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A Biason-Lauber

Showing results (1-10 of 19) with videos related to

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Molecular Aspects of Medicine|December 10, 1998
Molecular medicine of steroid hormone biosynthesisA Biason-Lauber
European Journal of Clinical Investigation|April 3, 2001
Intra-adrenal regulation of androgen synthesisD l'Allemand, A Biason-Lauber
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|November 7, 2008
WNT4 and sex developmentA Biason-Lauber, D Konrad
American Journal of Human Genetics|October 20, 2000
Apparently normal ovarian differentiation in a prepubertal girl with transcriptionally inactive steroidogenic factor 1 (NR5A1/SF-1) and adrenocortical insufficiencyA Biason-Lauber, E J Schoenle
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
A single amino acid substitution in the putative redox partner-binding site of P450c17 as cause of isolated 17,20-lyase deficiencyA Biason-Lauber, E Leiberman, M Zachmann
Endocrinology|April 4, 2000
Effect of leptin on CYP17 enzymatic activities in human adrenal cells: new insight in the onset of adrenarcheA Biason-Lauber, M Zachmann, E J Schoenle
Journal of Endocrinological Investigation|March 2, 2010
Defects of steroidogenesisA Biason-Lauber, M Boscaro, F Mantero, et al.
BJU International|January 8, 2009
A novel mutation inducing partial androgen-insensitivity syndrome with phenotypic diversityR Gobet, M Lang-Muritano, T Stallmach, et al.
Biochemical and Biophysical Research Communications|July 25, 2000
Genomic structure, chromosomal localization, and expression pattern of the human LIM-homeobox3 (LHX 3) geneS Schmitt, A Biason-Lauber, D Betts, et al.
Hormone Research|January 11, 2001
Apparent cortisone reductase deficiency: a rare cause of hyperandrogenemia and hypercortisolismA Biason-Lauber, S L Suter, C H Shackleton, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Molecular Aspects of Medicine|December 10, 1998
Molecular medicine of steroid hormone biosynthesisA Biason-Lauber
European Journal of Clinical Investigation|April 3, 2001
Intra-adrenal regulation of androgen synthesisD l'Allemand, A Biason-Lauber
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|November 7, 2008
WNT4 and sex developmentA Biason-Lauber, D Konrad
American Journal of Human Genetics|October 20, 2000
Apparently normal ovarian differentiation in a prepubertal girl with transcriptionally inactive steroidogenic factor 1 (NR5A1/SF-1) and adrenocortical insufficiencyA Biason-Lauber, E J Schoenle
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
A single amino acid substitution in the putative redox partner-binding site of P450c17 as cause of isolated 17,20-lyase deficiencyA Biason-Lauber, E Leiberman, M Zachmann
Endocrinology|April 4, 2000
Effect of leptin on CYP17 enzymatic activities in human adrenal cells: new insight in the onset of adrenarcheA Biason-Lauber, M Zachmann, E J Schoenle
Journal of Endocrinological Investigation|March 2, 2010
Defects of steroidogenesisA Biason-Lauber, M Boscaro, F Mantero, et al.
BJU International|January 8, 2009
A novel mutation inducing partial androgen-insensitivity syndrome with phenotypic diversityR Gobet, M Lang-Muritano, T Stallmach, et al.
Biochemical and Biophysical Research Communications|July 25, 2000
Genomic structure, chromosomal localization, and expression pattern of the human LIM-homeobox3 (LHX 3) geneS Schmitt, A Biason-Lauber, D Betts, et al.
Hormone Research|January 11, 2001
Apparent cortisone reductase deficiency: a rare cause of hyperandrogenemia and hypercortisolismA Biason-Lauber, S L Suter, C H Shackleton, et al.
Pageof 2