The FSHD region on human chromosome 4q35 contains potential coding regions among pseudogenes and a high density of repeat elements
about
Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHDDivergent origins and concerted expansion of two segmental duplications on chromosome 16SORBS2 transcription is activated by telomere position effect-over long distance upon telomere shortening in muscle cells from patients with facioscapulohumeral dystrophyA functional role for 4qA/B in the structural rearrangement of the 4q35 region and in the regulation of FRG1 and ANT1 in facioscapulohumeral dystrophy.Biphasic myopathic phenotype of mouse DUX, an ORF within conserved FSHD-related repeats.Myogenic enhancers regulate expression of the facioscapulohumeral muscular dystrophy-associated DUX4 gene.Hereditary Benign Intraepithelial Dyskeratosis: Report of a Case and Re-examination of the Evidence for Locus HeterogeneityAn optimized set of human telomere clones for studying telomere integrity and architecture.A cascade of complex subtelomeric duplications during the evolution of the hominoid and Old World monkey genomes.Chromatin loop domain organization within the 4q35 locus in facioscapulohumeral dystrophy patients versus normal human myoblasts.FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients.A nuclear matrix attachment site in the 4q35 locus has an enhancer-blocking activity in vivo: implications for the facio-scapulo-humeral dystrophy.Defective regulation of microRNA target genes in myoblasts from facioscapulohumeral dystrophy patients.The cell biology of disease: FSHD: copy number variations on the theme of muscular dystrophyEukaryotic enhancers: common features, regulation, and participation in diseases.Increasing D4Z4 repeat copy number compromises C2C12 myoblast differentiation.An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies.A transcript map encompassing a susceptibility locus for bipolar affective disorder on chromosome 4q35.
P2860
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P2860
The FSHD region on human chromosome 4q35 contains potential coding regions among pseudogenes and a high density of repeat elements
description
1999 nî lūn-bûn
@nan
1999 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
The FSHD region on human chrom ...... igh density of repeat elements
@ast
The FSHD region on human chrom ...... igh density of repeat elements
@en
The FSHD region on human chrom ...... igh density of repeat elements
@nl
type
label
The FSHD region on human chrom ...... igh density of repeat elements
@ast
The FSHD region on human chrom ...... igh density of repeat elements
@en
The FSHD region on human chrom ...... igh density of repeat elements
@nl
prefLabel
The FSHD region on human chrom ...... igh density of repeat elements
@ast
The FSHD region on human chrom ...... igh density of repeat elements
@en
The FSHD region on human chrom ...... igh density of repeat elements
@nl
P2093
P356
P1433
P1476
The FSHD region on human chrom ...... igh density of repeat elements
@en
P2093
P356
10.1006/GENO.1999.5942
P407
P577
1999-10-01T00:00:00Z