Imprinting of human H19: allele-specific CpG methylation, loss of the active allele in Wilms tumor, and potential for somatic allele switching.
about
NOEY2 (ARHI), an imprinted putative tumor suppressor gene in ovarian and breast carcinomasLong noncoding RNAs in cancer: mechanisms of action and technological advancementsLoss of IGF2 imprinting is associated with abrogation of long-range intrachromosomal interactions in human cancer cells.Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragmentsLong Noncoding RNAs as Biomarkers in Cancer.Roles of cell division and gene transcription in the methylation of CpG islands.Imprinted gene expression, transplantation medicine, and the "other" human embryonic stem cell.Dnmt1 overexpression causes genomic hypermethylation, loss of imprinting, and embryonic lethality.Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor.Epigenetic regulation of the cell type-specific gene 14-3-3sigma.Flipping the epigenetic switchAssessment of genomic imprinting of SLC38A4, NNAT, NAP1L5, and H19 in cattleTesting parental imprinting in insulin-dependent diabetes mellitus by the marker-association-segregation-chi 2 method.MTS1/p16/CDKN2 lesions in primary glioblastoma multiforme.A Common Polymorphism within the IGF2 Imprinting Control Region Is Associated with Parent of Origin Specific Effects in Infantile HemangiomasGenomic imprinting: mechanism and role in human pathology.Genomic landscape of human allele-specific DNA methylation.Carcinogenic nickel silences gene expression by chromatin condensation and DNA methylation: a new model for epigenetic carcinogens.Conditional deletions refine the embryonic requirement for Dlk1.Methylation similarities of two CpG sites within exon 5 of human H19 between normal tissues and testicular germ cell tumours of adolescents and adults, without correlation with allelic and total level of expression.A 5' 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development.To Wnt or Lose: The Missing Non-Coding Linc in Colorectal Cancer.Allele specific expression and methylation in the bumblebee, Bombus terrestris.New insights reveal complex mechanisms involved in genomic imprinting.Equivalent parental distribution of frequently lost alleles and biallelic expression of the H19 gene in human testicular germ cell tumors.
P2860
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P2860
Imprinting of human H19: allele-specific CpG methylation, loss of the active allele in Wilms tumor, and potential for somatic allele switching.
description
1993 nî lūn-bûn
@nan
1993 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
name
Imprinting of human H19: allel ...... for somatic allele switching.
@ast
Imprinting of human H19: allel ...... for somatic allele switching.
@en
type
label
Imprinting of human H19: allel ...... for somatic allele switching.
@ast
Imprinting of human H19: allel ...... for somatic allele switching.
@en
prefLabel
Imprinting of human H19: allel ...... for somatic allele switching.
@ast
Imprinting of human H19: allel ...... for somatic allele switching.
@en
P2093
P2860
P1476
Imprinting of human H19: allel ...... for somatic allele switching.
@en
P2093
P2860
P304
P407
P577
1993-07-01T00:00:00Z