Stem cell activation sustains hereditary hypertrophy in hamster cardiomyopathy

This publication has 38 references indexed in Scilit:

• The Dystrophin Glycoprotein Complex
  Circulation Research, 2004
• Smooth muscle cell–extrinsic vascular spasm arises from cardiomyocyte degeneration in sarcoglycan-deficient cardiomyopathy
  Journal of Clinical Investigation, 2004
• Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy
  Proceedings of the National Academy of Sciences, 2003
• Identification of a new missense mutation in the mtDNA of hereditary hypertrophic, but not dilated cardiomyopathic hamsters.
  Molecular and Cellular Biochemistry, 2003
• Phenotypic diversity in hypertrophic cardiomyopathy
  Human Molecular Genetics, 2002
• From Sarcomeric Mutations to Heart Disease: Understanding Familial Hypertrophic Cardiomyopathy
  Published by Cold Spring Harbor Laboratory ,2002
• Disruption of the Sarcoglycan–Sarcospan Complex in Vascular Smooth Muscle
  Cell, 1999
• Heart involvement in muscular dystrophies due to sarcoglycan gene mutations
  Muscle & Nerve, 1999
• Delineation of genomic deletion in cardiomyopathic hamster
  FEBS Letters, 1999
• Identification of the Syrian hamster cardiomyopathy gene
  Human Molecular Genetics, 1997