O-Mannosyl Glycan / Mammalian

General | Antibody | Glycoprotein | Glycolipid | Enzyme | Reference

7 reference for EP0002

sort by year Reference detail
1 Chai W, Yuen CT, Kogelberg H, Carruthers RA, Margolis RU, Feizi T, Lawson AM.
High prevalence of 2-mono- and 2,6-di-substituted manol-terminating sequences among O-glycans released from brain glycopeptides by reductive alkaline hydrolysis.
Eur J Biochem. 1999 Aug ;263(3):879-88
PMID: 10469154
2 Chiba A, Matsumura K, Yamada H, Inazu T, Shimizu T, Kusunoki S, Kanazawa I, Kobata A, Endo T.
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.
J Biol Chem. 1997 Jan 24;272(4):2156-62
PMID: 8999917
3 Kogelberg H, Chai W, Feizi T, Lawson AM.
NMR studies of mannitol-terminating oligosaccharides derived by reductive alkaline hydrolysis from brain glycoproteins.
Carbohydr Res. 2001 Apr 23;331(4):393-401
PMID: 11398981
4 Smalheiser NR, Haslam SM, Sutton-Smith M, Morris HR, Dell A.
Structural analysis of sequences O-linked to mannose reveals a novel Lewis X structure in cranin (dystroglycan) purified from sheep brain.
J Biol Chem. 1998 Sep 11;273(37):23698-703
PMID: 9726975
5 Ervasti JM, Campbell KP.
A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.
J Cell Biol. 1993 Aug ;122(4):809-23
PMID: 8349731
6 Schachter H, Vajsar J, Zhang W.
The role of defective glycosylation in congenital muscular dystrophy.
Glycoconj J. 2004 ;20(5):291-300
PMID: 15229394
7 Yoshida A, Kobayashi K, Manya H, Taniguchi K, Kano H, Mizuno M, Inazu T, Mitsuhashi H, Takahashi S, Takeuchi M, Herrmann R, Straub V, Talim B, Voit T, Topaloglu H, Toda T, Endo T.
Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1.
Dev Cell. 2001 Nov ;1(5):717-24
PMID: 11709191