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Volumn 232, Issue 2, 1997, Pages 317-322
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Adenosine A3 receptor agonists protect HL-60 and U-937 cells from apoptosis induced by A3 antagonists
a a b a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
ADENOSINE;
ADENOSINE A3 RECEPTOR;
ADENOSINE A3 RECEPTOR AGONIST;
ADENOSINE A3 RECEPTOR ANTAGONIST;
ADENOSINE RECEPTOR BLOCKING AGENT;
ADENOSINE RECEPTOR STIMULATING AGENT;
CELL PROTEIN;
DIHYDROPYRIDINE DERIVATIVE;
NAPHTHYRIDINE DERIVATIVE;
UNCLASSIFIED DRUG;
1,4 DIHYDRO 4 (2 ISOPROPYLPYRAZOLO[1,5 A]PYRIDIN 3 YL) 2,6 DIMETHYL 3,5 PYRIDINEDICARBOXYLIC ACID [2 (N BENZYL N METHYLAMINO)ETHYL] METHYL ESTER;
2 CHLORO N(6) (3 IODOBENZYL)ADENOSINE 5' N METHYLURONAMIDE;
2-CHLORO-N(6)-(3-IODOBENZYL)ADENOSINE-5'-N-METHYLURONAMIDE;
9 CHLORO 2 (2 FURYL) (1,2,4)TRIAZOLO(1,5 C)QUINAZOLIN 5 IMINE;
9-CHLORO-2-(2-FURYL)-(1,2,4)TRIAZOLO(1,5-C)QUINAZOLIN-5-IMINE;
ADENOSINE RECEPTOR;
DNA FRAGMENT;
DRUG DERIVATIVE;
N(6) (3 IODOBENZYL) 5' N METHYLCARBOXAMIDOADENOSINE;
N(6)-(3-IODOBENZYL)-5'-N-METHYLCARBOXAMIDOADENOSINE;
PYRAZOLE DERIVATIVE;
QUINAZOLINE DERIVATIVE;
TRIAZOLE DERIVATIVE;
APOPTOSIS;
ARTICLE;
CELL DEATH;
CELL PROTECTION;
CELL STRAIN HL 60;
CONTROLLED STUDY;
HUMAN;
HUMAN CELL;
LYMPHOMA CELL LINE;
PRIORITY JOURNAL;
PROTEIN EXPRESSION;
DOSE RESPONSE;
DRUG ANTAGONISM;
DRUG EFFECT;
DRUG POTENTIATION;
METABOLISM;
PATHOLOGY;
ADENOSINE;
APOPTOSIS;
DIHYDROPYRIDINES;
DNA FRAGMENTATION;
DOSE-RESPONSE RELATIONSHIP, DRUG;
HL-60 CELLS;
HUMANS;
PYRAZOLES;
QUINAZOLINES;
RECEPTORS, PURINERGIC P1;
TRIAZOLES;
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EID: 0031575663
PISSN: 0006291X
EISSN: None
Source Type: Journal
DOI: 10.1006/bbrc.1997.6290 Document Type: Article |
Times cited : (99)
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References (19)
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