Reciprocal expression of dystrophin and utrophin in muscles of Duchenne muscular dystrophy patients, female DMD-carriers and control subjects
- 1 October 1993
- journal article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 119 (1) , 43-52
- https://doi.org/10.1016/0022-510x(93)90190-a
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Glycoprotein‐binding site of dystrophin is confined to the cysteine‐rich domain and the first half of the carboxy‐terminal domainFEBS Letters, 1992
- Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cellsHuman Molecular Genetics, 1992
- Localization of the DMDL gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles, and in proliferating brain cell lines.The Journal of cell biology, 1991
- Dystrophin-related protein in the fetal and denervated skeletal muscles of normal and mdx miceBiochemical and Biophysical Research Communications, 1991
- Expression of dystrophin mRNA and the protein in the developing rat heartBiochemical and Biophysical Research Communications, 1990
- Immunocytochemical study of dystrophin at the myotendinous junctionMuscle & Nerve, 1990
- Dystrophin distribution in heterozygote mdx miceMuscle & Nerve, 1989
- Mosaic Expression of Dystrophin in Symptomatic Carriers of Duchenne's Muscular DystrophyNew England Journal of Medicine, 1989
- Immunohistochemical dystrophin reaction in synaptic regionsBrain & Development, 1989
- Characterization of Dystrophin in Muscle-Biopsy Specimens from Patients with Duchenne's or Becker's Muscular DystrophyNew England Journal of Medicine, 1988