Assembly defects of desmin disease mutants carrying deletions in the α-helical rod domain are rescued by wild type protein

This publication has 41 references indexed in Scilit:

• Desmin accumulation restrictive cardiomyopathy and atrioventricular block associated with desmin gene defects
  Published by Wiley ,2006
• Impact of Disease Mutations on the Desmin Filament Assembly Process
  Journal of Molecular Biology, 2006
• Forced expression of desmin and desmin mutants in cultured cells: Impact of myopathic missense mutations in the central coiled-coil domain on network formation
  Experimental Cell Research, 2006
• Severe muscle disease-causing desmin mutations interfere with in vitro filament assembly at distinct stages
  Proceedings of the National Academy of Sciences, 2005
• THE GENETIC BASIS FOR CARDIAC REMODELING
  Annual Review of Genomics and Human Genetics, 2005
• A novel desmin R355P mutation causes cardiac and skeletal myopathy
  Neuromuscular Disorders, 2005
• Pathogenic effects of a novel heterozygous R350P desmin mutation on the assembly of desmin intermediate filaments in vivo and in vitro
  Human Molecular Genetics, 2005
• The biology of desmin filaments: how do mutations affect their structure, assembly, and organisation?
  Journal of Structural Biology, 2004
• Desmin myopathy
  Brain, 2004
• Missense mutations in desmin associated with familial cardiac and skeletal myopathy
  Nature Genetics, 1998