Immunochemical study of connectin (titin) in neuromuscular diseases using a monoclonal antibody: connectin is degraded extensively in Duchenne muscular dystrophy
- 1 November 1989
- journal article
- review article
- Published by Elsevier
- Vol. 93 (2) , 147-156
- https://doi.org/10.1016/0022-510x(89)90185-8
Abstract
No abstract availableKeywords
Funding Information
- National Center of Neurology and Psychiatry
- Ministry of Education, Culture, Sports, Science and Technology (62-2, 62A-3-19, 62A-4-17)
- Ministry of Health, Labour and Welfare
This publication has 27 references indexed in Scilit:
- Molecular genetics in muscular dystrophy research: Revolutionary progressMuscle & Nerve, 1988
- Characterization of Dystrophin in Muscle-Biopsy Specimens from Patients with Duchenne's or Becker's Muscular DystrophyNew England Journal of Medicine, 1988
- The complete sequence of dystrophin predicts a rod-shaped cytoskeletal proteinCell, 1988
- Nebulin and titin expression in Duchenne muscular dystrophy appears normalFEBS Letters, 1987
- The positional stability of thick filaments in activated skeletal muscle depends on sarcomere length: evidence for the role of titin filaments.The Journal of cell biology, 1987
- Is Nebulin the Defective Gene Product in Duchenne Muscular Dystrophy?New England Journal of Medicine, 1987
- A physiological role for titin and nebulin in skeletal muscleNature, 1986
- Connectin filaments link thick filaments and Z lines in frog skeletal muscle as revealed by immunoelectron microscopy.The Journal of cell biology, 1985
- Purification and properties of native titinJournal of Molecular Biology, 1984
- Connectin filaments in stretched skinned fibers of frog skeletal muscle.The Journal of cell biology, 1984