Zobrazeno 1 - 10 of 49 pro vyhledávání: '"A.O. Bueverov"'
1
Akademický článek
Generation of an induced pluripotent stem cell line ICGi030-A from a Wilson's disease patient carrying a frameshift mutation p.Lys1013fs and missense mutation p.H1069Q in the ATP7B gene
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
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2
Akademický článek
Generation of two induced pluripotent stem cell lines from peripheral blood mononuclear cells of a patient with Wilson’s disease
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
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4
Generation of an induced pluripotent stem cell line ICGi030-A from a Wilson's disease patient carrying a frameshift mutation p.Lys1013fs and missense mutation p.H1069Q in the ATP7B gene
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
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8
Generation of two induced pluripotent stem cell lines from peripheral blood mononuclear cells of a patient with Wilson's disease
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
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9
Akademický článek
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10
Akademický článek
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