Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene
about
DNA damage, homology-directed repair, and DNA methylationDifferent binding properties and function of CXXC zinc finger domains in Dnmt1 and Tet1Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF)MCAF mediates MBD1-dependent transcriptional repressionTwo highly related p66 proteins comprise a new family of potent transcriptional repressors interacting with MBD2 and MBD3Modification of de novo DNA methyltransferase 3a (Dnmt3a) by SUMO-1 modulates its interaction with histone deacetylases (HDACs) and its capacity to repress transcriptionCo-operation and communication between the human maintenance and de novo DNA (cytosine-5) methyltransferasesDnmt3a binds deacetylases and is recruited by a sequence-specific repressor to silence transcriptionOverexpression of a splice variant of DNA methyltransferase 3b, DNMT3b4, associated with DNA hypomethylation on pericentromeric satellite regions during human hepatocarcinogenesis.Imprinting regulator DNMT3L is a transcriptional repressor associated with histone deacetylase activityLocus-specific control of asymmetric and CpNpG methylation by the DRM and CMT3 methyltransferase genesThe DNA methyltransferase-like protein DNMT3L stimulates de novo methylation by Dnmt3aCpG binding protein is crucial for early embryonic developmentMechanism of transcriptional regulation by methyl-CpG binding protein MBD1Isolation and characterization of a novel DNA methyltransferase complex linking DNMT3B with components of the mitotic chromosome condensation machineryGrowth retardation and premature aging phenotypes in mice with disruption of the SNF2-like gene, PASGDNA methylation profiling of human chromosomes 6, 20 and 22Structure of human DNMT2, an enigmatic DNA methyltransferase homolog that displays denaturant-resistant binding to DNAMutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing lossmiR-148 targets human DNMT3b protein coding regionSynergism of Xist RNA, DNA methylation, and histone hypoacetylation in maintaining X chromosome inactivationCGG-repeat expansion in the DIP2B gene is associated with the fragile site FRA12A on chromosome 12q13.1The molecular pathology of primary immunodeficienciesLack of involvement of known DNA methyltransferases in familial hydatidiform mole implies the involvement of other factors in establishment of imprinting in the human female germlineComputer aided analysis of additional chromosome aberrations in Philadelphia chromosome positive acute lymphoblastic leukaemia using a simplified computer readable cytogenetic notationNormal histone modifications on the inactive X chromosome in ICF and Rett syndrome cells: implications for methyl-CpG binding proteinsAnalysis of repetitive element DNA methylation by MethyLight.Permissive transcriptional activity at the centromere through pockets of DNA hypomethylation.Meiotically stable natural epialleles of Sadhu, a novel Arabidopsis retroposon.Modifiers and Readers of DNA Modifications and Their Impact on Genome Structure, Expression, and Stability in DiseaseMaking Sense of EpigeneticsStem Cell Models to Investigate the Role of DNA Methylation Machinery in Development of Neuropsychiatric DisordersTowards an understanding of the role of DNA methylation in rheumatoid arthritis: therapeutic and diagnostic implicationsDynamic DNA methylation in the brain: a new epigenetic mark for experience-dependent plasticityMechanisms and functions of Tet protein-mediated 5-methylcytosine oxidationCytosine modifications in neurodevelopment and diseasesEnzymatic DNA oxidation: mechanisms and biological significanceEvolutionary conservation and expression of human RNA-binding proteins and their role in human genetic diseaseDnmt3b Prefers Germ Line Genes and Centromeric Regions: Lessons from the ICF Syndrome and Cancer and Implications for DiseasesEpigenetics of Alzheimer's disease and frontotemporal dementia
P2860
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P2860
Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene
description
1999 nî lūn-bûn
@nan
1999 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի նոյեմբերին 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
Chromosome instability and imm ...... n a DNA methyltransferase gene
@ast
Chromosome instability and imm ...... n a DNA methyltransferase gene
@en
Chromosome instability and imm ...... n a DNA methyltransferase gene
@en-gb
Chromosome instability and imm ...... n a DNA methyltransferase gene
@nl
type
label
Chromosome instability and imm ...... n a DNA methyltransferase gene
@ast
Chromosome instability and imm ...... n a DNA methyltransferase gene
@en
Chromosome instability and imm ...... n a DNA methyltransferase gene
@en-gb
Chromosome instability and imm ...... n a DNA methyltransferase gene
@nl
prefLabel
Chromosome instability and imm ...... n a DNA methyltransferase gene
@ast
Chromosome instability and imm ...... n a DNA methyltransferase gene
@en
Chromosome instability and imm ...... n a DNA methyltransferase gene
@en-gb
Chromosome instability and imm ...... n a DNA methyltransferase gene
@nl
P2093
P2860
P3181
P356
P1433
P1476
Chromosome instability and imm ...... n a DNA methyltransferase gene
@en
P2093
E Viegas-Péquignot
T H Bestor
P2860
P2888
P304
P3181
P356
10.1038/46052
P407
P577
1999-11-11T00:00:00Z
P6179
1052544917