PMID-sentid Pub_year Sent_text comp_official_name comp_offset protein_name organism prot_offset 3133333-1 1988 The level of mRNA for carcinoembryonic antigen (CEA) and nonspecific crossreacting antigen (NCA) in human colon adenocarcinomas and normal colon mucosa was analyzed by Northern blot hybridization using as probes 32P-labeled CEA cDNA and synthetic oligodeoxyribonucleotides specific to CEA and NCA mRNA sequences. Phosphorus-32 212-215 CEA cell adhesion molecule 4 Homo sapiens 22-96 2480629-4 1989 The NCA epitope recognized by MAb 47D10 is well preserved in formalin-fixed and paraffin-embedded tissues. Formaldehyde 61-69 CEA cell adhesion molecule 4 Homo sapiens 4-7 2480629-4 1989 The NCA epitope recognized by MAb 47D10 is well preserved in formalin-fixed and paraffin-embedded tissues. Paraffin 80-88 CEA cell adhesion molecule 4 Homo sapiens 4-7 3390172-3 1988 The four cysteine residues detected in the NCA-50 molecule form disulfide bonds. Cysteine 9-17 CEA cell adhesion molecule 4 Homo sapiens 43-46 3390172-3 1988 The four cysteine residues detected in the NCA-50 molecule form disulfide bonds. Disulfides 64-73 CEA cell adhesion molecule 4 Homo sapiens 43-46 3390172-5 1988 There is strong evidence that NCA-50 is bound to a phosphatidyl-inositol glycan, via an amide linkage to ethanolamine at amino acid position 287, which has replaced the last 24 amino acids. Glycosylphosphatidylinositols 51-79 CEA cell adhesion molecule 4 Homo sapiens 30-33 3390172-5 1988 There is strong evidence that NCA-50 is bound to a phosphatidyl-inositol glycan, via an amide linkage to ethanolamine at amino acid position 287, which has replaced the last 24 amino acids. Amides 88-93 CEA cell adhesion molecule 4 Homo sapiens 30-33 3390172-5 1988 There is strong evidence that NCA-50 is bound to a phosphatidyl-inositol glycan, via an amide linkage to ethanolamine at amino acid position 287, which has replaced the last 24 amino acids. Ethanolamine 105-117 CEA cell adhesion molecule 4 Homo sapiens 30-33 3133333-1 1988 The level of mRNA for carcinoembryonic antigen (CEA) and nonspecific crossreacting antigen (NCA) in human colon adenocarcinomas and normal colon mucosa was analyzed by Northern blot hybridization using as probes 32P-labeled CEA cDNA and synthetic oligodeoxyribonucleotides specific to CEA and NCA mRNA sequences. Oligodeoxyribonucleotides 247-272 CEA cell adhesion molecule 4 Homo sapiens 22-96 33263310-0 2020 Novel graphitic sheets with ripple-like folds as an NCA cathode coating layer for high-energy-density lithium-ion batteries. Lithium 102-109 CEA cell adhesion molecule 4 Homo sapiens 52-55 3446083-0 1987 Gel filtration of carcinoembryonic antigen (CEA) and non-specific crossreacting antigen (NCA) on the Superose 12HR column: effect of guanidine hydrochloride. superose 101-109 CEA cell adhesion molecule 4 Homo sapiens 53-93 3446083-1 1987 CEA and NCA, which behave as dimeric molecules in SDS-polyacrylamide gel electrophoresis, were submitted to gel filtration on the Superose 12HR column in phosphate-buffered saline (PBS) pH 7.0 or in 6 M guanidine hydrochloride. Sodium Dodecyl Sulfate 50-53 CEA cell adhesion molecule 4 Homo sapiens 8-11 3446083-1 1987 CEA and NCA, which behave as dimeric molecules in SDS-polyacrylamide gel electrophoresis, were submitted to gel filtration on the Superose 12HR column in phosphate-buffered saline (PBS) pH 7.0 or in 6 M guanidine hydrochloride. polyacrylamide 54-68 CEA cell adhesion molecule 4 Homo sapiens 8-11 3446083-6 1987 These values were accordant with those obtained by other methods and suggested that guanidine dissociates NCA into subunits. Guanidine 84-93 CEA cell adhesion molecule 4 Homo sapiens 106-109 2426231-9 1986 Upon sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), molecular heterogeneity was observed among CEA or NCA preparations isolated from cell lysates. Sodium Dodecyl Sulfate 5-27 CEA cell adhesion molecule 4 Homo sapiens 125-128 2426231-9 1986 Upon sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), molecular heterogeneity was observed among CEA or NCA preparations isolated from cell lysates. polyacrylamide 28-42 CEA cell adhesion molecule 4 Homo sapiens 125-128 2426231-9 1986 Upon sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), molecular heterogeneity was observed among CEA or NCA preparations isolated from cell lysates. Sodium Dodecyl Sulfate 64-67 CEA cell adhesion molecule 4 Homo sapiens 125-128 3494003-1 1986 No-carrier-added (NCA)3-(2"-[18F]fluoroethyl)spiperone (5), a new dopamine receptor-binding radiopharmaceutical for positron emission tomography, was synthesized by two different methods. 3-(2"-[18f]fluoroethyl)spiperone 22-54 CEA cell adhesion molecule 4 Homo sapiens 18-21 3494003-2 1986 Alkylation of the amide nitrogen in spiperone by NCA [18F]fluorobromoethane in the presence of a strong base gave 5 (Method A). Amides 18-23 CEA cell adhesion molecule 4 Homo sapiens 49-52 3494003-2 1986 Alkylation of the amide nitrogen in spiperone by NCA [18F]fluorobromoethane in the presence of a strong base gave 5 (Method A). Nitrogen 24-32 CEA cell adhesion molecule 4 Homo sapiens 49-52 3494003-2 1986 Alkylation of the amide nitrogen in spiperone by NCA [18F]fluorobromoethane in the presence of a strong base gave 5 (Method A). Spiperone 36-45 CEA cell adhesion molecule 4 Homo sapiens 49-52 3494003-4 1986 These derivatives (4) reacted with NCA Ag18F, Cs18F or K18F/Kryptofix 222 in acetonitrile or DMSO to give 5 (Method B). acetonitrile 77-89 CEA cell adhesion molecule 4 Homo sapiens 35-38 6388311-6 1984 In normal pancreatic ducts, there was nonspecific cross-reacting antigen (NCA) or CEA-related substances containing antigenic determinants common to NCA, which were observed more easily in frozen sections than in paraffin sections. Paraffin 213-221 CEA cell adhesion molecule 4 Homo sapiens 38-78 6193387-1 1983 A proposed dopamine (DA) receptor labeling agent, [3H](-)N-chloroethylnorapomorphine (3H-NCA) underwent relatively little chemical change at 25 degrees C and pH 6.4 up to an hour of incubation. Tritium 51-53 CEA cell adhesion molecule 4 Homo sapiens 89-92 6193387-1 1983 A proposed dopamine (DA) receptor labeling agent, [3H](-)N-chloroethylnorapomorphine (3H-NCA) underwent relatively little chemical change at 25 degrees C and pH 6.4 up to an hour of incubation. n-chloroethylnorapomorphine 57-84 CEA cell adhesion molecule 4 Homo sapiens 89-92 6193387-1 1983 A proposed dopamine (DA) receptor labeling agent, [3H](-)N-chloroethylnorapomorphine (3H-NCA) underwent relatively little chemical change at 25 degrees C and pH 6.4 up to an hour of incubation. Tritium 86-88 CEA cell adhesion molecule 4 Homo sapiens 89-92 6193387-5 1983 Catechol-aporphines prevented binding of 3H-NCA to calf caudate membranes by up to 30%, but this effect was not stereoselective and was lost at concentrations of 3H-NCA above 100 nM. catechol 0-8 CEA cell adhesion molecule 4 Homo sapiens 44-47 6193387-5 1983 Catechol-aporphines prevented binding of 3H-NCA to calf caudate membranes by up to 30%, but this effect was not stereoselective and was lost at concentrations of 3H-NCA above 100 nM. catechol 0-8 CEA cell adhesion molecule 4 Homo sapiens 165-168 6193387-5 1983 Catechol-aporphines prevented binding of 3H-NCA to calf caudate membranes by up to 30%, but this effect was not stereoselective and was lost at concentrations of 3H-NCA above 100 nM. Aporphines 9-19 CEA cell adhesion molecule 4 Homo sapiens 44-47 6193387-5 1983 Catechol-aporphines prevented binding of 3H-NCA to calf caudate membranes by up to 30%, but this effect was not stereoselective and was lost at concentrations of 3H-NCA above 100 nM. Aporphines 9-19 CEA cell adhesion molecule 4 Homo sapiens 165-168 6193387-7 1983 The results suggest that while 3H-NCA may bind irreversibly, and possibly covalently, it does not have high selectivity for labeling dopamine D-3 or D-2 receptor sites, but may be partially selective for an aporphine binding site. aporphine 207-216 CEA cell adhesion molecule 4 Homo sapiens 34-37 6201714-6 1983 The molecular weight of purified NCA-2 was estimated to be 150,000 to 170,000 determined by SDS-PAGE. Sodium Dodecyl Sulfate 92-95 CEA cell adhesion molecule 4 Homo sapiens 33-36 6201714-8 1983 NCA-2 had amino acid and carbohydrate compositions similar to those of CEA and NFA-2. Carbohydrates 25-37 CEA cell adhesion molecule 4 Homo sapiens 0-3 77016-3 1978 The molecular weight of NCA determined by chromatography on Sephadex G-200 was approximately 100,000. sephadex 60-74 CEA cell adhesion molecule 4 Homo sapiens 24-27 77016-4 1978 The total amount of carbohydrate in NCA was 30%, compared to 60% in CEA. Carbohydrates 20-32 CEA cell adhesion molecule 4 Homo sapiens 36-39 77016-5 1978 NCA and CEA also differed in sugar composition. Sugars 29-34 CEA cell adhesion molecule 4 Homo sapiens 0-3 77016-6 1978 The amino acid composition of NCA was nearly identical to that of CEA, except for the apparent presence of methionine in NCA but not in CEA. Methionine 107-117 CEA cell adhesion molecule 4 Homo sapiens 121-124 77016-7 1978 The sequence of the first 26 NH2-terminal amino acids in NCA was identical to that of CEA except at position 21, where alanine was found in NCA instead of valine in CEA. Alanine 119-126 CEA cell adhesion molecule 4 Homo sapiens 57-60 77016-7 1978 The sequence of the first 26 NH2-terminal amino acids in NCA was identical to that of CEA except at position 21, where alanine was found in NCA instead of valine in CEA. Alanine 119-126 CEA cell adhesion molecule 4 Homo sapiens 140-143 77016-7 1978 The sequence of the first 26 NH2-terminal amino acids in NCA was identical to that of CEA except at position 21, where alanine was found in NCA instead of valine in CEA. Valine 155-161 CEA cell adhesion molecule 4 Homo sapiens 57-60 33656031-5 2021 At the same time, N-doped carbon in the Ge/NC-A microspheres can greatly improve the electrical conductivity and the structural stability. Carbon 26-32 CEA cell adhesion molecule 4 Homo sapiens 43-47 32935922-3 2021 Herein, a highly efficient strategy to access well-defined site-specific functionalized polypeptides is developed by combining Michael reaction with hydrogen-bonding organocatalytic ROP of NCA. Hydrogen 149-157 CEA cell adhesion molecule 4 Homo sapiens 189-192 6435631-0 1983 Minor serine tRNA containing anticodon NCA (C4 RNA) from human and mouse cells. Serine 6-12 CEA cell adhesion molecule 4 Homo sapiens 39-42 33925721-4 2021 By using Gr/PVdF suspensions, we fabricated highly dense LiNi0.85Co0.15Al0.05O2 (NCA) cathodes having a uniform distribution of conductive Gr sheets without CB nanoparticles, which was confirmed by scanning spreading resistance microscopy mode using atomic force microscopy. polyvinylidene fluoride 12-16 CEA cell adhesion molecule 4 Homo sapiens 81-84 33925721-5 2021 At a high content of 99 wt.% NCA, good cycling stability was shown with significantly improved areal capacity (Qareal) and volumetric capacity (Qvol), relative to the CB/PVdF-containing NCA electrode with a commercial-level of electrode parameters. polyvinylidene fluoride 170-174 CEA cell adhesion molecule 4 Homo sapiens 29-32 33925721-6 2021 The NCA electrodes using 1 wt.% Gr/PVdF (0.9:0.1) delivered a high Qareal of ~3.7 mAh cm-2 (~19% increment) and a high Qvol of ~774 mAh cm-3 (~18% increment) at a current rate of 0.2 C, as compared to the conventional NCA electrode. polyvinylidene fluoride 35-39 CEA cell adhesion molecule 4 Homo sapiens 4-7 33925721-6 2021 The NCA electrodes using 1 wt.% Gr/PVdF (0.9:0.1) delivered a high Qareal of ~3.7 mAh cm-2 (~19% increment) and a high Qvol of ~774 mAh cm-3 (~18% increment) at a current rate of 0.2 C, as compared to the conventional NCA electrode. polyvinylidene fluoride 35-39 CEA cell adhesion molecule 4 Homo sapiens 218-221 33542037-10 2021 TFPB prolonged the first-time request for NCA/PCA analgesia, and decreased the total number of pressing counts, compared with QLB III (22.5 (16.2 to 28.7) vs 11.7 (6.6 to 16.8), p<0.0001; 2.4 (1.3 to 3.6) vs 3.8 (2.8 to 4.8), p=0.0111, respectively). tfpb 0-4 CEA cell adhesion molecule 4 Homo sapiens 42-45 33315372-4 2020 As a result, the optimized lithium boron oxide-coated LiNi0.8Co0.15Al0.05O2 material exhibits a high initial discharge capacity of 202.1 mAh g-1 at 0.1 C with a great capacity retention of 93.59% after 100 cycles at 2 C. Thus, the uniform lithium boron oxide coating endows the NCA material with excellent structural stability and long-term cycling capability. Lithium boron oxide 27-46 CEA cell adhesion molecule 4 Homo sapiens 278-281 33263310-5 2020 Most importantly, this approach allows the preparation of GSFR@NCA with highly promising applications as a cathode for high-energy-density lithium-ion batteries, since in this contribution just simple equipment and a precursor with low cost are involved. Lithium 139-146 CEA cell adhesion molecule 4 Homo sapiens 63-66 33105125-0 2020 Novel graphitic sheets with ripple-like folds as NCA-cathode coating layer for high-energy-density lithium-ion batteries. Lithium 99-106 CEA cell adhesion molecule 4 Homo sapiens 49-52 33261159-4 2020 The synthesis of the graft copolypeptide was conducted via ROP of the Nepsilon-Boc-l-Lysine NCA while using n-hexylamine as the initiator, followed by the polymerization of Nepsilon-Fmoc-l-Lysine NCA. copolypeptide 27-40 CEA cell adhesion molecule 4 Homo sapiens 92-95 33261159-4 2020 The synthesis of the graft copolypeptide was conducted via ROP of the Nepsilon-Boc-l-Lysine NCA while using n-hexylamine as the initiator, followed by the polymerization of Nepsilon-Fmoc-l-Lysine NCA. copolypeptide 27-40 CEA cell adhesion molecule 4 Homo sapiens 196-199 33261159-4 2020 The synthesis of the graft copolypeptide was conducted via ROP of the Nepsilon-Boc-l-Lysine NCA while using n-hexylamine as the initiator, followed by the polymerization of Nepsilon-Fmoc-l-Lysine NCA. H-Lys(Fmoc)-OH 173-195 CEA cell adhesion molecule 4 Homo sapiens 196-199 33261159-5 2020 The last block was selectively deprotected under basic conditions, and the resulting epsilon-amines were used as the initiating species for the ROP of Nim-Trityl-l-Histidine NCA. epsilon-amines 85-99 CEA cell adhesion molecule 4 Homo sapiens 174-177 33261159-5 2020 The last block was selectively deprotected under basic conditions, and the resulting epsilon-amines were used as the initiating species for the ROP of Nim-Trityl-l-Histidine NCA. nim-trityl-l-histidine 151-173 CEA cell adhesion molecule 4 Homo sapiens 174-177 32969581-2 2020 In this work, the surface of LiNi 0.8 Co 0.15 Al 0.05 O 2 (NCA) was modified with a lithium phosphate coating to investigate its ability to protect the active material during electrode production. Lithium phosphate 84-101 CEA cell adhesion molecule 4 Homo sapiens 59-62 32969581-4 2020 Cells with water-based electrodes containing NCA with an optimized amount of lithium phosphate have a slightly lower specific discharge capacity as compared to cells with conventional N-Methyl-2-pyrrolidone-based electrodes. Water 11-16 CEA cell adhesion molecule 4 Homo sapiens 45-48 32969581-4 2020 Cells with water-based electrodes containing NCA with an optimized amount of lithium phosphate have a slightly lower specific discharge capacity as compared to cells with conventional N-Methyl-2-pyrrolidone-based electrodes. Lithium phosphate 77-94 CEA cell adhesion molecule 4 Homo sapiens 45-48 32969581-4 2020 Cells with water-based electrodes containing NCA with an optimized amount of lithium phosphate have a slightly lower specific discharge capacity as compared to cells with conventional N-Methyl-2-pyrrolidone-based electrodes. N-methylpyrrolidone 184-206 CEA cell adhesion molecule 4 Homo sapiens 45-48 33105125-5 2020 Most importantly, this approach allows the preparation of GSFR@NCA with highly promising applications as cathode for high-energy-density lithium-ion batteries, since in this contribution just simple equipment and precursor with low cost are involved. Lithium 137-144 CEA cell adhesion molecule 4 Homo sapiens 63-66 31708258-5 2020 FINDINGS: It has been found that the optimal condition for fabricating this NCA/OA/Fe3O4 aerogel is 0.4 wt% nanocellulose, 3 mg mL-1 OA and 0.5 wt% Fe3O4 in the aqueous solution. Oleic Acids 80-82 CEA cell adhesion molecule 4 Homo sapiens 76-79 32633486-1 2020 LiNi1-x-yCoxAlyO2 (NCA) possessing nano/micro hierarchical architecture delivers a high specific capacity of 200mAh/g with an upper cut-off voltage of 4.4V. lini1-x-ycoxalyo2 0-17 CEA cell adhesion molecule 4 Homo sapiens 19-22 32633486-4 2020 Nonetheless, getting aluminium concentration gradient in NCA-(OH)2 is difficult owing to the difference in the solubility constant and reaction kinetics of Al(OH)3 compared to that of NiCo-(OH)2. Aluminum 21-30 CEA cell adhesion molecule 4 Homo sapiens 57-60 32633486-4 2020 Nonetheless, getting aluminium concentration gradient in NCA-(OH)2 is difficult owing to the difference in the solubility constant and reaction kinetics of Al(OH)3 compared to that of NiCo-(OH)2. (oh)2 61-66 CEA cell adhesion molecule 4 Homo sapiens 57-60 32633486-8 2020 The graded NCA shows excellent reversibility of the H2 H3 phase leading to low impedance development confirming the reduced surface reconstruction during the initial cycles. h2 h3 52-57 CEA cell adhesion molecule 4 Homo sapiens 11-14 33049979-7 2020 Taking into account anti-cancer properties of studied NCA, it seems that the presence of hydroxyl groups had an influence on intermolecular interactions and the cytotoxic potential of the molecules, whereas the carboxyl group participated in the chelation of endogenous transition metal ions. Metals 281-286 CEA cell adhesion molecule 4 Homo sapiens 54-57 32691465-2 2020 Herein an elegant approach is presented for N-carboxyanhydride ring opening polymerization (NCA ROP) of Nepsilon-benzyloxycarbonyl-l-lysine (ZLL) and gamma-benzyl-l-glutamate (BLG) NCA in continuous flow. n-carboxyanhydride 44-62 CEA cell adhesion molecule 4 Homo sapiens 92-95 32691465-2 2020 Herein an elegant approach is presented for N-carboxyanhydride ring opening polymerization (NCA ROP) of Nepsilon-benzyloxycarbonyl-l-lysine (ZLL) and gamma-benzyl-l-glutamate (BLG) NCA in continuous flow. n-carboxyanhydride 44-62 CEA cell adhesion molecule 4 Homo sapiens 181-184 32691465-2 2020 Herein an elegant approach is presented for N-carboxyanhydride ring opening polymerization (NCA ROP) of Nepsilon-benzyloxycarbonyl-l-lysine (ZLL) and gamma-benzyl-l-glutamate (BLG) NCA in continuous flow. N(epsilon)-(benzyloxycarbonyl)lysine 104-139 CEA cell adhesion molecule 4 Homo sapiens 92-95 32691465-2 2020 Herein an elegant approach is presented for N-carboxyanhydride ring opening polymerization (NCA ROP) of Nepsilon-benzyloxycarbonyl-l-lysine (ZLL) and gamma-benzyl-l-glutamate (BLG) NCA in continuous flow. N(epsilon)-(benzyloxycarbonyl)lysine 104-139 CEA cell adhesion molecule 4 Homo sapiens 181-184 32691465-2 2020 Herein an elegant approach is presented for N-carboxyanhydride ring opening polymerization (NCA ROP) of Nepsilon-benzyloxycarbonyl-l-lysine (ZLL) and gamma-benzyl-l-glutamate (BLG) NCA in continuous flow. CHEMBL356841 141-144 CEA cell adhesion molecule 4 Homo sapiens 92-95 32691465-2 2020 Herein an elegant approach is presented for N-carboxyanhydride ring opening polymerization (NCA ROP) of Nepsilon-benzyloxycarbonyl-l-lysine (ZLL) and gamma-benzyl-l-glutamate (BLG) NCA in continuous flow. CHEMBL356841 141-144 CEA cell adhesion molecule 4 Homo sapiens 181-184 32691465-2 2020 Herein an elegant approach is presented for N-carboxyanhydride ring opening polymerization (NCA ROP) of Nepsilon-benzyloxycarbonyl-l-lysine (ZLL) and gamma-benzyl-l-glutamate (BLG) NCA in continuous flow. H-Glu(OBzl)-OH 150-174 CEA cell adhesion molecule 4 Homo sapiens 92-95 32691465-2 2020 Herein an elegant approach is presented for N-carboxyanhydride ring opening polymerization (NCA ROP) of Nepsilon-benzyloxycarbonyl-l-lysine (ZLL) and gamma-benzyl-l-glutamate (BLG) NCA in continuous flow. H-Glu(OBzl)-OH 150-174 CEA cell adhesion molecule 4 Homo sapiens 181-184 32691465-2 2020 Herein an elegant approach is presented for N-carboxyanhydride ring opening polymerization (NCA ROP) of Nepsilon-benzyloxycarbonyl-l-lysine (ZLL) and gamma-benzyl-l-glutamate (BLG) NCA in continuous flow. bulgecin a 176-179 CEA cell adhesion molecule 4 Homo sapiens 92-95 32691465-2 2020 Herein an elegant approach is presented for N-carboxyanhydride ring opening polymerization (NCA ROP) of Nepsilon-benzyloxycarbonyl-l-lysine (ZLL) and gamma-benzyl-l-glutamate (BLG) NCA in continuous flow. bulgecin a 176-179 CEA cell adhesion molecule 4 Homo sapiens 181-184 32736713-1 2020 The homogeneous dumbbell-like Au nanoparticles (DL-AuNPs) with large exposed active surfaces were obtained with a porous N-doped carbon aerogel (NCA). Carbon 129-135 CEA cell adhesion molecule 4 Homo sapiens 145-148 32736713-2 2020 Such coassembly of DL-AuNPs with NCA (NCA@DL-AuNPs) had a large specific surface area (788 m2/g), rich mesopores, and a high N content (4.93 at%). Nitrogen 24-25 CEA cell adhesion molecule 4 Homo sapiens 33-36 32736713-2 2020 Such coassembly of DL-AuNPs with NCA (NCA@DL-AuNPs) had a large specific surface area (788 m2/g), rich mesopores, and a high N content (4.93 at%). Nitrogen 24-25 CEA cell adhesion molecule 4 Homo sapiens 38-50 32736713-3 2020 The unique structures of NCA@DL-AuNPs yielded better electrocatalytic activity for the detection of H2O2 both in PBS and released from Hale cells than that of previously reported Au catalysts loaded on carbon materials, which demonstrates that such novel NCA@DL-AuNPs nanocomposite is promising for design of efficient nonenzymatic H2O2 biosensors. Hydrogen Peroxide 100-104 CEA cell adhesion molecule 4 Homo sapiens 25-37 32736713-3 2020 The unique structures of NCA@DL-AuNPs yielded better electrocatalytic activity for the detection of H2O2 both in PBS and released from Hale cells than that of previously reported Au catalysts loaded on carbon materials, which demonstrates that such novel NCA@DL-AuNPs nanocomposite is promising for design of efficient nonenzymatic H2O2 biosensors. Hydrogen Peroxide 100-104 CEA cell adhesion molecule 4 Homo sapiens 255-267 32736713-3 2020 The unique structures of NCA@DL-AuNPs yielded better electrocatalytic activity for the detection of H2O2 both in PBS and released from Hale cells than that of previously reported Au catalysts loaded on carbon materials, which demonstrates that such novel NCA@DL-AuNPs nanocomposite is promising for design of efficient nonenzymatic H2O2 biosensors. Lead 113-116 CEA cell adhesion molecule 4 Homo sapiens 25-37 32736713-3 2020 The unique structures of NCA@DL-AuNPs yielded better electrocatalytic activity for the detection of H2O2 both in PBS and released from Hale cells than that of previously reported Au catalysts loaded on carbon materials, which demonstrates that such novel NCA@DL-AuNPs nanocomposite is promising for design of efficient nonenzymatic H2O2 biosensors. Lead 113-116 CEA cell adhesion molecule 4 Homo sapiens 255-267 32736713-3 2020 The unique structures of NCA@DL-AuNPs yielded better electrocatalytic activity for the detection of H2O2 both in PBS and released from Hale cells than that of previously reported Au catalysts loaded on carbon materials, which demonstrates that such novel NCA@DL-AuNPs nanocomposite is promising for design of efficient nonenzymatic H2O2 biosensors. Gold 32-34 CEA cell adhesion molecule 4 Homo sapiens 255-267 32736713-3 2020 The unique structures of NCA@DL-AuNPs yielded better electrocatalytic activity for the detection of H2O2 both in PBS and released from Hale cells than that of previously reported Au catalysts loaded on carbon materials, which demonstrates that such novel NCA@DL-AuNPs nanocomposite is promising for design of efficient nonenzymatic H2O2 biosensors. Carbon 202-208 CEA cell adhesion molecule 4 Homo sapiens 25-37 32736713-3 2020 The unique structures of NCA@DL-AuNPs yielded better electrocatalytic activity for the detection of H2O2 both in PBS and released from Hale cells than that of previously reported Au catalysts loaded on carbon materials, which demonstrates that such novel NCA@DL-AuNPs nanocomposite is promising for design of efficient nonenzymatic H2O2 biosensors. Carbon 202-208 CEA cell adhesion molecule 4 Homo sapiens 255-267 32736713-3 2020 The unique structures of NCA@DL-AuNPs yielded better electrocatalytic activity for the detection of H2O2 both in PBS and released from Hale cells than that of previously reported Au catalysts loaded on carbon materials, which demonstrates that such novel NCA@DL-AuNPs nanocomposite is promising for design of efficient nonenzymatic H2O2 biosensors. Hydrogen Peroxide 332-336 CEA cell adhesion molecule 4 Homo sapiens 25-37 32736713-3 2020 The unique structures of NCA@DL-AuNPs yielded better electrocatalytic activity for the detection of H2O2 both in PBS and released from Hale cells than that of previously reported Au catalysts loaded on carbon materials, which demonstrates that such novel NCA@DL-AuNPs nanocomposite is promising for design of efficient nonenzymatic H2O2 biosensors. Hydrogen Peroxide 332-336 CEA cell adhesion molecule 4 Homo sapiens 255-267 32850629-0 2020 Development of Light-Responsive Poly(gamma-Benzyl-L-Glutamate) as Photo Switches by a One-Step NCA Method. poly(gamma-benzyl-l-glutamate) 32-62 CEA cell adhesion molecule 4 Homo sapiens 95-98 32850629-3 2020 Herein, light-responsive poly(gamma-benzyl-L-glutamate)s (PBLGs) is synthesized by a one-step NCA method using p-aminoazobenzene (m-AZO) and p-diaminoazobenzene (m-DAZO) as initiators. poly(gamma-benzyl-l-glutamate) 25-55 CEA cell adhesion molecule 4 Homo sapiens 94-97 32850629-3 2020 Herein, light-responsive poly(gamma-benzyl-L-glutamate)s (PBLGs) is synthesized by a one-step NCA method using p-aminoazobenzene (m-AZO) and p-diaminoazobenzene (m-DAZO) as initiators. p-Aminoazobenzene 111-128 CEA cell adhesion molecule 4 Homo sapiens 94-97 32850629-3 2020 Herein, light-responsive poly(gamma-benzyl-L-glutamate)s (PBLGs) is synthesized by a one-step NCA method using p-aminoazobenzene (m-AZO) and p-diaminoazobenzene (m-DAZO) as initiators. m-azo 130-135 CEA cell adhesion molecule 4 Homo sapiens 94-97 32850629-3 2020 Herein, light-responsive poly(gamma-benzyl-L-glutamate)s (PBLGs) is synthesized by a one-step NCA method using p-aminoazobenzene (m-AZO) and p-diaminoazobenzene (m-DAZO) as initiators. 4,4'-diaminoazobenzene 141-160 CEA cell adhesion molecule 4 Homo sapiens 94-97 32850629-3 2020 Herein, light-responsive poly(gamma-benzyl-L-glutamate)s (PBLGs) is synthesized by a one-step NCA method using p-aminoazobenzene (m-AZO) and p-diaminoazobenzene (m-DAZO) as initiators. m-dazo 162-168 CEA cell adhesion molecule 4 Homo sapiens 94-97 32627875-0 2020 High-Nickel NMA: A Cobalt-Free Alternative to NMC and NCA Cathodes for Lithium-Ion Batteries. Lithium 71-78 CEA cell adhesion molecule 4 Homo sapiens 54-57 32627875-2 2020 Both NMC and NCA contain cobalt, an expensive and scarce metal generally believed to be essential for their electrochemical performance. Cobalt 25-31 CEA cell adhesion molecule 4 Homo sapiens 13-16 32627875-2 2020 Both NMC and NCA contain cobalt, an expensive and scarce metal generally believed to be essential for their electrochemical performance. Metals 57-62 CEA cell adhesion molecule 4 Homo sapiens 13-16 32406453-3 2020 To overcome this shortcoming, a novel Ni concentration gradient LiNi0.8Co0.15Al0.05O2 (NCG-NCA) cathode material was successfully synthesized using the characteristic reaction of Ni2+ and dimethylglyoxime. Nickel(2+) 179-183 CEA cell adhesion molecule 4 Homo sapiens 91-94 32406453-3 2020 To overcome this shortcoming, a novel Ni concentration gradient LiNi0.8Co0.15Al0.05O2 (NCG-NCA) cathode material was successfully synthesized using the characteristic reaction of Ni2+ and dimethylglyoxime. dimethylglyoxime 188-204 CEA cell adhesion molecule 4 Homo sapiens 91-94 32202112-1 2020 Substituted Li layered transition metal oxide (LTMO) electrodes such as LixNiyMnzCo1-y-zO2 (NMC) and LixNiyCo1-y-zAlzO2 (NCA) show reduced first cycle Coulombic efficiency (90-87 % in standard cycling conditions) compared with archetypal LixCoO2 (LCO - ~98 % efficiency). lixniymnzco1-y-zo2 72-90 CEA cell adhesion molecule 4 Homo sapiens 121-124 32202112-1 2020 Substituted Li layered transition metal oxide (LTMO) electrodes such as LixNiyMnzCo1-y-zO2 (NMC) and LixNiyCo1-y-zAlzO2 (NCA) show reduced first cycle Coulombic efficiency (90-87 % in standard cycling conditions) compared with archetypal LixCoO2 (LCO - ~98 % efficiency). lixniyco1-y-zalzo2 101-119 CEA cell adhesion molecule 4 Homo sapiens 121-124 31708258-5 2020 FINDINGS: It has been found that the optimal condition for fabricating this NCA/OA/Fe3O4 aerogel is 0.4 wt% nanocellulose, 3 mg mL-1 OA and 0.5 wt% Fe3O4 in the aqueous solution. ferryl iron 83-88 CEA cell adhesion molecule 4 Homo sapiens 76-79 31708258-5 2020 FINDINGS: It has been found that the optimal condition for fabricating this NCA/OA/Fe3O4 aerogel is 0.4 wt% nanocellulose, 3 mg mL-1 OA and 0.5 wt% Fe3O4 in the aqueous solution. Oleic Acids 133-135 CEA cell adhesion molecule 4 Homo sapiens 76-79 31708258-5 2020 FINDINGS: It has been found that the optimal condition for fabricating this NCA/OA/Fe3O4 aerogel is 0.4 wt% nanocellulose, 3 mg mL-1 OA and 0.5 wt% Fe3O4 in the aqueous solution. ferryl iron 148-153 CEA cell adhesion molecule 4 Homo sapiens 76-79 31708258-8 2020 As a consequence, this hydrophobic magnetic NCA/OA/Fe3O4 aerogel is promising not only for easy oil and organic solvent adsorption but also potentially for other magnetic related applications. Oleic Acids 48-50 CEA cell adhesion molecule 4 Homo sapiens 44-47 31708258-8 2020 As a consequence, this hydrophobic magnetic NCA/OA/Fe3O4 aerogel is promising not only for easy oil and organic solvent adsorption but also potentially for other magnetic related applications. ferryl iron 51-56 CEA cell adhesion molecule 4 Homo sapiens 44-47 30973700-3 2019 With well-designed architecture and a uniform NASICON-type LZP nanolayer wrapping over the NCA microsphere, the entire electrode demonstrates exceptional Li+ diffusion and conductivity and suppresses the side reaction between electrolyte and electroactive NCA, stabilizing the phase interface with less Li+/Ni2+ cation mixing. Nickel(2+) 307-311 CEA cell adhesion molecule 4 Homo sapiens 91-94 31883232-8 2019 Moreover, oxygen consumption was higher in CA than in NCA (p < .001, d = 0.8). Oxygen 10-16 CEA cell adhesion molecule 4 Homo sapiens 54-57 31702887-3 2019 Here, we reveal surface structures and electrochemical properties of the exposed LiNi0.8Co0.15Al0.05O2 (NCA) cathodes and investigate systematically the impact of exposure humidity, temperature, and time on NCA cathodes. Lithium 81-85 CEA cell adhesion molecule 4 Homo sapiens 104-107 30897209-6 2019 NMR studies of monomer and trimer models showed that the NCalpha-gem-dimethylated groups exert complete cis control on the backbone amide conformation. Amides 132-137 CEA cell adhesion molecule 4 Homo sapiens 57-64 30995007-1 2019 The LiNi1- x- yCo xAl yO2 (NCA)-layered materials are regarded as a research focus of power lithium-ion batteries (LIBs) because of their high capacity. Lithium 92-99 CEA cell adhesion molecule 4 Homo sapiens 27-30 30973700-3 2019 With well-designed architecture and a uniform NASICON-type LZP nanolayer wrapping over the NCA microsphere, the entire electrode demonstrates exceptional Li+ diffusion and conductivity and suppresses the side reaction between electrolyte and electroactive NCA, stabilizing the phase interface with less Li+/Ni2+ cation mixing. Nickel(2+) 307-311 CEA cell adhesion molecule 4 Homo sapiens 256-259 30796795-7 2019 The most significant differences in the mean values of fatty acids of phospholipids between CA and NCA in patients with proximal tumor localization were noted. Fatty Acids 55-66 CEA cell adhesion molecule 4 Homo sapiens 99-102 30796795-7 2019 The most significant differences in the mean values of fatty acids of phospholipids between CA and NCA in patients with proximal tumor localization were noted. Phospholipids 70-83 CEA cell adhesion molecule 4 Homo sapiens 99-102 27852449-4 2017 Calculations for FeS-coated limestone dissolution experiments show that the process can be described as nCa.sol = At1/2 - nCa,gyp. Iron 17-20 CEA cell adhesion molecule 4 Homo sapiens 104-107 29587473-2 2018 Herein, an easily obtained catalyst system composed of zinc acetate and aniline was explored to mediate the fast ROP of gamma-benzyl-l-glutamate-N-carboxyanhydride (BLG-NCA) monomer, to produce poly(gamma-benzyl-l-glutamates) (PBLGs) with controllable molecular weights and narrow dispersity. Zinc Acetate 55-67 CEA cell adhesion molecule 4 Homo sapiens 169-172 29587473-2 2018 Herein, an easily obtained catalyst system composed of zinc acetate and aniline was explored to mediate the fast ROP of gamma-benzyl-l-glutamate-N-carboxyanhydride (BLG-NCA) monomer, to produce poly(gamma-benzyl-l-glutamates) (PBLGs) with controllable molecular weights and narrow dispersity. aniline 72-79 CEA cell adhesion molecule 4 Homo sapiens 169-172 29587473-2 2018 Herein, an easily obtained catalyst system composed of zinc acetate and aniline was explored to mediate the fast ROP of gamma-benzyl-l-glutamate-N-carboxyanhydride (BLG-NCA) monomer, to produce poly(gamma-benzyl-l-glutamates) (PBLGs) with controllable molecular weights and narrow dispersity. gamma-benzyl-l-glutamate-n-carboxyanhydride 120-163 CEA cell adhesion molecule 4 Homo sapiens 169-172 29587473-2 2018 Herein, an easily obtained catalyst system composed of zinc acetate and aniline was explored to mediate the fast ROP of gamma-benzyl-l-glutamate-N-carboxyanhydride (BLG-NCA) monomer, to produce poly(gamma-benzyl-l-glutamates) (PBLGs) with controllable molecular weights and narrow dispersity. poly-gamma-benzyl-L-glutamate 194-225 CEA cell adhesion molecule 4 Homo sapiens 169-172 29587473-2 2018 Herein, an easily obtained catalyst system composed of zinc acetate and aniline was explored to mediate the fast ROP of gamma-benzyl-l-glutamate-N-carboxyanhydride (BLG-NCA) monomer, to produce poly(gamma-benzyl-l-glutamates) (PBLGs) with controllable molecular weights and narrow dispersity. poly-gamma-benzyl-L-glutamate 227-232 CEA cell adhesion molecule 4 Homo sapiens 169-172 29587473-3 2018 Considering the excellent cooperative action of zinc acetate and a broad scope of aniline derivatives with different functional groups to control ROP of BLG-NCA, this method may offer a useful platform enabling the rapid generation of end-functionalized PBLG and block copolymers for numerous biomedical applications. Zinc Acetate 48-60 CEA cell adhesion molecule 4 Homo sapiens 157-160 29587473-3 2018 Considering the excellent cooperative action of zinc acetate and a broad scope of aniline derivatives with different functional groups to control ROP of BLG-NCA, this method may offer a useful platform enabling the rapid generation of end-functionalized PBLG and block copolymers for numerous biomedical applications. aniline 82-89 CEA cell adhesion molecule 4 Homo sapiens 157-160 29587473-3 2018 Considering the excellent cooperative action of zinc acetate and a broad scope of aniline derivatives with different functional groups to control ROP of BLG-NCA, this method may offer a useful platform enabling the rapid generation of end-functionalized PBLG and block copolymers for numerous biomedical applications. poly-gamma-benzyl-L-glutamate 254-258 CEA cell adhesion molecule 4 Homo sapiens 157-160 29587473-3 2018 Considering the excellent cooperative action of zinc acetate and a broad scope of aniline derivatives with different functional groups to control ROP of BLG-NCA, this method may offer a useful platform enabling the rapid generation of end-functionalized PBLG and block copolymers for numerous biomedical applications. copolymers 269-279 CEA cell adhesion molecule 4 Homo sapiens 157-160 28130978-0 2017 Novel ion exchange chromatography method for nca arsenic separation. Arsenic 49-56 CEA cell adhesion molecule 4 Homo sapiens 45-48 28130978-1 2017 A high-performance liquid chromatography (HPLC) device equipped with an anion exchange column was used to isolate nca 77As from reactor irradiated natGeO2 targets. natgeo2 147-154 CEA cell adhesion molecule 4 Homo sapiens 114-117 27852449-4 2017 Calculations for FeS-coated limestone dissolution experiments show that the process can be described as nCa.sol = At1/2 - nCa,gyp. Iron 17-20 CEA cell adhesion molecule 4 Homo sapiens 122-125 23943596-2 2014 First, the block copolymer poly(benzyl L-aspartate)-block-poly(ethylene glycol) (PBLA-b-PEG) is synthesized via ring-opening polymerization of beta-benzyl L-aspartate-N-carboxyanhydride (BLA-NCA) with alpha-methoxy-omega-aminopoly(ethylene glycol) (mPEG-NH2 ) as a macroinitiator. copolymer 17-26 CEA cell adhesion molecule 4 Homo sapiens 191-194 27840215-2 2017 The native-PAGE results showed that 4-chlorocinnamic acid (4-CCA), 4-ethoxycinnamic acid (4-ECA) and 4-nitrocinnamic acid (4-NCA) had inhibitory effects on tyrosinase. 4-eca 90-95 CEA cell adhesion molecule 4 Homo sapiens 125-128 27840215-2 2017 The native-PAGE results showed that 4-chlorocinnamic acid (4-CCA), 4-ethoxycinnamic acid (4-ECA) and 4-nitrocinnamic acid (4-NCA) had inhibitory effects on tyrosinase. 4-Nitrocinnamic acid 101-121 CEA cell adhesion molecule 4 Homo sapiens 125-128 27840215-7 2017 Meanwhile, 4-ECA and 4-NCA could chelate a copper ion of tyrosinase. Copper 43-49 CEA cell adhesion molecule 4 Homo sapiens 23-26 27936544-1 2016 A complete and ordered layered structure on the surface of LiNi0.815Co0.15Al0.035O2 (NCA) has been achieved via a facile surface-oxidation method with Na2S2O8. sodium persulfate 151-158 CEA cell adhesion molecule 4 Homo sapiens 85-88 27936544-2 2016 The field-emission transmission electron microscopy images clearly show that preoxidation of the hydroxide precursor can eliminate the crystal defects and convert Ni(OH)2 into layered beta-NiOOH, which leads to a highly ordered crystalline NCA, with its (006) planes perpendicular to the surface in the sintering process. hydroxide ion 97-106 CEA cell adhesion molecule 4 Homo sapiens 240-243 27936544-2 2016 The field-emission transmission electron microscopy images clearly show that preoxidation of the hydroxide precursor can eliminate the crystal defects and convert Ni(OH)2 into layered beta-NiOOH, which leads to a highly ordered crystalline NCA, with its (006) planes perpendicular to the surface in the sintering process. nickel hydroxide 163-170 CEA cell adhesion molecule 4 Homo sapiens 240-243 27936544-2 2016 The field-emission transmission electron microscopy images clearly show that preoxidation of the hydroxide precursor can eliminate the crystal defects and convert Ni(OH)2 into layered beta-NiOOH, which leads to a highly ordered crystalline NCA, with its (006) planes perpendicular to the surface in the sintering process. beta-niooh 184-194 CEA cell adhesion molecule 4 Homo sapiens 240-243 27564064-3 2016 The block copolymers were successfully obtained via click reaction to introduce peptide (alkynyl-GPLGVRGDG) into the end of PEG for initiating ring-opening polymerization of beta-benzyl l-aspartate N-carboxyanhydride (BLA-NCA) by terminal amino groups followed by partial hydrolysis of PBLA segments. copolymers 10-20 CEA cell adhesion molecule 4 Homo sapiens 222-225 27564064-3 2016 The block copolymers were successfully obtained via click reaction to introduce peptide (alkynyl-GPLGVRGDG) into the end of PEG for initiating ring-opening polymerization of beta-benzyl l-aspartate N-carboxyanhydride (BLA-NCA) by terminal amino groups followed by partial hydrolysis of PBLA segments. alkynyl-gplgvrgdg 89-106 CEA cell adhesion molecule 4 Homo sapiens 222-225 27564064-3 2016 The block copolymers were successfully obtained via click reaction to introduce peptide (alkynyl-GPLGVRGDG) into the end of PEG for initiating ring-opening polymerization of beta-benzyl l-aspartate N-carboxyanhydride (BLA-NCA) by terminal amino groups followed by partial hydrolysis of PBLA segments. Polyethylene Glycols 124-127 CEA cell adhesion molecule 4 Homo sapiens 222-225 27564064-3 2016 The block copolymers were successfully obtained via click reaction to introduce peptide (alkynyl-GPLGVRGDG) into the end of PEG for initiating ring-opening polymerization of beta-benzyl l-aspartate N-carboxyanhydride (BLA-NCA) by terminal amino groups followed by partial hydrolysis of PBLA segments. beta-benzyl l-aspartate n-carboxyanhydride 174-216 CEA cell adhesion molecule 4 Homo sapiens 222-225 27226071-0 2016 Modification of Ni-Rich FCG NMC and NCA Cathodes by Atomic Layer Deposition: Preventing Surface Phase Transitions for High-Voltage Lithium-Ion Batteries. Lithium 131-138 CEA cell adhesion molecule 4 Homo sapiens 36-39 27226071-2 2016 In this report, we show that atomic layer deposition (ALD) of titania (TiO2) and alumina (Al2O3) on Ni-rich FCG NMC and NCA active material particles could substantially improve LIB performance and allow for increased upper cutoff voltage (UCV) during charging, which delivers significantly increased specific energy utilization. titanium dioxide 71-75 CEA cell adhesion molecule 4 Homo sapiens 120-123 27226071-2 2016 In this report, we show that atomic layer deposition (ALD) of titania (TiO2) and alumina (Al2O3) on Ni-rich FCG NMC and NCA active material particles could substantially improve LIB performance and allow for increased upper cutoff voltage (UCV) during charging, which delivers significantly increased specific energy utilization. Aluminum Oxide 81-88 CEA cell adhesion molecule 4 Homo sapiens 120-123 27226071-2 2016 In this report, we show that atomic layer deposition (ALD) of titania (TiO2) and alumina (Al2O3) on Ni-rich FCG NMC and NCA active material particles could substantially improve LIB performance and allow for increased upper cutoff voltage (UCV) during charging, which delivers significantly increased specific energy utilization. Aluminum Oxide 90-95 CEA cell adhesion molecule 4 Homo sapiens 120-123 27226071-3 2016 Our results show that Al2O3 coating improved the NMC cycling performance by 40% and the NCA cycling performance by 34% at 1 C/-1 C with respectively 4.35 V and 4.4 V UCV in 2 Ah pouch cells. Aluminum Oxide 22-27 CEA cell adhesion molecule 4 Homo sapiens 88-91 24700120-5 2014 The presence of a proline residue contributes to an increased yield of ISD fragments originating from N-Calpha bond cleavage at Xxx1-Xxx2Pro, which is attributable to the cyclic structure of the proline residue. Proline 18-25 CEA cell adhesion molecule 4 Homo sapiens 102-110 24700120-5 2014 The presence of a proline residue contributes to an increased yield of ISD fragments originating from N-Calpha bond cleavage at Xxx1-Xxx2Pro, which is attributable to the cyclic structure of the proline residue. Proline 195-202 CEA cell adhesion molecule 4 Homo sapiens 102-110 24700120-6 2014 Our results suggest that the aminoketyl radical formed by MALDI-ISD generally induces the homolytic N-Calpha bond cleavage located on the C-terminal side of the radical site. aminoketyl radical 29-47 CEA cell adhesion molecule 4 Homo sapiens 100-108 23943596-2 2014 First, the block copolymer poly(benzyl L-aspartate)-block-poly(ethylene glycol) (PBLA-b-PEG) is synthesized via ring-opening polymerization of beta-benzyl L-aspartate-N-carboxyanhydride (BLA-NCA) with alpha-methoxy-omega-aminopoly(ethylene glycol) (mPEG-NH2 ) as a macroinitiator. poly(benzyl l-aspartate)-block-poly(ethylene glycol) 27-79 CEA cell adhesion molecule 4 Homo sapiens 191-194 23943596-2 2014 First, the block copolymer poly(benzyl L-aspartate)-block-poly(ethylene glycol) (PBLA-b-PEG) is synthesized via ring-opening polymerization of beta-benzyl L-aspartate-N-carboxyanhydride (BLA-NCA) with alpha-methoxy-omega-aminopoly(ethylene glycol) (mPEG-NH2 ) as a macroinitiator. pbla-b-peg 81-91 CEA cell adhesion molecule 4 Homo sapiens 191-194 21375808-4 2012 A synthesis method of conjugating poly(L-lysine) (PLL) derivatives with terminally galactose-graft-PEG was developed using ring-opening polymerization of N(epsilon)-benzyloxycarbonyl-L-lysine-N(alpha)-carboxyan-hydride (Z-Lys-NCA) initiated onto galactose graft amine-terminated PEG (galactose-PEG-NH2) as a macro-initiator. poly(l-lysine) 34-48 CEA cell adhesion molecule 4 Homo sapiens 226-229 24328203-6 2014 Extensive mapping with B3LYP, M06-2X, and MP2(frozen core) calculations of the potential energy surface of the ground doublet electronic state of (GLGGK + 2H)(+ ) provided transition-state and dissociation energies for backbone cleavages of the N-Calpha and amide C-N bonds leading to ion-molecule complexes. Deuterium 155-157 CEA cell adhesion molecule 4 Homo sapiens 245-253 21375808-4 2012 A synthesis method of conjugating poly(L-lysine) (PLL) derivatives with terminally galactose-graft-PEG was developed using ring-opening polymerization of N(epsilon)-benzyloxycarbonyl-L-lysine-N(alpha)-carboxyan-hydride (Z-Lys-NCA) initiated onto galactose graft amine-terminated PEG (galactose-PEG-NH2) as a macro-initiator. N-(3-hydroxy-1,2,3,4-tetrahydro-2-naphthyl)-N-(3-oxo-3-phenyl-2-methylpropyl)piperazine 50-53 CEA cell adhesion molecule 4 Homo sapiens 226-229 21375808-4 2012 A synthesis method of conjugating poly(L-lysine) (PLL) derivatives with terminally galactose-graft-PEG was developed using ring-opening polymerization of N(epsilon)-benzyloxycarbonyl-L-lysine-N(alpha)-carboxyan-hydride (Z-Lys-NCA) initiated onto galactose graft amine-terminated PEG (galactose-PEG-NH2) as a macro-initiator. Galactose 83-92 CEA cell adhesion molecule 4 Homo sapiens 226-229 21375808-4 2012 A synthesis method of conjugating poly(L-lysine) (PLL) derivatives with terminally galactose-graft-PEG was developed using ring-opening polymerization of N(epsilon)-benzyloxycarbonyl-L-lysine-N(alpha)-carboxyan-hydride (Z-Lys-NCA) initiated onto galactose graft amine-terminated PEG (galactose-PEG-NH2) as a macro-initiator. n(epsilon)-benzyloxycarbonyl-l-lysine-n(alpha)-carboxyan-hydride 154-218 CEA cell adhesion molecule 4 Homo sapiens 226-229 21646027-1 2011 For the first time, (nat)Hg2Cl2 target has been used to produce no-carrier-added-NCA (197,198,198m,199,200,201)Tl radionuclides using (nat)Hg(p,xn) reaction. calomel 25-31 CEA cell adhesion molecule 4 Homo sapiens 81-84 20000889-12 2010 Inhibition resulted in reduced clearances and prolonged elimination half-lives for tesofensine and itraconazole: using NCA, the actual study revealed an approximately 9% increase in exposure for the timeframe of the coadministration with itraconazole (the area under the plasma concentration-time curve (AUC) from 0 to 144 hours [AUC(144h)]), and the impact on exposure estimated to infinity (AUC(infinity)) was approximately 26%. Tesofensine 83-94 CEA cell adhesion molecule 4 Homo sapiens 119-122 20000889-12 2010 Inhibition resulted in reduced clearances and prolonged elimination half-lives for tesofensine and itraconazole: using NCA, the actual study revealed an approximately 9% increase in exposure for the timeframe of the coadministration with itraconazole (the area under the plasma concentration-time curve (AUC) from 0 to 144 hours [AUC(144h)]), and the impact on exposure estimated to infinity (AUC(infinity)) was approximately 26%. Itraconazole 99-111 CEA cell adhesion molecule 4 Homo sapiens 119-122 20000889-12 2010 Inhibition resulted in reduced clearances and prolonged elimination half-lives for tesofensine and itraconazole: using NCA, the actual study revealed an approximately 9% increase in exposure for the timeframe of the coadministration with itraconazole (the area under the plasma concentration-time curve (AUC) from 0 to 144 hours [AUC(144h)]), and the impact on exposure estimated to infinity (AUC(infinity)) was approximately 26%. Itraconazole 238-250 CEA cell adhesion molecule 4 Homo sapiens 119-122 15694771-4 2005 The N-Calpha bond dissociation and transition state energies in charge-stabilized NMA anions are 20-50 kJ mol(-1) greater than in the hydrogen atom adduct. N-methylacetamide 82-85 CEA cell adhesion molecule 4 Homo sapiens 4-12 20507711-7 2010 The anionic co-polymerization of gamma-benzyl-L-glutamate N-carboxyanhydride (BLG-NCA) using PEG-g-PEI as a macro-initiator was carried out, followed by aminolysis with 2-dimethylaminoethylamine to obtain the target water-soluble tri-block co-polymer. gamma-benzyl-l-glutamate n-carboxyanhydride 33-76 CEA cell adhesion molecule 4 Homo sapiens 82-85 20507711-7 2010 The anionic co-polymerization of gamma-benzyl-L-glutamate N-carboxyanhydride (BLG-NCA) using PEG-g-PEI as a macro-initiator was carried out, followed by aminolysis with 2-dimethylaminoethylamine to obtain the target water-soluble tri-block co-polymer. peg-g-pei 93-102 CEA cell adhesion molecule 4 Homo sapiens 82-85 20507711-7 2010 The anionic co-polymerization of gamma-benzyl-L-glutamate N-carboxyanhydride (BLG-NCA) using PEG-g-PEI as a macro-initiator was carried out, followed by aminolysis with 2-dimethylaminoethylamine to obtain the target water-soluble tri-block co-polymer. dimethylethylenediamine 169-194 CEA cell adhesion molecule 4 Homo sapiens 82-85 20507711-7 2010 The anionic co-polymerization of gamma-benzyl-L-glutamate N-carboxyanhydride (BLG-NCA) using PEG-g-PEI as a macro-initiator was carried out, followed by aminolysis with 2-dimethylaminoethylamine to obtain the target water-soluble tri-block co-polymer. Water 216-221 CEA cell adhesion molecule 4 Homo sapiens 82-85 19338581-3 2009 EXPERIMENTAL APPROACH: Functional and radioligand-binding assays were used to examine the interaction of two BA analogues, 3-(2,4-dimethoxybenzylidene)-anabaseine (DMXBA) and its primary metabolite 3-(4-hydroxy-2-methoxybenzylidene)-anabaseine (4OH-DMXBA) with both agonist and non-competitive antagonist (NCA)-binding sites on muscle-type nAChRs. Barium 109-111 CEA cell adhesion molecule 4 Homo sapiens 306-309 19338581-3 2009 EXPERIMENTAL APPROACH: Functional and radioligand-binding assays were used to examine the interaction of two BA analogues, 3-(2,4-dimethoxybenzylidene)-anabaseine (DMXBA) and its primary metabolite 3-(4-hydroxy-2-methoxybenzylidene)-anabaseine (4OH-DMXBA) with both agonist and non-competitive antagonist (NCA)-binding sites on muscle-type nAChRs. 3-(2,4-dimethoxybenzylidene)anabaseine 123-162 CEA cell adhesion molecule 4 Homo sapiens 306-309 19338581-10 2009 The NCA-binding site for BAs overlaps both the phencyclidine- and dizocilpine-binding sites in the desensitized Torpedo nAChR ion channel. Phencyclidine 47-60 CEA cell adhesion molecule 4 Homo sapiens 4-7 19338581-10 2009 The NCA-binding site for BAs overlaps both the phencyclidine- and dizocilpine-binding sites in the desensitized Torpedo nAChR ion channel. Dizocilpine Maleate 66-77 CEA cell adhesion molecule 4 Homo sapiens 4-7 18482800-3 2008 Neurocalcin alpha (NCalpha) is a member of neuronal calcium sensor (NCS) protein family and shows Ca(2+)-dependent binding to the cell membrane through N-terminal myristoyl moiety. Calcium 52-59 CEA cell adhesion molecule 4 Homo sapiens 19-26 16585946-7 2006 In response to weight loss, subjects with nCA/nCA haplotypes at SNPs 10076C>G/10171A>T showed greater reduction in FFA levels than those with CA/CA haplotype (CA/CA: C/C at SNP 10076 and A/A at SNP 10171, nCA: non-CA haplotype carrier). Fatty Acids, Nonesterified 121-124 CEA cell adhesion molecule 4 Homo sapiens 42-45 16585946-7 2006 In response to weight loss, subjects with nCA/nCA haplotypes at SNPs 10076C>G/10171A>T showed greater reduction in FFA levels than those with CA/CA haplotype (CA/CA: C/C at SNP 10076 and A/A at SNP 10171, nCA: non-CA haplotype carrier). Fatty Acids, Nonesterified 121-124 CEA cell adhesion molecule 4 Homo sapiens 46-49 16585946-7 2006 In response to weight loss, subjects with nCA/nCA haplotypes at SNPs 10076C>G/10171A>T showed greater reduction in FFA levels than those with CA/CA haplotype (CA/CA: C/C at SNP 10076 and A/A at SNP 10171, nCA: non-CA haplotype carrier). Fatty Acids, Nonesterified 121-124 CEA cell adhesion molecule 4 Homo sapiens 46-49 15820864-1 2005 The molecular structure and conformational properties of 1,2-dibromoethyl-trichlorosilane (CH2BrCHBrSiCl3) have been investigated using gas-phase electron diffraction (GED) data recorded at a temperature of 100 degrees C, together with ab initio molecular orbital (MO) and density functional theory (DFT) calculations, infrared (IR) and Raman spectroscopy in the liquid and solid phases, and normal coordinate analysis (NCA). 1,2-dibromoethyl-trichlorosilane 57-89 CEA cell adhesion molecule 4 Homo sapiens 420-423 15820864-1 2005 The molecular structure and conformational properties of 1,2-dibromoethyl-trichlorosilane (CH2BrCHBrSiCl3) have been investigated using gas-phase electron diffraction (GED) data recorded at a temperature of 100 degrees C, together with ab initio molecular orbital (MO) and density functional theory (DFT) calculations, infrared (IR) and Raman spectroscopy in the liquid and solid phases, and normal coordinate analysis (NCA). 1,2-dibromoethyl-trichlorosilane 91-105 CEA cell adhesion molecule 4 Homo sapiens 420-423 18482679-1 2008 INTRODUCTION: Non carrier added (NCA) 2-[(18)F]fluoromethyl-l-phenylalanine is currently used in a Phase I study. ]fluoromethyl-l-phenylalanine 46-75 CEA cell adhesion molecule 4 Homo sapiens 33-36 18482679-5 2008 NCA 3-(2-[(18)F(-)]Fluoromethyl-phenyl)-2-tert-butoxycarbonylamino-propionic acid tert-butyl ester recovered from HPLC was submitted to deprotection in TFA/CH(2)Cl(2) in the presence of CaCl(2). -)]fluoromethyl-phenyl)-2-tert-butoxycarbonylamino-propionic acid tert-butyl ester 16-98 CEA cell adhesion molecule 4 Homo sapiens 0-3 18482679-5 2008 NCA 3-(2-[(18)F(-)]Fluoromethyl-phenyl)-2-tert-butoxycarbonylamino-propionic acid tert-butyl ester recovered from HPLC was submitted to deprotection in TFA/CH(2)Cl(2) in the presence of CaCl(2). Trifluoroacetic Acid 152-155 CEA cell adhesion molecule 4 Homo sapiens 0-3 18482679-5 2008 NCA 3-(2-[(18)F(-)]Fluoromethyl-phenyl)-2-tert-butoxycarbonylamino-propionic acid tert-butyl ester recovered from HPLC was submitted to deprotection in TFA/CH(2)Cl(2) in the presence of CaCl(2). ch(2)cl 156-163 CEA cell adhesion molecule 4 Homo sapiens 0-3 18482679-5 2008 NCA 3-(2-[(18)F(-)]Fluoromethyl-phenyl)-2-tert-butoxycarbonylamino-propionic acid tert-butyl ester recovered from HPLC was submitted to deprotection in TFA/CH(2)Cl(2) in the presence of CaCl(2). cacl 186-190 CEA cell adhesion molecule 4 Homo sapiens 0-3 18482679-14 2008 CONCLUSION: The described synthetic route yields 40% of radiochemical pure NCA 2-[(18)F]fluoromethyl-l-phenylalanine within 105 min. 2-fluoromethylphenylalanine 79-116 CEA cell adhesion molecule 4 Homo sapiens 75-78 15694771-4 2005 The N-Calpha bond dissociation and transition state energies in charge-stabilized NMA anions are 20-50 kJ mol(-1) greater than in the hydrogen atom adduct. Hydrogen 134-142 CEA cell adhesion molecule 4 Homo sapiens 4-12 15694771-6 2005 A new mechanism is proposed for ECD of multiply charged peptide and protein cations in which the electron enters a charge-stabilized electronic state delocalized over the amide group, which is a superbase that abstracts a proton from a sterically proximate amino acid residue to form a labile aminoketyl radical that dissociates by N-Calpha bond cleavage. Amides 171-176 CEA cell adhesion molecule 4 Homo sapiens 332-340 15694771-6 2005 A new mechanism is proposed for ECD of multiply charged peptide and protein cations in which the electron enters a charge-stabilized electronic state delocalized over the amide group, which is a superbase that abstracts a proton from a sterically proximate amino acid residue to form a labile aminoketyl radical that dissociates by N-Calpha bond cleavage. aminoketyl radical 293-311 CEA cell adhesion molecule 4 Homo sapiens 332-340 15694771-7 2005 This mechanism explains the low selectivity of N-Calpha bond dissociations induced by electron capture, and is applicable to dissociations of peptide ions in which the charge carriers are metal ions or quaternary ammonium groups. Metals 188-193 CEA cell adhesion molecule 4 Homo sapiens 47-55 15694771-7 2005 This mechanism explains the low selectivity of N-Calpha bond dissociations induced by electron capture, and is applicable to dissociations of peptide ions in which the charge carriers are metal ions or quaternary ammonium groups. quaternary ammonium 202-221 CEA cell adhesion molecule 4 Homo sapiens 47-55 12115552-8 2002 NCA against NK-resistant (MCF-7, COLO-205, U937) and NK-sensitive (K562) cell lines was significantly lower in DBCP and much less augmented by in vitro preincubation with IL-2 or IL-12 compared to controls. 1,2-dibromo-3-chloropropane 111-115 CEA cell adhesion molecule 4 Homo sapiens 0-3 11350799-10 2001 These data suggest that lung fibroblasts may modulate inflammatory cell recruitment into the lung by releasing NCA and MCA in response to cyclophosphamide. Cyclophosphamide 138-154 CEA cell adhesion molecule 4 Homo sapiens 111-114 11782172-2 2002 The conformationally constrained peptide mimics that were used are cyclopropane-derived isosteres whereby a cyclopropane ring substitutes to the N-Calpha-Cbeta atoms of the phosphotyrosine. cyclopropane 67-79 CEA cell adhesion molecule 4 Homo sapiens 145-153 11782172-2 2002 The conformationally constrained peptide mimics that were used are cyclopropane-derived isosteres whereby a cyclopropane ring substitutes to the N-Calpha-Cbeta atoms of the phosphotyrosine. Phosphotyrosine 173-188 CEA cell adhesion molecule 4 Homo sapiens 145-153 10362718-2 1999 We postulated that bleomycin might stimulate A549 cells, a type II pneumocyte cell line, to release neutrophil and monocyte chemotactic activities (NCA and MCA, respectively). Bleomycin 19-28 CEA cell adhesion molecule 4 Homo sapiens 148-151 10600885-7 1999 Lipoxygenase inhibitors and cycloheximide inhibited the release of both NCA and MCA. Cycloheximide 28-41 CEA cell adhesion molecule 4 Homo sapiens 72-75 10600885-9 1999 NCA was inhibited by anti-human interleukin (IL)-8 and anti-granulocyte colony-stimulating factor antibodies and a leukotriene (LT) B(4)-receptor antagonist. Leukotrienes 115-126 CEA cell adhesion molecule 4 Homo sapiens 0-3 10362718-4 1999 A549 cell supernatant fluids showed NCA and MCA in response to bleomycin in a dose- and time-dependent manner (P < 0.05). Bleomycin 63-72 CEA cell adhesion molecule 4 Homo sapiens 36-39 10362718-6 1999 Partial characterization of the released NCA and MCA showed that the activities were partially heat labile, trypsin digested, and predominantly ethyl acetate extractable. ethyl acetate 144-157 CEA cell adhesion molecule 4 Homo sapiens 41-44 9041239-1 1997 BACKGROUND & AIMS: The nonspecific cross-reacting antigen (NCA) is a cell adhesion molecule, and the messenger RNA for NCA is overexpressed in 92% of colorectal carcinomas. Adenosine Monophosphate 12-15 CEA cell adhesion molecule 4 Homo sapiens 63-66 10229865-1 1999 We determined whether human lung fibroblasts might release chemotactic activity for neutrophils (NCA) and monocytes (MCA) in response to bleomycin. Bleomycin 137-146 CEA cell adhesion molecule 4 Homo sapiens 97-100 10229865-3 1999 Human lung fibroblasts released NCA and MCA in a dose- and time-dependent manner in response to bleomycin. Bleomycin 96-105 CEA cell adhesion molecule 4 Homo sapiens 32-35 10229865-5 1999 Partial characterization revealed that NCA was partly heat labile, trypsin sensitive, and predominantly ethyl acetate extractable. ethyl acetate 104-117 CEA cell adhesion molecule 4 Homo sapiens 39-42 10229865-14 1999 These data suggest that lung fibroblasts may modulate inflammatory cell recruitment into the lung by releasing NCA and MCA in response to bleomycin. Bleomycin 138-147 CEA cell adhesion molecule 4 Homo sapiens 111-114 9846980-7 1998 Partial characterization of NCA and MCA revealed that the activity was partly heat labile, trypsin sensitive, and ethyl acetate extractable. ethyl acetate 114-127 CEA cell adhesion molecule 4 Homo sapiens 28-31 9846980-8 1998 Lipoxygenase inhibitors and cycloheximide inhibited the release of NCA and MCA. Cycloheximide 28-41 CEA cell adhesion molecule 4 Homo sapiens 67-70 9846980-10 1998 NCA was inhibited by anti-human-interleukin (IL)-8 antibody, granulocyte colony-stimulating factor (G-CSF) antibody, or leukotriene (LT)B4 receptor antagonist. Leukotrienes 120-131 CEA cell adhesion molecule 4 Homo sapiens 0-3 7631812-1 1995 In the present investigation, we evaluated the potential of bradykinin (BK), histamine, and serotonin to induce the release of neutrophil and monocyte chemotactic activity (NCA and MCA) from bronchial epithelial cells (BEC). Histamine 77-86 CEA cell adhesion molecule 4 Homo sapiens 173-176 8890209-3 1996 In this study, we demonstrate that ligation of granulocyte NCA results in the activation of the cells, as measured by degranulation and the flux of intracellular calcium. Calcium 162-169 CEA cell adhesion molecule 4 Homo sapiens 59-62 8723147-7 1996 After apomorphine injection, the patients with early untreated probable PD showed significant improvement of Vmax, Amax, NCV, NCA, and UPDRS III scores. Apomorphine 6-17 CEA cell adhesion molecule 4 Homo sapiens 126-129 7631812-1 1995 In the present investigation, we evaluated the potential of bradykinin (BK), histamine, and serotonin to induce the release of neutrophil and monocyte chemotactic activity (NCA and MCA) from bronchial epithelial cells (BEC). Serotonin 92-101 CEA cell adhesion molecule 4 Homo sapiens 173-176 7631812-3 1995 Histamine weakly but significantly induced the release of both NCA and MCA in a similar fashion. Histamine 0-9 CEA cell adhesion molecule 4 Homo sapiens 63-66 7631812-7 1995 The releases of NCA and MCA in response to BK and histamine were inhibited by lipoxygenase inhibitors (P < 0.01). Histamine 50-59 CEA cell adhesion molecule 4 Homo sapiens 16-19 7631812-11 1995 These data suggest that BK and histamine may stimulate BEC to release NCA and MCA and may modulate neutrophil and monocyte recruitment into the airways in patients with asthma. Histamine 31-40 CEA cell adhesion molecule 4 Homo sapiens 70-73 7631812-11 1995 These data suggest that BK and histamine may stimulate BEC to release NCA and MCA and may modulate neutrophil and monocyte recruitment into the airways in patients with asthma. (2-boronoethyl)-cysteine 55-58 CEA cell adhesion molecule 4 Homo sapiens 70-73 24185974-3 1994 Use of the Vilsmeier reagent in acetonitrile, instead of the cyanuric fluoride, led to a N-Boc amino acid N-carboxyanhydride (Boc-NCA). acetonitrile 32-44 CEA cell adhesion molecule 4 Homo sapiens 130-133 24185974-3 1994 Use of the Vilsmeier reagent in acetonitrile, instead of the cyanuric fluoride, led to a N-Boc amino acid N-carboxyanhydride (Boc-NCA). cyanuric fluoride 61-78 CEA cell adhesion molecule 4 Homo sapiens 130-133 24185974-3 1994 Use of the Vilsmeier reagent in acetonitrile, instead of the cyanuric fluoride, led to a N-Boc amino acid N-carboxyanhydride (Boc-NCA). n-boc amino acid n-carboxyanhydride 89-124 CEA cell adhesion molecule 4 Homo sapiens 130-133 24185974-4 1994 From a mixed N-Z,N-Boc amino acid salt a N-Z,N-Boc amino acid fluoride and a Z-NCA were respectively obtained. n-z,n-boc amino acid salt 13-38 CEA cell adhesion molecule 4 Homo sapiens 79-82 1566862-3 1992 Thus, we postulated that acetylcholine (ACh) stimulates bronchial epithelial cells (BEC) to release neutrophil and monocyte chemotactic activity (NCA and MCA). Acetylcholine 25-38 CEA cell adhesion molecule 4 Homo sapiens 146-149 18472935-6 1994 Preincubation of the monocyte cultures with the lipoxygenase inhibitors nordihydroguaiaretic acid (10(-4) M) or diethylcarbamazine (10(-9) M) completely abolished the appearance of NCA and MCA. Masoprocol 72-97 CEA cell adhesion molecule 4 Homo sapiens 181-184 18472935-6 1994 Preincubation of the monocyte cultures with the lipoxygenase inhibitors nordihydroguaiaretic acid (10(-4) M) or diethylcarbamazine (10(-9) M) completely abolished the appearance of NCA and MCA. Diethylcarbamazine 112-130 CEA cell adhesion molecule 4 Homo sapiens 181-184 1431336-5 1992 Treatment of LoVo/Dx with differentiating agents (dimethylformamide and retinoic acid) led to a decreased expression of the adhesion molecules, including NCA, accompanied by increased resistance to LAK-mediated lysis. lovo 13-17 CEA cell adhesion molecule 4 Homo sapiens 154-157 1431336-5 1992 Treatment of LoVo/Dx with differentiating agents (dimethylformamide and retinoic acid) led to a decreased expression of the adhesion molecules, including NCA, accompanied by increased resistance to LAK-mediated lysis. Dimethylformamide 50-67 CEA cell adhesion molecule 4 Homo sapiens 154-157 1431336-5 1992 Treatment of LoVo/Dx with differentiating agents (dimethylformamide and retinoic acid) led to a decreased expression of the adhesion molecules, including NCA, accompanied by increased resistance to LAK-mediated lysis. Tretinoin 72-85 CEA cell adhesion molecule 4 Homo sapiens 154-157 8460091-2 1993 To analyse the molecular nature of these glycoproteins further, a lambda gt11 expression library has been constructed from the GER pancreatic adenocarcinoma cell line and screened with an NCA sequence-specific oligonucleotide probe. Oligonucleotides 210-225 CEA cell adhesion molecule 4 Homo sapiens 188-191 1625062-1 1992 Using a panel of polyclonal and monoclonal antibodies to CEA-related antigens in paraffin-processed cervical biopsies, CEA and NCA expression has been demonstrated on the cell membrane of normal mature cervical squames. Paraffin 81-89 CEA cell adhesion molecule 4 Homo sapiens 127-130 1566862-3 1992 Thus, we postulated that acetylcholine (ACh) stimulates bronchial epithelial cells (BEC) to release neutrophil and monocyte chemotactic activity (NCA and MCA). Acetylcholine 40-43 CEA cell adhesion molecule 4 Homo sapiens 146-149 1566862-5 1992 BEC released NCA and MCA in response to ACh in a dose-dependent and time-dependent manner. Acetylcholine 40-43 CEA cell adhesion molecule 4 Homo sapiens 13-16 1566862-6 1992 Molecular sieve column chromatography revealed that ACh induced a single low-molecular-weight peak (near 400) for NCA and two low-molecular-weight peaks (near 12,000 and 400) for MCA. Acetylcholine 52-55 CEA cell adhesion molecule 4 Homo sapiens 114-117 1566862-7 1992 The release of NCA and MCA was inhibited by the lipoxygenase inhibitors, nordihydroguaiaretic acid and diethylcarbamazine. Masoprocol 73-98 CEA cell adhesion molecule 4 Homo sapiens 15-18 1566862-7 1992 The release of NCA and MCA was inhibited by the lipoxygenase inhibitors, nordihydroguaiaretic acid and diethylcarbamazine. Diethylcarbamazine 103-121 CEA cell adhesion molecule 4 Homo sapiens 15-18 1566862-11 1992 In contrast, atropine and the M1 receptor antagonist, pirenzepine, inhibited the release of NCA. Atropine 13-21 CEA cell adhesion molecule 4 Homo sapiens 92-95 1566862-11 1992 In contrast, atropine and the M1 receptor antagonist, pirenzepine, inhibited the release of NCA. Pirenzepine 54-65 CEA cell adhesion molecule 4 Homo sapiens 92-95 1566862-12 1992 These data demonstrate that ACh stimulates BEC to release lipoxygenase-derived NCA and MCA through the muscarinic receptor. Acetylcholine 28-31 CEA cell adhesion molecule 4 Homo sapiens 79-82 34731511-10 2022 Longer PCA/NCA duration was associated with higher initial morphine requirements (rho=0.46(95%CI 0.35,0.57)); subsequent increased pain and need for ketamine co-analgesia (118/364 episodes with opioid/ketamine 13.9(9.8-22.2) days vs opioid alone 6.0(3.9-10.8) days; median(IQR)); but not with age or sex. Morphine 59-67 CEA cell adhesion molecule 4 Homo sapiens 11-14 1370882-0 1992 Three different NCA species, CGM6/CD67, NCA-95, and NCA-90, are comprised in the major 90 to 100-kDa band of granulocyte NCA detectable upon SDS-polyacrylamide gel electrophoresis. Sodium Dodecyl Sulfate 141-144 CEA cell adhesion molecule 4 Homo sapiens 16-19 1370882-0 1992 Three different NCA species, CGM6/CD67, NCA-95, and NCA-90, are comprised in the major 90 to 100-kDa band of granulocyte NCA detectable upon SDS-polyacrylamide gel electrophoresis. Sodium Dodecyl Sulfate 141-144 CEA cell adhesion molecule 4 Homo sapiens 40-43 1370882-0 1992 Three different NCA species, CGM6/CD67, NCA-95, and NCA-90, are comprised in the major 90 to 100-kDa band of granulocyte NCA detectable upon SDS-polyacrylamide gel electrophoresis. Sodium Dodecyl Sulfate 141-144 CEA cell adhesion molecule 4 Homo sapiens 40-43 1370882-0 1992 Three different NCA species, CGM6/CD67, NCA-95, and NCA-90, are comprised in the major 90 to 100-kDa band of granulocyte NCA detectable upon SDS-polyacrylamide gel electrophoresis. polyacrylamide 145-159 CEA cell adhesion molecule 4 Homo sapiens 16-19 1370882-0 1992 Three different NCA species, CGM6/CD67, NCA-95, and NCA-90, are comprised in the major 90 to 100-kDa band of granulocyte NCA detectable upon SDS-polyacrylamide gel electrophoresis. polyacrylamide 145-159 CEA cell adhesion molecule 4 Homo sapiens 40-43 1370882-0 1992 Three different NCA species, CGM6/CD67, NCA-95, and NCA-90, are comprised in the major 90 to 100-kDa band of granulocyte NCA detectable upon SDS-polyacrylamide gel electrophoresis. polyacrylamide 145-159 CEA cell adhesion molecule 4 Homo sapiens 40-43 1370882-4 1992 This component was reactive with an anti-CD67 antibody as well as polyclonal anti-NCA and released from the cell surface with phosphatidylinositol-specific phospholipase C, indicating that the 100-kDa NCA species is CD67. Phosphatidylinositols 126-146 CEA cell adhesion molecule 4 Homo sapiens 201-204 1370882-5 1992 Both antibodies revealed high binding activities with a recombinant protein of CGM6, which has been identified in a leukocyte cDNA library as an NCA gene and found to encode a glycosyl-phosphatidylinositol-anchored heterotypic cell adhesion molecule. Phosphatidylinositols 185-205 CEA cell adhesion molecule 4 Homo sapiens 145-148 1706327-0 1991 The high lysability by LAK cells of colon-carcinoma cells resistant to doxorubicin is associated with a high expression of ICAM-1, LFA-3, NCA and a less-differentiated phenotype. Doxorubicin 71-82 CEA cell adhesion molecule 4 Homo sapiens 138-141 2341397-5 1990 This approach showed that TEX and NCA were identical with respect to primary sequence and provided direct evidence that 11 of the 12 predicted asparagine-linked glycosylation sites were glycosylated in both TEX and NCA. Asparagine 143-153 CEA cell adhesion molecule 4 Homo sapiens 34-37 2341397-5 1990 This approach showed that TEX and NCA were identical with respect to primary sequence and provided direct evidence that 11 of the 12 predicted asparagine-linked glycosylation sites were glycosylated in both TEX and NCA. Asparagine 143-153 CEA cell adhesion molecule 4 Homo sapiens 215-218 2341397-8 1990 The large difference in the molecular weights of glycosylated TEX and NCA suggests significant variations in their oligosaccharide structures. Oligosaccharides 115-130 CEA cell adhesion molecule 4 Homo sapiens 70-73 2178978-3 1990 Binding of the bacteria to CEA and NCA was completely abolished in the presence of 10 mM alpha-methyl D-mannopyranoside. alpha-methyl d-mannopyranoside 89-119 CEA cell adhesion molecule 4 Homo sapiens 35-38 2178978-6 1990 These findings indicate that the E. coli strains bind to D-mannosyl residues in CEA and NCA. Deuterium 57-58 CEA cell adhesion molecule 4 Homo sapiens 88-91 2178978-6 1990 These findings indicate that the E. coli strains bind to D-mannosyl residues in CEA and NCA. mannosyl 59-67 CEA cell adhesion molecule 4 Homo sapiens 88-91 2187320-7 1990 The antigenicity of CEA and NCA in normal tissues was significantly lost after paraffin embedding as compared to frozen sections. Paraffin 79-87 CEA cell adhesion molecule 4 Homo sapiens 28-31 2187320-8 1990 NCA was consistently demonstrated in eccrine sweat glands embedded in paraffin. Paraffin 70-78 CEA cell adhesion molecule 4 Homo sapiens 0-3 2187320-9 1990 In various tumor tissues, CEA and NCA were colocalized and expression increased sufficiently to be detected in paraffin sections. Paraffin 111-119 CEA cell adhesion molecule 4 Homo sapiens 34-37 23030464-2 2012 First, Val-Tyr-OH dipeptide was synthesized by a novel chemical method in two steps involving preparation of NCA-Val. val-tyr-oh dipeptide 7-27 CEA cell adhesion molecule 4 Homo sapiens 109-112 34731511-10 2022 Longer PCA/NCA duration was associated with higher initial morphine requirements (rho=0.46(95%CI 0.35,0.57)); subsequent increased pain and need for ketamine co-analgesia (118/364 episodes with opioid/ketamine 13.9(9.8-22.2) days vs opioid alone 6.0(3.9-10.8) days; median(IQR)); but not with age or sex. Ketamine 149-157 CEA cell adhesion molecule 4 Homo sapiens 11-14 34731511-10 2022 Longer PCA/NCA duration was associated with higher initial morphine requirements (rho=0.46(95%CI 0.35,0.57)); subsequent increased pain and need for ketamine co-analgesia (118/364 episodes with opioid/ketamine 13.9(9.8-22.2) days vs opioid alone 6.0(3.9-10.8) days; median(IQR)); but not with age or sex. Ketamine 201-209 CEA cell adhesion molecule 4 Homo sapiens 11-14 34638671-6 2021 To the best of our knowledge, this is the first report on an NCA/Si@G pouch cell cycled at the 5C rate that delivers specific capacity values of 87 mAh g-1. Silicon 65-67 CEA cell adhesion molecule 4 Homo sapiens 61-64 34672572-2 2021 This study reports, for the first time, NCA formation when gas-phase ozone reacts with human surfaces. Ozone 69-74 CEA cell adhesion molecule 4 Homo sapiens 40-43 34672572-3 2021 In an occupied climate-controlled chamber, we detected NCA only when ozone was present. Ozone 69-74 CEA cell adhesion molecule 4 Homo sapiens 55-58 34672572-5 2021 Ozone-initiated chemistry with human skin lipids (particularly their primary surface reaction products) is the key mechanism driving NCA emissions, as evidenced by positive correlations with squalene in human skin wipe samples and known gaseous products from ozonolysis of skin lipids. Ozone 0-5 CEA cell adhesion molecule 4 Homo sapiens 133-136 34672572-5 2021 Ozone-initiated chemistry with human skin lipids (particularly their primary surface reaction products) is the key mechanism driving NCA emissions, as evidenced by positive correlations with squalene in human skin wipe samples and known gaseous products from ozonolysis of skin lipids. Squalene 191-199 CEA cell adhesion molecule 4 Homo sapiens 133-136 34672572-6 2021 Oxidation by OH radicals, autoxidation reactions, and human-emitted NH3 may also play a role in NCA formation. oh radicals 13-24 CEA cell adhesion molecule 4 Homo sapiens 96-99 34672572-6 2021 Oxidation by OH radicals, autoxidation reactions, and human-emitted NH3 may also play a role in NCA formation. Ammonia 68-71 CEA cell adhesion molecule 4 Homo sapiens 96-99 34402193-7 2021 Following, five hub genes (CRYBB1, RIMBP3C, CEACAM4, HAMP, and LYL1) were identified for their strong relationships with sunitinib and immune infiltration in ccRCC. Sunitinib 121-130 CEA cell adhesion molecule 4 Homo sapiens 44-51 34402193-8 2021 Further validations in external data refined CRYBB1, CEACAM4, and HAMP which play a vital role in sunitinib resistance, immune infiltrations in ccRCC, and the development and progression of ccRCC. Sunitinib 98-107 CEA cell adhesion molecule 4 Homo sapiens 53-60 34392611-11 2022 Average total postoperative opioid use during hospital stay was reduced by 53.7% in the NCA cohort, with an average use of 501.6 morphine milligram equivalents (MME) (SD 410.3) among PCA patients and an average use of 232.0 MME (SD 216.5) among NCA patients (p = 0.003). Morphine 129-137 CEA cell adhesion molecule 4 Homo sapiens 88-91 35131499-1 2022 In this work, a strategy of using fast co-precipitation method has been developed to synthesize stable Al doped alpha-phase NiCo layered double hydroxides (NCA-LDH). Aluminum 103-105 CEA cell adhesion molecule 4 Homo sapiens 156-159 35131499-1 2022 In this work, a strategy of using fast co-precipitation method has been developed to synthesize stable Al doped alpha-phase NiCo layered double hydroxides (NCA-LDH). Niacin 124-128 CEA cell adhesion molecule 4 Homo sapiens 156-159 35306183-2 2022 In this work, we recorded the successful preparation of well-defined theranostic amphiliphilic bottlebrush copolymers composing of fluorescent backbone of PF and tunable enzyme-degradable side chains of polytyrosine (PTyr) and POEGMA by integrating Suzuki coupling, NCA ROP and ATRP techniques. bottlebrush copolymers 95-117 CEA cell adhesion molecule 4 Homo sapiens 266-269 35306183-2 2022 In this work, we recorded the successful preparation of well-defined theranostic amphiliphilic bottlebrush copolymers composing of fluorescent backbone of PF and tunable enzyme-degradable side chains of polytyrosine (PTyr) and POEGMA by integrating Suzuki coupling, NCA ROP and ATRP techniques. pf 155-157 CEA cell adhesion molecule 4 Homo sapiens 266-269 35306183-2 2022 In this work, we recorded the successful preparation of well-defined theranostic amphiliphilic bottlebrush copolymers composing of fluorescent backbone of PF and tunable enzyme-degradable side chains of polytyrosine (PTyr) and POEGMA by integrating Suzuki coupling, NCA ROP and ATRP techniques. polytyrosine 203-215 CEA cell adhesion molecule 4 Homo sapiens 266-269 35306183-2 2022 In this work, we recorded the successful preparation of well-defined theranostic amphiliphilic bottlebrush copolymers composing of fluorescent backbone of PF and tunable enzyme-degradable side chains of polytyrosine (PTyr) and POEGMA by integrating Suzuki coupling, NCA ROP and ATRP techniques. polytyrosine 217-221 CEA cell adhesion molecule 4 Homo sapiens 266-269 35306183-9 2022 This study therefore not only developed a universal strategy for the construction of multifunction polymeric vehicles based on the conjugated polymer of PF and degradable polypeptide by integrated Suzuki coupling and NCA ROP, but also emphasized the better stability of micelles endowed by the branched hydrophilic brushes than linear ones. Polymers 142-149 CEA cell adhesion molecule 4 Homo sapiens 217-220 35306183-9 2022 This study therefore not only developed a universal strategy for the construction of multifunction polymeric vehicles based on the conjugated polymer of PF and degradable polypeptide by integrated Suzuki coupling and NCA ROP, but also emphasized the better stability of micelles endowed by the branched hydrophilic brushes than linear ones. pf 153-155 CEA cell adhesion molecule 4 Homo sapiens 217-220