Amelioration of muscular dystrophy by transgenic expression of Niemann-Pick C1. - Wikidata - awgldk - TriplyDB

Amelioration of muscular dystrophy by transgenic expression of Niemann-Pick C1.

Amelioration of muscular dystrophy by transgenic expression of Niemann-Pick C1.

http://www.wikidata.org/entity/Q37035048

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Automated drug screening with contractile muscle tissue engineered from dystrophic myoblasts Dystrophin deficiency leads to disturbance of LAMP1-vesicle-associated protein secretion.

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Amelioration of muscular dystrophy by transgenic expression of Niemann-Pick C1.

http://www.wikidata.org/entity/Q37035048

description

article científic

@ca

article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 22 October 2008

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Amelioration of muscular dystrophy by transgenic expression of Niemann-Pick C1.

@en

Amelioration of muscular dystrophy by transgenic expression of Niemann-Pick C1.

@nl

type

label

Amelioration of muscular dystrophy by transgenic expression of Niemann-Pick C1.

@en

Amelioration of muscular dystrophy by transgenic expression of Niemann-Pick C1.

@nl

prefLabel

Amelioration of muscular dystrophy by transgenic expression of Niemann-Pick C1.

@en

Amelioration of muscular dystrophy by transgenic expression of Niemann-Pick C1.

@nl

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MBC.E08-08-0811

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Molecular Biology of the Cell

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Amelioration of muscular dystrophy by transgenic expression of Niemann-Pick C1.

@en

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Marvin E Adams

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Michelle S Steen

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Stanley C Froehner

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Yan Tesch

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P2860

Caveolin-3 directly interacts with the C-terminal tail of beta -dystroglycan. Identification of a central WW-like domain within caveolin family members

Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy

Gene expression comparison of biopsies from Duchenne muscular dystrophy (DMD) and normal skeletal muscle

Absence of alpha-syntrophin leads to structurally aberrant neuromuscular synapses deficient in utrophin

A chronic inflammatory response dominates the skeletal muscle molecular signature in dystrophin-deficient mdx mice

Interaction of neuronal nitric-oxide synthase with caveolin-3 in skeletal muscle. Identification of a novel caveolin scaffolding/inhibitory domain

Caveolin regulates endocytosis of the muscle repair protein, dysferlin

Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy

Expression of caveolin-3 in skeletal, cardiac, and smooth muscle cells. Caveolin-3 is a component of the sarcolemma and co-fractionates with dystrophin and dystrophin-associated glycoproteins

X chromosome-linked muscular dystrophy (mdx) in the mouse

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146-152

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scholarly article

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10.1091/MBC.E08-08-0811

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1

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20

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2008-10-22T00:00:00Z

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18946078

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2613093

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