Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Alexandra Gudkova"'
Autor:
Aleksandr Khudiakov, Daria Kostina, Anna Zlotina, Tatiana Nikulina, Alexey Sergushichev, Alexandra Gudkova, Alexey Tomilin, Anna Malashicheva, Anna Kostareva
Publikováno v:
Stem Cell Research, Vol 24, Iss C, Pp 77-80 (2017)
Human iPSC line was generated from patient-specific adipose tissue-derived mesenchymal multipotent stromal cells carrying desmin (DES) gene heterozygous splice site mutation using non-integrative reprogramming method. Reprogramming factors OCT4, KLF4
Externí odkaz:
https://doaj.org/article/45f0b317b1c54f84a10dff71d781ba17
Autor:
Diana Cimiotti, Setsuko Fujita-Becker, Desirée Möhner, Natalia Smolina, Heidi Budde, Aline Wies, Lisa Morgenstern, Alexandra Gudkova, Thomas Sejersen, Gunnar Sjöberg, Andreas Mügge, Marc M Nowaczyk, Peter Reusch, Gabriele Pfitzer, Robert Stehle, Rasmus R Schröder, Hans G Mannherz, Anna Kostareva, Kornelia Jaquet
Publikováno v:
PLoS ONE, Vol 15, Iss 3, p e0229227 (2020)
TNNI3 encoding cTnI, the inhibitory subunit of the troponin complex, is the main target for mutations leading to restrictive cardiomyopathy (RCM). Here we investigate two cTnI-R170G/W amino acid replacements, identified in infantile RCM patients, whi
Externí odkaz:
https://doaj.org/article/bb47d502141e46aba86a3a8e42223132
Autor:
Anna Kostareva, Artem Kiselev, Alexandra Gudkova, Goar Frishman, Andreas Ruepp, Dmitrij Frishman, Natalia Smolina, Svetlana Tarnovskaya, Daniel Nilsson, Anna Zlotina, Tatiana Khodyuchenko, Tatiana Vershinina, Tatiana Pervunina, Alexandra Klyushina, Andrey Kozlenok, Gunnar Sjoberg, Irina Golovljova, Thomas Sejersen, Eugeniy Shlyakhto
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0163362 (2016)
BACKGROUND:Cardiomyopathies represent a rare group of disorders often of genetic origin. While approximately 50% of genetic causes are known for other types of cardiomyopathies, the genetic spectrum of restrictive cardiomyopathy (RCM) is largely unkn
Externí odkaz:
https://doaj.org/article/764033b189314c3c94b73bc07e66efb8
Autor:
Diana Cimiotti, Setsuko Fujita-Becker, Desirée Möhner, Natalia Smolina, Heidi Budde, Aline Wies, Lisa Morgenstern, Alexandra Gudkova, Thomas Sejersen, Gunnar Sjöberg, Andreas Mügge, Marc M Nowaczyk, Peter Reusch, Gabriele Pfitzer, Robert Stehle, Rasmus R Schröder, Hans G Mannherz, Anna Kostareva, Kornelia Jaquet
Publikováno v:
PLoS ONE
PLoS ONE, Vol 15, Iss 3, p e0229227 (2020)
PLoS ONE, Vol 15, Iss 3, p e0229227 (2020)
TNNI3 encoding cTnI, the inhibitory subunit of the troponin complex, is the main target for mutations leading to restrictive cardiomyopathy (RCM). Here we investigate two cTnI-R170G/W amino acid replacements, identified in infantile RCM patients, whi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::6de7e8e3f0e6e531c4746fac5a161a62
https://pubmed.ncbi.nlm.nih.gov/32182250
https://pubmed.ncbi.nlm.nih.gov/32182250
Autor:
Gunnar Sjöberg, Joseph Bruton, Shi-Jin Zhang, Johanna Balogh, Alexandra Gudkova, Birgitta Hedberg, Lars Edström, Håkan Westerblad, Thomas Sejersen
Publikováno v:
Journal of Muscle Research & Cell Motility; Jan2008, Vol. 29 Issue 1, p25-36, 12p