Mutant glycosyltransferase and altered glycosylation of α-dystroglycan in the myodystrophy mouse
- 1 June 2001
- journal article
- letter
- Published by Springer Nature in Nature Genetics
- Vol. 28 (2) , 151-154
- https://doi.org/10.1038/88865
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophyHuman Molecular Genetics, 2000
- Direct interaction of Smn with dp103, a putative RNA helicase: a role for Smn in transcription regulation?Human Molecular Genetics, 2000
- Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapsesNature Genetics, 1999
- The fukutin protein family – predicted enzymes modifying cell-surface moleculesCurrent Biology, 1999
- Genetic mapping near the myd locus on mouse Chromosome 8Mammalian Genome, 1995
- Mouse myodystrophy (myd) mutation: Refined mapping in an interval flanked by homology with distal human 4qMuscle & Nerve, 1995
- CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choiceNucleic Acids Research, 1994
- Dystroglycan is a binding protein of laminin and merosin in peripheral nerveFEBS Letters, 1994
- Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrixNature, 1992
- Membrane organization of the dystrophin-glycoprotein complexCell, 1991