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N de Roux

Showing results (11-20 of 22) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|October 1, 1996
Analysis of the thyrotropin receptor as a candidate gene in familial Graves' diseaseN de Roux, D C Shields, M Misrahi, et al.
Journal of Cardiovascular Pharmacology|January 1, 1990
Pathophysiological role of the vascular smooth muscle cellJ B Michel, N De Roux, D Plissonnier, et al.
The Journal of Clinical Endocrinology and Metabolism|June 1, 1996
A neomutation of the thyroid-stimulating hormone receptor in a severe neonatal hyperthyroidismN de Roux, M Polak, J Couet, et al.
Gut|July 17, 2003
Lack of association between HFE gene mutations and hepatocellular carcinoma in patients with cirrhosisV Boige, L Castéra, N de Roux, et al.
Hormone Research|January 1, 1997
Gonadotrophin and thyrotrophin receptorsE Milgrom, N de Roux, N Ghinea, et al.
European Journal of Endocrinology|September 2, 1998
Absence of activating mutations in the GnRH receptor gene in human pituitary gonadotroph adenomasP Chanson, N De Roux, J Young, et al.
Annales D'Endocrinologie|August 24, 1999
Gonadotropin receptorsM V Hai, N De Roux, N Ghinea, et al.
Neurology|April 25, 2008
The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndromeJ Nectoux, N Bahi-Buisson, I Guellec, et al.
Human Molecular Genetics|May 18, 2000
MECP2 mutations account for most cases of typical forms of Rett syndromeT Bienvenu, A Carrié, N de Roux, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1996
Four families with loss of function mutations of the thyrotropin receptorN de Roux, M Misrahi, R Brauner, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
The Journal of Clinical Endocrinology and Metabolism|October 1, 1996
Analysis of the thyrotropin receptor as a candidate gene in familial Graves' diseaseN de Roux, D C Shields, M Misrahi, et al.
Journal of Cardiovascular Pharmacology|January 1, 1990
Pathophysiological role of the vascular smooth muscle cellJ B Michel, N De Roux, D Plissonnier, et al.
The Journal of Clinical Endocrinology and Metabolism|June 1, 1996
A neomutation of the thyroid-stimulating hormone receptor in a severe neonatal hyperthyroidismN de Roux, M Polak, J Couet, et al.
Gut|July 17, 2003
Lack of association between HFE gene mutations and hepatocellular carcinoma in patients with cirrhosisV Boige, L Castéra, N de Roux, et al.
Hormone Research|January 1, 1997
Gonadotrophin and thyrotrophin receptorsE Milgrom, N de Roux, N Ghinea, et al.
European Journal of Endocrinology|September 2, 1998
Absence of activating mutations in the GnRH receptor gene in human pituitary gonadotroph adenomasP Chanson, N De Roux, J Young, et al.
Annales D'Endocrinologie|August 24, 1999
Gonadotropin receptorsM V Hai, N De Roux, N Ghinea, et al.
Neurology|April 25, 2008
The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndromeJ Nectoux, N Bahi-Buisson, I Guellec, et al.
Human Molecular Genetics|May 18, 2000
MECP2 mutations account for most cases of typical forms of Rett syndromeT Bienvenu, A Carrié, N de Roux, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1996
Four families with loss of function mutations of the thyrotropin receptorN de Roux, M Misrahi, R Brauner, et al.
Pageof 3