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Ralf Werner

Showing results (21-30 of 62) with videos related to

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Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 7, 2020
Spectrum of Pathogenic Variants in SRD5A2 in Indian Children with 46,XY Disorders of Sex Development and Clinically Suspected Steroid 5α-Reductase 2 DeficiencyAnil Kumar, Rajni Sharma, Mohammed Faruq, et al.
The Journal of Clinical Endocrinology and Metabolism|June 29, 2006
The A645D mutation in the hinge region of the human androgen receptor (AR) gene modulates AR activity, depending on the context of the polymorphic glutamine and glycine repeatsRalf Werner, Paul-Martin Holterhus, Gerhard Binder, et al.
Clinical Endocrinology|March 8, 2026
Clinical Characterization and Molecular Profiling by Targeted Next-Generation Sequencing in a Large Indian Cohort With 46,XY Differences in Sex DevelopmentVandana Jain, Sukanya Priyadarshini, Rajni Sharma, et al.
Molecular Genetics & Genomic Medicine|March 25, 2015
A positive genotype-phenotype correlation in a large cohort of patients with Pseudohypoparathyroidism Type Ia and Pseudo-pseudohypoparathyroidism and 33 newly identified mutations in the GNAS geneSusanne Thiele, Ralf Werner, Joachim Grötzinger, et al.
Molecular and Cellular Endocrinology|March 13, 2012
RWDD1 interacts with the ligand binding domain of the androgen receptor and acts as a coactivator of androgen-dependent transactivationHelga Grötsch, Marlene Kunert, Katrin A Mooslehner, et al.
Scientific Reports|May 31, 2020
CYP17A1 deficient XY mice display susceptibility to atherosclerosis, altered lipidomic profile and atypical sex developmentRedouane Aherrahrou, Alexandra E Kulle, Natalia Alenina, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 26, 2006
Cell-line and tissue-specific signatures of androgen receptor-coregulator transcriptionJan-Hendrik Bebermeier, James D Brooks, Samuel E DePrimo, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|November 18, 2014
Preserved fertility in a patient with gynecomastia associated with the p.Pro695Ser mutation in the androgen receptorReginaldo J Petroli, Olaf Hiort, Dagmar Struve, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 31, 2009
Apolipoprotein D (APOD) is a putative biomarker of androgen receptor function in androgen insensitivity syndromeMahesh Appari, Ralf Werner, Lutz Wünsch, et al.
Human Mutation|October 10, 2018
In vitro functional characterization of the novel DHH mutations p.(Asn337Lysfs*24) and p.(Glu212Lys) associated with gonadal dysgenesisAsma Tajouri, Maher Kharrat, Syrine Hizem, et al.
Pageof 7

Showing results (21-30 of 62) with videos related to

Sort By:
Pageof 7
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 7, 2020
Spectrum of Pathogenic Variants in SRD5A2 in Indian Children with 46,XY Disorders of Sex Development and Clinically Suspected Steroid 5α-Reductase 2 DeficiencyAnil Kumar, Rajni Sharma, Mohammed Faruq, et al.
The Journal of Clinical Endocrinology and Metabolism|June 29, 2006
The A645D mutation in the hinge region of the human androgen receptor (AR) gene modulates AR activity, depending on the context of the polymorphic glutamine and glycine repeatsRalf Werner, Paul-Martin Holterhus, Gerhard Binder, et al.
Clinical Endocrinology|March 8, 2026
Clinical Characterization and Molecular Profiling by Targeted Next-Generation Sequencing in a Large Indian Cohort With 46,XY Differences in Sex DevelopmentVandana Jain, Sukanya Priyadarshini, Rajni Sharma, et al.
Molecular Genetics & Genomic Medicine|March 25, 2015
A positive genotype-phenotype correlation in a large cohort of patients with Pseudohypoparathyroidism Type Ia and Pseudo-pseudohypoparathyroidism and 33 newly identified mutations in the GNAS geneSusanne Thiele, Ralf Werner, Joachim Grötzinger, et al.
Molecular and Cellular Endocrinology|March 13, 2012
RWDD1 interacts with the ligand binding domain of the androgen receptor and acts as a coactivator of androgen-dependent transactivationHelga Grötsch, Marlene Kunert, Katrin A Mooslehner, et al.
Scientific Reports|May 31, 2020
CYP17A1 deficient XY mice display susceptibility to atherosclerosis, altered lipidomic profile and atypical sex developmentRedouane Aherrahrou, Alexandra E Kulle, Natalia Alenina, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 26, 2006
Cell-line and tissue-specific signatures of androgen receptor-coregulator transcriptionJan-Hendrik Bebermeier, James D Brooks, Samuel E DePrimo, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|November 18, 2014
Preserved fertility in a patient with gynecomastia associated with the p.Pro695Ser mutation in the androgen receptorReginaldo J Petroli, Olaf Hiort, Dagmar Struve, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 31, 2009
Apolipoprotein D (APOD) is a putative biomarker of androgen receptor function in androgen insensitivity syndromeMahesh Appari, Ralf Werner, Lutz Wünsch, et al.
Human Mutation|October 10, 2018
In vitro functional characterization of the novel DHH mutations p.(Asn337Lysfs*24) and p.(Glu212Lys) associated with gonadal dysgenesisAsma Tajouri, Maher Kharrat, Syrine Hizem, et al.
Pageof 7