<p>The locations of ACTC mutations associated with cardiomyopathies are shown in black (HCM) and red (DCM) letters. The regions of molecular effects are circled and spacefilling models presented in red (protein stability changes), green (actin polymerization changed), and blue (no significant intrinsic property changes). Those residues shown in grey have not been characterized. Coordinate data for ATP-bound TMR-actin (1J6Z) <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0036821#pone.0036821-Graceffa1" target="_blank">[39]</a> were visualized using PyMol <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0036821#pone.0036821-Schrodinger1" target="_blank">[40]</a>.</p
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiovascular disease that could res...
Hypertrophic and restrictive cardiomyopathies are congenital cardiac diseases that have an incidence...
The cardiac thin filament (CTF) is known as the regulatory unit of cardiac muscle. Point mutations t...
<p><b><i>A</i></b><i>.</i> The protein structure of actin (PDB 1J6Z) <a href="http://www.plosone.org...
Determining the molecular mechanisms that lead to the development of heart failure will help us gain...
Determining the molecular mechanisms that lead to the development of heart failure will help us gain...
Mutations in the cardiac actin gene (ACTC1) are associated with the development of hypertrophic card...
†<p>labeled with tetramethylrhodamine.</p>*<p><i>p</i><0.05 by <i>t</i>–test.</p>**<p><i>p</i><0.15 ...
<p>Actin and myosin amino acid numbers are according to human numbering <b>(A)</b> Backbone represen...
Hypertrophic cardiomyopathy (HCM) is an inherited cardiovascular disease (CD) that commonly causes a...
Familial hypertrophic and dilated cardiomyopathies (HCM and DCM, respectively) are diseases which ac...
Cardiac contraction at the level of the sarcomere is regulated by the thin filament (TF) composed of...
The two genes most commonly associated with mutations linked to hypertrophic or dilated cardiomyopat...
The inherited cardiac diseases hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) ca...
Point mutations within sarcomeric proteins have been associated with altered function and cardiomyop...
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiovascular disease that could res...
Hypertrophic and restrictive cardiomyopathies are congenital cardiac diseases that have an incidence...
The cardiac thin filament (CTF) is known as the regulatory unit of cardiac muscle. Point mutations t...
<p><b><i>A</i></b><i>.</i> The protein structure of actin (PDB 1J6Z) <a href="http://www.plosone.org...
Determining the molecular mechanisms that lead to the development of heart failure will help us gain...
Determining the molecular mechanisms that lead to the development of heart failure will help us gain...
Mutations in the cardiac actin gene (ACTC1) are associated with the development of hypertrophic card...
†<p>labeled with tetramethylrhodamine.</p>*<p><i>p</i><0.05 by <i>t</i>–test.</p>**<p><i>p</i><0.15 ...
<p>Actin and myosin amino acid numbers are according to human numbering <b>(A)</b> Backbone represen...
Hypertrophic cardiomyopathy (HCM) is an inherited cardiovascular disease (CD) that commonly causes a...
Familial hypertrophic and dilated cardiomyopathies (HCM and DCM, respectively) are diseases which ac...
Cardiac contraction at the level of the sarcomere is regulated by the thin filament (TF) composed of...
The two genes most commonly associated with mutations linked to hypertrophic or dilated cardiomyopat...
The inherited cardiac diseases hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) ca...
Point mutations within sarcomeric proteins have been associated with altered function and cardiomyop...
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiovascular disease that could res...
Hypertrophic and restrictive cardiomyopathies are congenital cardiac diseases that have an incidence...
The cardiac thin filament (CTF) is known as the regulatory unit of cardiac muscle. Point mutations t...