Related references
Note: Only part of the references are listed.PLN-encoded phospholamban mutation in a large cohort of hypertrophic cardiomyopathy cases: Summary of the literature and implications for genetic testing
Andrew P. Landstrom et al.
AMERICAN HEART JOURNAL (2011)
Mutations in NEXN, a Z-Disc Gene, Are Associated with Hypertrophic Cardiomyopathy
Hu Wang et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
Research Priorities in Hypertrophic Cardiomyopathy Report of a Working Group of the National Heart, Lung, and Blood Institute
Thomas Force et al.
CIRCULATION (2010)
Is genotype clinically useful in predicting prognosis in hypertrophic cardiomyopathy? Genetics and Clinical Destiny: Improving Care in Hypertrophic Cardiomyopathy
Carolyn Y. Ho
CIRCULATION (2010)
The Cardiac Myosin Binding Protein C Arg502Trp Mutation A Common Cause of Hypertrophic Cardiomyopathy
Adam J. Saltzman et al.
CIRCULATION RESEARCH (2010)
A Common MLP (Muscle LIM Protein) Variant Is Associated With Cardiomyopathy
Ralph Knoell et al.
CIRCULATION RESEARCH (2010)
DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness model
Sarah Wordsworth et al.
EUROPEAN HEART JOURNAL (2010)
Cardiac fibrosis in mice with hypertrophic cardiomyopathy is mediated by non-myocyte proliferation and requires Tgf-β
Polakit Teekakirikul et al.
JOURNAL OF CLINICAL INVESTIGATION (2010)
Mutations in Alpha-Actinin-2 Cause Hypertrophic Cardiomyopathy A Genome-Wide Analysis
Christine Chiu et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2010)
Heterogeneous myocyte enhancer factor-2 (Mef2) activation in myocytes predicts focal scarring in hypertrophic cardiomyopathy
Tetsuo Konno et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Cardiac Myosin-Binding Protein C Mutations and Hypertrophic Cardiomyopathy Haploinsufficiency, Deranged Phosphorylation, and Cardiomyocyte Dysfunction
Sabine J. van Dijk et al.
CIRCULATION (2009)
Evidence From Human Myectomy Samples That MYBPC3 Mutations Cause Hypertrophic Cardiomyopathy Through Haploinsufficiency
Steven Marston et al.
CIRCULATION RESEARCH (2009)
Cardiac Ankyrin Repeat Protein Gene (ANKRD1) Mutations in Hypertrophic Cardiomyopathy
Takuro Arimura et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2009)
A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia
Perundurai S. Dhandapany et al.
NATURE GENETICS (2009)
Genetic diagnosis by whole exome capture and massively parallel DNA sequencing
Murim Choi et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Role of Animal Models in HCM Research
Rhian Shephard et al.
JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH (2009)
Insights into Human β-Cardiac Myosin Function from Single Molecule and Single Cell Studies
Sivaraj Sivaramakrishnan et al.
JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH (2009)
Hypertrophic cardiomyopathy: lessons from history
C. J. Coats et al.
HEART (2008)
Hypertrophic and dilated cardiomyopathy mutations differentially affect the molecular force generation of mouse α-cardiac myosin in the laser trap assay
Edward P. Debold et al.
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY (2007)
Polony multiplex analysis of gene expression (PMAGE) in mouse hypertrophic cardiomyopathy
Jae Bum Kim et al.
SCIENCE (2007)
A molecular screening strategy based on β-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy
Francesca Girolami et al.
JOURNAL OF CARDIOVASCULAR MEDICINE (2006)
A missense mutation in a ubiquitously expressed protein, vinculin, confers susceptibility to hypertrophic cardiomyopathy
Vlad C. Vasile et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)
Genotype-phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethonin
JM Bos et al.
MOLECULAR GENETICS AND METABOLISM (2006)
Lifelong left ventricular remodeling of hypertrophic cardiomyopathy caused by a founder frameshift deletion mutation in the cardiac myosin-binding protein c gene among Japanese
T Kubo et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2005)
α-Myosin heavy chain -: A sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy
E Carniel et al.
CIRCULATION (2005)
Sarcomeric proteins and familial hypertrophic cardiomyopathy: Linking mutations in structural proteins to complex cardiovascular phenotypes
JC Tardiff
HEART FAILURE REVIEWS (2005)
Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy
T Hayashi et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2004)
Genetics of hypertrophic cardiomyopathy in eastern Finland: few founder mutations with benign or intermediary phenotypes
P Jaaskelainen et al.
ANNALS OF MEDICINE (2004)
The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands
M Alders et al.
EUROPEAN HEART JOURNAL (2003)
An abnormal Ca2+ response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy
D Fatkin et al.
JOURNAL OF CLINICAL INVESTIGATION (2000)
Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy
TM Olson et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2000)
Share Paper
