Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophy
- 1 May 2001
- journal article
- research article
- Published by Elsevier in Neuromuscular Disorders
- Vol. 11 (4) , 350-359
- https://doi.org/10.1016/s0960-8966(00)00203-0
Abstract
No abstract availableKeywords
Funding Information
- Core Research for Evolutional Science and Technology
- Ministry of Health and Welfare
- Uehara Memorial Foundation
- Japan Science and Technology Corporation
This publication has 38 references indexed in Scilit:
- Diminished Expression of CD59 on Activated CD8+ T Cells Undergoing Apoptosis in Systemic Lupus Erythematosus and Sjogren's SyndromeScandinavian Journal of Immunology, 2000
- Akt Phosphorylation Site Found in Human Caspase-9 Is Absent in Mouse Caspase-9Biochemical and Biophysical Research Communications, 1999
- Presence of Laminin α5 Chain and Lack of Laminin α1 Chain during Human Muscle Development and in Muscular DystrophiesJournal of Biological Chemistry, 1997
- Integrins (alpha7beta1) in muscle function and survival. Disrupted expression in merosin-deficient congenital muscular dystrophy.Journal of Clinical Investigation, 1997
- Myonuclear apoptosis in dystrophic mdx muscle occurs by perforin-mediated cytotoxicity.Journal of Clinical Investigation, 1997
- Congenital muscular dystrophy with primary laminin α2 (merosin) deficiency presenting as inflammatory myopathyAnnals of Neurology, 1996
- Deficiency of Merosin (Laminin M or α2) in Congenital Muscular Dystrophy Associated with Cerebral White Matter AlterationsNeuropediatrics, 1995
- Deficiency of laminin α2‐Chain mRNA in muscle in a patient with merosin‐negative congenital muscular dystrophyMuscle & Nerve, 1995
- Proceedings of the 27th ENMC sponsored workshop on congenital muscular dystrophy 22–24 April 1994, The NetherlandsNeuromuscular Disorders, 1995
- Somatosensory and Visual Evoked Potentials in Congenital Muscular Dystrophy: Correlation with MRI Changes and Muscle Merosin StatusNeuropediatrics, 1995