Mutagenesis at the α-β interface impairs the cleavage of the dystroglycan precursor
Author:
Publisher
Wiley
Subject
Cell Biology,Molecular Biology,Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1742-4658.2009.07196.x/fullpdf
Reference45 articles.
1. Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix;Ibraghimov-Beskrovnaya;Nature,1992
2. Dystroglycan: from biosynthesis to pathogenesis of human disease;Barresi;J Cell Sci,2006
3. Dystroglycan: important player in skeletal muscle and beyond;Cohn;Neuromuscul Disord,2005
4. Biochemical characterization of the epithelial dystroglycan complex;Durbeej;J Biol Chem,1999
5. Dystroglycan is essential for early embryonic development: disruption of Reichert’s membrane in Dag1-null mice;Williamson;Hum Mol Genet,1997
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1. Evaluation of the effect of a floxed Neo cassette within the dystroglycan (Dag1) gene;BMC Research Notes;2017-11-21
2. The evolution of the dystroglycan complex, a major mediator of muscle integrity;Biology Open;2015-08-28
3. The Structure of the T190M Mutant of Murine α-Dystroglycan at High Resolution: Insight into the Molecular Basis of a Primary Dystroglycanopathy;PLOS ONE;2015-05-01
4. A new monoclonal antibody DAG-6F4 against human alpha-dystroglycan reveals reduced core protein in some, but not all, dystroglycanopathy patients;Neuromuscular Disorders;2015-01
5. Genetic Engineering of Dystroglycan in Animal Models of Muscular Dystrophy;BioMed Research International;2015
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