hiPSC-Derived Cardiomyocyte Model of LQT2 Syndrome Derived from Asymptomatic and Symptomatic Mutation Carriers Reproduces Clinical Differences in Aggregates but Not in Single Cells.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
07 05 2020
Historique:
received: 26 02 2020
revised: 29 04 2020
accepted: 02 05 2020
entrez: 13 5 2020
pubmed: 13 5 2020
medline: 26 2 2021
Statut: epublish

Résumé

Mutations in the

Identifiants

pubmed: 32392813
pii: cells9051153
doi: 10.3390/cells9051153
pmc: PMC7290503
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Références

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Auteurs

Disheet Shah (D)

Faculty of Medicine and Health Technology and BioMediTech Institute, Tampere University, Tampere 33520, Finland.

Chandra Prajapati (C)

Faculty of Medicine and Health Technology and BioMediTech Institute, Tampere University, Tampere 33520, Finland.

Kirsi Penttinen (K)

Faculty of Medicine and Health Technology and BioMediTech Institute, Tampere University, Tampere 33520, Finland.

Reeja Maria Cherian (RM)

Faculty of Medicine and Health Technology and BioMediTech Institute, Tampere University, Tampere 33520, Finland.

Jussi T Koivumäki (JT)

Faculty of Medicine and Health Technology and BioMediTech Institute, Tampere University, Tampere 33520, Finland.

Anna Alexanova (A)

Faculty of Medicine and Health Technology and BioMediTech Institute, Tampere University, Tampere 33520, Finland.

Jari Hyttinen (J)

Faculty of Medicine and Health Technology and BioMediTech Institute, Tampere University, Tampere 33520, Finland.

Katriina Aalto-Setälä (K)

Faculty of Medicine and Health Technology and BioMediTech Institute, Tampere University, Tampere 33520, Finland.
Heart Hospital, Tampere University Hospital, Tampere 33520, Finland.

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Classifications MeSH