Demonstration of mammalian protein O-mannosyltransferase activity: Coexpression of POMT1 and POMT2 required for enzymatic activity

Defects in O-mannosylation of α-dystroglycan are thought to cause certain types of congenital muscular dystrophies with neuronal migration disorders. Among these muscular dystrophies, Walker–Warburg syndrome is caused by mutations in the gene encoding putative protein O-mannosyltransferase 1 (POMT1)...

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שמור ב:
מידע ביבליוגרפי
Main Authors: Manya, Hiroshi, Chiba, Atsuro, Yoshida, Aruto, Wang, Xiaohui, Chiba, Yasunori, Jigami, Yoshifumi, Margolis, Richard U., Endo, Tamao
פורמט: Artigo
שפה:Inglês
יצא לאור: National Academy of Sciences 2004
נושאים:
Biological Sciences
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC327176/
https://ncbi.nlm.nih.gov/pubmed/14699049
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0307228101
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