Androgens inhibit the proliferation of a variant of the human prostate cancer cell line LNCaP
Joly-Pharaboz, Marie-O., Soave, Marie-C., Nicolas, Brigitte, Mebarki, Farida, Renaud, Mélanie, Foury, Olivier, Morel, Yves, Andre, Jean G.
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Published in The Journal of steroid biochemistry and molecular biology (01.10.1995)
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Genome Sequence of the Atypical Symbiotic Frankia R43 Strain, a Nitrogen-Fixing and Hydrogen-Producing Actinobacterium
Pujic, Petar, Bolotin, Alexander, Fournier, Pascale, Sorokin, Alexei, Lapidus, Alla, Richau, Kerstin H, Briolay, Jerome, Mebarki, Farida, Normand, Philippe, Sellstedt, Anita
Published in Genome announcements (Washington, DC) (25.11.2015)
Published in Genome announcements (Washington, DC) (25.11.2015)
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Partial androgen insensitivity with phenotypic variation caused by androgen receptor mutations that disrupt activation function 2 and the NH 2- and carboxyl-terminal interaction
Quigley, Charmian A., Tan, Jiann-an, He, Bin, Zhou, Zhong-xun, Mebarki, Farida, Morel, Yves, Forest, Maguelone G., Chatelain, Pierre, Ritzén, E. Martin, French, Frank S., Wilson, Elizabeth M.
Published in Mechanisms of ageing and development (01.10.2004)
Published in Mechanisms of ageing and development (01.10.2004)
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Partial androgen insensitivity with phenotypic variation caused by androgen receptor mutations that disrupt activation function 2 and the NH2- and carboxyl-terminal interaction
Quigley, Charmian A., Tan, Jiann-an, He, Bin, Zhou, Zhong-xun, Mebarki, Farida, Morel, Yves, Forest, Maguelone G., Chatelain, Pierre, Ritzén, E. Martin, French, Frank S., Wilson, Elizabeth M.
Published in Mechanisms of ageing and development (01.10.2004)
Published in Mechanisms of ageing and development (01.10.2004)
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Congenital adrenal hyperplasia due to point mutations in the type II 3β-hydroxysteroid dehydrogenase gene
Rhéaume, Eric, Forest, Maguelone G, Labrie, Fernand, Morel, Yves, Simard, Jacques, Zachmann, Milo, Mebarki, Farida, New, Maria I
Published in Nature genetics (01.07.1992)
Published in Nature genetics (01.07.1992)
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Different phenotypes in a family with androgen insensitivity caused by the same M780I point mutation in the androgen receptor gene
RODIEN, P, MEBARKI, F, MOWSZOWICZ, I, CHAUSSAIN, J.-L, YOUNG, J, MOREL, Y, SCHAISON, G
Published in The journal of clinical endocrinology and metabolism (01.08.1996)
Published in The journal of clinical endocrinology and metabolism (01.08.1996)
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Anti-müllerian hormone in children with androgen insensitivity
Rey, R, Mebarki, F, Forest, M G, Mowszowicz, I, Cate, R L, Morel, Y, Chaussain, J L, Josso, N
Published in The journal of clinical endocrinology and metabolism (01.10.1994)
Published in The journal of clinical endocrinology and metabolism (01.10.1994)
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Partial androgen insensitivity with phenotypic variation caused by androgen receptor mutations that disrupt activation function 2 and the NH2- and carboxyl-terminal interaction: Hormone receptors, genes, ageing and Arun Roy: A tribute to Professor Arun K. Roy
QUIGLEY, Charmian A, TAN, Jiann-An, WILSON, Elizabeth M, BIN HE, ZHOU, Zhong-Xun, MEBARKI, Farida, MOREL, Yves, FOREST, Maguelone G, CHATELAIN, Pierre, RITZEN, E. Martin, FRENCH, Frank S
Published in Mechanisms of ageing and development (2004)
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Published in Mechanisms of ageing and development (2004)
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Molecular basis of human 3β-hydroxysteroid dehydrogenase deficiency
Simard, Jacques, Rheaume, Eric, Mebarki, Farida, Sanchez, Rocio, New, Maria I., Morel, Yves, Labrie, Fernand
Published in Journal of steroid biochemistry and molecular biology (01.06.1995)
Published in Journal of steroid biochemistry and molecular biology (01.06.1995)
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Conference Proceeding
Partial androgen insensitivity with phenotypic variation caused by androgen receptor mutations that disrupt activation function 2 and the NH(2)- and carboxyl-terminal interaction
Quigley, Charmian A, Tan, Jiann-an, He, Bin, Zhou, Zhong-xun, Mebarki, Farida, Morel, Yves, Forest, Maguelone G, Chatelain, Pierre, Ritzén, E Martin, French, Frank S, Wilson, Elizabeth M
Published in Mechanisms of ageing and development (01.10.2004)
Published in Mechanisms of ageing and development (01.10.2004)
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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
Rhéaume, E, Sanchez, R, Mébarki, F, Gagnon, E, Carel, J C, Chaussain, J L, Morel, Y, Labrie, F, Simard, J
Published in Biochemistry (Easton) (07.03.1995)
Published in Biochemistry (Easton) (07.03.1995)
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Structure-function relationships and molecular genetics of the 3β-hydroxysteroid dehydrogenase gene family
Simard, Jacques, Sanchez, Rocio, Durocher, Francine, Rhéaume, Eric, Turgeon, Carl, Labrie, Yvan, Luu-The, Van, Mebarki, Farida, Morel, Yves, de Launoit, Yvan, Labrie, Fernand
Published in Journal of steroid biochemistry and molecular biology (01.12.1995)
Published in Journal of steroid biochemistry and molecular biology (01.12.1995)
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Conference Proceeding
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
Rheaume, Eric, Sanchez, Rocio, Mebarki, Farida, Gagnon, Eve, Carel, Jean-Claude, Chaussain, Jean-Louis, Morel, Yves, Labrie, Fernand, Simard, Jacques
Published in Biochemistry (Easton) (01.03.1995)
Published in Biochemistry (Easton) (01.03.1995)
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New insight into the molecular basis of 3β-hydroxysteroid dehydrogenase deficiency: Identification of eight mutations in the HSD3B2 gene in eleven patients from seven new families and comparison of the functional properties of twenty-five mutant enzymes
MOISAN, A. M, RICKETTS, M. L, PETER, M, MOREL, Y, SIMARD, J, TARDY, V, DESROCHERS, M, MEBARKI, F, CHAUSSAIN, J.-L, CABROL, S, RAUX-DEMAY, M. C, FOREST, M. G, SIPPELL, W. G
Published in The journal of clinical endocrinology and metabolism (1999)
Published in The journal of clinical endocrinology and metabolism (1999)
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Structure-function relationships of 3β-hydroxysteroid dehydrogenase: Contribution made by the molecular genetics of 3β-hydroxysteroid dehydrogenase deficiency
Morel, Yves, Mébarki, Farida, Rhéaume, Eric, Sanchez, Rocio, Forest, Maguelone G., Simard, Jacques
Published in Steroids (1997)
Published in Steroids (1997)
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Conference Proceeding
Nonsalt-losing male pseudohermaphroditism due to the novel homozygous N100S mutation in the type II 3 beta-hydroxysteroid dehydrogenase gene
Mébarki, F, Sanchez, R, Rhéaume, E, Laflamme, N, Simard, J, Forest, M G, Bey-Omar, F, David, M, Labrie, F, Morel, Y
Published in The journal of clinical endocrinology and metabolism (01.07.1995)
Published in The journal of clinical endocrinology and metabolism (01.07.1995)
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New Insight into the Molecular Basis of 3β-Hydroxysteroid Dehydrogenase Deficiency: Identification of Eight Mutations in the HSD3B2 Gene in Eleven Patients from Seven New Families and Comparison of the Functional Properties of Twenty-Five Mutant Enzymes1
Moisan, Anne Marie, Ricketts, Marie Louise, Tardy, Véronique, Desrochers, Marc, Mébarki, Farida, Chaussain, Jean-Louis, Cabrol, Sylvie, Raux-Demay, Marie Charles, Forest, Maguelone G, Sippell, Wolfgang G, Peter, Michael, Morel, Yves, Simard, Jacques
Published in The journal of clinical endocrinology and metabolism (01.12.1999)
Published in The journal of clinical endocrinology and metabolism (01.12.1999)
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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
Sanchez, R, Mébarki, F, Rhéaume, E, Laflamme, N, Forest, M G, Bey-Omard, F, David, M, Morel, Y, Labrie, F, Simard, J
Published in Human molecular genetics (01.09.1994)
Published in Human molecular genetics (01.09.1994)
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