Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57
about
A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprintsCoevolution of retroelements and tandem zinc finger genesEpigenetics: a molecular link between environmental factors and type 2 diabetesMaintaining memory of silencing at imprinted differentially methylated regionsSpotting the enemy within: Targeted silencing of foreign DNA in mammalian genomes by the Krüppel-associated box zinc finger protein familyNew insights from monogenic diabetes for "common" type 2 diabetesRole of ZAC1 in transient neonatal diabetes mellitus and glucose metabolismGenomic imprinting in mammalsThe GNAS complex locus and human diseases associated with loss-of-function mutations or epimutations within this imprinted geneNew insights into establishment and maintenance of DNA methylation imprints in mammalsThe specification of imprints in mammalsMendelian disorders of the epigenetic machinery: tipping the balance of chromatin statesImprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted lociAbnormalities of the DNA methylation mark and its machinery: an emerging cause of neurologic dysfunctionTranslational implications of the β-cell epigenome in diabetes mellitusNeonatal diabetes: an expanding list of genes allows for improved diagnosis and treatmentChromatin regulators of genomic imprintingKAP1 regulates gene networks controlling T-cell development and responsiveness.An atomic model of Zfp57 recognition of CpG methylation within a specific DNA sequenceDNA Recognition of 5-Carboxylcytosine by a Zfp57 Mutant at an Atomic Resolution of 0.97 ÅImprinted gene expression in hybrids: perturbed mechanisms and evolutionary implications.Regulatory links between imprinted genes: evolutionary predictions and consequencesSilver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular EtiologyThe KRAB zinc finger protein RSL1 regulates sex- and tissue-specific promoter methylation and dynamic hormone-responsive chromatin configurationGenome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genesSelf/nonself perception, reproduction and the extended MHCChild health, developmental plasticity, and epigenetic programmingA statistical method for single sample analysis of HumanMethylation450 array data: genome-wide methylation analysis of patients with imprinting disorders.Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).The ancient mammalian KRAB zinc finger gene cluster on human chromosome 8q24.3 illustrates principles of C2H2 zinc finger evolution associated with unique expression profiles in human tissues.The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.A pair of mouse KRAB zinc finger proteins modulates multiple indicators of female reproduction.Forced expression of DNA methyltransferases during oocyte growth accelerates the establishment of methylation imprints but not functional genomic imprinting.Asymmetric DNA methylation of CpG dyads is a feature of secondary DMRs associated with the Dlk1/Gtl2 imprinting cluster in mouseZNF300 tight self-regulation and functioning through DNA methylation and histone acetylationSuccessful computational prediction of novel imprinted genes from epigenomic features.A gene-rich, transcriptionally active environment and the pre-deposition of repressive marks are predictive of susceptibility to KRAB/KAP1-mediated silencing.Characterisation of marsupial PHLDA2 reveals eutherian specific acquisition of imprinting.Mammalian genomic imprinting.Genome-wide gene and pathway analysis.
P2860
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P2860
Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57
description
2008 nî lūn-bûn
@nan
2008 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Hypomethylation of multiple im ...... ciated with mutations in ZFP57
@ast
Hypomethylation of multiple im ...... ciated with mutations in ZFP57
@en
Hypomethylation of multiple im ...... ciated with mutations in ZFP57
@en-gb
Hypomethylation of multiple im ...... ciated with mutations in ZFP57
@nl
type
label
Hypomethylation of multiple im ...... ciated with mutations in ZFP57
@ast
Hypomethylation of multiple im ...... ciated with mutations in ZFP57
@en
Hypomethylation of multiple im ...... ciated with mutations in ZFP57
@en-gb
Hypomethylation of multiple im ...... ciated with mutations in ZFP57
@nl
prefLabel
Hypomethylation of multiple im ...... ciated with mutations in ZFP57
@ast
Hypomethylation of multiple im ...... ciated with mutations in ZFP57
@en
Hypomethylation of multiple im ...... ciated with mutations in ZFP57
@en-gb
Hypomethylation of multiple im ...... ciated with mutations in ZFP57
@nl
P2093
P2860
P50
P3181
P356
P1433
P1476
Hypomethylation of multiple im ...... ciated with mutations in ZFP57
@en
P2093
Ahmed F Masoud
Andreas P Haemers
David O Robinson
Deborah J G Mackay
Elsebet Oestergaard
Helen E White
Helen V Firth
I Karen Temple
Johanne M D Hahnemann
John Storr
P2860
P2888
P304
P3181
P356
10.1038/NG.187
P407
P577
2008-08-01T00:00:00Z
P6179
1040383462