Perturbations of chromatin structure in human genetic disease: recent advances.
about
Nucleosome recognition by the Piccolo NuA4 histone acetyltransferase complex.From silencing to gene expression: real-time analysis in single cellsEvolutionary genomic remodelling of the human 4q subtelomere (4q35.2).Altered intra-nuclear organisation of heterochromatin and genes in ICF syndrome.Long-range control of gene expression: emerging mechanisms and disruption in disease.Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia.Facioscapulohumeral muscular dystrophy as a model for epigenetic regulation and diseaseConnections between epigenetic gene silencing and human disease.Bromodomain protein Brd4 associated with acetylated chromatin is important for maintenance of higher-order chromatin structure.The 4q subtelomere harboring the FSHD locus is specifically anchored with peripheral heterochromatin unlike most human telomeresExpression of human Cfdp1 gene in Drosophila reveals new insights into the function of the evolutionarily conserved BCNT protein family.Site specificity analysis of Piccolo NuA4-mediated acetylation for different histone complexes.Gene clusters, molecular evolution and disease: a speculation.Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?Role of microRNAs and long-non-coding RNAs in CD4(+) T-cell differentiation.The Bucentaur (BCNT) protein family: a long-neglected class of essential proteins required for chromatin/chromosome organization and function.Genomic properties of chromosomal bands are linked to evolutionary rearrangements and new centromere formation in primates.When chromatin organisation floats astray: the Srcap gene and Floating-Harbor syndrome.Telomere shortening and telomere position effect in mild ring 17 syndrome.Two new de novo interstitial duplications covering 2p14-p22.1: clinical and molecular analysis.Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy.Epigenetics and Human Disease.
P2860
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P2860
Perturbations of chromatin structure in human genetic disease: recent advances.
description
2003 nî lūn-bûn
@nan
2003 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Perturbations of chromatin structure in human genetic disease: recent advances.
@ast
Perturbations of chromatin structure in human genetic disease: recent advances.
@en
type
label
Perturbations of chromatin structure in human genetic disease: recent advances.
@ast
Perturbations of chromatin structure in human genetic disease: recent advances.
@en
prefLabel
Perturbations of chromatin structure in human genetic disease: recent advances.
@ast
Perturbations of chromatin structure in human genetic disease: recent advances.
@en
P2860
P356
P1476
Perturbations of chromatin structure in human genetic disease: recent advances
@en
P2093
Wendy A Bickmore
P2860
P304
P356
10.1093/HMG/DDG260
P478
12 Spec No 2
P577
2003-08-05T00:00:00Z