RNA granules: The good, the bad and the ugly

[1]  I. Mackenzie,et al.  ALS‐associated fused in sarcoma (FUS) mutations disrupt Transportin‐mediated nuclear import , 2010, The EMBO journal.

[2]  M. Mishima,et al.  Drosophila PAT1 is required for Kinesin-1 to transport cargo and to maximize its motility , 2010, Development.

[3]  Francesca Tuorto,et al.  RNA methylation by Dnmt2 protects transfer RNAs against stress-induced cleavage. , 2010, Genes & development.

[4]  Huilin Zhou,et al.  ALS-associated mutations in TDP-43 increase its stability and promote TDP-43 complexes with FUS/TLS , 2010, Proceedings of the National Academy of Sciences.

[5]  Richard J Harrison,et al.  Fusel Alcohols Regulate Translation Initiation by Inhibiting eIF2B to Reduce Ternary Complex in a Mechanism That May Involve Altering the Integrity and Dynamics of the eIF2B Body , 2010, Molecular biology of the cell.

[6]  Y. Yoneda,et al.  Identification of importin alpha1 as a novel constituent of RNA stress granules. , 2010, Biochimica et biophysica acta.

[7]  M. Hallak,et al.  The arginylation-dependent association of calreticulin with stress granules is regulated by calcium. , 2010, The Biochemical journal.

[8]  G. Hart,et al.  Site‐specific interplay between O‐GlcNAcylation and phosphorylation in cellular regulation , 2010, FEBS letters.

[9]  A. Bertolin,et al.  Drosophila Genome-Wide RNAi Screen Identifies Multiple Regulators of HIF–Dependent Transcription in Hypoxia , 2010, PLoS genetics.

[10]  S. Goldenberg,et al.  A population of tRNA-derived small RNAs is actively produced in Trypanosoma cruzi and recruited to specific cytoplasmic granules. , 2010, Molecular and biochemical parasitology.

[11]  G. Biamonti,et al.  Nuclear stress bodies. , 2010, Cold Spring Harbor perspectives in biology.

[12]  Roy Parker,et al.  Dcp2 phosphorylation by Ste20 modulates stress granule assembly and mRNA decay in Saccharomyces cerevisiae , 2010, The Journal of cell biology.

[13]  Aaron J. Bell,et al.  Short- and Long-Term Memory Are Modulated by Multiple Isoforms of the Fragile X Mental Retardation Protein , 2010, The Journal of Neuroscience.

[14]  I. Fetka,et al.  The structure of the Myo4p globular tail and its function in ASH1 mRNA localization , 2010, The Journal of cell biology.

[15]  N. Dixon,et al.  The ROQUIN family of proteins localizes to stress granules via the ROQ domain and binds target mRNAs , 2010, The FEBS journal.

[16]  R. Parker,et al.  Localization to, and Effects of Pbp1, Pbp4, Lsm12, Dhh1, and Pab1 on Stress Granules in Saccharomyces cerevisiae , 2010, PloS one.

[17]  S. Ceman,et al.  Arginines of the RGG box regulate FMRP association with polyribosomes and mRNA. , 2010, Human molecular genetics.

[18]  N. Tsai,et al.  RhoA/ROCK1 signaling regulates stress granule formation and apoptosis. , 2010, Cellular signalling.

[19]  P. Ivanov,et al.  eIF5A Promotes Translation Elongation, Polysome Disassembly and Stress Granule Assembly , 2010, PloS one.

[20]  Justin N Vaughn,et al.  The h subunit of eIF3 promotes reinitiation competence during translation of mRNAs harboring upstream open reading frames. , 2010, RNA.

[21]  P. Sarnow,et al.  OGFOD1, a Novel Modulator of Eukaryotic Translation Initiation Factor 2α Phosphorylation and the Cellular Response to Stress , 2010, Molecular and Cellular Biology.

[22]  Eric R. Kandel,et al.  Aplysia CPEB Can Form Prion-like Multimers in Sensory Neurons that Contribute to Long-Term Facilitation , 2010, Cell.

[23]  Pavel Ivanov,et al.  Angiogenin-induced tRNA-derived Stress-induced RNAs Promote Stress-induced Stress Granule Assembly* , 2010, The Journal of Biological Chemistry.

[24]  G. Stoecklin,et al.  On track with P-bodies. , 2010, Biochemical Society transactions.

[25]  Ilan Davis,et al.  Transmitting the message: intracellular mRNA localization. , 2010, Current opinion in cell biology.

[26]  L. Ajamian,et al.  Novel Staufen1 ribonucleoproteins prevent formation of stress granules but favour encapsidation of HIV-1 genomic RNA , 2010, Journal of Cell Science.

[27]  C. Bagni,et al.  Fragile X mental retardation protein control of neuronal mRNA metabolism: Insights into mRNA stability , 2010, Molecular and Cellular Neuroscience.

[28]  A. Aronheim,et al.  A Novel c-Jun N-terminal Kinase (JNK)-binding Protein WDR62 Is Recruited to Stress Granules and Mediates a Nonclassical JNK Activation , 2010, Molecular biology of the cell.

[29]  R. Parker,et al.  Eukaryotic stress granules: the ins and outs of translation. , 2009, Molecular cell.

[30]  Joerg E Braun,et al.  DCP1 forms asymmetric trimers to assemble into active mRNA decapping complexes in metazoa , 2009, Proceedings of the National Academy of Sciences.

[31]  C. Holt,et al.  Subcellular mRNA Localization in Animal Cells and Why It Matters , 2009, Science.

[32]  D. Ito,et al.  Characterization of Alternative Isoforms and Inclusion Body of the TAR DNA-binding Protein-43* , 2009, The Journal of Biological Chemistry.

[33]  Mariela Loschi,et al.  Dynein and kinesin regulate stress-granule and P-body dynamics , 2009, Journal of Cell Science.

[34]  E. Buratti,et al.  TDP‐43 is recruited to stress granules in conditions of oxidative insult , 2009, Journal of neurochemistry.

[35]  Y. Yoneda,et al.  Microscopic dissection of the process of stress granule assembly. , 2009, Biochimica et biophysica acta.

[36]  J. Hoeijmakers,et al.  MicroRNA responses and stress granule formation modulate the DNA damage response , 2009, Cell cycle.

[37]  Yuyu Song,et al.  Axonal Transport Defects in Neurodegenerative Diseases , 2009, The Journal of Neuroscience.

[38]  P. Silver,et al.  Metazoan stress granule assembly is mediated by P-eIF2alpha-dependent and -independent mechanisms. , 2009, RNA.

[39]  W. Tarn,et al.  A role for transportin in deposition of TTP to cytoplasmic RNA granules and , 2009 .

[40]  Q. Qin,et al.  Mammalian Orthoreovirus Particles Induce and Are Recruited into Stress Granules at Early Times Postinfection , 2009, Journal of Virology.

[41]  J. Weissman,et al.  Regulated Ire1-dependent decay of messenger RNAs in mammalian cells , 2009, The Journal of cell biology.

[42]  E. Izaurralde,et al.  The GW182 protein family in animal cells: new insights into domains required for miRNA-mediated gene silencing. , 2009, RNA.

[43]  Andrew D. Ellington,et al.  Widespread reorganization of metabolic enzymes into reversible assemblies upon nutrient starvation , 2009, Proceedings of the National Academy of Sciences.

[44]  Masayuki Nashimoto,et al.  Modulation of Gene Expression by Human Cytosolic tRNase ZL through 5′-Half-tRNA , 2009, PloS one.

[45]  P. Ivanov,et al.  Robust heat shock induces eIF2α-phosphorylation-independent assembly of stress granules containing eIF3 and 40S ribosomal subunits in budding yeast, Saccharomyces cerevisiae , 2009, Journal of Cell Science.

[46]  Jerry Pelletier,et al.  Uncoupling stress granule assembly and translation initiation inhibition. , 2009, Molecular biology of the cell.

[47]  R. Parker,et al.  The RNase Rny1p cleaves tRNAs and promotes cell death during oxidative stress in Saccharomyces cerevisiae , 2009, The Journal of cell biology.

[48]  S. Yamasaki,et al.  Angiogenin cleaves tRNA and promotes stress-induced translational repression , 2009, The Journal of cell biology.

[49]  Diego Peretti,et al.  KIF4 Mediates Anterograde Translocation and Positioning of Ribosomal Constituents to Axons* , 2009, Journal of Biological Chemistry.

[50]  E. Izaurralde,et al.  The RRM domain in GW182 proteins contributes to miRNA-mediated gene silencing , 2009, Nucleic acids research.

[51]  N. -P. Tsai,et al.  Dynein motor contributes to stress granule dynamics in primary neurons , 2009, Neuroscience.

[52]  Shoudong Zhang,et al.  The Phloem-Delivered RNA Pool Contains Small Noncoding RNAs and Interferes with Translation1[W][OA] , 2009, Plant Physiology.

[53]  K. Martin,et al.  mRNA Localization: Gene Expression in the Spatial Dimension , 2009, Cell.

[54]  M. A. Desbats,et al.  Mammalian Staufen 1 is recruited to stress granules and impairs their assembly , 2009, Journal of Cell Science.

[55]  M. Molinari,et al.  Dendritic LSm1/CBP80-mRNPs mark the early steps of transport commitment and translational control , 2009, The Journal of cell biology.

[56]  D. Pincus,et al.  Messenger RNA targeting to endoplasmic reticulum stress signalling sites. , 2009, Nature.

[57]  Chao Zhang,et al.  The unfolded protein response signals through high-order assembly of Ire1 , 2009, Nature.

[58]  A. Rishi,et al.  Microtubule-dependent association of AKAP350A and CCAR1 with RNA stress granules. , 2009, Experimental cell research.

[59]  P. Sarnow,et al.  Stable Formation of Compositionally Unique Stress Granules in Virus-Infected Cells , 2009, Journal of Virology.

[60]  Yi Tie,et al.  Stress induces tRNA cleavage by angiogenin in mammalian cells , 2009, FEBS letters.

[61]  N. Sonenberg,et al.  Translational Control of Long-Lasting Synaptic Plasticity and Memory , 2009, Neuron.

[62]  E. Elliott,et al.  Dcp1a phosphorylation along neuronal development and stress , 2009, FEBS letters.

[63]  W. Filipowicz,et al.  Dendrites of Mammalian Neurons Contain Specialized P-Body-Like Structures That Respond to Neuronal Activation , 2008, The Journal of Neuroscience.

[64]  J. Lykke-Andersen,et al.  The control of mRNA decapping and P-body formation. , 2008, Molecular cell.

[65]  R. Wek,et al.  Stress response pathways in protozoan parasites , 2008, Cellular microbiology.

[66]  Florence Besse,et al.  Translational control of localized mRNAs: restricting protein synthesis in space and time , 2008, Nature Reviews Molecular Cell Biology.

[67]  Roy Parker,et al.  P bodies promote stress granule assembly in Saccharomyces cerevisiae , 2008, The Journal of cell biology.

[68]  A. Aguilera,et al.  A novel class of mRNA-containing cytoplasmic granules are produced in response to UV-irradiation. , 2008, Molecular biology of the cell.

[69]  T. Abel,et al.  A loss of function allele for murine Staufen1 leads to impairment of dendritic Staufen1-RNP delivery and dendritic spine morphogenesis , 2008, Proceedings of the National Academy of Sciences.

[70]  Xinfu Jiao,et al.  Drosophila processing bodies in oogenesis. , 2008, Developmental biology.

[71]  H. Saito,et al.  Formation of stress granules inhibits apoptosis by suppressing stress-responsive MAPK pathways , 2008, Nature Cell Biology.

[72]  Robert H Singer,et al.  The dynamics of mammalian P body transport, assembly, and disassembly in vivo. , 2008, Molecular biology of the cell.

[73]  M. Jinek,et al.  The C-terminal region of Ge-1 presents conserved structural features required for P-body localization. , 2008, RNA.

[74]  Pamela J Green,et al.  tRNA cleavage is a conserved response to oxidative stress in eukaryotes. , 2008, RNA.

[75]  D. Weil,et al.  Translationally repressed mRNA transiently cycles through stress granules during stress. , 2008, Molecular biology of the cell.

[76]  Hui Zhou,et al.  Stress-induced tRNA-derived RNAs: a novel class of small RNAs in the primitive eukaryote Giardia lamblia , 2008, Nucleic acids research.

[77]  J. Hoheisel,et al.  Heat shock causes a decrease in polysomes and the appearance of stress granules in trypanosomes independently of eIF2α phosphorylation at Thr169 , 2008, Journal of Cell Science.

[78]  Sarah Tisdale,et al.  A functional RNAi screen links O-GlcNAc modification of ribosomal proteins to stress granule and processing body assembly , 2008, Nature Cell Biology.

[79]  J. Shabanowitz,et al.  Codependent functions of RSK2 and the apoptosis-promoting factor TIA-1 in stress granule assembly and cell survival. , 2008, Molecular cell.

[80]  W. Zerges,et al.  Stress induces the assembly of RNA granules in the chloroplast of Chlamydomonas reinhardtii , 2008, The Journal of cell biology.

[81]  Martin A. M. Reijns,et al.  A role for Q/N-rich aggregation-prone regions in P-body localization , 2008, Journal of Cell Science.

[82]  M. Kiebler,et al.  Dynamic Interaction between P-Bodies and Transport Ribonucleoprotein Particles in Dendrites of Mature Hippocampal Neurons , 2008, The Journal of Neuroscience.

[83]  S. Pestka,et al.  Chaperone Hsp27, a Novel Subunit of AUF1 Protein Complexes, Functions in AU-Rich Element-Mediated mRNA Decay , 2008, Molecular and Cellular Biology.

[84]  Christopher M. Gallo,et al.  Large P body-like RNPs form in C. elegans oocytes in response to arrested ovulation, heat shock, osmotic stress, and anoxia and are regulated by the major sperm protein pathway. , 2008, Developmental biology.

[85]  S. Lindquist,et al.  A yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDP-43 aggregation and cellular toxicity , 2008, Proceedings of the National Academy of Sciences.

[86]  C. Beckham,et al.  P bodies, stress granules, and viral life cycles. , 2008, Cell host & microbe.

[87]  Stephen J Benkovic,et al.  Reversible Compartmentalization of de Novo Purine Biosynthetic Complexes in Living Cells , 2008, Science.

[88]  Peter F. Stadler,et al.  Small ncRNA transcriptome analysis from Aspergillus fumigatus suggests a novel mechanism for regulation of protein synthesis , 2008, Nucleic acids research.

[89]  Ping-Chih Ho,et al.  Regulation of stress granule dynamics by Grb7 and FAK signalling pathway , 2008, The EMBO journal.

[90]  X. Roucou,et al.  Prion protein aggresomes are poly(A)+ ribonucleoprotein complexes that induce a PKR-mediated deficient cell stress response. , 2008, Biochimica et biophysica acta.

[91]  F. Kano,et al.  Identification of PCBP2, a facilitator of IRES-mediated translation, as a novel constituent of stress granules and processing bodies. , 2008, RNA.

[92]  P. Anderson,et al.  Stress granules: the Tao of RNA triage. , 2008, Trends in biochemical sciences.

[93]  Samara L. Reck-Peterson,et al.  Myo2p, a class V myosin in budding yeast, associates with a large ribonucleic acid-protein complex that contains mRNAs and subunits of the RNA-processing body. , 2008, RNA.

[94]  Tobias M. H. Schenk,et al.  Intracellular localization of human Ins(1,3,4,5,6)P5 2-kinase. , 2007, The Biochemical journal.

[95]  P. Matthias,et al.  The deacetylase HDAC6 is a novel critical component of stress granules involved in the stress response. , 2007, Genes & development.

[96]  S. Jang,et al.  Anti‐inflammatory lipid mediator 15d‐PGJ2 inhibits translation through inactivation of eIF4A , 2007, The EMBO journal.

[97]  C. Arias,et al.  Rotavirus Infection Induces the Phosphorylation of eIF2α but Prevents the Formation of Stress Granules , 2007, Journal of Virology.

[98]  R. Lloyd,et al.  Inhibition of cytoplasmic mRNA stress granule formation by a viral proteinase. , 2007, Cell host & microbe.

[99]  R. Parker,et al.  Edc3p and a glutamine/asparagine-rich domain of Lsm4p function in processing body assembly in Saccharomyces cerevisiae , 2007, The Journal of cell biology.

[100]  A. Isaacs,et al.  Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease , 2007, The Journal of cell biology.

[101]  Peer Bork,et al.  Target-specific requirements for enhancers of decapping in miRNA-mediated gene silencing. , 2007, Genes & development.

[102]  S. Campbell,et al.  Stress-dependent relocalization of translationally primed mRNPs to cytoplasmic granules that are kinetically and spatially distinct from P-bodies , 2007, The Journal of cell biology.

[103]  Steffen Schmidt,et al.  A Divergent Sm Fold in EDC3 Proteins Mediates DCP1 Binding and P-Body Targeting , 2007, Molecular and Cellular Biology.

[104]  B. A. Castilho,et al.  Novel Membrane-Bound eIF2α Kinase in the Flagellar Pocket of Trypanosoma brucei , 2007, Eukaryotic Cell.

[105]  H. Le Hir,et al.  The exon-junction-complex-component metastatic lymph node 51 functions in stress-granule assembly , 2007, Journal of Cell Science.

[106]  A. Frasch,et al.  Recruitment of mRNAs to cytoplasmic ribonucleoprotein granules in trypanosomes , 2007, Molecular microbiology.

[107]  Orna Elroy-Stein,et al.  Ribosomal Slowdown Mediates Translational Arrest during Cellular Division , 2007, Molecular and Cellular Biology.

[108]  J. Gall,et al.  U bodies are cytoplasmic structures that contain uridine-rich small nuclear ribonucleoproteins and associate with P bodies , 2007, Proceedings of the National Academy of Sciences.

[109]  R. Kaufman,et al.  Inhibition of the ubiquitin-proteasome system induces stress granule formation. , 2007, Molecular biology of the cell.

[110]  M. Emara,et al.  Interaction of TIA-1/TIAR with West Nile and dengue virus products in infected cells interferes with stress granule formation and processing body assembly , 2007, Proceedings of the National Academy of Sciences.

[111]  J. Rafols,et al.  Convergence of stress granules and protein aggregates in hippocampal cornu ammonis 1 at later reperfusion following global brain ischemia , 2007, Neuroscience.

[112]  R. Parker,et al.  Accumulation of polyadenylated mRNA, Pab1p, eIF4E, and eIF4G with P-bodies in Saccharomyces cerevisiae. , 2007, Molecular biology of the cell.

[113]  M. Raaben,et al.  Mouse hepatitis coronavirus replication induces host translational shutoff and mRNA decay, with concomitant formation of stress granules and processing bodies , 2007, Cellular microbiology.

[114]  K. Nader,et al.  eIF2α Phosphorylation Bidirectionally Regulates the Switch from Short- to Long-Term Synaptic Plasticity and Memory , 2007, Cell.

[115]  Isabelle Behm-Ansmant,et al.  P-Body Formation Is a Consequence, Not the Cause, of RNA-Mediated Gene Silencing , 2007, Molecular and Cellular Biology.

[116]  H. Lehrach,et al.  Ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granules. , 2007, Molecular biology of the cell.

[117]  P. S. Ray,et al.  Macromolecular complexes as depots for releasable regulatory proteins. , 2007, Trends in biochemical sciences.

[118]  J. Lykke-Andersen,et al.  TTP and BRF proteins nucleate processing body formation to silence mRNAs with AU-rich elements. , 2007, Genes & development.

[119]  Jung-Chun Lin,et al.  Cell stress modulates the function of splicing regulatory protein RBM4 in translation control , 2007, Proceedings of the National Academy of Sciences.

[120]  M. David,et al.  Distinct Structural Features ofCaprin-1 Mediate Its Interaction with G3BP-1 and Its Induction of Phosphorylation of Eukaryotic Translation InitiationFactor 2α, Entry to Cytoplasmic Stress Granules, and Selective Interaction with a Subset of mRNAs , 2007, Molecular and Cellular Biology.

[121]  H. Akiyama,et al.  TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. , 2006, Biochemical and biophysical research communications.

[122]  T. Takumi,et al.  Myosin-Va Facilitates the Accumulation of mRNA/Protein Complex in Dendritic Spines , 2006, Current Biology.

[123]  N. Chua,et al.  Arabidopsis DCP2, DCP1, and VARICOSE Form a Decapping Complex Required for Postembryonic Development[W] , 2006, The Plant Cell Online.

[124]  Anthony K. L. Leung,et al.  Quantitative analysis of Argonaute protein reveals microRNA-dependent localization to stress granules , 2006, Proceedings of the National Academy of Sciences.

[125]  Stefan Hüttelmaier,et al.  ZBP1 regulates mRNA stability during cellular stress , 2006, The Journal of cell biology.

[126]  B. Daignan-Fornier,et al.  Actin bodies in yeast quiescent cells: an immediately available actin reserve? , 2006, Molecular biology of the cell.

[127]  Jun O. Liu,et al.  Eukaryotic Initiation Factor 2α-independent Pathway of Stress Granule Induction by the Natural Product Pateamine A* , 2006, Journal of Biological Chemistry.

[128]  Bruce L. Miller,et al.  Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis , 2006, Science.

[129]  E. Schuman,et al.  Dendritic Protein Synthesis, Synaptic Plasticity, and Memory , 2006, Cell.

[130]  J. Pelletier,et al.  Inhibition of ribosome recruitment induces stress granule formation independently of eukaryotic initiation factor 2alpha phosphorylation. , 2006, Molecular biology of the cell.

[131]  N. Kedersha,et al.  Polysome-Bound Endonuclease PMR1 Is Targeted to Stress Granules via Stress-Specific Binding to TIA-1 , 2006, Molecular and Cellular Biology.

[132]  Jonathan S Weissman,et al.  Decay of Endoplasmic Reticulum-Localized mRNAs During the Unfolded Protein Response , 2006, Science.

[133]  O. Steward,et al.  Synaptic Regulation of Translation of Dendritic mRNAs , 2006, The Journal of Neuroscience.

[134]  Ralf Dahm,et al.  Dendritic Localization of the Translational Repressor Pumilio 2 and Its Contribution to Dendritic Stress Granules , 2006, The Journal of Neuroscience.

[135]  W. Filipowicz,et al.  Relief of microRNA-Mediated Translational Repression in Human Cells Subjected to Stress , 2006, Cell.

[136]  C. Bagni,et al.  mRNPs, polysomes or granules: FMRP in neuronal protein synthesis , 2006, Current Opinion in Neurobiology.

[137]  M. Gorospe,et al.  Translational Repression by RNA-Binding Protein TIAR , 2006, Molecular and Cellular Biology.

[138]  S. Campbell,et al.  Localization of the Translational Guanine Nucleotide Exchange Factor eIF2B: A Common Theme for GEFs? , 2006, Cell cycle.

[139]  M. Katze,et al.  Reovirus Induces and Benefits from an Integrated Cellular Stress Response , 2006, Journal of Virology.

[140]  T. Anthony,et al.  Coping with stress: eIF2 kinases and translational control. , 2006, Biochemical Society transactions.

[141]  J. Rafols,et al.  Prolonged translation arrest in reperfused hippocampal cornu Ammonis 1 is mediated by stress granules , 2005, Neuroscience.

[142]  K. Collins,et al.  Starvation-induced Cleavage of the tRNA Anticodon Loop in Tetrahymena thermophila* , 2005, Journal of Biological Chemistry.

[143]  G. Boccaccio,et al.  Mammalian Smaug Is a Translational Repressor That Forms Cytoplasmic Foci Similar to Stress Granules* , 2005, Journal of Biological Chemistry.

[144]  J. Lykke-Andersen,et al.  Multiple processing body factors and the ARE binding protein TTP activate mRNA decapping. , 2005, Molecular cell.

[145]  J. Alwine,et al.  Production of Infectious Human Cytomegalovirus Virions Is Inhibited by Drugs That Disrupt Calcium Homeostasis in the Endoplasmic Reticulum , 2005, Journal of Virology.

[146]  K. Bloch,et al.  Ge-1 is a central component of the mammalian cytoplasmic mRNA processing body. , 2005, RNA.

[147]  Geppino Falco,et al.  Identification and Functional Outcome of mRNAs Associated with RNA-Binding Protein TIA-1 , 2005, Molecular and Cellular Biology.

[148]  Roy Parker,et al.  Movement of Eukaryotic mRNAs Between Polysomes and Cytoplasmic Processing Bodies , 2005, Science.

[149]  N. Hoyle,et al.  Dynamic cycling of eIF2 through a large eIF2B-containing cytoplasmic body , 2005, Journal of Cell Biology.

[150]  K. Nader,et al.  Translational control of hippocampal synaptic plasticity and memory by the eIF2α kinase GCN2 , 2005, Nature.

[151]  S. Nakano,et al.  Messenger RNA degradation may be inhibited in sporadic inclusion body myositis , 2005, Neurology.

[152]  P. Anderson,et al.  Importance of eIF2alpha phosphorylation and stress granule assembly in alphavirus translation regulation. , 2005, Molecular biology of the cell.

[153]  Randal J. Kaufman,et al.  Stress granules and processing bodies are dynamically linked sites of mRNP remodeling , 2005, The Journal of cell biology.

[154]  W. Greenough,et al.  From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome , 2005, Nature Reviews Neuroscience.

[155]  Randal J. Kaufman,et al.  Heme-regulated Inhibitor Kinase-mediated Phosphorylation of Eukaryotic Translation Initiation Factor 2 Inhibits Translation, Induces Stress Granule Formation, and Mediates Survival upon Arsenite Exposure* , 2005, Journal of Biological Chemistry.

[156]  N. Sonenberg,et al.  Translational control in stress and apoptosis , 2005, Nature Reviews Molecular Cell Biology.

[157]  R. Parker,et al.  Processing bodies require RNA for assembly and contain nontranslating mRNAs. , 2005, RNA.

[158]  S. Jang,et al.  Sequestration of TRAF2 into Stress Granules Interrupts Tumor Necrosis Factor Signaling under Stress Conditions , 2005, Molecular and Cellular Biology.

[159]  D. Weil,et al.  The translational regulator CPEB1 provides a link between dcp1 bodies and stress granules , 2005, Journal of Cell Science.

[160]  Luc DesGroseillers,et al.  Mammalian Staufen1 Recruits Upf1 to Specific mRNA 3′UTRs so as to Elicit mRNA Decay , 2005, Cell.

[161]  P. Anderson,et al.  Stress granule assembly is mediated by prion-like aggregation of TIA-1. , 2004, Molecular biology of the cell.

[162]  J. Correale,et al.  Staufen recruitment into stress granules does not affect early mRNA transport in oligodendrocytes. , 2004, Molecular biology of the cell.

[163]  E. Chan,et al.  GW182 is critical for the stability of GW bodies expressed during the cell cycle and cell proliferation , 2004, Journal of Cell Science.

[164]  M. Hentze,et al.  Molecular mechanisms of translational control , 2004, Nature Reviews Molecular Cell Biology.

[165]  B. Roizman,et al.  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 RNAs , 2004, Journal of Virology.

[166]  Y. Hua,et al.  Survival motor neuron protein facilitates assembly of stress granules , 2004, FEBS letters.

[167]  B. Semler,et al.  Multimerization of poly(rC) binding protein 2 is required for translation initiation mediated by a viral IRES. , 2004, RNA.

[168]  G. Hart,et al.  O-GlcNAcylation regulates phosphorylation of tau: a mechanism involved in Alzheimer's disease. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[169]  M. Dewhirst,et al.  Radiation activates HIF-1 to regulate vascular radiosensitivity in tumors: role of reoxygenation, free radicals, and stress granules. , 2004, Cancer cell.

[170]  P. Anderson,et al.  MK2‐induced tristetraprolin:14‐3‐3 complexes prevent stress granule association and ARE‐mRNA decay , 2004, The EMBO journal.

[171]  Y. Hua,et al.  Rpp20 interacts with SMN and is re-distributed into SMN granules in response to stress. , 2004, Biochemical and biophysical research communications.

[172]  M. Vigneron,et al.  Stress-induced transcription of satellite III repeats , 2004, The Journal of cell biology.

[173]  E. Kandel,et al.  A Neuronal Isoform of the Aplysia CPEB Has Prion-Like Properties , 2003, Cell.

[174]  É. Khandjian,et al.  Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs. , 2003, Human molecular genetics.

[175]  S. Riva,et al.  Transcriptional activation of a constitutive heterochromatic domain of the human genome in response to heat shock. , 2003, Molecular biology of the cell.

[176]  E. Nadezhdina,et al.  Disruption of microtubules inhibits cytoplasmic ribonucleoprotein stress granule formation. , 2003, Experimental cell research.

[177]  O. Steward,et al.  Compartmentalized Synthesis and Degradation of Proteins in Neurons , 2003, Neuron.

[178]  Jane-Jane Chen,et al.  Autophosphorylation of threonine 485 in the activation loop is essential for attaining eIF2alpha kinase activity of HRI. , 2003, Biochemistry.

[179]  K. Chébli,et al.  The RasGAP-associated endoribonuclease G3BP assembles stress granules , 2003, The Journal of cell biology.

[180]  Ann-Shyn Chiang,et al.  The staufen/pumilio Pathway Is Involved in Drosophila Long-Term Memory , 2003, Current Biology.

[181]  D. Ron,et al.  Mammalian stress granules represent sites of accumulation of stalled translation initiation complexes. , 2003, American journal of physiology. Cell physiology.

[182]  B. Séraphin,et al.  Human Dcp2: a catalytically active mRNA decapping enzyme located in specific cytoplasmic structures , 2002, The EMBO journal.

[183]  R. Lührmann,et al.  The human LSm1-7 proteins colocalize with the mRNA-degrading enzymes Dcp1/2 and Xrnl in distinct cytoplasmic foci. , 2002, RNA.

[184]  É. Khandjian,et al.  Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repression. , 2002, Human molecular genetics.

[185]  O. Steward.  mRNA at Synapses, Synaptic Plasticity, and Memory Consolidation , 2002, Neuron.

[186]  C. Norbury,et al.  Sum1, a component of the fission yeast eIF3 translation initiation complex, is rapidly relocalized during environmental stress and interacts with components of the 26S proteasome. , 2002, Molecular biology of the cell.

[187]  Raymond Kaempfer,et al.  Human Interferon-γ mRNA Autoregulates Its Translation through a Pseudoknot that Activates the Interferon-Inducible Protein Kinase PKR , 2002, Cell.

[188]  S. Riva,et al.  Stress-induced nuclear bodies are sites of accumulation of pre-mRNA processing factors. , 2001, Molecular biology of the cell.

[189]  H. Lehrach,et al.  Accumulation of mutant huntingtin fragments in aggresome-like inclusion bodies as a result of insufficient protein degradation. , 2001, Molecular biology of the cell.

[190]  M. Tohyama,et al.  Activation of Caspase-12, an Endoplastic Reticulum (ER) Resident Caspase, through Tumor Necrosis Factor Receptor-associated Factor 2-dependent Mechanism in Response to the ER Stress* , 2001, The Journal of Biological Chemistry.

[191]  David E. Golan,et al.  Dynamic Shuttling of Tia-1 Accompanies the Recruitment of mRNA to Mammalian Stress Granules , 2000, The Journal of cell biology.

[192]  R. Cuesta,et al.  Chaperone hsp27 inhibits translation during heat shock by binding eIF4G and facilitating dissociation of cap-initiation complexes. , 2000, Genes & development.

[193]  Wei Li,et al.  RNA-Binding Proteins Tia-1 and Tiar Link the Phosphorylation of Eif-2α to the Assembly of Mammalian Stress Granules , 1999, The Journal of cell biology.

[194]  E. Sztul,et al.  Characterization and Dynamics of Aggresome Formation by a Cytosolic Gfp-Chimera✪ , 1999, The Journal of cell biology.

[195]  Phuong B Tran,et al.  Aggregates in neurodegenerative disease: crowds and power? , 1999, Trends in Neurosciences.

[196]  R. M. Marión,et al.  A Human Sequence Homologue of Staufen Is an RNA-Binding Protein That Is Associated with Polysomes and Localizes to the Rough Endoplasmic Reticulum , 1999, Molecular and Cellular Biology.

[197]  M. Kiebler,et al.  The Mammalian Staufen Protein Localizes to the Somatodendritic Domain of Cultured Hippocampal Neurons: Implications for Its Involvement in mRNA Transport , 1999, The Journal of Neuroscience.

[198]  B. Pettmann,et al.  Subcellular distribution of survival motor neuron (SMN) protein: possible involvement in nucleocytoplasmic and dendritic transport , 1999, The European journal of neuroscience.

[199]  R. Kopito,et al.  Aggresomes: A Cellular Response to Misfolded Proteins , 1998, The Journal of cell biology.

[200]  Jean-Marie Buerstedde,et al.  A Mouse Cytoplasmic Exoribonuclease (mXRN1p) with Preference for G4 Tetraplex Substrates , 1997, The Journal of cell biology.

[201]  O. Steward,et al.  mRNA Localization in Neurons: A Multipurpose Mechanism? , 1997, Neuron.

[202]  R. Morimoto,et al.  Activation of Heat Shock Gene Transcription by Heat Shock Factor 1 Involves Oligomerization, Acquisition of DNA-Binding Activity, and Nuclear Localization and Can Occur in the Absence of Stress , 1993, Molecular and cellular biology.

[203]  Y. Lutz,et al.  Rapid effect of heat shock on two heterogeneous nuclear ribonucleoprotein-associated antigens in HeLa cells , 1989, The Journal of cell biology.

[204]  J. Mandel,et al.  Cells lacking the fragile X mental retardation protein (FMRP) have normal RISC activity but exhibit altered stress granule assembly. , 2009, Molecular biology of the cell.

[205]  P. V. John,et al.  ネズミのスタウフェン1に対する機能消失対立遺伝子は,樹状突起のStaufen1‐RNP配送や樹状突起棘の形態形成の障害を誘導する , 2008 .

[206]  C. Press.  Cell host & microbe , 2007 .

[207]  P. Anderson,et al.  Mammalian stress granules and processing bodies. , 2007, Methods in enzymology.

[208]  E. Izaurralde,et al.  P bodies: at the crossroads of post-transcriptional pathways , 2007, Nature Reviews Molecular Cell Biology.

[209]  E. Fisher,et al.  Decapping and Decay of Messenger RNA Occur in Cytoplasmic Processing Bodies , 2003 .

[210]  Wei Li,et al.  Evidence that ternary complex (eIF2-GTP-tRNA(i)(Met))-deficient preinitiation complexes are core constituents of mammalian stress granules. , 2002, Molecular biology of the cell.

[211]  M. Saraste,et al.  FEBS Lett , 2000 .