Phenotypes of myopathy-related beta-tropomyosin mutants in human and mouse tissue cultures. - Wikidata - awgldk - TriplyDB

Phenotypes of myopathy-related beta-tropomyosin mutants in human and mouse tissue cultures.

Phenotypes of myopathy-related beta-tropomyosin mutants in human and mouse tissue cultures.

http://www.wikidata.org/entity/Q34988373

about

Myosin Storage Myopathy in C. elegans and Human Cultured Muscle Cells.Proteomic identification of moesin upon exposure to acrolein.

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P2860

Phenotypes of myopathy-related beta-tropomyosin mutants in human and mouse tissue cultures.

http://www.wikidata.org/entity/Q34988373

description

2013 nî lūn-bûn

@nan

2013 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

Phenotypes of myopathy-related ...... man and mouse tissue cultures.

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Phenotypes of myopathy-related ...... man and mouse tissue cultures.

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Phenotypes of myopathy-related ...... man and mouse tissue cultures.

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type

label

Phenotypes of myopathy-related ...... man and mouse tissue cultures.

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Phenotypes of myopathy-related ...... man and mouse tissue cultures.

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Phenotypes of myopathy-related ...... man and mouse tissue cultures.

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prefLabel

Phenotypes of myopathy-related ...... man and mouse tissue cultures.

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Phenotypes of myopathy-related ...... man and mouse tissue cultures.

@en

Phenotypes of myopathy-related ...... man and mouse tissue cultures.

@nl

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JOURNAL.PONE.0072396

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Phenotypes of myopathy-related ...... man and mouse tissue cultures.

@en

P2093

Ali-Reza Moslemi

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

Homa Tajsharghi

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

Karin Rahl

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

Saba Abdul-Hussein

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

P2860

Phenotypes of myopathy-related actin mutants in differentiated C2C12 myotubes

Evidence for a dominant-negative effect in ACTA1 nemaline myopathy caused by abnormal folding, aggregation and altered polymerization of mutant actin isoforms

Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromes

Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy

Vertebrate tropomyosin: distribution, properties and function

Cap disease due to mutation of the beta-tropomyosin gene (TPM2)

Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2)

Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemaline and cap myopathy

Tropomyosin isoforms: divining rods for actin cytoskeleton function

Distal arthrogryposis and muscle weakness associated with a beta-tropomyosin mutation

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e72396

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scholarly article

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10.1371/JOURNAL.PONE.0072396

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9

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8

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2013-09-10T00:00:00Z

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24039757

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3769345

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