TY - JOUR

T1 - Generation of two iPSC lines (FAMRCi004-A and FAMRCi004-B) from patient with familial progressive cardiac conduction disorder carrying genetic variant DSP p.His1684Arg.

AU - Khudiakov, Aleksandr

AU - Perepelina, Kseniya

AU - Klauzen, Polina

AU - Zlotina, Anna

AU - Gusev, Konstantin

AU - Kaznacheyeva, Elena

AU - Malashicheva, Anna

AU - Kostareva, Anna

PY - 2020/3

Y1 - 2020/3

N2 - Human iPSC cell lines (FAMRCi004-A and FAMRCi004-B) were generated from patient with progressive cardiac conduction disease and sick sinus syndrome carrying DSP p.His1684Arg genetic variant. Patient-specific adipose tissue-derived mesenchymal multipotent stromal cells were reprogrammed using non-integrative Sendai viruses. Established iPSC lines showed normal karyotype, expressed pluripotent markers and were able to differentiate toward three germ layers in vitro. The reported iPSC lines could be useful tool for in vitro modeling of progressive cardiac conduction disease associated with mutations in desmosomal genes.

AB - Human iPSC cell lines (FAMRCi004-A and FAMRCi004-B) were generated from patient with progressive cardiac conduction disease and sick sinus syndrome carrying DSP p.His1684Arg genetic variant. Patient-specific adipose tissue-derived mesenchymal multipotent stromal cells were reprogrammed using non-integrative Sendai viruses. Established iPSC lines showed normal karyotype, expressed pluripotent markers and were able to differentiate toward three germ layers in vitro. The reported iPSC lines could be useful tool for in vitro modeling of progressive cardiac conduction disease associated with mutations in desmosomal genes.

UR - http://www.scopus.com/inward/record.url?scp=85079230033&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/61a48400-14d3-3193-b2d0-84cf9b6803e7/

U2 - 10.1016/j.scr.2020.101720

DO - 10.1016/j.scr.2020.101720

M3 - Editorial

C2 - 32062131

AN - SCOPUS:85079230033

VL - 43

JO - Stem Cell Research

JF - Stem Cell Research

SN - 1873-5061

M1 - 101720

ER -