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Ralf Werner

Showing results (31-40 of 62) with videos related to

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Journal of Clinical Medicine|August 26, 2022
MYRF: A New Regulator of Cardiac and Early Gonadal Development-Insights from Single Cell RNA Sequencing AnalysisVerónica Calonga-Solís, Helena Fabbri-Scallet, Fabian Ott, et al.
Endocrine|October 6, 2021
Pubertal development in 46,XY patients with NR5A1 mutationsIsabel Mönig, Julia Schneidewind, Trine H Johannsen, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 2015
46,XY Gonadal Dysgenesis due to a Homozygous Mutation in Desert Hedgehog (DHH) Identified by Exome SequencingRalf Werner, Hartmut Merz, Wiebke Birnbaum, et al.
The Journal of Clinical Endocrinology and Metabolism|October 28, 2004
Homozygous disruption of P450 side-chain cleavage (CYP11A1) is associated with prematurity, complete 46,XY sex reversal, and severe adrenal failureOlaf Hiort, Paul-Martin Holterhus, Ralf Werner, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 26, 2011
Gsα activity is reduced in erythrocyte membranes of patients with psedohypoparathyroidism due to epigenetic alterations at the GNAS locusCelia Zazo, Susanne Thiele, Cesar Martín, et al.
Plos One|May 2, 2017
New NR5A1 mutations and phenotypic variations of gonadal dysgenesisRalf Werner, Isabel Mönig, Ralf Lünstedt, et al.
Nature|March 27, 2023
Formin-mediated nuclear actin at androgen receptors promotes transcriptionJulian Knerr, Ralf Werner, Carsten Schwan, et al.
BMC Genomics|July 3, 2009
Disorders of sex development expose transcriptional autonomy of genetic sex and androgen-programmed hormonal sex in human blood leukocytesPaul-Martin Holterhus, Jan-Hendrik Bebermeier, Ralf Werner, et al.
European Journal of Medical Genetics|November 21, 2017
Novel mosaic variants in two patients with Cornelia de Lange syndromeJelena Pozojevic, Ilaria Parenti, Luitgard Graul-Neumann, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|June 20, 2014
46,XY disorder of sex development in a sudanese patient caused by a novel mutation in the HSD17B3 geneMona Ellaithi, Ralf Werner, Felix G Riepe, et al.
Pageof 7

Showing results (31-40 of 62) with videos related to

Sort By:
Pageof 7
Journal of Clinical Medicine|August 26, 2022
MYRF: A New Regulator of Cardiac and Early Gonadal Development-Insights from Single Cell RNA Sequencing AnalysisVerónica Calonga-Solís, Helena Fabbri-Scallet, Fabian Ott, et al.
Endocrine|October 6, 2021
Pubertal development in 46,XY patients with NR5A1 mutationsIsabel Mönig, Julia Schneidewind, Trine H Johannsen, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 2015
46,XY Gonadal Dysgenesis due to a Homozygous Mutation in Desert Hedgehog (DHH) Identified by Exome SequencingRalf Werner, Hartmut Merz, Wiebke Birnbaum, et al.
The Journal of Clinical Endocrinology and Metabolism|October 28, 2004
Homozygous disruption of P450 side-chain cleavage (CYP11A1) is associated with prematurity, complete 46,XY sex reversal, and severe adrenal failureOlaf Hiort, Paul-Martin Holterhus, Ralf Werner, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 26, 2011
Gsα activity is reduced in erythrocyte membranes of patients with psedohypoparathyroidism due to epigenetic alterations at the GNAS locusCelia Zazo, Susanne Thiele, Cesar Martín, et al.
Plos One|May 2, 2017
New NR5A1 mutations and phenotypic variations of gonadal dysgenesisRalf Werner, Isabel Mönig, Ralf Lünstedt, et al.
Nature|March 27, 2023
Formin-mediated nuclear actin at androgen receptors promotes transcriptionJulian Knerr, Ralf Werner, Carsten Schwan, et al.
BMC Genomics|July 3, 2009
Disorders of sex development expose transcriptional autonomy of genetic sex and androgen-programmed hormonal sex in human blood leukocytesPaul-Martin Holterhus, Jan-Hendrik Bebermeier, Ralf Werner, et al.
European Journal of Medical Genetics|November 21, 2017
Novel mosaic variants in two patients with Cornelia de Lange syndromeJelena Pozojevic, Ilaria Parenti, Luitgard Graul-Neumann, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|June 20, 2014
46,XY disorder of sex development in a sudanese patient caused by a novel mutation in the HSD17B3 geneMona Ellaithi, Ralf Werner, Felix G Riepe, et al.
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