Related references
Note: Only part of the references are listed.DIAGNOSTIC OVERVIEW OF BLOOD-BASED DYSFERLIN PROTEIN ASSAY FOR DYSFERLINOPATHIES
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MUSCLE & NERVE (2014)
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ANNALS OF NEUROLOGY (2013)
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Update on the Treatment of Duchenne Muscular Dystrophy
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被撤回的出版物: Modular Dispensability of Dysferlin C2 Domains Reveals Rational Design for Mini-dysferlin Molecules (Retracted article. See vol. 292, pg. 12543, 2017)
Bilal A. Azakir et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2012)
Dantrolene Enhances Antisense-Mediated Exon Skipping in Human and Mouse Models of Duchenne Muscular Dystrophy
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SCIENCE TRANSLATIONAL MEDICINE (2012)
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TRAFFIC (2012)
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Proinflammatory Signals and the Loss of Lymphatic Vessel Hyaluronan Receptor-1 (LYVE-1) in the Early Pathogenesis of Laminin Alpha2-deficient Skeletal Muscle
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JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY (2011)
Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study
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MOLECULAR MEDICINE (2011)
Systemic Administration of PRO051 in Duchenne's Muscular Dystrophy
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PLOS ONE (2011)
Dysferlin Forms a Dimer Mediated by the C2 Domains and the Transmembrane Domain In Vitro and in Living Cells
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FEBS JOURNAL (2010)
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Characterization of Lipid Binding Specificities of Dysferlin C2 Domains Reveals Novel Interactions with Phosphoinositides
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Membrane Repair Defects in Muscular Dystrophy Are Linked to Altered Interaction between MG53, Caveolin-3, and Dysferlin
Chuanxi Cai et al.
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NUCLEIC ACIDS RESEARCH (2009)
DMD pseudoexon mutations: Splicing efficiency, phenotype, and potential therapy
Olga L. Gurvich et al.
ANNALS OF NEUROLOGY (2008)
Cell-lineage regulated myogenesis for dystrophin replacement: a novel therapeutic approach for treatment of muscular dystrophy
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HUMAN MOLECULAR GENETICS (2008)
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Dysferlin and muscle membrane repair
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TRAFFIC (2007)
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FASEB JOURNAL (2007)
AHNAR, a novel component of the dysferlin protein complex, redistributes to the cytoplasm with dysferlin during skeletal muscle regeneration
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FASEB JOURNAL (2007)
Lariat branch point mutation in the dysferlin gene with mild limb-girdle muscular dystrophy
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Systemic delivery of morpholino oligonucleotide restores dystrophin expression bodywide and improves dystrophic pathology
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Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage display
YC Huang et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2005)
Dysferlin interacts with affixin (β-parvin) at the sarcolemma
C Matsuda et al.
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SH Laval et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2004)
Dysferlin interacts with Annexins A1 and A2 and mediates sarcolemmal wound-healing
NJ Lennon et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Therapeutic antisense-induced exon skipping in cultured muscle cells from six different DMD patients
A Aartsma-Rus et al.
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Predictive identification of exonic splicing enhancers in human genes
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SCIENCE (2002)
The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle
C Matsuda et al.
HUMAN MOLECULAR GENETICS (2001)