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P M Holterhus

Showing results (21-30 of 42) with videos related to

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Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|March 12, 2009
Mutation analysis of FOXF2 in patients with disorders of sex development (DSD) in combination with cleft palateU Jochumsen, R Werner, N Miura, et al.
European Journal of Endocrinology|March 5, 2005
Novel insertion frameshift mutation of the LH receptor gene: problematic clinical distinction of Leydig cell hypoplasia from enzyme defects primarily affecting testosterone biosynthesisA Richter-Unruh, E Korsch, O Hiort, et al.
Anatomy and Embryology|May 30, 1998
Immunohistochemistry and in situ hybridization of the androgen receptor in the developing human prostateG Aumüller, P M Holterhus, L Konrad, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 31, 2006
Tissue-specific transcription profiles of sex steroid biosynthesis enzymes and the androgen receptorU Hoppe, P-M Holterhus, L Wünsch, et al.
European Journal of Pediatrics|September 15, 1999
Expression of two functionally different androgen receptors in a patient with androgen insensitivityP M Holterhus, G H Sinnecker, H A Wollmann, et al.
European Journal of Endocrinology|August 29, 2015
LC-MS/MS based determination of basal- and ACTH-stimulated plasma concentrations of 11 steroid hormones: implications for detecting heterozygote CYP21A2 mutation carriersA E Kulle, F G Riepe, J Hedderich, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 12, 2005
Molecular features and clinical phenotypes in androgen insensitivity syndrome in the absence and presence of androgen receptor gene mutationsP M Holterhus, R Werner, U Hoppe, et al.
The Journal of Clinical Endocrinology and Metabolism|August 18, 2000
Significance of mutations in the androgen receptor gene in males with idiopathic infertilityO Hiort, P M Holterhus, T Horter, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|June 5, 2008
Hypophosphatemic rickets with hypercalciuria due to mutation in SLC34A3/NaPi-IIc can be masked by vitamin D deficiency and can be associated with renal calcificationsB Kremke, C Bergwitz, W Ahrens, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
Mosaicism due to a somatic mutation of the androgen receptor gene determines phenotype in androgen insensitivity syndromeP M Holterhus, H T Brüggenwirth, O Hiort, et al.
Pageof 5

Showing results (21-30 of 42) with videos related to

Sort By:
Pageof 5
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|March 12, 2009
Mutation analysis of FOXF2 in patients with disorders of sex development (DSD) in combination with cleft palateU Jochumsen, R Werner, N Miura, et al.
European Journal of Endocrinology|March 5, 2005
Novel insertion frameshift mutation of the LH receptor gene: problematic clinical distinction of Leydig cell hypoplasia from enzyme defects primarily affecting testosterone biosynthesisA Richter-Unruh, E Korsch, O Hiort, et al.
Anatomy and Embryology|May 30, 1998
Immunohistochemistry and in situ hybridization of the androgen receptor in the developing human prostateG Aumüller, P M Holterhus, L Konrad, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 31, 2006
Tissue-specific transcription profiles of sex steroid biosynthesis enzymes and the androgen receptorU Hoppe, P-M Holterhus, L Wünsch, et al.
European Journal of Pediatrics|September 15, 1999
Expression of two functionally different androgen receptors in a patient with androgen insensitivityP M Holterhus, G H Sinnecker, H A Wollmann, et al.
European Journal of Endocrinology|August 29, 2015
LC-MS/MS based determination of basal- and ACTH-stimulated plasma concentrations of 11 steroid hormones: implications for detecting heterozygote CYP21A2 mutation carriersA E Kulle, F G Riepe, J Hedderich, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 12, 2005
Molecular features and clinical phenotypes in androgen insensitivity syndrome in the absence and presence of androgen receptor gene mutationsP M Holterhus, R Werner, U Hoppe, et al.
The Journal of Clinical Endocrinology and Metabolism|August 18, 2000
Significance of mutations in the androgen receptor gene in males with idiopathic infertilityO Hiort, P M Holterhus, T Horter, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|June 5, 2008
Hypophosphatemic rickets with hypercalciuria due to mutation in SLC34A3/NaPi-IIc can be masked by vitamin D deficiency and can be associated with renal calcificationsB Kremke, C Bergwitz, W Ahrens, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
Mosaicism due to a somatic mutation of the androgen receptor gene determines phenotype in androgen insensitivity syndromeP M Holterhus, H T Brüggenwirth, O Hiort, et al.
Pageof 5