Parental-origin-specific epigenetic modification of the mouse H19 gene.
about
Cloning of a mammalian transcriptional activator that binds unmethylated CpG motifs and shares a CXXC domain with DNA methyltransferase, human trithorax, and methyl-CpG binding domain protein 1.CpG binding protein is crucial for early embryonic developmentImprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in human myeloid malignanciesMouse U2af1-rs1 is a neomorphic imprinted geneEvolution and function of genomic imprinting in plantsCTCF: the protein, the binding partners, the binding sites and their chromatin loopsA non-coding RNA within the Rasgrf1 locus in mouse is imprinted and regulated by its homologous chromosome in transCTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locusAn analytical pipeline for genomic representations used for cytosine methylation studiesEstablishment of functional imprinting of the H19 gene in human developing placentaeRole of CTCF binding sites in the Igf2/H19 imprinting control regionRetrotransposon silencing by DNA methylation can drive mammalian genomic imprintingA silencer element identified in Drosophila is required for imprinting of H19 reporter transgenes in mice.A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes.A novel mutation in the maternally imprinted PEG3 domain results in a loss of MIMT1 expression and causes abortions and stillbirths in cattle (Bos taurus).Relationship between DNA methylation, histone H4 acetylation and gene expression in the mouse imprinted Igf2-H19 domain.A role for Insulin-like growth factor 2 in specification of the fast skeletal muscle fibre.Genomic imprinting: implications for human disease.Novel three-dimensional in vitro models of ovarian endometriosis.The importance of imprinting in the human placenta.H19 imprinting control region methylation requires an imprinted environment only in the male germ line.Fate of induced pluripotent stem cells following transplantation to murine seminiferous tubulesMosaic uniparental disomy in Beckwith-Wiedemann syndrome.Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster.An alternative promoter in the mouse major histocompatibility complex class II I-Abeta gene: implications for the origin of CpG islandsCharacterization of novel parent-specific epigenetic modifications upstream of the imprinted mouse H19 gene.Forced expression of DNA methyltransferases during oocyte growth accelerates the establishment of methylation imprints but not functional genomic imprinting.The tendency to recreate ancestral CG dinucleotides in the human genomeImprinted genes as potential genetic and epigenetic toxicologic targetsEmbryonic germ cells induce epigenetic reprogramming of somatic nucleus in hybrid cellsCompetition--a common motif for the imprinting mechanism?C(m)C(a/t)GG methylation: a new epigenetic mark in mammalian DNA?Parental allele-specific chromatin configuration in a boundary-imprinting-control element upstream of the mouse H19 geneRoles of cell division and gene transcription in the methylation of CpG islands.The absence of enhancer competition between Igf2 and H19 following transfer into differentiated cells.Regulatory mechanisms at the mouse Igf2/H19 locus.The ontogeny of allele-specific methylation associated with imprinted genes in the mouse.Dynamic stage-specific changes in imprinted differentially methylated regions during early mammalian development and prevalence of non-CpG methylation in oocytesEpigenetic control of the genome-lessons from genomic imprinting
P2860
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P2860
Parental-origin-specific epigenetic modification of the mouse H19 gene.
description
1993 nî lūn-bûn
@nan
1993 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Parental-origin-specific epigenetic modification of the mouse H19 gene.
@ast
Parental-origin-specific epigenetic modification of the mouse H19 gene.
@en
Parental-origin-specific epigenetic modification of the mouse H19 gene.
@nl
type
label
Parental-origin-specific epigenetic modification of the mouse H19 gene.
@ast
Parental-origin-specific epigenetic modification of the mouse H19 gene.
@en
Parental-origin-specific epigenetic modification of the mouse H19 gene.
@nl
prefLabel
Parental-origin-specific epigenetic modification of the mouse H19 gene.
@ast
Parental-origin-specific epigenetic modification of the mouse H19 gene.
@en
Parental-origin-specific epigenetic modification of the mouse H19 gene.
@nl
P2093
P356
P1433
P1476
Parental-origin-specific epigenetic modification of the mouse H19 gene.
@en
P2093
Cattanach BM
Ferguson-Smith AC
P2888
P304
P356
10.1038/362751A0
P407
P577
1993-04-01T00:00:00Z
P6179
1023758371