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Kseniya Perepelina
Kseniya Perepelina
Almazov National Medical Research Centre
Verified email at almazovcentre.ru
Title
Cited by
Cited by
Year
Diversity of nuclear lamin A/C action as a key to tissue-specific regulation of cellular identity in health and disease
A Malashicheva, K Perepelina
Frontiers in cell and developmental biology 9, 761469, 2021
362021
Sodium current abnormalities and deregulation of Wnt/β-catenin signaling in iPSC-derived cardiomyocytes generated from patient with arrhythmogenic cardiomyopathy harboring …
A Khudiakov, A Zaytseva, K Perepelina, N Smolina, T Pervunina, ...
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1866 (11), 165915, 2020
202020
Tissue-specific influence of lamin A mutations on notch signaling and osteogenic phenotype of primary human mesenchymal cells
K Perepelina, P Klauzen, A Kostareva, A Malashicheva
Cells 8 (3), 266, 2019
192019
Impact of the DSP-H1684R genetic variant on ion channels activity in iPSC-derived cardiomyocytes
K Gusev, A Khudiakov, A Zaytseva, K Perepelina, S Makeenok, ...
Cell. Physiol. Biochem 54, 696-706, 2020
122020
Extracellular micrornas and mitochondrial DNA as potential biomarkers of arrhythmogenic cardiomyopathy
AA Khudiakov, NA Smolina, KI Perepelina, AB Malashicheva, ...
Biochemistry (Moscow) 84 (3), 272-282, 2019
122019
Generation of two iPSC lines (FAMRCi006-A and FAMRCi006-B) from patient with dilated cardiomyopathy and Emery–Dreifuss muscular dystrophy associated with genetic variant LMNAp …
K Perepelina, P Klauzen, A Khudiakov, A Zlotina, Y Fomicheva, ...
Stem Cell Research 43, 101714, 2020
62020
LMNA mutation leads to cardiac sodium channel dysfunction in the Emery-Dreifuss muscular dystrophy patient
K Perepelina, A Zaytseva, A Khudiakov, I Neganova, E Vasichkina, ...
Frontiers in Cardiovascular Medicine 9, 932956, 2022
52022
Generation of iPSC line (FAMRCi009-A) from patient with familial progressive cardiac conduction disorder carrying genetic variant FLNC p. Val2264Met
N Rodina, A Khudiakov, K Perepelina, A Muravyev, A Boytsov, A Zlotina, ...
Stem Cell Research 59, 102640, 2022
52022
Generation of two iPSC lines (FAMRCi007-A and FAMRCi007-B) from patient with Emery–Dreifuss muscular dystrophy and heart rhythm abnormalities carrying genetic variant LMNA p …
K Perepelina, A Kostina, P Klauzen, A Khudiakov, M Rabino, S Crasto, ...
Stem Cell Research 47, 101895, 2020
52020
Generation of iPSC line FAMRCi010-A from patient with restrictive cardiomyopathy carrying genetic variant FLNC p. Gly2011Arg
K Perepelina, A Khudiakov, N Rodina, A Boytsov, T Vavilova, A Zlotina, ...
Stem Cell Research 59, 102639, 2022
32022
Generation of two iPSC lines (FAMRCi004-A and FAMRCi004-B) from patient with familial progressive cardiac conduction disorder carrying genetic variant DSP p. His1684Arg.
A Khudiakov, K Perepelina, P Klauzen, A Zlotina, K Gusev, ...
Stem Cell Research 43, 101720, 2020
32020
The Role of Mechanical Properties of the Nucleus in Maintaining Tissue Homeostasis
SV Lavrushkina, NL Ovsyannikova, AS Yudina, OS Strelkova, ...
Cell and Tissue Biology 13, 237-241, 2019
32019
R482L Mutation of the LMNA Gene Affects Dynamics of C2C12 Myogenic Differentiation and Stimulates Formation of Intramuscular Lipid Droplets
NV Khromova, KI Perepelina, OA Ivanova, AB Malashicheva, ...
Biochemistry (Moscow) 84, 241-249, 2019
32019
The role of LMNA mutations in myogenic differentiation of C2C12 and primary satellite cells
KI Perepelina, NA Smolina, AS Zabirnik, RI Dmitrieva, AB Malashicheva, ...
Cell and Tissue Biology 11 (3), 213-219, 2017
32017
THE ROLE OF LMNA MUTATIONS IN MYOGENIC DIFFERENTIATION OF PRIMARY SATELLITE CELLS AND C2C12 CELLS.
KI Perepelina, NA Smolina, AS Zabirnik, RI Dmitrieva, AB Malashicheva, ...
Tsitologiia 59 (2), 117-124, 2017
32017
Внеклеточные микроРНК и митохондриальная ДНК как потенциальные биомаркеры аритмогенной кардиомиопатии
АА Худяков, НА Смолина, КИ Перепелина, АБ Малашичева, ...
Биохимия 84 (3), 392-403, 2019
22019
Роль механических свойств ядра в поддержании гомеостаза тканей
СВ Лаврушкина, НЛ Овсянникова, АС Юдина, ОС Стрелкова, ...
Цитология 60 (11), 911-915, 2018
22018
Generation of two induced pluripotent stem cell lines (FAMRCi005-A and FAMRCi005-B) from patient carrying genetic variant LMNA p. Asp357Val.
P Klauzen, K Perepelina, A Khudiakov, A Zlotina, Y Fomicheva, ...
Stem Cell Research 43, 101719, 2020
12020
Analysis of the role of Na v 1.5 slow inactivation in the development of inherited cardiac pathology
AK Zaytseva, KI Perepelina, AA Kostareva
Citologiâ 66 (1), 54-63, 2024
2024
Analysis of Slow Inactivation of Nav1.5 Channels in the Development of Hereditary Heart Pathology
AK Zaitseva, KI Perepelina, AA Kostareva
Cell and Tissue Biology 18 (3), 324-333, 2024
2024
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