Proteins encoded by human Down syndrome critical region gene 1-like 2 (DSCR1L2) mRNA and by a novel DSCR1L2 mRNA isoform interact with cardiac troponin I (TNNI3) (original) (raw)

Isolation and Characterization of the Human Cardiac Troponin I Gene (TNNI3

Pankaj Bhavsar

Genomics, 1996

Structure and regulation of the mouse cardiac troponin I gene

M. Vitadello

The Journal of biological chemistry, 1994

Human cardiac troponin complex. Structure and functions

Ivan Katrukha

Biochemistry (Moscow), 2013

Structural Consequences of Cardiac Troponin I Phosphorylation

Douglas Ward

Journal of Biological Chemistry, 2002

Ca ²⁺ -desensitizing effect of a deletion mutation ΔK210 in cardiac troponin T that causes familial dilated cardiomyopathy

Proceedings of the National Academy of Sciences of the United States of America, 2002

The functional significance of the last 5 residues of the C-terminus of cardiac troponin I

Aldrin Gomes

Archives of biochemistry and biophysics, 2016

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

2013

A Novel Mutation in TNNC1-ENCODED Cardiac Troponin C Predisposes to Hypertrophic Cardiomyopathy and Recurrent Episodes of Aborted Sudden Cardiac Death

Michelle Parvatiyar

Biophysical Journal, 2011

Different Functional Properties of Troponin T Mutants That Cause Dilated Cardiomyopathy

James d. Potter

Journal of Biological Chemistry, 2003

A point mutation (R192H) in the C-terminus of human cardiac troponin I causes diastolic dysfunction in transgenic mice

Archives of Biochemistry and Biophysics, 2006

doi:10.1155/2010/350706 Review Article Cardiac Troponin Mutations and Restrictive Cardiomyopathy

Michelle Parvatiyar

2013

Functional analysis of a unique troponin c mutation, GLY159ASP, that causes familial dilated cardiomyopathy, studied in explanted heart muscle

Douglas Ward

2009

Allele and species dependent contractile defects by restrictive and hypertrophic cardiomyopathy-linked troponin I mutants

Terri Edwards

Journal of Molecular and Cellular Cardiology, 2008

Troponin I Mutations R146G and R21C Alter Cardiac Troponin Function, Contractile Properties and Modulation by PKA-mediated Phosphorylation

Lucas Oxenford

The Journal of biological chemistry, 2015

A model for the function of the bisphosphorylated heart-specific troponin-I N-terminus

Michael Czisch

Journal of muscle research and cell motility, 1998

In Vivo and In Vitro analysis of cardiac troponin I phosphorylation

Paul Rosevear

Journal of Biological Chemistry, 2004

Functional Consequences of the Mutations in Human Cardiac Troponin I Gene Found in Familial Hypertrophic Cardiomyopathy

Journal of Molecular and Cellular Cardiology, 2001

Cardiomyopathy-Causing Deletion K210 in Cardiac Troponin T Alters Phosphorylation Propensity of Sarcomeric Proteins

Liliana Duke

Biophysical Journal, 2010

The Functional Properties of Human Slow Skeletal Troponin T Isoforms in Cardiac Muscle Regulation

Michelle Parvatiyar

Journal of Biological Chemistry, 2012

Structural Kinetics of Cardiac Troponin C Mutants Linked to Familial Hypertrophic and Dilated Cardiomyopathy in Troponin Complexes

Yexin Ouyang

Journal of Biological Chemistry, 2007

Effects of Troponin I Phosphorylation on Conformational Exchange in the Regulatory Domain of Cardiac Troponin C

Paul Rosevear

Journal of Biological Chemistry, 1999

Proteolytic N-terminal Truncation of Cardiac Troponin I Enhances Ventricular Diastolic Function

Shah.Md.Moazzem Hossain

Journal of Biological Chemistry, 2005

Cardiac Troponin I Gene Knockout : A Mouse Model of Myocardial Troponin I Deficiency

Circulation Research, 1999

Troponin Mutation Caused Diastolic Dysfunction and Experimental Treatment in Transgenic Mice with Cardiomyopathy

GSTF Journal of Advances in Medical Research, 2014

Troponin I, cardiac diastolic dysfunction and restrictive cardiomyopathy

Acta pharmacologica Sinica, 2004

Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T–tropomyosin interaction and causes a Ca2+ desensitization

Journal of Molecular and Cellular Cardiology, 2003

Restrictive Cardiomyopathy Caused by Troponin Mutations: Application of Disease Animal Models in Translational Studies

Frontiers in physiology, 2016

Gene-Targeted Mice with the Human Troponin T R141W Mutation Develop Dilated Cardiomyopathy with Calcium Desensitization

Guy Salama

PloS one, 2016