Genomic structure and parent-of-origin-specific methylation of Peg1.
about
Isoform-specific imprinting of the human PEG1/MEST geneExpression of the imprinted genes MEST/Mest in human and murine placenta suggests a role in angiogenesisAn imprinted PEG1/MEST antisense expressed predominantly in human testis and in mature spermatozoaMesoderm-specific transcript is associated with fat mass expansion in response to a positive energy balanceDiet-induced adipose tissue expansion is mitigated in mice with a targeted inactivation of mesoderm specific transcript (Mest).Embryonic germ cells induce epigenetic reprogramming of somatic nucleus in hybrid cellsRole of epigenetics in mental disorders.An extended domain of Kcnq1ot1 silencing revealed by an imprinted fluorescent reporter.Establishment and maintenance of genomic methylation patterns in mouse embryonic stem cells by Dnmt3a and Dnmt3b.Glycogen synthase kinase-3 (Gsk-3) plays a fundamental role in maintaining DNA methylation at imprinted loci in mouse embryonic stem cells.Tissue-specific alternative polyadenylation at the imprinted gene Mest regulates allelic usage at Copg2Epigenetic and phenotypic consequences of a truncation disrupting the imprinted domain on distal mouse chromosome 7.Disruption of the interaction between transcriptional intermediary factor 1{beta} and heterochromatin protein 1 leads to a switch from DNA hyper- to hypomethylation and H3K9 to H3K27 trimethylation on the MEST promoter correlating with gene reactivaAn extensive genetic program occurring during postnatal growth in multiple tissuesAn imprinted GFP insertion reveals long-range epigenetic regulation in embryonic lineages.Mest/Peg1 Is Essential for the Development and Maintenance of a SNc Neuronal Subset.Inter-individual variation of dietary fat-induced mesoderm specific transcript in adipose tissue within inbred mice is not caused by altered promoter methylation.Maternal vitamin D, DNA methylation at imprint regulatory regions and offspring weight at birth, 1 year and 3 years.Peg1/Mest in obese adipose tissue is expressed from the paternal allele in an isoform-specific manner.Effects of maternal folic acid supplementation on gene methylation and being small for gestational age.Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest.Maintenance of Mest imprinted methylation in blastocyst-stage mouse embryos is less stable than other imprinted loci following superovulation or embryo culture.Aberrant DNA methylation of imprinted loci in superovulated oocytes.Oocyte growth-dependent progression of maternal imprinting in mice.Dynamic CpG and non-CpG methylation of the Peg1/Mest gene in the mouse oocyte and preimplantation embryo.
P2860
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P2860
Genomic structure and parent-of-origin-specific methylation of Peg1.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Genomic structure and parent-of-origin-specific methylation of Peg1.
@en
type
label
Genomic structure and parent-of-origin-specific methylation of Peg1.
@en
prefLabel
Genomic structure and parent-of-origin-specific methylation of Peg1.
@en
P2093
P2860
P356
P1476
Genomic structure and parent-of-origin-specific methylation of Peg1.
@en
P2093
P2860
P304
P356
10.1093/HMG/6.11.1907
P50
P577
1997-10-01T00:00:00Z