An important role for RUNX3 in human L1 transcription and retrotransposition - Test2 - elhamkhani - TriplyDB

An important role for RUNX3 in human L1 transcription and retrotransposition

An important role for RUNX3 in human L1 transcription and retrotransposition

http://www.wikidata.org/entity/Q24670621

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The impact of retrotransposons on human genome evolution Many LINE1 elements contribute to the transcriptome of human somatic cells L1 retrotransposon-mediated stable gene silencing A potential role for RNA interference in controlling the activity of the human LINE-1 retrotransposon Restricting retrotransposons: a review Guardian of the Human Genome: Host Defense Mechanisms against LINE-1 Retrotransposition Roles for retrotransposon insertions in human disease The Fine LINE: Methylation Drawing the Cancer Landscape Response of transposable elements to environmental stressors The Influence of LINE-1 and SINE Retrotransposons on Mammalian Genomes Expressing genes do not forget their LINEs: transposable elements and gene expression Molecular epigenetic switches in neurodevelopment in health and disease Regulation of L1 expression and retrotransposition by melatonin and its receptor: implications for cancer risk associated with light exposure at night L1 retrotransposons, cancer stem cells and oncogenesis In vitro screening for compounds that enhance human L1 mobilization Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the DPYD enigma LINE-1 elements in structural variation and disease Mapping the LINE1 ORF1 protein interactome reveals associated inhibitors of human retrotransposition Reactivation of L1 retrotransposon by benzo(a)pyrene involves complex genetic and epigenetic regulation Mutagenesis in rodents using the L1 retrotransposon The RNA polymerase dictates ORF1 requirement and timing of LINE and SINE retrotransposition.The impact of CpG island on defining transcriptional activation of the mouse L1 retrotransposable elements.Importance of RNA analysis in interpretation of reporter gene expression data.Intronic L1 retrotransposons and nested genes cause transcriptional interference by inducing intron retention, exonization and cryptic polyadenylation.All y'all need to know 'bout retroelements in cancer.De novo LINE-1 retrotransposition in HepG2 cells preferentially targets gene poor regions of chromosome 13 Modulation of LINE-1 and Alu/SVA retrotransposition by Aicardi-Goutières syndrome-related SAMHD1.LINE-1 RNA splicing and influences on mammalian gene expression.Long interspersed nucleotide element-1 hypomethylation in folate-deficient mouse embryonic stem cells.L1 retrotransposition is suppressed by endogenously encoded small interfering RNAs in human cultured cells.Extensive individual variation in L1 retrotransposition capability contributes to human genetic diversity An S/MAR-based L1 retrotransposition cassette mediates sustained levels of insertional mutagenesis without suffering from epigenetic silencing of DNA methylation The take and give between retrotransposable elements and their hosts.The potential regulation of L1 mobility by RNA interference.DNA damage and L1 retrotransposition Intrinsic restriction activity by apolipoprotein B mRNA editing enzyme APOBEC1 against the mobility of autonomous retrotransposons.Restless genomes humans as a model organism for understanding host-retrotransposable element dynamics.L1 expression and regulation in humans and rodents.Drawing a fine line on endogenous retroelement activity Retroelements versus APOBEC3 family members: No great escape from the magnificent seven

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P2860

An important role for RUNX3 in human L1 transcription and retrotransposition

http://www.wikidata.org/entity/Q24670621

description

2003 nî lūn-bûn

@nan

2003 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի օգոստոսին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

An important role for RUNX3 in human L1 transcription and retrotransposition

@ast

An important role for RUNX3 in human L1 transcription and retrotransposition

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An important role for RUNX3 in human L1 transcription and retrotransposition

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type

label

An important role for RUNX3 in human L1 transcription and retrotransposition

@ast

An important role for RUNX3 in human L1 transcription and retrotransposition

@en

An important role for RUNX3 in human L1 transcription and retrotransposition

@nl

prefLabel

An important role for RUNX3 in human L1 transcription and retrotransposition

@ast

An important role for RUNX3 in human L1 transcription and retrotransposition

@en

An important role for RUNX3 in human L1 transcription and retrotransposition

@nl

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Nucleic Acids Research

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An important role for RUNX3 in human L1 transcription and retrotransposition

@en

P2093

Haig H Kazazian

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

Lin Zhang

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

Nuo Yang

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

Yue Zhang

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

P2860

Initial sequencing and analysis of the human genome

Members of the SRY family regulate the human LINE retrotransposons

Hot L1s account for the bulk of retrotransposition in the human population

Initial sequencing and comparative analysis of the mouse genome

CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

AML1, AML2, and AML3, the human members of the runt domain gene-family: cDNA structure, expression, and chromosomal localization

Positional cloning of the gene for X-linked retinitis pigmentosa 2

Antisense promoter of human L1 retrotransposon drives transcription of adjacent cellular genes

Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis

A RUNX2/PEBP2alpha A/CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia

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4929-40

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scholarly article

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1803866

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10.1093/NAR/GKG663

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16

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31

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2003-08-15T00:00:00Z

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10621939

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12907736

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169909

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