Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca2+ sensitivity

DCM-Causing Mutation E361G in Actin Slows Myofibril Relaxation Kinetics and Uncouples Myofibril Ca2+ Sensitivity from Protein Phosphorylation

(2013) Petr G. Vikhorev et al.   BIOPHYSICAL JOURNAL

Myofibrillar Ca2+ sensitivity is uncoupled from troponin I phosphorylation in hypertrophic obstructive cardiomyopathy due to abnormal troponin T

(2012) Christopher R. Bayliss et al.   CARDIOVASCULAR RESEARCH

The Rates of Ca2+Dissociation and Cross-bridge Detachment from Ventricular Myofibrils as Reported by a Fluorescent Cardiac Troponin C

(2012) Sean C. Little et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Truncations of Titin Causing Dilated Cardiomyopathy

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

Functional Characterization ofTNNC1Rare Variants Identified in Dilated Cardiomyopathy

(2011) Jose Renato Pinto et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Molecular Mechanism of the E99K Mutation in Cardiac Actin (ACTCGene) That Causes Apical Hypertrophy in Man and Mouse

(2011) Weihua Song et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

How Do Mutations in Contractile Proteins Cause the Primary Familial Cardiomyopathies?

(2011) Steven B. Marston   Journal of Cardiovascular Translational Research

Investigation of a transgenic mouse model of familial dilated cardiomyopathy

(2010) Weihua Song 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

Functional aberration of myofibrils by cardiomyopathy-causing mutations in the coiled-coil region of the troponin-core domain

(2009) Fumiko Matsumoto et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Identification and Functional Characterization of Cardiac Troponin I As a Novel Disease Gene in Autosomal Dominant Dilated Cardiomyopathy

(2009) Sebastian Carballo et al.   CIRCULATION RESEARCH

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

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy

(2009) Daniel Vega Møller et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Stress-induced dilated cardiomyopathy in a knock-in mouse model mimicking human titin-based disease

(2009) Michael Gramlich et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

Human actin mutations associated with hypertrophic and dilated cardiomyopathies demonstrate distinct thin filament regulatory properties in vitro

(2009) Edward P. Debold et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

From genotype to phenotype: a longitudinal study of a patient with hypertrophic cardiomyopathy due to a mutation in the MYBPC3 gene

(2009) Adam Jacques et al.   JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY

The unique functions of cardiac troponin I in the control of cardiac muscle contraction and relaxation

(2008) R. John Solaro et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

The changes of the cardiac structure and function in cTnTR141W transgenic mice

(2008) Feng Juan et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY