scholarly article | Q13442814 |
P356 | DOI | 10.1016/J.CUB.2009.03.013 |
P8608 | Fatcat ID | release_o5vnh2k3qnduvkwi3vb3tqzqmi |
P698 | PubMed publication ID | 19467203 |
P5875 | ResearchGate publication ID | 26238750 |
P2093 | author name string | Nancy Kedersha | |
Paul Anderson | |||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | R397-8 | |
P577 | publication date | 2009-05-01 | |
P1433 | published in | Current Biology | Q1144851 |
P1476 | title | Stress granules | |
P478 | volume | 19 |
Q57929129 | A Review of the Recent Advances Made with SIRT6 and its Implications on Aging Related Processes, Major Human Diseases, and Possible Therapeutic Targets |
Q33745691 | A global profiling of uncapped mRNAs under cold stress reveals specific decay patterns and endonucleolytic cleavages in Brachypodium distachyon |
Q36190490 | A novel origin for granulovacuolar degeneration in aging and Alzheimer's disease: parallels to stress granules |
Q35531069 | A novel role for hSMG-1 in stress granule formation |
Q47647790 | ALS-Related Mutant FUS Protein Is Mislocalized to Cytoplasm and Is Recruited into Stress Granules of Fibroblasts from Asymptomatic FUS P525L Mutation Carriers |
Q28114329 | ATPase activity of the DEAD-box protein Dhh1 controls processing body formation |
Q26753006 | Alphaherpesvirus Subversion of Stress-Induced Translational Arrest |
Q24604643 | Altered ribostasis: RNA-protein granules in degenerative disorders |
Q40054445 | Analysis of the Cellular Stress Response During Ebola Virus Infection by Immunofluorescence |
Q36624735 | Angiogenin Mediates Cell-Autonomous Translational Control under Endoplasmic Reticulum Stress and Attenuates Kidney Injury |
Q33796328 | Angiogenin-induced tRNA-derived stress-induced RNAs promote stress-induced stress granule assembly |
Q41982994 | Angiogenin-mediated rRNA transcription in cancer and neurodegeneration |
Q48094339 | Arabidopsis CML38, a Calcium Sensor That Localizes to Ribonucleoprotein Complexes under Hypoxia Stress |
Q57035312 | Biomolecular Assemblies: Moving from Observation to Predictive Design |
Q34194399 | C. elegans sirtuin SIR-2.4 and its mammalian homolog SIRT6 in stress response |
Q28553977 | Calcineurin Targets Involved in Stress Survival and Fungal Virulence |
Q36431066 | Can we observe changes in mRNA "state"? Overview of methods to study mRNA interactions with regulatory proteins relevant in cancer related processes |
Q92455023 | Cellular stress leads to the formation of membraneless stress assemblies in eukaryotic cells |
Q30010040 | Chikungunya virus nsP3 blocks stress granule assembly by recruitment of G3BP into cytoplasmic foci |
Q37549637 | Chromatin and beyond: the multitasking roles for SIRT6 |
Q92286575 | Clinical Significance of Ubiquitin-associated Protein 2-like in Patients With Uterine Cervical Cancer |
Q30390208 | Combined structural, biochemical and cellular evidence demonstrates that both FGDF motifs in alphavirus nsP3 are required for efficient replication |
Q98627154 | Critical role for G3BP1 in infectious bursal disease virus (IBDV)-induced stress granule formation and viral replication |
Q24337086 | Critical roles of RNA helicase DDX3 and its interactions with eIF4E/PABP1 in stress granule assembly and stress response |
Q51912877 | Different requirements for conserved post-transcriptional regulators in planarian regeneration and stem cell maintenance. |
Q36959103 | Do nucleic acids moonlight as molecular chaperones? |
Q48057821 | Dual functions of the nucleus-encoded factor TDA1 in trapping and translation activation of atpA transcripts in Chlamydomonas reinhardtii chloroplasts |
Q37174456 | Ebola Virus Does Not Induce Stress Granule Formation during Infection and Sequesters Stress Granule Proteins within Viral Inclusions |
Q40107518 | Effects of oxidative and thermal stresses on stress granule formation in human induced pluripotent stem cells. |
Q26827965 | Emerging functions of the unfolded protein response in immunity |
Q36460968 | Emerging roles of interferon-stimulated genes in the innate immune response to hepatitis C virus infection |
Q36412456 | Endogenous TDP-43, but not FUS, contributes to stress granule assembly via G3BP |
Q39638326 | Evidence That G-quadruplex DNA Accumulates in the Cytoplasm and Participates in Stress Granule Assembly in Response to Oxidative Stress. |
Q37531676 | FUS Mislocalization and Vulnerability to DNA Damage in ALS Patients Derived hiPSCs and Aging Motoneurons. |
Q30577079 | FUS/TLS assembles into stress granules and is a prosurvival factor during hyperosmolar stress |
Q39621474 | Formation of antiviral cytoplasmic granules during orthopoxvirus infection |
Q35394777 | G3BP1 promotes stress-induced RNA granule interactions to preserve polyadenylated mRNA. |
Q31104690 | Gene expression responses to FUS, EWS, and TAF15 reduction and stress granule sequestration analyses identifies FET-protein non-redundant functions |
Q38803351 | Granulovacuolar degeneration: a neurodegenerative change that accompanies tau pathology |
Q27932557 | Heat shock-induced accumulation of translation elongation and termination factors precedes assembly of stress granules in S. cerevisiae |
Q30010035 | Hepatitis C virus (HCV) induces formation of stress granules whose proteins regulate HCV RNA replication and virus assembly and egress |
Q35834793 | How do trypanosomes change gene expression in response to the environment? |
Q34533688 | Hsp70 architecture: the formation of novel polymeric structures of Hsp70.1 and Hsc70 after proteotoxic stress. |
Q39330119 | Hydrogen peroxide induces stress granule formation independent of eIF2α phosphorylation |
Q38762159 | Identification of Neuregulin-2 as a novel stress granule component |
Q33623745 | Impaired embryonic development in mice overexpressing the RNA-binding protein TIAR. |
Q37560020 | Inflammation: cytokines and RNA-based regulation |
Q57469914 | Inhibition of Stress Granule Formation by Middle East Respiratory Syndrome Coronavirus 4a Accessory Protein Facilitates Viral Translation, Leading to Efficient Virus Replication |
Q42030945 | Inhibition of autophagy, lysosome and VCP function impairs stress granule assembly |
Q34194441 | Inhibition of eukaryotic translation elongation by the antitumor natural product Mycalamide B. |
Q36348491 | Integrative genomics positions MKRN1 as a novel ribonucleoprotein within the embryonic stem cell gene regulatory network |
Q91440749 | Interplay between potato virus X and RNA granules in Nicotiana benthamiana |
Q30496858 | Intracellular localization and interaction of mRNA binding proteins as detected by FRET |
Q28118644 | La-related Protein 1 (LARP1) Represses Terminal Oligopyrimidine (TOP) mRNA Translation Downstream of mTOR Complex 1 (mTORC1) |
Q38977612 | Long-term memory consolidation: The role of RNA-binding proteins with prion-like domains |
Q28118582 | Mammalian microtubule P-body dynamics are mediated by nesprin-1. |
Q34544246 | Mechanistic insights into mammalian stress granule dynamics. |
Q93016366 | Membrane-Bound Meet Membraneless in Health and Disease |
Q64230213 | Metazoan tsRNAs: Biogenesis, Evolution and Regulatory Functions |
Q38432162 | Methods for the characterization of stress granules in virus infected cells |
Q28750201 | Microvesicles derived from adult human bone marrow and tissue specific mesenchymal stem cells shuttle selected pattern of miRNAs |
Q36501665 | Modulation of hepatitis C virus RNA abundance and virus release by dispersion of processing bodies and enrichment of stress granules |
Q52316968 | Modulation of the secretory pathway by amino-acid starvation. |
Q64263070 | Molecular Mechanisms of TDP-43 Misfolding and Pathology in Amyotrophic Lateral Sclerosis |
Q39106402 | Multiple mechanisms repress N-Bak mRNA translation in the healthy and apoptotic neurons |
Q30499108 | Myosin Va is required for P body but not stress granule formation |
Q38222192 | Nervous translation, do you get the message? A review of mRNPs, mRNA-protein interactions and translational control within cells of the nervous system |
Q38225814 | Nucleoli and stress granules: connecting distant relatives. |
Q38700722 | Old versus New Mechanisms in the Pathogenesis of ALS. |
Q38191702 | Oxidative stress response pathways: Fission yeast as archetype |
Q36084461 | Pdcd4 Is Involved in the Formation of Stress Granule in Response to Oxidized Low-Density Lipoprotein or High-Fat Diet. |
Q64067598 | Pharmacological systems analysis defines EIF4A3 functions in cell-cycle and RNA stress granule formation |
Q28588090 | Phase separation by low complexity domains promotes stress granule assembly and drives pathological fibrillization |
Q96230238 | Phosphorylation of eukaryotic initiation factor-2α (eIF2α) in autophagy |
Q38286581 | Poliovirus switches to an eIF2-independent mode of translation during infection |
Q38238685 | PolyQ-mediated regulation of mRNA granules assembly |
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 |
Q48465245 | Preferential binding of a stable G3BP ribonucleoprotein complex to intron-retaining transcripts in mouse brain and modulation of their expression in the cerebellum |
Q35838747 | Probes for intracellular RNA imaging in live cells |
Q41655789 | Protease 2A induces stress granule formation during coxsackievirus B3 and enterovirus 71 infections |
Q51421031 | Protein clustering in chemically stressed HeLa cells studied by infrared nanospectroscopy. |
Q27674307 | Pub1p C-Terminal RRM Domain Interacts with Tif4631p through a Conserved Region Neighbouring the Pab1p Binding Site |
Q64072874 | RNA as a key factor in driving or preventing self-assembly of the TAR DNA-binding protein 43 |
Q38238681 | RNA granules and cytoskeletal links. |
Q34835670 | RNA recognition and stress granule formation by TIA proteins |
Q42956867 | RNAs as chaperones |
Q36165348 | Rabies Virus Infection Induces the Formation of Stress Granules Closely Connected to the Viral Factories. |
Q64084547 | Rbfox2 dissociation from stress granules suppresses cancer progression |
Q39240888 | Reduction of polyglutamine toxicity by TDP-43, FUS and progranulin in Huntington's disease models. |
Q54551156 | Reversible translocation of ASK1 to a Triton-X100 insoluble cytoplasmic compartment during cardiac myocyte cell stress. |
Q34356753 | Ribonuclease/angiogenin inhibitor 1 regulates stress-induced subcellular localization of angiogenin to control growth and survival |
Q34140237 | Role of the RNA-binding protein Nrd1 in stress granule formation and its implication in the stress response in fission yeast |
Q34271670 | Roles of the respiratory syncytial virus trailer region: effects of mutations on genome production and stress granule formation |
Q106464739 | SARS-CoV-2 nucleocapsid protein phase separates with G3BPs to disassemble stress granules and facilitate viral production |
Q30009987 | Sequestration of G3BP coupled with efficient translation inhibits stress granules in Semliki Forest virus infection |
Q27318590 | Spatio-temporal Dynamics and Mechanisms of Stress Granule Assembly |
Q51758735 | Stress granules counteract senescence by sequestration of PAI-1. |
Q38099065 | Stress granules in neurodegeneration--lessons learnt from TAR DNA binding protein of 43 kDa and fused in sarcoma |
Q35689148 | Stress granules, P-bodies and cancer. |
Q39328150 | Stress out the LINEs |
Q40839064 | Subtilase cytotoxin produced by locus of enterocyte effacement-negative Shiga-toxigenic Escherichia coli induces stress granule formation |
Q42229837 | Sumoylation of eIF4A2 affects stress granule formation. |
Q34430583 | Suppression of Her2/neu expression through ILK inhibition is regulated by a pathway involving TWIST and YB-1 |
Q57083958 | Systemic control of protein synthesis through sequestration of translation and ribosome biogenesis factors during severe heat stress |
Q27332459 | TDP-1/TDP-43 regulates stress signaling and age-dependent proteotoxicity in Caenorhabditis elegans |
Q34155890 | TDP-43 is directed to stress granules by sorbitol, a novel physiological osmotic and oxidative stressor |
Q64229631 | TDP-43 proteinopathy in Theiler's murine encephalomyelitis virus infection |
Q53818684 | TDP-43 regulation of stress granule dynamics in neurodegenerative disease-relevant cell types. |
Q39047518 | TIA-1 Is a Functional Prion-Like Protein. |
Q91775774 | The Leader Protein of Theiler's Virus Prevents the Activation of PKR |
Q46302852 | The Physiological and Pathological Implications of the Formation of Hydrogels, with a Specific Focus on Amyloid Polypeptides |
Q33700385 | The QKI-6 RNA Binding Protein Localizes with the MBP mRNAs in Stress Granules of Glial Cells |
Q41568959 | The helicase, DDX3X, interacts with poly(A)-binding protein 1 (PABP1) and caprin-1 at the leading edge of migrating fibroblasts and is required for efficient cell spreading |
Q35192670 | The leader protein of cardioviruses inhibits stress granule assembly. |
Q41900852 | The mRNAs associated to a zinc finger protein from Trypanosoma cruzi shift during stress conditions. |
Q42065558 | The role of molecular microtubule motors and the microtubule cytoskeleton in stress granule dynamics |
Q39332333 | The translation inhibitor pateamine A prevents cachexia-induced muscle wasting in mice |
Q47952877 | The wisdom of crowds: regulating cell function through condensed states of living matter. |
Q53659772 | Transfer RNA fragmentation and protein translation dynamics in the course of kidney injury. |
Q36606866 | Translational control in Plasmodium and toxoplasma parasites |
Q35393305 | Translational coregulation of 5'TOP mRNAs by TIA-1 and TIAR. |
Q37940420 | Turnover of AU-rich-containing mRNAs during stress: a matter of survival. |
Q64356590 | UBAP2L arginine methylation by PRMT1 modulates stress granule assembly |
Q37327483 | Vinca alkaloid drugs promote stress-induced translational repression and stress granule formation |
Q38019323 | Viral modulation of stress granules |
Q26700102 | Who Regulates Whom? An Overview of RNA Granules and Viral Infections |
Q37210975 | YB-1 regulates tiRNA-induced Stress Granule formation but not translational repression |
Q37396140 | mRNA redistribution during permanent focal cerebral ischemia |
Q26824181 | tRNA fragments in human health and disease |
Q125199561 | mRNAs sequestered in stress granules recover nearly completely for translation | main subject | P921 |
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