Generation of an Induced Pluripotent Stem Cell Line TNRMCi001-A by Reprogramming Fibroblasts from a Homozygous F508del Cystic Fibrosis Patient
Zhigalina, D. I., Kireeva, T. N., Nikitina, T. V., Odinokova, O. N., Kolesnikov, N. A., Malakhova, A. A., Savchenko, R. R., Zhalsanova, I. Zh, Valiahmetov, N. R., Postrigan, A. E., Vovk, S. L., Torkhova, N. B., Frolova, A. A., Stepanov, V. A., Skryabin, N. A.
Published in Russian journal of developmental biology (01.12.2023)
Published in Russian journal of developmental biology (01.12.2023)
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Associations of genes of DNA repair systems with Parkinson’s disease
Babushkina, N. P., Nikitina, M. A., Bragina, E. Yu, Alifirova, V. M., Postrigan, A. E., Deviatkina, Ye. A., Gomboeva, D. E., Nazarenko, M. S.
Published in Acta biomedica scientifica (29.12.2022)
Published in Acta biomedica scientifica (29.12.2022)
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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
Zhigalina, D.I., Malakhova, A.A., Vasilyeva, O.Yu, Grigor'eva, E.V., Sivtsev, A.A., Kolesnikov, N.A., Lopatkina, M.E., Savchenko, R.R., Zhalsanova, I.Zh, Postrigan', A.E., Zarubin, A.A., Nikitina, T.V., Bueverov, A.O., Bogomolov, P.O., Zakian, S.M., Skryabin, N.A.
Published in Stem cell research (01.12.2021)
Published in Stem cell research (01.12.2021)
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Analysis of mutations spectrum in the ATP7B gene in patients with Wilson disease using massively parallel sequencing
Sivtsev, A A, Zhalsanova, I Zh, Postrigan, A E, Fonova, E A, Vasilyeva, O Yu, Zarubin, A A, Minaicheva, L I, Agafonova, A A, Petrova, V V, Ravzhaeva, E G, Salyukova, O A, Skryabin, N A
Published in Klinicheskaia laboratornaia diagnostika (17.04.2022)
Published in Klinicheskaia laboratornaia diagnostika (17.04.2022)
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Clinical and Genetic Characteristics of Congenital Long QT Syndrome
Postrigan, A. E., Babushkina, N. P., Svintsova, L. I., Plotnikova, I. V., Skryabin, N. A.
Published in Russian journal of genetics (01.10.2022)
Published in Russian journal of genetics (01.10.2022)
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Modifier Genes as a Cause of Wilson–Konovalov Disease Clinical Polymorphism
Postrigan, A. E., Zhalsanova, I. Zh, Fonova, E. A., Skryabin, N. A.
Published in Russian journal of genetics (01.05.2021)
Published in Russian journal of genetics (01.05.2021)
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