Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Viktoriia KYRYCHENKO"'
Comparative Analysis of Physical Fitness of Physical Education Major Romanian and Ukrainian Students
Autor:
Viktoriia KYRYCHENKO, Grațiela-Flavia DEAK, Nicolae Horațiu POP, Leon GOMBOȘ, Olena ANDRIEIEVA, Inna KHRYPKO
Publikováno v:
Studia Universitatis Babeş-Bolyai: Educatio Artis Gymnasticae, Vol 68, Iss 3 (2023)
Introduction: The aim of the present study was to compare the level of physical fitness of physical education majors from two universities based in Romania and Ukraine respectively. Materials and methods: A total of 201 university students participat
Externí odkaz:
https://doaj.org/article/c83401f38d5348f08fe7b0b5d0887864
Autor:
Olena Andrieieva, Anastasia Nahorna, Olena Yarmak, Liubov Yerakova, Viktoriia Kyrychenko, Svitlana Drozdovska, Oleksandr Petrachkov, Anatolii Buznik
Publikováno v:
Sport Mont, Vol 19, Iss S2, Pp 75-81 (2021)
The objective of this study was to identify informative anthropometric and functional indicators for design- ing self-training exercise programs for middle-aged obese women. The study involved 105 women with an average age of 38.9 and was conducted a
Externí odkaz:
https://doaj.org/article/78d74f0bb3d54f85b73d334dbfe7d537
Autor:
Qing-Jun Zhang, Tram Anh T. Tran, Ming Wang, Mark J. Ranek, Kristen M. Kokkonen-Simon, Jason Gao, Xiang Luo, Wei Tan, Viktoriia Kyrychenko, Lan Liao, Jianming Xu, Joseph A. Hill, Eric N. Olson, David A. Kass, Elisabeth D. Martinez, Zhi-Ping Liu
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-12 (2018)
Histone lysine demethylases (KDMs) can mediate transcriptional reprogramming in disease states. Here the authors show that KDM3A promotes left ventricular hypertrophy and cardiac fibrosis by activating the transcription of Timp1, and that pharmacolog
Externí odkaz:
https://doaj.org/article/7518fe10d5ab4b61a96ce3487b11c73b
Autor:
Wei Tan, Kristen M. Kokkonen-Simon, David A. Kass, Jason Gao, Viktoriia Kyrychenko, Elisabeth D. Martinez, Zhi Ping Liu, Lan Liao, Joseph A. Hill, Qing Jun Zhang, Tram Anh T. Tran, Mark J. Ranek, Jianming Xu, Xiang Luo, Eric N. Olson, Ming Wang
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-12 (2018)
Nature Communications
Nature Communications
Left ventricular hypertrophy (LVH) is a major risk factor for cardiovascular morbidity and mortality. Pathological LVH engages transcriptional programs including reactivation of canonical fetal genes and those inducing fibrosis. Histone lysine demeth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5a58d7ae7adcbc4db51c02b441cffab
http://link.springer.com/article/10.1038/s41467-018-07173-2
http://link.springer.com/article/10.1038/s41467-018-07173-2
Autor:
Thomas G. Gillette, Alfredo Criollo, Min Xie, Jay W. Schneider, Joseph A. Hill, Viktoriia Kyrychenko, Xiang Luo, Herman I. May, Nan Jiang, Wei Tan, Dan L. Li, Zhao V. Wang, Guanqiao Ding
Publikováno v:
Circulation. 133:1668-1687
Background— The clinical use of doxorubicin is limited by cardiotoxicity. Histopathological changes include interstitial myocardial fibrosis and the appearance of vacuolated cardiomyocytes. Whereas dysregulation of autophagy in the myocardium has b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad6c638429c0d87ddd1a6e13021a6c55
https://doi.org/10.1161/circulationaha.115.017443
https://doi.org/10.1161/circulationaha.115.017443
Autor:
Beverly A. Rothermel, Jay W. Schneider, Dan Tong, Carolina Hernández-Fuentes, David Rotter, Joseph A. Hill, Zully Pedrozo, Sergio Lavandero, Francisco Altamirano, Verónica Eisner, Valentina Parra, Viktoriia Kyrychenko
Publikováno v:
Circulation Research. 122
Rationale: The regulator of calcineurin 1 (RCAN1) inhibits CN (calcineurin), a Ca 2+ -activated protein phosphatase important in cardiac remodeling. In humans, RCAN1 is located on chromosome 21 in proximity to the Down syndrome critical region. The h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4eea105f2f084742ebabccf6291b65f7
https://doi.org/10.1161/circresaha.117.311522
https://doi.org/10.1161/circresaha.117.311522
Publikováno v:
Cell Calcium. 58:186-195
Duchenne muscular dystrophy (DMD) is a progressive muscle disease with severe cardiac complications. It is believed that cellular oxidative stress and augmented Ca(2+) signaling drives the development of cardiac pathology. Some mitochondrial and meta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ecc56213677b13440acac21a01dc106
https://doi.org/10.1016/j.ceca.2015.04.006
https://doi.org/10.1016/j.ceca.2015.04.006
Autor:
Yu Zhang, Norman Y. Liaw, Jay W. Schneider, Eric N. Olson, Malte Tiburcy, Cristina Rodriguez-Caycedo, John M. Shelton, Chengzu Long, Wolfram-Hubertus Zimmermann, Rhonda Bassel-Duby, Hui Li, Huanyu Zhou, Pradeep P.A. Mammen, Yi Li Min, Viktoriia Kyrychenko
Publikováno v:
Science Advances
CRISPR-mediated genome editing efficiently corrected cardiac abnormalities associated with DMD in human engineered heart tissue.
Genome editing with CRISPR/Cas9 is a promising new approach for correcting or mitigating disease-causing mutations.
Genome editing with CRISPR/Cas9 is a promising new approach for correcting or mitigating disease-causing mutations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9b1fb73c74f1ee3de08568327f19243
https://doi.org/10.1126/sciadv.aap9004
https://doi.org/10.1126/sciadv.aap9004
Autor:
Malte Tiburcy, John M. Shelton, Viktoriia Kyrychenko, Rhonda Bassel-Duby, Sergii Kyrychenko, Wolfram-Hubertus Zimmermann, Chengzu Long, Jay W. Schneider, Eric N. Olson
Publikováno v:
JCI Insight. 2
Dystrophin maintains the integrity of striated muscles by linking the actin cytoskeleton with the cell membrane. Duchenne muscular dystrophy (DMD) is caused by mutations in the dystrophin gene (DMD) that result in progressive, debilitating muscle wea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a726db94e8b22bfb4c2ccfeec63eea9
https://doi.org/10.1172/jci.insight.95918
https://doi.org/10.1172/jci.insight.95918
Deficit in PINK1/PARKIN-mediated mitochondrial autophagy at late stages of dystrophic cardiomyopathy
Publikováno v:
Cardiovascular research. 114(1)
Aims Duchenne muscular dystrophy (DMD) is an inherited devastating muscle disease with severe and often lethal cardiac complications. Emerging evidence suggests that the evolution of the pathology in DMD is accompanied by the accumulation of mitochon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e4d34ce58d170eb89af98a6dc57ec04
https://pubmed.ncbi.nlm.nih.gov/29036556
https://pubmed.ncbi.nlm.nih.gov/29036556