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

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

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

http://www.wikidata.org/entity/Q28285889

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DUX4c is up-regulated in FSHD. It induces the MYF5 protein and human myoblast proliferation Facioscapulohumeral dystrophy: the path to consensus on pathophysiology Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD DNaseI hypersensitivity at gene-poor, FSH dystrophy-linked 4q35.2 Transgenic Drosophila for Investigating DUX4 and FRG1, Two Genes Associated with Facioscapulohumeral Muscular Dystrophy (FSHD)Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy The mosaic structure of human pericentromeric DNA: a strategy for characterizing complex regions of the human genome [Facioscapulohumeral muscular dystrophy. Clinical picture, atypical forms, diagnostics, genetics].Novel contrasting and labeling procedures for correlative microscopy of thawed cryosections.A functional role for 4qA/B in the structural rearrangement of the 4q35 region and in the regulation of FRG1 and ANT1 in facioscapulohumeral dystrophy.Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation Biphasic myopathic phenotype of mouse DUX, an ORF within conserved FSHD-related repeats.Facioscapulohumeral muscular dystrophy region gene-1 (FRG-1) is an actin-bundling protein associated with muscle-attachment sites.Genomic identification of regulatory elements by evolutionary sequence comparison and functional analysis DUX4, a candidate gene for facioscapulohumeral muscular dystrophy, causes p53-dependent myopathy in vivo Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere.Muscular dystrophy candidate gene FRG1 is critical for muscle development.The spreading of X inactivation into autosomal material of an x;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA 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 Perturbations of chromatin structure in human genetic disease: recent advances.FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients.Emerging preclinical animal models for FSHD.Alternative splicing and muscular dystrophy.Epigenetic mechanisms of facioscapulohumeral muscular dystrophy.FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy.The cell biology of disease: FSHD: copy number variations on the theme of muscular dystrophy Wnt/β-catenin signaling suppresses DUX4 expression and prevents apoptosis of FSHD muscle cells.Current status and future prospect of FSHD region gene 1.Direct interplay between two candidate genes in FSHD muscular dystrophy.RNA interference improves myopathic phenotypes in mice over-expressing FSHD region gene 1 (FRG1).Increasing D4Z4 repeat copy number compromises C2C12 myoblast differentiation.Molecular basis of genetic heterogeneity: role of the clinical neurologist.An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies.RNAPol-ChIP analysis of transcription from FSHD-linked tandem repeats and satellite DNA.Increased FSHD region gene1 expression reduces in vitro cell migration, invasion, and angiogenesis, ex vivo supported by reduced expression in tumors.The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8.A transcript map encompassing a susceptibility locus for bipolar affective disorder on chromosome 4q35.

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P2860

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

http://www.wikidata.org/entity/Q28285889

description

1996 nî lūn-bûn

@nan

1996 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

1996 թվականի մայիսին հրատարակված գիտական հոդված

@hy

1996年の論文

@ja

1996年論文

@yue

1996年論文

@zh-hant

1996年論文

@zh-hk

1996年論文

@zh-mo

1996年論文

@zh-tw

1996年论文

@wuu

name

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

@ast

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

@en

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

@nl

type

label

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

@ast

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

@en

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

@nl

prefLabel

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

@ast

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

@en

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

@nl

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P1433

Human Molecular Genetics

P1476

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

@en

P2093

G W Padberg

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

H G Dauwerse

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J C van Deutekom

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J E Hewitt

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M H Hofker

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M van Geel

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P K Grewal

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R J Lemmers

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R R Frants

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S Romberg

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P304

581-90

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scholarly article

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10.1093/HMG/5.5.581

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P407

P433

5

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P478

5

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P577

1996-05-01T00:00:00Z

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P5875

14469629

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P698

8733123

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