Muscular dystrophy candidate gene FRG1 is critical for muscle development. - Wikidata - awgldk - TriplyDB

Muscular dystrophy candidate gene FRG1 is critical for muscle development.

Muscular dystrophy candidate gene FRG1 is critical for muscle development.

http://www.wikidata.org/entity/Q34244856

about

DUX4c is up-regulated in FSHD. It induces the MYF5 protein and human myoblast proliferation Transgenic Drosophila for Investigating DUX4 and FRG1, Two Genes Associated with Facioscapulohumeral Muscular Dystrophy (FSHD)Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD)Facioscapulohumeral muscular dystrophy region gene-1 (FRG-1) is an actin-bundling protein associated with muscle-attachment sites.Testing the effects of FSHD candidate gene expression in vertebrate muscle development.Decreased proliferation kinetics of mouse myoblasts overexpressing FRG1.Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a dynamic nuclear and sarcomeric protein.FHL1 reduces dystrophy in transgenic mice overexpressing FSHD muscular dystrophy region gene 1 (FRG1).Facioscapulohumeral muscular dystrophy region gene 1 is a dynamic RNA-associated and actin-bundling protein.DUX4 promotes transcription of FRG2 by directly activating its promoter in facioscapulohumeral muscular dystrophy AAV6-mediated systemic shRNA delivery reverses disease in a mouse model of facioscapulohumeral muscular dystrophy Alternative splicing and muscular dystrophy.FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy.Prenatal diagnosis of 4p and 4q subtelomeric microdeletion in de novo ring chromosome 4.Altered Tnnt3 characterizes selective weakness of fast fibers in mice overexpressing FSHD region gene 1 (FRG1)Heterochromatin dysregulation in human diseases.The cell biology of disease: FSHD: copy number variations on the theme of muscular dystrophy Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?In junk we trust: repetitive DNA, epigenetics and facioscapulohumeral muscular dystrophy.Current status and future prospect of FSHD region gene 1.Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) expression and possible function in mouse tooth germ development.Direct interplay between two candidate genes in FSHD muscular dystrophy.RNA interference improves myopathic phenotypes in mice over-expressing FSHD region gene 1 (FRG1).FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis.Increased FSHD region gene1 expression reduces in vitro cell migration, invasion, and angiogenesis, ex vivo supported by reduced expression in tumors.Facioscapulohumeral Muscular Dystrophy.

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P2860

Muscular dystrophy candidate gene FRG1 is critical for muscle development.

http://www.wikidata.org/entity/Q34244856

description

2009 nî lūn-bûn

@nan

2009 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

Muscular dystrophy candidate gene FRG1 is critical for muscle development.

@ast

Muscular dystrophy candidate gene FRG1 is critical for muscle development.

@en

Muscular dystrophy candidate gene FRG1 is critical for muscle development.

@nl

type

label

Muscular dystrophy candidate gene FRG1 is critical for muscle development.

@ast

Muscular dystrophy candidate gene FRG1 is critical for muscle development.

@en

Muscular dystrophy candidate gene FRG1 is critical for muscle development.

@nl

prefLabel

Muscular dystrophy candidate gene FRG1 is critical for muscle development.

@ast

Muscular dystrophy candidate gene FRG1 is critical for muscle development.

@en

Muscular dystrophy candidate gene FRG1 is critical for muscle development.

@nl

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P1433

Developmental Dynamics

P1476

Muscular dystrophy candidate gene FRG1 is critical for muscle development.

@en

P2093

Meredith L Hanel

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

P2860

FRG1P is localised in the nucleolus, Cajal bodies, and speckles

The mesenchymal cell, its role in the embryo, and the remarkable signaling mechanisms that create it

Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35

Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1

Genome-wide RNAi screening in Caenorhabditis elegans

In situ hybridization: an improved whole-mount method for Xenopus embryos

Inappropriate Gene Activation in FSHD

Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation.

Formation and differentiation of the avian dermomyotome.

FRG1P-mediated aggregation of proteins involved in pre-mRNA processing.

P304

1502-1512

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scholarly article

P356

10.1002/DVDY.21830

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6

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238

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Ryan D. Wuebbles

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2009-06-01T00:00:00Z

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23678120

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19097195

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2964887

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