| Literature DB >> 31398660 |
Manuela Mura1, Federica Pisano2, Manuela Stefanello1, Monia Ginevrino3, Marina Boni4, Federica Calabrò1, Lia Crotti5, Enza Maria Valente3, Peter J Schwartz6, Paul A Brink7, Massimiliano Gnecchi8.
Abstract
We generated PSMi001-A and PSMi008-A hiPSC lines from two individuals belonging to a South African (SA) founder population in which the malignant KCNQ1-A341V mutation cosegregates with the Long QT Syndrome (LQTS) phenotype. PSMi001-A was derived from an asymptomatic KCNQ1-A341V mutation carrier, whereas PSMi008-A was derived from a healthy non-mutation carrier, heterozygous for the minor variant rs16847548 on the NOS1AP gene, associated with QT prolongation in the general population, and with a greater risk for cardiac arrest in the affected members of the SA founder population. The hiPSCs, generated using the Yamanaka's retroviruses, display pluripotent stem cell features and trilineage differentiation potential.Entities:
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Year: 2019 PMID: 31398660 DOI: 10.1016/j.scr.2019.101510
Source DB: PubMed Journal: Stem Cell Res ISSN: 1873-5061 Impact factor: 2.020