Does utrophin expression in muscles of mdx mice during postnatal development functionally compensate for dystrophin deficiency?
- 30 April 1994
- journal article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 122 (2) , 162-170
- https://doi.org/10.1016/0022-510x(94)90295-x
Abstract
No abstract availableKeywords
This publication has 38 references indexed in Scilit:
- Immunoblot analysis of dystrophin-related protein (DRP)Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1993
- Fiber regeneration is not persistent in dystrophic (mdx) mouse skeletal muscleDevelopmental Biology, 1991
- Dystrophin-related protein in the fetal and denervated skeletal muscles of normal and mdx miceBiochemical and Biophysical Research Communications, 1991
- A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal and mdx mice Immunological evidenceFEBS Letters, 1991
- Immunohistochemical dystrophin reaction in synaptic regionsBrain & Development, 1989
- Ultrastructure of the skeletal muscle in the X chromosome-linked dystrophic (mdx) mouseActa Neuropathologica, 1988
- Slow myosin in developing rat skeletal muscle.The Journal of cell biology, 1987
- Muscle regeneration and satellite cells in fukuyama type congenital muscular dystrophyMuscle & Nerve, 1986
- Local changes in myosin types in diseased human atrial myocardium: a quantitative immunofluorescence study.Circulation, 1985
- Structural changes in the early stages of Duchenne muscular dystrophyJournal of Neurology, Neurosurgery & Psychiatry, 1972