Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Anastasia Knyazeva"'
Autor:
Artem Kiselev, Raquel Vaz, Anastasia Knyazeva, Alexey Sergushichev, Renata Dmitrieva, Aleksandr Khudiakov, John Jorholt, Natalia Smolina, Ksenia Sukhareva, Yulia Fomicheva, Evgeny Mikhaylov, Lubov Mitrofanova, Alexander Predeus, Gunnar Sjoberg, Dmitriy Rudenko, Thomas Sejersen, Anna Lindstrand, Anna Kostareva
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Even though genetic studies of individuals with neuromuscular diseases have uncovered the molecular background of many cardiac disorders such as cardiomyopathies and inherited arrhythmic syndromes, the genetic cause of a proportion of cardiomyopathie
Externí odkaz:
https://doaj.org/article/22d8647acd1744329fe82c3504bbe1a7
Autor:
Anastasia Knyazeva, Alexander Krutikov, Alexey Golovkin, Alexander Mishanin, Georgii Pavlov, Natalia Smolina, Anastasia Hushkina, Thomas Sejersen, Gunnar Sjoberg, Mikhail Galagudza, Anna Kostareva
Publikováno v:
Frontiers in Genetics, Vol 9 (2019)
Mechanotransduction is an essential mechanism of transforming external mechanical stimulus to biochemical response. In cardiomyocytes mechanotransduction plays an important role in contraction, stretch sensing and homeostasis regulation. One of the m
Externí odkaz:
https://doaj.org/article/0f698ef063d84f8bbfd3b7803c3a117c
Autor:
Xiaotong Jia, Anastasia Knyazeva, Yu Zhang, Sergio Castro-Gonzalez, Shuhei Nakamura, Lars-Anders Carlson, Tamotsu Yoshimori, Dale P. Corkery, Yao-Wen Wu
Pore-forming toxins (PFTs) are important virulence factors produced by many pathogenic bacteria. Here, we show that the Vibrio cholerae toxin MakA is a novel cholesterol-binding PFT that induces non-canonical autophagy in a pH-dependent manner. MakA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d88893f84a19275237662a729eff3cb
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-200014
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-200014
Autor:
Anna Kostareva, Aleksey Muravyev, Anastasia Knyazeva, Aleksandr Khudiakov, Raquel Vaz, Ksenia Sukhareva, Thomas Sejersen
Publikováno v:
Genes
Volume 11
Issue 11
Genes, Vol 11, Iss 1343, p 1343 (2020)
Volume 11
Issue 11
Genes, Vol 11, Iss 1343, p 1343 (2020)
Filamin C (FLNC), being one of the major actin-binding proteins, is involved in the maintenance of key muscle cell functions. Inherited skeletal muscle and cardiac disorders linked to genetic variants in FLNC have attracted attention because of their
Autor:
Artem, Kiselev, Raquel, Vaz, Anastasia, Knyazeva, Alexey, Sergushichev, Renata, Dmitrieva, Aleksandr, Khudiakov, John, Jorholt, Natalia, Smolina, Ksenia, Sukhareva, Yulia, Fomicheva, Evgeny, Mikhaylov, Lubov, Mitrofanova, Alexander, Predeus, Gunnar, Sjoberg, Dmitriy, Rudenko, Thomas, Sejersen, Anna, Lindstrand, Anna, Kostareva
Publikováno v:
Frontiers in Genetics
Even though genetic studies of individuals with neuromuscular diseases have uncovered the molecular background of many cardiac disorders such as cardiomyopathies and inherited arrhythmic syndromes, the genetic cause of a proportion of cardiomyopathie
Autor:
Tatiana Vershinina, Tatiana Pervunina, Artem Kiselev, Sergey Kazakov, S. I. Tarnovskaya, Natalia Smolina, Dmitriy Rudenko, Dmitrij Frishman, Thomas Sejersen, Aleksandr Khudiakov, Jiao Liu, Alexey Sergushichev, Raquel Vaz, Anastasia Knyazeva, Anders Arner, Gunnar Sjöberg, John Jorholt, Anna Lindstrand, Anna Kostareva
Publikováno v:
Human mutation. 39(9)
Mutations in FLNC for a long time are known in connection to neuromuscular disorders and only recently were described in association with various cardiomyopathies. Here, we report a new clinical phenotype of filaminopathy in four unrelated patients w