| scholarly article | Q13442814 |
| P2093 | author name string | Paul J Anderson | |
| Marta M Fay | |||
| P2860 | cites work | The Nuclear-Retained Noncoding RNA MALAT1 Regulates Alternative Splicing by Modulating SR Splicing Factor Phosphorylation | Q24297656 |
| An architectural role for a nuclear noncoding RNA: NEAT1 RNA is essential for the structure of paraspeckles | Q24310786 | ||
| ZBP1 regulates mRNA stability during cellular stress | Q24314843 | ||
| MK2-induced tristetraprolin:14-3-3 complexes prevent stress granule association and ARE-mRNA decay | Q24316111 | ||
| A novel phosphorylation-dependent RNase activity of GAP-SH3 binding protein: a potential link between signal transduction and RNA stability | Q24522539 | ||
| 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 | ||
| Direct visualization of the co-transcriptional assembly of a nuclear body by noncoding RNAs | Q24623900 | ||
| Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS | Q24633692 | ||
| A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD | Q24634583 | ||
| MENepsilon/beta noncoding RNAs are essential for structural integrity of nuclear paraspeckles | Q24646100 | ||
| Altered nuclear retention of mRNAs containing inverted repeats in human embryonic stem cells: functional role of a nuclear noncoding RNA | Q24648896 | ||
| Assembly of snRNP-containing coiled bodies is regulated in interphase and mitosis--evidence that the coiled body is a kinetic nuclear structure | Q24651270 | ||
| The histidyl-tRNA synthetase-related sequence in the eIF-2 alpha protein kinase GCN2 interacts with tRNA and is required for activation in response to starvation for different amino acids | Q24651464 | ||
| MEN epsilon/beta nuclear-retained non-coding RNAs are up-regulated upon muscle differentiation and are essential components of paraspeckles | Q24651886 | ||
| Stress granules and processing bodies are dynamically linked sites of mRNP remodeling | Q24678779 | ||
| G3BP-Caprin1-USP10 complexes mediate stress granule condensation and associate with 40S subunits | Q27309029 | ||
| Characterizing mRNA interactions with RNA granules during translation initiation inhibition | Q27342467 | ||
| Lysine acetylation targets protein complexes and co-regulates major cellular functions | Q27860589 | ||
| Edc3p and a glutamine/asparagine-rich domain of Lsm4p function in processing body assembly in Saccharomyces cerevisiae | Q27930894 | ||
| ATPase-Modulated Stress Granules Contain a Diverse Proteome and Substructure. | Q27936710 | ||
| Phase separation in biology; functional organization of a higher order | Q28071484 | ||
| Regulation of translation initiation in eukaryotes: mechanisms and biological targets | Q28111696 | ||
| The structure of human SFPQ reveals a coiled-coil mediated polymer essential for functional aggregation in gene regulation | Q28118784 | ||
| Context-Dependent and Disease-Specific Diversity in Protein Interactions within Stress Granules | Q49649749 | ||
| Intrinsically Disordered Regions Can Contribute Promiscuous Interactions to RNP Granule Assembly | Q50098070 | ||
| High-Density Proximity Mapping Reveals the Subcellular Organization of mRNA-Associated Granules and Bodies. | Q50209860 | ||
| Stress-Triggered Phase Separation Is an Adaptive, Evolutionarily Tuned Response. | Q50963829 | ||
| The coilin interactome identifies hundreds of small noncoding RNAs that traffic through Cajal bodies. | Q51502949 | ||
| RNA catalysis through compartmentalization. | Q53356383 | ||
| A Liquid-to-Solid Phase Transition of the ALS Protein FUS Accelerated by Disease Mutation. | Q53368534 | ||
| Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy | Q55670526 | ||
| RNA self-assembly contributes to stress granule formation and defining the stress granule transcriptome | Q60017421 | ||
| Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member | Q68100373 | ||
| Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat | Q74281230 | ||
| De novo formation of a subnuclear body | Q79696419 | ||
| Phase Transitions in the Assembly and Function of Human miRISC | Q88167003 | ||
| Vinca alkaloid drugs promote stress-induced translational repression and stress granule formation | Q37327483 | ||
| RNA Controls PolyQ Protein Phase Transitions. | Q37573060 | ||
| Repeat expansion disease: progress and puzzles in disease pathogenesis | Q37696972 | ||
| Structural Characteristics of Simple RNA Repeats Associated with Disease and their Deleterious Protein Interactions | Q37747172 | ||
| Perk is essential for translational regulation and cell survival during the unfolded protein response | Q28140062 | ||
| Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9 | Q28210917 | ||
| The fate of dsRNA in the nucleus: a p54(nrb)-containing complex mediates the nuclear retention of promiscuously A-to-I edited RNAs | Q28214585 | ||
| Stress granules: sites of mRNA triage that regulate mRNA stability and translatability | Q28215404 | ||
| The translational regulator CPEB1 provides a link between dcp1 bodies and stress granules | Q28236721 | ||
| Identifying and quantifying in vivo methylation sites by heavy methyl SILAC | Q28241075 | ||
| A proteome-wide, quantitative survey of in vivo ubiquitylation sites reveals widespread regulatory roles | Q28247080 | ||
| Movement of eukaryotic mRNAs between polysomes and cytoplasmic processing bodies | Q28270553 | ||
| Regulating gene expression through RNA nuclear retention | Q28278213 | ||
| A functional RNAi screen links O-GlcNAc modification of ribosomal proteins to stress granule and processing body assembly | Q28294112 | ||
| Heme-regulated inhibitor kinase-mediated phosphorylation of eukaryotic translation initiation factor 2 inhibits translation, induces stress granule formation, and mediates survival upon arsenite exposure | Q28305175 | ||
| Phase separation by low complexity domains promotes stress granule assembly and drives pathological fibrillization | Q28588090 | ||
| Paraspeckles are subpopulation-specific nuclear bodies that are not essential in mice | Q28591342 | ||
| A muscleblind knockout model for myotonic dystrophy | Q28592365 | ||
| The regulated retrotransposon transcriptome of mammalian cells | Q29614444 | ||
| Cell-free formation of RNA granules: low complexity sequence domains form dynamic fibers within hydrogels | Q29614781 | ||
| 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 | ||
| Protein arginine methylation in mammals: who, what, and why | Q29617309 | ||
| Eukaryotic stress granules: the ins and outs of translation | Q29619569 | ||
| Arginine Demethylation of G3BP1 Promotes Stress Granule Assembly | Q30008866 | ||
| Viral and cellular proteins containing FGDF motifs bind G3BP to block stress granule formation | Q30009233 | ||
| Both G3BP1 and G3BP2 contribute to stress granule formation | Q30009952 | ||
| Quantitative proteomics and dynamic imaging reveal that G3BP-mediated stress granule assembly is poly(ADP-ribose)-dependent following exposure to MNNG-induced DNA alkylation | Q30010053 | ||
| 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 | ||
| RNA phase transitions in repeat expansion disorders | Q30224330 | ||
| Polar Positioning of Phase-Separated Liquid Compartments in Cells Regulated by an mRNA Competition Mechanism. | Q30313887 | ||
| RNA seeds higher-order assembly of FUS protein | Q30457170 | ||
| Nucleic acid-binding specificity of human FUS protein | Q30459673 | ||
| G-quadruplex RNA structure as a signal for neurite mRNA targeting | Q30502060 | ||
| Phosphorylation-regulated binding of RNA polymerase II to fibrous polymers of low-complexity domains | Q30577537 | ||
| Liquid demixing of intrinsically disordered proteins is seeded by poly(ADP-ribose). | Q30663823 | ||
| Cloning of the essential myotonic dystrophy region and mapping of the putative defect | Q30985550 | ||
| Targeting vertebrate intron-encoded box C/D 2'-O-methylation guide RNAs into the Cajal body. | Q33698657 | ||
| C9orf72 nucleotide repeat structures initiate molecular cascades of disease. | Q33715387 | ||
| The amyloid state of proteins in human diseases | Q37994283 | ||
| Cajal bodies: where form meets function | Q38050096 | ||
| Protein arginine methyltransferases and cancer | Q38067063 | ||
| Unusual biophysics of intrinsically disordered proteins | Q38069936 | ||
| Stress granules and cell signaling: more than just a passing phase? | Q38136844 | ||
| Liquid-liquid phase separation in biology | Q38257388 | ||
| TDP-43 and FUS RNA-binding proteins bind distinct sets of cytoplasmic messenger RNAs and differently regulate their post-transcriptional fate in motoneuron-like cells. | Q38326803 | ||
| Stress-specific differences in assembly and composition of stress granules and related foci | Q38720884 | ||
| Protein methylation and stress granules: posttranslational remodeler or innocent bystander? | Q38755430 | ||
| Unusual semi-extractability as a hallmark of nuclear body-associated architectural noncoding RNAs | Q38839533 | ||
| Quantifying mRNA targeting to P-bodies in living human cells reveals their dual role in mRNA decay and storage | Q38965527 | ||
| Phosphorothioate oligonucleotides can displace NEAT1 RNA and form nuclear paraspeckle-like structures | Q38976436 | ||
| c9orf72 Disease-Related Foci Are Each Composed of One Mutant Expanded Repeat RNA. | Q38993039 | ||
| Biomolecular condensates: organizers of cellular biochemistry | Q39146409 | ||
| Poly(ADP-ribose) regulates stress responses and microRNA activity in the cytoplasm. | Q39265687 | ||
| Unravelling the ultrastructure of stress granules and associated P-bodies in human cells. | Q39297506 | ||
| Cell-free formation of RNA granules: bound RNAs identify features and components of cellular assemblies. | Q39349822 | ||
| The C9ORF72 GGGGCC expansion forms RNA G-quadruplex inclusions and sequesters hnRNP H to disrupt splicing in ALS brains. | Q39396328 | ||
| Alu element-mediated gene silencing | Q39408863 | ||
| Characterization and prediction of protein nucleolar localization sequences. | Q39675144 | ||
| mRNA escape from stress granule sequestration is dictated by localization to the endoplasmic reticulum | Q39706103 | ||
| A common sequence motif determines the Cajal body-specific localization of box H/ACA scaRNAs. | Q39831945 | ||
| A conserved charged single α-helix with a putative steric role in paraspeckle formation. | Q40475971 | ||
| Poly(ADP-ribose): an organizer of cellular architecture | Q40485657 | ||
| Phase transition of a disordered nuage protein generates environmentally responsive membraneless organelles | Q41277254 | ||
| Nuclear speckles: molecular organization, biological function and role in disease | Q41924562 | ||
| Granules harboring translationally active mRNAs provide a platform for P-body formation following stress. | Q42115920 | ||
| Transcription-dependent colocalization of the U1, U2, U4/U6, and U5 snRNPs in coiled bodies | Q42119478 | ||
| Promiscuous interactions and protein disaggregases determine the material state of stress-inducible RNP granules | Q42208957 | ||
| Adaptation to Stressors by Systemic Protein Amyloidogenesis. | Q42373056 | ||
| C9orf72 hexanucleotide repeat associated with amyotrophic lateral sclerosis and frontotemporal dementia forms RNA G-quadruplexes | Q42424866 | ||
| Identification of functional tetramolecular RNA G-quadruplexes derived from transfer RNAs. | Q42636887 | ||
| P-body formation is a consequence, not the cause, of RNA-mediated gene silencing | Q42738042 | ||
| Phosphorylation of eukaryotic translation initiation factor 2 mediates apoptosis in response to activation of the double-stranded RNA-dependent protein kinase | Q42833009 | ||
| The long noncoding RNA Neat1 is required for mammary gland development and lactation. | Q43015249 | ||
| An improved MS2 system for accurate reporting of the mRNA life cycle | Q45072785 | ||
| Coilin-dependent snRNP assembly is essential for zebrafish embryogenesis | Q47073237 | ||
| Paraspeckles: Where Long Noncoding RNA Meets Phase Separation. | Q47242675 | ||
| ALS/FTD-Associated C9ORF72 Repeat RNA Promotes Phase Transitions In Vitro and in Cells | Q47270745 | ||
| Quantitative analysis of multilayer organization of proteins and RNA in nuclear speckles at super resolution. | Q47352667 | ||
| The Stress Granule Transcriptome Reveals Principles of mRNA Accumulation in Stress Granules | Q47411868 | ||
| P-Body Purification Reveals the Condensation of Repressed mRNA Regulons | Q47665335 | ||
| Nanoscale Analysis Reveals the Maturation of Neurodegeneration-Associated Protein Aggregates: Grown in mRNA Granules then Released by Stress Granule Proteins | Q48058822 | ||
| p21(WAF1/CIP1) upregulation through the stress granule-associated protein CUGBP1 confers resistance to bortezomib-mediated apoptosis | Q33921377 | ||
| Free mRNA in excess upon polysome dissociation is a scaffold for protein multimerization to form stress granules | Q33983718 | ||
| Cajal bodies: the first 100 years | Q34059715 | ||
| Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2. | Q34094021 | ||
| Angiogenin-induced tRNA fragments inhibit translation initiation | Q34209434 | ||
| Highly ordered spatial organization of the structural long noncoding NEAT1 RNAs within paraspeckle nuclear bodies | Q34313582 | ||
| Discovery of a biomarker and lead small molecules to target r(GGGGCC)-associated defects in c9FTD/ALS. | Q34512451 | ||
| Coexisting Liquid Phases Underlie Nucleolar Subcompartments | Q34527840 | ||
| Mechanistic insights into mammalian stress granule dynamics. | Q34544246 | ||
| Programmable RNA Tracking in Live Cells with CRISPR/Cas9. | Q34676404 | ||
| Active liquid-like behavior of nucleoli determines their size and shape in Xenopus laevis oocytes | Q34694194 | ||
| NOPdb: Nucleolar Proteome Database--2008 update | Q34872544 | ||
| Relationship of GW/P-bodies with stress granules. | Q35049975 | ||
| Compromised paraspeckle formation as a pathogenic factor in FUSopathies | Q35066217 | ||
| An overview of pre-ribosomal RNA processing in eukaryotes | Q35180630 | ||
| P-body assembly requires DDX6 repression complexes rather than decay or Ataxin2/2L complexes | Q35849087 | ||
| ALS-Causing Mutations Significantly Perturb the Self-Assembly and Interaction with Nucleic Acid of the Intrinsically Disordered Prion-Like Domain of TDP-43. | Q35886826 | ||
| Modified deoxyoligonucleotides stable to exonuclease degradation in serum | Q35913882 | ||
| Phase transitions in the assembly of multivalent signalling proteins | Q35932499 | ||
| Prion-like domains in RNA binding proteins are essential for building subnuclear paraspeckles | Q35965458 | ||
| Formation and Maturation of Phase-Separated Liquid Droplets by RNA-Binding Proteins | Q36172705 | ||
| A triple helix stabilizes the 3' ends of long noncoding RNAs that lack poly(A) tails | Q36374180 | ||
| RNA-mediated neuromuscular disorders | Q36507582 | ||
| Nucleophosmin integrates within the nucleolus via multi-modal interactions with proteins displaying R-rich linear motifs and rRNA. | Q36673676 | ||
| The disease-associated r(GGGGCC)n repeat from the C9orf72 gene forms tract length-dependent uni- and multimolecular RNA G-quadruplex structures | Q36742244 | ||
| Translationally repressed mRNA transiently cycles through stress granules during stress. | Q36914216 | ||
| Mammalian stress granules and processing bodies | Q36965220 | ||
| Interleukin-1β induced Stress Granules Sequester COX-2 mRNA and Regulates its Stability and Translation in Human OA Chondrocytes | Q36980832 | ||
| Repeat-associated non-ATG (RAN) translation in neurological disease | Q37195032 | ||
| Uncoupling stress granule assembly and translation initiation inhibition | Q37207715 | ||
| Distinct stages in stress granule assembly and disassembly | Q37238978 | ||
| Paraspeckles modulate the intranuclear distribution of paraspeckle-associated Ctn RNA. | Q37282006 | ||
| Structural, super-resolution microscopy analysis of paraspeckle nuclear body organization | Q37285424 | ||
| P433 | issue | 23 | |
| P1104 | number of pages | 17 | |
| P304 | page(s) | 4685-4701 | |
| P577 | publication date | 2018-05-10 | |
| P1433 | published in | Journal of Molecular Biology | Q925779 |
| P1476 | title | The Role of RNA in Biological Phase Separations | |
| P478 | volume | 430 |
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