Generation of induced pluripotent stem cell line ICGi018-A from peripheral blood mononuclear cells of a patient with Huntington's disease

Summary

Huntington's disease (HD) is an autosomal dominant neurodegenerative disease caused by CAG repeat expansion in the HTT gene. HD patient-specific induced pluripotent stem cells (iPSCs) represent an excellent model for the disease study. We generated iPSC line from blood mononuclear cells of HD patient with 38 CAG repeats in the HTT exon 1 using integration free episomal plasmids expressing Yamanaka factors. The iPSC line retained the disease causing mutation and expressed pluripotency markers. It also displayed a normal karyotype and the ability to differentiate into derivatives of three germ layers. Copyright © 2020 The Authors. Published by Elsevier B.V. All rights reserved.

Authors Malakhova AA, Grigor'eva EV, Malankhanova TB, Pavlova SV, Valetdinova KR, Abramycheva NY, Vetchinova AS, Illarioshkin SN, Zakian SM
Journal Stem cell research
Publication Date 2020 Feb 21;44:101743
PubMed 32179492
DOI 10.1016/j.scr.2020.101743

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