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Ralf Werner

Showing results (11-20 of 62) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|June 1, 2014
Different pattern of epigenetic changes of the GNAS gene locus in patients with pseudohypoparathyroidism type Ic confirm the heterogeneity of underlying pathomechanisms in this subgroup of pseudohypoparathyroidism and the demand for a new classification of GNAS-related disordersBettina Brix, Ralf Werner, Pia Staedt, et al.
The Journal of Clinical Endocrinology and Metabolism|February 15, 2007
A disruptive mutation in exon 3 of the GNAS gene with albright hereditary osteodystrophy, normocalcemic pseudohypoparathyroidism, and selective long transcript variant Gsalpha-L deficiencySusanne Thiele, Ralf Werner, Wiebke Ahrens, et al.
Berliner Und Munchener Tierarztliche Wochenschrift|August 19, 2015
[Detection of Coxiella burnetii in dairy cattle bulk tank milk and single tank milk samples by confirmatory testing]Angela Hilbert, Tatjana Andres, Ralf Werner, et al.
Hormone Research in Paediatrics|December 13, 2016
Pubertal Development in
17Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency
Olaf Hiort, Louise Marshall, Wiebke Birnbaum, et al.
The Journal of Steroid Biochemistry and Molecular Biology|August 26, 2006
Androgen receptor gene mutations in androgen insensitivity syndrome cause distinct patterns of reduced activation of androgen-responsive promoter constructsRalf Werner, Jenny Schütt, Sabine Hannema, et al.
European Journal of Endocrinology|February 1, 2023
Persistence of foetal testicular features in patients with defective androgen signallingMostafa Al-Sharkawi, Verónica Calonga-Solís, Franz F Dressler, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|October 24, 2021
Clinical, Biochemical, and Molecular Characterization of Indian Children with Clinically Suspected Androgen Insensitivity SyndromeAnil Kumar, Rajni Sharma, Mohammed Faruq, et al.
Nature Reviews. Endocrinology|July 16, 2014
Management of disorders of sex developmentOlaf Hiort, Wiebke Birnbaum, Louise Marshall, et al.
Human Mutation|April 14, 2011
Functional characterization of GNAS mutations found in patients with pseudohypoparathyroidism type Ic defines a new subgroup of pseudohypoparathyroidism affecting selectively Gsα-receptor interactionSusanne Thiele, Luisa de Sanctis, Ralf Werner, et al.
Cerebrovascular Diseases (Basel, Switzerland)|June 15, 2007
Functional outcome and prevalence of recurrent ischemic events in patients with acute ischemic stroke due to aortic plaquesChristian Rainer Baumann, Ralf Werner Baumgartner, Hans-Christian von Büdingen, et al.
Pageof 7

Showing results (11-20 of 62) with videos related to

Sort By:
Pageof 7
The Journal of Clinical Endocrinology and Metabolism|June 1, 2014
Different pattern of epigenetic changes of the GNAS gene locus in patients with pseudohypoparathyroidism type Ic confirm the heterogeneity of underlying pathomechanisms in this subgroup of pseudohypoparathyroidism and the demand for a new classification of GNAS-related disordersBettina Brix, Ralf Werner, Pia Staedt, et al.
The Journal of Clinical Endocrinology and Metabolism|February 15, 2007
A disruptive mutation in exon 3 of the GNAS gene with albright hereditary osteodystrophy, normocalcemic pseudohypoparathyroidism, and selective long transcript variant Gsalpha-L deficiencySusanne Thiele, Ralf Werner, Wiebke Ahrens, et al.
Berliner Und Munchener Tierarztliche Wochenschrift|August 19, 2015
[Detection of Coxiella burnetii in dairy cattle bulk tank milk and single tank milk samples by confirmatory testing]Angela Hilbert, Tatjana Andres, Ralf Werner, et al.
Hormone Research in Paediatrics|December 13, 2016
Pubertal Development in
17Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency
Olaf Hiort, Louise Marshall, Wiebke Birnbaum, et al.
The Journal of Steroid Biochemistry and Molecular Biology|August 26, 2006
Androgen receptor gene mutations in androgen insensitivity syndrome cause distinct patterns of reduced activation of androgen-responsive promoter constructsRalf Werner, Jenny Schütt, Sabine Hannema, et al.
European Journal of Endocrinology|February 1, 2023
Persistence of foetal testicular features in patients with defective androgen signallingMostafa Al-Sharkawi, Verónica Calonga-Solís, Franz F Dressler, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|October 24, 2021
Clinical, Biochemical, and Molecular Characterization of Indian Children with Clinically Suspected Androgen Insensitivity SyndromeAnil Kumar, Rajni Sharma, Mohammed Faruq, et al.
Nature Reviews. Endocrinology|July 16, 2014
Management of disorders of sex developmentOlaf Hiort, Wiebke Birnbaum, Louise Marshall, et al.
Human Mutation|April 14, 2011
Functional characterization of GNAS mutations found in patients with pseudohypoparathyroidism type Ic defines a new subgroup of pseudohypoparathyroidism affecting selectively Gsα-receptor interactionSusanne Thiele, Luisa de Sanctis, Ralf Werner, et al.
Cerebrovascular Diseases (Basel, Switzerland)|June 15, 2007
Functional outcome and prevalence of recurrent ischemic events in patients with acute ischemic stroke due to aortic plaquesChristian Rainer Baumann, Ralf Werner Baumgartner, Hans-Christian von Büdingen, et al.
Pageof 7