Genotype-specific pathogenic effects in human dilated cardiomyopathy-Reference-Cited by-同舟云学术

Genotype-specific pathogenic effects in human dilated cardiomyopathy

Published:2017-06-01 Issue:14 Volume:595 Page:4677-4693
ISSN:0022-3751
Container-title:The Journal of Physiology
language:en
Short-container-title:J Physiol

Author:

Bollen Ilse A. E.¹^ORCID,Schuldt Maike¹,Harakalova Magdalena²,Vink Aryan³,Asselbergs Folkert W.²⁴⁵,Pinto Jose R.⁶,Krüger Martina⁷,Kuster Diederik W. D.¹,van der Velden Jolanda¹⁸

Affiliation:

1. Department of Physiology, Amsterdam Cardiovascular Sciences; VU University Medical Center; Amsterdam the Netherlands

2. Department of Cardiology; Division of Heart and Lungs, University of Utrecht; University Medical Center Utrecht; Utrecht the Netherlands

3. Department of Pathology; University Medical Center Utrecht; Utrecht the Netherlands

4. Durrer Center for Cardiogenetic Research; ICIN-Netherlands Heart Institute; Utrecht the Netherlands

5. Institute of Cardiovascular Science, Faculty of Population Health Sciences; University College London; London UK

6. Department of Biomedical Sciences; College of Medicine; Florida State University; Tallahassee FL USA

7. Institute of Cardiovascular Physiology; Heinrich Heine University Düsseldorf; Düsseldorf Germany

8. Netherlands Heart Institute; Utrecht the Netherlands

Funder

National Heart, Lung, and Blood Institute

Rembrandt Institute for Cardiovascular Sciences

Hartstichting

UCL Hospitals NIHR Biomedical Research Centre

Publisher

Wiley

Subject

Physiology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1113/JP274145/fullpdf

Reference54 articles.

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2. Analysis of the molecular pathogenesis of cardiomyopathy-causing cTnT mutants I79N, DeltaE96, and DeltaK210;Bai;Biophys J,2013

3. A mutation in the glutamate-rich region of RNA-binding motif protein 20 causes dilated cardiomyopathy through missplicing of titin and impaired Frank-Starling mechanism;Beqqali;Cardiovasc Res,2016

4. Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy;Carballo;Circ Res,2009

5. Knock-in mouse model of dilated cardiomyopathy caused by troponin mutation;Du;Circ Res,2007

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