Identification of a Post-translational Modification with Ribitol-Phosphate and Its Defect in Muscular Dystrophy
Top Cited Papers
Open Access
- 25 February 2016
- journal article
- research article
- Published by Elsevier BV in Cell Reports
- Vol. 14 (9), 2209-2223
- https://doi.org/10.1016/j.celrep.2016.02.017
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycanNature Genetics, 2012
- ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndromeNature Genetics, 2012
- Like-acetylglucosaminyltransferase (LARGE)-dependent modification of dystroglycan at Thr-317/319 is required for laminin binding and arenavirus infectionProceedings of the National Academy of Sciences of the United States of America, 2011
- Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophyNature, 2011
- Synthetic, Structural, and Biosynthetic Studies of an Unusual Phospho-Glycopeptide Derived from α-DystroglycanJournal of the American Chemical Society, 2011
- A Dystroglycan Mutation Associated with Limb-Girdle Muscular DystrophyNew England Journal of Medicine, 2011
- Tumor suppressor function of laminin-binding α-dystroglycan requires a distinct β3- N -acetylglucosaminyltransferaseProceedings of the National Academy of Sciences of the United States of America, 2009
- Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophyNature, 2002
- Post-translational disruption of dystroglycan–ligand interactions in congenital muscular dystrophiesNature, 2002
- Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrixNature, 1992