| scholarly article | Q13442814 |
| P356 | DOI | 10.1128/JVI.02220-10 |
| P8608 | Fatcat ID | release_sgjmslpz6vdpnldpwduszwyq2a |
| P932 | PMC publication ID | 3028890 |
| P698 | PubMed publication ID | 21106737 |
| P5875 | ResearchGate publication ID | 49634968 |
| P2093 | author name string | Eric Jan | |
| Anthony Khong | |||
| P2860 | cites work | A polyadenylate binding protein localized to the granules of cytolytic lymphocytes induces DNA fragmentation in target cells | Q24311760 |
| MK2-induced tristetraprolin:14-3-3 complexes prevent stress granule association and ARE-mRNA decay | Q24316111 | ||
| Dynein and kinesin regulate stress-granule and P-body dynamics | Q24329224 | ||
| A phosphorylated cytoplasmic autoantigen, GW182, associates with a unique population of human mRNAs within novel cytoplasmic speckles | Q24515264 | ||
| A crucial role for GW182 and the DCP1:DCP2 decapping complex in miRNA-mediated gene silencing | Q24537488 | ||
| 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 | Q24538975 | ||
| The human LSm1-7 proteins colocalize with the mRNA-degrading enzymes Dcp1/2 and Xrnl in distinct cytoplasmic foci | Q24540163 | ||
| mRNA degradation by miRNAs and GW182 requires both CCR4:NOT deadenylase and DCP1:DCP2 decapping complexes | Q24554481 | ||
| Stress granule assembly is mediated by prion-like aggregation of TIA-1 | Q24559953 | ||
| A role for the P-body component GW182 in microRNA function | Q24669847 | ||
| The RasGAP-associated endoribonuclease G3BP assembles stress granules | Q24671936 | ||
| Inhibition of ribosome recruitment induces stress granule formation independently of eukaryotic initiation factor 2alpha phosphorylation | Q24674083 | ||
| Stress granules and processing bodies are dynamically linked sites of mRNP remodeling | Q24678779 | ||
| The deacetylase HDAC6 is a novel critical component of stress granules involved in the stress response | Q24680794 | ||
| Gawky is a component of cytoplasmic mRNA processing bodies required for early Drosophila development. | Q24683077 | ||
| Interaction of TIA-1/TIAR with West Nile and dengue virus products in infected cells interferes with stress granule formation and processing body assembly | Q27478442 | ||
| P bodies promote stress granule assembly in Saccharomyces cerevisiae | Q27937387 | ||
| RNA granules: post-transcriptional and epigenetic modulators of gene expression | Q28245899 | ||
| A metagenomic survey of microbes in honey bee colony collapse disorder | Q28247041 | ||
| Multivesicular bodies associate with components of miRNA effector complexes and modulate miRNA activity | Q28255255 | ||
| The RNA silencing endonuclease Argonaute 2 mediates specific antiviral immunity in Drosophila melanogaster | Q28271770 | ||
| P bodies: at the crossroads of post-transcriptional pathways | Q28280058 | ||
| A functional RNAi screen links O-GlcNAc modification of ribosomal proteins to stress granule and processing body assembly | Q28294112 | ||
| Rasputin, more promiscuous than ever: a review of G3BP | Q28298633 | ||
| Mammalian stress granules represent sites of accumulation of stalled translation initiation complexes | Q28504910 | ||
| P bodies and the control of mRNA translation and degradation | Q29547253 | ||
| 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 | ||
| Eukaryotic stress granules: the ins and outs of translation | Q29619569 | ||
| 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 | ||
| Stable formation of compositionally unique stress granules in virus-infected cells. | Q30156978 | ||
| Quantitative analysis of Argonaute protein reveals microRNA-dependent localization to stress granules | Q30479192 | ||
| Cricket paralysis virus antagonizes Argonaute 2 to modulate antiviral defense in Drosophila | Q30556603 | ||
| eIF5A promotes translation elongation, polysome disassembly and stress granule assembly | Q33550797 | ||
| Angiogenin-induced tRNA-derived stress-induced RNAs promote stress-induced stress granule assembly | Q33796328 | ||
| Genome-wide RNAi screen reveals a specific sensitivity of IRES-containing RNA viruses to host translation inhibition | Q33848936 | ||
| Importance of eIF2alpha phosphorylation and stress granule assembly in alphavirus translation regulation | Q33911149 | ||
| Naturally occurring dicistronic cricket paralysis virus RNA is regulated by two internal ribosome entry sites | Q33964548 | ||
| hnRNP A1 relocalization to the stress granules reflects a role in the stress response. | Q34548446 | ||
| 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 | ||
| Translation-independent inhibition of mRNA deadenylation during stress in Saccharomyces cerevisiae | Q35057506 | ||
| Divergent IRES elements in invertebrates | Q36322302 | ||
| Translationally repressed mRNA transiently cycles through stress granules during stress. | Q36914216 | ||
| Suppression of HIV-1 Nef translation by Sam68 mutant-induced stress granules and nef mRNA sequestration | Q37101393 | ||
| P bodies, stress granules, and viral life cycles | Q37136680 | ||
| Uncoupling stress granule assembly and translation initiation inhibition | Q37207715 | ||
| Cellular microRNA and P bodies modulate host-HIV-1 interactions | Q37391014 | ||
| Dicistroviruses | Q37644491 | ||
| Novel Staufen1 ribonucleoproteins prevent formation of stress granules but favour encapsidation of HIV-1 genomic RNA. | Q39755331 | ||
| Metazoan stress granule assembly is mediated by P-eIF2alpha-dependent and -independent mechanisms | Q39815877 | ||
| Rotavirus infection induces the phosphorylation of eIF2alpha but prevents the formation of stress granules | Q40046408 | ||
| Inhibition of cytoplasmic mRNA stress granule formation by a viral proteinase | Q40051185 | ||
| Eukaryotic initiation factor 2alpha-independent pathway of stress granule induction by the natural product pateamine A. | Q40236014 | ||
| The anti-HIV-1 editing enzyme APOBEC3G binds HIV-1 RNA and messenger RNAs that shuttle between polysomes and stress granules | Q40247992 | ||
| Mammalian orthoreovirus particles induce and are recruited into stress granules at early times postinfection | Q41844888 | ||
| Host and viral translational mechanisms during cricket paralysis virus infection | Q41973562 | ||
| Double-stranded RNA is produced by positive-strand RNA viruses and DNA viruses but not in detectable amounts by negative-strand RNA viruses | Q42425012 | ||
| Mammalian Staufen 1 is recruited to stress granules and impairs their assembly | Q42563125 | ||
| GW182 interaction with Argonaute is essential for miRNA-mediated translational repression and mRNA decay | Q46698175 | ||
| Mouse hepatitis coronavirus replication induces host translational shutoff and mRNA decay, with concomitant formation of stress granules and processing bodies | Q57279989 | ||
| P433 | issue | 4 | |
| P304 | page(s) | 1439-1451 | |
| P577 | publication date | 2010-11-24 | |
| P1433 | published in | Journal of Virology | Q1251128 |
| P1476 | title | Modulation of stress granules and P bodies during dicistrovirus infection | |
| P478 | volume | 85 |
| Q42934329 | 1st International Symposium on Stress-associated RNA Granules in Human Disease and Viral Infection |
| Q35901563 | A Polymorphism in the Processing Body Component Ge-1 Controls Resistance to a Naturally Occurring Rhabdovirus in Drosophila |
| Q39319522 | ALS-associated ataxin 2 polyQ expansions enhance stress-induced caspase 3 activation and increase TDP-43 pathological modifications |
| Q26314623 | Alphavirus Infection: Host Cell Shut-Off and Inhibition of Antiviral Responses |
| Q38242934 | Antiviral innate immunity and stress granule responses |
| Q30010040 | Chikungunya virus nsP3 blocks stress granule assembly by recruitment of G3BP into cytoplasmic foci |
| Q36901471 | Cytoplasmic RNA Granules and Viral Infection |
| Q53688283 | Defense Mechanisms against Viral Infection in Drosophila: RNAi and Non-RNAi. |
| Q40399861 | Disruption of Stress Granule Formation by the Multifunctional Cricket Paralysis Virus 1A Protein. |
| Q36727541 | Diversion of stress granules and P-bodies during viral infection |
| Q40107518 | Effects of oxidative and thermal stresses on stress granule formation in human induced pluripotent stem cells. |
| Q34508040 | Genetic interaction of hnRNPA2B1 and DNAJB6 in a Drosophila model of multisystem proteinopathy |
| Q36172058 | Hepatitis C virus infection alters P-body composition but is independent of P-body granules |
| Q42318129 | Hippo signaling promotes JNK-dependent cell migration |
| Q34325495 | How do viruses interact with stress-associated RNA granules? |
| Q52666773 | Inclusion bodies of human parainfluenza virus type 3 inhibit antiviral stress granule formation by shielding viral RNAs. |
| Q36506918 | Induction of stress granule-like structures in vesicular stomatitis virus-infected cells |
| Q34789415 | Mechanism of translation initiation by Dicistroviridae IGR IRESs |
| Q24701749 | Mosquito Rasputin interacts with chikungunya virus nsP3 and determines the infection rate in Aedes albopictus |
| Q92859918 | Mouse Norovirus Infection Arrests Host Cell Translation Uncoupled from the Stress Granule-PKR-eIF2α Axis |
| Q36619471 | Movements of HIV-1 genomic RNA-APOBEC3F complexes and PKR reveal cytoplasmic and nuclear PKR defenses and HIV-1 evasion strategies |
| Q52664442 | Natural Variation in Resistance to Virus Infection in Dipteran Insects. |
| Q37736003 | Porcine Reproductive and Respiratory Syndrome Virus Infection Induces Stress Granule Formation Depending on Protein Kinase R-like Endoplasmic Reticulum Kinase (PERK) in MARC-145 Cells |
| Q30009523 | Production of a dominant-negative fragment due to G3BP1 cleavage contributes to the disruption of mitochondria-associated protective stress granules during CVB3 infection |
| Q36165348 | Rabies Virus Infection Induces the Formation of Stress Granules Closely Connected to the Viral Factories. |
| Q36839842 | Regulation of stress granules and P-bodies during RNA virus infection |
| Q37992291 | Regulation of stress granules in virus systems |
| Q37618198 | Relationships between Stress Granules, Oxidative Stress, and Neurodegenerative Diseases. |
| Q38590100 | Stress Granules and Virus Replication |
| Q35066495 | Therapeutic modulation of eIF2α phosphorylation rescues TDP-43 toxicity in amyotrophic lateral sclerosis disease models |
| Q38064834 | Tinkering with translation: protein synthesis in virus-infected cells |
| Q64247484 | Viral Regulation of RNA Granules in Infected Cells |
| Q33553603 | Viral and Cellular mRNA Translation in Coronavirus-Infected Cells |
| Q38019323 | Viral modulation of stress granules |
| Q37946208 | Viral subversion of the host protein synthesis machinery |
| Q26998819 | Viruses and antiviral immunity in Drosophila |
| Q26700102 | Who Regulates Whom? An Overview of RNA Granules and Viral Infections |
| Q30635379 | YB-1 regulates stress granule formation and tumor progression by translationally activating G3BP1. |
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