Fukutin-related Protein Associates with the Sarcolemmal Dystrophin-Glycoprotein Complex
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference30 articles.
1. Mutations in the Fukutin-Related Protein Gene (FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan
2. Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C
3. The Childhood Limb-Girdle Muscular Dystrophies
4. An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy
5. The fukutin protein family – predicted enzymes modifying cell-surface molecules
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1. Mouse models of human ocular disease for translational research;PLOS ONE;2017-08-31
2. Autologous intramuscular transplantation of engineered satellite cells induces exosome-mediated systemic expression of Fukutin-related protein and rescues disease phenotype in a murine model of limb-girdle muscular dystrophy type 2I;Human Molecular Genetics;2017-06-29
3. Efficacy of Gene Therapy Is Dependent on Disease Progression in Dystrophic Mice with Mutations in the FKRP Gene;Molecular Therapy - Methods & Clinical Development;2017-06
4. AAV-mediated transfer of FKRP shows therapeutic efficacy in a murine model but requires control of gene expression;Human Molecular Genetics;2017-03-03
5. Structural basis of laminin binding to the LARGE glycans on dystroglycan;Nature Chemical Biology;2016-08-15
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