review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Georg Stoecklin | Q43093535 |
P2093 | author name string | Nancy Kedersha | |
P2860 | cites work | Human retroviral host restriction factors APOBEC3G and APOBEC3F localize to mRNA processing bodies | Q21090536 |
Multiple processing body factors and the ARE binding protein TTP activate mRNA decapping | Q24299303 | ||
Ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granules | Q24301077 | ||
P-body formation is a consequence, not the cause, of RNA-mediated gene silencing | Q42738042 | ||
Plant stress granules and mRNA processing bodies are distinct from heat stress granules | Q46471562 | ||
Mouse hepatitis coronavirus replication induces host translational shutoff and mRNA decay, with concomitant formation of stress granules and processing bodies | Q57279989 | ||
Evidence for general stabilization of mRNAs in response to UV light | Q78553219 | ||
RNA-associated protein 55 (RAP55) localizes to mRNA processing bodies and stress granules | Q24305036 | ||
GW182 is critical for the stability of GW bodies expressed during the cell cycle and cell proliferation | Q24307714 | ||
ZBP1 regulates mRNA stability during cellular stress | Q24314843 | ||
MK2-induced tristetraprolin:14-3-3 complexes prevent stress granule association and ARE-mRNA decay | Q24316111 | ||
Localization of the developmental timing regulator Lin28 to mRNP complexes, P-bodies and stress granules | Q24317757 | ||
Importin 8 is a gene silencing factor that targets argonaute proteins to distinct mRNAs | Q24321397 | ||
Dynein and kinesin regulate stress-granule and P-body dynamics | Q24329224 | ||
Human Pat1b connects deadenylation with mRNA decapping and controls the assembly of processing bodies | Q24336741 | ||
Mammalian Smaug is a translational repressor that forms cytoplasmic foci similar to stress granules | Q24338191 | ||
A phosphorylated cytoplasmic autoantigen, GW182, associates with a unique population of human mRNAs within novel cytoplasmic speckles | Q24515264 | ||
A role for eIF4E and eIF4E-transporter in targeting mRNPs to mammalian processing bodies | Q24537397 | ||
The human LSm1-7 proteins colocalize with the mRNA-degrading enzymes Dcp1/2 and Xrnl in distinct cytoplasmic foci | Q24540163 | ||
Human Dcp2: a catalytically active mRNA decapping enzyme located in specific cytoplasmic structures | Q24543188 | ||
Stress granule assembly is mediated by prion-like aggregation of TIA-1 | Q24559953 | ||
Cytoplasmic heat shock granules are formed from precursor particles and are associated with a specific set of mRNAs | Q24633797 | ||
A role for the P-body component GW182 in microRNA function | Q24669847 | ||
The RasGAP-associated endoribonuclease G3BP assembles stress granules | Q24671936 | ||
Cytoplasmic foci are sites of mRNA decay in human cells | Q24677437 | ||
Stress granules and processing bodies are dynamically linked sites of mRNP remodeling | Q24678779 | ||
MicroRNA-dependent localization of targeted mRNAs to mammalian P-bodies | Q24681266 | ||
Edc3p and a glutamine/asparagine-rich domain of Lsm4p function in processing body assembly in Saccharomyces cerevisiae | Q27930894 | ||
Decapping and Decay of Messenger RNA Occur in Cytoplasmic Processing Bodies | Q27931286 | ||
Stress-dependent relocalization of translationally primed mRNPs to cytoplasmic granules that are kinetically and spatially distinct from P-bodies | Q27935514 | ||
P bodies promote stress granule assembly in Saccharomyces cerevisiae | Q27937387 | ||
Targeting of aberrant mRNAs to cytoplasmic processing bodies | Q27939158 | ||
Robust heat shock induces eIF2alpha-phosphorylation-independent assembly of stress granules containing eIF3 and 40S ribosomal subunits in budding yeast, Saccharomyces cerevisiae. | Q27940310 | ||
TTP and BRF proteins nucleate processing body formation to silence mRNAs with AU-rich elements | Q28117692 | ||
Analysis of the function, expression, and subcellular distribution of human tristetraprolin | Q28214476 | ||
The translational regulator CPEB1 provides a link between dcp1 bodies and stress granules | Q28236721 | ||
Relief of microRNA-mediated translational repression in human cells subjected to stress | Q28246349 | ||
Argonaute 2/RISC resides in sites of mammalian mRNA decay known as cytoplasmic bodies | Q28252216 | ||
A functional RNAi screen links O-GlcNAc modification of ribosomal proteins to stress granule and processing body assembly | Q28294112 | ||
A mouse cytoplasmic exoribonuclease (mXRN1p) with preference for G4 tetraplex substrates | Q28304600 | ||
Mammalian stress granules represent sites of accumulation of stalled translation initiation complexes | Q28504910 | ||
Deadenylation is prerequisite for P-body formation and mRNA decay in mammalian cells | Q28508125 | ||
Roquin binds inducible costimulator mRNA and effectors of mRNA decay to induce microRNA-independent post-transcriptional repression | Q28512151 | ||
Fragile X mental retardation protein shifts between polyribosomes and stress granules after neuronal injury by arsenite stress or in vivo hippocampal electrode insertion | Q28771391 | ||
Processing bodies require RNA for assembly and contain nontranslating mRNAs | Q29615264 | ||
RNA-binding proteins TIA-1 and TIAR link the phosphorylation of eIF-2 alpha to the assembly of mammalian stress granules | Q29615265 | ||
Translational control in stress and apoptosis | Q29615497 | ||
Evidence that ternary complex (eIF2-GTP-tRNA(i)(Met))-deficient preinitiation complexes are core constituents of mammalian stress granules | Q30014820 | ||
Dynamic shuttling of TIA-1 accompanies the recruitment of mRNA to mammalian stress granules | Q30014821 | ||
Quantitative analysis of Argonaute protein reveals microRNA-dependent localization to stress granules | Q30479192 | ||
The dynamics of mammalian P body transport, assembly, and disassembly in vivo | Q30483777 | ||
Sequestration of TRAF2 into stress granules interrupts tumor necrosis factor signaling under stress conditions | Q33707613 | ||
HuR binding to cytoplasmic mRNA is perturbed by heat shock | Q33895914 | ||
CPEB: a life in translation | Q34003974 | ||
Global analysis of stress-regulated mRNA turnover by using cDNA arrays | Q34075278 | ||
The ROQUIN family of proteins localizes to stress granules via the ROQ domain and binds target mRNAs | Q34111526 | ||
Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repression | Q34157806 | ||
Antiviral protein APOBEC3G localizes to ribonucleoprotein complexes found in P bodies and stress granules | Q34590679 | ||
Identification of PCBP2, a facilitator of IRES-mediated translation, as a novel constituent of stress granules and processing bodies | Q34732992 | ||
Formation of stress granules inhibits apoptosis by suppressing stress-responsive MAPK pathways | Q34845865 | ||
Hsp90 regulates the function of argonaute 2 and its recruitment to stress granules and P-bodies | Q34982175 | ||
Translation-independent inhibition of mRNA deadenylation during stress in Saccharomyces cerevisiae | Q35057506 | ||
Probing the mRNA processing body using protein macroarrays and "autoantigenomics". | Q35752843 | ||
Analysis of P-body assembly in Saccharomyces cerevisiae | Q35810641 | ||
Translationally repressed mRNA transiently cycles through stress granules during stress. | Q36914216 | ||
Cells lacking the fragile X mental retardation protein (FMRP) have normal RISC activity but exhibit altered stress granule assembly | Q37035053 | ||
Regulation of translation by stress granules and processing bodies | Q37726443 | ||
Neural RNA-binding protein Musashi1 inhibits translation initiation by competing with eIF4G for PABP. | Q38517787 | ||
Unravelling the ultrastructure of stress granules and associated P-bodies in human cells. | Q39297506 | ||
Interaction with 14-3-3 adaptors regulates the sorting of hMex-3B RNA-binding protein to distinct classes of RNA granules. | Q39941914 | ||
GW body disassembly triggered by siRNAs independently of their silencing activity. | Q40112935 | ||
AU-rich-element-mediated upregulation of translation by FXR1 and Argonaute 2. | Q40154871 | ||
The anti-HIV-1 editing enzyme APOBEC3G binds HIV-1 RNA and messenger RNAs that shuttle between polysomes and stress granules | Q40247992 | ||
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 197-211 | |
P577 | publication date | 2013-01-01 | |
P1433 | published in | Advances in Experimental Medicine and Biology | Q4686385 |
P1476 | title | Relationship of GW/P-bodies with stress granules | |
P478 | volume | 768 |
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