Zobrazeno 1 - 8 of 8 pro vyhledávání: '"O. E. Karpicheva"'
2
Hallmark Features of the Tropomyosin Regulatory Function in Several Variants of Congenital Myopathy
Autor: O. E. Karpicheva
Publikováno v: Journal of Evolutionary Biochemistry and Physiology. 57:646-665
Congenital myopathies are a group of clinically and genetically heterogeneous diseases, which are united by primary lesions of skeletal muscles and are characterized by progressive muscle weakness and hypotension, as well as morphological changes in
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5547e8bbb428f02e59ebb63f793c9338
https://doi.org/10.1134/s0022093021030133
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4
[Abnormal tropomyosin function in ATPase cycle in hypertrophic and dilated cardiomyopathies]
Autor: Iu S, Borovikov, O E, Karpicheva, N A, Rysev, C S, Redwood
Publikováno v: Rossiiskii fiziologicheskii zhurnal imeni I.M. Sechenova. 99(1)
Pathogenesis of most myopathies including inherited hypertrophic (HCM) and dilated (DCM) cardiomyopathies is based on modification of structural state of contractile proteins induced by point mutations, such as mutations in alpha-tropomyosin (TM). To
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b69d3087695d7fb8bd2baebad67c2d42
https://pubmed.ncbi.nlm.nih.gov/23659058
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5
Akademický článek
Dilated cardiomyopathy-associated skeletal muscle actin (ACTA1) mutation R256H disrupts actin structure and function and causes cardiomyocyte hypocontractility.
Autor: Garg, Ankit, Jansen, Silvia, Greenberg, Lina, Rui Zhang, Lavine, Kory J., Greenberg, Michael J.
Publikováno v: Proceedings of the National Academy of Sciences of the United States of America; 11/12/2024, Vol. 121 Issue 46, p1-12, 36p
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