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Y Morel

Showing results (101-110 of 138) with videos related to

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Clinical Genetics|November 22, 2008
Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney diseaseL Michel-Calemard, F Dijoud, M Till, et al.
The Journal of Biological Chemistry|December 5, 1989
Regulation of the gene for estrogenic 17-ketosteroid reductase lying on chromosome 17cen----q25Y Tremblay, G E Ringler, Y Morel, et al.
The Journal of Clinical Endocrinology and Metabolism|June 6, 2003
Follow-up of 68 children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: relevance of genotype for managementG Pinto, V Tardy, C Trivin, et al.
Hormone Research|September 6, 2000
Mutational analysis in Lebanese patients with congenital adrenal hyperplasia due to a deficit in 21-hydroxylaseV Delague, N Souraty, E Khallouf, et al.
Nature Genetics|July 1, 1992
Congenital adrenal hyperplasia due to point mutations in the type II 3 beta-hydroxysteroid dehydrogenase geneE Rhéaume, J Simard, Y Morel, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1989
Gene conversions and rearrangements cause discordance between inheritance of forms of 21-hydroxylase deficiency and HLA typesY Morel, M David, M G Forest, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1994
Anti-müllerian hormone in children with androgen insensitivityR Rey, F Mebarki, M G Forest, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1998
Isolated aldosterone synthase deficiency caused by simultaneous E198D and V386A mutations in the CYP11B2 geneS Portrat-Doyen, J Tourniaire, O Richard, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1988
Human adrenodoxin reductase: two mRNAs encoded by a single gene on chromosome 17cen----q25 are expressed in steroidogenic tissuesS B Solish, J Picado-Leonard, Y Morel, et al.
The Journal of Steroid Biochemistry and Molecular Biology|October 1, 1995
Androgens inhibit the proliferation of a variant of the human prostate cancer cell line LNCaPM O Joly-Pharaboz, M C Soave, B Nicolas, et al.
Pageof 14

Showing results (101-110 of 138) with videos related to

Sort By:
Pageof 14
Clinical Genetics|November 22, 2008
Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney diseaseL Michel-Calemard, F Dijoud, M Till, et al.
The Journal of Biological Chemistry|December 5, 1989
Regulation of the gene for estrogenic 17-ketosteroid reductase lying on chromosome 17cen----q25Y Tremblay, G E Ringler, Y Morel, et al.
The Journal of Clinical Endocrinology and Metabolism|June 6, 2003
Follow-up of 68 children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: relevance of genotype for managementG Pinto, V Tardy, C Trivin, et al.
Hormone Research|September 6, 2000
Mutational analysis in Lebanese patients with congenital adrenal hyperplasia due to a deficit in 21-hydroxylaseV Delague, N Souraty, E Khallouf, et al.
Nature Genetics|July 1, 1992
Congenital adrenal hyperplasia due to point mutations in the type II 3 beta-hydroxysteroid dehydrogenase geneE Rhéaume, J Simard, Y Morel, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1989
Gene conversions and rearrangements cause discordance between inheritance of forms of 21-hydroxylase deficiency and HLA typesY Morel, M David, M G Forest, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1994
Anti-müllerian hormone in children with androgen insensitivityR Rey, F Mebarki, M G Forest, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1998
Isolated aldosterone synthase deficiency caused by simultaneous E198D and V386A mutations in the CYP11B2 geneS Portrat-Doyen, J Tourniaire, O Richard, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1988
Human adrenodoxin reductase: two mRNAs encoded by a single gene on chromosome 17cen----q25 are expressed in steroidogenic tissuesS B Solish, J Picado-Leonard, Y Morel, et al.
The Journal of Steroid Biochemistry and Molecular Biology|October 1, 1995
Androgens inhibit the proliferation of a variant of the human prostate cancer cell line LNCaPM O Joly-Pharaboz, M C Soave, B Nicolas, et al.
Pageof 14