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Imprinted genes as potential genetic and epigenetic toxicologic targets

Imprinted genes as potential genetic and epigenetic toxicologic targets

http://www.wikidata.org/entity/Q33852775

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Epigenetic reprogramming and imprinting in origins of disease Techniques used in studies of epigenome dysregulation due to aberrant DNA methylation: an emphasis on fetal-based adult diseases.Prenatal arsenic exposure and drowning among children in Bangladesh.What is an epigenetic transgenerational phenotype? F3 or F2.Regulation of the metastasis suppressor gene MKK4 in ovarian cancer.Epigenetics and transcriptomics to detect adverse drug effects in model systems of human development.H19 gene methylation study in Indian buffalo (Bubalus bubalis).Valuing the Ozone-Related Health Benefits of Methane Emission Controls

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Imprinted genes as potential genetic and epigenetic toxicologic targets

http://www.wikidata.org/entity/Q33852775

description

2000 nî lūn-bûn

@nan

2000 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի մարտին 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

Imprinted genes as potential genetic and epigenetic toxicologic targets

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Imprinted genes as potential genetic and epigenetic toxicologic targets

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type

label

Imprinted genes as potential genetic and epigenetic toxicologic targets

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Imprinted genes as potential genetic and epigenetic toxicologic targets

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prefLabel

Imprinted genes as potential genetic and epigenetic toxicologic targets

@ast

Imprinted genes as potential genetic and epigenetic toxicologic targets

@en

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Environmental Health Perspectives

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Imprinted genes as potential genetic and epigenetic toxicologic targets

@en

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R L Jirtle

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

S K Murphy

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

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An imprinted, mammalian bicistronic transcript encodes two independent proteins

The human DNA methyltransferases (DNMTs) 1, 3a and 3b: coordinate mRNA expression in normal tissues and overexpression in tumors

Parental imprinting of the mouse H19 gene

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

UBE3A/E6-AP mutations cause Angelman syndrome

IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes

Frequent loss of heterozygosity on 6q at the mannose 6-phosphate/insulin-like growth factor II receptor locus in human hepatocellular tumors

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

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5-11

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

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scholarly article

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10.1289/EHP.00108S15

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108 Suppl 1

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2000-03-01T00:00:00Z

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12616389

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10698719

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regulation of gene expression

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1637779

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