Genetic mutations and mechanisms in dilated cardiomyopathy

Evaluating Pathogenicity of Rare Variants From Dilated Cardiomyopathy in the Exome Era

(2012) Nadine Norton et al.   Circulation-Cardiovascular Genetics

The National Institutes of Health Undiagnosed Diseases Program: insights into rare diseases

(2012) William A. Gahl et al.   GENETICS IN MEDICINE

Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations

(2012) Enkhsaikhan Purevjav et al.   HUMAN MOLECULAR GENETICS

Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers

(2012) Ingrid A.W. van Rijsingen et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Truncations of Titin Causing Dilated Cardiomyopathy

(2012) Daniel S. Herman et al.   NEW ENGLAND JOURNAL OF MEDICINE

Review and Metaanalysis of the Frequency of Familial Dilated Cardiomyopathy

(2011) Mario Petretta et al.   AMERICAN JOURNAL OF CARDIOLOGY

Genetic Variation in Titin in Arrhythmogenic Right Ventricular Cardiomyopathy–Overlap Syndromes

(2011) Matthew Taylor et al.   CIRCULATION

Thin Filament Mutations

(2011) Jil C. Tardiff   CIRCULATION RESEARCH

A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy

(2011) Eric Villard et al.   EUROPEAN HEART JOURNAL

Cytoskeletal protein kinases: titin and its relations in mechanosensing

(2011) Mathias Gautel   PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY

Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation

(2011) T. P. Cappola et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Common Variants in HSPB7 and FRMD4B Associated With Advanced Heart Failure

(2010) Thomas P. Cappola et al.   Circulation-Cardiovascular Genetics

Nesprins LINC the nucleus and cytoskeleton

(2010) Jason A Mellad et al.   CURRENT OPINION IN CELL BIOLOGY

Transforming growth factor (TGF)-β signaling in cardiac remodeling

(2010) Marcin Dobaczewski et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

Familial Dilated Cardiomyopathy Caused by an Alpha-Tropomyosin Mutation

(2010) Neal K. Lakdawala et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations

(2010) Francesca Girolami et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Myocardial Fibrosis as an Early Manifestation of Hypertrophic Cardiomyopathy

(2010) Carolyn Y. Ho et al.   NEW ENGLAND JOURNAL OF MEDICINE

Distinct genetic regions modify specific muscle groups in muscular dystrophy

(2010) Kayleigh A. Swaggart et al.   PHYSIOLOGICAL GENOMICS

Altered Chromosomal Positioning, Compaction, and Gene Expression with a Lamin A/C Gene Mutation

(2010) Stephanie K. Mewborn et al.   PLoS One

The Pediatric Cardiomyopathy Registry and Heart Failure: Key Results from the First 15 Years

(2010) James D. Wilkinson et al.   Heart Failure Clinics

Sarcomere Mutations in Cardiomyopathy With Left Ventricular Hypertrabeculation

(2009) Lisa M. Dellefave et al.   Circulation-Cardiovascular Genetics

Functional Analysis of a Unique Troponin C Mutation, GLY159ASP, that Causes Familial Dilated Cardiomyopathy, Studied in Explanted Heart Muscle

(2009) Emma C. Dyer et al.   Circulation-Heart Failure

Lamin A/C deficiency as a cause of familial dilated cardiomyopathy

(2009) Rohit Malhotra et al.   CURRENT OPINION IN CARDIOLOGY

Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathy

(2009) Laëtitia Duboscq-Bidot et al.   EUROPEAN HEART JOURNAL

Lamin A/C–mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy

(2009) Alexandre Méjat et al.   JOURNAL OF CELL BIOLOGY

Latent TGF-β–binding protein 4 modifies muscular dystrophy in mice

(2009) Ahlke Heydemann et al.   JOURNAL OF CLINICAL INVESTIGATION

Nesprin-1 mutations in human and murine cardiomyopathy

(2009) Megan J. Puckelwartz et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

ANKRD1, the Gene Encoding Cardiac Ankyrin Repeat Protein, Is a Novel Dilated Cardiomyopathy Gene

(2009) Mousumi Moulik et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy

(2009) David Hassel et al.   NATURE MEDICINE

Tnni3k Modifies Disease Progression in Murine Models of Cardiomyopathy

(2009) Ferrin C. Wheeler et al.   PLoS Genetics

Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction

(2008) Sabine Klaassen et al.   CIRCULATION