Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Antje Kathrin Huebner"'
Autor:
Alena Maul, Antje Kathrin Huebner, Nicola Strenzke, Tobias Moser, Rudolf Rübsamen, Saša Jovanovic, Christian A Hübner
Publikováno v:
eLife, Vol 11 (2022)
Before hearing onset (postnatal day 12 in mice), inner hair cells (IHCs) spontaneously fire action potentials, thereby driving pre-sensory activity in the ascending auditory pathway. The rate of IHC action potential bursts is modulated by inner suppo
Externí odkaz:
https://doaj.org/article/e773dfc29cac45ce8b2c34b18aa35f2f
Autor:
Alena, Maul, Antje Kathrin, Huebner, Nicola, Strenzke, Tobias, Moser, Rudolf, Rübsamen, Saša, Jovanovic, Christian A, Hübner
Publikováno v:
eLife. 11
Before hearing onset (postnatal day 12 in mice), inner hair cells (IHCs) spontaneously fire action potentials, thereby driving pre-sensory activity in the ascending auditory pathway. The rate of IHC action potential bursts is modulated by inner suppo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f7e1b6ccb2137041ee1ac3a475e4513a
https://pubmed.ncbi.nlm.nih.gov/35129434
https://pubmed.ncbi.nlm.nih.gov/35129434
Autor:
Thorsten Marquardt, Braulio Martínez, Otmar Huber, J. Christopher Hennings, Patricia Franzka, José M. Morales, Julia von Maltzahn, Susann Groth, Joachim Weis, M. Juliane Jung, Osvaldo M. Mutchinick, Christoph Kaether, Christian A. Hübner, Takfarinas Kentache, Istvan Katona, Rüdiger Horstkorte, Alessandro Ori, Svenja C. Schüler, Tanja Herrmann, Lutz Liebmann, Sonnhild Mittag, Lennart Gresing, Henriette Henze, Karina Biskup, Véronique Blanchard, Antje-Kathrin Huebner
Publikováno v:
The Journal of clinical investigation, Vol. 131, no.9, p. e139076 [1-19] (2021)
J Clin Invest
J Clin Invest
GDP-mannose-pyrophosphorylase-B (GMPPB) facilitates the generation of GDP-mannose, a sugar donor required for glycosylation. GMPPB defects cause muscle disease due to hypoglycosylation of α-dystroglycan (α-DG). Alpha-DG is part of a protein complex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7371ca3152f7966570f88d506b8d035
https://hdl.handle.net/2078.1/264486
https://hdl.handle.net/2078.1/264486
Autor:
Antje-Kathrin Huebner, Michaela Schweizer, Rizwan Mumtaz, Geraldine Zimmer, Christian A. Hübner, Kathrin N. Karle, Sandor Nietzsche, Ingo Kurth, Victoria Alvarez, Christoph Redies, Nicole Koch, Andrey Irintchev, Michael M. Kessels, Christian Beetz, Britta Qualmann, Nicole Hertel, Thomas Deufel, Elisabeth Dirren, Martin Westermann, Mukhran Khundadze
Publikováno v:
The journal of clinical investigation 124(6), 2809-2809 (2014). doi:10.1172/JCI76634
The journal of clinical investigation 123(10), 4273-4282 (2013). doi:10.1172/JCI65665
The journal of clinical investigation 123(10), 4273-4282 (2013). doi:10.1172/JCI65665
Axonopathies are a group of clinically diverse disorders characterized by the progressive degeneration of the axons of specific neurons. In hereditary spastic paraplegia (HSP), the axons of cortical motor neurons degenerate and cause a spastic moveme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a47658ecbb9814f0b78de8b5c323b66
https://doi.org/10.1172/jci65665
https://doi.org/10.1172/jci65665