Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Nadine Hornig"'
Autor:
Julian Knerr, Ralf Werner, Carsten Schwan, Hong Wang, Peter Gebhardt, Helga Grötsch, Almuth Caliebe, Malte Spielmann, Paul-Martin Holterhus, Robert Grosse, Nadine Hornig
Steroid hormone receptors are ligand-binding transcription factors essential for mammalian physiology. The androgen receptor (AR) binds androgens mediating gene expression for sexual, somatic, and behavioral functions, and is involved in various cond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a91d5032f23dbd127f2a3b360fa8032
https://doi.org/10.21203/rs.3.rs-1664650/v1
https://doi.org/10.21203/rs.3.rs-1664650/v1
Autor:
Andreas Rosenwald, Chris Lawerenz, Matthias Schlesner, Birgit Burkhardt, Monika Szczepanowski, Ole Ammerpohl, Jan O. Korbel, Dieter Kube, Gordana Apic, Markus Kreuz, René Scholtysik, Marius Rohde, Hans G. Drexler, Bernhard Radlwimmer, Roland Eils, Dirk Hasenclever, Markus Loeffler, Maren Paulsen, Simone Picelli, Katharina Meyer, Simone Lipinski, Peter Lichter, Rabea Wagener, Peter F. Stadler, Ralf Küppers, Stephan H. Bernhart, Markus Schilhabel, Maciej Rosolowski, Philip Rosenstiel, Sabine Adam-Klages, Roderick A.F. MacLeod, Julia Richter, Thorsten Zenz, Jasmin Lisfeld, Michael Hummel, Rainer Spang, Benedikt Brors, David Langenberger, Heiko Trautmann, Arndt Borkhardt, Lorenz Trümper, Volker Hovestadt, Reiner Siebert, Wolfram Klapper, Robert B. Russell, Ellen Leich, Tobias Rausch, Stefan Schreiber, Peter Möller, Nadine Hornig, Steve Hoffmann, Dido Lenze, Alexander Claviez, Christiane Pott, Jordan Pischimarov
Burkitt lymphoma is a mature aggressive B-cell lymphoma derived from germinal center B cells(1). Its cytogenetic hallmark is the Burkitt translocation t(8;14)(q24;q32) and its variants, which juxtapose the MYC oncogene with one of the three immunoglo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ec004da4bd0355aa90004cc684fa938
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/79434
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/79434
Autor:
Paul-Martin Holterhus, Eva Maria Murga Penas, Olaf Hiort, Anne Katrin Eckstein, Almuth Caliebe, Pascal Rodens, Ralf Werner, Jeta Demiri, Hans-Udo Schweikert, Nadine Hornig, Alexandra Kulle, Ole Ammerpohl, Laura Audí
Publikováno v:
The Journal of clinical endocrinology and metabolism. 104(10)
Context Molecular mechanisms causing the broad phenotypic diversity of external masculinization in individuals with 45,X/46,XY mosaicism are poorly understood. Objective Analysis of androgen receptor (AR) expression and function as a putative influen
Sexual differentiation of genital anatomy in the male occurs under strict hormonal control of the fetal testes and is confined to a developmental time window between the 8th and 12th week of gestation. Wolffian ducts will develop into epididymis, vas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2e0818d84e86f786ad710ca194a1c28
https://doi.org/10.1016/b978-0-12-801238-3.65372-2
https://doi.org/10.1016/b978-0-12-801238-3.65372-2
Autor:
H. U. Schweikert, Olaf Hiort, Ole Ammerpohl, Susanne Bens, Hendrik G. Stunnenberg, Alexandra Kulle, Paul-Martin Holterhus, Nina C. Hubner, Ralf Werner, Anne Katrin Eckstein, Annemarie Verrijn-Stuart, Martine Cools, Helmuth G. Dörr, Susanne Gonzalves, Reiner Siebert, Nadine Hornig, Maik Welzel, Pascal Rodens
Publikováno v:
The Journal of clinical endocrinology and metabolism, 103(12), 4617. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 103, 12, pp. 4617-4627
Journal of Clinical Endocrinology and Metabolism, 103, 4617-4627
Journal of Clinical Endocrinology and Metabolism, 103, 12, pp. 4617-4627
Journal of Clinical Endocrinology and Metabolism, 103, 4617-4627
Contains fulltext : 197541.pdf (Publisher’s version ) (Closed access) Context: Inactivating mutations within the AR-gene are present in only around 40% of individuals with clinically and hormonally diagnosed androgen insensitivity syndrome (AIS). P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62e58acb268e331df0c790daa943f487
https://dspace.library.uu.nl/handle/1874/373771
https://dspace.library.uu.nl/handle/1874/373771
Autor:
Paul-Martin Holterhus, Nadine Hornig
Publikováno v:
Molecular and Cellular Endocrinology. 523:111146
Individuals with complete androgen insensitivity syndrome show a female genital phenotype despite 46, XY gonosomes and the presence of androgen producing testes. This clinical observation indicates the resistance of the body and its cells to androgen
Autor:
Thomas Reinehr, Marek Niedziela, Alexandra Kulle, Nadine Hornig, Christoph Borzikowsky, Paul-Martin Holterhus, Gunter Simic-Schleicher, Maciej Flader, Dominika Zalas, Halit Ilker Akkurt, Sabine Heger
Publikováno v:
Hormone research in paediatrics. 89(4)
Background/Aims: The high complexity of pediatric reference ranges across age, sex, and units impairs clinical application and comparability of steroid hormone data, e.g., in congenital adrenal hyperplasia (CAH). We developed a multiples-of-median (M
Autor:
Reiner Siebert, Martine Cools, Ole Ammerpohl, Gaby Wehner, Lisa Worch, Elke Muller-Roszberg, Laura Audí, Nadine Hornig, Ahmed T Hadidi, C. Seif, Desiree Dunstheimer, Jeta Demiri, Alexandra Kulle, Thomas Reinehr, Hans-Udo Schweikert, S Faisal Ahmed, Ralf Werner, Martine Ukat, Stenvert L. S. Drop, Paul-Martin Holterhus, Pascal Rodens, Ieuan A Hughes, Olaf Hiort, der Horst Christof van, Anne Katrin Eckstein
Publikováno v:
Endocrine Abstracts.
Autor:
Thomas Reinehr, Paul-Martin Holterhus, Alexandra Kulle, Nadine Hornig, Gunter Simic-Schleicher
Publikováno v:
The Journal of clinical endocrinology and metabolism. 102(1)
Background: Dehydroepiandrosterone sulfate (DHEAS) and 17-hydroxypregnenolone (17OHPreg) are important for understanding the Δ5 pathway (e.g., in adrenarche and obesity). Although mass spectrometry has become the state-of-the-art method for quantify
Autor:
Friederike Denzer, Nadine Hornig, Hans-Udo Schweikert, Olaf Hiort, Ralf Werner, Ole Ammerpohl, Alexandra Kulle, Reiner Siebert, Martine Cools, Martin Ukat, Laura Audí, Carine de Beaufort, Martin Wabitsch, Paul-Martin Holterhus
Publikováno v:
PLoS ONE, 11(4). San Franscisco, CA: Public Library of Science (2016).
PLoS ONE, Vol 11, Iss 4, p e0154158 (2016)
PLOS ONE
PLoS ONE
PLoS ONE, Vol 11, Iss 4, p e0154158 (2016)
PLOS ONE
PLoS ONE
A subset of patients with monogenic disorders lacks disease causing mutations in the protein coding region of the corresponding gene. Here we describe a recurrent germline mutation found in two unrelated patients with complete androgen insensitivity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c50e2933c1331ce3ffacdb7a20e7ad01
http://orbilu.uni.lu/handle/10993/27172
http://orbilu.uni.lu/handle/10993/27172