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Results: 13

Authors: VIGUIER M PODER N TEULON JM GENETET F SEGUIN P DARBOURET B
Citation: M. Viguier et al., FREE PROSTATE-SPECIFIC ANTIGEN (FPSA) DETERMINATION USING TRACE(R) TECHNOLOGY, Clinical chemistry, 44, 1998, pp. 151-151

Authors: BOYER T FOURNEL L NICOLAI E TEULON JM
Citation: T. Boyer et al., NEW PROCESS FOR THE SYNTHESIS OF UP-269-6, A 1,2,4-TRIAZOLO[1,5-C]PYRIMIDINE DERIVATIVE AS A POTENT ORALLY-ACTIVE ANGIOTENSIN-II ANTAGONIST, Journal of heterocyclic chemistry, 33(4), 1996, pp. 1307-1311

Authors: DELAGE V TEULON JM BELLANGER L SEGUIN P DESCOTES F SAEZ S
Citation: V. Delage et al., MICROTITER PLATE IMMUNOENZYMOMETRIC ASSAY FOR ESTROGEN-RECEPTOR, Clinical chemistry, 42(12), 1996, pp. 1955-1960

Authors: NICOLAI E CURE G GOYARD J KIRCHNER M TEULON JM VERSIGNY A CAZES M VIRONEODDOS A CAUSSADE F CLOAREC A
Citation: E. Nicolai et al., SYNTHESIS AND ANGIOTENSIN-II RECEPTOR ANTAGONIST ACTIVITY OF C-LINKEDPYRIMIDINE-DERIVATIVES, European journal of medicinal chemistry, 30(5), 1995, pp. 365-375

Authors: SARTORI E CAMY F TEULON JM CAMBORDE F MEIGNEN J HERTZ F CLOAREC A
Citation: E. Sartori et al., SYNTHESIS AND ANALGESIC ACTIVITIES OF UREA DERIVATIVES OF ALPHA-AMINO-N-PYRIDYL BENZENE PROPANAMIDE, European journal of medicinal chemistry, 29(6), 1994, pp. 431-439

Authors: GUNGOR T MALABRE P TEULON JM
Citation: T. Gungor et al., NEW SYNTHESIS OF 1-SUBSTITUTED 3-(2-AMINOETHYL) INDOLES, Synthetic communications, 24(16), 1994, pp. 2247-2256

Authors: GUNGOR T MALABRE P TEULON JM CAMBORDE F MEIGNEN J HERTZ F VIRONEODDOS A CAUSSADE F CLOAREC A
Citation: T. Gungor et al., N6-SUBSTITUTED ADENOSINE RECEPTOR AGONISTS - SYNTHESIS AND PHARMACOLOGICAL ACTIVITY AS POTENT ANTINOCICEPTIVE AGENTS, Journal of medicinal chemistry, 37(25), 1994, pp. 4307-4316

Authors: NICOLAI E CURE G GOYARD J KIRCHNER M TEULON JM VERSIGNY A CAZES M CAUSSADE F VIRONEODDOS A CLOAREC A
Citation: E. Nicolai et al., SYNTHESIS AND SAR STUDIES OF NOVEL TRIAZOLOPYRIMIDINE DERIVATIVES AS POTENT, ORALLY-ACTIVE ANGIOTENSIN-II RECEPTOR ANTAGONISTS, Journal of medicinal chemistry, 37(15), 1994, pp. 2371-2386

Authors: NICOLAI E CLAUDE S TEULON JM
Citation: E. Nicolai et al., NEW PROCESS FOR THE SYNTHESIS OF IMIDAZO[4,5-B]PYRIDINE DERIVATIVES AS POTENT ORALLY-ACTIVE THROMBOXANE-A2 RECEPTOR ANTAGONISTS, Journal of heterocyclic chemistry, 31(1), 1994, pp. 73-75

Authors: NICOLAI E CURE G GOYARD J KIRCHNER M TEULON JM VERSIGNY A CAZES M VIRONEODDOS A CAUSSADE F CLOAREC A
Citation: E. Nicolai et al., SYNTHESIS AND ANGIOTENSIN-II RECEPTOR ANTAGONIST ACTIVITY OF C-LINKEDPYRAZOLE DERIVATIVES, Chemical and Pharmaceutical Bulletin, 42(8), 1994, pp. 1617-1630

Authors: SARTORI E CAMY F TEULON JM CAUSSADE F VIRONEODDOS A CLOAREC A
Citation: E. Sartori et al., SYNTHESIS AND ACTIVITIES OF NEW ARYLSULFONAMIDO THROMBOXANE-A(2)-RECEPTOR ANTAGONISTS, European journal of medicinal chemistry, 28(7-8), 1993, pp. 625-632

Authors: RODIER N CEOLIN R AGAFONOV V TOSCANI S DUGUE J NICOLAI E TEULON JM
Citation: N. Rodier et al., 4-(6-CHLORO-3-(4-CHLOROBENZYL)IMIDAZO[4,5 -D]PYRIDIN-2-YL)-3,3-DIMETHYLBUTANOIC ACID, Acta crystallographica. Section C, Crystal structure communications, 49, 1993, pp. 2034-2037

Authors: NICOLAI E GOYARD J BENCHETRIT T TEULON JM CAUSSADE F VIRONE A DELCHAMBRE C CLOAREC A
Citation: E. Nicolai et al., SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF NOVEL BENZIMIDAZOLEAND IMIDAZO[4,5-B]PYRIDINE ACID-DERIVATIVES AS THROMBOXANE-A(2) RECEPTOR ANTAGONISTS, Journal of medicinal chemistry, 36(9), 1993, pp. 1175-1187
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