PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
23686875-1	2001	The potential activation by electron capture of H2+CO2 or CO+H2O reactions, leading to HCOOH (formic acid), and of CO+NH3, HCN+H2O and HNC+H2O reactions, leading to HC(O)NH2 (formamide), have been studied theoretically.	formamide	175-184	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	123-126
9829975-4	1998	The reflection coefficients (sigma) of urea, glycerol, acetamide, and formamide at 23 degreesC were: AQP0: 1, 1, 0.8, 0.6; AQP1: 1, 0.8, 1, 1; AQP2: 1, 0.8, 1, 1; AQP3: 1, 0.2, 0.7, 0.4; AQP4: 1, 0.9, 1, 1; and AQP5: 1, 1, 1, 0.8.	formamide	70-79	major intrinsic protein of lens fiber S homeolog	Xenopus laevis	101-105
10960471-15	2000	), indicate that the most likely positioning of fMLF in the binding pocket of FPR is approximately parallel to the fifth transmembrane helix with the formamide group of fMLF hydrogen-bonded to both Asp-106 and Arg-201, the leucine side chain pointing toward the second transmembrane region, and the COOH-terminal carboxyl group of fMLF ion-paired with Arg-205.	formamide	150-159	formyl peptide receptor 1	Homo sapiens	78-81
11000274-4	2000	We show here that, while the HTZ1 gene encoding H2A.Z is not essential in budding yeast, its disruption results in slow growth and formamide sensitivity.	formamide	131-140	histone H2AZ	Saccharomyces cerevisiae S288C	29-33
11121269-5	2001	Based on the experimentally measured enthalpies of immersion in n-heptane, water, and formamide per unit BET specific surface area, estimates could be made of the apolar, Lewis acid, and Lewis base contributions to the total surface enthalpy of MCM-41 materials.	formamide	86-95	delta/notch like EGF repeat containing	Homo sapiens	105-108
10893716-4	2000	We have found that the following factors influence oligoribonucleotide hydrolysis: (i) single-stranded structure of RNA flanking the scissile phosphodiester bond, (ii) the substituent on atom C-5 of the uridine adjacent to the cleaved internucleotide bond, (iii) the position of the scissile UA phosphodiester bond within a hairpin loop, (iv) the concentration of formamide, urea, ethanol and sodium chloride.	formamide	364-373	complement C5	Homo sapiens	192-195
1520336-2	1992	The PCR products of the transthyretin gene were denatured in the presence of formamide and electrophoresed in a non-denaturing polyacrylamide gel to detect an electrophoretic change due to a sequence variation.	formamide	77-86	transthyretin	Homo sapiens	24-37
9680064-2	1998	The model reaction of DCC-activated coupling of Boc-Ala-Phe-OH with H-Ala-OBu(t) has been carried out in dioxane, dimethylsulfoxide and formamide, as well as in mixtures (90%/10%, v/v) of dioxane with acetonitrile, dimethylformamide, dimethylsulfoxide and formamide.	formamide	136-145	DCC netrin 1 receptor	Homo sapiens	22-25
9680064-2	1998	The model reaction of DCC-activated coupling of Boc-Ala-Phe-OH with H-Ala-OBu(t) has been carried out in dioxane, dimethylsulfoxide and formamide, as well as in mixtures (90%/10%, v/v) of dioxane with acetonitrile, dimethylformamide, dimethylsulfoxide and formamide.	formamide	223-232	DCC netrin 1 receptor	Homo sapiens	22-25
9493911-5	1998	We show that YY1 can be sequestered in vivo into a high-molecular-weight complex and can be dislodged from this complex either by treatment with formamide or by incubation with an oligonucleotide containing the YY1 DNA binding site sequence.	formamide	145-154	YY1 transcription factor	Homo sapiens	13-16
9364937-1	1997	We report here that 3-aminobenzamide and other amides, such as formamide, acetamide and nicotinamide, specifically induce a high rate of transcription at the 93D puff (the hsr omega heat shock gene) in polytene chromosomes of Drosophila melanogaster.	formamide	63-72	Heat shock RNA omega	Drosophila melanogaster	172-181
1444430-1	1992	Products observed during anaerobic cyanide transformation are consistent with a hydrolytic pathway (HCN + H2O <--> HCONH2 + H2O <--> HCOOH + NH3).	formamide	121-127	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	100-103
9729823-2	1998	The use of formamide and a low concentration of acrylamide increased resolution and sharpness of HUMARA alleles in silver-stained polyacrylamide gels.	formamide	11-20	androgen receptor	Homo sapiens	97-103
8138179-4	1994	Those genes susceptible to giving rise to formamide-sensitive alleles include the structural gene for DNA ligase, CDC9, and the structural gene for arginine permease, CAN1.	formamide	42-51	DNA ligase (ATP) CDC9	Saccharomyces cerevisiae S288C	114-118
8138179-4	1994	Those genes susceptible to giving rise to formamide-sensitive alleles include the structural gene for DNA ligase, CDC9, and the structural gene for arginine permease, CAN1.	formamide	42-51	arginine permease CAN1	Saccharomyces cerevisiae S288C	167-171
2263626-6	1990	SDP1 DNA-binding activity was restored by treating a protein fraction containing SDP1 and I-SDP1 with the dissociating agent formamide.	formamide	125-134	mitogen-activated protein kinase tyrosine protein phosphatase SDP1	Saccharomyces cerevisiae S288C	0-4
1686201-4	1991	Gd3+ (450 microM) applied to normal or formamide-treated cutaneous pectoris nerve-muscle preparations induced, after a short delay, a complete block of neuromuscular transmission.	formamide	39-48	GRDX	Homo sapiens	0-3
2003925-0	1991	Use of formamide to improve amplification of HLA DQ alpha sequences.	formamide	7-16	major histocompatibility complex, class II, DQ alpha 1	Homo sapiens	45-57
2263626-6	1990	SDP1 DNA-binding activity was restored by treating a protein fraction containing SDP1 and I-SDP1 with the dissociating agent formamide.	formamide	125-134	mitogen-activated protein kinase tyrosine protein phosphatase SDP1	Saccharomyces cerevisiae S288C	81-85
2263626-6	1990	SDP1 DNA-binding activity was restored by treating a protein fraction containing SDP1 and I-SDP1 with the dissociating agent formamide.	formamide	125-134	mitogen-activated protein kinase tyrosine protein phosphatase SDP1	Saccharomyces cerevisiae S288C	81-85
1969856-7	1990	The POMC-directed 24-mer probe had a theoretical melting point (Tm) of 49.4 degrees C (in the absence of formamide) and four individual experimental determinations of Tm produced a mean value of 48.9 degrees C. Detection of the biotinylated probe was best accomplished with monoclonal antibiotin antibodies and the alkaline phosphatase-anti-alkaline phosphatase (APAAP) system.	formamide	105-114	proopiomelanocortin	Rattus norvegicus	4-8
2539429-5	1989	With porin as the channel, formamide requires an osmotic gradient about ten times that required with urea, which is approximately 1/40th as permeant as formamide through bare lipid membrane.	formamide	27-36	voltage dependent anion channel 1	Homo sapiens	5-10
35537261-1	2022	In this work we present a time-resolved FTIR spectroscopic study on kinetics of atomic and molecular species, specifically CO, CN radical, N2, HCN and CO2 generated in a glow discharge of formamide-nitrogen-water mixture in a helium buffer gas.	formamide	188-197	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	143-146
3129195-3	1988	By using a variety of protocols involving the dissociating agents sodium desoxycholate and formamide, as much cytosolic NF-kappa B can be found in the fraction from unstimulated 70Z/3 pre-B cells as is found in the nuclear extract from phorbol ester-activated cells.	formamide	91-100	nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105	Mus musculus	120-130
2444283-3	1987	Although the four small hsps show considerable sequence homology in their coding sequences, antisense hsp 23 RNA was shown to specifically inhibit hsp 23 mRNA translation under both high (formamide, 45 degrees C) and low stringency (37 degrees C) conditions.	formamide	188-197	Heat shock protein 23	Drosophila melanogaster	102-108
2444283-3	1987	Although the four small hsps show considerable sequence homology in their coding sequences, antisense hsp 23 RNA was shown to specifically inhibit hsp 23 mRNA translation under both high (formamide, 45 degrees C) and low stringency (37 degrees C) conditions.	formamide	188-197	Heat shock protein 23	Drosophila melanogaster	147-153
6604155-10	1983	Formamide, which is known to abolish excitation-contraction coupling, also abolished the Ca2+ transient.	formamide	0-9	carbonic anhydrase 2	Homo sapiens	89-92
6182256-4	1982	Formamide sucrose gradient centrifugation analysis indicated that the mRNA which codes for IFN-gamma sediments at around 15 S. The profile, however, suggested a size heterogeneity of IFN-specific mRNA.	formamide	0-9	interferon gamma	Homo sapiens	91-100
6182256-4	1982	Formamide sucrose gradient centrifugation analysis indicated that the mRNA which codes for IFN-gamma sediments at around 15 S. The profile, however, suggested a size heterogeneity of IFN-specific mRNA.	formamide	0-9	interferon alpha 1	Homo sapiens	91-94
6152854-4	1981	Fractionation of the RNA on formamide-containing sucrose gradients before translation indicates that the desmin messenger RNA is larger than the vimentin messenger RNA and contains an extensive noncoding segment.	formamide	28-37	desmin	Oryctolagus cuniculus	105-111
7329416-3	1981	Heterogeneous nuclear RNA carrying the sequences of ceruloplasmin mRNA sedimented in sucrose gradients containing formamide, as a broad zone around the 56S peak.	formamide	114-123	ceruloplasmin	Rattus norvegicus	52-65
6254766-1	1980	actin complex by formamide.	formamide	17-26	actin	Oryctolagus cuniculus	0-5
6254766-3	1980	It was used to demonstrate that actin can be released from DNAse-I-agarose by 35--40% formamide.	formamide	86-95	actin	Oryctolagus cuniculus	32-37
6254766-3	1980	It was used to demonstrate that actin can be released from DNAse-I-agarose by 35--40% formamide.	formamide	86-95	deoxyribonuclease-1	Oryctolagus cuniculus	59-66
986157-2	1976	This highly purified myosin mRNP-tcRNA is shown to have a molecular weight of 10 000 on formamide-acrylamide gels, and reacts stoichometrically (on a 1:1 mole ratio) with myosin mRNA.	formamide	88-97	myosin, heavy chain 15	Gallus gallus	21-27
488117-1	1979	Purified vitellogenin mRNA of Xenopus laevis was incubated with mechanically sheared DNA in high concentrations of formamide and the resulting R-loops (i.e. RNA .	formamide	115-124	a1-a	Xenopus laevis	9-21
1002695-5	1976	Pure albumin mRNA migrated as an 18 S peak on 85% formamide-containing linear sucrose gradients and as a 22 S peak on 2.5% polyacrylamide gels in sodium dodecyl sulfate.	formamide	50-59	albumin	Rattus norvegicus	5-12
947754-4	1976	On 99% formamide 3.4% polyacrylamide gels vitellogenin mRNA has an Mr of 2.4-2.5 X 10(6) and codes for a peptide of Mr 240000, which under our incubation conditions is partially degraded to smaller peptides.	formamide	7-16	putative uncharacterized protein LOC400499	Homo sapiens	42-54
658040-1	1978	cDNA synthesized on purified vitellogenin mRNA from Xenopus liver was hybridized to the template in formamide/urea at 22 degrees C to avoid degradation of the RNA.	formamide	100-109	a1-a	Xenopus laevis	29-41
560211-2	1977	It has a poly(A) content of 8.6% and a molecular weight, estimated by formamide gel electrophoresis, of 260 000. mRNA with a molecular weight of around 143 000 would be sufficient to code for leghemoglobin.	formamide	70-79	leghemoglobin A	Glycine max	192-205
33130073-9	2021	METHODS: We used two experimental models: A) formamide-induced acute "detubulation", where VM retain functional RyR2 and SERCA2, but lack T-tubules-associated LCC and NCX.	formamide	45-54	ryanodine receptor 2	Rattus norvegicus	112-116
1112793-6	1975	The molar ratio of the alpha- and beta-globin mRNAs, as determined by quantitating the bands on the formamide gels, is similar to that of the cytoplasmic mRNAs.	formamide	100-109	hemoglobin alpha, adult chain 1	Mus musculus	23-45
4415727-0	1974	Separation of alpha- and beta-globin messenger RNAs by formamide gel electrophoresis.	formamide	55-64	hemoglobin subunit alpha 2	Homo sapiens	14-36
13745891-0	1961	Denaturation of catalase by formamide and urea related to the subunit make-up of the molecule.	formamide	28-37	catalase	Homo sapiens	16-24
13755318-2	1961	Activation of methemoglobin and catalase by formamide and guanidine.	formamide	44-53	hemoglobin subunit gamma 2	Homo sapiens	14-27
13755318-2	1961	Activation of methemoglobin and catalase by formamide and guanidine.	formamide	44-53	catalase	Homo sapiens	32-40
33427846-3	2021	Herein, beta-phase anhydrous guanine (beta-AG) microrods were formed in mixed solvents of formamide and water in the presence of small organic molecules such as uric acid, pyrrole (Py), N-methyl-2-pyrrolidone (NMP), N-vinyl-2-pyrrolidone (NVP).	formamide	90-99	N-methylpurine DNA glycosylase	Homo sapiens	38-45
33130073-9	2021	METHODS: We used two experimental models: A) formamide-induced acute "detubulation", where VM retain functional RyR2 and SERCA2, but lack T-tubules-associated LCC and NCX.	formamide	45-54	ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2	Rattus norvegicus	121-127
32586715-0	2020	Formic acid, the precursor of formamide, from serpentinization: Comment on the paper: "Mineral self-organization on a lifeless planet" by Juan Manuel Garcia-Ruiz, Mark A. van Zuilen and Wolfgang Bach.	formamide	30-39	acyl-CoA thioesterase 7	Homo sapiens	195-199
32266913-2	2020	Under the physicochemical conditions of primordial Earth, formamide could have undergone decomposition, either via dehydration (HCN + H2O) or via decarbonylation (CO + NH3).	formamide	58-67	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	128-131
32748908-4	2020	In a delaminated state, the colloidal suspension of SDC0.05OS0.95-LDH in formamide (FM) also gives a blue emission at 444 nm in comparison to the 451/468 nm emissions of the FM solution of free SDC2- anions, and the luminescence intensity of the exfoliated composite is ~28 times higher than that of the SDC2- anions.	formamide	73-82	syndecan 2	Homo sapiens	194-198
32748908-4	2020	In a delaminated state, the colloidal suspension of SDC0.05OS0.95-LDH in formamide (FM) also gives a blue emission at 444 nm in comparison to the 451/468 nm emissions of the FM solution of free SDC2- anions, and the luminescence intensity of the exfoliated composite is ~28 times higher than that of the SDC2- anions.	formamide	73-82	syndecan 2	Homo sapiens	304-308
32748908-4	2020	In a delaminated state, the colloidal suspension of SDC0.05OS0.95-LDH in formamide (FM) also gives a blue emission at 444 nm in comparison to the 451/468 nm emissions of the FM solution of free SDC2- anions, and the luminescence intensity of the exfoliated composite is ~28 times higher than that of the SDC2- anions.	formamide	84-86	syndecan 2	Homo sapiens	194-198
32748908-4	2020	In a delaminated state, the colloidal suspension of SDC0.05OS0.95-LDH in formamide (FM) also gives a blue emission at 444 nm in comparison to the 451/468 nm emissions of the FM solution of free SDC2- anions, and the luminescence intensity of the exfoliated composite is ~28 times higher than that of the SDC2- anions.	formamide	84-86	syndecan 2	Homo sapiens	304-308
32790302-4	2020	Between 250 and 400  C, HCONH2 decomposes by dehydration (major pathway) and decarbonylation (minor pathway) to liberate toxic HCN and CO, respectively.	formamide	24-30	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	127-130
33988653-9	2020	CONCLUSION: Using Tris-glucose-citrate-egg yolk extender, formamide, EG and DMSO could substitute glycerol as permeable CPAs for cat epididymal sperm cryopreservation.	formamide	58-67	catalase	Homo sapiens	129-132
30092492-0	2019	Infrared spectroscopic and computational studies on formamide solutions of Ca2+.	formamide	52-61	carbonic anhydrase 2	Homo sapiens	75-78
30092492-1	2019	Vibrational frequencies of formamide and modes of coordination to Ca2.	formamide	27-36	carbonic anhydrase 2	Homo sapiens	66-69
30092492-2	2019	Infrared spectroscopy for formamide (FA) solutions of Ca(ClO4)2 shows that both CN stretch (nuCN) and CO stretch (nuCO) bands of FA undergo upshifts in the presence of Ca2+.	formamide	26-35	carbonic anhydrase 2	Homo sapiens	168-171
28194158-9	2017	Surprisingly, AcdS was shown to confer the ability to utilize formamide and some dipeptides as sole nitrogen source.	formamide	62-71	1-aminocyclopropane-1-carboxylate deaminase	Sinorhizobium meliloti	14-18
28936535-3	2017	Previously, exposure of DNA to ionizing radiation found ~50% of the dOG exists as a tandem lesion with an adjacent formamide site.	formamide	115-124	dog	Drosophila melanogaster	68-71
28936535-4	2017	The present work explored oxidation of dOG in a tandem lesion with a THF abasic site analog (F) that models the formamide on either the 5" or 3" side.	formamide	112-121	dog	Drosophila melanogaster	39-42
24832217-1	2014	The efficient formation of HCN/HNC from formamide (FM) combining the advantages of water-assistance, self-catalyzed reactions, and the mineral surfaces was investigated.	formamide	40-49	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	27-30
27640164-6	2016	The newly designed vanA probe displayed highly specific hybridization with vanA-positive Enterococcus faecalis tested at 46  C, 55 % formamide, and 0.020 M NaCl stringency conditions.	formamide	133-142	VanA	Enterococcus faecalis	19-23
27016454-2	2016	Is it energetically favorable for formamidic acid, the first hydration product of HCN, to tautomerize into formamide under standard conditions?	formamide	107-116	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	82-85
27016454-8	2016	We also find that for HCN trimerization, although the planar sp(2) six-membered ring is more stable compared to its monomers, the reverse is true for the nonplanar sp(3) six-membered rings formed by trimerization of formamidic acid or formamide.	formamide	235-244	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	22-25
25192494-3	2014	Formamide, a hydrolysis product of HCN, was taken as starting material for the formation of nucleobases.	formamide	0-9	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	35-38
24762164-0	2014	Palladium-catalyzed C(sp2)-H arylation using formamide as a transformable directing group.	formamide	45-54	Sp2 transcription factor	Homo sapiens	20-25
24147593-3	2013	On the basis of a step-by-step mechanism of the reaction pathways, formamide is suggested to be more reactive in addition reactions than HCN.	formamide	67-76	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	137-140
24460097-5	2014	Lyman-alpha photolysis of H2O:HCONH2 mixed ices increases OCN(-) and CO production, suggesting a catalytic role of H2O.	formamide	30-36	bone gamma-carboxyglutamate protein	Homo sapiens	58-61
22455515-5	2012	Likewise, atmospherically generated HCN was undoubtedly converted in these aquifers to formamide and ammonium formate, precursors for RNA nucleobases.	formamide	87-96	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	36-39
23873588-6	2013	The consequence is that typical bases like aniline or formamide lead to BeX2 complexes that are stronger acids than phosphoric or chloric acids.	formamide	54-63	brain expressed X-linked 2	Homo sapiens	72-76
23889466-4	2013	Formation of HCN and HNC from dehydration of neutral and protonated formamide via formimic acid and aminohydroxymethylene isomers has higher energy barriers.	formamide	68-77	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	13-16
23889466-6	2013	The most probable pathways for HCN and HNC generation are found to be dehydration of formamide in the T1 state.	formamide	85-94	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	31-34
22738728-1	2012	Formamide provides the raw material and the reaction leads connecting hydrogen cyanide HCN chemistry with higher complexity molecular structures.	formamide	0-9	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	87-90
22219802-0	2011	Hexa-kis-(dimethyl-formamide-kappaO)manganese(II) mu-oxido-bis-[trichlorido-ferrate(III)].	formamide	18-28	hexosaminidase subunit alpha	Homo sapiens	0-4
22474011-2	2012	As a potential partial solution, we report the spontaneous polymerization of 3",5"-cyclic GMP in water, in formamide, in dimethylformamide, and (in water) in the presence of a Bronsted base such as 1,8-diazabicycloundec-7-ene.	formamide	107-116	5'-nucleotidase, cytosolic II	Homo sapiens	90-93
22129168-4	2012	We show that, albeit both the pyrimidine and purine ring formation utilizes the undissociated form of formamide, the dehydration product of formamide, HCN, may also play a key role in the mechanism.	formamide	102-111	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	151-154
22129168-4	2012	We show that, albeit both the pyrimidine and purine ring formation utilizes the undissociated form of formamide, the dehydration product of formamide, HCN, may also play a key role in the mechanism.	formamide	140-149	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	151-154
21480791-2	2011	Formamide, a hydrolysis product of HCN, is known as the precursor of various biologically important compounds, for example, nucleobases (purines and pyrimidines).	formamide	0-9	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	35-38
21573300-1	2011	The linear and two-dimensional infrared (2DIR) responses of the amide I vibrational mode in liquid formamide are investigated experimentally and theoretically using molecular dynamics simulations.	formamide	99-108	arginine vasopressin receptor 2	Homo sapiens	42-45
21573300-5	2011	We point out that, at variance with liquid water, the 2DIR spectral profile of formamide is determined more by the excitonic nature of the vibrational states than by the fast structural dynamics responsible for the frequency fluctuations.	formamide	79-88	arginine vasopressin receptor 2	Homo sapiens	55-58
20132793-6	2010	We found that the presence of AQP8 increased by threefold mitochondrial formamide transport.	formamide	72-81	aquaporin 8	Rattus norvegicus	30-34
21344931-0	2011	HNC/HCN ratio in acetonitrile, formamide, and BrCN discharge.	formamide	31-40	metastasis associated lung adenocarcinoma transcript 1	Homo sapiens	4-7
20132793-7	2010	AQP8-facilitated mitochondrial formamide transport in rat native tissue was confirmed in liver (a mitochondrial AQP8-expressing tissue) vs. brain (a mitochondrial AQP8 non-expressing tissue).	formamide	31-40	aquaporin 8	Rattus norvegicus	0-4
20132793-7	2010	AQP8-facilitated mitochondrial formamide transport in rat native tissue was confirmed in liver (a mitochondrial AQP8-expressing tissue) vs. brain (a mitochondrial AQP8 non-expressing tissue).	formamide	31-40	aquaporin 8	Rattus norvegicus	112-116
20132793-7	2010	AQP8-facilitated mitochondrial formamide transport in rat native tissue was confirmed in liver (a mitochondrial AQP8-expressing tissue) vs. brain (a mitochondrial AQP8 non-expressing tissue).	formamide	31-40	aquaporin 8	Rattus norvegicus	112-116
20132793-8	2010	Comparative studies indicated that the AQP8-mediated mitochondrial movement of formamide was markedly higher than that of water.	formamide	79-88	aquaporin 8	Rattus norvegicus	39-43
19159242-2	2009	Here, weak complexes between formamide and acetylene are studied, and three 1:1 complexes with binding energies of -2.96, -2.46, and -1.79 kcal/mol have been found at the MP2 level of theory (MP2/cc-pVTZ + ZPE + BSSE).	formamide	29-38	tryptase pseudogene 1	Homo sapiens	171-174
19159242-2	2009	Here, weak complexes between formamide and acetylene are studied, and three 1:1 complexes with binding energies of -2.96, -2.46, and -1.79 kcal/mol have been found at the MP2 level of theory (MP2/cc-pVTZ + ZPE + BSSE).	formamide	29-38	tryptase pseudogene 1	Homo sapiens	192-195
17506977-4	2007	Stopped-flow light-scattering measurements indicated high UT-B permeability to urea and chemical analogues formamide, acetamide, methylurea, methylformamide, ammonium carbamate, and acrylamide, each with P(s)>5.0 x 10(-6) cm/s at 10 degrees C. UT-B genetic knockout and phloretin treatment of wildtype erythrocytes similarly reduced urea analogue permeabilities.	formamide	107-116	solute carrier family 14 (urea transporter), member 1	Mus musculus	58-62
17764303-1	2007	By incorporating effective basis sets containing diffuse functions only in the interaction region of hydrogen-bonded complexes into the simple extrapolation scheme suitable for such basis sets, an accurate estimation of the MP2 basis set limit hydrogen-bonding energies of formic acid tetramer, formamide tetramer, alanine-water, phenol-water, and guanine-cytosine base pair is made with all estimates falling within 0.1-0.3 kcalmol of the reference basis set limits.	formamide	295-304	tryptase pseudogene 1	Homo sapiens	224-227
17506977-5	2007	Strong temperature dependencies of formamide, acetamide, acrylamide and butyramide transport across UT-B-null membranes (E(a)>10 kcal/mol) suggested efficient diffusion of these amides across lipid bilayers.	formamide	35-44	solute carrier family 14 (urea transporter), member 1	Mus musculus	100-104
14622406-4	2003	Both ts mutants were formamide-sensitive which supports a structural relatedness of Act3p/Arp4p to actin; they were also hypersensitive against hydroxyurea and ultraviolet irradiation pointing to a possible role of Act3p/Arp4p in DNA replication and repair.	formamide	21-30	Arp4p	Saccharomyces cerevisiae S288C	84-89
15948717-8	2006	rAQP8 and hAQP8 proteoliposomes did not transport glycerol or urea but were permeable to formamide, which was also inhibited by mercuric chloride.	formamide	89-98	aquaporin 8	Rattus norvegicus	0-5
15948717-8	2006	rAQP8 and hAQP8 proteoliposomes did not transport glycerol or urea but were permeable to formamide, which was also inhibited by mercuric chloride.	formamide	89-98	aquaporin 8	Homo sapiens	10-15
15948717-13	2006	Moreover, hAQP8 is permeable to ammonium analogues (formamide and methylammonium).	formamide	52-61	aquaporin 8	Homo sapiens	10-15
16363796-8	2005	In constrast, AtNIP6;1 showed no measurable water permeability but transported glycerol, formamide, as well as larger solutes that were impermeable to nodulin 26.	formamide	89-98	NOD26-like intrinsic protein 6;1	Arabidopsis thaliana	14-22
14581240-1	2003	Formamide-induced detubulation of rat ventricular myocytes was used to investigate the functional distribution of the Na/Ca exchanger (NCX) and Na/K-ATPase between the t-tubules and external sarcolemma.	formamide	0-9	solute carrier family 8 member A1	Rattus norvegicus	118-133
14581240-1	2003	Formamide-induced detubulation of rat ventricular myocytes was used to investigate the functional distribution of the Na/Ca exchanger (NCX) and Na/K-ATPase between the t-tubules and external sarcolemma.	formamide	0-9	solute carrier family 8 member A1	Rattus norvegicus	135-138
12182318-6	2002	For the cis isomer, the formamide is in a syn conformation and two hydrogen bonds with adenine are formed.	formamide	24-33	synemin	Homo sapiens	42-45
11798324-8	2002	Using formamide, further acceleration was achieved in the presence of Yb(OTf)(3) (5 mol %).	formamide	6-15	POU class 5 homeobox 1	Homo sapiens	70-80