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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-д хэвлэсэн:	Proc Natl Acad Sci U S A
Үндсэн зохиолчид:	Manya, Hiroshi, Chiba, Atsuro, Yoshida, Aruto, Wang, Xiaohui, Chiba, Yasunori, Jigami, Yoshifumi, Margolis, Richard U., Endo, Tamao
Формат:	Artigo
Хэл сонгох:	Inglês
Хэвлэсэн:	National Academy of Sciences 2003
Нөхцлүүд:	Biological Sciences
Онлайн хандалт:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC327176/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/14699049/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.0307228101
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