Zobrazeno 1 - 10
of 2 199
pro vyhledávání: '"L, Zech"'
Autor:
Antonia T. L. Zech, Maksymilian Prondzynski, Sonia R. Singh, Niels Pietsch, Ellen Orthey, Erda Alizoti, Josefine Busch, Alexandra Madsen, Charlotta S. Behrens, Moritz Meyer-Jens, Giulia Mearini, Marc D. Lemoine, Elisabeth Krämer, Diogo Mosqueira, Sanamjeet Virdi, Daniela Indenbirken, Maren Depke, Manuela Gesell Salazar, Uwe Völker, Ingke Braren, William T. Pu, Thomas Eschenhagen, Elke Hammer, Saskia Schlossarek, Lucie Carrier
Publikováno v:
Cells, Vol 11, Iss 17, p 2745 (2022)
Genetic variants in α-actinin-2 (ACTN2) are associated with several forms of (cardio)myopathy. We previously reported a heterozygous missense (c.740C>T) ACTN2 gene variant, associated with hypertrophic cardiomyopathy, and characterized by an electro
Externí odkaz:
https://doaj.org/article/109fa3ab16674cf981367758f4aa3eb1
Autor:
James W. McNamara, Benjamin L. Parker, Holly K. Voges, Neda R. Mehdiabadi, Francesca Bolk, Feroz Ahmad, Jin D. Chung, Natalie Charitakis, Jeffrey Molendijk, Antonia T. L. Zech, Sean Lal, Mirana Ramialison, Kathy Karavendzas, Hayley L. Pointer, Petros Syrris, Luis R. Lopes, Perry M. Elliott, Gordon S. Lynch, Richard J. Mills, James E. Hudson, Kevin I. Watt, Enzo R. Porrello, David A. Elliott
Publikováno v:
Nature Cardiovascular Research. 2:159-173
Muscle contraction is driven by the molecular machinery of the sarcomere. As phosphorylation is a critical regulator of muscle function, the identification of regulatory kinases is important for understanding sarcomere biology. Pathogenic variants in
Autor:
András Horváth, Torsten Christ, Jussi T. Koivumäki, Maksymilian Prondzynski, Antonia T. L. Zech, Michael Spohn, Umber Saleem, Ingra Mannhardt, Bärbel Ulmer, Evaldas Girdauskas, Christian Meyer, Arne Hansen, Thomas Eschenhagen, Marc D. Lemoine
Publikováno v:
Cells, Vol 9, Iss 1, p 253 (2020)
Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) represent an unlimited source of human CMs that could be a standard tool in drug research. However, there is concern whether hiPSC-CMs express all cardiac ion channels at physiolo
Externí odkaz:
https://doaj.org/article/3763edddbe7747caaa9a423b5f025cfe
Autor:
Antonia T. L. Zech, Maksymilian Prondzynski, Sonia R. Singh, Ellen Orthey, Erda Alizoti, Josefine Busch, Alexandra Madsen, Charlotta S. Behrens, Giulia Mearini, Marc D. Lemoine, Elisabeth Krämer, Diogo Mosqueira, Sanamjeet Virdi, Daniela Indenbirken, Maren Depke, Manuela Gesell Salazar, Uwe Völker, Ingke Braren, William T. Pu, Thomas Eschenhagen, Elke Hammer, Saskia Schlossarek, Lucie Carrier
Genetic variants in α-actinin-2 (ACTN2) are associated with several forms of (cardio)myopathy. We previously reported a heterozygous missense (c.740C>T) ACTN2 gene variant, associated with hypertrophic cardiomyopathy, and characterized by an electro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4de4d821144b4a5d36d21f3d0d284ec
https://doi.org/10.1101/2021.10.28.466251
https://doi.org/10.1101/2021.10.28.466251
Akademický článek
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Publikováno v:
Pharmacopsychiatry.
For four decades investigators have been using radio- and stable isotopes to help them understand aspects of mineral and trace element metabolism. In particular issues such as storage sites, absorption mechanisms, control mechanisms and control point
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fa53ea11164ee85eac2a21caf41bc5b
https://doi.org/10.1201/9780367811716-37
https://doi.org/10.1201/9780367811716-37
Publikováno v:
Journal of Lipid Research, Vol 35, Iss 12, Pp 2280-2291 (1994)
Apolipoprotein (apo) A-IV is an intestinally derived apolipoprotein that plays a potentially important role in lipoprotein metabolism and reverse cholesterol transport. However, the factors that regulate its plasma concentrations are not well underst
Externí odkaz:
https://doaj.org/article/e736d7dd3f634677aa369291ea787c1e
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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K zobrazení výsledku je třeba se přihlásit.
Autor:
Sonia R, Singh, Antonia T L, Zech, Birgit, Geertz, Silke, Reischmann-Düsener, Hanna, Osinska, Maksymilian, Prondzynski, Elisabeth, Krämer, Qinghang, Meng, Charles, Redwood, Jolanda, van der Velden, Jeffrey, Robbins, Saskia, Schlossarek, Lucie, Carrier
Publikováno v:
Circulation. Heart failure. 10(10)
Alterations in autophagy have been reported in hypertrophic cardiomyopathy (HCM) caused by Danon disease, Vici syndrome, or LEOPARD syndrome, but not in HCM caused by mutations in genes encoding sarcomeric proteins, which account for most of HCM case