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M Lobaccaro

Showing results (21-30 of 51) with videos related to

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Molecular and Cellular Endocrinology|April 25, 1997
Trafficking of the androgen receptor in living cells with fused green fluorescent protein-androgen receptorV Georget, J M Lobaccaro, B Terouanne, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1993
[Familial form of partial androgen insensitivity (Reifenstein syndrome): arginine-histidine mutation in position 840 in the androgen receptor]S Lumbroso, J M Lobaccaro, C Belon, et al.
Clinical Endocrinology|August 1, 1995
A new deletion of the 5 alpha-reductase type 2 gene in a Turkish family with 5 alpha-reductase deficiencyC Boudon, J M Lobaccaro, S Lumbroso, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|December 1, 1995
5 alpha-reductase activity in cultured epithelial and stromal cells from normal and hyperplastic human prostates--effect of finasteride (Proscar), a 5 alpha-reductase inhibitorC Boudon, J M Lobaccaro, S Lumbroso, et al.
Hormone Research|January 1, 1992
Molecular analysis of the sex-determining region from the Y chromosome in two patients with Frasier syndromeP Berta, D Morin, F Poulat, et al.
Annales D'Endocrinologie|January 1, 1997
[5 alpha-reductase and prostate]J M Lobaccaro, C Boudon, S Lumbroso, et al.
European Journal of Endocrinology|April 1, 1994
Molecular prenatal exclusion of familial partial androgen insensitivity (Reifenstein syndrome)S Lumbroso, J M Lobaccaro, C Belon, et al.
Endocrinology|January 14, 1999
Transcriptional interferences between normal or mutant androgen receptors and the activator protein 1--dissection of the androgen receptor functional domainsJ M Lobaccaro, N Poujol, B Térouanne, et al.
The Journal of Biological Chemistry|May 9, 2000
Human white/murine ABC8 mRNA levels are highly induced in lipid-loaded macrophages. A transcriptional role for specific oxysterolsA Venkateswaran, J J Repa, J M Lobaccaro, et al.
Molecular and Cellular Endocrinology|April 28, 1995
Complete androgen insensitivity syndrome due to a new frameshift deletion in exon 4 of the androgen receptor gene: functional analysis of the mutant receptorJ M Lobaccaro, S Lumbroso, N Poujol, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
Molecular and Cellular Endocrinology|April 25, 1997
Trafficking of the androgen receptor in living cells with fused green fluorescent protein-androgen receptorV Georget, J M Lobaccaro, B Terouanne, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1993
[Familial form of partial androgen insensitivity (Reifenstein syndrome): arginine-histidine mutation in position 840 in the androgen receptor]S Lumbroso, J M Lobaccaro, C Belon, et al.
Clinical Endocrinology|August 1, 1995
A new deletion of the 5 alpha-reductase type 2 gene in a Turkish family with 5 alpha-reductase deficiencyC Boudon, J M Lobaccaro, S Lumbroso, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|December 1, 1995
5 alpha-reductase activity in cultured epithelial and stromal cells from normal and hyperplastic human prostates--effect of finasteride (Proscar), a 5 alpha-reductase inhibitorC Boudon, J M Lobaccaro, S Lumbroso, et al.
Hormone Research|January 1, 1992
Molecular analysis of the sex-determining region from the Y chromosome in two patients with Frasier syndromeP Berta, D Morin, F Poulat, et al.
Annales D'Endocrinologie|January 1, 1997
[5 alpha-reductase and prostate]J M Lobaccaro, C Boudon, S Lumbroso, et al.
European Journal of Endocrinology|April 1, 1994
Molecular prenatal exclusion of familial partial androgen insensitivity (Reifenstein syndrome)S Lumbroso, J M Lobaccaro, C Belon, et al.
Endocrinology|January 14, 1999
Transcriptional interferences between normal or mutant androgen receptors and the activator protein 1--dissection of the androgen receptor functional domainsJ M Lobaccaro, N Poujol, B Térouanne, et al.
The Journal of Biological Chemistry|May 9, 2000
Human white/murine ABC8 mRNA levels are highly induced in lipid-loaded macrophages. A transcriptional role for specific oxysterolsA Venkateswaran, J J Repa, J M Lobaccaro, et al.
Molecular and Cellular Endocrinology|April 28, 1995
Complete androgen insensitivity syndrome due to a new frameshift deletion in exon 4 of the androgen receptor gene: functional analysis of the mutant receptorJ M Lobaccaro, S Lumbroso, N Poujol, et al.
Pageof 6