Distribution of ten laminin chains in dystrophic and regenerating muscles
- 1 October 1999
- journal article
- Published by Elsevier in Neuromuscular Disorders
- Vol. 9 (6-7) , 423-433
- https://doi.org/10.1016/s0960-8966(99)00033-4
Abstract
No abstract availableKeywords
This publication has 60 references indexed in Scilit:
- Presence of Laminin α5 Chain and Lack of Laminin α1 Chain during Human Muscle Development and in Muscular DystrophiesJournal of Biological Chemistry, 1997
- Emery-Dreifuss syndromeCurrent Opinion in Neurology, 1997
- Changes of laminin β2 chain expression in congenital muscular dystrophyNeuromuscular Disorders, 1997
- Early onset autosomal dominant myopathy with rigidity of the spine: a possible role for laminin β1?Neuromuscular Disorders, 1997
- Increased laminin a expression in regenerating myofibers neuromuscular disordersMuscle & Nerve, 1995
- Primary structure and expression of a novel human laminin α4 chainFEBS Letters, 1995
- Localization of the Gene (LAMA4) to Chromosome 6q21 and Isolation of a Partial cDNA Encoding a Variant Laminin A ChainGenomics, 1994
- Monoclonal antibodies against laminin A chain fragment E3 and their effects on binding to cells and proteoglycan and on kidney developmentExperimental Cell Research, 1992
- Kalinin: an epithelium-specific basement membrane adhesion molecule that is a component of anchoring filaments.The Journal of cell biology, 1991
- Fetal myosin heavy chains in regenerating muscleNature, 1982