potential ecological risk of Cd2+ is higher than that of Cr6+.	Carbon	28-34	CD2 molecule	Homo sapiens	55-58
29959734-8	2018	The speciation on activated carbon was mainly residual Cd2+ and Cr6+, and the potential ecological risk of Cd2+ is higher than that of Cr6+.	Carbon	28-34	CD2 molecule	Homo sapiens	107-110
29959734-9	2018	The adsorptions of Cd2+ and Cr6+ on activated carbon were dominated by chelation and ion exchange, respectively.	Carbon	46-52	CD2 molecule	Homo sapiens	19-22
29660878-0	2018	Investigation of the behaviour of zero-valent iron nanoparticles and their interactions with Cd2+ in wastewater by single particle ICP-MS. Zero-valent iron nanoparticles (nZVI) exhibit great potential for the removal of metal contaminants from wastewater.	Iron	46-50	CD2 molecule	Homo sapiens	93-96
29702319-1	2018	Since adsorption and nanomaterials had been respectively found to be the most promising technique and the preferred adsorbents for heavy metal ions removal, in this study, novel mesoporous silica-calcium phosphate (MS-CP) hybrid nanoparticles were synthesized by a facile one-pot method, and subsequently assessed as adsorbent for Cd2+ removal from aqueous solution.	ms-cp	215-220	CD2 molecule	Homo sapiens	331-334
29702319-5	2018	The Cd2+ removal experiments demonstrated that MS-CP had a high adsorption capacity due to electrostatic interaction between Cd2+ and silanol groups on MS-CP surface, as well as ion-exchange between Cd2+ and calcium in MS-CP.	ms-cp	47-52	CD2 molecule	Homo sapiens	4-7
29702319-5	2018	The Cd2+ removal experiments demonstrated that MS-CP had a high adsorption capacity due to electrostatic interaction between Cd2+ and silanol groups on MS-CP surface, as well as ion-exchange between Cd2+ and calcium in MS-CP.	ms-cp	47-52	CD2 molecule	Homo sapiens	125-128
29702319-5	2018	The Cd2+ removal experiments demonstrated that MS-CP had a high adsorption capacity due to electrostatic interaction between Cd2+ and silanol groups on MS-CP surface, as well as ion-exchange between Cd2+ and calcium in MS-CP.	ms-cp	47-52	CD2 molecule	Homo sapiens	125-128
29702319-7	2018	The maximum adsorption capacity of Cd2+ by MS-CP was above 153 mg/L.	ms-cp	43-48	CD2 molecule	Homo sapiens	35-38
29702319-8	2018	These results suggested that the as-synthesized MS-CP could be promising adsorbent for Cd2+ removal from aqueous solution.	ms-cp	48-53	CD2 molecule	Homo sapiens	87-90
29710586-0	2018	Efficient removal of Cd2+ and Pb2+ from aqueous solution with amino- and thiol-functionalized activated carbon: Isotherm and kinetics modeling.	Sulfhydryl Compounds	73-78	CD2 molecule	Homo sapiens	21-24
29710586-0	2018	Efficient removal of Cd2+ and Pb2+ from aqueous solution with amino- and thiol-functionalized activated carbon: Isotherm and kinetics modeling.	Carbon	104-110	CD2 molecule	Homo sapiens	21-24
30084020-1	2018	A novel fluorescent probe (NT) was developed by merging 2-hydrazinylbenzothiazole with 2-hydroxy-1-naphthaldehyde for the detection of Cd2+ and Cu2+.	2-hydrazinobenzothiazole	56-81	CD2 molecule	Homo sapiens	135-138
30084020-1	2018	A novel fluorescent probe (NT) was developed by merging 2-hydrazinylbenzothiazole with 2-hydroxy-1-naphthaldehyde for the detection of Cd2+ and Cu2+.	2-hydroxy-1-naphthaldehyde	87-113	CD2 molecule	Homo sapiens	135-138
30084020-5	2018	Based on fluorescence spectra and ESI-MS analysis, the binding modes between NT and Cd2+/Cu2+ were proposed.	cupric ion	89-93	CD2 molecule	Homo sapiens	84-87
29710586-12	2018	The overall results demonstrated that both N-AC and S-AC could be the promising efficient candidates for removing Cd2+ and Pb2+ from contaminated water.	n-ac	43-47	CD2 molecule	Homo sapiens	114-117
29660878-0	2018	Investigation of the behaviour of zero-valent iron nanoparticles and their interactions with Cd2+ in wastewater by single particle ICP-MS. Zero-valent iron nanoparticles (nZVI) exhibit great potential for the removal of metal contaminants from wastewater.	Iron	151-155	CD2 molecule	Homo sapiens	93-96
29710586-12	2018	The overall results demonstrated that both N-AC and S-AC could be the promising efficient candidates for removing Cd2+ and Pb2+ from contaminated water.	Actinium	52-56	CD2 molecule	Homo sapiens	114-117
29710586-12	2018	The overall results demonstrated that both N-AC and S-AC could be the promising efficient candidates for removing Cd2+ and Pb2+ from contaminated water.	Water	146-151	CD2 molecule	Homo sapiens	114-117
29660878-8	2018	Consequently, Cd2+ was more efficiently (86%) removed from effluent wastewater than from synthetic wastewater (73%), while its removal from Milli-Q water was inefficient (19%).	Water	73-78	CD2 molecule	Homo sapiens	14-17
29660878-9	2018	The trace amounts of Cd2+ that remained in the remediated water were either dissolved or sorbed to residual nZVI.	Water	58-63	CD2 molecule	Homo sapiens	21-24
29786906-1	2018	A dimethylxanthene-based phosphine/borane frustrated Lewis pair (FLP) is shown to effect reversible C-H activation, cleaving phenylacetylene, PhCCH, to give an equilibrium mixture of the free FLP and phosphonium acetylide in CD2 Cl2 solution at room temperature.	Dimethyl-9H-xanthene	2-18	CD2 molecule	Homo sapiens	225-228
32255071-5	2018	Interestingly, the addition of Zn2+ or Cd2+ can connect the nanospheres to form large aggregates, so a unique second increase of AEE from GSH-AuNCs appears, while the emission of SiNPs remains constant to act as an internal reference.	aspirin eugenol ester	129-132	CD2 molecule	Homo sapiens	39-42
32255071-5	2018	Interestingly, the addition of Zn2+ or Cd2+ can connect the nanospheres to form large aggregates, so a unique second increase of AEE from GSH-AuNCs appears, while the emission of SiNPs remains constant to act as an internal reference.	Glutathione	138-141	CD2 molecule	Homo sapiens	39-42
32255071-6	2018	The fluorescence ratios (I570/I450) of SiNPs@GSH-AuNCs are positively correlated with Zn2+ or Cd2+ with the linear range from 1.5 muM to 500 muM.	Glutathione	45-48	CD2 molecule	Homo sapiens	94-97
32255071-6	2018	The fluorescence ratios (I570/I450) of SiNPs@GSH-AuNCs are positively correlated with Zn2+ or Cd2+ with the linear range from 1.5 muM to 500 muM.	Zinc	86-90	CD2 molecule	Homo sapiens	94-97
29753966-3	2018	Meanwhile, probe 1 displays selectivity for Cd2+ over other metal ions and anions in DMF by emission spectrum.	Metals	60-65	CD2 molecule	Homo sapiens	44-47
29753966-3	2018	Meanwhile, probe 1 displays selectivity for Cd2+ over other metal ions and anions in DMF by emission spectrum.	Dimethylformamide	85-88	CD2 molecule	Homo sapiens	44-47
29923039-1	2018	Cadmium (Cd2+) is toxic to living organisms because it causes the malfunction of essential proteins and induces oxidative stress.	Cadmium	0-7	CD2 molecule	Homo sapiens	9-12
29923039-3	2018	Intriguingly, the effects of Cd2+ on the activity of IDH are both positive and negative, and to understand the molecular basis, we determined the crystal structure of NADP+-dependent cytosolic IDH in the presence of Cd2+.	NADP	167-172	CD2 molecule	Homo sapiens	29-32
29923039-3	2018	Intriguingly, the effects of Cd2+ on the activity of IDH are both positive and negative, and to understand the molecular basis, we determined the crystal structure of NADP+-dependent cytosolic IDH in the presence of Cd2+.	NADP	167-172	CD2 molecule	Homo sapiens	216-219
29923039-4	2018	The structure includes two Cd2+ ions, one coordinated by active site residues and another near a cysteine residue.	Cysteine	97-105	CD2 molecule	Homo sapiens	27-30
29923039-5	2018	Cd2+ presumably inactivates IDH due to its high affinity for thiols, leading to a covalent enzyme modification.	Sulfhydryl Compounds	61-67	CD2 molecule	Homo sapiens	0-3
29923039-7	2018	Inactivation of IDH by Cd2+ is less effective when the enzyme is activated with Cd2+ than Mg2+.	magnesium ion	90-94	CD2 molecule	Homo sapiens	23-26
29923039-9	2018	Glutathione, a cellular sulphydryl reductant, has a moderate affinity for Cd2+, allowing IDH to be activated with residual Cd2+, unlike dithiothreitol, which has a much higher affinity.	Glutathione	0-11	CD2 molecule	Homo sapiens	74-77
29923039-9	2018	Glutathione, a cellular sulphydryl reductant, has a moderate affinity for Cd2+, allowing IDH to be activated with residual Cd2+, unlike dithiothreitol, which has a much higher affinity.	Glutathione	0-11	CD2 molecule	Homo sapiens	123-126
30037402-0	2018	Relating Cd2+ binding by humic acids to molecular weight: A modeling and spectroscopic study.	Humic Substances	25-36	CD2 molecule	Homo sapiens	9-12
30037402-8	2018	Moreover, the distribution of cadmium speciation indicated that the phenolic groups were responsible for the variations in binding of Cd2+ among different Mw fractions.	Cadmium	30-37	CD2 molecule	Homo sapiens	134-137
29759217-6	2018	These generic columns were modified with iminodiacetate to create complexing functionalities on the polymer surface, being further used for online solid-phase extraction of Cu2+, Pb2+ and Cd2+ from natural, tap and drinking waters prior to their determination by stripping chronopotentiometry.	Polymers	100-107	CD2 molecule	Homo sapiens	188-191
29805037-7	2018	Among the cations tested, Cd2+ and Mn2+ bind most tightly, and comparison of three new Cd2+-bound crystal structures suggests that these riboswitches achieve selectivity by enforcing heptacoordination (favored by high-spin Cd2+ and Mn2+, but otherwise uncommon) in the softer site.	Manganese(2+)	232-236	CD2 molecule	Homo sapiens	87-90
29805037-7	2018	Among the cations tested, Cd2+ and Mn2+ bind most tightly, and comparison of three new Cd2+-bound crystal structures suggests that these riboswitches achieve selectivity by enforcing heptacoordination (favored by high-spin Cd2+ and Mn2+, but otherwise uncommon) in the softer site.	Manganese(2+)	232-236	CD2 molecule	Homo sapiens	87-90
29805037-8	2018	Remarkably, the Cd2+- and Mn2+-selective bacterial transcription factor MntR also uses heptacoordination within a binuclear site to achieve selectivity.	Manganese(2+)	26-30	CD2 molecule	Homo sapiens	16-19
30062355-0	2018	Experimental and theoretical investigations of infrared multiple photon dissociation spectra of arginine complexes with Zn2+ and Cd2.	Arginine	96-104	CD2 molecule	Homo sapiens	129-132
30062355-1	2018	Arginine (Arg) complexes with Zn2+ and Cd2+ were examined by infrared multiple photon dissociation (IRMPD) action spectroscopy using light from a free electron laser.	Arginine	0-8	CD2 molecule	Homo sapiens	39-42
30062355-1	2018	Arginine (Arg) complexes with Zn2+ and Cd2+ were examined by infrared multiple photon dissociation (IRMPD) action spectroscopy using light from a free electron laser.	Arginine	0-3	CD2 molecule	Homo sapiens	39-42
29525715-0	2018	Graphene oxide-facilitated transport of Pb2+ and Cd2+ in saturated porous media.	graphene oxide	0-14	CD2 molecule	Homo sapiens	49-52
29525715-1	2018	This paper provides an overview of the effect of graphene oxide (GO) on sorption, transport, and remobilization of Pb2+ and Cd2+ ions in saturated porous media.	graphene oxide	49-63	CD2 molecule	Homo sapiens	124-127
29525715-1	2018	This paper provides an overview of the effect of graphene oxide (GO) on sorption, transport, and remobilization of Pb2+ and Cd2+ ions in saturated porous media.	graphene oxide	65-67	CD2 molecule	Homo sapiens	124-127
29525715-2	2018	The affinity of GO to Pb2+ and Cd2+ ions was investigated via kinetic and isothermal sorption experiments.	graphene oxide	16-18	CD2 molecule	Homo sapiens	31-34
29525715-6	2018	On the other hand, while GO improved the transport ability of Pb2+ and Cd2+, both ions reduced the mobility of GO in saturated porous media.	graphene oxide	25-27	CD2 molecule	Homo sapiens	71-74
29525715-7	2018	Data from the elution experiment revealed that the high affinity of GO toward the metal ions led to the remobilization of the presorbed Pb2+ and Cd2+ ions onto the quartz sand surfaces and their concurrent migration across the sand column.	Metals	82-87	CD2 molecule	Homo sapiens	145-148
29525715-9	2018	The cotransport of Pb2+ and Cd2+ ions with GO in the saturated quartz sand was successfully simulated by the advection-dispersion-reaction equation.	graphene oxide	43-45	CD2 molecule	Homo sapiens	28-31
29786906-1	2018	A dimethylxanthene-based phosphine/borane frustrated Lewis pair (FLP) is shown to effect reversible C-H activation, cleaving phenylacetylene, PhCCH, to give an equilibrium mixture of the free FLP and phosphonium acetylide in CD2 Cl2 solution at room temperature.	phosphine	25-34	CD2 molecule	Homo sapiens	225-228
29786906-1	2018	A dimethylxanthene-based phosphine/borane frustrated Lewis pair (FLP) is shown to effect reversible C-H activation, cleaving phenylacetylene, PhCCH, to give an equilibrium mixture of the free FLP and phosphonium acetylide in CD2 Cl2 solution at room temperature.	Boranes	35-41	CD2 molecule	Homo sapiens	225-228
29786906-1	2018	A dimethylxanthene-based phosphine/borane frustrated Lewis pair (FLP) is shown to effect reversible C-H activation, cleaving phenylacetylene, PhCCH, to give an equilibrium mixture of the free FLP and phosphonium acetylide in CD2 Cl2 solution at room temperature.	phenylacetylene	125-140	CD2 molecule	Homo sapiens	225-228
29786906-1	2018	A dimethylxanthene-based phosphine/borane frustrated Lewis pair (FLP) is shown to effect reversible C-H activation, cleaving phenylacetylene, PhCCH, to give an equilibrium mixture of the free FLP and phosphonium acetylide in CD2 Cl2 solution at room temperature.	phcch	142-147	CD2 molecule	Homo sapiens	225-228
29786906-1	2018	A dimethylxanthene-based phosphine/borane frustrated Lewis pair (FLP) is shown to effect reversible C-H activation, cleaving phenylacetylene, PhCCH, to give an equilibrium mixture of the free FLP and phosphonium acetylide in CD2 Cl2 solution at room temperature.	phosphonium acetylide	200-221	CD2 molecule	Homo sapiens	225-228
29627672-3	2018	The Cd2+ resistant mutant strain C2, which was irradiated by the 12C6+ beams, can grow in Cd medium ranging from 20 to 100 mg L-1 when compared with the original strain.	cd medium	90-99	CD2 molecule	Homo sapiens	4-7
29978884-2	2018	Herein, the in situ formation of CdS quantum dots integrated into a metallogel formed through the coordination of Cd2+ with two pyrimidine nucleobases is reported.	Cadmium	33-36	CD2 molecule	Homo sapiens	114-117
29978884-2	2018	Herein, the in situ formation of CdS quantum dots integrated into a metallogel formed through the coordination of Cd2+ with two pyrimidine nucleobases is reported.	pyrimidine nucleobases	128-150	CD2 molecule	Homo sapiens	114-117
29978884-3	2018	Thymine and uracil formed spontaneous hydrogels with nanofibrous morphology through coordinative interaction with Cd2+ ions at alkaline pH.	Thymine	0-7	CD2 molecule	Homo sapiens	114-117
29978884-3	2018	Thymine and uracil formed spontaneous hydrogels with nanofibrous morphology through coordinative interaction with Cd2+ ions at alkaline pH.	Uracil	12-18	CD2 molecule	Homo sapiens	114-117
29627672-8	2018	The expression of SOD peaked at 24 h in high concentrations of Cd2+; the content of GSH increased gradually and was significantly affected by cultivation time.	Glutathione	84-87	CD2 molecule	Homo sapiens	63-66
29770942-0	2018	Facile preparation of nitrogen and sulfur co-doped graphene-based aerogel for simultaneous removal of Cd2+ and organic dyes.	Nitrogen	22-30	CD2 molecule	Homo sapiens	102-105
29770942-0	2018	Facile preparation of nitrogen and sulfur co-doped graphene-based aerogel for simultaneous removal of Cd2+ and organic dyes.	Sulfur	35-41	CD2 molecule	Homo sapiens	102-105
29770942-0	2018	Facile preparation of nitrogen and sulfur co-doped graphene-based aerogel for simultaneous removal of Cd2+ and organic dyes.	Graphite	51-59	CD2 molecule	Homo sapiens	102-105
29770942-2	2018	A nitrogen (N) and sulfur (S) co-doped graphene-based aerogel (GBA) modified with 2,5-dithiobisurea was synthesized hydrothermally for simultaneous adsorption of Cd2+ and organic dyes-safranin-O (SO), crystal violet (CV), and methylene blue (MB).	Nitrogen	2-10	CD2 molecule	Homo sapiens	162-165
29770942-2	2018	A nitrogen (N) and sulfur (S) co-doped graphene-based aerogel (GBA) modified with 2,5-dithiobisurea was synthesized hydrothermally for simultaneous adsorption of Cd2+ and organic dyes-safranin-O (SO), crystal violet (CV), and methylene blue (MB).	Sulfur	19-25	CD2 molecule	Homo sapiens	162-165
29770942-2	2018	A nitrogen (N) and sulfur (S) co-doped graphene-based aerogel (GBA) modified with 2,5-dithiobisurea was synthesized hydrothermally for simultaneous adsorption of Cd2+ and organic dyes-safranin-O (SO), crystal violet (CV), and methylene blue (MB).	Graphite	39-47	CD2 molecule	Homo sapiens	162-165
29770942-2	2018	A nitrogen (N) and sulfur (S) co-doped graphene-based aerogel (GBA) modified with 2,5-dithiobisurea was synthesized hydrothermally for simultaneous adsorption of Cd2+ and organic dyes-safranin-O (SO), crystal violet (CV), and methylene blue (MB).	based aerogel	48-61	CD2 molecule	Homo sapiens	162-165
29770942-2	2018	A nitrogen (N) and sulfur (S) co-doped graphene-based aerogel (GBA) modified with 2,5-dithiobisurea was synthesized hydrothermally for simultaneous adsorption of Cd2+ and organic dyes-safranin-O (SO), crystal violet (CV), and methylene blue (MB).	8-bromoadenosine	63-66	CD2 molecule	Homo sapiens	162-165
29770942-2	2018	A nitrogen (N) and sulfur (S) co-doped graphene-based aerogel (GBA) modified with 2,5-dithiobisurea was synthesized hydrothermally for simultaneous adsorption of Cd2+ and organic dyes-safranin-O (SO), crystal violet (CV), and methylene blue (MB).	2,5-dithiobisurea	82-99	CD2 molecule	Homo sapiens	162-165
29770942-4	2018	The adsorption mechanism of GBA towards Cd2+ and organic dyes was studied by Dumwald-Wagner models and the results showed that surface and intraparticle diffusion was the key factor in controlling the rate of adsorption.	8-bromoadenosine	28-31	CD2 molecule	Homo sapiens	40-43
29770942-5	2018	The maximum adsorption capacities of GBA towards Cd2+, SO, CV, and MB comprised 1.755, 0.949, 0.538, and 0.389 mmol/g in monocomponent system, respectively.	8-bromoadenosine	37-40	CD2 molecule	Homo sapiens	49-52
29770942-7	2018	The performance of GBA with respect to Cd2+ removal from binary solutions, Cd2+-SO, Cd2+-CV, and Cd2+-MB, was enhanced by the presence of the dyes significantly, while the adsorption capacities towards the dyes were not affected by the presence of Cd2+.	8-bromoadenosine	19-22	CD2 molecule	Homo sapiens	39-42
29770942-7	2018	The performance of GBA with respect to Cd2+ removal from binary solutions, Cd2+-SO, Cd2+-CV, and Cd2+-MB, was enhanced by the presence of the dyes significantly, while the adsorption capacities towards the dyes were not affected by the presence of Cd2+.	8-bromoadenosine	19-22	CD2 molecule	Homo sapiens	75-78
29770942-7	2018	The performance of GBA with respect to Cd2+ removal from binary solutions, Cd2+-SO, Cd2+-CV, and Cd2+-MB, was enhanced by the presence of the dyes significantly, while the adsorption capacities towards the dyes were not affected by the presence of Cd2+.	8-bromoadenosine	19-22	CD2 molecule	Homo sapiens	75-78
29770942-7	2018	The performance of GBA with respect to Cd2+ removal from binary solutions, Cd2+-SO, Cd2+-CV, and Cd2+-MB, was enhanced by the presence of the dyes significantly, while the adsorption capacities towards the dyes were not affected by the presence of Cd2+.	8-bromoadenosine	19-22	CD2 molecule	Homo sapiens	75-78
29770942-7	2018	The performance of GBA with respect to Cd2+ removal from binary solutions, Cd2+-SO, Cd2+-CV, and Cd2+-MB, was enhanced by the presence of the dyes significantly, while the adsorption capacities towards the dyes were not affected by the presence of Cd2+.	8-bromoadenosine	19-22	CD2 molecule	Homo sapiens	75-78
29501167-4	2018	An electrochemical sensor was constructed based on glass carbon electrode (GCE) modified by MoS2 nanosheets obtained in DMF, which exhibits relatively higher sensitivity to Cd2+ detection and lower cytotoxicity against MCF-7 cells.	Carbon	57-63	CD2 molecule	Homo sapiens	173-176
29806770-2	2018	Wet pretreatments of the CIGS absorbers with NH4OH, H2O, and/or aqueous solution of Cd2+ ions were explored to improve the quality of the CIGS/ZnTiO interface, and their effects on the chemical state of the absorber and the final performance of Cd-free CIGS devices were investigated.	cigs	25-29	CD2 molecule	Homo sapiens	84-87
29806770-5	2018	However, the addition of Cd2+ ions to the NH4OH aqueous solution suppressed the etching of the OVC by NH4OH, explaining why such a negative effect of NH4OH is not present in the conventional chemical bath deposition of CdS.	Ammonium Hydroxide	42-47	CD2 molecule	Homo sapiens	25-28
29806770-5	2018	However, the addition of Cd2+ ions to the NH4OH aqueous solution suppressed the etching of the OVC by NH4OH, explaining why such a negative effect of NH4OH is not present in the conventional chemical bath deposition of CdS.	Ammonium Hydroxide	102-107	CD2 molecule	Homo sapiens	25-28
29806770-5	2018	However, the addition of Cd2+ ions to the NH4OH aqueous solution suppressed the etching of the OVC by NH4OH, explaining why such a negative effect of NH4OH is not present in the conventional chemical bath deposition of CdS.	Ammonium Hydroxide	102-107	CD2 molecule	Homo sapiens	25-28
29806770-5	2018	However, the addition of Cd2+ ions to the NH4OH aqueous solution suppressed the etching of the OVC by NH4OH, explaining why such a negative effect of NH4OH is not present in the conventional chemical bath deposition of CdS.	Cadmium	219-222	CD2 molecule	Homo sapiens	25-28
29691744-9	2018	The affinity coefficient (Kf) of the Freundlich model of Fh2-200 series arranged in descending order is Fh2-200-Mgs&gt; Fh2-200-Cas&gt; Fh2-200s, showing that the Cd2+ adsorption capacity of Fh2-200 was relatively weak, while that of Fh2-200-Ca series and Fh2-200-Mg series was relatively strong, which was confirmed by the experimental results.	fh2	57-60	CD2 molecule	Homo sapiens	163-166
29691744-9	2018	The affinity coefficient (Kf) of the Freundlich model of Fh2-200 series arranged in descending order is Fh2-200-Mgs&gt; Fh2-200-Cas&gt; Fh2-200s, showing that the Cd2+ adsorption capacity of Fh2-200 was relatively weak, while that of Fh2-200-Ca series and Fh2-200-Mg series was relatively strong, which was confirmed by the experimental results.	fh2	104-107	CD2 molecule	Homo sapiens	163-166
29549808-3	2018	For diamagnetic alpha-glycine, the 2H NMR spectrum collected at 198 K was separated into two components from static -CD2- and dynamic -ND3.	2-azaniumylacetate	16-29	CD2 molecule	Homo sapiens	117-120
29549808-3	2018	For diamagnetic alpha-glycine, the 2H NMR spectrum collected at 198 K was separated into two components from static -CD2- and dynamic -ND3.	Deuterium	35-37	CD2 molecule	Homo sapiens	117-120
30065136-0	2018	Behavior of bentonite in an aqueous electrolytic solution - evaluation of electrolytic aggregation for adsorption capacity of Cd2+ ions onto bentonite.	Bentonite	12-21	CD2 molecule	Homo sapiens	126-129
30065136-0	2018	Behavior of bentonite in an aqueous electrolytic solution - evaluation of electrolytic aggregation for adsorption capacity of Cd2+ ions onto bentonite.	Bentonite	141-150	CD2 molecule	Homo sapiens	126-129
30065136-1	2018	In this study, we used aqueous solutions containing 1 mg/L of Cd2+ for electrolysis while varying the current density (CD), amount of bentonite added and the effective submerged area to investigate the adsorption capacity of Cd2+ ions onto bentonite by electrolytic aggregation.	Bentonite	134-143	CD2 molecule	Homo sapiens	225-228
30065136-2	2018	The adsorption of Cd2+ ions increased with increasing amount of bentonite added to the electrolytic solution.	Bentonite	64-73	CD2 molecule	Homo sapiens	18-21
29032710-0	2018	Phase I dose escalation study of the anti-CD2 monoclonal antibody, siplizumab, with DA-EPOCH-R in aggressive peripheral T-cell lymphomas.	da-epoch-r	84-94	CD2 molecule	Homo sapiens	42-45
29762494-1	2018	A simple and easy method was implemented for the contemporary detection of cadmium (Cd2+) and lead (Pb2+) ions using 1,3,6,8-pyrenetetrasulfonic acid sodium salt-functionalized carbon nanotubes nanocomposites (PyTS-CNTs).	Cadmium	75-82	CD2 molecule	Homo sapiens	84-87
29762494-1	2018	A simple and easy method was implemented for the contemporary detection of cadmium (Cd2+) and lead (Pb2+) ions using 1,3,6,8-pyrenetetrasulfonic acid sodium salt-functionalized carbon nanotubes nanocomposites (PyTS-CNTs).	1,3,6,8-pyrenetetrasulfonic acid sodium salt	117-161	CD2 molecule	Homo sapiens	84-87
29762494-1	2018	A simple and easy method was implemented for the contemporary detection of cadmium (Cd2+) and lead (Pb2+) ions using 1,3,6,8-pyrenetetrasulfonic acid sodium salt-functionalized carbon nanotubes nanocomposites (PyTS-CNTs).	Carbon	177-183	CD2 molecule	Homo sapiens	84-87
29762494-1	2018	A simple and easy method was implemented for the contemporary detection of cadmium (Cd2+) and lead (Pb2+) ions using 1,3,6,8-pyrenetetrasulfonic acid sodium salt-functionalized carbon nanotubes nanocomposites (PyTS-CNTs).	pyts-cnts	210-219	CD2 molecule	Homo sapiens	84-87
29762494-6	2018	Under the optimal condition, the stripping peak current of the PyTS-CNTs/Nafion/PGE varies linearly with the heavy metal ion concentration, ranging from 1.0 mug L-1 to 90 mug L-1 for Cd2+ and from 1.0 mug L-1 to 110 mug L-1 for Pb2+.	perfluorosulfonic acid	73-79	CD2 molecule	Homo sapiens	183-186
29762494-6	2018	Under the optimal condition, the stripping peak current of the PyTS-CNTs/Nafion/PGE varies linearly with the heavy metal ion concentration, ranging from 1.0 mug L-1 to 90 mug L-1 for Cd2+ and from 1.0 mug L-1 to 110 mug L-1 for Pb2+.	phenylglycidyl ether	80-83	CD2 molecule	Homo sapiens	183-186
29762494-6	2018	Under the optimal condition, the stripping peak current of the PyTS-CNTs/Nafion/PGE varies linearly with the heavy metal ion concentration, ranging from 1.0 mug L-1 to 90 mug L-1 for Cd2+ and from 1.0 mug L-1 to 110 mug L-1 for Pb2+.	Metals	115-120	CD2 molecule	Homo sapiens	183-186
29762494-8	2018	The proposed PyTS-CNTs/Nafion/PGE can be used as a rapid, simple, and controllable electrochemical sensor for the determination of toxic Cd2+ and Pb2+.	pyts	13-17	CD2 molecule	Homo sapiens	137-140
29762494-8	2018	The proposed PyTS-CNTs/Nafion/PGE can be used as a rapid, simple, and controllable electrochemical sensor for the determination of toxic Cd2+ and Pb2+.	perfluorosulfonic acid	23-29	CD2 molecule	Homo sapiens	137-140
29762494-8	2018	The proposed PyTS-CNTs/Nafion/PGE can be used as a rapid, simple, and controllable electrochemical sensor for the determination of toxic Cd2+ and Pb2+.	phenylglycidyl ether	30-33	CD2 molecule	Homo sapiens	137-140
29501167-4	2018	An electrochemical sensor was constructed based on glass carbon electrode (GCE) modified by MoS2 nanosheets obtained in DMF, which exhibits relatively higher sensitivity to Cd2+ detection and lower cytotoxicity against MCF-7 cells.	Dimethylformamide	120-123	CD2 molecule	Homo sapiens	173-176
29501167-7	2018	The high selectivity of the sensor is attributed to the coordination reaction between Cd2+ and O donor atoms of DMF adsorbed on MoS2 nanosheets.	Dimethylformamide	112-115	CD2 molecule	Homo sapiens	86-89
29501167-8	2018	The robust anti-interference is ascribed to the strong binding energy of Cd2+ and O atoms of DMF.	Dimethylformamide	93-96	CD2 molecule	Homo sapiens	73-76
29314196-2	2018	Research suggests that the impurity Cu2+ replaces the host Cd2+ and undergoes the local rhombic elongation distortion, characterized by the axial elongation ratios of 4.1%, and 3.8% along the z-axis and the planar bond length variation ratios of 3.8%, and 3.1% along the x-axis and y-axis, for Cu2+ Centers, I and II, respectively.	cupric ion	36-40	CD2 molecule	Homo sapiens	59-62
29527648-0	2018	The toxicity of cadmium ion (Cd2+) to phycocyanin: an in vitro spectroscopic study.	Cadmium	16-23	CD2 molecule	Homo sapiens	29-32
29527648-5	2018	The synchronous fluorescence spectra are used to study the change in amino acid residues of PC molecules, indicating that the effect of Cd2+ on the Trp of PC is more significant than the Tyr.	Tryptophan	148-151	CD2 molecule	Homo sapiens	136-139
29527648-6	2018	The UV-Vis absorbance of tetrapyrrole decreases from 0.26 to 0.23 cps with increasing Cd2+ concentration, suggesting that Cd2+ affects the light adsorption and the photosynthesis function of PC.	Tetrapyrroles	25-37	CD2 molecule	Homo sapiens	86-89
29527648-6	2018	The UV-Vis absorbance of tetrapyrrole decreases from 0.26 to 0.23 cps with increasing Cd2+ concentration, suggesting that Cd2+ affects the light adsorption and the photosynthesis function of PC.	Tetrapyrroles	25-37	CD2 molecule	Homo sapiens	122-125
28934999-1	2018	A simple vortex-assisted modified dispersive liquid-liquid microextraction procedure is proposed for the enrichment of cadmium (Cd+2) in surface (stored rainwater) and groundwater of the Tharparkar district in Pakistan, before analysis by flame atomic absorption spectrometry.	Cadmium	119-126	CD2 molecule	Homo sapiens	128-132
28934999-2	2018	Ammonium pyrrolidinedithiocarbamate was used as a ligand to make a hydrophobic complex of Cd+2, which was extracted in an ionic liquid (1-butyl-3-methylimidazolium hexafluorophosphate), and the nonionic surfactant Triton X-114 was applied as a dispersing medium.	pyrrolidine dithiocarbamic acid	0-35	CD2 molecule	Homo sapiens	90-94
28934999-2	2018	Ammonium pyrrolidinedithiocarbamate was used as a ligand to make a hydrophobic complex of Cd+2, which was extracted in an ionic liquid (1-butyl-3-methylimidazolium hexafluorophosphate), and the nonionic surfactant Triton X-114 was applied as a dispersing medium.	1-butyl-3-methylimidazolium hexafluorophosphate	136-183	CD2 molecule	Homo sapiens	90-94
28934999-2	2018	Ammonium pyrrolidinedithiocarbamate was used as a ligand to make a hydrophobic complex of Cd+2, which was extracted in an ionic liquid (1-butyl-3-methylimidazolium hexafluorophosphate), and the nonionic surfactant Triton X-114 was applied as a dispersing medium.	Nonidet P-40	214-226	CD2 molecule	Homo sapiens	90-94
28934999-9	2018	The observed results revealed that the concentration of Cd+2 in groundwater was higher than the World Health Organization recommended value of 3 microg/L for drinking water.	Water	70-75	CD2 molecule	Homo sapiens	56-60
29502412-0	2018	Experimental and Theoretical Investigations of Infrared Multiple Photon Dissociation Spectra of Aspartic Acid Complexes with Zn2+ and Cd2.	Aspartic Acid	96-109	CD2 molecule	Homo sapiens	134-137
29716227-10	2018	While the CD2+ complex exactly mimics the resonance behaviors (local and hyperspherical modes) of the bound and quasibound CH2+ complex, the CHD+(CDH+) complex reveals only the local mode behaviors at low energies and significantly less number of resonance structures at high energies.	ch2+	123-127	CD2 molecule	Homo sapiens	10-13
29716227-11	2018	Lifetime analysis of the isotopic variants implies that the CD2+ complex survives much longer than the CHD+(CDH+) complex and concludes the work by noting the following order in the decay profile of the deuterated CH2+ resonances as CH2+&gt;CHD+(CDH+) &gt;CD2+.	ch2+	214-218	CD2 molecule	Homo sapiens	60-63
29716227-11	2018	Lifetime analysis of the isotopic variants implies that the CD2+ complex survives much longer than the CHD+(CDH+) complex and concludes the work by noting the following order in the decay profile of the deuterated CH2+ resonances as CH2+&gt;CHD+(CDH+) &gt;CD2+.	ch2+	214-218	CD2 molecule	Homo sapiens	256-259
29716227-11	2018	Lifetime analysis of the isotopic variants implies that the CD2+ complex survives much longer than the CHD+(CDH+) complex and concludes the work by noting the following order in the decay profile of the deuterated CH2+ resonances as CH2+&gt;CHD+(CDH+) &gt;CD2+.	CDw17 antigen	246-249	CD2 molecule	Homo sapiens	60-63
29716227-11	2018	Lifetime analysis of the isotopic variants implies that the CD2+ complex survives much longer than the CHD+(CDH+) complex and concludes the work by noting the following order in the decay profile of the deuterated CH2+ resonances as CH2+&gt;CHD+(CDH+) &gt;CD2+.	CDw17 antigen	246-249	CD2 molecule	Homo sapiens	256-259
29502412-1	2018	Complexes of aspartic acid (Asp) cationized with Zn2+: Zn(Asp-H)+, Zn(Asp-H)+(ACN) where ACN = acetonitrile, and Zn(Asp-H)+(Asp); as well as with Cd2+, CdCl+(Asp), were examined by infrared multiple photon dissociation (IRMPD) action spectroscopy using light generated from a free electron laser.	Aspartic Acid	13-26	CD2 molecule	Homo sapiens	146-149
29502412-1	2018	Complexes of aspartic acid (Asp) cationized with Zn2+: Zn(Asp-H)+, Zn(Asp-H)+(ACN) where ACN = acetonitrile, and Zn(Asp-H)+(Asp); as well as with Cd2+, CdCl+(Asp), were examined by infrared multiple photon dissociation (IRMPD) action spectroscopy using light generated from a free electron laser.	Aspartic Acid	28-31	CD2 molecule	Homo sapiens	146-149
29502412-8	2018	Further, comparison of the current work to that of Zn2+ and Cd2+ complexes of asparagine (Asn) allows additional conclusions regarding populated conformers and effects of carboxamide versus carboxylic acid binding to be drawn.	Asparagine	78-88	CD2 molecule	Homo sapiens	60-63
29502412-8	2018	Further, comparison of the current work to that of Zn2+ and Cd2+ complexes of asparagine (Asn) allows additional conclusions regarding populated conformers and effects of carboxamide versus carboxylic acid binding to be drawn.	Asparagine	90-93	CD2 molecule	Homo sapiens	60-63
29546911-2	2018	It demonstrates superior efficiency for rapid, capacitive and simultaneous removal of multiple heavy metal ions such as Pb2+, Cd2+, Cu2+ and Zn2+.	Metals	101-106	CD2 molecule	Homo sapiens	126-129
29546911-3	2018	The adsorption is exceptionally rapid, showing 100% removal of Cu2+ in 10 min, and 100% removal of Pb2+ and Cd2+ in 20 min in water with a wide range of concentrations from 0.1 to 5 mmol L-1.	Water	126-131	CD2 molecule	Homo sapiens	108-111
29596360-2	2018	Sensor H4L could show fluorescence turn-on response rapidly and significant selectivity to Cd2+ over many other metallic ions (Cu2+, Ba2+, Ca2+, K+, Cr3+, Mn2+, Sr2+, Co2+, Na+, Li+, Ni2+, Ag+, and Zn2+), and a clear change in color from colorless to yellow that can be very easily observed via the naked eyes in the existence of Cd2+, while other metallic ions do not induce such a change.	Cobalt(2+)	167-171	CD2 molecule	Homo sapiens	91-94
29501697-5	2018	They T4, T3, T5, T15, T11 and T10 genotypes have a high potential for pathogenicity and a very high degree of virulence due to their production of serine proteases and extracellular cysteine enzymes involved in tissue degradation of the host.	Cysteine	182-190	CD2 molecule	Homo sapiens	22-25
29596360-0	2018	A Reversible Bis(Salamo)-Based Fluorescence Sensor for Selective Detection of Cd2+ in Water-Containing Systems and Food Samples.	bis(salamo)	13-24	CD2 molecule	Homo sapiens	78-81
29596360-2	2018	Sensor H4L could show fluorescence turn-on response rapidly and significant selectivity to Cd2+ over many other metallic ions (Cu2+, Ba2+, Ca2+, K+, Cr3+, Mn2+, Sr2+, Co2+, Na+, Li+, Ni2+, Ag+, and Zn2+), and a clear change in color from colorless to yellow that can be very easily observed via the naked eyes in the existence of Cd2+, while other metallic ions do not induce such a change.	Nickel(2+)	183-187	CD2 molecule	Homo sapiens	91-94
29596360-0	2018	A Reversible Bis(Salamo)-Based Fluorescence Sensor for Selective Detection of Cd2+ in Water-Containing Systems and Food Samples.	Water	86-91	CD2 molecule	Homo sapiens	78-81
29596360-2	2018	Sensor H4L could show fluorescence turn-on response rapidly and significant selectivity to Cd2+ over many other metallic ions (Cu2+, Ba2+, Ca2+, K+, Cr3+, Mn2+, Sr2+, Co2+, Na+, Li+, Ni2+, Ag+, and Zn2+), and a clear change in color from colorless to yellow that can be very easily observed via the naked eyes in the existence of Cd2+, while other metallic ions do not induce such a change.	Zinc	198-202	CD2 molecule	Homo sapiens	91-94
29174648-3	2018	As expected, the synthesized Zn-MOF exhibited fluorescence enhancement for cadmium ion (Cd2+) and sensing of nitrobenzene (NB) through fluorescence quenching.	zn-mof	29-35	CD2 molecule	Homo sapiens	88-91
29596360-1	2018	A novel, simple, highly selective, and sensitive fluorescence chemosensor for detecting Cd2+ that was constructed from a bis(salamo)-type compound (H4L) with two N2O2 chelating moieties as ionophore was successfully developed.	dioxohydrazine	162-166	CD2 molecule	Homo sapiens	88-91
29584471-4	2018	Also, the maximum adsorption of Cd2+ for RS (5.87 mg/g) was slightly bigger than that for NS (5.36 mg/g).	rs	41-43	CD2 molecule	Homo sapiens	32-35
29584471-4	2018	Also, the maximum adsorption of Cd2+ for RS (5.87 mg/g) was slightly bigger than that for NS (5.36 mg/g).	ns	90-92	CD2 molecule	Homo sapiens	32-35
29584471-5	2018	In Freundlich isotherm, the Kf of the adsorption of Cd2+ to surface of the RS components was higher than that of the NS, indicating stronger attraction between Cd2+ and components of the RS.	rs	75-77	CD2 molecule	Homo sapiens	52-55
29584471-5	2018	In Freundlich isotherm, the Kf of the adsorption of Cd2+ to surface of the RS components was higher than that of the NS, indicating stronger attraction between Cd2+ and components of the RS.	rs	75-77	CD2 molecule	Homo sapiens	160-163
29126942-1	2018	A simple electrochemical DNA- based biosensor was designed for determination of Cd2+ using ethyl green (EG) as a DNA hybridization indicator on the surface of carbon paste electrode (CPE).	brilliant green	91-102	CD2 molecule	Homo sapiens	80-83
29126942-1	2018	A simple electrochemical DNA- based biosensor was designed for determination of Cd2+ using ethyl green (EG) as a DNA hybridization indicator on the surface of carbon paste electrode (CPE).	brilliant green	104-106	CD2 molecule	Homo sapiens	80-83
29126942-1	2018	A simple electrochemical DNA- based biosensor was designed for determination of Cd2+ using ethyl green (EG) as a DNA hybridization indicator on the surface of carbon paste electrode (CPE).	Carbon	159-165	CD2 molecule	Homo sapiens	80-83
29126942-2	2018	The interaction of Cd2+ with double strand DNA (dsDNA) led to the destabilizing of dsDNA and the increase in the reduction peak currents of EG.	brilliant green	140-142	CD2 molecule	Homo sapiens	19-22
29575493-0	2018	Duplex Healing of Selectively Thiolated Guanosine Mismatches through a Cd2+ Chemical Stimulus.	Guanosine	40-49	CD2 molecule	Homo sapiens	71-74
29174648-3	2018	As expected, the synthesized Zn-MOF exhibited fluorescence enhancement for cadmium ion (Cd2+) and sensing of nitrobenzene (NB) through fluorescence quenching.	Cadmium	75-82	CD2 molecule	Homo sapiens	88-91
29191651-4	2018	Here we report a crystal structure of A3F-CD2 in complex with a 10-nucleotide ssDNA composed of poly-thymine, which reveals a novel positively charged nucleic acid binding site distal to the active center that plays a key role in substrate DNA binding and catalytic activity.	10-nucleotide	64-77	CD2 molecule	Homo sapiens	42-45
29243315-2	2018	In CD2 Cl2 solutions, both tetraurea-calix[4]pyrroles self-assemble into dimeric capsules by encapsulating one molecule of a suitable bis-N-oxide or two molecules of a mono-N-oxide.	tetraurea	27-36	CD2 molecule	Homo sapiens	3-6
29243315-2	2018	In CD2 Cl2 solutions, both tetraurea-calix[4]pyrroles self-assemble into dimeric capsules by encapsulating one molecule of a suitable bis-N-oxide or two molecules of a mono-N-oxide.	calix(4)pyrrole	37-53	CD2 molecule	Homo sapiens	3-6
29243315-2	2018	In CD2 Cl2 solutions, both tetraurea-calix[4]pyrroles self-assemble into dimeric capsules by encapsulating one molecule of a suitable bis-N-oxide or two molecules of a mono-N-oxide.	mono-n-oxide	168-180	CD2 molecule	Homo sapiens	3-6
29208290-0	2018	Synthesis, spectroscopic, thermal and molecular modeling studies of Zn2+, Cd2+ and UO22+ complexes of Schiff bases containing triazole moiety.	Schiff Bases	102-114	CD2 molecule	Homo sapiens	74-77
29208290-0	2018	Synthesis, spectroscopic, thermal and molecular modeling studies of Zn2+, Cd2+ and UO22+ complexes of Schiff bases containing triazole moiety.	Triazoles	126-134	CD2 molecule	Homo sapiens	74-77
29208290-2	2018	A novel series of Zn2+, Cd2+ and UO22+ complexes of ligands namely 1-[(5-mercapto-1H-1,2,4-triazole-3-ylimino) methyl]naphthalene-2-ol (HL1) and [(1H-1,2,4-triazole-3-ylimino) methyl] naphthalene-2-ol (HL2) have been prepared and characterized by different analytical and spectral techniques.	1-[(5-mercapto-1h-1,2,4-triazole-3-ylimino) methyl]naphthalene-2-ol	67-134	CD2 molecule	Homo sapiens	24-27
29136875-4	2018	This turn-on CICSs device was applied to detect cadmium ions (Cd2+).	cicss	13-18	CD2 molecule	Homo sapiens	62-65
29136875-4	2018	This turn-on CICSs device was applied to detect cadmium ions (Cd2+).	Cadmium	48-55	CD2 molecule	Homo sapiens	62-65
29100878-0	2018	N-acetyl-l-cysteine and Mn2+ attenuate Cd2+-induced disturbance of the intracellular free calcium homeostasis in cultured cerebellar granule neurons.	Manganese(2+)	24-28	CD2 molecule	Homo sapiens	39-42
29100878-0	2018	N-acetyl-l-cysteine and Mn2+ attenuate Cd2+-induced disturbance of the intracellular free calcium homeostasis in cultured cerebellar granule neurons.	Calcium	90-97	CD2 molecule	Homo sapiens	39-42
29100878-4	2018	Using Fluo-4 AM, measurements of intracellular calcium ions demonstrated that 24h-exposure to Cd2+ induced intensive increase of Fluo-4 fluorescence in neurons accompanied by mitochondria swelling.	fluo-4 am	6-15	CD2 molecule	Homo sapiens	94-97
29100878-4	2018	Using Fluo-4 AM, measurements of intracellular calcium ions demonstrated that 24h-exposure to Cd2+ induced intensive increase of Fluo-4 fluorescence in neurons accompanied by mitochondria swelling.	Calcium	47-54	CD2 molecule	Homo sapiens	94-97
29100878-4	2018	Using Fluo-4 AM, measurements of intracellular calcium ions demonstrated that 24h-exposure to Cd2+ induced intensive increase of Fluo-4 fluorescence in neurons accompanied by mitochondria swelling.	9-(3-hydroxy-2-phosphonomethoxypropyl)guanine	78-81	CD2 molecule	Homo sapiens	94-97
29100878-4	2018	Using Fluo-4 AM, measurements of intracellular calcium ions demonstrated that 24h-exposure to Cd2+ induced intensive increase of Fluo-4 fluorescence in neurons accompanied by mitochondria swelling.	Fluo 4	6-12	CD2 molecule	Homo sapiens	94-97
29107029-1	2018	We studied the effects of Cd2+ on TCDD-mediated induction of the cytochrome P450 1A1 (cyp1a1) gene using a zebrafish liver cell line (ZFL).	Polychlorinated Dibenzodioxins	34-38	CD2 molecule	Homo sapiens	26-29
29279115-0	2018	A novel voltammetric sensor for the simultaneous detection of Cd2+ and Pb2+ using graphene oxide/kappa-carrageenan/l-cysteine nanocomposite.	graphene oxide	82-96	CD2 molecule	Homo sapiens	62-65
29279115-0	2018	A novel voltammetric sensor for the simultaneous detection of Cd2+ and Pb2+ using graphene oxide/kappa-carrageenan/l-cysteine nanocomposite.	Carrageenan	97-114	CD2 molecule	Homo sapiens	62-65
29279115-0	2018	A novel voltammetric sensor for the simultaneous detection of Cd2+ and Pb2+ using graphene oxide/kappa-carrageenan/l-cysteine nanocomposite.	Cysteine	115-125	CD2 molecule	Homo sapiens	62-65
29279115-1	2018	Simultaneous determination of Cd2+ and Pb2+ was achieved by using graphene oxide/kappa-carrageenan/l-cysteine (GO/kappa-Car/l-Cys) nanocomposite modified glassy carbon electrode (GCE) by Square Wave Anodic Stripping Voltammetry (SWASV).	graphene oxide	66-80	CD2 molecule	Homo sapiens	30-33
29279115-1	2018	Simultaneous determination of Cd2+ and Pb2+ was achieved by using graphene oxide/kappa-carrageenan/l-cysteine (GO/kappa-Car/l-Cys) nanocomposite modified glassy carbon electrode (GCE) by Square Wave Anodic Stripping Voltammetry (SWASV).	Carrageenan	81-98	CD2 molecule	Homo sapiens	30-33
29279115-1	2018	Simultaneous determination of Cd2+ and Pb2+ was achieved by using graphene oxide/kappa-carrageenan/l-cysteine (GO/kappa-Car/l-Cys) nanocomposite modified glassy carbon electrode (GCE) by Square Wave Anodic Stripping Voltammetry (SWASV).	Cysteine	99-109	CD2 molecule	Homo sapiens	30-33
29279115-1	2018	Simultaneous determination of Cd2+ and Pb2+ was achieved by using graphene oxide/kappa-carrageenan/l-cysteine (GO/kappa-Car/l-Cys) nanocomposite modified glassy carbon electrode (GCE) by Square Wave Anodic Stripping Voltammetry (SWASV).	l	4-5	CD2 molecule	Homo sapiens	30-33
29279115-1	2018	Simultaneous determination of Cd2+ and Pb2+ was achieved by using graphene oxide/kappa-carrageenan/l-cysteine (GO/kappa-Car/l-Cys) nanocomposite modified glassy carbon electrode (GCE) by Square Wave Anodic Stripping Voltammetry (SWASV).	Cysteine	126-129	CD2 molecule	Homo sapiens	30-33
29279115-1	2018	Simultaneous determination of Cd2+ and Pb2+ was achieved by using graphene oxide/kappa-carrageenan/l-cysteine (GO/kappa-Car/l-Cys) nanocomposite modified glassy carbon electrode (GCE) by Square Wave Anodic Stripping Voltammetry (SWASV).	Carbon	161-167	CD2 molecule	Homo sapiens	30-33
29279115-6	2018	The modified electrode has been applied to the detection of Cd2+ and Pb2+ present in water and milk samples, and the accessed results were satisfactory with that of AAS.	Water	85-90	CD2 molecule	Homo sapiens	60-63
29435667-1	2018	BACKGROUND: The coexistence of Cd2+ and Zn2+ ions in nature has a significant influence on their environmental behaviors in soils and bioavailability for plants.	Zinc	40-44	CD2 molecule	Homo sapiens	31-34
29435667-4	2018	These results indicated that Cd2+ and Zn2+ have a strong capacity to adsorb in the solid phase at the soil-water interface of boggy soil and yellow brown soil, respectively.	Water	107-112	CD2 molecule	Homo sapiens	29-32
29435667-7	2018	A 1:1 ratio of Cd2+ to Zn2+ promotes the mutual inhibition of their retentions.	Zinc	23-27	CD2 molecule	Homo sapiens	15-18
29435667-11	2018	In the combined system, Cd2+ and Zn2+ restrain each other, resulting in the weaker binding force between ions and soil particles at a 1:1 ratio of Cd2+-Zn2+.	Zinc	33-37	CD2 molecule	Homo sapiens	147-150
29435667-11	2018	In the combined system, Cd2+ and Zn2+ restrain each other, resulting in the weaker binding force between ions and soil particles at a 1:1 ratio of Cd2+-Zn2+.	Zinc	152-156	CD2 molecule	Homo sapiens	24-27
29435667-11	2018	In the combined system, Cd2+ and Zn2+ restrain each other, resulting in the weaker binding force between ions and soil particles at a 1:1 ratio of Cd2+-Zn2+.	Zinc	152-156	CD2 molecule	Homo sapiens	147-150
28941888-0	2018	Efficiency of the intermolecular interaction of salicylic acid neutral form and monoanion with Cd2+ ion studied by methods of absorption and fluorescence.	Salicylic Acid	48-62	CD2 molecule	Homo sapiens	95-98
28941888-0	2018	Efficiency of the intermolecular interaction of salicylic acid neutral form and monoanion with Cd2+ ion studied by methods of absorption and fluorescence.	monoanion	80-89	CD2 molecule	Homo sapiens	95-98
28941888-1	2018	The methods of absorption and fluorescence were used to study the efficiency of the interaction between salicylic acid derivatives SAD (neutral SA form and SA monoanion) and Cd2+ ions (in CdBr2 salt) within the range rN=1.5/8.	Salicylic Acid	104-118	CD2 molecule	Homo sapiens	174-177
28941888-1	2018	The methods of absorption and fluorescence were used to study the efficiency of the interaction between salicylic acid derivatives SAD (neutral SA form and SA monoanion) and Cd2+ ions (in CdBr2 salt) within the range rN=1.5/8.	cdbr2 salt	188-198	CD2 molecule	Homo sapiens	174-177
28941888-6	2018	These factors are: (1) the decrease in rN after addition of CdBr2 to the SAD solution, (2) the decrease in the efficiency of the N-bonding of SAD molecules to the water ones, and (3) the existence of electrostatic ion-ion interaction between the NSal- monoanion and the Cd2+ ion.	Cadmium dibromide	60-65	CD2 molecule	Homo sapiens	270-273
28941888-7	2018	The bimolecular fluorescence quenching constants Kq of NSal- monoanion fluorescence quenching by the Cd2+ ion appeared to be substantially less than those of the quenching which would follow either the dynamic (diffusion) or the concentration (static) mechanisms.	monoanion	61-70	CD2 molecule	Homo sapiens	101-104
28818764-6	2018	The ratiometric displacement of Cd2+ ions by Zn2+ ions shows an excellent selectivity towards in-situ detection of Zn2+ ions.	Zinc	45-49	CD2 molecule	Homo sapiens	32-35
28818764-6	2018	The ratiometric displacement of Cd2+ ions by Zn2+ ions shows an excellent selectivity towards in-situ detection of Zn2+ ions.	Zinc	115-119	CD2 molecule	Homo sapiens	32-35
29191651-4	2018	Here we report a crystal structure of A3F-CD2 in complex with a 10-nucleotide ssDNA composed of poly-thymine, which reveals a novel positively charged nucleic acid binding site distal to the active center that plays a key role in substrate DNA binding and catalytic activity.	poly-thymine	96-108	CD2 molecule	Homo sapiens	42-45
30023584-4	2017	Using molecular dynamics simulations, it was found that the Cd2+ ion preferred to bind to the thymine exposed in the major groove.	Thymine	94-101	CD2 molecule	Homo sapiens	60-63
29161651-8	2018	Release of Cd2+ from nanocomposites depended to solubility and particle degradation of CdS nanoparticles were considered to be the main cause of these cytotoxicity.	Cadmium	87-90	CD2 molecule	Homo sapiens	11-14
28915474-5	2017	The interaction of heavy metal ions showed that the increase of initial Zn2+ concentration adversely affects on Cd2+ removal.	Metals	25-30	CD2 molecule	Homo sapiens	112-115
28915474-5	2017	The interaction of heavy metal ions showed that the increase of initial Zn2+ concentration adversely affects on Cd2+ removal.	Zinc	72-76	CD2 molecule	Homo sapiens	112-115
28915474-7	2017	Single sulfate and binary anion systems exert a more positive effect on Cd2+ and Zn2+ removal because of the stronger charge neutralization and destabilization of iron hydroxide flocs.	Sulfates	7-14	CD2 molecule	Homo sapiens	72-75
28915474-7	2017	Single sulfate and binary anion systems exert a more positive effect on Cd2+ and Zn2+ removal because of the stronger charge neutralization and destabilization of iron hydroxide flocs.	Ferrous hydroxide	163-177	CD2 molecule	Homo sapiens	72-75
28683540-7	2017	In addition, the absorption and emission optical properties of Zn x Cd1 - x S QDs were red shifted with increasing the amount of Cd2+ in the alloyed nanocrystals, which have also increased the quantum yield compared to pure CdS and ZnS nanoparticles.	Zinc	63-65	CD2 molecule	Homo sapiens	129-132
28683540-7	2017	In addition, the absorption and emission optical properties of Zn x Cd1 - x S QDs were red shifted with increasing the amount of Cd2+ in the alloyed nanocrystals, which have also increased the quantum yield compared to pure CdS and ZnS nanoparticles.	Cadmium	224-227	CD2 molecule	Homo sapiens	129-132
28683540-7	2017	In addition, the absorption and emission optical properties of Zn x Cd1 - x S QDs were red shifted with increasing the amount of Cd2+ in the alloyed nanocrystals, which have also increased the quantum yield compared to pure CdS and ZnS nanoparticles.	Zinc	232-235	CD2 molecule	Homo sapiens	129-132
28635101-0	2017	A simply synthesized biphenyl substituted piperidin-4-one for the fluorescence chemosensing of Cd2.	biphenyl substituted piperidin-4-one	21-57	CD2 molecule	Homo sapiens	95-98
28635101-3	2017	We report in this paper a piperidine-4-one-based fluorescent chemosensor of Cd2+ ions, designed and synthesized by a simple method.	piperidine-4-one	26-42	CD2 molecule	Homo sapiens	76-79
28635101-7	2017	Piperidine-4-one shows a 1:1 stoichiometric binding to Cd2+ .	piperidine-4-one	0-16	CD2 molecule	Homo sapiens	55-58
28795537-5	2017	Then labeled digested proteins adsorb by Polyflux 140H and Polyflux 14L with 13 CD2 O and NaCNBD3 (light labeling, L) and CD2 O and NaCNBH3 (heavy labeling, H), respectively.	polyflux 14l	59-71	CD2 molecule	Homo sapiens	80-83
29234692-0	2018	Characterization and isotherm data for adsorption of Cd2+ from aqueous solution by adsorbent from mixture of bagasse-bentonite.	bagasse-bentonite	109-126	CD2 molecule	Homo sapiens	53-56
29234692-10	2018	The acquired data indicated that the adsorption of Cd2+ by the adsorbent prepared from mixture of bagasse-bentonite is a promising technique for treating Cd-bearing wastewaters.	bagasse-bentonite	98-115	CD2 molecule	Homo sapiens	51-54
29099186-1	2017	A thermally stable cadmium-based chiral metal-organic framework (MOF), {[Cd2(L)(H2O)(DMF)] 3DMF 2H2O}n (1; DMF = N,N-dimethylformamide), has been synthesized from an achiral ligand by spontaneous resolution.	Cadmium	19-26	CD2 molecule	Homo sapiens	73-76
28577240-0	2017	A Rhodamine-Based Fluorescent Chemosensor for the Detection of Pb2+, Hg2+ and Cd2.	Rhodamines	2-11	CD2 molecule	Homo sapiens	78-81
29099088-1	2017	This work reports on a novel fluorescent sensor 1 for Cd2+ ion based on the fluorophore of tetramethyl substituted bis(difluoroboron)-1,2-bis[(1H-pyrrol-2-yl)methylene]hydrazine (Me4BOPHY), which is modified with an electron donor moiety of N,N-bis(pyridin-2-ylmethyl)benzenamine.	tetramethyl substituted bis(difluoroboron)-1,2-bis[(1h-pyrrol-2-yl)methylene]hydrazine	91-177	CD2 molecule	Homo sapiens	54-57
29099088-1	2017	This work reports on a novel fluorescent sensor 1 for Cd2+ ion based on the fluorophore of tetramethyl substituted bis(difluoroboron)-1,2-bis[(1H-pyrrol-2-yl)methylene]hydrazine (Me4BOPHY), which is modified with an electron donor moiety of N,N-bis(pyridin-2-ylmethyl)benzenamine.	me4bophy	179-187	CD2 molecule	Homo sapiens	54-57
29099088-1	2017	This work reports on a novel fluorescent sensor 1 for Cd2+ ion based on the fluorophore of tetramethyl substituted bis(difluoroboron)-1,2-bis[(1H-pyrrol-2-yl)methylene]hydrazine (Me4BOPHY), which is modified with an electron donor moiety of N,N-bis(pyridin-2-ylmethyl)benzenamine.	N,N-Bis(2-pyridylmethyl)aniline	241-279	CD2 molecule	Homo sapiens	54-57
29099088-7	2017	The sensor also demonstrates a high selectivity towards Cd2+ in comparison to other interferent metal ions.	Metals	96-101	CD2 molecule	Homo sapiens	56-59
29382003-0	2017	Hemoglobin Hornchurch [beta43 (CD2) Glu &gt; Lys; HBB: c.130G &gt; A] in a Chinese boy complicated with thrombocytopenia: A case report and literature review.	Glutamic Acid	36-39	CD2 molecule	Homo sapiens	31-34
29382003-0	2017	Hemoglobin Hornchurch [beta43 (CD2) Glu &gt; Lys; HBB: c.130G &gt; A] in a Chinese boy complicated with thrombocytopenia: A case report and literature review.	Lysine	45-48	CD2 molecule	Homo sapiens	31-34
28925966-2	2017	After being modified with 2% chitosan-acetate for 2 h at 30  C, significant uptake of Cd2+ could be achieved.	chitosan-acetate	29-45	CD2 molecule	Homo sapiens	86-89
28925966-6	2017	The equilibrium Cd2+ concentration was &lt;5 mug/L, which meets the requirements of "Standards for Irrigation Water Quality" (GB5084-2005) (10 mug/L) and MCL and MCLG for groundwater and drinking water (5 mug/L) set by United States Environmental Protection Agency.	Water	177-182	CD2 molecule	Homo sapiens	16-19
28782951-0	2017	Rapid Simultaneous Removal of Toxic Anions [HSeO3]-, [SeO3]2-, and [SeO4]2-, and Metals Hg2+, Cu2+, and Cd2+ by MoS42- Intercalated Layered Double Hydroxide.	seo4	68-72	CD2 molecule	Homo sapiens	104-107
28782951-0	2017	Rapid Simultaneous Removal of Toxic Anions [HSeO3]-, [SeO3]2-, and [SeO4]2-, and Metals Hg2+, Cu2+, and Cd2+ by MoS42- Intercalated Layered Double Hydroxide.	hydroxide ion	147-156	CD2 molecule	Homo sapiens	104-107
28782951-1	2017	We demonstrate fast, highly efficient concurrent removal of toxic oxoanions of Se(VI) (SeO42-) and Se(IV) (SeO32-/HSeO3-) and heavy metal ions of Hg2+, Cu2+, and Cd2+ by the MoS42- intercalated Mg/Al layered double hydroxide (MgAl-MoS4-LDH, abbr.	abbr	241-245	CD2 molecule	Homo sapiens	162-165
28782951-3	2017	Using the MoS4-LDH as a sorbent, we observe that the presence of Hg2+ ions greatly promotes the capture of SeO42-, while the three metal ions (Hg2+, Cu2+, Cd2+) enable a remarkable improvement in the removal of SeO32-/HSeO3-.	seo32	211-216	CD2 molecule	Homo sapiens	155-158
28782951-3	2017	Using the MoS4-LDH as a sorbent, we observe that the presence of Hg2+ ions greatly promotes the capture of SeO42-, while the three metal ions (Hg2+, Cu2+, Cd2+) enable a remarkable improvement in the removal of SeO32-/HSeO3-.	hseo3	218-223	CD2 molecule	Homo sapiens	155-158
28782951-10	2017	The sorptions of Se(VI)+Hg and Se(IV)+M (M = Hg2+, Cu2+, Cd2+) are exceptionally rapid, showing &gt;99.5% removals for Hg2+ within 1 min and ~99.0% removal for Se(VI) within 30 min, as well as &gt;99.5% removals for pairs Cu2+ and Se(IV) within 10 min, and Cd2+ and Se(IV) within 30 min.	Selenium	17-19	CD2 molecule	Homo sapiens	57-60
28782951-10	2017	The sorptions of Se(VI)+Hg and Se(IV)+M (M = Hg2+, Cu2+, Cd2+) are exceptionally rapid, showing &gt;99.5% removals for Hg2+ within 1 min and ~99.0% removal for Se(VI) within 30 min, as well as &gt;99.5% removals for pairs Cu2+ and Se(IV) within 10 min, and Cd2+ and Se(IV) within 30 min.	Selenium	17-19	CD2 molecule	Homo sapiens	257-260
28782951-10	2017	The sorptions of Se(VI)+Hg and Se(IV)+M (M = Hg2+, Cu2+, Cd2+) are exceptionally rapid, showing &gt;99.5% removals for Hg2+ within 1 min and ~99.0% removal for Se(VI) within 30 min, as well as &gt;99.5% removals for pairs Cu2+ and Se(IV) within 10 min, and Cd2+ and Se(IV) within 30 min.	Mercuric cation	119-123	CD2 molecule	Homo sapiens	57-60
28782951-13	2017	The intercalated material of MoS4-LDH is very promising as a highly effective filter for decontamination of water with toxic Se(IV)/Se(VI) oxoanions along with heavy metals such as Hg2+, Cd2+, and Cu2+.	Water	108-113	CD2 molecule	Homo sapiens	187-190
29085018-2	2017	In this study, different concentrations of cadmium ion (Cd2+) were applied to study toxic effects of Cd2+ and responses of tall fescue by soilless culture.	Cadmium	43-50	CD2 molecule	Homo sapiens	56-59
29085018-2	2017	In this study, different concentrations of cadmium ion (Cd2+) were applied to study toxic effects of Cd2+ and responses of tall fescue by soilless culture.	Cadmium	43-50	CD2 molecule	Homo sapiens	101-104
29085018-4	2017	Additionally, the treatment with high concentration of Cd2+ leaded to decreased chlorophyll contents, production of reactive oxygen species (ROS) and lipid peroxidation, as well as damage of cell membrane, necrosis and apoptosis in tall fescue roots, and toxicity of Cd2+ on physiologic properties of tall fescue has been well discussed.	Chlorophyll	80-91	CD2 molecule	Homo sapiens	55-58
29085018-4	2017	Additionally, the treatment with high concentration of Cd2+ leaded to decreased chlorophyll contents, production of reactive oxygen species (ROS) and lipid peroxidation, as well as damage of cell membrane, necrosis and apoptosis in tall fescue roots, and toxicity of Cd2+ on physiologic properties of tall fescue has been well discussed.	Reactive Oxygen Species	116-139	CD2 molecule	Homo sapiens	55-58
29085018-4	2017	Additionally, the treatment with high concentration of Cd2+ leaded to decreased chlorophyll contents, production of reactive oxygen species (ROS) and lipid peroxidation, as well as damage of cell membrane, necrosis and apoptosis in tall fescue roots, and toxicity of Cd2+ on physiologic properties of tall fescue has been well discussed.	Reactive Oxygen Species	141-144	CD2 molecule	Homo sapiens	55-58
29085018-5	2017	Moreover, in photosystem II electron donor side, electron transport from oxygen evolution complex (OEC) to Yz residue of D1 protein was inhibited under high Cd2+ treatments, which may be due to the Cd2+ induced ROS production and the replacement of Ca2+ in the core of OEC.	Oxygen	73-79	CD2 molecule	Homo sapiens	157-160
29085018-5	2017	Moreover, in photosystem II electron donor side, electron transport from oxygen evolution complex (OEC) to Yz residue of D1 protein was inhibited under high Cd2+ treatments, which may be due to the Cd2+ induced ROS production and the replacement of Ca2+ in the core of OEC.	Oxygen	73-79	CD2 molecule	Homo sapiens	198-201
29085018-5	2017	Moreover, in photosystem II electron donor side, electron transport from oxygen evolution complex (OEC) to Yz residue of D1 protein was inhibited under high Cd2+ treatments, which may be due to the Cd2+ induced ROS production and the replacement of Ca2+ in the core of OEC.	Reactive Oxygen Species	211-214	CD2 molecule	Homo sapiens	157-160
29085018-5	2017	Moreover, in photosystem II electron donor side, electron transport from oxygen evolution complex (OEC) to Yz residue of D1 protein was inhibited under high Cd2+ treatments, which may be due to the Cd2+ induced ROS production and the replacement of Ca2+ in the core of OEC.	Reactive Oxygen Species	211-214	CD2 molecule	Homo sapiens	198-201
29085018-6	2017	In electron acceptor side, electron transport efficiency from quinone B to photosystem I acceptors increased under high Cd2+ treatments, which may be an important response for plants against Cd2+ toxicity and its mechanism needs our further study.	quinone	62-69	CD2 molecule	Homo sapiens	120-123
29085018-6	2017	In electron acceptor side, electron transport efficiency from quinone B to photosystem I acceptors increased under high Cd2+ treatments, which may be an important response for plants against Cd2+ toxicity and its mechanism needs our further study.	quinone	62-69	CD2 molecule	Homo sapiens	191-194
28820257-8	2017	We then introduced the optimized-enhanced aromatic sequons into other glycoproteins and observed an enhancement in N-glycan occupancy that was further supported by modeling the high-affinity interaction between the optimized sequence on hCD2ad and a human oligosaccharyltransferase (OST) subunit.	n-glycan	115-123	CD2 molecule	Homo sapiens	237-241
28577240-2	2017	The receptor can selectively recognize and sense Pb2+, Hg2+ and Cd2+ by showing different fluorescence characteristics.	Lead	49-53	CD2 molecule	Homo sapiens	64-67
28577240-3	2017	In ethanol/HEPES buffer medium, the addition of Cd2+ caused a yellowish-green fluorescence, while the presence of Pb2+ or Hg2+ gave rise to an orange fluorescence.	Ethanol	3-10	CD2 molecule	Homo sapiens	48-51
28577240-3	2017	In ethanol/HEPES buffer medium, the addition of Cd2+ caused a yellowish-green fluorescence, while the presence of Pb2+ or Hg2+ gave rise to an orange fluorescence.	HEPES	11-16	CD2 molecule	Homo sapiens	48-51
28671628-0	2017	Direct Quantification of Cd2+ in the Presence of Cu2+ by a Combination of Anodic Stripping Voltammetry Using a Bi-Film-Modified Glassy Carbon Electrode and an Artificial Neural Network.	cupric ion	49-53	CD2 molecule	Homo sapiens	25-28
28702563-2	2017	Previous studies have revealed that Cd2+, Hg2+ and CH3Hg+ are taken up by red blood cells (RBCs) and bind to cytosolic glutathione (GSH) and/or hemoglobin (Hb).	Glutathione	119-130	CD2 molecule	Homo sapiens	36-39
28702563-2	2017	Previous studies have revealed that Cd2+, Hg2+ and CH3Hg+ are taken up by red blood cells (RBCs) and bind to cytosolic glutathione (GSH) and/or hemoglobin (Hb).	Glutathione	132-135	CD2 molecule	Homo sapiens	36-39
28621934-1	2017	A quinoline-based heptadentate ligand, N,N,N",N"-tetrakis(2-quinolylmethyl)-3-oxa-1,5-pentanediamine (TQOPEN), exhibits a fluorescence increase (ICd/I0 = 25, phiCd = 0.017) at 428 nm upon addition of 1 equiv of Cd2+.	quinoline	2-11	CD2 molecule	Homo sapiens	211-214
28621934-3	2017	In comparison with TQOPEN, the thia and aza derivatives TQSPEN and TQNPEN exhibit improved Cd2+/Zn2+ selectivity and higher Cd2+-binding affinity, respectively.	thia	31-35	CD2 molecule	Homo sapiens	91-94
28621934-3	2017	In comparison with TQOPEN, the thia and aza derivatives TQSPEN and TQNPEN exhibit improved Cd2+/Zn2+ selectivity and higher Cd2+-binding affinity, respectively.	thia	31-35	CD2 molecule	Homo sapiens	124-127
28621934-3	2017	In comparison with TQOPEN, the thia and aza derivatives TQSPEN and TQNPEN exhibit improved Cd2+/Zn2+ selectivity and higher Cd2+-binding affinity, respectively.	Azathioprine	40-43	CD2 molecule	Homo sapiens	91-94
28621934-3	2017	In comparison with TQOPEN, the thia and aza derivatives TQSPEN and TQNPEN exhibit improved Cd2+/Zn2+ selectivity and higher Cd2+-binding affinity, respectively.	Azathioprine	40-43	CD2 molecule	Homo sapiens	124-127
28621934-5	2017	Although the crystal structure of the TQOPEN-Cd2+ complex exhibits a six-coordinate metal center, in which one quinoline weakly interacts with the Cd center (Cd   Nquinoline = 3.303(3) A), a 1H NMR study at 233 K suggests that all quinolines interact with the Cd center to form a symmetrical seven-coordinate structure in solution.	quinoline	111-120	CD2 molecule	Homo sapiens	45-48
28621934-5	2017	Although the crystal structure of the TQOPEN-Cd2+ complex exhibits a six-coordinate metal center, in which one quinoline weakly interacts with the Cd center (Cd   Nquinoline = 3.303(3) A), a 1H NMR study at 233 K suggests that all quinolines interact with the Cd center to form a symmetrical seven-coordinate structure in solution.	cd   nquinoline	158-173	CD2 molecule	Homo sapiens	45-48
28621934-5	2017	Although the crystal structure of the TQOPEN-Cd2+ complex exhibits a six-coordinate metal center, in which one quinoline weakly interacts with the Cd center (Cd   Nquinoline = 3.303(3) A), a 1H NMR study at 233 K suggests that all quinolines interact with the Cd center to form a symmetrical seven-coordinate structure in solution.	Hydrogen	191-193	CD2 molecule	Homo sapiens	45-48
28621934-5	2017	Although the crystal structure of the TQOPEN-Cd2+ complex exhibits a six-coordinate metal center, in which one quinoline weakly interacts with the Cd center (Cd   Nquinoline = 3.303(3) A), a 1H NMR study at 233 K suggests that all quinolines interact with the Cd center to form a symmetrical seven-coordinate structure in solution.	Quinolines	231-241	CD2 molecule	Homo sapiens	45-48
28475982-0	2017	A circular dichroism sensor for selective detection of Cd2+ and S2- based on the in-situ generation of chiral CdS quantum dots.	Cadmium	110-113	CD2 molecule	Homo sapiens	55-58
28475982-1	2017	We demonstrate an advance in the fabrication of circular dichroism (CD) sensors for detection of Cd2+ and S2- based on chiral CdS quantum dots (QDs) generated by a facile in-situ reaction.	Cadmium	126-129	CD2 molecule	Homo sapiens	97-100
28475982-5	2017	The sensor is applied in real water samples with results comparing favorably with those obtained from ICP-OES (for Cd2+) and HPLC (for S2-).	Water	30-35	CD2 molecule	Homo sapiens	115-118
28745503-0	2017	Correction to "Experimental and Theoretical Investigations of Infrared Multiple Photon Dissociation Spectra of Asparagine Complexes with Zn2+ and Cd2+ and Their Deamidation Processes".	Asparagine	111-121	CD2 molecule	Homo sapiens	146-149
27860110-0	2017	Core-shell structured CdTe/CdS@SiO2 @CdTe@SiO2 composite fluorescent spheres: Synthesis and application for Cd2+ detection.	cadmium telluride	22-26	CD2 molecule	Homo sapiens	108-111
27860110-0	2017	Core-shell structured CdTe/CdS@SiO2 @CdTe@SiO2 composite fluorescent spheres: Synthesis and application for Cd2+ detection.	Cadmium	27-30	CD2 molecule	Homo sapiens	108-111
27860110-0	2017	Core-shell structured CdTe/CdS@SiO2 @CdTe@SiO2 composite fluorescent spheres: Synthesis and application for Cd2+ detection.	Silicon Dioxide	31-35	CD2 molecule	Homo sapiens	108-111
27860110-0	2017	Core-shell structured CdTe/CdS@SiO2 @CdTe@SiO2 composite fluorescent spheres: Synthesis and application for Cd2+ detection.	cadmium telluride	37-41	CD2 molecule	Homo sapiens	108-111
27860110-0	2017	Core-shell structured CdTe/CdS@SiO2 @CdTe@SiO2 composite fluorescent spheres: Synthesis and application for Cd2+ detection.	Silicon Dioxide	42-46	CD2 molecule	Homo sapiens	108-111
27860110-6	2017	Upon addition of Cd2+ to the S2- -quenched CdTe/CdS@SiO2 @CdTe@SiO2 system, the responding signal at 550 nm was dramatically restored, whereas the emission at 630 nm remained almost unchanged; this response could be used as a ratiometric "off-on" fluorescent probe for the detection of Cd2+ .	cadmium telluride	43-47	CD2 molecule	Homo sapiens	17-20
27860110-6	2017	Upon addition of Cd2+ to the S2- -quenched CdTe/CdS@SiO2 @CdTe@SiO2 system, the responding signal at 550 nm was dramatically restored, whereas the emission at 630 nm remained almost unchanged; this response could be used as a ratiometric "off-on" fluorescent probe for the detection of Cd2+ .	cadmium telluride	43-47	CD2 molecule	Homo sapiens	286-289
27860110-6	2017	Upon addition of Cd2+ to the S2- -quenched CdTe/CdS@SiO2 @CdTe@SiO2 system, the responding signal at 550 nm was dramatically restored, whereas the emission at 630 nm remained almost unchanged; this response could be used as a ratiometric "off-on" fluorescent probe for the detection of Cd2+ .	Cadmium	48-51	CD2 molecule	Homo sapiens	17-20
27860110-6	2017	Upon addition of Cd2+ to the S2- -quenched CdTe/CdS@SiO2 @CdTe@SiO2 system, the responding signal at 550 nm was dramatically restored, whereas the emission at 630 nm remained almost unchanged; this response could be used as a ratiometric "off-on" fluorescent probe for the detection of Cd2+ .	Cadmium	48-51	CD2 molecule	Homo sapiens	286-289
27860110-6	2017	Upon addition of Cd2+ to the S2- -quenched CdTe/CdS@SiO2 @CdTe@SiO2 system, the responding signal at 550 nm was dramatically restored, whereas the emission at 630 nm remained almost unchanged; this response could be used as a ratiometric "off-on" fluorescent probe for the detection of Cd2+ .	Silicon Dioxide	52-56	CD2 molecule	Homo sapiens	17-20
27860110-6	2017	Upon addition of Cd2+ to the S2- -quenched CdTe/CdS@SiO2 @CdTe@SiO2 system, the responding signal at 550 nm was dramatically restored, whereas the emission at 630 nm remained almost unchanged; this response could be used as a ratiometric "off-on" fluorescent probe for the detection of Cd2+ .	Silicon Dioxide	52-56	CD2 molecule	Homo sapiens	286-289
27860110-6	2017	Upon addition of Cd2+ to the S2- -quenched CdTe/CdS@SiO2 @CdTe@SiO2 system, the responding signal at 550 nm was dramatically restored, whereas the emission at 630 nm remained almost unchanged; this response could be used as a ratiometric "off-on" fluorescent probe for the detection of Cd2+ .	cadmium telluride	58-62	CD2 molecule	Homo sapiens	17-20
27860110-6	2017	Upon addition of Cd2+ to the S2- -quenched CdTe/CdS@SiO2 @CdTe@SiO2 system, the responding signal at 550 nm was dramatically restored, whereas the emission at 630 nm remained almost unchanged; this response could be used as a ratiometric "off-on" fluorescent probe for the detection of Cd2+ .	cadmium telluride	58-62	CD2 molecule	Homo sapiens	286-289
27860110-6	2017	Upon addition of Cd2+ to the S2- -quenched CdTe/CdS@SiO2 @CdTe@SiO2 system, the responding signal at 550 nm was dramatically restored, whereas the emission at 630 nm remained almost unchanged; this response could be used as a ratiometric "off-on" fluorescent probe for the detection of Cd2+ .	Silicon Dioxide	63-67	CD2 molecule	Homo sapiens	17-20
27860110-6	2017	Upon addition of Cd2+ to the S2- -quenched CdTe/CdS@SiO2 @CdTe@SiO2 system, the responding signal at 550 nm was dramatically restored, whereas the emission at 630 nm remained almost unchanged; this response could be used as a ratiometric "off-on" fluorescent probe for the detection of Cd2+ .	Silicon Dioxide	63-67	CD2 molecule	Homo sapiens	286-289
28661524-0	2017	Correction: Zn2+ and Cd2+ cationized serine complexes: infrared multiple photon dissociation spectroscopy and density functional theory investigations.	Serine	37-43	CD2 molecule	Homo sapiens	21-24
28661524-1	2017	Correction for "Zn2+ and Cd2+ cationized serine complexes: infrared multiple photon dissociation spectroscopy and density functional theory investigations" by Rebecca A. Coates et al., Phys.	Serine	41-47	CD2 molecule	Homo sapiens	25-28
28682399-0	2017	Correction: Experimental and theoretical investigations of infrared multiple photon dissociation spectra of glutamic acid complexes with Zn2+ and Cd2.	Glutamic Acid	108-121	CD2 molecule	Homo sapiens	146-149
28682399-1	2017	Correction for "Experimental and theoretical investigations of infrared multiple photon dissociation spectra of glutamic acid complexes with Zn2+ and Cd2+" by Georgia C. Boles et al., Phys.	Glutamic Acid	112-125	CD2 molecule	Homo sapiens	150-153
28671628-2	2017	The influence of the Cu2+ concentration on the stripping response to Cd2+ was studied.	cupric ion	21-25	CD2 molecule	Homo sapiens	69-72
28671628-3	2017	In addition, the effect of the ferrocyanide concentration on the SWASV detection of Cd2+ in the presence of Cu2+ was investigated.	hexacyanoferrate II	31-43	CD2 molecule	Homo sapiens	84-87
28671628-4	2017	A BP-ANN with two inputs and one output was used to establish the nonlinear relationship between the concentration of Cd2+ and the stripping peak currents of Cu2+ and Cd2+.	bp-ann	2-8	CD2 molecule	Homo sapiens	118-121
28671628-4	2017	A BP-ANN with two inputs and one output was used to establish the nonlinear relationship between the concentration of Cd2+ and the stripping peak currents of Cu2+ and Cd2+.	bp-ann	2-8	CD2 molecule	Homo sapiens	167-170
28671628-4	2017	A BP-ANN with two inputs and one output was used to establish the nonlinear relationship between the concentration of Cd2+ and the stripping peak currents of Cu2+ and Cd2+.	cupric ion	158-162	CD2 molecule	Homo sapiens	118-121
28671628-4	2017	A BP-ANN with two inputs and one output was used to establish the nonlinear relationship between the concentration of Cd2+ and the stripping peak currents of Cu2+ and Cd2+.	cupric ion	158-162	CD2 molecule	Homo sapiens	167-170
28621934-5	2017	Although the crystal structure of the TQOPEN-Cd2+ complex exhibits a six-coordinate metal center, in which one quinoline weakly interacts with the Cd center (Cd   Nquinoline = 3.303(3) A), a 1H NMR study at 233 K suggests that all quinolines interact with the Cd center to form a symmetrical seven-coordinate structure in solution.	Cadmium	147-149	CD2 molecule	Homo sapiens	45-48
28671628-0	2017	Direct Quantification of Cd2+ in the Presence of Cu2+ by a Combination of Anodic Stripping Voltammetry Using a Bi-Film-Modified Glassy Carbon Electrode and an Artificial Neural Network.	Carbon	135-141	CD2 molecule	Homo sapiens	25-28
28671628-1	2017	Abstract: In this study, a novel method based on a Bi/glassy carbon electrode (Bi/GCE) for quantitatively and directly detecting Cd2+ in the presence of Cu2+ without further electrode modifications by combining square-wave anodic stripping voltammetry (SWASV) and a back-propagation artificial neural network (BP-ANN) has been proposed.	Carbon	61-67	CD2 molecule	Homo sapiens	129-132
28671628-1	2017	Abstract: In this study, a novel method based on a Bi/glassy carbon electrode (Bi/GCE) for quantitatively and directly detecting Cd2+ in the presence of Cu2+ without further electrode modifications by combining square-wave anodic stripping voltammetry (SWASV) and a back-propagation artificial neural network (BP-ANN) has been proposed.	cupric ion	153-157	CD2 molecule	Homo sapiens	129-132
28509528-5	2017	The added Zn2+ or Cd2+ could react with the surface thioglycollic acid to form Zn-thiol or Cd-thiol complex passivation shell, which restored surface defects and suppressed nonradiative recombination pathway.	2-mercaptoacetate	52-70	CD2 molecule	Homo sapiens	18-21
28574251-3	2017	Here, we used a non-native metal ion, Cd2+, in lieu of Ca2+ to gain insight into the contributions made by long-range Coulombic interactions and direct metal ion-lipid bridging to membrane binding.	Metals	27-32	CD2 molecule	Homo sapiens	38-41
28574251-6	2017	In contrast, electron paramagnetic resonance experiments revealed that Cd2+ does support membrane binding of the C2 domains in full-length synaptotagmin 1, where the high local lipid concentrations that result from membrane tethering can partially compensate for lack of a full complement of divalent metal ions and specific lipid coordination in Cd2+-complexed C2A/B domains.	Metals	301-306	CD2 molecule	Homo sapiens	71-74
28509528-5	2017	The added Zn2+ or Cd2+ could react with the surface thioglycollic acid to form Zn-thiol or Cd-thiol complex passivation shell, which restored surface defects and suppressed nonradiative recombination pathway.	zn-thiol	79-87	CD2 molecule	Homo sapiens	18-21
28509528-5	2017	The added Zn2+ or Cd2+ could react with the surface thioglycollic acid to form Zn-thiol or Cd-thiol complex passivation shell, which restored surface defects and suppressed nonradiative recombination pathway.	cd-thiol	91-99	CD2 molecule	Homo sapiens	18-21
28510419-3	2017	We show that 83.0 +- 0.2% of hazardous cadmium ion (Cd2+) was released from the commercial cadmium sulfoselenide pigment (i.e., cadmium red) in aqueous suspension within 24 h under simulated sunlit conditions.	Cadmium	39-46	CD2 molecule	Homo sapiens	52-55
28510419-3	2017	We show that 83.0 +- 0.2% of hazardous cadmium ion (Cd2+) was released from the commercial cadmium sulfoselenide pigment (i.e., cadmium red) in aqueous suspension within 24 h under simulated sunlit conditions.	selanylidenecadmium;sulfanylidenecadmium	91-112	CD2 molecule	Homo sapiens	52-55
28510419-3	2017	We show that 83.0 +- 0.2% of hazardous cadmium ion (Cd2+) was released from the commercial cadmium sulfoselenide pigment (i.e., cadmium red) in aqueous suspension within 24 h under simulated sunlit conditions.	cadmium red	128-139	CD2 molecule	Homo sapiens	52-55
28510419-9	2017	The fast release of Cd2+ from the pigment was further confirmed in river water under natural sunlight, with 38.6 +- 0.1% of the cadmium released within 4 h. Overall, this study underscores the importance to account for photochemical effects to inform risk assessments and regulations of cadmium pigments which are currently based on their low solubility.	Water	73-78	CD2 molecule	Homo sapiens	20-23
28510419-9	2017	The fast release of Cd2+ from the pigment was further confirmed in river water under natural sunlight, with 38.6 +- 0.1% of the cadmium released within 4 h. Overall, this study underscores the importance to account for photochemical effects to inform risk assessments and regulations of cadmium pigments which are currently based on their low solubility.	Cadmium	128-135	CD2 molecule	Homo sapiens	20-23
28510419-9	2017	The fast release of Cd2+ from the pigment was further confirmed in river water under natural sunlight, with 38.6 +- 0.1% of the cadmium released within 4 h. Overall, this study underscores the importance to account for photochemical effects to inform risk assessments and regulations of cadmium pigments which are currently based on their low solubility.	Cadmium	287-294	CD2 molecule	Homo sapiens	20-23
28462956-0	2017	Experimental and theoretical investigations of infrared multiple photon dissociation spectra of glutamic acid complexes with Zn2+ and Cd2.	Glutamic Acid	96-109	CD2 molecule	Homo sapiens	134-137
28365425-5	2017	The results showed that both the binding of Pb2+ and Cd2+ to bacteria with EPS had a similar kinetics process, however Pb2+ bound to bacterial surface without EPS more firmly compared with Cd2+.	Lead	119-123	CD2 molecule	Homo sapiens	53-56
28462956-1	2017	Complexes of glutamic acid (Glu) cationized with Zn2+ and Cd2+ were examined by infrared multiple photon dissociation (IRMPD) action spectroscopy using light generated from a free electron laser.	Glutamic Acid	13-26	CD2 molecule	Homo sapiens	58-61
28462956-1	2017	Complexes of glutamic acid (Glu) cationized with Zn2+ and Cd2+ were examined by infrared multiple photon dissociation (IRMPD) action spectroscopy using light generated from a free electron laser.	Glutamic Acid	28-31	CD2 molecule	Homo sapiens	58-61
28541940-0	2017	Efficient removal of Cd2+ ion from water by calcium alginate hydrogel filtration membrane.	Water	35-40	CD2 molecule	Homo sapiens	21-24
28524876-5	2017	Ligand LA (VRu2+X, V=bisterpyridine, X=tetraterpyridine, Ru=Ruthenium) was initially used for the self-assembly of an anticipated hexagram upon reaction with Cd2+ or Fe2+; however, unexpected pentagonal structures were formed, that is, [Cd5LA5]30+ and [Fe5LA5]30+.	bisterpyridine	21-35	CD2 molecule	Homo sapiens	158-161
28524876-5	2017	Ligand LA (VRu2+X, V=bisterpyridine, X=tetraterpyridine, Ru=Ruthenium) was initially used for the self-assembly of an anticipated hexagram upon reaction with Cd2+ or Fe2+; however, unexpected pentagonal structures were formed, that is, [Cd5LA5]30+ and [Fe5LA5]30+.	tetraterpyridine	39-55	CD2 molecule	Homo sapiens	158-161
28524876-5	2017	Ligand LA (VRu2+X, V=bisterpyridine, X=tetraterpyridine, Ru=Ruthenium) was initially used for the self-assembly of an anticipated hexagram upon reaction with Cd2+ or Fe2+; however, unexpected pentagonal structures were formed, that is, [Cd5LA5]30+ and [Fe5LA5]30+.	Ruthenium	12-14	CD2 molecule	Homo sapiens	158-161
28524876-5	2017	Ligand LA (VRu2+X, V=bisterpyridine, X=tetraterpyridine, Ru=Ruthenium) was initially used for the self-assembly of an anticipated hexagram upon reaction with Cd2+ or Fe2+; however, unexpected pentagonal structures were formed, that is, [Cd5LA5]30+ and [Fe5LA5]30+.	Ruthenium	60-69	CD2 molecule	Homo sapiens	158-161
28524876-5	2017	Ligand LA (VRu2+X, V=bisterpyridine, X=tetraterpyridine, Ru=Ruthenium) was initially used for the self-assembly of an anticipated hexagram upon reaction with Cd2+ or Fe2+; however, unexpected pentagonal structures were formed, that is, [Cd5LA5]30+ and [Fe5LA5]30+.	ammonium ferrous sulfate	166-170	CD2 molecule	Homo sapiens	158-161
28524876-5	2017	Ligand LA (VRu2+X, V=bisterpyridine, X=tetraterpyridine, Ru=Ruthenium) was initially used for the self-assembly of an anticipated hexagram upon reaction with Cd2+ or Fe2+; however, unexpected pentagonal structures were formed, that is, [Cd5LA5]30+ and [Fe5LA5]30+.	fe5la5	253-259	CD2 molecule	Homo sapiens	158-161
28189897-1	2017	We synthesized fluorescent Cd nanoclusters (CdNCs) through a protein-directed method, and the synthesis method was utilized for a homogeneous, ultrasensitive, and selective detection of cadmium ion (Cd2+).	Cadmium	27-29	CD2 molecule	Homo sapiens	199-202
28189897-1	2017	We synthesized fluorescent Cd nanoclusters (CdNCs) through a protein-directed method, and the synthesis method was utilized for a homogeneous, ultrasensitive, and selective detection of cadmium ion (Cd2+).	cdncs	44-49	CD2 molecule	Homo sapiens	199-202
28189897-1	2017	We synthesized fluorescent Cd nanoclusters (CdNCs) through a protein-directed method, and the synthesis method was utilized for a homogeneous, ultrasensitive, and selective detection of cadmium ion (Cd2+).	Cadmium	186-193	CD2 molecule	Homo sapiens	199-202
28189897-6	2017	The fluorescence of the CdNCs increased with increasing Cd2+ concentrations, and the limit of detection in deionized water was 15.68 fM.	cdncs	24-29	CD2 molecule	Homo sapiens	56-59
28189897-7	2017	This method enables the detection of Cd2+ through the Cd concentration-dependent formation of fluorescent CdNCs in tap, fountain, and pond water samples with detection limits of 0.75, 7.65, and 48.2 fM, respectively.	cdncs	106-111	CD2 molecule	Homo sapiens	37-40
28189897-7	2017	This method enables the detection of Cd2+ through the Cd concentration-dependent formation of fluorescent CdNCs in tap, fountain, and pond water samples with detection limits of 0.75, 7.65, and 48.2 fM, respectively.	Water	139-144	CD2 molecule	Homo sapiens	37-40
28409428-0	2017	Evaluation of zeolite-supported microscale zero-valent iron as a potential adsorbent for Cd2+ and Pb2+ removal in permeable reactive barriers.	Zeolites	14-21	CD2 molecule	Homo sapiens	89-92
28409428-0	2017	Evaluation of zeolite-supported microscale zero-valent iron as a potential adsorbent for Cd2+ and Pb2+ removal in permeable reactive barriers.	Iron	55-59	CD2 molecule	Homo sapiens	89-92
28409428-1	2017	A new composite adsorbent, zeolite-supported microscale zero-valent iron (Z-mZVI) was evaluated as a potential adsorbent for the removal of Cd2+ and Pb2+ from aqueous solution using batch and column experiments.	Zeolites	27-34	CD2 molecule	Homo sapiens	140-143
28409428-1	2017	A new composite adsorbent, zeolite-supported microscale zero-valent iron (Z-mZVI) was evaluated as a potential adsorbent for the removal of Cd2+ and Pb2+ from aqueous solution using batch and column experiments.	Iron	68-72	CD2 molecule	Homo sapiens	140-143
28409428-4	2017	The coexistence of Cd2+ and Pb2+ caused the reduction of Cd2+ removal efficiency, but not for Pb2+.	Lead	28-32	CD2 molecule	Homo sapiens	57-60
28409428-5	2017	Z-mZVI has a high removal capacity for Cd2+ and Pb2+ over a wide pH range (3.0-6.8) as well as in the presence of competitive Ca2+ or Mg2+ ions (&lt;2 mmol/L).	z-mzvi	0-6	CD2 molecule	Homo sapiens	39-42
28409428-6	2017	Moreover, Z-mZVI shows a high immobilization capacity for the adsorbed Cd2+ and Pb2+ products, even at the acid solution (pH = 3.95).	z-mzvi	10-16	CD2 molecule	Homo sapiens	71-74
28409428-7	2017	Column experiment confirmed that Z-mZVI could simultaneously remove Cd2+ and Pb2+ from solution efficiently.	z-mzvi	33-39	CD2 molecule	Homo sapiens	68-71
28409428-8	2017	Thomas model can simulate the equilibrium adsorption capacity of Cd2+ and Pb2+ of the Z-mZVI column well.	Lead	74-78	CD2 molecule	Homo sapiens	65-68
28409428-9	2017	This study demonstrates that Z-mZVI is an efficient and promising reactive material in permeable reactive barriers for Cd2+ and Pb2+ removal from aqueous solution.	z-mzvi	29-35	CD2 molecule	Homo sapiens	119-122
28220278-0	2017	Rhodamine Diaminomaleonitrile Conjugate as a Novel Colorimetric Fluorescent Sensor for Recognition of Cd2+ Ion.	rhodamine diaminomaleonitrile	0-29	CD2 molecule	Homo sapiens	102-105
28220278-1	2017	Rhodamine diaminomaleonitrile linked probe (RD-1) shows highly sensitive colorimetric and selective turn-on fluorescent response to Cd2+ over other metal ions.	rhodamine diaminomaleonitrile	0-29	CD2 molecule	Homo sapiens	132-135
28220278-1	2017	Rhodamine diaminomaleonitrile linked probe (RD-1) shows highly sensitive colorimetric and selective turn-on fluorescent response to Cd2+ over other metal ions.	Metals	148-153	CD2 molecule	Homo sapiens	132-135
28220278-3	2017	The probe RD-1 was preliminarily applied to the determination of Cd2+ ion in water samples from river and tap water with satisfying results.	Water	77-82	CD2 molecule	Homo sapiens	65-68
28220278-3	2017	The probe RD-1 was preliminarily applied to the determination of Cd2+ ion in water samples from river and tap water with satisfying results.	Water	110-115	CD2 molecule	Homo sapiens	65-68
28541940-0	2017	Efficient removal of Cd2+ ion from water by calcium alginate hydrogel filtration membrane.	Alginates	44-60	CD2 molecule	Homo sapiens	21-24
28049053-8	2017	It was found to be effective in the extraction of Cd2+ ions with near 100% cadmium removal, as well as being selective since no Ca2+ ions were extracted.	Cadmium	75-82	CD2 molecule	Homo sapiens	50-53
28009932-0	2017	Luminescent Metal-Organic Framework Sensor: Exceptional Cd2+ Turn-On Detection and First In Situ Visualization of Cd2+ Ion Diffusion into a Crystal.	Metals	12-17	CD2 molecule	Homo sapiens	56-59
28009932-0	2017	Luminescent Metal-Organic Framework Sensor: Exceptional Cd2+ Turn-On Detection and First In Situ Visualization of Cd2+ Ion Diffusion into a Crystal.	Metals	12-17	CD2 molecule	Homo sapiens	114-117
28009932-2	2017	A metal-organic framework (MOF) chemosensor has been prepared that serves as an efficient platform for the selective detection of Cu2+ and Cd2+ ions over other metal ions.	Metals	2-7	CD2 molecule	Homo sapiens	139-142
28009932-2	2017	A metal-organic framework (MOF) chemosensor has been prepared that serves as an efficient platform for the selective detection of Cu2+ and Cd2+ ions over other metal ions.	Metals	160-165	CD2 molecule	Homo sapiens	139-142
28009932-3	2017	In particular, this framework shows the highest fluorescence enhancement ( 60-fold relative to Cd-free MOF) for the hazardous metal ion Cd2+ among luminescent MOFs and displays excellent reusability in repeated cycles.	Cadmium	95-97	CD2 molecule	Homo sapiens	136-139
28009932-3	2017	In particular, this framework shows the highest fluorescence enhancement ( 60-fold relative to Cd-free MOF) for the hazardous metal ion Cd2+ among luminescent MOFs and displays excellent reusability in repeated cycles.	Metals	126-131	CD2 molecule	Homo sapiens	136-139
28247897-0	2017	Solvothermal self-assembly of Cd2+ coordination polymers with supramolecular networks involving N-donor ligands and aromatic dicarboxylates: synthesis, crystal structure and photoluminescence studies.	Polymers	48-56	CD2 molecule	Homo sapiens	30-33
28247897-3	2017	The structure of CP2 revealed an undulated 2D sql net comprising Cd2+ nodes bridged by the ditopic N-donor, BTTMB and dicarboxylate BrIP involved in mu2-eta1eta1eta1eta1 coordination.	cp2	17-20	CD2 molecule	Homo sapiens	65-68
28247897-0	2017	Solvothermal self-assembly of Cd2+ coordination polymers with supramolecular networks involving N-donor ligands and aromatic dicarboxylates: synthesis, crystal structure and photoluminescence studies.	Nitrogen	96-97	CD2 molecule	Homo sapiens	30-33
28247897-0	2017	Solvothermal self-assembly of Cd2+ coordination polymers with supramolecular networks involving N-donor ligands and aromatic dicarboxylates: synthesis, crystal structure and photoluminescence studies.	malonic acid	125-139	CD2 molecule	Homo sapiens	30-33
28132769-3	2017	Intravenous administration of cyclophosphamide (37.5 mg/kg body weight) resulted in immunosuppresion induction, as significant drops were observed in blood leukocytes and lymphocyte subset counts (CD2+, CD4+, CD8+, CD19+), lasting 3-10 days after its administration.	Cyclophosphamide	30-46	CD2 molecule	Homo sapiens	197-200
28221392-0	2017	A 4,5-quinolimide-based fluorescent sensor for the turn-on detection of Cd2+ with live-cell imaging.	4,5-quinolimide	2-17	CD2 molecule	Homo sapiens	72-75
28221392-1	2017	A 4,5-quinolimide derivative, BNA, bearing the amide-DPA receptor, was synthesized as a turn-on fluorescent sensor for Cd2+.	4,5-quinolimide	2-17	CD2 molecule	Homo sapiens	119-122
28221392-1	2017	A 4,5-quinolimide derivative, BNA, bearing the amide-DPA receptor, was synthesized as a turn-on fluorescent sensor for Cd2+.	2-Naphthylamine	30-33	CD2 molecule	Homo sapiens	119-122
28221392-2	2017	Under physiological conditions, BNA could distinguish Cd2+ from Zn2+, showing turn-on fluorescence behaviour and an increased fluorescence lifetime.	2-Naphthylamine	32-35	CD2 molecule	Homo sapiens	54-57
28221392-4	2017	Furthermore, BNA was utilized for fluorescence imaging of Cd2+ in live cells.	2-Naphthylamine	13-16	CD2 molecule	Homo sapiens	58-61
28154862-0	2017	Intracellular detection of hazardous Cd2+ through a fluorescence imaging technique by using a nontoxic coumarin based sensor.	coumarin	103-111	CD2 molecule	Homo sapiens	37-40
28165100-5	2017	The ultra-fast introduction of Cd2+ and Hg2+ (70 minutes for Cd2+ and 19 minutes for Hg2+) was realized at room temperature; other metal ions such as Ag+, Cu2+ and Pb2+ can be buried at 50  C. This mild reaction temperature offers a solution for introducing impurities without sacrificing the interfacial structure of nanocrystals.	Mercuric cation	40-44	CD2 molecule	Homo sapiens	61-64
28165100-5	2017	The ultra-fast introduction of Cd2+ and Hg2+ (70 minutes for Cd2+ and 19 minutes for Hg2+) was realized at room temperature; other metal ions such as Ag+, Cu2+ and Pb2+ can be buried at 50  C. This mild reaction temperature offers a solution for introducing impurities without sacrificing the interfacial structure of nanocrystals.	Lead	164-168	CD2 molecule	Homo sapiens	31-34
28154862-1	2017	A new coumarin based turn on fluorescent sensor (R1) was reported for the detection of highly hazardous Cd2+ with excellent selectivity and sensitivity without any interference of other metal ions.	coumarin	6-14	CD2 molecule	Homo sapiens	104-107
28154862-1	2017	A new coumarin based turn on fluorescent sensor (R1) was reported for the detection of highly hazardous Cd2+ with excellent selectivity and sensitivity without any interference of other metal ions.	Metals	186-191	CD2 molecule	Homo sapiens	104-107
27875763-7	2017	In addition, the bio-char removal efficiency of Cd2+ from soapstock pyrolysis in presence of bentonite was 27.4wt.% higher than without bentonite.	Bentonite	93-102	CD2 molecule	Homo sapiens	48-51
27875763-7	2017	In addition, the bio-char removal efficiency of Cd2+ from soapstock pyrolysis in presence of bentonite was 27.4wt.% higher than without bentonite.	Bentonite	136-145	CD2 molecule	Homo sapiens	48-51
27824176-4	2017	This was more influenced by the new molecular conformation and modified spin-orbit coupling imposed by the binding of the Cd2+ ions to the phenazine molecules.	phenazine	139-148	CD2 molecule	Homo sapiens	122-125
28009167-2	2017	We explore the effects of using small concentrations of Cd2+ and unusually high concentrations of methylammonium iodide during the growth of MAPbI3 in the two-step solution process.	mapbi3	141-147	CD2 molecule	Homo sapiens	56-59
27611473-1	2017	A dual-functional platform for the sensing of acetylcholinesterase (AChE) activity and cadmium ions (Cd2+) was developed based on the fluorescence resonance energy transfer (FRET) between NaYF4:Yb,Er upconversion nanoparticles (UCNPs) and gold nanoparticles (AuNPs) via glutathione regulation.	Cadmium	87-94	CD2 molecule	Homo sapiens	101-104
27802590-0	2017	Reactions of the Zn Proteome with Cd2+ and Other Xenobiotics: Trafficking and Toxicity.	Zinc	17-19	CD2 molecule	Homo sapiens	34-37
27802590-3	2017	The hypothesis is evaluated that Cd2+ damages cells by replacing Zn2+ in key Zn proteins.	Zinc	65-69	CD2 molecule	Homo sapiens	33-36
27802590-3	2017	The hypothesis is evaluated that Cd2+ damages cells by replacing Zn2+ in key Zn proteins.	Zinc	65-67	CD2 molecule	Homo sapiens	33-36
27981329-0	2017	Replacement of quinolines with isoquinolines affords target metal ion switching from Zn2+ to Cd2+ in the fluorescent sensor TQLN (N,N,N",N"-tetrakis(2-quinolylmethyl)-2,6-bis(aminomethyl)pyridine).	Quinolines	15-25	CD2 molecule	Homo sapiens	93-96
27981329-0	2017	Replacement of quinolines with isoquinolines affords target metal ion switching from Zn2+ to Cd2+ in the fluorescent sensor TQLN (N,N,N",N"-tetrakis(2-quinolylmethyl)-2,6-bis(aminomethyl)pyridine).	Isoquinolines	31-44	CD2 molecule	Homo sapiens	93-96
27981329-0	2017	Replacement of quinolines with isoquinolines affords target metal ion switching from Zn2+ to Cd2+ in the fluorescent sensor TQLN (N,N,N",N"-tetrakis(2-quinolylmethyl)-2,6-bis(aminomethyl)pyridine).	Metals	60-65	CD2 molecule	Homo sapiens	93-96
27981329-0	2017	Replacement of quinolines with isoquinolines affords target metal ion switching from Zn2+ to Cd2+ in the fluorescent sensor TQLN (N,N,N",N"-tetrakis(2-quinolylmethyl)-2,6-bis(aminomethyl)pyridine).	Zinc	85-89	CD2 molecule	Homo sapiens	93-96
27981329-0	2017	Replacement of quinolines with isoquinolines affords target metal ion switching from Zn2+ to Cd2+ in the fluorescent sensor TQLN (N,N,N",N"-tetrakis(2-quinolylmethyl)-2,6-bis(aminomethyl)pyridine).	tqln	124-128	CD2 molecule	Homo sapiens	93-96
27981329-2	2017	In contrast, the isoquinoline counterpart 1-isoTQLN exhibits a Cd2+-specific fluorescence increase at 365 nm attributable to monomer emission (ICd/I0 = 83, IZn/ICd = 19%, phiCd = 0.015).	isoquinoline	17-29	CD2 molecule	Homo sapiens	63-66
27981329-2	2017	In contrast, the isoquinoline counterpart 1-isoTQLN exhibits a Cd2+-specific fluorescence increase at 365 nm attributable to monomer emission (ICd/I0 = 83, IZn/ICd = 19%, phiCd = 0.015).	1-isotqln	42-51	CD2 molecule	Homo sapiens	63-66
27611473-1	2017	A dual-functional platform for the sensing of acetylcholinesterase (AChE) activity and cadmium ions (Cd2+) was developed based on the fluorescence resonance energy transfer (FRET) between NaYF4:Yb,Er upconversion nanoparticles (UCNPs) and gold nanoparticles (AuNPs) via glutathione regulation.	Glutathione	270-281	CD2 molecule	Homo sapiens	101-104
27611473-6	2017	When Cd2+ is added into the stable mixture of AuNPs, GSH and AChE/ATC, Cd2+ could interact with GSH to form a spherical shaped (GSH)4Cd complex, which decreases the free GSH on the surface of AuNPs to weaken the stability of AuNPs and lead to the easily aggregation of them in the system.	Glutathione	53-56	CD2 molecule	Homo sapiens	5-8
27611473-6	2017	When Cd2+ is added into the stable mixture of AuNPs, GSH and AChE/ATC, Cd2+ could interact with GSH to form a spherical shaped (GSH)4Cd complex, which decreases the free GSH on the surface of AuNPs to weaken the stability of AuNPs and lead to the easily aggregation of them in the system.	Glutathione	53-56	CD2 molecule	Homo sapiens	71-74
27611473-6	2017	When Cd2+ is added into the stable mixture of AuNPs, GSH and AChE/ATC, Cd2+ could interact with GSH to form a spherical shaped (GSH)4Cd complex, which decreases the free GSH on the surface of AuNPs to weaken the stability of AuNPs and lead to the easily aggregation of them in the system.	Glutathione	96-99	CD2 molecule	Homo sapiens	5-8
27611473-6	2017	When Cd2+ is added into the stable mixture of AuNPs, GSH and AChE/ATC, Cd2+ could interact with GSH to form a spherical shaped (GSH)4Cd complex, which decreases the free GSH on the surface of AuNPs to weaken the stability of AuNPs and lead to the easily aggregation of them in the system.	Glutathione	96-99	CD2 molecule	Homo sapiens	71-74
27611473-6	2017	When Cd2+ is added into the stable mixture of AuNPs, GSH and AChE/ATC, Cd2+ could interact with GSH to form a spherical shaped (GSH)4Cd complex, which decreases the free GSH on the surface of AuNPs to weaken the stability of AuNPs and lead to the easily aggregation of them in the system.	(gsh)4cd	127-135	CD2 molecule	Homo sapiens	5-8
27611473-6	2017	When Cd2+ is added into the stable mixture of AuNPs, GSH and AChE/ATC, Cd2+ could interact with GSH to form a spherical shaped (GSH)4Cd complex, which decreases the free GSH on the surface of AuNPs to weaken the stability of AuNPs and lead to the easily aggregation of them in the system.	(gsh)4cd	127-135	CD2 molecule	Homo sapiens	71-74
27611473-6	2017	When Cd2+ is added into the stable mixture of AuNPs, GSH and AChE/ATC, Cd2+ could interact with GSH to form a spherical shaped (GSH)4Cd complex, which decreases the free GSH on the surface of AuNPs to weaken the stability of AuNPs and lead to the easily aggregation of them in the system.	Glutathione	96-99	CD2 molecule	Homo sapiens	5-8
27611473-6	2017	When Cd2+ is added into the stable mixture of AuNPs, GSH and AChE/ATC, Cd2+ could interact with GSH to form a spherical shaped (GSH)4Cd complex, which decreases the free GSH on the surface of AuNPs to weaken the stability of AuNPs and lead to the easily aggregation of them in the system.	Glutathione	96-99	CD2 molecule	Homo sapiens	71-74
27611473-9	2017	The small molecules regulated dual-functional platform based on UCNPs/AuNPs is a simple, label-free method and can be applied for the turn-on fluorescence detection of AChE activity in human serum and Cd2+ in real water samples.	Water	214-219	CD2 molecule	Homo sapiens	201-204
29965059-1	2017	The influence of Cd on the degradation of nonylphenol (NP) by P.aeruginosa SH1 was investigated in this study.The investigation revealed that biomass of the strain was significantly declined with the increase of Cd2+ concentration.The biomass was declined by 27.1% in the presence of 10 mg L-1Cd2+ after 24 h.The addition of Cd2+ had a great influence on adsorption of NP by the strain.As for the effect of living stain,adsorption by P.aeruginosa SH1 cells was stimulated at low concentrations of Cd2+(0.5 mg L-1),while inhibited at higher levels (&gt;=5 mg L-1).As for inactivation of microbes,adsorption by cells was stimulated at higher concentrations,but was only slightly influenced at low levels.The results showed that the intracellular enzymes had much greater degradation rate than the living cells.Different concentrations of Cd2+ had different effects on bacteria and intracellular enzyme degradation of NP separately.The degradation efficiency when using intracellular enzymes and bacteria was inhibited at higher levels of Cd2+ and the intracellular enzyme inhibition was more significant.Degradation by cells was stimulated at low concentrations of Cd2+,but no significant impact was found on that by intracellular enzymes.The degradation process of NP by intracellular enzymes of the strain conformed to the first-order kinetic model.The highest reaction rate was achieved when the concentrations of Cd2+ was 0.5 mg L-1 and the half-life of this substrate was 5.5 h.However,the degradation process of NP by the strain did not conform to the first-order kinetic model.	nonylphenol	42-53	CD2 molecule	Homo sapiens	212-215
29965059-1	2017	The influence of Cd on the degradation of nonylphenol (NP) by P.aeruginosa SH1 was investigated in this study.The investigation revealed that biomass of the strain was significantly declined with the increase of Cd2+ concentration.The biomass was declined by 27.1% in the presence of 10 mg L-1Cd2+ after 24 h.The addition of Cd2+ had a great influence on adsorption of NP by the strain.As for the effect of living stain,adsorption by P.aeruginosa SH1 cells was stimulated at low concentrations of Cd2+(0.5 mg L-1),while inhibited at higher levels (&gt;=5 mg L-1).As for inactivation of microbes,adsorption by cells was stimulated at higher concentrations,but was only slightly influenced at low levels.The results showed that the intracellular enzymes had much greater degradation rate than the living cells.Different concentrations of Cd2+ had different effects on bacteria and intracellular enzyme degradation of NP separately.The degradation efficiency when using intracellular enzymes and bacteria was inhibited at higher levels of Cd2+ and the intracellular enzyme inhibition was more significant.Degradation by cells was stimulated at low concentrations of Cd2+,but no significant impact was found on that by intracellular enzymes.The degradation process of NP by intracellular enzymes of the strain conformed to the first-order kinetic model.The highest reaction rate was achieved when the concentrations of Cd2+ was 0.5 mg L-1 and the half-life of this substrate was 5.5 h.However,the degradation process of NP by the strain did not conform to the first-order kinetic model.	Cadmium	17-19	CD2 molecule	Homo sapiens	212-215
29965059-1	2017	The influence of Cd on the degradation of nonylphenol (NP) by P.aeruginosa SH1 was investigated in this study.The investigation revealed that biomass of the strain was significantly declined with the increase of Cd2+ concentration.The biomass was declined by 27.1% in the presence of 10 mg L-1Cd2+ after 24 h.The addition of Cd2+ had a great influence on adsorption of NP by the strain.As for the effect of living stain,adsorption by P.aeruginosa SH1 cells was stimulated at low concentrations of Cd2+(0.5 mg L-1),while inhibited at higher levels (&gt;=5 mg L-1).As for inactivation of microbes,adsorption by cells was stimulated at higher concentrations,but was only slightly influenced at low levels.The results showed that the intracellular enzymes had much greater degradation rate than the living cells.Different concentrations of Cd2+ had different effects on bacteria and intracellular enzyme degradation of NP separately.The degradation efficiency when using intracellular enzymes and bacteria was inhibited at higher levels of Cd2+ and the intracellular enzyme inhibition was more significant.Degradation by cells was stimulated at low concentrations of Cd2+,but no significant impact was found on that by intracellular enzymes.The degradation process of NP by intracellular enzymes of the strain conformed to the first-order kinetic model.The highest reaction rate was achieved when the concentrations of Cd2+ was 0.5 mg L-1 and the half-life of this substrate was 5.5 h.However,the degradation process of NP by the strain did not conform to the first-order kinetic model.	nonylphenol	42-53	CD2 molecule	Homo sapiens	293-296
29965059-1	2017	The influence of Cd on the degradation of nonylphenol (NP) by P.aeruginosa SH1 was investigated in this study.The investigation revealed that biomass of the strain was significantly declined with the increase of Cd2+ concentration.The biomass was declined by 27.1% in the presence of 10 mg L-1Cd2+ after 24 h.The addition of Cd2+ had a great influence on adsorption of NP by the strain.As for the effect of living stain,adsorption by P.aeruginosa SH1 cells was stimulated at low concentrations of Cd2+(0.5 mg L-1),while inhibited at higher levels (&gt;=5 mg L-1).As for inactivation of microbes,adsorption by cells was stimulated at higher concentrations,but was only slightly influenced at low levels.The results showed that the intracellular enzymes had much greater degradation rate than the living cells.Different concentrations of Cd2+ had different effects on bacteria and intracellular enzyme degradation of NP separately.The degradation efficiency when using intracellular enzymes and bacteria was inhibited at higher levels of Cd2+ and the intracellular enzyme inhibition was more significant.Degradation by cells was stimulated at low concentrations of Cd2+,but no significant impact was found on that by intracellular enzymes.The degradation process of NP by intracellular enzymes of the strain conformed to the first-order kinetic model.The highest reaction rate was achieved when the concentrations of Cd2+ was 0.5 mg L-1 and the half-life of this substrate was 5.5 h.However,the degradation process of NP by the strain did not conform to the first-order kinetic model.	nonylphenol	42-53	CD2 molecule	Homo sapiens	293-296
29965059-1	2017	The influence of Cd on the degradation of nonylphenol (NP) by P.aeruginosa SH1 was investigated in this study.The investigation revealed that biomass of the strain was significantly declined with the increase of Cd2+ concentration.The biomass was declined by 27.1% in the presence of 10 mg L-1Cd2+ after 24 h.The addition of Cd2+ had a great influence on adsorption of NP by the strain.As for the effect of living stain,adsorption by P.aeruginosa SH1 cells was stimulated at low concentrations of Cd2+(0.5 mg L-1),while inhibited at higher levels (&gt;=5 mg L-1).As for inactivation of microbes,adsorption by cells was stimulated at higher concentrations,but was only slightly influenced at low levels.The results showed that the intracellular enzymes had much greater degradation rate than the living cells.Different concentrations of Cd2+ had different effects on bacteria and intracellular enzyme degradation of NP separately.The degradation efficiency when using intracellular enzymes and bacteria was inhibited at higher levels of Cd2+ and the intracellular enzyme inhibition was more significant.Degradation by cells was stimulated at low concentrations of Cd2+,but no significant impact was found on that by intracellular enzymes.The degradation process of NP by intracellular enzymes of the strain conformed to the first-order kinetic model.The highest reaction rate was achieved when the concentrations of Cd2+ was 0.5 mg L-1 and the half-life of this substrate was 5.5 h.However,the degradation process of NP by the strain did not conform to the first-order kinetic model.	nonylphenol	42-53	CD2 molecule	Homo sapiens	293-296
29965059-1	2017	The influence of Cd on the degradation of nonylphenol (NP) by P.aeruginosa SH1 was investigated in this study.The investigation revealed that biomass of the strain was significantly declined with the increase of Cd2+ concentration.The biomass was declined by 27.1% in the presence of 10 mg L-1Cd2+ after 24 h.The addition of Cd2+ had a great influence on adsorption of NP by the strain.As for the effect of living stain,adsorption by P.aeruginosa SH1 cells was stimulated at low concentrations of Cd2+(0.5 mg L-1),while inhibited at higher levels (&gt;=5 mg L-1).As for inactivation of microbes,adsorption by cells was stimulated at higher concentrations,but was only slightly influenced at low levels.The results showed that the intracellular enzymes had much greater degradation rate than the living cells.Different concentrations of Cd2+ had different effects on bacteria and intracellular enzyme degradation of NP separately.The degradation efficiency when using intracellular enzymes and bacteria was inhibited at higher levels of Cd2+ and the intracellular enzyme inhibition was more significant.Degradation by cells was stimulated at low concentrations of Cd2+,but no significant impact was found on that by intracellular enzymes.The degradation process of NP by intracellular enzymes of the strain conformed to the first-order kinetic model.The highest reaction rate was achieved when the concentrations of Cd2+ was 0.5 mg L-1 and the half-life of this substrate was 5.5 h.However,the degradation process of NP by the strain did not conform to the first-order kinetic model.	nonylphenol	42-53	CD2 molecule	Homo sapiens	293-296
29965059-1	2017	The influence of Cd on the degradation of nonylphenol (NP) by P.aeruginosa SH1 was investigated in this study.The investigation revealed that biomass of the strain was significantly declined with the increase of Cd2+ concentration.The biomass was declined by 27.1% in the presence of 10 mg L-1Cd2+ after 24 h.The addition of Cd2+ had a great influence on adsorption of NP by the strain.As for the effect of living stain,adsorption by P.aeruginosa SH1 cells was stimulated at low concentrations of Cd2+(0.5 mg L-1),while inhibited at higher levels (&gt;=5 mg L-1).As for inactivation of microbes,adsorption by cells was stimulated at higher concentrations,but was only slightly influenced at low levels.The results showed that the intracellular enzymes had much greater degradation rate than the living cells.Different concentrations of Cd2+ had different effects on bacteria and intracellular enzyme degradation of NP separately.The degradation efficiency when using intracellular enzymes and bacteria was inhibited at higher levels of Cd2+ and the intracellular enzyme inhibition was more significant.Degradation by cells was stimulated at low concentrations of Cd2+,but no significant impact was found on that by intracellular enzymes.The degradation process of NP by intracellular enzymes of the strain conformed to the first-order kinetic model.The highest reaction rate was achieved when the concentrations of Cd2+ was 0.5 mg L-1 and the half-life of this substrate was 5.5 h.However,the degradation process of NP by the strain did not conform to the first-order kinetic model.	nonylphenol	42-53	CD2 molecule	Homo sapiens	293-296
29965059-1	2017	The influence of Cd on the degradation of nonylphenol (NP) by P.aeruginosa SH1 was investigated in this study.The investigation revealed that biomass of the strain was significantly declined with the increase of Cd2+ concentration.The biomass was declined by 27.1% in the presence of 10 mg L-1Cd2+ after 24 h.The addition of Cd2+ had a great influence on adsorption of NP by the strain.As for the effect of living stain,adsorption by P.aeruginosa SH1 cells was stimulated at low concentrations of Cd2+(0.5 mg L-1),while inhibited at higher levels (&gt;=5 mg L-1).As for inactivation of microbes,adsorption by cells was stimulated at higher concentrations,but was only slightly influenced at low levels.The results showed that the intracellular enzymes had much greater degradation rate than the living cells.Different concentrations of Cd2+ had different effects on bacteria and intracellular enzyme degradation of NP separately.The degradation efficiency when using intracellular enzymes and bacteria was inhibited at higher levels of Cd2+ and the intracellular enzyme inhibition was more significant.Degradation by cells was stimulated at low concentrations of Cd2+,but no significant impact was found on that by intracellular enzymes.The degradation process of NP by intracellular enzymes of the strain conformed to the first-order kinetic model.The highest reaction rate was achieved when the concentrations of Cd2+ was 0.5 mg L-1 and the half-life of this substrate was 5.5 h.However,the degradation process of NP by the strain did not conform to the first-order kinetic model.	nonylphenol	42-53	CD2 molecule	Homo sapiens	293-296
29965059-1	2017	The influence of Cd on the degradation of nonylphenol (NP) by P.aeruginosa SH1 was investigated in this study.The investigation revealed that biomass of the strain was significantly declined with the increase of Cd2+ concentration.The biomass was declined by 27.1% in the presence of 10 mg L-1Cd2+ after 24 h.The addition of Cd2+ had a great influence on adsorption of NP by the strain.As for the effect of living stain,adsorption by P.aeruginosa SH1 cells was stimulated at low concentrations of Cd2+(0.5 mg L-1),while inhibited at higher levels (&gt;=5 mg L-1).As for inactivation of microbes,adsorption by cells was stimulated at higher concentrations,but was only slightly influenced at low levels.The results showed that the intracellular enzymes had much greater degradation rate than the living cells.Different concentrations of Cd2+ had different effects on bacteria and intracellular enzyme degradation of NP separately.The degradation efficiency when using intracellular enzymes and bacteria was inhibited at higher levels of Cd2+ and the intracellular enzyme inhibition was more significant.Degradation by cells was stimulated at low concentrations of Cd2+,but no significant impact was found on that by intracellular enzymes.The degradation process of NP by intracellular enzymes of the strain conformed to the first-order kinetic model.The highest reaction rate was achieved when the concentrations of Cd2+ was 0.5 mg L-1 and the half-life of this substrate was 5.5 h.However,the degradation process of NP by the strain did not conform to the first-order kinetic model.	nonylphenol	55-57	CD2 molecule	Homo sapiens	212-215
29965059-1	2017	The influence of Cd on the degradation of nonylphenol (NP) by P.aeruginosa SH1 was investigated in this study.The investigation revealed that biomass of the strain was significantly declined with the increase of Cd2+ concentration.The biomass was declined by 27.1% in the presence of 10 mg L-1Cd2+ after 24 h.The addition of Cd2+ had a great influence on adsorption of NP by the strain.As for the effect of living stain,adsorption by P.aeruginosa SH1 cells was stimulated at low concentrations of Cd2+(0.5 mg L-1),while inhibited at higher levels (&gt;=5 mg L-1).As for inactivation of microbes,adsorption by cells was stimulated at higher concentrations,but was only slightly influenced at low levels.The results showed that the intracellular enzymes had much greater degradation rate than the living cells.Different concentrations of Cd2+ had different effects on bacteria and intracellular enzyme degradation of NP separately.The degradation efficiency when using intracellular enzymes and bacteria was inhibited at higher levels of Cd2+ and the intracellular enzyme inhibition was more significant.Degradation by cells was stimulated at low concentrations of Cd2+,but no significant impact was found on that by intracellular enzymes.The degradation process of NP by intracellular enzymes of the strain conformed to the first-order kinetic model.The highest reaction rate was achieved when the concentrations of Cd2+ was 0.5 mg L-1 and the half-life of this substrate was 5.5 h.However,the degradation process of NP by the strain did not conform to the first-order kinetic model.	nonylphenol	55-57	CD2 molecule	Homo sapiens	293-296
29965059-1	2017	The influence of Cd on the degradation of nonylphenol (NP) by P.aeruginosa SH1 was investigated in this study.The investigation revealed that biomass of the strain was significantly declined with the increase of Cd2+ concentration.The biomass was declined by 27.1% in the presence of 10 mg L-1Cd2+ after 24 h.The addition of Cd2+ had a great influence on adsorption of NP by the strain.As for the effect of living stain,adsorption by P.aeruginosa SH1 cells was stimulated at low concentrations of Cd2+(0.5 mg L-1),while inhibited at higher levels (&gt;=5 mg L-1).As for inactivation of microbes,adsorption by cells was stimulated at higher concentrations,but was only slightly influenced at low levels.The results showed that the intracellular enzymes had much greater degradation rate than the living cells.Different concentrations of Cd2+ had different effects on bacteria and intracellular enzyme degradation of NP separately.The degradation efficiency when using intracellular enzymes and bacteria was inhibited at higher levels of Cd2+ and the intracellular enzyme inhibition was more significant.Degradation by cells was stimulated at low concentrations of Cd2+,but no significant impact was found on that by intracellular enzymes.The degradation process of NP by intracellular enzymes of the strain conformed to the first-order kinetic model.The highest reaction rate was achieved when the concentrations of Cd2+ was 0.5 mg L-1 and the half-life of this substrate was 5.5 h.However,the degradation process of NP by the strain did not conform to the first-order kinetic model.	nonylphenol	55-57	CD2 molecule	Homo sapiens	293-296
29965059-1	2017	The influence of Cd on the degradation of nonylphenol (NP) by P.aeruginosa SH1 was investigated in this study.The investigation revealed that biomass of the strain was significantly declined with the increase of Cd2+ concentration.The biomass was declined by 27.1% in the presence of 10 mg L-1Cd2+ after 24 h.The addition of Cd2+ had a great influence on adsorption of NP by the strain.As for the effect of living stain,adsorption by P.aeruginosa SH1 cells was stimulated at low concentrations of Cd2+(0.5 mg L-1),while inhibited at higher levels (&gt;=5 mg L-1).As for inactivation of microbes,adsorption by cells was stimulated at higher concentrations,but was only slightly influenced at low levels.The results showed that the intracellular enzymes had much greater degradation rate than the living cells.Different concentrations of Cd2+ had different effects on bacteria and intracellular enzyme degradation of NP separately.The degradation efficiency when using intracellular enzymes and bacteria was inhibited at higher levels of Cd2+ and the intracellular enzyme inhibition was more significant.Degradation by cells was stimulated at low concentrations of Cd2+,but no significant impact was found on that by intracellular enzymes.The degradation process of NP by intracellular enzymes of the strain conformed to the first-order kinetic model.The highest reaction rate was achieved when the concentrations of Cd2+ was 0.5 mg L-1 and the half-life of this substrate was 5.5 h.However,the degradation process of NP by the strain did not conform to the first-order kinetic model.	nonylphenol	55-57	CD2 molecule	Homo sapiens	293-296
29965059-1	2017	The influence of Cd on the degradation of nonylphenol (NP) by P.aeruginosa SH1 was investigated in this study.The investigation revealed that biomass of the strain was significantly declined with the increase of Cd2+ concentration.The biomass was declined by 27.1% in the presence of 10 mg L-1Cd2+ after 24 h.The addition of Cd2+ had a great influence on adsorption of NP by the strain.As for the effect of living stain,adsorption by P.aeruginosa SH1 cells was stimulated at low concentrations of Cd2+(0.5 mg L-1),while inhibited at higher levels (&gt;=5 mg L-1).As for inactivation of microbes,adsorption by cells was stimulated at higher concentrations,but was only slightly influenced at low levels.The results showed that the intracellular enzymes had much greater degradation rate than the living cells.Different concentrations of Cd2+ had different effects on bacteria and intracellular enzyme degradation of NP separately.The degradation efficiency when using intracellular enzymes and bacteria was inhibited at higher levels of Cd2+ and the intracellular enzyme inhibition was more significant.Degradation by cells was stimulated at low concentrations of Cd2+,but no significant impact was found on that by intracellular enzymes.The degradation process of NP by intracellular enzymes of the strain conformed to the first-order kinetic model.The highest reaction rate was achieved when the concentrations of Cd2+ was 0.5 mg L-1 and the half-life of this substrate was 5.5 h.However,the degradation process of NP by the strain did not conform to the first-order kinetic model.	nonylphenol	55-57	CD2 molecule	Homo sapiens	293-296
29965059-1	2017	The influence of Cd on the degradation of nonylphenol (NP) by P.aeruginosa SH1 was investigated in this study.The investigation revealed that biomass of the strain was significantly declined with the increase of Cd2+ concentration.The biomass was declined by 27.1% in the presence of 10 mg L-1Cd2+ after 24 h.The addition of Cd2+ had a great influence on adsorption of NP by the strain.As for the effect of living stain,adsorption by P.aeruginosa SH1 cells was stimulated at low concentrations of Cd2+(0.5 mg L-1),while inhibited at higher levels (&gt;=5 mg L-1).As for inactivation of microbes,adsorption by cells was stimulated at higher concentrations,but was only slightly influenced at low levels.The results showed that the intracellular enzymes had much greater degradation rate than the living cells.Different concentrations of Cd2+ had different effects on bacteria and intracellular enzyme degradation of NP separately.The degradation efficiency when using intracellular enzymes and bacteria was inhibited at higher levels of Cd2+ and the intracellular enzyme inhibition was more significant.Degradation by cells was stimulated at low concentrations of Cd2+,but no significant impact was found on that by intracellular enzymes.The degradation process of NP by intracellular enzymes of the strain conformed to the first-order kinetic model.The highest reaction rate was achieved when the concentrations of Cd2+ was 0.5 mg L-1 and the half-life of this substrate was 5.5 h.However,the degradation process of NP by the strain did not conform to the first-order kinetic model.	nonylphenol	55-57	CD2 molecule	Homo sapiens	293-296
29965059-1	2017	The influence of Cd on the degradation of nonylphenol (NP) by P.aeruginosa SH1 was investigated in this study.The investigation revealed that biomass of the strain was significantly declined with the increase of Cd2+ concentration.The biomass was declined by 27.1% in the presence of 10 mg L-1Cd2+ after 24 h.The addition of Cd2+ had a great influence on adsorption of NP by the strain.As for the effect of living stain,adsorption by P.aeruginosa SH1 cells was stimulated at low concentrations of Cd2+(0.5 mg L-1),while inhibited at higher levels (&gt;=5 mg L-1).As for inactivation of microbes,adsorption by cells was stimulated at higher concentrations,but was only slightly influenced at low levels.The results showed that the intracellular enzymes had much greater degradation rate than the living cells.Different concentrations of Cd2+ had different effects on bacteria and intracellular enzyme degradation of NP separately.The degradation efficiency when using intracellular enzymes and bacteria was inhibited at higher levels of Cd2+ and the intracellular enzyme inhibition was more significant.Degradation by cells was stimulated at low concentrations of Cd2+,but no significant impact was found on that by intracellular enzymes.The degradation process of NP by intracellular enzymes of the strain conformed to the first-order kinetic model.The highest reaction rate was achieved when the concentrations of Cd2+ was 0.5 mg L-1 and the half-life of this substrate was 5.5 h.However,the degradation process of NP by the strain did not conform to the first-order kinetic model.	nonylphenol	55-57	CD2 molecule	Homo sapiens	293-296
27815852-8	2017	The presence of Ca2+ or Cd2+ significantly increased arsenic removal at higher pH.	Arsenic	53-60	CD2 molecule	Homo sapiens	24-27
28348509-3	2017	The adsorption behavior of the modified product for Cd2+ in aqueous solution was studied as a function of pH, initial metal concentration, equilibrium time, and temperature.	Metals	118-123	CD2 molecule	Homo sapiens	52-55
27743328-6	2017	The content of zerovalent iron decreased after Cd2+ adsorption as a result of iron oxidation during Cd2+ adsorption.	Iron	26-30	CD2 molecule	Homo sapiens	47-50
27743328-6	2017	The content of zerovalent iron decreased after Cd2+ adsorption as a result of iron oxidation during Cd2+ adsorption.	Iron	26-30	CD2 molecule	Homo sapiens	100-103
27743328-6	2017	The content of zerovalent iron decreased after Cd2+ adsorption as a result of iron oxidation during Cd2+ adsorption.	Iron	78-82	CD2 molecule	Homo sapiens	47-50
27743328-6	2017	The content of zerovalent iron decreased after Cd2+ adsorption as a result of iron oxidation during Cd2+ adsorption.	Iron	78-82	CD2 molecule	Homo sapiens	100-103
29313432-0	2017	Hb Hornchurch [beta43(CD2)Glu Lys; HBB: c.130G&gt;A] Compromises the Molecular Diagnosis of beta-Thalassemia in a Chinese Family.	Lysine	30-33	CD2 molecule	Homo sapiens	22-25
27771568-8	2017	This carbon surface coverage can control the release of Cd2+ ions in CdO-2 compared to non-covered CdO-1 nanoparticles and hence mitigate the toxicity in the case of CdO-2.	Carbon	5-11	CD2 molecule	Homo sapiens	56-59
27771568-8	2017	This carbon surface coverage can control the release of Cd2+ ions in CdO-2 compared to non-covered CdO-1 nanoparticles and hence mitigate the toxicity in the case of CdO-2.	cdo-2	69-74	CD2 molecule	Homo sapiens	56-59
27771568-8	2017	This carbon surface coverage can control the release of Cd2+ ions in CdO-2 compared to non-covered CdO-1 nanoparticles and hence mitigate the toxicity in the case of CdO-2.	cdo-2	166-171	CD2 molecule	Homo sapiens	56-59
27629588-1	2017	Cadmium ions (Cd2+) are a widespread and easily absorbed toxin to both humans and animals that can be spread via food, water, and air pollution.	Cadmium	0-7	CD2 molecule	Homo sapiens	14-17
27936541-3	2016	In this study, based on the charge-discharge principle of the supercapacitor and excellent adsorption properties of birnessite, a birnessite-based electrode was used to remove Cd2+ from aqueous solutions.	birnessite	116-126	CD2 molecule	Homo sapiens	176-179
27871888-2	2017	As compared to the extensive research in Cd tissue accumulation, little was known about the elimination of Cd, particularly its toxic form, Cd ion (Cd2+).	Cadmium	107-109	CD2 molecule	Homo sapiens	148-151
27871888-2	2017	As compared to the extensive research in Cd tissue accumulation, little was known about the elimination of Cd, particularly its toxic form, Cd ion (Cd2+).	Cadmium	107-109	CD2 molecule	Homo sapiens	148-151
27871888-5	2017	The cells overexpressing MATEs showed a 2-4 fold increase of Cd2+ uptake that could be blocked by the MATE inhibitor cimetidine.	Cimetidine	117-127	CD2 molecule	Homo sapiens	61-64
27871888-7	2017	Cd2+ could inhibit the uptake of metformin, a substrate of MATE transporters, with the half maximal inhibitory concentration (IC50) of 97.5+-6.0muM, 20.2+-2.6muM, and 49.9+-6.9muM in HEK-hMATE1, HEK-hMATE2-K, and HEK-mMate1 cells, respectively.	Metformin	33-42	CD2 molecule	Homo sapiens	0-3
27973834-0	2016	Experimental and Theoretical Investigations of Infrared Multiple Photon Dissociation Spectra of Asparagine Complexes with Zn2+ and Cd2+ and Their Deamidation Processes.	Asparagine	96-106	CD2 molecule	Homo sapiens	131-134
27973834-1	2016	Complexes of asparagine (Asn) cationized with Zn2+ and Cd2+ were examined by infrared multiple photon dissociation (IRMPD) action spectroscopy using light generated from a free electron laser.	Asparagine	13-23	CD2 molecule	Homo sapiens	55-58
30034028-5	2017	Variable-pressure 2H T1 measurements reveal site-dependent interactions in the cation with strengths in the order MD3 &gt; CD3 &gt; CD2, indicating dissimilarities in the electric field gradients along the alkyl chain, with the CD2 sites having the largest gradient.	Deuterium	18-20	CD2 molecule	Homo sapiens	132-135
30034028-5	2017	Variable-pressure 2H T1 measurements reveal site-dependent interactions in the cation with strengths in the order MD3 &gt; CD3 &gt; CD2, indicating dissimilarities in the electric field gradients along the alkyl chain, with the CD2 sites having the largest gradient.	Deuterium	18-20	CD2 molecule	Homo sapiens	228-231
27973834-1	2016	Complexes of asparagine (Asn) cationized with Zn2+ and Cd2+ were examined by infrared multiple photon dissociation (IRMPD) action spectroscopy using light generated from a free electron laser.	Asparagine	25-28	CD2 molecule	Homo sapiens	55-58
27936541-3	2016	In this study, based on the charge-discharge principle of the supercapacitor and excellent adsorption properties of birnessite, a birnessite-based electrode was used to remove Cd2+ from aqueous solutions.	birnessite	130-140	CD2 molecule	Homo sapiens	176-179
27936541-5	2016	The results showed that Cd2+ was adsorbed on the surfaces and interlayers of birnessite, and the maximum electrosorption capacity of birnessite for Cd2+ was about 900.7 mg g-1 (8.01 mmol g-1), which was significantly higher than the adsorption isotherm capacity of birnessite (125.8 mg g-1).	birnessite	77-87	CD2 molecule	Homo sapiens	24-27
27936541-5	2016	The results showed that Cd2+ was adsorbed on the surfaces and interlayers of birnessite, and the maximum electrosorption capacity of birnessite for Cd2+ was about 900.7 mg g-1 (8.01 mmol g-1), which was significantly higher than the adsorption isotherm capacity of birnessite (125.8 mg g-1).	birnessite	133-143	CD2 molecule	Homo sapiens	24-27
27936541-5	2016	The results showed that Cd2+ was adsorbed on the surfaces and interlayers of birnessite, and the maximum electrosorption capacity of birnessite for Cd2+ was about 900.7 mg g-1 (8.01 mmol g-1), which was significantly higher than the adsorption isotherm capacity of birnessite (125.8 mg g-1).	birnessite	133-143	CD2 molecule	Homo sapiens	148-151
27936541-5	2016	The results showed that Cd2+ was adsorbed on the surfaces and interlayers of birnessite, and the maximum electrosorption capacity of birnessite for Cd2+ was about 900.7 mg g-1 (8.01 mmol g-1), which was significantly higher than the adsorption isotherm capacity of birnessite (125.8 mg g-1).	birnessite	133-143	CD2 molecule	Homo sapiens	24-27
27936541-5	2016	The results showed that Cd2+ was adsorbed on the surfaces and interlayers of birnessite, and the maximum electrosorption capacity of birnessite for Cd2+ was about 900.7 mg g-1 (8.01 mmol g-1), which was significantly higher than the adsorption isotherm capacity of birnessite (125.8 mg g-1).	birnessite	133-143	CD2 molecule	Homo sapiens	148-151
27936541-6	2016	The electrosorption specific capacity of birnessite for Cd2+ increased with an increase in initial Cd2+ concentration and decreased with an increase in the loading of active birnessite.	birnessite	41-51	CD2 molecule	Homo sapiens	56-59
27936541-6	2016	The electrosorption specific capacity of birnessite for Cd2+ increased with an increase in initial Cd2+ concentration and decreased with an increase in the loading of active birnessite.	birnessite	41-51	CD2 molecule	Homo sapiens	99-102
27759950-7	2016	The association constant of the 7+  OHBP4 complex in 1:1 (v/v) [D6 ]acetone/CD2 Cl2 solution is up to 3100+-300 m-1 .	7+  ohbp4	32-41	CD2 molecule	Homo sapiens	76-79
27759950-7	2016	The association constant of the 7+  OHBP4 complex in 1:1 (v/v) [D6 ]acetone/CD2 Cl2 solution is up to 3100+-300 m-1 .	[d6 ]acetone	63-75	CD2 molecule	Homo sapiens	76-79
27846987-3	2016	A glassy carbon electrode modified by the nanocomposite was evaluated as a new platform for the simultaneous detection of trace amounts of Cd2+ and Pb2+ using differential pulse anodic stripping voltammetry (DPASV).	Carbon	9-15	CD2 molecule	Homo sapiens	139-142
27846987-5	2016	Under the optimal conditions, good linear relationships were obtained for Cd2+ in a range of 0.05-60 mug L-1, with the detection limit (S/N = 3) of 0.02 mug L-1, and for Pb2+ in a range of 0.1-60 mug L-1, with the detection limit (S/N = 3) of 0.05 mug L-1.	Lead	170-174	CD2 molecule	Homo sapiens	74-77
27846987-6	2016	The new electrode was successfully applied to real water samples for simultaneous detection of Cd2+ and Pb2+ with good recovery rates.	Water	51-56	CD2 molecule	Homo sapiens	95-98
27624665-4	2016	The syntheses of stable-labelled [13 C6 ]BMS-725519 and [13 CD313 CD2 ]BMS-812204 synthesized from of [13 C6 ]4-chloroacetophenone and [13 CD313 CD2 ]iodoethane, respectively, are also described.	4-chloroacetophenone	109-130	CD2 molecule	Homo sapiens	66-69
27624665-4	2016	The syntheses of stable-labelled [13 C6 ]BMS-725519 and [13 CD313 CD2 ]BMS-812204 synthesized from of [13 C6 ]4-chloroacetophenone and [13 CD313 CD2 ]iodoethane, respectively, are also described.	iodoethane	149-160	CD2 molecule	Homo sapiens	66-69
31964065-5	2016	Analysis of the Job plot data, the fluorescence lifetimes, and experiments on varying micellar shape and pH, confirms that the coordination volume of the resulting octahedral metal complex and formation of a five-membered chelate ring are critical factors for Cd2+ interference.	Metals	175-180	CD2 molecule	Homo sapiens	260-263
27597743-0	2016	Fabrication of magnetic macroporous chitosan-g-poly (acrylic acid) hydrogel for removal of Cd2+ and Pb2.	carbopol 940	47-66	CD2 molecule	Homo sapiens	91-94