about
Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 regionAn imprinted PEG1/MEST antisense expressed predominantly in human testis and in mature spermatozoaIdentification of a large novel imprinted gene cluster on mouse proximal chromosome 6.Evaluation of allelic expression of imprinted genes in adult human blood.Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome.Variable imprinting of the MEST gene in human preimplantation embryos.Maternally inherited genetic variants of CADPS2 are present in autism spectrum disorders and intellectual disability patients.Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions.G-quadruplex structures and CpG methylation cause drop-out of the maternal allele in polymerase chain reaction amplification of the imprinted MEST gene promoter.Near-haploidy and subsequent polyploidization characterize the progression of peripheral chondrosarcoma.Structural Analysis of G-Quadruplex Formation at the Human MEST Promoter.Metabolic programming of MEST DNA methylation by intrauterine exposure to gestational diabetes mellitus.Epigenetics of gestational diabetes mellitus and offspring health: the time for action is in early stages of life.Genome-wide histone state profiling of fibroblasts from the opossum, Monodelphis domestica, identifies the first marsupial-specific imprinted gene.Systemic analysis of osteoblast-specific DNA methylation marks reveals novel epigenetic basis of osteoblast differentiation.Imprinting regulation of the murine Meg1/Grb10 and human GRB10 genes; roles of brain-specific promoters and mouse-specific CTCF-binding sites.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.Hypermethylation of the non-imprinted maternal MEG3 and paternal MEST alleles is highly variable among normal individuals.Methylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15Characterization of the aryl hydrocarbon receptor repressor gene and association of its Pro185Ala polymorphism with micropenis.Imprinted survival genes preclude loss of heterozygosity of chromosome 7 in cancer cells.Impairment of sperm DNA methylation in male infertility: a meta-analytic study.Evidence for mitochondrial genetic control of autosomal gene expression.Analysis of imprinted messenger RNA expression during bovine preimplantation development.Transcriptional regulation of metabolism in disease: From transcription factors to epigenetics.Allele-specific methylation of imprinted genes in fetal cord blood is influenced by cis-acting genetic variants and parental factors
P2860
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P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հունվարին 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
Isoform-specific imprinting of the human PEG1/MEST gene
@ast
Isoform-specific imprinting of the human PEG1/MEST gene
@en
Isoform-specific imprinting of the human PEG1/MEST gene
@nl
type
label
Isoform-specific imprinting of the human PEG1/MEST gene
@ast
Isoform-specific imprinting of the human PEG1/MEST gene
@en
Isoform-specific imprinting of the human PEG1/MEST gene
@nl
prefLabel
Isoform-specific imprinting of the human PEG1/MEST gene
@ast
Isoform-specific imprinting of the human PEG1/MEST gene
@en
Isoform-specific imprinting of the human PEG1/MEST gene
@nl
P2093
P2860
P356
P1476
Isoform-specific imprinting of the human PEG1/MEST gene
@en
P2093
P2860
P304
P356
10.1086/302712
P407
P577
2000-01-01T00:00:00Z