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Molecular organization of sarcoglycan complex in mouse myotubes in culture

Molecular organization of sarcoglycan complex in mouse myotubes in culture

http://www.wikidata.org/entity/Q24685886

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Sarcoglycan subcomplex expression in normal human smooth muscle Biglycan binds to alpha- and gamma-sarcoglycan and regulates their expression during development Filamin 2 (FLN2): A muscle-specific sarcoglycan interacting protein Sarcoglycan isoforms in skeletal muscle Defective assembly of sarcoglycan complex in patients with beta-sarcoglycan gene mutations. Study of aneural and innervated cultured myotubes Localization of sarcoglycan, neuronal nitric oxide synthase, beta-dystroglycan, and dystrophin molecules in normal skeletal myofiber: triple immunogold labeling electron microscopy The Dystrophin Complex: Structure, Function, and Implications for Therapy Formation of the neuromuscular junction. Agrin and its unusual receptors.Sarcoglycans in muscular dystrophy.The molecular neuropathology of the muscular dystrophies: a review and update.Rescue of sarcoglycan mutations by inhibition of endoplasmic reticulum quality control is associated with minimal structural modifications.Post-Natal knockdown of fukutin-related protein expression in muscle by long-termRNA interference induces dystrophic pathology [corrected]Fibrosis and inflammation are greater in muscles of beta-sarcoglycan-null mouse than mdx mouse.Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E Forskolin Regulates L-Type Calcium Channel through Interaction between Actinin 4 and β3 Subunit in Osteoblasts.Sarcoglycanopathies: molecular pathogenesis and therapeutic prospects A Haplotype of Two Novel Polymorphisms in δ-Sarcoglycan Gene Increases Risk of Dilated Cardiomyopathy in Mongoloid Population A novel isoform of delta-sarcoglycan is localized at the sarcoplasmic reticulum of mouse skeletal muscle.Reengineering a transmembrane protein to treat muscular dystrophy using exon skipping Processing and assembly of the dystrophin glycoprotein complex.Inhibition of proteasome activity promotes the correct localization of disease-causing alpha-sarcoglycan mutants in HEK-293 cells constitutively expressing beta-, gamma-, and delta-sarcoglycan.Animal models of muscular dystrophy From scrawny to brawny: the quest for neomusculogenesis; smart surfaces and scaffolds for muscle tissue engineering.The neurobiology of the dystrophin-associated glycoprotein complex.AAV-directed muscular dystrophy gene therapy.δ-Sarcoglycan-deficient muscular dystrophy: from discovery to therapeutic approaches.Cell-matrix interactions in muscle disease.Finding the sweet spot: assembly and glycosylation of the dystrophin-associated glycoprotein complex.What do mouse models of muscular dystrophy tell us about the DAPC and its components?Smooth muscle cell-extrinsic vascular spasm arises from cardiomyocyte degeneration in sarcoglycan-deficient cardiomyopathy delta- and gamma-Sarcoglycan localization in the sarcoplasmic reticulum of skeletal muscle.Dystroglycan is not required for localization of dystrophin, syntrophin, and neuronal nitric-oxide synthase at the sarcolemma but regulates integrin alpha 7B expression and caveolin-3 distribution.Sarcoglycan complex in human normal and pathological prostatic tissue: an immunohistochemical and RT-PCR study.Characterization of the dystrophin-glycoprotein complex in airway smooth muscle: role of δ-sarcoglycan in airway responsiveness.Efficient exon skipping of SGCG mutations mediated by phosphorodiamidate morpholino oligomers.

P2860

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P2860

Molecular organization of sarcoglycan complex in mouse myotubes in culture

http://www.wikidata.org/entity/Q24685886

description

1998 nî lūn-bûn

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1998 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1998 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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1998年の論文

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1998年論文

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1998年論文

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1998年論文

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1998年論文

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1998年論文

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1998年论文

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name

Molecular organization of sarcoglycan complex in mouse myotubes in culture

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Molecular organization of sarcoglycan complex in mouse myotubes in culture

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Molecular organization of sarcoglycan complex in mouse myotubes in culture

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type

label

Molecular organization of sarcoglycan complex in mouse myotubes in culture

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Molecular organization of sarcoglycan complex in mouse myotubes in culture

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Molecular organization of sarcoglycan complex in mouse myotubes in culture

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prefLabel

Molecular organization of sarcoglycan complex in mouse myotubes in culture

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Molecular organization of sarcoglycan complex in mouse myotubes in culture

@en

Molecular organization of sarcoglycan complex in mouse myotubes in culture

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P1433

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Journal of Cell Biology

P1476

Molecular organization of sarcoglycan complex in mouse myotubes in culture

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P2093

C G Bönnemann

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H G Lidov

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L M Kunkel

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Y M Chan

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P2860

Expression of recombinant dystrophin and its localization to the cell membrane

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

Human epsilon-sarcoglycan is highly related to alpha-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene

Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein

Syntrophin binds to an alternatively spliced exon of dystrophin

Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12

Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12

epsilon-Sarcoglycan, a broadly expressed homologue of the gene mutated in limb-girdle muscular dystrophy 2D

Identification and characterization of the dystrophin anchoring site on beta-dystroglycan

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

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2033-44

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scholarly article

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10.1083/JCB.143.7.2033

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7

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143

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13424470

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9864373

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2175228

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