Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Larysa Sivitskaya"'
Autor:
Ewa Matczyńska, Marta Beć-Gajowniczek, Larysa Sivitskaya, Elżbieta Gregorczyk, Przemysław Łyszkiewicz, Robert Szymańczak, Maria Jędrzejowska, Edward Wylęgała, Maciej R. Krawczyński, Sławomir Teper, Anna Boguszewska-Chachulska
Publikováno v:
Biomedicines, Vol 12, Iss 6, p 1355 (2024)
Advances in gene therapy and genome editing give hope that new treatments will soon be available for inherited eye diseases that together affect a significant proportion of the adult population. New solutions are needed to make genetic diagnosis fast
Externí odkaz:
https://doaj.org/article/983efdecb6184a87ae87baa8abda4dfd
Autor:
Larysa Sivitskaya, Tatiyana Vaikhanskaya, Nina Danilenko, Aleh Liaudanski, Oleg Davydenko, Nikolai Zhelev
Publikováno v:
Folia Medica, Vol 64, Iss 5, Pp 853-862 (2022)
Danon disease (DD), a rare X-linked genetic illness with a poor prognosis, is caused by a mutation in the lysosome-associated membrane protein 2 gene (LAMP2). Three main clinical features of this pathology are cardiomyopathy, skeletal myopathy, and m
Externí odkaz:
https://doaj.org/article/3b1fc7c1713f4fdf9a05f63edb0ae9f9
Autor:
Alena Kushniarevich, Larysa Sivitskaya, Nina Danilenko, Tadeush Novogrodskii, Iosif Tsybovsky, Anna Kiseleva, Svetlana Kotova, Gyaneshwer Chaubey, Ene Metspalu, Hovhannes Sahakyan, Ardeshir Bahmanimehr, Maere Reidla, Siiri Rootsi, Jüri Parik, Tuuli Reisberg, Alessandro Achilli, Baharak Hooshiar Kashani, Francesca Gandini, Anna Olivieri, Doron M Behar, Antonio Torroni, Oleg Davydenko, Richard Villems
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e66499 (2013)
Ethnic Belarusians make up more than 80% of the nine and half million people inhabiting the Republic of Belarus. Belarusians together with Ukrainians and Russians represent the East Slavic linguistic group, largest both in numbers and territory, inha
Externí odkaz:
https://doaj.org/article/5cb77446c9ed41729d9a142975024038
Autor:
Larysa Sivitskaya
Publikováno v:
Russian Heart Failure Journal. 17:201-211
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::026f4a48845e2a3771ad043507905a3a
https://doi.org/10.18087/rhfj.2016.3.2223
https://doi.org/10.18087/rhfj.2016.3.2223
Autor:
Larysa Sivitskaya
Publikováno v:
Russian Heart Failure Journal. 16:344-359
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47583098a6cc1524b84787812fefb0ba
https://doi.org/10.18087/rhfj.2015.6.2165
https://doi.org/10.18087/rhfj.2015.6.2165
Publikováno v:
Scopus-Elsevier
Acta Myologica
Acta Myologica
Desmoplakin is encoded by DSP gene, whose altered function leads to skin and hair abnormalities, and heart diseases. The whole triad of these traits characterizes the Carvajal syndrome (CS). CS is an autosomal recessive genetic disorder, mapping on c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::6284d569a678e3b3301f3f94a606a3ea
http://www.scopus.com/inward/record.url?eid=2-s2.0-85062684401&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-85062684401&partnerID=MN8TOARS
