Mutations of the POMT1 gene found in patients with Walker–Warburg syndrome lead to a defect of protein O-mannosylation
- 3 December 2004
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 325 (1) , 75-79
- https://doi.org/10.1016/j.bbrc.2004.10.001
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Dystrophin-Glycoprotein Complex: Post-translational Processing and Dystroglycan FunctionJournal of Biological Chemistry, 2003
- Targeting Dystroglycan in the BrainNeuron, 2003
- Post-translational disruption of dystroglycan–ligand interactions in congenital muscular dystrophiesNature, 2002
- The muscular dystrophiesPublished by Elsevier ,2002
- Muscular Dystrophy—Reason for Optimism?Cell, 2002
- The complexities of dystroglycanTrends in Biochemical Sciences, 2001
- Morphogenesis, Adhesive Properties, and Antifungal Resistance Depend on the Pmt6 Protein Mannosyltransferase in the Fungal Pathogen Candida albicansJournal of Bacteriology, 2000
- Protein O-mannosylationBiochimica et Biophysica Acta (BBA) - General Subjects, 1999
- Multiple Functions of Pmt1p-mediated ProteinO-Mannosylation in the Fungal Pathogen Candida albicansJournal of Biological Chemistry, 1998
- Structures of Sialylated O-Linked Oligosaccharides of Bovine Peripheral Nerve α-DystroglycanJournal of Biological Chemistry, 1997