Characterization of heterozygous and homozygous mouse models with the most common hypertrophic cardiomyopathy mutation MYBPC3 in the Netherlands-Reference-Cited by-同舟云学术

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Characterization of heterozygous and homozygous mouse models with the most common hypertrophic cardiomyopathy mutation MYBPC3 in the Netherlands

Published:2023-12 Issue: Volume:185 Page:65-76
ISSN:0022-2828
Container-title:Journal of Molecular and Cellular Cardiology
language:en
Short-container-title:Journal of Molecular and Cellular Cardiology

Author:

Hilderink Sarah,Schuldt Maike,Goebel Max,Jansen Valentijn J.,Manders Emmy,Moorman Stan,Dorsch Larissa M.,van Steenbeek Frank G.,van der Velden Jolanda,Kuster Diederik W.D.

Funder

Dutch CardioVascular Alliance

NWO

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Molecular Biology

Reference59 articles.

1. New perspectives on the prevalence of hypertrophic cardiomyopathy;Semsarian;J. Am. Coll. Cardiol.,2015

2. Cardiac disorders and pathophysiology of Sarcomeric proteins;van der Velden;Physiol. Rev.,2019

3. What causes hypertrophic cardiomyopathy?;Maron;Am. J. Cardiol.,2022

4. The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands;Alders;Eur. Heart J.,2003

5. Contractile dysfunction irrespective of the mutant protein in human hypertrophic cardiomyopathy with normal systolic function;van Dijk;Circ. Heart Fail.,2012

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1. Localized translation and sarcomere maintenance requires ribosomal protein SA in mice;Journal of Clinical Investigation;2024-05-14

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