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Ralf Werner

Showing results (41-50 of 62) with videos related to

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Journal of Medical Genetics|October 13, 2022
Disruption of the topologically associated domain at Xp21.2 is related to 46,XY gonadal dysgenesisJakob A Meinel, Verónica Yumiceba, Axel Künstner, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|December 10, 2019
Clinical Findings and Follow-Up of 46,XY and 45,X/46,XY Testicular DysgenesisJuliana G R Andrade, Helena Fabbri-Scallet, Ana P Dos Santos, et al.
Circulation|July 13, 2006
Early recurrent ischemic stroke in stroke patients undergoing intravenous thrombolysisDimitrios Georgiadis, Stefan Engelter, Barbara Tettenborn, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|June 28, 2022
Can Non-Coding NR5A1 Gene Variants Explain Phenotypes of Disorders of Sex Development?Helena Fabbri-Scallet, Ralf Werner, Mara S Guaragna, et al.
Endocrine|March 8, 2022
Metabolic effects of estradiol versus testosterone in complete androgen insensitivity syndromeMatthias K Auer, Wiebke Birnbaum, Michaela F Hartmann, et al.
BMC Genomics|October 20, 2007
Intrinsic androgen-dependent gene expression patterns revealed by comparison of genital fibroblasts from normal males and individuals with complete and partial androgen insensitivity syndromePaul-Martin Holterhus, Uta Deppe, Ralf Werner, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|December 19, 2015
Novel Insights into 46,XY Disorders of Sex Development due to NR5A1 Gene MutationRalf Werner, Isabel Mönig, Julia August, et al.
European Journal of Human Genetics : EJHG|March 13, 2015
European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA studyIntza Garin, Giovanna Mantovani, Urko Aguirre, et al.
European Journal of Human Genetics : EJHG|July 10, 2014
European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA studyIntza Garin, Giovanna Mantovani, Urko Aguirre, et al.
Scientific Reports|February 13, 2026
Exploring the underlying gene expression profiles of differences of sex development phenotypes through transcriptome analysisHelena Fabbri-Scallet, Verónica Calonga-Solís, Gil Guerra-Júnior, et al.
Pageof 7

Showing results (41-50 of 62) with videos related to

Sort By:
Pageof 7
Journal of Medical Genetics|October 13, 2022
Disruption of the topologically associated domain at Xp21.2 is related to 46,XY gonadal dysgenesisJakob A Meinel, Verónica Yumiceba, Axel Künstner, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|December 10, 2019
Clinical Findings and Follow-Up of 46,XY and 45,X/46,XY Testicular DysgenesisJuliana G R Andrade, Helena Fabbri-Scallet, Ana P Dos Santos, et al.
Circulation|July 13, 2006
Early recurrent ischemic stroke in stroke patients undergoing intravenous thrombolysisDimitrios Georgiadis, Stefan Engelter, Barbara Tettenborn, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|June 28, 2022
Can Non-Coding NR5A1 Gene Variants Explain Phenotypes of Disorders of Sex Development?Helena Fabbri-Scallet, Ralf Werner, Mara S Guaragna, et al.
Endocrine|March 8, 2022
Metabolic effects of estradiol versus testosterone in complete androgen insensitivity syndromeMatthias K Auer, Wiebke Birnbaum, Michaela F Hartmann, et al.
BMC Genomics|October 20, 2007
Intrinsic androgen-dependent gene expression patterns revealed by comparison of genital fibroblasts from normal males and individuals with complete and partial androgen insensitivity syndromePaul-Martin Holterhus, Uta Deppe, Ralf Werner, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|December 19, 2015
Novel Insights into 46,XY Disorders of Sex Development due to NR5A1 Gene MutationRalf Werner, Isabel Mönig, Julia August, et al.
European Journal of Human Genetics : EJHG|March 13, 2015
European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA studyIntza Garin, Giovanna Mantovani, Urko Aguirre, et al.
European Journal of Human Genetics : EJHG|July 10, 2014
European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA studyIntza Garin, Giovanna Mantovani, Urko Aguirre, et al.
Scientific Reports|February 13, 2026
Exploring the underlying gene expression profiles of differences of sex development phenotypes through transcriptome analysisHelena Fabbri-Scallet, Verónica Calonga-Solís, Gil Guerra-Júnior, et al.
Pageof 7