Expression of NCAM and its polysialylated isoforms during mdx mouse muscle regeneration and in vitro myogenesis-Reference-Cited by-同舟云学术

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Expression of NCAM and its polysialylated isoforms during mdx mouse muscle regeneration and in vitro myogenesis

Published:1994-05 Issue:3 Volume:4 Page:171-182
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Dubois C.,Figarella-Branger D.,Pastoret C.,Rampini C.,Karpati G.,Rougon G.

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference40 articles.

1. X chromosome-linked muscular dystrophy (mdx) in the mouse;Bulfield,1984

2. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organisation of the DMD gene in normal and affected individuals;Koenig;Cell,1987

3. Dystrophin: the protein product of the Duchenne muscular dystrophy locus;Hoffman;Cell,1987

4. Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface;Bonilla;Cell,1988

5. Immunoelectron microscopic localization of dystrophin in myofibres;Watkins;Nature,1988

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