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J Simard

Showing results (201-210 of 314) with videos related to

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Molecular and Cellular Endocrinology|April 28, 1995
Occurrence of cytochrome P450c17 mRNA and dehydroepiandrosterone biosynthesis in the rat gastrointestinal tractL Dalla Valle, J Couët, Y Labrie, et al.
Endocrine Research|February 24, 2001
A new insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiencyJ Simard, M L Ricketts, A M Moisan, et al.
Molecular Endocrinology (Baltimore, Md.)|April 1, 1989
Inhibitory effect of estrogens on GCDFP-15 mRNA levels and secretion in ZR-75-1 human breast cancer cellsJ Simard, A C Hatton, C Labrie, et al.
Atherosclerosis|April 20, 1999
Fine mapping of low-density lipoprotein receptor gene by genetic linkage on chromosome 19p13.1-p13.3 and study of the founder effect of four French Canadian low-density lipoprotein receptor gene mutationsP Couture, J Morissette, D Gaudet, et al.
The Journal of Clinical Endocrinology and Metabolism|June 8, 2000
A novel A10E homozygous mutation in the HSD3B2 gene causing severe salt-wasting 3beta-hydroxysteroid dehydrogenase deficiency in 46,XX and 46,XY French-Canadians: evaluation of gonadal function after pubertyN Alos, A M Moisan, L Ward, et al.
Aging|October 19, 2012
Down regulation of miR-124 in both Werner syndrome DNA helicase mutant mice and mutant Caenorhabditis elegans wrn-1 reveals the importance of this microRNA in accelerated agingAlexandra Dallaire, Chantal Garand, Eric R Paquel, et al.
EMBO Reports|September 15, 2023
Casein kinase 1 and 2 phosphorylate Argonaute proteins to regulate miRNA-mediated gene silencingVivek Nilesh Shah, Julia Neumeier, Miguel Quévillon Huberdeau, 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.
Molecular and Cellular Endocrinology|February 1, 1991
Characterization of macaque 3 beta-hydroxy-5-ene steroid dehydrogenase/delta 5-delta 4 isomerase: structure and expression in steroidogenic and peripheral tissues in primateJ Simard, M H Melner, N Breton, et al.
Current Biology : CB|February 23, 2005
A member of the polymerase beta nucleotidyltransferase superfamily is required for RNA interference in C. elegansChun-Chieh G Chen, Martin J Simard, Hiroaki Tabara, et al.
Pageof 32

Showing results (201-210 of 314) with videos related to

Sort By:
Pageof 32
Molecular and Cellular Endocrinology|April 28, 1995
Occurrence of cytochrome P450c17 mRNA and dehydroepiandrosterone biosynthesis in the rat gastrointestinal tractL Dalla Valle, J Couët, Y Labrie, et al.
Endocrine Research|February 24, 2001
A new insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiencyJ Simard, M L Ricketts, A M Moisan, et al.
Molecular Endocrinology (Baltimore, Md.)|April 1, 1989
Inhibitory effect of estrogens on GCDFP-15 mRNA levels and secretion in ZR-75-1 human breast cancer cellsJ Simard, A C Hatton, C Labrie, et al.
Atherosclerosis|April 20, 1999
Fine mapping of low-density lipoprotein receptor gene by genetic linkage on chromosome 19p13.1-p13.3 and study of the founder effect of four French Canadian low-density lipoprotein receptor gene mutationsP Couture, J Morissette, D Gaudet, et al.
The Journal of Clinical Endocrinology and Metabolism|June 8, 2000
A novel A10E homozygous mutation in the HSD3B2 gene causing severe salt-wasting 3beta-hydroxysteroid dehydrogenase deficiency in 46,XX and 46,XY French-Canadians: evaluation of gonadal function after pubertyN Alos, A M Moisan, L Ward, et al.
Aging|October 19, 2012
Down regulation of miR-124 in both Werner syndrome DNA helicase mutant mice and mutant Caenorhabditis elegans wrn-1 reveals the importance of this microRNA in accelerated agingAlexandra Dallaire, Chantal Garand, Eric R Paquel, et al.
EMBO Reports|September 15, 2023
Casein kinase 1 and 2 phosphorylate Argonaute proteins to regulate miRNA-mediated gene silencingVivek Nilesh Shah, Julia Neumeier, Miguel Quévillon Huberdeau, 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.
Molecular and Cellular Endocrinology|February 1, 1991
Characterization of macaque 3 beta-hydroxy-5-ene steroid dehydrogenase/delta 5-delta 4 isomerase: structure and expression in steroidogenic and peripheral tissues in primateJ Simard, M H Melner, N Breton, et al.
Current Biology : CB|February 23, 2005
A member of the polymerase beta nucleotidyltransferase superfamily is required for RNA interference in C. elegansChun-Chieh G Chen, Martin J Simard, Hiroaki Tabara, et al.
Pageof 32