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C Jaillard

Showing results (31-40 of 38) with videos related to

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Journal of Molecular Endocrinology|December 1, 1991
ACTH and angiotensin II regulation of insulin-like growth factor-I and its binding proteins in cultured bovine adrenal cellsA Penhoat, P Leduque, C Jaillard, et al.
Endocrine Research|November 1, 1996
Characterization of the human ACTH receptor gene and in vitro expressionD Naville, A Penhoat, L Barjhoux, et al.
Annales D'Endocrinologie|January 1, 1996
[Mutations of ACTH receptor gene and familial syndrome of glucocorticoid deficiency]D Naville, L Barjhoux, C Jaillard, 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.
Nature Genetics|August 31, 2001
Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndromeB Moghadaszadeh, N Petit, C Jaillard, et al.
Cell Death and Differentiation|February 9, 2010
The disruption of the rod-derived cone viability gene leads to photoreceptor dysfunction and susceptibility to oxidative stressT Cronin, W Raffelsberger, I Lee-Rivera, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 11, 2005
Edg8/S1P5: an oligodendroglial receptor with dual function on process retraction and cell survivalC Jaillard, S Harrison, B Stankoff, et al.
Brain Research. Molecular Brain Research|February 20, 2003
Molecular cloning and characterisation of a novel GABAB-related G-protein coupled receptorA R Calver, D Michalovich, T T Testa, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Journal of Molecular Endocrinology|December 1, 1991
ACTH and angiotensin II regulation of insulin-like growth factor-I and its binding proteins in cultured bovine adrenal cellsA Penhoat, P Leduque, C Jaillard, et al.
Endocrine Research|November 1, 1996
Characterization of the human ACTH receptor gene and in vitro expressionD Naville, A Penhoat, L Barjhoux, et al.
Annales D'Endocrinologie|January 1, 1996
[Mutations of ACTH receptor gene and familial syndrome of glucocorticoid deficiency]D Naville, L Barjhoux, C Jaillard, 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.
Nature Genetics|August 31, 2001
Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndromeB Moghadaszadeh, N Petit, C Jaillard, et al.
Cell Death and Differentiation|February 9, 2010
The disruption of the rod-derived cone viability gene leads to photoreceptor dysfunction and susceptibility to oxidative stressT Cronin, W Raffelsberger, I Lee-Rivera, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 11, 2005
Edg8/S1P5: an oligodendroglial receptor with dual function on process retraction and cell survivalC Jaillard, S Harrison, B Stankoff, et al.
Brain Research. Molecular Brain Research|February 20, 2003
Molecular cloning and characterisation of a novel GABAB-related G-protein coupled receptorA R Calver, D Michalovich, T T Testa, et al.
Pageof 4