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S Lumbroso

Showing results (41-50 of 66) with videos related to

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European Journal of Endocrinology|May 1, 1996
Immunohistochemical localization and immunoblotting of androgen receptor in spinal neurons of male and female ratsS Lumbroso, F Sandillon, V Georget, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2001
Macroorchidism due to autonomous hyperfunction of Sertoli cells and G(s)alpha gene mutation: an unusual expression of McCune-Albright syndrome in a prepubertal boyR Coutant, S Lumbroso, R Rey, et al.
Hormone Research|January 1, 1997
Molecular analysis of the androgen receptor gene in Kennedy's disease. Report of two families and review of the literatureS Lumbroso, J M Lobaccaro, C Vial, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1995
[Genetics and endocrinology of male sex differentiation: application to molecular study of male pseudohermaphroditism]C Sultan, S Lumbroso, N Poujol, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|June 1, 1996
Effect of finasteride (Proscar) on the proliferation of cultured epithelial and stromal cells from normal and hyperplastic human prostatesJ M Lobaccaro, C Boudon, E Lechevallier, et al.
Journal of Molecular Endocrinology|June 3, 2004
A new mutation of the androgen receptor, P817A, causing partial androgen insensitivity syndrome: in vitro and structural analysisS Lumbroso, A Wagschal, W Bourguet, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1995
Molecular study of the 5 alpha-reductase type 2 gene in three European families with 5 alpha-reductase deficiencyC Boudon, S Lumbroso, J M Lobaccaro, et al.
Human Reproduction Update|June 8, 2001
Disorders linked to insufficient androgen action in male childrenC Sultan, F Paris, B Terouanne, et al.
Journal of Endocrinological Investigation|June 1, 2010
The IVS1-2A>G mutation in the SRD5A2 gene predominates in Cypriot patients with 5α reductase deficiencyN Skordis, V Neocleous, A Kyriakou, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1996
A novel substitution (Leu707Arg) in exon 4 of the androgen receptor gene causes complete androgen resistanceS Lumbroso, J M Lobaccaro, V Georget, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
European Journal of Endocrinology|May 1, 1996
Immunohistochemical localization and immunoblotting of androgen receptor in spinal neurons of male and female ratsS Lumbroso, F Sandillon, V Georget, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2001
Macroorchidism due to autonomous hyperfunction of Sertoli cells and G(s)alpha gene mutation: an unusual expression of McCune-Albright syndrome in a prepubertal boyR Coutant, S Lumbroso, R Rey, et al.
Hormone Research|January 1, 1997
Molecular analysis of the androgen receptor gene in Kennedy's disease. Report of two families and review of the literatureS Lumbroso, J M Lobaccaro, C Vial, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1995
[Genetics and endocrinology of male sex differentiation: application to molecular study of male pseudohermaphroditism]C Sultan, S Lumbroso, N Poujol, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|June 1, 1996
Effect of finasteride (Proscar) on the proliferation of cultured epithelial and stromal cells from normal and hyperplastic human prostatesJ M Lobaccaro, C Boudon, E Lechevallier, et al.
Journal of Molecular Endocrinology|June 3, 2004
A new mutation of the androgen receptor, P817A, causing partial androgen insensitivity syndrome: in vitro and structural analysisS Lumbroso, A Wagschal, W Bourguet, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1995
Molecular study of the 5 alpha-reductase type 2 gene in three European families with 5 alpha-reductase deficiencyC Boudon, S Lumbroso, J M Lobaccaro, et al.
Human Reproduction Update|June 8, 2001
Disorders linked to insufficient androgen action in male childrenC Sultan, F Paris, B Terouanne, et al.
Journal of Endocrinological Investigation|June 1, 2010
The IVS1-2A>G mutation in the SRD5A2 gene predominates in Cypriot patients with 5α reductase deficiencyN Skordis, V Neocleous, A Kyriakou, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1996
A novel substitution (Leu707Arg) in exon 4 of the androgen receptor gene causes complete androgen resistanceS Lumbroso, J M Lobaccaro, V Georget, et al.
Pageof 7