about
To edit or not to edit: regulation of ADAR editing specificity and efficiencyA-to-I RNA Editing: Current Knowledge Sources and Computational Approaches with Special Emphasis on Non-Coding RNA MoleculesRNA editome in rhesus macaque shaped by purifying selectionKnowledge in the Investigation of A-to-I RNA Editing SignalsA genome-wide map of hyper-edited RNA reveals numerous new sitesConstraint and opportunity in genome innovationRADAR: a rigorously annotated database of A-to-I RNA editingDarned in 2013: inclusion of model organisms and linking with WikipediaAlu elements shape the primate transcriptome by cis-regulation of RNA editingA distant cis acting intronic element induces site-selective RNA editing.Prediction of constitutive A-to-I editing sites from human transcriptomes in the absence of genomic sequences.VIRGO: visualization of A-to-I RNA editing sites in genomic sequences.Dynamic response of RNA editing to temperature in Drosophila.One hundred million adenosine-to-inosine RNA editing sites: hearing through the noise.The emerging role of RNA editing in plasticity.Identification of General and Heart-Specific miRNAs in Sheep (Ovis aries)Transcriptome-wide identification of A > I RNA editing sites by inosine specific cleavageRNA-DNA differences are generated in human cells within seconds after RNA exits polymerase IIADAR regulates RNA editing, transcript stability, and gene expression.A-to-I RNA editing occurs at over a hundred million genomic sites, located in a majority of human genes.Multi-level regulation of cellular recognition of viral dsRNA.Identification of human RNA editing sites: A historical perspective.Endogenous Retroelements and the Host Innate Immune Sensors.RNA Editing, ADAR1, and the Innate Immune Response.RNA editing generates cellular subsets with diverse sequence within populations.Genome-wide mapping of infection-induced SINE RNAs reveals a role in selective mRNA export.Genome-wide analysis of Alu editability.Noncoding regions of C. elegans mRNA undergo selective adenosine to inosine deamination and contain a small number of editing sites per transcript.Massive A-to-I RNA editing is common across the Metazoa and correlates with dsRNA abundance.Editing inducer elements increases A-to-I editing efficiency in the mammalian transcriptome.Deletion of the RNA-editing enzyme ADAR1 causes regression of established chronic myelogenous leukemia in mice.Linkage of A-to-I RNA editing in metazoans and the impact on genome evolution.Rewriting the transcriptome: adenosine-to-inosine RNA editing by ADARs.Elucidating the editome: bioinformatics approaches for RNA editing detection.Decreased A-to-I RNA editing as a source of keratinocytes dsRNA in psoriasis.Increased RNA Editing May Provide a Source for Autoantigens in Systemic Lupus Erythematosus.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Identification of widespread ultra-edited human RNAs.
@ast
Identification of widespread ultra-edited human RNAs.
@en
Identification of widespread ultra-edited human RNAs.
@nl
type
label
Identification of widespread ultra-edited human RNAs.
@ast
Identification of widespread ultra-edited human RNAs.
@en
Identification of widespread ultra-edited human RNAs.
@nl
prefLabel
Identification of widespread ultra-edited human RNAs.
@ast
Identification of widespread ultra-edited human RNAs.
@en
Identification of widespread ultra-edited human RNAs.
@nl
P2860
P1433
P1476
Identification of widespread ultra-edited human RNAs
@en
P2093
Itamar Borukhov
P2860
P304
P356
10.1371/JOURNAL.PGEN.1002317
P577
2011-10-20T00:00:00Z