Pages that link to "Q28215026"
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The following pages link to The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle (Q28215026):
Displaying 50 items.
- Calcium-sensitive phospholipid binding properties of normal and mutant ferlin C2 domains (Q24294673) (← links)
- Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patients (Q24317669) (← links)
- Reduced plasma membrane expression of dysferlin mutants is attributed to accelerated endocytosis via a syntaxin-4-associated pathway (Q24337100) (← links)
- AHNAK, a novel component of the dysferlin protein complex, redistributes to the cytoplasm with dysferlin during skeletal muscle regeneration (Q24337859) (← links)
- Caveolinopathies: from the biology of caveolin-3 to human diseases (Q24599074) (← links)
- Dysferlin at transverse tubules regulates Ca(2+) homeostasis in skeletal muscle (Q26866519) (← links)
- Ferlins: regulators of vesicle fusion for auditory neurotransmission, receptor trafficking and membrane repair (Q27022787) (← links)
- The caveolin-cavin system plays a conserved and critical role in mechanoprotection of skeletal muscle (Q27310248) (← links)
- Solution structure of the inner DysF domain of myoferlin and implications for limb girdle muscular dystrophy type 2b (Q27650651) (← links)
- Crystal structures of the human Dysferlin inner DysF domain (Q27681383) (← links)
- (Q28183797) (redirect page) (← links)
- Limb-girdle muscular dystrophy (Q28200887) (← links)
- Defective membrane repair in dysferlin-deficient muscular dystrophy (Q28203095) (← links)
- Dysferlin Interacts with Annexins A1 and A2 and Mediates Sarcolemmal Wound-healing (Q28204713) (← links)
- Characterisation of the dysferlin skeletal muscle promoter (Q28210130) (← links)
- Caveolin regulates endocytosis of the muscle repair protein, dysferlin (Q28261848) (← links)
- The multiple faces of caveolae (Q29618099) (← links)
- Rapid actin-cytoskeleton-dependent recruitment of plasma membrane-derived dysferlin at wounds is critical for muscle membrane repair (Q30583899) (← links)
- Comparison of dysferlin expression in human skeletal muscle with that in monocytes for the diagnosis of dysferlin myopathy. (Q31043843) (← links)
- Sarcolemmal repair is a slow process and includes EHD2. (Q31063871) (← links)
- Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage display (Q31159589) (← links)
- Dysferlin interacts with tubulin and microtubules in mouse skeletal muscle (Q33559890) (← links)
- Clinical and pathological characteristics of four Korean patients with limb-girdle muscular dystrophy type 2B. (Q33631614) (← links)
- Proteomic analysis of the dysferlin protein complex unveils its importance for sarcolemmal maintenance and integrity (Q33747737) (← links)
- Expression levels of sarcolemmal membrane repair proteins following prolonged exercise training in mice (Q33878140) (← links)
- Retracted: Dysferlin Interacts with Histone Deacetylase 6 and Increases alpha-Tubulin Acetylation (Q34103199) (← links)
- Contribution of dysferlin deficiency to skeletal muscle pathology in asymptomatic and severe dystroglycanopathy models: generation of a new model for Fukuyama congenital muscular dystrophy (Q34149744) (← links)
- Dysferlin-deficient immortalized human myoblasts and myotubes as a useful tool to study dysferlinopathy (Q34172739) (← links)
- Modular dispensability of dysferlin C2 domains reveals rational design for mini-dysferlin molecules (Q34318021) (← links)
- Expression of myoferlin in human airway epithelium and its role in cell adhesion and zonula occludens-1 expression (Q34342055) (← links)
- Novel diagnostic features of dysferlinopathies (Q34513720) (← links)
- Genetic diseases of muscle (Q34997853) (← links)
- Protein defects in neuromuscular diseases (Q35114795) (← links)
- Muscular dystrophies: genes to pathogenesis (Q35145855) (← links)
- From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies (Q35166268) (← links)
- The 10 autosomal recessive limb-girdle muscular dystrophies (Q35201105) (← links)
- Repairing the tears: dysferlin in muscle membrane repair (Q35203020) (← links)
- Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic (Q35227523) (← links)
- Ultrastructural changes in dysferlinopathy support defective membrane repair mechanism (Q35588331) (← links)
- Muscular dystrophy overview: genetics and diagnosis (Q35638579) (← links)
- Limb-girdle muscular dystrophies--from genetics to molecular pathology (Q35714351) (← links)
- GRAF1 deficiency blunts sarcolemmal injury repair and exacerbates cardiac and skeletal muscle pathology in dystrophin-deficient mice (Q35753474) (← links)
- GRAF1 promotes ferlin-dependent myoblast fusion (Q35949289) (← links)
- Diagnostic immunohistochemistry in neuromuscular disorders (Q36012956) (← links)
- The absence of dysferlin induces the expression of functional connexin-based hemichannels in human myotubes (Q36031274) (← links)
- Dysferlin and muscle membrane repair. (Q36282549) (← links)
- Neural cell adhesion molecule (NCAM) marks adult myogenic cells committed to differentiation (Q36288517) (← links)
- Therapy insight: cardiovascular complications associated with muscular dystrophies (Q36304335) (← links)
- Comparative proteomics reveals abnormal binding of ATGL and dysferlin on lipid droplets from pressure overload-induced dysfunctional rat hearts (Q36501131) (← links)
- Molecular mechanisms of muscular dystrophies: old and new players (Q36593241) (← links)