Muscular Dystrophy—Reason for Optimism?

This publication has 16 references indexed in Scilit:

• Mutations in the Fukutin-Related Protein Gene (FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan
  American Journal of Human Genetics, 2001
• Muscular Dystrophy and Neuronal Migration Disorder Caused by Mutations in a Glycosyltransferase, POMGnT1
  Developmental Cell, 2001
• An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy
  Nature, 2001
• The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
  Nature Genetics, 2001
• Reconstructing Myotonic Dystrophy
  Science, 2001
• Selective deficiency of α-dystroglycan in Fukuyama-type congenital muscular dystrophy
  Neurology, 2001
• Mutant glycosyltransferase and altered glycosylation of α-dystroglycan in the myodystrophy mouse
  Nature Genetics, 2001
• Syncoilin, a Novel Member of the Intermediate Filament Superfamily That Interacts with α-Dystrobrevin in Skeletal Muscle
  Journal of Biological Chemistry, 2001
• Localized Igf-1 transgene expression sustains hypertrophy and regeneration in senescent skeletal muscle
  Nature Genetics, 2001
• Expression of full-length utrophin prevents muscular dystrophy in mdx mice
  Nature Medicine, 1998