about
Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolutionA novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical regionIsoform-specific imprinting of the human PEG1/MEST geneThe imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndromeThe epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprintedMutation screening and imprinting analysis of four candidate genes for autism in the 7q32 regionFrequent loss of imprinting of IGF2 and MEST in lung adenocarcinomaAn imprinted PEG1/MEST antisense expressed predominantly in human testis and in mature spermatozoaLead exposure induces changes in 5-hydroxymethylcytosine clusters in CpG islands in human embryonic stem cells and umbilical cord bloodMesoderm-specific transcript is associated with fat mass expansion in response to a positive energy balancemiR-335 orchestrates cell proliferation, migration and differentiation in human mesenchymal stem cells.Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.Genomic imprinting: implications for human disease.Genomic imprinting: concept and clinical consequences.Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7.Association of specific language impairment (SLI) to the region of 7q31.Convergent and divergent evolution of genomic imprinting in the marsupial Monodelphis domesticaImprinted genes and mental dysfunction.Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome.Variable imprinting of the MEST gene in human preimplantation embryos.Differential decay of parent-of-origin-specific genomic sharing in cystic fibrosis-affected sib pairs maps a paternally imprinted locus to 7q34.Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions.Maternal stress, preterm birth, and DNA methylation at imprint regulatory sequences in humans.Imprinting disorders: non-Mendelian mechanisms affecting growth.Population models of genomic imprinting. II. Maternal and fertility selection.The role of imprinted genes in fetal growth abnormalities.G-quadruplex structures and CpG methylation cause drop-out of the maternal allele in polymerase chain reaction amplification of the imprinted MEST gene promoter.Epigenetic regulation by RARα maintains ligand-independent transcriptional activity.Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome geneQ-RRBS: a quantitative reduced representation bisulfite sequencing method for single-cell methylome analyses.Mesoderm-specific transcript (MEST) is a negative regulator of human adipocyte differentiationStructural Analysis of G-Quadruplex Formation at the Human MEST Promoter.Increased Histone Deacetylase Activity Involved in the Suppressed Invasion of Cancer Cells Survived from ALA-Mediated Photodynamic Treatment.Transcriptome profiling of granulosa cells of bovine ovarian follicles during growth from small to large antral sizes.Genome-wide histone state profiling of fibroblasts from the opossum, Monodelphis domestica, identifies the first marsupial-specific imprinted gene.Epigenetic modifications at DMRs of placental genes are subjected to variations in normal gestation, pathological conditions and folate supplementation.Quantitative expression of developmental genes, Pou5f1 (Oct4) and Mest (Peg1), in vitrified mouse embryos.Quantitative Assessment of Sialo-Glycoproteins and N-Glycans during Cardiomyogenic Differentiation of Human Induced Pluripotent Stem Cells.Complete meiosis from human induced pluripotent stem cells.Imprinting regulation of the murine Meg1/Grb10 and human GRB10 genes; roles of brain-specific promoters and mouse-specific CTCF-binding sites.
P2860
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P2860
description
1997 nî lūn-bûn
@nan
1997 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի մայիսին հրատարակված գիտական հոդված
@hy
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
name
Human PEG1/MEST, an imprinted gene on chromosome 7
@ast
Human PEG1/MEST, an imprinted gene on chromosome 7
@en
Human PEG1/MEST, an imprinted gene on chromosome 7
@en-gb
Human PEG1/MEST, an imprinted gene on chromosome 7
@nl
type
label
Human PEG1/MEST, an imprinted gene on chromosome 7
@ast
Human PEG1/MEST, an imprinted gene on chromosome 7
@en
Human PEG1/MEST, an imprinted gene on chromosome 7
@en-gb
Human PEG1/MEST, an imprinted gene on chromosome 7
@nl
prefLabel
Human PEG1/MEST, an imprinted gene on chromosome 7
@ast
Human PEG1/MEST, an imprinted gene on chromosome 7
@en
Human PEG1/MEST, an imprinted gene on chromosome 7
@en-gb
Human PEG1/MEST, an imprinted gene on chromosome 7
@nl
P2093
P2860
P356
P1476
Human PEG1/MEST, an imprinted gene on chromosome 7
@en
P2093
O Tsutsumi
S Kobayashi
T Kaneko-Ishino
P2860
P356
10.1093/HMG/6.5.781
P407
P577
1997-05-01T00:00:00Z