A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes. - Wikidata - wikimedia - TriplyDB

A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes.

A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes.

http://www.wikidata.org/entity/Q30830058

about

DNA methylation profiling of the human major histocompatibility complex: a pilot study for the human epigenome project Reduced representation bisulfite sequencing for comparative high-resolution DNA methylation analysis SWAN: Subset-quantile within array normalization for illumina infinium HumanMethylation450 BeadChips DNA methylation profiling of human chromosomes 6, 20 and 22 Hypomethylation and aberrant expression of the glioma pathogenesis-related 1 gene in Wilms tumors Computational and experimental identification of novel human imprinted genes A phase I study of hydralazine to demethylate and reactivate the expression of tumor suppressor genes Epigenetics of cervical cancer. An overview and therapeutic perspectives Modifiers and Readers of DNA Modifications and Their Impact on Genome Structure, Expression, and Stability in Disease Roles for retrotransposon insertions in human disease SVA retrotransposons as potential modulators of neuropeptide gene expression Flow-Dependent Epigenetic DNA Methylation in Endothelial Gene Expression and Atherosclerosis Mammalian small nucleolar RNAs are mobile genetic elements Novel retrotransposed imprinted locus identified at human 6p25 Epigenetic mechanisms in mammals Active human retrotransposons: variation and disease Monoallelic expression of multiple genes in the CNS.A novel CpG island set identifies tissue-specific methylation at developmental gene loci.Massive parallel bisulfite sequencing of CG-rich DNA fragments reveals that methylation of many X-chromosomal CpG islands in female blood DNA is incomplete.The new field of epigenomics: implications for cancer and other common disease research.Gradual transition from mosaic to global DNA methylation patterns during deuterostome evolution The tendency to recreate ancestral CG dinucleotides in the human genome Flow-dependent epigenetic DNA methylation regulates endothelial gene expression and atherosclerosis.Genome-wide prediction of imprinted murine genes Association of tissue-specific differentially methylated regions (TDMs) with differential gene expression.SVA retrotransposons: Evolution and genetic instability The emerging science of epigenomics.Natural genetic variation caused by transposable elements in humans A novel approach identifies new differentially methylated regions (DMRs) associated with imprinted genes Increased DNA methylation at the AXIN1 gene in a monozygotic twin from a pair discordant for a caudal duplication anomaly DNMT1 and AIM1 Imprinting in human placenta revealed through a genome-wide screen for allele-specific DNA methylation.Fidelity of the methylation pattern and its variation in the genome.Genome-scale approaches to the epigenetics of common human disease.Extensive epigenetic reprogramming in human somatic tissues between fetus and adult DNA sequence explains seemingly disordered methylation levels in partially methylated domains of Mammalian genomes.Retrotransposition of marked SVA elements by human L1s in cultured cells.Genome-wide mapping of imprinted differentially methylated regions by DNA methylation profiling of human placentas from triploidies.Genome-wide assays that identify and quantify modified cytosines in human disease studies A comprehensive analysis of allelic methylation status of CpG islands on human chromosome 21q Linkage analysis of adult height with parent-of-origin effects in the Framingham Heart Study

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A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes.

http://www.wikidata.org/entity/Q30830058

description

2002 nî lūn-bûn

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2002 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2002 թվականի ապրիլին հրատարակված գիտական հոդված

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2002年の論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年论文

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name

A genome-wide screen for norma ...... dentify novel imprinted genes.

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A genome-wide screen for norma ...... dentify novel imprinted genes.

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type

label

A genome-wide screen for norma ...... dentify novel imprinted genes.

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A genome-wide screen for norma ...... dentify novel imprinted genes.

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prefLabel

A genome-wide screen for norma ...... dentify novel imprinted genes.

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A genome-wide screen for norma ...... dentify novel imprinted genes.

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Genome Research

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A genome-wide screen for norma ...... dentify novel imprinted genes.

@en

P2093

Andrew P Feinberg

http://www.w3.org/2001/XMLSchema#string

Elizabeth Perlman

http://www.w3.org/2001/XMLSchema#string

Folke Flam

http://www.w3.org/2001/XMLSchema#string

Liora Z Strichman-Almashanu

http://www.w3.org/2001/XMLSchema#string

Matthew B Frieman

http://www.w3.org/2001/XMLSchema#string

Patrick O Onyango

http://www.w3.org/2001/XMLSchema#string

Richard S Lee

http://www.w3.org/2001/XMLSchema#string

P2860

Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein

Identification and characterization of Elongin A2, a new member of the Elongin family of transcription elongation factors, specifically expressed in the testis

Regulation of histone deacetylase 4 by binding of 14-3-3 proteins

Binding of the von Hippel-Lindau tumor suppressor protein to Elongin B and C

A variable number of tandem repeats locus within the human complement C2 gene is associated with a retroposon derived from a human endogenous retrovirus

Basic local alignment search tool

CpG islands in vertebrate genomes

CpG-rich islands and the function of DNA methylation

CTCF is a uniquely versatile transcription regulator linked to epigenetics and disease

Structure and genetics of the partially duplicated gene RP located immediately upstream of the complement C4A and the C4B genes in the HLA class III region. Molecular cloning, exon-intron structure, composite retroposon, and breakpoint of gene dupli

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543-554

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10.1101/GR.224102

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4

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12

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11932239

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187522

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