Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse
about
An antisense RNA regulates the bidirectional silencing property of the Kcnq1 imprinting control regionBidirectional action of the Igf2r imprint control element on upstream and downstream imprinted genesThe Air noncoding RNA: an imprinted cis-silencing transcriptChromatin dynamics during epigenetic reprogramming in the mouse germ lineImprinting: silently crossing the boundary.The evolution of the DLK1-DIO3 imprinted domain in mammalsTargeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange-Nielsen Syndrome.Antisense transcripts with FANTOM2 clone set and their implications for gene regulation.Gene expression profile of neuronal progenitor cells derived from hESCs: activation of chromosome 11p15.5 and comparison to human dopaminergic neurons.Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome.Structural and functional analysis of a 0.5-Mb chicken region orthologous to the imprinted mammalian Ascl2/Mash2-Igf2-H19 region.Imprinted genes: identification by chromosome rearrangements and post-genomic strategies.A novel variant of Inpp5f is imprinted in brain, and its expression is correlated with differential methylation of an internal CpG island.Loss of CpG methylation is strongly correlated with loss of histone H3 lysine 9 methylation at DMR-LIT1 in patients with Beckwith-Wiedemann syndrome.Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes.DNA methylation in genomic imprinting, development, and disease.The absence of Tssc6, a member of the tetraspanin superfamily, does not affect lymphoid development but enhances in vitro T-cell proliferative responses.Extra-embryonic-specific imprinted expression is restricted to defined lineages in the post-implantation embryo.Identification of novel imprinted genes in a genome-wide screen for maternal methylation.Regulation of supply and demand for maternal nutrients in mammals by imprinted genes.Chromosome-wide analysis of parental allele-specific chromatin and DNA methylation.Depletion of Kcnq1ot1 non-coding RNA does not affect imprinting maintenance in stem cells.The potential role of gene duplications in the evolution of imprinting mechanisms.Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control regionComparative analysis of sequence characteristics of imprinted genes in human, mouse, and cattle.Gene density and transcription influence the localization of chromatin outside of chromosome territories detectable by FISH.Two distinct mechanisms of silencing by the KvDMR1 imprinting control region.Genomic imprinting in the placenta.Expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 and the methylation patterns at the KvDMR1 and H19/IGF2 imprinting control regions is conserved between human and bovine.The interval between Ins2 and Ascl2 is dispensable for imprinting centre function in the murine Beckwith-Wiedemann region.An imprinted GFP insertion reveals long-range epigenetic regulation in embryonic lineages.The placental imprintome and imprinted gene function in the trophoblast glycogen cell lineageThe H19 differentially methylated region marks the parental origin of a heterologous locus without gametic DNA methylation.Genomic imprinting mechanisms in embryonic and extraembryonic mouse tissuesA survey of tissue-specific genomic imprinting in mammals.What does genetics tell us about imprinting and the placenta connection?Comparative sequence analysis of the imprinted Dlk1-Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2-H19 region.Biallelic expression of Tssc4, Nap1l4, Phlda2 and Osbpl5 in adult cattle.A novel TRPM2 isoform inhibits calcium influx and susceptibility to cell death.Evolution of the Beckwith-Wiedemann syndrome region in vertebrates.
P2860
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P2860
Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse
description
2000 nî lūn-bûn
@nan
2000 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Sequence conservation and vari ...... ene cluster in human and mouse
@ast
Sequence conservation and vari ...... ene cluster in human and mouse
@en
Sequence conservation and vari ...... ene cluster in human and mouse
@nl
type
label
Sequence conservation and vari ...... ene cluster in human and mouse
@ast
Sequence conservation and vari ...... ene cluster in human and mouse
@en
Sequence conservation and vari ...... ene cluster in human and mouse
@nl
prefLabel
Sequence conservation and vari ...... ene cluster in human and mouse
@ast
Sequence conservation and vari ...... ene cluster in human and mouse
@en
Sequence conservation and vari ...... ene cluster in human and mouse
@nl
P2093
P356
P1476
Sequence conservation and vari ...... ene cluster in human and mouse
@en
P2093
M Strödicke
O El-Maarri
R Reinhardt
S Engemann
P304
P356
10.1093/HMG/9.12.1829
P407
P50
P577
2000-07-22T00:00:00Z