Zobrazeno 1 - 10
of 45
pro vyhledávání: '"A M, Matyushenko"'
Autor:
Victoria V. Nefedova, Sergey Y. Kleymenov, Irina V. Safenkova, Dmitrii I. Levitsky, Alexander M. Matyushenko
Publikováno v:
Biomolecules, Vol 14, Iss 1, p 85 (2024)
Neurofilaments are neuron-specific proteins that belong to the intermediate filament (IFs) protein family, with the neurofilament light chain protein (NFL) being the most abundant. The IFs structure typically includes a central coiled-coil rod domain
Externí odkaz:
https://doaj.org/article/75f5457c99a04118980c5d18599a76f3
Autor:
Victoria V. Nefedova, Daria S. Yampolskaya, Sergey Y. Kleymenov, Natalia A. Chebotareva, Alexander M. Matyushenko, Dmitrii I. Levitsky
Publikováno v:
Biochemistry (Moscow). 88:610-620
Publikováno v:
Journal of Evolutionary Biochemistry and Physiology. 58:S82-S91
Autor:
Daria S, Yampolskaya, Galina V, Kopylova, Daniil V, Shchepkin, Sergey Y, Bershitsky, Alexander M, Matyushenko, Dmitrii I, Levitsky
Publikováno v:
Biochemistry (Moscow). 87:1260-1267
Abstract The effects of cardiomyopathic mutations E56G, M149V, and E177G in the MYL3 gene encoding essential light chain of human ventricular myosin (ELCv), on the functional properties of cardiac myosin and its isolated head (myosin subfragment 1, S
Autor:
Galina V. Kopylova, Anastasia M. Kochurova, Daria S. Yampolskaya, Victoria V. Nefedova, Andrey K. Tsaturyan, Natalia A. Koubassova, Sergey Y. Kleymenov, Dmitrii I. Levitsky, Sergey Y. Bershitsky, Alexander M. Matyushenko, Daniil V. Shchepkin
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 9; Pages: 8340
In the myocardium, the TPM1 gene expresses two isoforms of tropomyosin (Tpm), alpha (αTpm; Tpm 1.1) and kappa (κTpm; Tpm 1.2). κTpm is the result of alternative splicing of the TPM1 gene. We studied the structural features of κTpm and its regulat
Autor:
Andrey K. Tsaturyan, Elena V. Zaklyazminskaya, Margarita E. Polyak, Galina V. Kopylova, Daniil V. Shchepkin, Anastasia M. Kochurova, Anastasiia D. Gonchar, Sergey Y. Kleymenov, Natalia A. Koubasova, Sergey Y. Bershitsky, Alexander M. Matyushenko, Dmitrii I. Levitsky
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 1; Pages: 18
Hypertrophic cardiomyopathy (HCM), caused by mutations in thin filament proteins, manifests as moderate cardiac hypertrophy and is associated with sudden cardiac death (SCD). We identified a new de novo variant, c.656A>T (p.D219V), in the TPM1 gene e
Publikováno v:
Вестник Кемеровского государственного университета, Vol 0, Iss 2-2, Pp 162-168 (2014)
The paper examines the question of connection between psychological protection and type of relations. The greatest quantity of psychological protections occurs in distrustful, obedient and shy, and dependent and obedient types. Intellectualization is
Externí odkaz:
https://doaj.org/article/8f9093193aa74b3386f5ed63bae4b6ea
Publikováno v:
Вестник Кемеровского государственного университета, Vol 0, Iss 2-1, Pp 160-166 (2014)
In the article is examined a question about the leading activity from the point of view of psychology and its signs, and as it influences the formation of nature.
Externí odkaz:
https://doaj.org/article/c74b1982a56a4d41bf23a0820ae7a59e
Autor:
Dmitrii I. Levitsky, Valentina Y. Berg, Galina V. Kopylova, Alexander M. Matyushenko, Sergey Y. Bershitsky, D. V. Shchepkin
Publikováno v:
Journal of Muscle Research and Cell Motility. 42:343-353
Phosphorylation of α-tropomyosin (Tpm1.1), a predominant Tpm isoform in the myocardium, is one of the regulatory mechanisms of the heart contractility. The Tpm 1.1 molecule has one site of phosphorylation, Ser283. The degree of the Tpm phosphorylati
Autor:
Valentina Y. Berg, Alexander M. Matyushenko, Anastasia M. Kochurova, Dmitrii I. Levitsky, Sergey Yu. Kleymenov, Anastasiia D. Gonchar, Andrey K. Tsaturyan, Galina V. Kopylova, Natalia A. Koubasova, D. V. Shchepkin
Publikováno v:
Biochemical and Biophysical Research Communications. 534:8-13
Tropomyosin (Tpm) is an actin-binding protein that plays a crucial role in the regulation of muscle contraction. Numerous point mutations in the TPM3 gene encoding Tpm of slow skeletal muscles (Tpm 3.12 or γ-Tpm) are associated with the genesis of v