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Results: 1-12 |
Results: 12
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
DIFFERENT PHENOTYPES IN A FAMILY WITH ANDROGEN INSENSITIVITY CAUSED BY THE SAME M780I POINT MUTATION IN THE ANDROGEN RECEPTOR GENE
Authors: RODIEN P MEBARKI F MOWSZOWICZ I CHAUSSAIN JL YOUNG J MOREL Y SCHAISON G
Citation: P. Rodien et al., DIFFERENT PHENOTYPES IN A FAMILY WITH ANDROGEN INSENSITIVITY CAUSED BY THE SAME M780I POINT MUTATION IN THE ANDROGEN RECEPTOR GENE, The Journal of clinical endocrinology and metabolism, 81(8), 1996, pp. 2994-2998
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
ANDROGENS INHIBIT THE PROLIFERATION OF A VARIANT OF THE HUMAN PROSTATE-CANCER CELL-LINE LNCAP
Authors: JOLYPHARABOZ MO SOAVE MC NICOLAS B MEBARKI F RENAUD M FOURY O MOREL Y ANDRE JG
Citation: Mo. Jolypharaboz et al., ANDROGENS INHIBIT THE PROLIFERATION OF A VARIANT OF THE HUMAN PROSTATE-CANCER CELL-LINE LNCAP, Journal of steroid biochemistry and molecular biology, 55(1), 1995, pp. 67-76
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
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
WHAT ARE THE INDICATIONS FOR PRENATAL-DIAGNOSIS IN THE ANDROGEN INSENSITIVITY SYNDROME - FACING CLINICAL HETEROGENEITY OF PHENOTYPES FOR THE SAME GENOTYPE
Authors: MOREL Y MEBARKI F FOREST MG
Citation: Y. Morel et al., WHAT ARE THE INDICATIONS FOR PRENATAL-DIAGNOSIS IN THE ANDROGEN INSENSITIVITY SYNDROME - FACING CLINICAL HETEROGENEITY OF PHENOTYPES FOR THE SAME GENOTYPE, European journal of endocrinology, 130(4), 1994, pp. 325-326
ANTI-MULLERIAN HORMONE IN CHILDREN WITH ANDROGEN INSENSITIVITY
Authors: REY R MEBARKI F FOREST MG MOWSZOWICZ I CATE RL MOREL Y CHAUSSAIN JL JOSSO N
Citation: R. Rey et al., ANTI-MULLERIAN HORMONE IN CHILDREN WITH ANDROGEN INSENSITIVITY, The Journal of clinical endocrinology and metabolism, 79(4), 1994, pp. 960-964
ANTI-MULLERIAN HORMONE IN CHILDREN WITH ANDROGEN INSENSITIVITY
Authors: REY R MEBARKI F FOREST MG MOWSZOWICZ I CATE RL MOREL Y CHAUSSAIN JL JOSSO N
Citation: R. Rey et al., ANTI-MULLERIAN HORMONE IN CHILDREN WITH ANDROGEN INSENSITIVITY, The Journal of clinical endocrinology and metabolism, 79(4), 1994, pp. 960-964
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