Lectin-binding characterizes the healthy human skeletal muscle glycophenotype and identifies disease-specific changes in dystrophic muscle.

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Lectin-binding characterizes the healthy human skeletal muscle glycophenotype and identifies disease-specific changes in dystrophic muscle.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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Lectin-binding characterizes t ...... changes in dystrophic muscle.

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Lectin-binding characterizes t ...... changes in dystrophic muscle.

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Lectin-binding characterizes t ...... changes in dystrophic muscle.

@en

Lectin-binding characterizes t ...... changes in dystrophic muscle.

@nl

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Lectin-binding characterizes t ...... changes in dystrophic muscle.

@en

Lectin-binding characterizes t ...... changes in dystrophic muscle.

@nl

P1476

Lectin-binding characterizes t ...... c changes in dystrophic muscle

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Brian J McMorran

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Linda G Baum

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M Carrie Miceli

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P2860

Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE

Mutations in the integrin alpha7 gene cause congenital myopathy

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

Absence of integrin alpha 7 causes a novel form of muscular dystrophy

The potential of sarcospan in adhesion complex replacement therapeutics for the treatment of muscular dystrophy

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy

Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

Structural basis of laminin binding to the LARGE glycans on dystroglycan.

Overexpression of the cytotoxic T cell GalNAc transferase in skeletal muscle inhibits muscular dystrophy in mdx mice

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1134-1143

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scholarly article

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10.1093/GLYCOB/CWX073

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P433

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P478

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2017-08-23T00:00:00Z

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28973355

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6283322

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