๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

The molecular and biochemical basis of Duchenne muscular dystrophy

โœ Scribed by Anderson, MaryDilys S.; Kunkel, Louis M.


Book ID
121929681
Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
799 KB
Volume
17
Category
Article
ISSN
0968-0004

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Defective growth in vitro of Duchenne mu
โœ Mariarosa A.B. Melone; Gianfranco Peluso; Orsolina Petillo; Umberto Galderisi; R ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 234 KB ๐Ÿ‘ 1 views

As the molecular basis of Duchenne Muscular Dystrophy (DMD) was being discovered, increasing focus was placed on the mechanisms of progressive failure of myoregeneration. In this study, we propose a pathogenesis model for DMD, where an autocrine growth factor release of TGF-โค1-from necrotic myofiber

Molecular analysis of Duchenne and Becke
โœ Ronald G. Worton ๐Ÿ“‚ Article ๐Ÿ“… 1987 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 818 KB

Duchenne muscular dystrophy (DMD) is a progressive and lethal neuromuscular disorder caused by a defective gene on the X chromosome. There is no effective treatment and the biochemical defect is yet unknown. Mapping of the DMD locus to band Xp21 in the short arm of the X chromosome has given rise to