Contractile Dysfunction Irrespective of the Mutant Protein in Human Hypertrophic Cardiomyopathy With Normal Systolic Function-Reference-Cited by-同舟云学术

Contractile Dysfunction Irrespective of the Mutant Protein in Human Hypertrophic Cardiomyopathy With Normal Systolic Function

Published:2012-01 Issue:1 Volume:5 Page:36-46
ISSN:1941-3289
Container-title:Circulation: Heart Failure
language:en
Short-container-title:Circ Heart Fail

Author:

van Dijk Sabine J.¹,Paalberends E. Rosalie¹,Najafi Aref¹,Michels Michelle¹,Sadayappan Sakthivel¹,Carrier Lucie¹,Boontje Nicky M.¹,Kuster Diederik W.D.¹,van Slegtenhorst Marjon¹,Dooijes Dennis¹,dos Remedios Cris¹,ten Cate Folkert J.¹,Stienen Ger J.M.¹,van der Velden Jolanda¹

Affiliation:

1. From the Laboratory for Physiology, Institute for Cardiovascular Research, VU University Medical Center, Amsterdam, The Netherlands (S.J.D., E.R.P., A.N., N.M.B., D.W.D.K., G.J.M.S., J.V.); Department of Physics and Astronomy, VU University Amsterdam, De Boelelaan 1081, Amsterdam, The Netherlands (G.J.M.S.); Thorax Center (M.M., F.J.C.) and Clinical Genetics (M.S.), Erasmus Medical Center Rotterdam, The Netherlands; Department of Cell and Molecular Physiology, Loyola University Chicago, Chicago, IL ...

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

Reference48 articles.

1. Genetic basis of hypertrophic cardiomyopathy: from bench to the clinics;Alcalai R;J Cardiovasc Electrophysiol,2008

2. Hypertrophic Cardiomyopathy

3. Narrative Review: Harnessing Molecular Genetics for the Diagnosis and Management of Hypertrophic Cardiomyopathy

4. The ubiquitin-proteasome system and nonsense-mediated mRNA decay in hypertrophic cardiomyopathy

5. Hypertrophic Cardiomyopathy

Cited by 112 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Characterization of heterozygous and homozygous mouse models with the most common hypertrophic cardiomyopathy mutation MYBPC3 in the Netherlands;Journal of Molecular and Cellular Cardiology;2023-12

2. Nonsense mediated decay factor UPF3B is associated with cMyBP-C haploinsufficiency in hypertrophic cardiomyopathy patients;Journal of Molecular and Cellular Cardiology;2023-12

3. Mavacamten, a precision medicine for hypertrophic cardiomyopathy: From a motor protein to patients;Science Advances;2023-07-28

4. A pathogenic nonsense mutation (c.1522C>T) of the MYBPC3 gene is implicated with hypertrophic cardiomyopathy;ESC Heart Failure;2023-06-04

5. Mechano-energetic uncoupling in hypertrophic cardiomyopathy: Pathophysiological mechanisms and therapeutic opportunities;Journal of Molecular and Cellular Cardiology Plus;2023-06