Muscular dystrophy meets protein biochemistry, the mother of invention.

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Linker proteins restore basement membrane and correct LAMA2-related muscular dystrophy in mice.

P2860

Q47164258-9A646632-4D6C-4F5F-9A85-55CAF441EB4C

P2860

Muscular dystrophy meets protein biochemistry, the mother of invention.

Item

http://www.wikidata.org/entity/Q51130563

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Muscular dystrophy meets protein biochemistry, the mother of invention.

@en

Muscular dystrophy meets protein biochemistry, the mother of invention.

@nl

type

Item

label

Muscular dystrophy meets protein biochemistry, the mother of invention.

@en

Muscular dystrophy meets protein biochemistry, the mother of invention.

@nl

prefLabel

Muscular dystrophy meets protein biochemistry, the mother of invention.

@en

Muscular dystrophy meets protein biochemistry, the mother of invention.

@nl

P1476

Muscular dystrophy meets protein biochemistry, the mother of invention.

@en

P2093

Jeffrey H Miner

http://www.w3.org/2001/XMLSchema#string

Steven D Funk

http://www.w3.org/2001/XMLSchema#string

P2860

Distribution and function of laminins in the neuromuscular system of developing, adult, and mutant mice

Amelioration of laminin-alpha2-deficient congenital muscular dystrophy by somatic gene transfer of miniagrin.

An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy.

Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum.

Self-assembly and calcium-binding sites in laminin. A three-arm interaction model.

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

Laminin-111 protein therapy reduces muscle pathology and improves viability of a mouse model of merosin-deficient congenital muscular dystrophy

Linker molecules between laminins and dystroglycan ameliorate laminin-alpha2-deficient muscular dystrophy at all disease stages

Laminin polymerization induces a receptor-cytoskeleton network

The cell biology of disease: cellular and molecular mechanisms underlying muscular dystrophy.

P304

798-800

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scholarly article

P356

10.1172/JCI92847

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English

P433

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P478

127

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P577

2017-02-20T00:00:00Z

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P698

28218619

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P932

5330736

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Muscular dystrophy meets protein biochemistry, the mother of invention.

about

P2860

P2860

Muscular dystrophy meets protein biochemistry, the mother of invention.

description

name

type

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prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P932