Somatic reversion/suppression of the mouse mdx phenotype in vivo

This publication has 28 references indexed in Scilit:

• Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus
  Nature, 1989
• Mosaic Expression of Dystrophin in Symptomatic Carriers of Duchenne's Muscular Dystrophy
  New England Journal of Medicine, 1989
• The gypsy retrotransposon ofDrosophila melanogaster: Mechanisms of mutagenesis and interaction with thesuppressor of Hairy-wing locus
  Developmental Genetics, 1989
• Molecular analysis of ethyl methanesulfonate-induced reversion of a chromosomally integrated mutant shuttle vector gene in mammalian cells.
  Molecular and Cellular Biology, 1988
• Duchenne muscular dystrophy: Deficiency of dystrophin at the muscle cell surface
  Cell, 1988
• The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs
  Nature, 1988
• Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide
  Nature, 1988
• THE mdx MOUSE SKELETAL MUSCLE MYOPATHY: I. A HISTOLOGICAL, MORPHOMETRIC AND BIOCHEMICAL INVESTIGATION
  Neuropathology and Applied Neurobiology, 1988
• Dystrophin: The protein product of the duchenne muscular dystrophy locus
  Cell, 1987
• Excision of the DBA ecotropic provirus in dilute coat-color revertants of mice occurs by homologous recombination involving the viral LTRs
  Cell, 1983