The RNA-binding protein TIAR is translocated from the nucleus to the cytoplasm during Fas-mediated apoptotic cell death
about
Fas-activated serine/threonine kinase (FAST) phosphorylates TIA-1 during Fas-mediated apoptosisStructure-function analysis of Qk1: a lethal point mutation in mouse quaking prevents homodimerization.Novel DNA-binding properties of the RNA-binding protein TIAR.Sendai virus trailer RNA binds TIAR, a cellular protein involved in virus-induced apoptosisCell proteins TIA-1 and TIAR interact with the 3' stem-loop of the West Nile virus complementary minus-strand RNA and facilitate virus replication.Herpes simplex virus 1 induces cytoplasmic accumulation of TIA-1/TIAR and both synthesis and cytoplasmic accumulation of tristetraprolin, two cellular proteins that bind and destabilize AU-rich RNAsCytotoxicity-dependent APO-1 (Fas/CD95)-associated proteins form a death-inducing signaling complex (DISC) with the receptorU1 snRNP-dependent function of TIAR in the regulation of alternative RNA processing of the human calcitonin/CGRP pre-mRNAFunctions of the 3' and 5' genome RNA regions of members of the genus FlavivirusMutation of Mapped TIA-1/TIAR Binding Sites in the 3' Terminal Stem-Loop of West Nile Virus Minus-Strand RNA in an Infectious Clone Negatively Affects Genomic RNA AmplificationTIA-1 or TIAR is required for DT40 cell viabilityTIA-1 and TIAR activate splicing of alternative exons with weak 5' splice sites followed by a U-rich stretch on their own pre-mRNAsCompetition of PTB with TIA proteins for binding to a U-rich cis-element determines tissue-specific splicing of the myosin phosphatase targeting subunit 1RNA-binding protein TIAR is essential for primordial germ cell developmentThe RNA-binding protein TIA-1 is a novel mammalian splicing regulator acting through intron sequences adjacent to a 5' splice siteRNA-binding proteins TIA-1 and TIAR link the phosphorylation of eIF-2 alpha to the assembly of mammalian stress granulesSequestration of G3BP coupled with efficient translation inhibits stress granules in Semliki Forest virus infectionEvidence that ternary complex (eIF2-GTP-tRNA(i)(Met))-deficient preinitiation complexes are core constituents of mammalian stress granulesiCLIP predicts the dual splicing effects of TIA-RNA interactions.Infectious bronchitis virus 3a protein localizes to a novel domain of the smooth endoplasmic reticulum.Importance of eIF2alpha phosphorylation and stress granule assembly in alphavirus translation regulationIdentification of global gene expression differences between human lens epithelial and cortical fiber cells reveals specific genes and their associated pathways important for specialized lens cell functionsTranslational control of cytochrome c by RNA-binding proteins TIA-1 and HuRStructure, tissue distribution and genomic organization of the murine RRM-type RNA binding proteins TIA-1 and TIAR.Noncovalent functionalization of carbon nanotubes for highly specific electronic biosensors.Polysome-bound endonuclease PMR1 is targeted to stress granules via stress-specific binding to TIA-1.The involvement of mRNA processing factors TIA-1, TIAR, and PABP-1 during mammalian hibernation.Apigenin prevents UVB-induced cyclooxygenase 2 expression: coupled mRNA stabilization and translational inhibition.RBM45 Modulates the Antioxidant Response in Amyotrophic Lateral Sclerosis through Interactions with KEAP1.Immunohistological analysis of immune cells in blistering skin lesions.Design and bioinformatics analysis of genome-wide CLIP experiments.Apoptosis in the trophoblast--role of apoptosis in placental morphogenesis.Proteins phosphorylated during stress-induced apoptosis are common targets for autoantibody production in patients with systemic lupus erythematosus.Association of phosphorylated serine/arginine (SR) splicing factors with the U1-small ribonucleoprotein (snRNP) autoantigen complex accompanies apoptotic cell death.PTB and TIAR binding to insulin mRNA 3'- and 5'UTRs; implications for insulin biosynthesis and messenger stability.p53 and little brother p53/47: linking IRES activities with protein functions.Replication cycle and molecular biology of the West Nile virus.The role of RNA processing in the pathogenesis of motor neuron degeneration.Dissecting functional roles of p53 N-terminal transactivation domains by microarray expression analysis.Targeted Knockdown of RNA-Binding Protein TIAR for Promoting Self-Renewal and Attenuating Differentiation of Mouse Embryonic Stem Cells.
P2860
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P2860
The RNA-binding protein TIAR is translocated from the nucleus to the cytoplasm during Fas-mediated apoptotic cell death
description
1995 nî lūn-bûn
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1995 թուականի Փետրուարին հրատարակուած գիտական յօդուած
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1995 թվականի փետրվարին հրատարակված գիտական հոդված
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1995年の論文
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1995年学术文章
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1995年学术文章
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1995年学术文章
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1995年学术文章
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1995年学术文章
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1995年學術文章
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The RNA-binding protein TIAR i ...... -mediated apoptotic cell death
@ast
The RNA-binding protein TIAR i ...... -mediated apoptotic cell death
@en
The RNA-binding protein TIAR i ...... -mediated apoptotic cell death
@nl
type
label
The RNA-binding protein TIAR i ...... -mediated apoptotic cell death
@ast
The RNA-binding protein TIAR i ...... -mediated apoptotic cell death
@en
The RNA-binding protein TIAR i ...... -mediated apoptotic cell death
@nl
prefLabel
The RNA-binding protein TIAR i ...... -mediated apoptotic cell death
@ast
The RNA-binding protein TIAR i ...... -mediated apoptotic cell death
@en
The RNA-binding protein TIAR i ...... -mediated apoptotic cell death
@nl
P2093
P2860
P3181
P356
P1476
The RNA-binding protein TIAR i ...... -mediated apoptotic cell death
@en
P2093
P2860
P304
P3181
P356
10.1073/PNAS.92.5.1629
P407
P577
1995-02-28T00:00:00Z