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D Naville

Showing results (41-50 of 47) with videos related to

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Journal of Molecular Medicine (Berlin, Germany)|July 12, 2002
Functional relationships between three novel homozygous mutations in the ACTH receptor gene and familial glucocorticoid deficiencyA Penhoat, D Naville, H El Mourabit, et al.
Endocrinology|October 1, 1990
Transforming growth factor-beta inhibits steroid 17 alpha-hydroxylase cytochrome P-450 expression in ovine adrenocortical cellsW E Rainey, D Naville, J M Saez, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1996
Demonstration by transfection studies that mutations in the adrenocorticotropin receptor gene are one cause of the hereditary syndrome of glucocorticoid deficiencyD Naville, L Barjhoux, C Jaillard, et al.
Molecular and Cellular Endocrinology|September 1, 1991
3 beta-hydroxysteroid dehydrogenase/delta 5----4-isomerase expression in rat and characterization of the testis isoformM C Lorence, D Naville, S E Graham-Lorence, et al.
Endocrinology|September 10, 2003
Study of the alteration of gene expression in adipose tissue of diet-induced obese mice by microarray and reverse transcription-polymerase chain reaction analysesR C Moraes, A Blondet, K Birkenkamp-Demtroeder, et al.
The Journal of Steroid Biochemistry and Molecular Biology|December 1, 1993
Regulation of expression of the 3 beta-hydroxysteroid dehydrogenases of human placenta and fetal adrenalJ I Mason, K Ushijima, K M Doody, et al.
Nature Genetics|November 4, 2000
Mutant WD-repeat protein in triple-A syndromeA Tullio-Pelet, R Salomon, S Hadj-Rabia, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Journal of Molecular Medicine (Berlin, Germany)|July 12, 2002
Functional relationships between three novel homozygous mutations in the ACTH receptor gene and familial glucocorticoid deficiencyA Penhoat, D Naville, H El Mourabit, et al.
Endocrinology|October 1, 1990
Transforming growth factor-beta inhibits steroid 17 alpha-hydroxylase cytochrome P-450 expression in ovine adrenocortical cellsW E Rainey, D Naville, J M Saez, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1996
Demonstration by transfection studies that mutations in the adrenocorticotropin receptor gene are one cause of the hereditary syndrome of glucocorticoid deficiencyD Naville, L Barjhoux, C Jaillard, et al.
Molecular and Cellular Endocrinology|September 1, 1991
3 beta-hydroxysteroid dehydrogenase/delta 5----4-isomerase expression in rat and characterization of the testis isoformM C Lorence, D Naville, S E Graham-Lorence, et al.
Endocrinology|September 10, 2003
Study of the alteration of gene expression in adipose tissue of diet-induced obese mice by microarray and reverse transcription-polymerase chain reaction analysesR C Moraes, A Blondet, K Birkenkamp-Demtroeder, et al.
The Journal of Steroid Biochemistry and Molecular Biology|December 1, 1993
Regulation of expression of the 3 beta-hydroxysteroid dehydrogenases of human placenta and fetal adrenalJ I Mason, K Ushijima, K M Doody, et al.
Nature Genetics|November 4, 2000
Mutant WD-repeat protein in triple-A syndromeA Tullio-Pelet, R Salomon, S Hadj-Rabia, et al.
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