Zobrazeno 1 - 10
of 19
pro vyhledávání: '"O.Yu. Vasilyeva"'
Autor:
D.I. Zhigalina, A.A. Malakhova, O.Yu. Vasilyeva, E.V. Grigor'eva, A.A. Sivtsev, N.A. Kolesnikov, M.E. Lopatkina, R.R. Savchenko, I.Zh. Zhalsanova, A.E. Postrigan', A.A. Zarubin, T.V. Nikitina, A.O. Bueverov, P.O. Bogomolov, S.M. Zakian, N.A. Skryabin
Publikováno v:
Stem Cell Research, Vol 57, Iss , Pp 102556- (2021)
Wilson’s disease is a rare autosomal recessive disorder of copper metabolism. The copper accumulation in the viscera appears due to the functional impairment of copper-transporting ATPase, which is encoded by the ATP7B gene. In this study, PBMCs of
Externí odkaz:
https://doaj.org/article/8d6c5d2f67e44c1bbd16929bb4e7e7d8
Autor:
A.A. Malakhova, E.V. Grigor'eva, O.Yu. Vasilyeva, D.I. Zhigalina, N.A. Skryabin, A.A. Sivtcev, N.A. Kolesnikov, A.O. Bueverov, I.N. Lebedev, P.O. Bogomolov, S.M. Zakian
Publikováno v:
Stem Cell Research, Vol 47, Iss , Pp 101922- (2020)
Wilson’s disease is an inherited disorder associated with copper accumulation in the liver, brain and other vital organs. Wilson’s disease is caused by mutations in the ATP7B gene. Over 300 mutations of ATP7B have been described. Despite the dise
Externí odkaz:
https://doaj.org/article/6219fd4c424b43dfa5a476939c0ccfbd
Publikováno v:
Acta Horticulturae. :143-150
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c29982bf67db2451c2623201060dee4a
https://doi.org/10.17660/actahortic.2021.1324.22
https://doi.org/10.17660/actahortic.2021.1324.22
Publikováno v:
Scientific Works of North Caucasian Federal Scientific Center of Horticulture, Viticulture, Wine-making. 28:101-104
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09150db4ba46e37dc9a07aeb86452128
https://doi.org/10.30679/2587-9847-2020-28-101-104
https://doi.org/10.30679/2587-9847-2020-28-101-104
Autor:
M.V. Komarova, O.Yu. Vasilyeva
Publikováno v:
Review of Omsk State Pedagogical University. Humanitarian research. :61-65
In the article the naming units denoting means of transportation are considered in the framework of the linguoculturological approach, which allowed to identify the specifics of the formation of both the regional nominative fund and national thinking
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41b6a00bf95009a167f2082ab256c805
https://doi.org/10.36809/2309-9380-2020-28-61-65
https://doi.org/10.36809/2309-9380-2020-28-61-65
Autor:
O.Yu. Vasilyeva, A.V. Lyapina
Publikováno v:
Review of Omsk State Pedagogical University. Humanitarian research. :9-12
The hunting ritual, which has a long tradition of studying, is for the first time considered from the standpoint of the value-oriented system of values of the world by the authors of Russian journal essays of the late 19th century. The distinctive fe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a111620d5f77eb98482d374136af25f
https://doi.org/10.36809/2309-9380-2020-29-9-12
https://doi.org/10.36809/2309-9380-2020-29-9-12
Autor:
A.A. Malakhova, Alexei A. Zarubin, D. I. Zhigalina, I.Zh. Zhalsanova, A.O. Bueverov, E.V. Grigor'eva, R. R. Savchenko, Suren M. Zakian, A.E. Postrigan, O.Yu. Vasilyeva, N.A. Skryabin, A.A. Sivtsev, M.E. Lopatkina, N.A. Kolesnikov, T. V. Nikitina, P.O. Bogomolov
Publikováno v:
Stem Cell Research, Vol 57, Iss, Pp 102556-(2021)
Wilson’s disease is a rare autosomal recessive disorder of copper metabolism. The copper accumulation in the viscera appears due to the functional impairment of copper-transporting ATPase, which is encoded by the ATP7B gene. In this study, PBMCs of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::204c838ad42b7004955414b4aab2abd0
https://pubmed.ncbi.nlm.nih.gov/34736038
https://pubmed.ncbi.nlm.nih.gov/34736038
Autor:
O.Yu. Vasilyeva, Suren M. Zakian, D. I. Zhigalina, N.A. Skryabin, I. N. Lebedev, N.A. Kolesnikov, A.O. Bueverov, E.V. Grigor'eva, A.A. Sivtcev, A.A. Malakhova, P.O. Bogomolov
Publikováno v:
Stem Cell Research, Vol 47, Iss, Pp 101922-(2020)
Wilson’s disease is an inherited disorder associated with copper accumulation in the liver, brain and other vital organs. Wilson’s disease is caused by mutations in the ATP7B gene. Over 300 mutations of ATP7B have been described. Despite the dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37256cc2d17110225d9909ae5ab5ca2e
https://pubmed.ncbi.nlm.nih.gov/32738633
https://pubmed.ncbi.nlm.nih.gov/32738633
Autor:
I.Zh. Zhalsanova, N.A. Skryabin, O.Yu. Vasilyeva, Vadim Stepanov, A.A. Agafonova, G.N. Seitova, L.I. Minaicheva, Lyudmila P. Nazarenko, A.A. Sivtsev, Elena O. Belyaeva, V.V. Petrova, M.N. Filimonova, A.E. Postrigan
Publikováno v:
Nauchno-prakticheskii zhurnal «Medicinskaia genetika».
Using massively parallel sequencing, the COL1A1 and COL1A2 genes were analyzed in 16 patients from 10 families with osteogenesis imperfecta types I, III, and IV. To analyze the mutations in these genes, a panel of primers was developed for sequencing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7422de00d0b9bc3fbc846ee2122f9402
https://doi.org/10.25557/2073-7998.2020.01.38-45
https://doi.org/10.25557/2073-7998.2020.01.38-45
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