Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Petr G. Vikhorev"'
Autor:
Petr G. Vikhorev, Natalia Smoktunowicz, Alex B. Munster, O’ Neal Copeland, Sawa Kostin, Cecile Montgiraud, Andrew E. Messer, Mohammad R. Toliat, Amy Li, Cristobal G. dos Remedios, Sean Lal, Cheavar A. Blair, Kenneth S. Campbell, Maya Guglin, Manfred Richter, Ralph Knöll, Steven B. Marston
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-2 (2018)
A correction to this article has been published and is linked from the HTML and PDF versions of this paper. The error has been fixed in the paper.
Externí odkaz:
https://doaj.org/article/7e904c4780cb44de9c6ada44be61cfe2
Autor:
Petr G. Vikhorev, Natalia N. Vikhoreva
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 8, p 2234 (2018)
About half of hypertrophic and dilated cardiomyopathies cases have been recognized as genetic diseases with mutations in sarcomeric proteins. The sarcomeric proteins are involved in cardiomyocyte contractility and its regulation, and play a structura
Externí odkaz:
https://doaj.org/article/534dce83898d4869b2f108dbf4be4229
Autor:
Pieter de Tombe, Sean Lal, Natalia N. Vikhoreva, Kenneth S. Campbell, Magdi H. Yacoub, WaiChun Yeung, Amy Li, Steven B. Marston, Petr G. Vikhorev, Maya Guglin, Cristobal G. dos Remedios, Cheavar A. Blair
Publikováno v:
Cardiovascular Research
Aims Dilated cardiomyopathy (DCM) is associated with mutations in many genes encoding sarcomere proteins. Truncating mutations in the titin gene TTN are the most frequent. Proteomic and functional characterizations are required to elucidate the origi
Autor:
Hannah Karp, J. Carter Ralphe, Zachery R. Gregorich, Willem J. de Lange, Timothy J. Kamp, Ying Ge, Elizabeth F. Bayne, Trisha Tucholski, Wenxuan Cai, Joshua L. Hermsen, Sean J. McIlwain, Amy Li, Steven B. Marston, Stanford D. Mitchell, Petr G. Vikhorev, Zachary Hite, Cristobal G. dos Remedios, Max Wrobbel, Sean Lal, Takushi Kohmoto, Richard L. Moss
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Significance Hypertrophic cardiomyopathy (HCM) is a common genetic heart disease and a leading cause of sudden cardiac death in young adults. HCM has been linked to mutations in genes encoding sarcomeric proteins, but how different mutations can resu
Autor:
Petr G. Vikhorev, Natalia Smoktunowicz, Alex B. Munster, O’Neal Copeland, Sawa Kostin, Cecile Montgiraud, Andrew E. Messer, Mohammad R. Toliat, Amy Li, Cristobal G. dos Remedios, Sean Lal, Cheavar A. Blair, Kenneth S. Campbell, Maya Guglin, Manfred Richter, Ralph Knöll, Steven B. Marston
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
Dilated cardiomyopathy (DCM) is an important cause of heart failure. Single gene mutations in at least 50 genes have been proposed to account for 25–50% of DCM cases and up to 25% of inherited DCM has been attributed to truncating mutations in the
Autor:
O' Neal Copeland, Sawa Kostin, Cécile Montgiraud, Andrew E. Messer, Natalia Smoktunowicz, Manfred Richter, Maya Guglin, Alex B Munster, Kenneth S. Campbell, Steven B. Marston, Ralph Knöll, Amy Li, Petr G. Vikhorev, Cristobal G. dos Remedios, Cheavar A. Blair, Sean Lal, Mohammad R. Toliat
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-2 (2018)
A correction to this article has been published and is linked from the HTML and PDF versions of this paper. The error has been fixed in the paper.
Autor:
Natalia N. Vikhoreva, Petr G. Vikhorev
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 19, Iss 8, p 2234 (2018)
International Journal of Molecular Sciences, Vol 19, Iss 8, p 2234 (2018)
About half of hypertrophic and dilated cardiomyopathies cases have been recognized as genetic diseases with mutations in sarcomeric proteins. The sarcomeric proteins are involved in cardiomyocyte contractility and its regulation, and play a structura
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::458069b6b26288ff55665665913d379c
http://hdl.handle.net/10044/1/62693
http://hdl.handle.net/10044/1/62693
Publikováno v:
62nd Annual Meeting of the Biophysical-Society
498A
498A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a28e3f93fb4b7a157f330592092c3d69
http://hdl.handle.net/10044/1/60774
http://hdl.handle.net/10044/1/60774
Autor:
Weihua Song, Christina Rowlands, Nancy A. Curtin, Steven B. Marston, Roger C. Woledge, Michael A. Ferenczi, Petr G. Vikhorev, Kenneth T. MacLeod, Mavin N Kashyap
Publikováno v:
AJP: Heart and Circulatory Physiology; Vol 304
AJP: Heart and Circulatory Physiology
AJP: Heart and Circulatory Physiology
We compared the contractile performance of papillary muscle from a mouse model of hypertrophic cardiomyopathy [α-cardiac actin ( ACTC) E99K mutation] with nontransgenic (non-TG) littermates. In isometric twitches, ACTC E99K papillary muscle produced
Autor:
Kenneth Liljesson, Mark Sundberg, Nuria Albet-Torres, Alf Månsson, Sven Tågerud, Natalia N. Vikhoreva, Anders Kvennefors, Leif Nilsson, Lars Montelius, Martina Balaz, Pär Omling, R Bunk, Ian A. Nicholls, Petr G. Vikhorev
Publikováno v:
Langmuir. 24:13509-13517
The interaction between cytoskeletal filaments (e.g., actin filaments) and molecular motors (e.g., myosin) is the basis for many aspects of cell motility and organization of the cell interior. In the in vitro motility assay (IVMA), cytoskeletal filam