The dystrophin-associated protein complex

Journal of Cell Science

Volumn 115, Issue 14, 2002, Pages 2801-2803

  Ehmsen, Jeffrey ^a   Poon, Ellen ^a   Davies, Kay ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADHALIN; CALMODULIN; CAVEOLIN 3; DESMIN; DYSTROBREVIN; DYSTROGLYCAN; DYSTROPHIN; F ACTIN; GROWTH FACTOR RECEPTOR BOUND PROTEIN 2; MEROSIN; NITRIC OXIDE; NITRIC OXIDE SYNTHASE; SARCOGLYCAN; SIGNAL PEPTIDE; SODIUM CHANNEL; SYNTROPHIN; UTROPHIN;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CONSENSUS SEQUENCE; CONTROLLED STUDY; DUCHENNE MUSCULAR DYSTROPHY; GENE DELETION; GENE MUTATION; GENETIC CONSERVATION; HUMAN; HUMAN CELL; HUMAN TISSUE; MOUSE; MUSCLE BLOOD FLOW; NONHUMAN; NONSENSE MUTATION; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN GLYCOSYLATION; PROTEIN PROCESSING; PROTEIN PROTEIN INTERACTION; PROTEIN STRUCTURE; SARCOLEMMA; SEQUENCE ANALYSIS;

ANIMALS; CYTOSKELETON; EXTRACELLULAR MATRIX; HUMANS; MUSCLE PROTEINS; MUSCLE, SKELETAL; MUSCULAR DYSTROPHY, DUCHENNE; MUTATION;

ANIMALIA;

EID: 0037099030     PISSN: 00219533     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (26)

1. Absence of alpha-syntrophin leads to structurally aberrant neuromuscular synapses deficient in utrophin
2. In vivo requirement of the α-syntrophin PDZ domain for the sarcolemmal localization of nNOS and aquaporin-4
3. A cluster of basic repeats in the dystrophin rod domain binds F-actin through an electrostatic interaction
4. Making sense of the limb-girdle muscular dystrophies
5. Molecular organization of sarcoglycan complex in mouse myotubes in culture
6. Muscular dystrophy in mdx mice despite lack of neuronal nitric oxide synthase
7. Assembly of the dystrophin-associated protein complex does not require the dystrophin COOH-terminal domain
8. Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
9. mdx muscle pathology is independent of nNOS perturbation
10. Caveolae and caveolin-3 in muscular dystrophy
11. Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins
12. Role for alpha-dystrobrevin in the pathogenesis of dystrophin-dependent muscular dystrophies
13. Mutant glycosyltransferase and altered glycosylation of α-dystroglycan in the myodystrophy mouse
14. Modular flexibility of dystrophin: Implications for gene therapy of Duchenne muscular dystrophy
15. alpha1-syntrophin gene disruption results in the absence of neuronal-type nitric-oxide synthase at the sarcolemma but does not induce muscle degeneration
16. Sarcospan-deficient mice maintain normal muscle function
17. Alternative splicing of dystrobrevin regulates the stoichiometry of syntrophin binding to the dystrophin protein complex
18. Syncoilin, a novel member of the intermediate filament superfamily that interacts with alpha-dystrobrevin in skeletal muscle
19. The structure of the N-terminal actin-binding domain of human dystrophin and how mutations in this domain may cause Duchenne or Becker muscular dystrophy
20. Laminins of the neuromuscular system
21. Dystrophin protects the sarcolemma from stresses developed during muscle contraction
22. Association of syncoilin and desmin: Linking intermediate filament proteins to the dystrophin-associated protein complex
23. The dystrophin-glycoprotein complex, cellular signalling, and the regulation of cell survival in the muscular dystrophies
24. Voltage-gated sodium channel (SkM1) content in dystrophin-deficient muscle
25. Dystroglycan is essential for early embryonic development: Disruption of Reichert's membrane in Dag1-null mice
26. The complexities of dystroglycan