FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy.
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DUX4c is up-regulated in FSHD. It induces the MYF5 protein and human myoblast proliferationIntrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHDTransgenic 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.BAC TG-EMBED: one-step method for high-level, copy-number-dependent, position-independent transgene expression.Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a dynamic nuclear and sarcomeric protein.Determining the role of sarcomeric proteins in facioscapulohumeral muscular dystrophy: a study protocol.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.AAV6-mediated systemic shRNA delivery reverses disease in a mouse model of facioscapulohumeral muscular dystrophyCombined treatment with intravitreal bevacizumab and laser photocoagulation for exudative maculopathy in facioscapulohumeral muscular dystrophy.Alternative splicing and muscular dystrophy.The cell biology of disease: FSHD: copy number variations on the theme of muscular dystrophyFacioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?In junk we trust: repetitive DNA, epigenetics and facioscapulohumeral muscular dystrophy.Deciphering transcription dysregulation in FSH muscular dystrophy.Prospect for pharmacological therapies to treat skeletal muscle dysfunction.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
FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy.
description
article científic
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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 21 April 2009
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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
FSHD region gene 1 (FRG1) is c ...... rophy-associated vasculopathy.
@en
FSHD region gene 1
@nl
type
label
FSHD region gene 1 (FRG1) is c ...... rophy-associated vasculopathy.
@en
FSHD region gene 1
@nl
prefLabel
FSHD region gene 1 (FRG1) is c ...... rophy-associated vasculopathy.
@en
FSHD region gene 1
@nl
P2860
P356
P1476
FSHD region gene 1 (FRG1) is c ...... rophy-associated vasculopathy.
@en
P2093
Meredith L Hanel
P2860
P304
P356
10.1242/DMM.002261
P577
2009-04-21T00:00:00Z