Literature DB >> 31398660

Generation of two human induced pluripotent stem cell (hiPSC) lines from a long QT syndrome South African founder population.

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.
Copyright © 2019 The Authors. Published by Elsevier B.V. All rights reserved.

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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


  1 in total

1.  NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesis.

Authors:  Carlotta Ronchi; Joyce Bernardi; Manuela Mura; Manuela Stefanello; Beatrice Badone; Marcella Rocchetti; Lia Crotti; Paul Brink; Peter J Schwartz; Massimiliano Gnecchi; Antonio Zaza
Journal:  Cardiovasc Res       Date:  2021-01-21       Impact factor: 10.787

  1 in total

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