O-Mannose and O–N-acetyl galactosamine glycosylation of mammalian α-dystroglycan is conserved in a region-specific manner
Author:
Publisher
Oxford University Press (OUP)
Subject
Biochemistry
Link
http://academic.oup.com/glycob/article-pdf/22/11/1413/16655425/cws109.pdf
Reference33 articles.
1. Dystroglycan: From biosynthesis to pathogenesis of human disease;Barresi;J Cell Sci,2006
2. Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndrome;Beltran-Valero de Bernabe;J Med Genet,2004
3. Initiation of mammalian O-mannosylation in vivo is independent of a consensus sequence and controlled by peptide regions within and upstream of the alpha-dystroglycan mucin domain;Breloy;J Biol Chem,2008
4. Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan;Brockington;Am J Hum Genet,2001
5. Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin;Chiba;J Biol Chem,1997
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2. A universal gene correction approach for FKRP-associated dystroglycanopathies to enable autologous cell therapy;Cell Reports;2021-07
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4. Functional implications of MIR domains in protein O-mannosylation;eLife;2020-12-24
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