Glycosylation defects and muscular dystrophy
- PMID: 16400811
- DOI: 10.1007/0-387-25515-X_15
Glycosylation defects and muscular dystrophy
Similar articles
-
[Dystroglycan glycosylation and muscular dystrophy].Seikagaku. 2014 Aug;86(4):452-63. Seikagaku. 2014. PMID: 25255627 Review. Japanese. No abstract available.
-
Glycosylation defects: a new mechanism for muscular dystrophy?Hum Mol Genet. 2003 Oct 15;12 Spec No 2:R259-64. doi: 10.1093/hmg/ddg272. Epub 2003 Aug 12. Hum Mol Genet. 2003. PMID: 12925572 Review.
-
Impaired viability of muscle precursor cells in muscular dystrophy with glycosylation defects and amelioration of its severe phenotype by limited gene expression.Hum Mol Genet. 2013 Aug 1;22(15):3003-15. doi: 10.1093/hmg/ddt157. Epub 2013 Apr 4. Hum Mol Genet. 2013. PMID: 23562821
-
Congenital muscular dystrophy with glycosylation defects of alpha-dystroglycan in Japan.Neuromuscul Disord. 2005 May;15(5):342-8. doi: 10.1016/j.nmd.2005.01.009. Neuromuscul Disord. 2005. PMID: 15833426
-
[Alpha-dystroglycanopathy (FCMD, MEB, etc): abnormal glycosylation and muscular dystrophy].Rinsho Shinkeigaku. 2005 Nov;45(11):932-4. Rinsho Shinkeigaku. 2005. PMID: 16447766 Japanese.
Cited by
-
Modulation of p38 mitogen-activated protein kinase cascade and metalloproteinase activity in diaphragm muscle in response to free radical scavenger administration in dystrophin-deficient Mdx mice.Am J Pathol. 2007 Feb;170(2):633-43. doi: 10.2353/ajpath.2007.060344. Am J Pathol. 2007. PMID: 17255331 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical