Different Functional Properties of Troponin T Mutants That Cause Dilated Cardiomyopathy

This publication has 38 references indexed in Scilit:

• Molecular Mechanisms of Inherited Cardiomyopathies
  Physiological Reviews, 2002
• A novel mutation Lys273Glu in the cardiac troponin T gene shows high degree of penetrance and transition from hypertrophic to dilated cardiomyopathy
  Published by Elsevier ,2002
• Novel Cardiac Troponin T Mutation as a Cause of Familial Dilated Cardiomyopathy
  Circulation, 2001
• The Genetic Basis for Cardiomyopathy: from Mutation Identification to Mechanistic Paradigms
  Published by Elsevier ,2001
• Mutations in Sarcomere Protein Genes as a Cause of Dilated Cardiomyopathy
  New England Journal of Medicine, 2000
• Actin Mutations in Dilated Cardiomyopathy, a Heritable Form of Heart Failure
  Science, 1998
• Molecular Switches in Troponin
  Published by Springer Nature ,1998
• Report of the National Heart, Lung, and Blood Institute Special Emphasis Panel on Heart Failure Research
  Circulation, 1997
• Thin Filament-Mediated Regulation of Cardiac Contraction
  Annual Review of Physiology, 1996
• Structural Aspects of Troponin-Tropomyosin Regulation of Skeletal Muscle Contraction
  Annual Review of Biophysics, 1987