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Literature DB >> 9330892

Functions of dystrophin and dystrophin associated proteins.

Abstract

Dystrophin is a protein product of the X-linked gene mutation that is responsible for Duchenne and Becker muscular dystrophies. The protein binds actin and associates with dystrophin-glycoprotein complex to link the cytoskeleton to the extracellular matrix. Defects in the components of the dystrophin-glycoprotein complex are responsible for several phenotypes of muscular dystrophy.

Entities: Disease Gene

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Year: 1997 PMID： 9330892 DOI： 10.1097/00019052-199710000-00014

Source DB: PubMed Journal: Curr Opin Neurol ISSN： 1350-7540 Impact factor: 5.710

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Cited

9 in total

1. short stop is allelic to kakapo, and encodes rod-like cytoskeletal-associated proteins required for axon extension.

Authors: S Lee; K L Harris; P M Whitington; P A Kolodziej
Journal: J Neurosci Date: 2000-02-01 Impact factor: 6.167

2. A transcriptome-based assessment of the astrocytic dystrophin-associated complex in the developing human brain.

Authors: Matthew J Simon; Charles Murchison; Jeffrey J Iliff
Journal: J Neurosci Res Date: 2017-05-16 Impact factor: 4.164

3. A mutation in dVps28 reveals a link between a subunit of the endosomal sorting complex required for transport-I complex and the actin cytoskeleton in Drosophila.

Authors: Evgueni A Sevrioukov; Nabil Moghrabi; Mary Kuhn; Helmut Krämer
Journal: Mol Biol Cell Date: 2005-02-23 Impact factor: 4.138

4. Selective deficits in verbal working memory associated with a known genetic etiology: the neuropsychological profile of duchenne muscular dystrophy.

Authors: V J Hinton; D C De Vivo; N E Nereo; E Goldstein; Y Stern
Journal: J Int Neuropsychol Soc Date: 2001-01 Impact factor: 2.892

9. Novel inhibitor candidates of TRPV2 prevent damage of dystrophic myocytes and ameliorate against dilated cardiomyopathy in a hamster model.

Authors: Yuko Iwata; Yoshimi Katayama; Yasushi Okuno; Shigeo Wakabayashi
Journal: Oncotarget Date: 2018-02-08

9 in total

Functions of dystrophin and dystrophin associated proteins.

1. short stop is allelic to kakapo, and encodes rod-like cytoskeletal-associated proteins required for axon extension.

2. A transcriptome-based assessment of the astrocytic dystrophin-associated complex in the developing human brain.

3. A mutation in dVps28 reveals a link between a subunit of the endosomal sorting complex required for transport-I complex and the actin cytoskeleton in Drosophila.

4. Selective deficits in verbal working memory associated with a known genetic etiology: the neuropsychological profile of duchenne muscular dystrophy.

5. The expression of dystrophin and alpha1-syntrophin during skeletal muscle regeneration.

6. Guanine analogues enhance antisense oligonucleotide-induced exon skipping in dystrophin gene in vitro and in vivo.

7. Pericytes in Muscular Dystrophies.

Review 8. Blockade of TRPV2 is a Novel Therapy for Cardiomyopathy in Muscular Dystrophy.

9. Novel inhibitor candidates of TRPV2 prevent damage of dystrophic myocytes and ameliorate against dilated cardiomyopathy in a hamster model.