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Results: 1-16 |
Results: 16
THE ROLE OF CASPASES IN T-CELL DEVELOPMENT AND THE CONTROL OF IMMUNE-RESPONSES
Authors: DENIS F RHEAUME E AOUAD SM ALAM A SEKALY RP COHEN LY
Citation: F. Denis et al., THE ROLE OF CASPASES IN T-CELL DEVELOPMENT AND THE CONTROL OF IMMUNE-RESPONSES, Cellular and molecular life sciences, 54(9), 1998, pp. 1005-1019
THE LARGE SUBUNIT OF REPLICATION FACTOR-C IS A SUBSTRATE FOR CASPASE-3 IN-VITRO AND IS CLEAVED BY A CASPASE-3-LIKE PROTEASE DURING FAS-MEDIATED APOPTOSIS
Authors: RHEAUME E COHEN LY UHLMANN F LAZURE C ALAM A HURWITZ J SEKALY PP DENIS F
Citation: E. Rheaume et al., THE LARGE SUBUNIT OF REPLICATION FACTOR-C IS A SUBSTRATE FOR CASPASE-3 IN-VITRO AND IS CLEAVED BY A CASPASE-3-LIKE PROTEASE DURING FAS-MEDIATED APOPTOSIS, EMBO journal, 16(21), 1997, pp. 6346-6354
STRUCTURE-FUNCTION-RELATIONSHIPS OF 3-BETA-HYDROXYSTEROID DEHYDROGENASE - CONTRIBUTION MADE BY THE MOLECULAR-GENETICS OF 3-BETA-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY
Authors: MOREL Y MEBARKI F RHEAUME E SANCHEZ R FOREST MG SIMARD J
Citation: Y. Morel et al., STRUCTURE-FUNCTION-RELATIONSHIPS OF 3-BETA-HYDROXYSTEROID DEHYDROGENASE - CONTRIBUTION MADE BY THE MOLECULAR-GENETICS OF 3-BETA-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY, Steroids, 62(1), 1997, pp. 176-184
MOLECULAR-BIOLOGY AND GENETICS OF THE 3-BETA-HYDROXYSTEROID DEHYDROGENASE DELTA-5-DELTA-4 ISOMERASE GENE FAMILY
Authors: SIMARD J DUROCHER F MEBARKI F TURGEON C SANCHEZ R LABRIE Y COUET J TRUDEL C RHEAUME E MOREL Y LUUTHE V LABRIE F
Citation: J. Simard et al., MOLECULAR-BIOLOGY AND GENETICS OF THE 3-BETA-HYDROXYSTEROID DEHYDROGENASE DELTA-5-DELTA-4 ISOMERASE GENE FAMILY, Journal of Endocrinology, 150, 1996, pp. 189-207
STRUCTURE-FUNCTION-RELATIONSHIPS AND MOLECULAR-GENETICS OF THE 3-BETA-HYDROXYSTEROID DEHYDROGENASE GENE FAMILY
Authors: SIMARD J SANCHEZ R DUROCHER F RHEAUME E TURGEON C LABRIE Y LUUTHE V MEBARKI F MOREL Y DELAUNOIT Y LABRIE F
Citation: J. Simard et al., STRUCTURE-FUNCTION-RELATIONSHIPS AND MOLECULAR-GENETICS OF THE 3-BETA-HYDROXYSTEROID DEHYDROGENASE GENE FAMILY, Journal of steroid biochemistry and molecular biology, 55(5-6), 1995, pp. 489-505
MOLECULAR-BASIS OF HUMAN 3-BETA-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY
Authors: SIMARD J RHEAUME E MEBARKI F SANCHEZ R NEW MI MOREL Y LABRIE F
Citation: J. Simard et al., MOLECULAR-BASIS OF HUMAN 3-BETA-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY, Journal of steroid biochemistry and molecular biology, 53(1-6), 1995, pp. 127-138
GENETIC-LINKAGE MAPPING OF HSD3B1 AND HSD3B2 ENCODING HUMAN TYPE-I AND TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASE DELTA-5-DELTA-4-ISOMERASE CLOSE TO D1S514 AND THE CENTROMERIC D1Z5 LOCUS/
Authors: MORISSETTE J RHEAUME E LEBLANC JF LUUTHE V LABRIE F SIMARD J
Citation: J. Morissette et al., GENETIC-LINKAGE MAPPING OF HSD3B1 AND HSD3B2 ENCODING HUMAN TYPE-I AND TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASE DELTA-5-DELTA-4-ISOMERASE CLOSE TO D1S514 AND THE CENTROMERIC D1Z5 LOCUS/, Cytogenetics and cell genetics, 69(1-2), 1995, pp. 59-62
NONSALT-LOSING MALE PSEUDOHERMAPHRODITISM DUE TO THE NOVEL HOMOZYGOUSN100S MUTATION IN THE TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASE GENE
Authors: MEBARKI F SANCHEZ R RHEAUME E LAFLAMME N SIMARD J FOREST MG BEYOMAR F DAVID M LABRIE F MOREL Y
Citation: F. Mebarki et al., NONSALT-LOSING MALE PSEUDOHERMAPHRODITISM DUE TO THE NOVEL HOMOZYGOUSN100S MUTATION IN THE TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASE GENE, The Journal of clinical endocrinology and metabolism, 80(7), 1995, pp. 2127-2134
IDENTIFICATION AND CHARACTERIZATION OF THE G15D MUTATION FOUND IN A MALE-PATIENT WITH 3-BETA-HYDROXYSTEROID DEHYDROGENASE (3-BETA-HSD) DEFICIENCY - ALTERATION OF THE PUTATIVE NAD-BINDING DOMAIN OF TYPE-II 3-BETA-HSD
Authors: RHEAUME E SANCHEZ R MEBARKI F GAGNON E CAREL JC CHAUSSAIN JL MOREL Y LABRIE F SIMARD J
Citation: E. Rheaume et al., IDENTIFICATION AND CHARACTERIZATION OF THE G15D MUTATION FOUND IN A MALE-PATIENT WITH 3-BETA-HYDROXYSTEROID DEHYDROGENASE (3-BETA-HSD) DEFICIENCY - ALTERATION OF THE PUTATIVE NAD-BINDING DOMAIN OF TYPE-II 3-BETA-HSD, Biochemistry, 34(9), 1995, pp. 2893-2900
FUNCTIONAL-CHARACTERIZATION OF THE NOVEL L108W AND P186L MUTATIONS DETECTED IN THE TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASE GENE OF A MALE PSEUDOHERMAPHRODITE WITH CONGENITAL ADRENAL-HYPERPLASIA
Authors: SANCHEZ R MEBARKI F RHEAUME E LAFLAMME N FOREST MG BEYOMARD F DAVID M MOREL Y LABRIE F SIMARD J
Citation: R. Sanchez et al., FUNCTIONAL-CHARACTERIZATION OF THE NOVEL L108W AND P186L MUTATIONS DETECTED IN THE TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASE GENE OF A MALE PSEUDOHERMAPHRODITE WITH CONGENITAL ADRENAL-HYPERPLASIA, Human molecular genetics, 3(9), 1994, pp. 1639-1645
CONGENITAL ADRENAL-HYPERPLASIA CAUSED BY A NOVEL HOMOZYGOUS FRAMESHIFT MUTATION 273-DELTA-AA IN TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASEGENE (HSD3B2) IN 3 MALE-PATIENTS OF AFGHAN PAKISTANI ORIGIN/
Authors: SIMARD J RHEAUME E LEBLANC JF WALLIS SC JOPLIN GF GILBEY S ALLANSON J METTLER G BETTENDORF M HEINRICH U LABRIE F
Citation: J. Simard et al., CONGENITAL ADRENAL-HYPERPLASIA CAUSED BY A NOVEL HOMOZYGOUS FRAMESHIFT MUTATION 273-DELTA-AA IN TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASEGENE (HSD3B2) IN 3 MALE-PATIENTS OF AFGHAN PAKISTANI ORIGIN/, Human molecular genetics, 3(2), 1994, pp. 327-330
NO EVIDENCE OF MUTATIONS IN THE GENES FOR TYPE-I AND TYPE-II 3-HYDROXYSTEROID DEHYDROGENASE (3-BETA-HSD) IN NONCLASSICAL 3-BETA-HSD DEFICIENCY
Authors: ZERAH M RHEAUME E MANI P SCHRAM P SIMARD J LABRIE F NEW MI
Citation: M. Zerah et al., NO EVIDENCE OF MUTATIONS IN THE GENES FOR TYPE-I AND TYPE-II 3-HYDROXYSTEROID DEHYDROGENASE (3-BETA-HSD) IN NONCLASSICAL 3-BETA-HSD DEFICIENCY, The Journal of clinical endocrinology and metabolism, 79(6), 1994, pp. 1811-1817
MOLECULAR-BASIS OF CONGENITAL ADRENAL-HYPERPLASIA IN 2 SIBLINGS WITH CLASSICAL NONSALT-LOSING 3-BETA-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY
Authors: RHEAUME E SANCHEZ R SIMARD J CHANG YT WANG J PANG SY LABRIE F
Citation: E. Rheaume et al., MOLECULAR-BASIS OF CONGENITAL ADRENAL-HYPERPLASIA IN 2 SIBLINGS WITH CLASSICAL NONSALT-LOSING 3-BETA-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY, The Journal of clinical endocrinology and metabolism, 79(4), 1994, pp. 1012-1018
MOLECULAR-BASIS OF CONGENITAL ADRENAL-HYPERPLASIA IN 2 SIBLINGS WITH CLASSICAL NONSALT-LOSING 3-BETA-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY
Authors: RHEAUME E SANCHEZ R SIMARD J CHANG YT WANG J PANG SY LABRIE F
Citation: E. Rheaume et al., MOLECULAR-BASIS OF CONGENITAL ADRENAL-HYPERPLASIA IN 2 SIBLINGS WITH CLASSICAL NONSALT-LOSING 3-BETA-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY, The Journal of clinical endocrinology and metabolism, 79(4), 1994, pp. 1012-1018
DETECTION AND FUNCTIONAL-CHARACTERIZATION OF THE NOVEL MISSENSE MUTATION Y254D IN TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASE (3-BETA-HSD) GENE OF A FEMALE-PATIENT WITH NONSALT-LOSING 3-BETA-HSD DEFICIENCY
Authors: SANCHEZ R RHEAUME E LAFLAMME N ROSENFIELD RL LABRIE F SIMARD J
Citation: R. Sanchez et al., DETECTION AND FUNCTIONAL-CHARACTERIZATION OF THE NOVEL MISSENSE MUTATION Y254D IN TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASE (3-BETA-HSD) GENE OF A FEMALE-PATIENT WITH NONSALT-LOSING 3-BETA-HSD DEFICIENCY, The Journal of clinical endocrinology and metabolism, 78(3), 1994, pp. 561-567
MOLECULAR-BASIS OF CONGENITAL ADRENAL-HYPERPLASIA DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY
Authors: SIMARD J RHEAUME E SANCHEZ R LAFLAMME N DELAUNOIT Y LUUTHE V VANSETERS AP GORDON RD BETTENDORF M HEINRICH U MOSHANG T NEW MI LABRIE F
Citation: J. Simard et al., MOLECULAR-BASIS OF CONGENITAL ADRENAL-HYPERPLASIA DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY, Molecular endocrinology, 7(5), 1993, pp. 716-728
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