Quantitative mass spectrometry of DENV-2 RNA-interacting proteins reveals that the DEAD-box RNA helicase DDX6 binds the DB1 and DB2 3' UTR structures. - Wikidata - wikimedia - TriplyDB

Quantitative mass spectrometry of DENV-2 RNA-interacting proteins reveals that the DEAD-box RNA helicase DDX6 binds the DB1 and DB2 3' UTR structures.

Quantitative mass spectrometry of DENV-2 RNA-interacting proteins reveals that the DEAD-box RNA helicase DDX6 binds the DB1 and DB2 3' UTR structures.

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Identification of RNA Binding Proteins Associated with Dengue Virus RNA in Infected Cells Reveals Temporally Distinct Host Factor Requirements Who Regulates Whom? An Overview of RNA Granules and Viral Infections Functions of the 3' and 5' genome RNA regions of members of the genus Flavivirus Interplay between Inflammation and Cellular Stress Triggered by Flaviviridae Viruses The Golgi associated ERI3 is a Flavivirus host factor Zika virus produces noncoding RNAs using a multi-pseudoknot structure that confounds a cellular exonuclease Use of Cellular Decapping Activators by Positive-Strand RNA Viruses Viral activation of MK2-hsp27-p115RhoGEF-RhoA signaling axis causes cytoskeletal rearrangements, p-body disruption and ARE-mRNA stabilization Zika virus disrupts molecular fingerprinting of human neurospheres IRAV (FLJ11286), an Interferon Stimulated Gene with Antiviral Activity Against Dengue Virus, Interacts with MOV10 Functional Information Stored in the Conserved Structural RNA Domains of Flavivirus Genomes MicroRNA-23b Targets Ras GTPase-Activating Protein SH3 Domain-Binding Protein 2 to Alleviate Fibrosis and Albuminuria in Diabetic Nephropathy Stress granule components G3BP1 and G3BP2 play a proviral role early in Chikungunya virus replication.Identification of Proteins Bound to Dengue Viral RNA In Vivo Reveals New Host Proteins Important for Virus Replication.G3BP1, G3BP2 and CAPRIN1 are required for translation of interferon stimulated mRNAs and are targeted by a dengue virus non-coding RNA.Structured RNAs that evade or confound exonucleases: function follows form.In-Cell Western Assays to Evaluate Hantaan Virus Replication as a Novel Approach to Screen Antiviral Molecules and Detect Neutralizing Antibody Titers.HIV-1 Gag co-opts a cellular complex containing DDX6, a helicase that facilitates capsid assembly How do viruses interact with stress-associated RNA granules?Quantitative interaction screen of telomeric repeat-containing RNA reveals novel TERRA regulators.Flaviviral RNAs: weapons and targets in the war between virus and host.Host cell transcriptome profile during wild-type and attenuated dengue virus infection.Modulation of hepatitis C virus RNA accumulation and translation by DDX6 and miR-122 are mediated by separate mechanisms Dengue virus RNA structure specialization facilitates host adaptation.Overlapping local and long-range RNA-RNA interactions modulate dengue virus genome cyclization and replication Clinical outcome and genetic differences within a monophyletic Dengue virus type 2 population Ribonomic approaches to study the RNA-binding proteome.Dengue subgenomic RNA binds TRIM25 to inhibit interferon expression for epidemiological fitness.Quantitative mass spectrometry and PAR-CLIP to identify RNA-protein interactions.Cleavage and polyadenylation specificity factor 1 (CPSF1) regulates alternative splicing of interleukin 7 receptor (IL7R) exon 6.Modulation of hepatitis C virus RNA abundance and virus release by dispersion of processing bodies and enrichment of stress granules.Japanese encephalitis virus core protein inhibits stress granule formation through an interaction with Caprin-1 and facilitates viral propagation Tissue-specific control of brain-enriched miR-7 biogenesis Diversion of stress granules and P-bodies during viral infection.Structural complexity of Dengue virus untranslated regions: cis-acting RNA motifs and pseudoknot interactions modulating functionality of the viral genome.Regulation of stress granules and P-bodies during RNA virus infection.Cytoplasmic RNA Granules and Viral Infection.A novel coding-region RNA element modulates infectious dengue virus particle production in both mammalian and mosquito cells and regulates viral replication in Aedes aegypti mosquitoes Replacement of conserved or variable sequences of the mosquito-borne dengue virus 3' UTR with homologous sequences from Modoc virus does not change infectivity for mosquitoes Identifying proteins that bind to specific RNAs - focus on simple repeat expansion diseases.

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P2860

Quantitative mass spectrometry of DENV-2 RNA-interacting proteins reveals that the DEAD-box RNA helicase DDX6 binds the DB1 and DB2 3' UTR structures.

http://www.wikidata.org/entity/Q39466005

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2011 nî lūn-bûn

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2011年の論文

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name

Quantitative mass spectrometry ...... DB1 and DB2 3' UTR structures.

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Quantitative mass spectrometry ...... DB1 and DB2 3' UTR structures.

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type

label

Quantitative mass spectrometry ...... DB1 and DB2 3' UTR structures.

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Quantitative mass spectrometry ...... DB1 and DB2 3' UTR structures.

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prefLabel

Quantitative mass spectrometry ...... DB1 and DB2 3' UTR structures.

@en

Quantitative mass spectrometry ...... DB1 and DB2 3' UTR structures.

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Quantitative mass spectrometry ...... DB1 and DB2 3' UTR structures.

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Alex Michael Ward

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Ang Yinglin

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Jayantha Gunaratne

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Katell Bidet

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Kelly Hogue

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

Mariano A Garcia-Blanco

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Siok Ghee Ler

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Walter Blackstock

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P2860

Translation repression in human cells by microRNA-induced gene silencing requires RCK/p54

RNA Secondary Structure in the Coding Region of Dengue Virus Type 2 Directs Translation Start Codon Selection and Is Required for Viral Replication

Control of Translation by the 5'- and 3'-Terminal Regions of the Dengue Virus Genome

A 5' RNA element promotes dengue virus RNA synthesis on a circular genome

Characterization of the interactions between mammalian PAZ PIWI domain proteins and Dicer

Mfold web server for nucleic acid folding and hybridization prediction

A role for eIF4E and eIF4E-transporter in targeting mRNPs to mammalian processing bodies.

Cell proteins TIA-1 and TIAR interact with the 3' stem-loop of the West Nile virus complementary minus-strand RNA and facilitate virus replication.

DDX6 (Rck/p54) is required for efficient hepatitis C virus replication but not for internal ribosome entry site-directed translation

STRING 8--a global view on proteins and their functional interactions in 630 organisms

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10.4161/RNA.8.6.17836

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6

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21957497

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3256426

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