Identification of MYLK3 mutations in familial dilated cardiomyopathy
Published 2017 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Identification of MYLK3 mutations in familial dilated cardiomyopathy
Authors
Keywords
-
Journal
Scientific Reports
Volume 7, Issue 1, Pages -
Publisher
Springer Nature
Online
2017-12-07
DOI
10.1038/s41598-017-17769-1
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C
- (2016) Eyal Reinstein et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Human genetic variation database, a reference database of genetic variations in the Japanese population
- (2016) Koichiro Higasa et al. JOURNAL OF HUMAN GENETICS
- Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies
- (2016) Martín F. Ortiz-Genga et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Translation readthrough mitigation
- (2016) Joshua A. Arribere et al. NATURE
- Analysis of protein-coding genetic variation in 60,706 humans
- (2016) Monkol Lek et al. NATURE
- Inferring gene-to-phenotype and gene-to-disease relationships at Mouse Genome Informatics: challenges and solutions
- (2016) Susan M. Bello et al. Journal of Biomedical Semantics
- Degradation of Stop Codon Read-through Mutant Proteins via the Ubiquitin-Proteasome System Causes Hereditary Disorders
- (2015) Norihito Shibata et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals
- (2015) Masao Nagasaki et al. Nature Communications
- Ventricular myosin modifies in vitro step-size when phosphorylated
- (2014) Yihua Wang et al. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
- Guidelines for investigating causality of sequence variants in human disease
- (2014) D. G. MacArthur et al. NATURE
- A general framework for estimating the relative pathogenicity of human genetic variants
- (2014) Martin Kircher et al. NATURE GENETICS
- 2013 ACCF/AHA Guideline for the Management of Heart Failure: Executive Summary
- (2013) Clyde W. Yancy et al. CIRCULATION
- Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy
- (2013) Roberta Roncarati et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Genetic mutations and mechanisms in dilated cardiomyopathy
- (2013) Elizabeth M. McNally et al. JOURNAL OF CLINICAL INVESTIGATION
- Rare-disease genetics in the era of next-generation sequencing: discovery to translation
- (2013) Kym M. Boycott et al. NATURE REVIEWS GENETICS
- Myosin Light Chain Phosphorylation Is Critical for Adaptation to Cardiac Stress
- (2012) Sonisha A. Warren et al. CIRCULATION
- Genetics of Hypertrophic Cardiomyopathy After 20 Years
- (2012) Barry J. Maron et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Dom34:Hbs1 Plays a General Role in Quality-Control Systems by Dissociation of a Stalled Ribosome at the 3′ End of Aberrant mRNA
- (2012) Tatsuhisa Tsuboi et al. MOLECULAR CELL
- Update 2011: Clinical and Genetic Issues in Familial Dilated Cardiomyopathy
- (2011) Ray E. Hershberger et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Prevalence and Prognostic Significance of Left Ventricular Reverse Remodeling in Dilated Cardiomyopathy Receiving Tailored Medical Treatment
- (2011) Marco Merlo et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Integrative genomics viewer
- (2011) James T Robinson et al. NATURE BIOTECHNOLOGY
- Cardiac Myosin Light Chain Kinase Is Necessary for Myosin Regulatory Light Chain Phosphorylation and Cardiac Performancein Vivo
- (2010) Peiguo Ding et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The Sequence Alignment/Map format and SAMtools
- (2009) H. Li et al. BIOINFORMATICS
- Identification of Cardiac-Specific Myosin Light Chain Kinase
- (2008) Jason Y. Chan et al. CIRCULATION RESEARCH
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreDiscover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversation