Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Charlotta Sophie Behrens"'
Autor:
Charlotta Sophie Behrens, Maximilian Kolbe, Julia Freese, Sophia Hanke, Maria Köhne, Andreas Huge, Aya Shibamiya, Arne Hansen, Lucie Carrier, Bärbel Ulmer, Thomas Eschenhagen
Publikováno v:
Journal of Molecular and Cellular Cardiology. 173:155-156
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29120090dae1a59e580a624dcac6c530
https://doi.org/10.1016/j.yjmcc.2022.08.307
https://doi.org/10.1016/j.yjmcc.2022.08.307
Autor:
Maria Köhne, Charlotta Sophie Behrens, Tim Stüdemann, Constantin von Bibra, Eva Querdel, Aya Shibamiya, Birgit Geertz, Jakob Olfe, Ida Hüners, Stefan Jockenhövel, Michael Hübler, Thomas Eschenhagen, Jörg Siegmar Sachweh, Florian Weinberger, Daniel Biermann
Publikováno v:
European journal of cardio-thoracic surgery 62(2), (2022). doi:10.1093/ejcts/ezac111
European journal of cardio-thoracic surgery 62(2), (2022). doi:10.1093/ejcts/ezac111
Published by Oxford Univ. Press, Oxford
Published by Oxford Univ. Press, Oxford
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::905ef2f096d428d62784805785e2a1ab
Autor:
Charlotta Sophie Behrens, Julia Freese, Antonia T.L. Zech, Maria Köhne, Christoph Krisp, Ingke Braren, Malte Loos, Maximilian Kolbe, Andreas Huge, Hartmut Schlüter, Arne Hansen, Lucie Carrier, Bärbel Ulmer, Thomas Eschenhagen
Publikováno v:
Journal of Molecular and Cellular Cardiology. 173:110
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1393a91978cc874bf098c16b3d25f28a
https://doi.org/10.1016/j.yjmcc.2022.08.218
https://doi.org/10.1016/j.yjmcc.2022.08.218
Autor:
Marina Reinsch, Thomas G. Schulze, Anika E Knaust, Aya Shibamiya, Florian Weinberger, Sandra D. Laufer, Birgit Klampe, Christiane Neuber, Simone Steuck, Giulia Mearini, Elisabeth Schulze, Malte Loos, Ingra Mannhardt, Mirja L Schulze, Charlotta Sophie Behrens, Bärbel M. Ulmer, Arne Hansen, Dana Krauß, Tessa Werner, Marta Lemme, Umber Saleem, Christa Augustin, Sigrid Fuchs, Thomas Eschenhagen
Publikováno v:
Current Protocols in Stem Cell Biology. 55
The reproducibility of stem cell research relies on the constant availability of quality-controlled cells. As the quality of human induced pluripotent stem cells (hiPSCs) can deteriorate in the course of a few passages, cell banking is key to achieve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb5236c1a3d53cab08e444c75ce55de4
https://doi.org/10.1002/cpsc.127
https://doi.org/10.1002/cpsc.127
Autor:
Kenneth S. Ginsburg, Charlotta Sophie Behrens, Renee G.C. Maas, Michaela Schweizer, Larissa Hörmann, Bence Hegyi, Joseph C. Wu, Wesley L. McKeithan, Risto Pekka Pölönen, Christine Wahlquist, Christian M. Metallo, Francesca Briganti, Matthew Greenhaw, Zhandi Liao, Ricardo Serrano, Arne A. N. Bruyneel, Mark Mercola, Dries A. M. Feyen, Chi Keung Lam, Daniel Bernstein, Hui Zhang, Alexander Kreymerman, Michelle Vu, Sean Spiering, Donald M. Bers, Prashila L Amatya, Thomas Eschenhagen, Bärbel M. Ulmer, Sara Ranjbarvaziri
Publikováno v:
Cell reports
Cell reports, vol 32, iss 3
Cell reports, vol 32, iss 3
SUMMARY Induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) have enormous potential for the study of human cardiac disorders. However, their physiological immaturity severely limits their utility as a model system and their adoption for d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23942c1aa9af3e3932c03e8e88fdc9e1
https://pubmed.ncbi.nlm.nih.gov/32697997
https://pubmed.ncbi.nlm.nih.gov/32697997
Autor:
Elisabeth Krämer, Christiane Neuber, Nele Warnecke, Jirko Kühnisch, Sandra D. Laufer, Aya Shibamiya, Bärbel M. Ulmer, Giulia Mearini, Monica Patten-Hamel, Sabine Klaassen, Charlotta Sophie Behrens, Thomas Eschenhagen, Sophia Hanke, Lucie Carrier, Julia Münch, Malte Loos
Publikováno v:
Stem Cell Research, Vol 55, Iss, Pp 102489-(2021)
MYBPC3 is the most frequently affected gene in hypertrophic cardiomyopathy (HCM), which is an autosomal-dominant cardiac disease caused by mutations in sarcomeric proteins. Bi-allelic truncating MYBPC3 mutations are associated with severe forms of ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4caf4b42cd533ca8882523bebc7825d
https://doi.org/10.1016/j.scr.2021.102489
https://doi.org/10.1016/j.scr.2021.102489