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N De Roux

Showing results (1-10 of 24) with videos related to

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Frontiers of Hormone Research|April 15, 2010
FGFR1 mutations in Kallmann syndromeC Villanueva, N de Roux
Molecular and Cellular Endocrinology|June 23, 2001
Inherited disorders of GnRH and gonadotropin receptorsN de Roux, E Milgrom
Molecular and Cellular Endocrinology|June 8, 2011
GnRH receptor mutations in isolated gonadotropic deficiencyL Chevrier, F Guimiot, N de Roux
La Revue Du Praticien|September 17, 1999
[Genetic anomalies of the gonadotropic axis]N de Roux, Y Morel, J P Hardelin
Annales D'Endocrinologie|February 10, 2009
[Congenital hypogonadotropic hypogonadism]C Roze, P Touraine, J Leger, et al.
Molecular and Cellular Endocrinology|March 25, 1996
Microsatellites and PCR primers for genetic studies and genomic sequencing of the human TSH receptor geneN de Roux, M Misrahi, N Chatelain, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 4, 2000
Loss of function mutations of the GnRH receptor: a new cause of hypogonadotropic hypogonadismN de Roux, J Young, M Misrahi, et al.
British Journal of Haematology|June 1, 1990
Clinical and biochemical characterization of antithrombin III Franconville, a variant with Pro 41 Leu mutationN de Roux, G Chadeuf, P Molho-Sabatier, et al.
The Journal of Biological Chemistry|July 25, 1991
Na+/H+ antiporter gene expression during monocytic differentiation of HL60 cellsG N Rao, N de Roux, C Sardet, et al.
The Journal of Clinical Endocrinology and Metabolism|February 18, 1999
The same molecular defects of the gonadotropin-releasing hormone receptor determine a variable degree of hypogonadism in affected kindredN de Roux, J Young, S Brailly-Tabard, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Frontiers of Hormone Research|April 15, 2010
FGFR1 mutations in Kallmann syndromeC Villanueva, N de Roux
Molecular and Cellular Endocrinology|June 23, 2001
Inherited disorders of GnRH and gonadotropin receptorsN de Roux, E Milgrom
Molecular and Cellular Endocrinology|June 8, 2011
GnRH receptor mutations in isolated gonadotropic deficiencyL Chevrier, F Guimiot, N de Roux
La Revue Du Praticien|September 17, 1999
[Genetic anomalies of the gonadotropic axis]N de Roux, Y Morel, J P Hardelin
Annales D'Endocrinologie|February 10, 2009
[Congenital hypogonadotropic hypogonadism]C Roze, P Touraine, J Leger, et al.
Molecular and Cellular Endocrinology|March 25, 1996
Microsatellites and PCR primers for genetic studies and genomic sequencing of the human TSH receptor geneN de Roux, M Misrahi, N Chatelain, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 4, 2000
Loss of function mutations of the GnRH receptor: a new cause of hypogonadotropic hypogonadismN de Roux, J Young, M Misrahi, et al.
British Journal of Haematology|June 1, 1990
Clinical and biochemical characterization of antithrombin III Franconville, a variant with Pro 41 Leu mutationN de Roux, G Chadeuf, P Molho-Sabatier, et al.
The Journal of Biological Chemistry|July 25, 1991
Na+/H+ antiporter gene expression during monocytic differentiation of HL60 cellsG N Rao, N de Roux, C Sardet, et al.
The Journal of Clinical Endocrinology and Metabolism|February 18, 1999
The same molecular defects of the gonadotropin-releasing hormone receptor determine a variable degree of hypogonadism in affected kindredN de Roux, J Young, S Brailly-Tabard, et al.
Pageof 3