about
DUX4c is up-regulated in FSHD. It induces the MYF5 protein and human myoblast proliferationFacioscapulohumeral dystrophy: the path to consensus on pathophysiologyIntrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHDDUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophySpecific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophyDNaseI hypersensitivity at gene-poor, FSH dystrophy-linked 4q35.2The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure.Decoding the non-coding genome: elucidating genetic risk outside the coding genomeA muscle stem cell for every muscle: variability of satellite cell biology among different muscle groupsPolycomb Group (PcG) Proteins and Human Cancers: Multifaceted Functions and Therapeutic ImplicationsChromosome boundary elements and regulation of heterochromatin spreadingFacioscapulohumeral muscular dystrophy: consequences of chromatin relaxationIncreased expression of PcG protein YY1 negatively regulates B cell development while allowing accumulation of myeloid cells and LT-HSC cellsTransgenic Drosophila for Investigating DUX4 and FRG1, Two Genes Associated with Facioscapulohumeral Muscular Dystrophy (FSHD)Deregulation of the protocadherin gene FAT1 alters muscle shapes: implications for the pathogenesis of facioscapulohumeral dystrophyPhenotypic consequences of copy number variation: insights from Smith-Magenis and Potocki-Lupski syndrome mouse modelsMolecular and cellular changes in the lumbar spinal cord following thoracic injury: regulation by treadmill locomotor trainingDiscovery and characterization of human exonic transcriptional regulatory elementsA unifying genetic model for facioscapulohumeral muscular dystrophyThe Polycomb Ezh2 methyltransferase regulates muscle gene expression and skeletal muscle differentiationRbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD)Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophyRNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophyDNA methylation and human diseaseNovel checkpoint response to genotoxic stress mediated by nucleolin-replication protein a complex formation.Molecular cloning and functional characterization of the transcription factor YY2.The role of mitochondrial DNA mutations in mammalian agingEvolutionary genomic remodelling of the human 4q subtelomere (4q35.2).Down-regulation of NF-kappaB target genes by the AP-1 and STAT complex during the innate immune response in Drosophila.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.The D4Z4 macrosatellite repeat acts as a CTCF and A-type lamins-dependent insulator in facio-scapulo-humeral dystrophy.Hypermethylation of genomic 3.3-kb repeats is frequent event in HPV-positive cervical cancer.Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD).Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiationBiphasic myopathic phenotype of mouse DUX, an ORF within conserved FSHD-related repeats.Myogenic enhancers regulate expression of the facioscapulohumeral muscular dystrophy-associated DUX4 gene.Polycomb repressive complex 1 provides a molecular explanation for repeat copy number dependency in FSHD muscular dystrophy.Neurogenic to Gliogenic Fate Transition Perturbed by Loss of HMGB2.FSHD: a repeat contraction disease finally ready to expand (our understanding of its pathogenesis)
P2860
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P2860
description
2002 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
artikull shkencor
@sq
artículu científicu espublizáu en 2002
@ast
im August 2002 veröffentlichter wissenschaftlicher Artikel
@de
scientific article (publication date: August 2002)
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в серпні 2002
@uk
مقالة علمية (نشرت في أغسطس 2002)
@ar
name
Inappropriate Gene Activation in FSHD
@ast
Inappropriate Gene Activation in FSHD
@en
type
label
Inappropriate Gene Activation in FSHD
@ast
Inappropriate Gene Activation in FSHD
@en
prefLabel
Inappropriate Gene Activation in FSHD
@ast
Inappropriate Gene Activation in FSHD
@en
P3181
P1433
P1476
Inappropriate Gene Activation in FSHD
@en
P2093
Michael R. Green
P304
P3181
P356
10.1016/S0092-8674(02)00826-7
P407
P577
2002-08-01T00:00:00Z