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RNA granules: post-transcriptional and epigenetic modulators of gene expression
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1 of the 77 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-04): 10.1083/jcb.200212128 (notice 2023-09-06).
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bies.10247openalex-snapshot
Transcriptional silencing and translational control: key features of early germline development
inferredcites →https://doi.org/10.1016/j.ceb.2008.02.004openalex-snapshot
Mechanisms and cellular roles of local protein synthesis in mammalian cells
inferredcites →https://doi.org/10.1016/j.cell.2004.12.038openalex-snapshot
Involvement of MicroRNA in AU-Rich Element-Mediated mRNA Instability
inferredcites →https://doi.org/10.1016/j.cell.2006.04.031openalex-snapshot
Relief of microRNA-Mediated Translational Repression in Human Cells Subjected to Stress
inferredcites →https://doi.org/10.1016/j.cell.2006.04.037openalex-snapshot
Targeting of Aberrant mRNAs to Cytoplasmic Processing Bodies
inferredcites →https://doi.org/10.1016/j.cell.2008.09.022openalex-snapshot
Retrotransposons Revisited: The Restraint and Rehabilitation of Parasites
inferredcites →https://doi.org/10.1016/j.cub.2008.05.009openalex-snapshot
A C. elegans Piwi, PRG-1, Regulates 21U-RNAs during Spermatogenesis
inferredcites →https://doi.org/10.1016/j.mod.2008.06.005openalex-snapshot
Isolation of new polar granule components in Drosophila reveals P body and ER associated proteins
inferredcites →https://doi.org/10.1016/j.molcel.2005.10.031openalex-snapshot
Multiple Processing Body Factors and the ARE Binding Protein TTP Activate mRNA Decapping
inferredcites →https://doi.org/10.1016/j.molcel.2007.02.011openalex-snapshot
P Bodies and the Control of mRNA Translation and Degradation
inferredcites →https://doi.org/10.1016/j.molcel.2007.09.005openalex-snapshot
Inosine-Containing dsRNA Binds a Stress-Granule-like Complex and Downregulates Gene Expression In trans
inferredcites →https://doi.org/10.1016/j.molcel.2008.06.002openalex-snapshot
PRG-1 and 21U-RNAs Interact to Form the piRNA Complex Required for Fertility in C. elegans
inferredcites →https://doi.org/10.1016/j.molcel.2008.11.001openalex-snapshot
The Control of mRNA Decapping and P-Body Formation
inferredcites →https://doi.org/10.1016/j.neuron.2006.10.028openalex-snapshot
Staufen- and FMRP-Containing Neuronal RNPs Are Structurally and Functionally Related to Somatic P Bodies
inferredcites →https://doi.org/10.1016/j.tcb.2008.11.001openalex-snapshot
CGH-1 and the control of maternal mRNAs
inferredcites →https://doi.org/10.1016/j.tibs.2007.04.004openalex-snapshot
CPEB: a life in translation
inferredcites →https://doi.org/10.1016/j.tibs.2007.12.003openalex-snapshot
Stress granules: the Tao of RNA triage
inferredcites →https://doi.org/10.1016/j.ydbio.2008.02.059openalex-snapshot
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
inferredcites →https://doi.org/10.1016/j.ydbio.2008.07.008openalex-snapshot
Processing bodies and germ granules are distinct RNA granules that interact in C. elegans embryos
inferredcites →https://doi.org/10.1016/j.ydbio.2008.07.033openalex-snapshot
Drosophila processing bodies in oogenesis
inferredcites →https://doi.org/10.1016/s0014-4827(03)00290-8openalex-snapshot
Disruption of microtubules inhibits cytoplasmic ribonucleoprotein stress granule formation
inferredcites →https://doi.org/10.1038/nature06263openalex-snapshot
An epigenetic activation role of Piwi and a Piwi-associated piRNA in Drosophila melanogaster
inferredcites →https://doi.org/10.1038/ncb1265openalex-snapshot
Argonaute 2/RISC resides in sites of mammalian mRNA decay known as cytoplasmic bodies
inferredcites →https://doi.org/10.1038/ncb1274openalex-snapshot
MicroRNA-dependent localization of targeted mRNAs to mammalian P-bodies
inferredcites →https://doi.org/10.1038/ncb1723openalex-snapshot
Mature ribosomes are selectively degraded upon starvation by an autophagy pathway requiring the Ubp3p/Bre5p ubiquitin protease
inferredcites →https://doi.org/10.1038/ncb1783openalex-snapshot
A functional RNAi screen links O-GlcNAc modification of ribosomal proteins to stress granule and processing body assembly
inferredcites →https://doi.org/10.1038/nrm2080openalex-snapshot
P bodies: at the crossroads of post-transcriptional pathways
inferredcites →https://doi.org/10.1038/nrm2081openalex-snapshot
The chromatoid body: a germ-cell-specific RNA-processing centre
inferredcites →https://doi.org/10.1038/nsmb1016openalex-snapshot
Concerted action of poly(A) nucleases and decapping enzyme in mammalian mRNA turnover
inferredcites →https://doi.org/10.1038/sj.emboj.7601977openalex-snapshot
Messenger RNA regulation: to translate or to degrade
inferredcites →https://doi.org/10.1038/sj.embor.7400783openalex-snapshot
Formation of GW bodies is a consequence of microRNA genesis
inferredcites →https://doi.org/10.1038/sj.onc.1204553openalex-snapshot
Ras–GAP SH3 domain binding protein (G3BP) is a modulator of USP10, a novel human ubiquitin specific protease
inferredcites →https://doi.org/10.1042/bst0300963openalex-snapshot
Stress granules: sites of mRNA triage that regulate mRNA stability and translatability
inferredcites →https://doi.org/10.1073/pnas.0509333103openalex-snapshot
The chromatoid body of male germ cells: Similarity with processing bodies and presence of Dicer and microRNA pathway components
inferredcites →https://doi.org/10.1073/pnas.0510928103openalex-snapshot
MicroRNAs direct rapid deadenylation of mRNA
inferredcites →https://doi.org/10.1074/jbc.m601901200openalex-snapshot
The Anti-HIV-1 Editing Enzyme APOBEC3G Binds HIV-1 RNA and Messenger RNAs That Shuttle between Polysomes and Stress Granules
inferredcites →https://doi.org/10.1083/jcb.147.7.1431openalex-snapshot
RNA-Binding Proteins Tia-1 and Tiar Link the Phosphorylation of Eif-2α to the Assembly of Mammalian Stress Granules
inferredcites →https://doi.org/10.1083/jcb.151.6.1257openalex-snapshot
Dynamic Shuttling of Tia-1 Accompanies the Recruitment of mRNA to Mammalian Stress Granules
inferredcites →https://doi.org/10.1083/jcb.200212128openalex-snapshot
RETRACTED: The RasGAP-associated endoribonuclease G3BP assembles stress granules
inferredcites →https://doi.org/10.1083/jcb.200502088openalex-snapshot
Stress granules and processing bodies are dynamically linked sites of mRNP remodeling
inferredcites →https://doi.org/10.1083/jcb.200608071openalex-snapshot
ZBP1 regulates mRNA stability during cellular stress
inferredcites →https://doi.org/10.1083/jcb.200704147openalex-snapshot
Edc3p and a glutamine/asparagine-rich domain of Lsm4p function in processing body assembly in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1083/jcb.200707010openalex-snapshot
Stress-dependent relocalization of translationally primed mRNPs to cytoplasmic granules that are kinetically and spatially distinct from P-bodies
inferredcites →https://doi.org/10.1083/jcb.200801183openalex-snapshot
Protection of specific maternal messenger RNAs by the P body protein CGH-1 (Dhh1/RCK) during Caenorhabditis elegans oogenesis
inferredcites →https://doi.org/10.1083/jcb.200801196openalex-snapshot
Deadenylation is prerequisite for P-body formation and mRNA decay in mammalian cells
inferredcites →https://doi.org/10.1083/jcb.200802128openalex-snapshot
Maternal mRNAs are regulated by diverse P body–related mRNP granules during early Caenorhabditis elegans development
inferredcites →https://doi.org/10.1083/jcb.200807043openalex-snapshot
P bodies promote stress granule assembly in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1091/mbc.01-05-0221openalex-snapshot
Evidence That Ternary Complex (eIF2-GTP-tRNA i Met )–Deficient Preinitiation Complexes Are Core Constituents of Mammalian Stress Granules
inferredcites →https://doi.org/10.1091/mbc.e04-08-0715openalex-snapshot
Stress Granule Assembly Is Mediated by Prion-like Aggregation of TIA-1
inferredcites →https://doi.org/10.1091/mbc.e08-05-0513openalex-snapshot
The Dynamics of Mammalian P Body Transport, Assembly, and Disassembly In Vivo
inferredcites →https://doi.org/10.1101/gad.461107openalex-snapshot
The deacetylase HDAC6 is a novel critical component of stress granules involved in the stress response
inferredcites →https://doi.org/10.1101/sqb.2006.71.049openalex-snapshot
Function and Localization of MicroRNAs in Mammalian Cells
inferredcites →https://doi.org/10.1126/science.1111443openalex-snapshot
From Birth to Death: The Complex Lives of Eukaryotic mRNAs
inferredcites →https://doi.org/10.1126/science.1115079openalex-snapshot
Inhibition of Translational Initiation by Let-7 MicroRNA in Human Cells
inferredcites →https://doi.org/10.1126/science.1115791openalex-snapshot
Movement of Eukaryotic mRNAs Between Polysomes and Cytoplasmic Processing Bodies
inferredcites →https://doi.org/10.1126/science.1165171openalex-snapshot
An Epigenetic Role for Maternally Inherited piRNAs in Transposon Silencing
inferredcites →https://doi.org/10.1128/jvi.00287-08openalex-snapshot
Comparison of Cellular Ribonucleoprotein Complexes Associated with the APOBEC3F and APOBEC3G Antiviral Proteins
inferredcites →https://doi.org/10.1128/jvi.02287-06openalex-snapshot
Antiviral Protein APOBEC3G Localizes to Ribonucleoprotein Complexes Found in P Bodies and Stress Granules
inferredcites →https://doi.org/10.1128/mcb.00128-07openalex-snapshot
P-Body Formation Is a Consequence, Not the Cause, of RNA-Mediated Gene Silencing
inferredcites →https://doi.org/10.1128/mcb.00332-07openalex-snapshot
LINE-1 ORF1 Protein Localizes in Stress Granules with Other RNA-Binding Proteins, Including Components of RNA Interference RNA-Induced Silencing Complex
inferredcites →https://doi.org/10.1128/mcb.02300-06openalex-snapshot
Distinct Structural Features ofCaprin-1 Mediate Its Interaction with G3BP-1 and Its Induction of Phosphorylation of Eukaryotic Translation InitiationFactor 2 α , Entry to Cytoplasmic Stress Granules, and Selective Interaction with a Subset of mRNAs
inferredcites →https://doi.org/10.1128/mcb.25.21.9520-9531.2005openalex-snapshot
Identification and Functional Outcome of mRNAs Associated with RNA-Binding Protein TIA-1
inferredcites →https://doi.org/10.1128/mcb.26.7.2716-2727.2006openalex-snapshot
Translational Repression by RNA-Binding Protein TIAR
inferredcites →https://doi.org/10.1128/mcb.9.3.1298openalex-snapshot
Cytoplasmic Heat Shock Granules Are Formed from Precursor Particles and Are Associated with a Specific Set of mRNAs
inferredcites →https://doi.org/10.1139/o08-034openalex-snapshot
eIF4E, the mRNA cap-binding protein: from basic discovery to translational researchThis paper is one of a selection of papers published in this Special Issue, entitled CSBMCB — Systems and Chemical Biology, and has undergone the Journal's usual peer review process.
inferredcites →https://doi.org/10.1146/annurev.genet.35.102401.090756openalex-snapshot
Translational Regulation and RNA Localization in Drosophila Oocytes and Embryos
inferredcites →https://doi.org/10.1242/dev.128.8.1287openalex-snapshot
Analysis of RNA associated with P granules in germ cells of C. elegans adults
inferredcites →https://doi.org/10.1242/jcs.01692openalex-snapshot
The translational regulator CPEB1 provides a link between dcp1 bodies and stress granules
inferredcites →https://doi.org/10.1242/jcs.024976openalex-snapshot
A role for Q/N-rich aggregation-prone regions in P-body localization
inferredcites →https://doi.org/10.1261/rna.665008openalex-snapshot
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
inferredcites →https://doi.org/10.1371/journal.pbio.0040210openalex-snapshot
Translation Repression in Human Cells by MicroRNA-Induced Gene Silencing Requires RCK/p54
inferredcites →https://doi.org/10.1371/journal.ppat.0020041openalex-snapshot
Human Retroviral Host Restriction Factors APOBEC3G and APOBEC3F Localize to mRNA Processing Bodies
inferredcites →https://doi.org/10.1523/jneurosci.0104-08.2008openalex-snapshot
Dynamic Interaction between P-Bodies and Transport Ribonucleoprotein Particles in Dendrites of Mature Hippocampal Neurons
inferredcites →https://doi.org/10.4161/cc.7.22.6977openalex-snapshot
The chromatoid body of male germ cells: Epigenetic control and miRNA pathway
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Modulation of Stress Granule Dynamics by Phosphorylation and Ubiquitination in Plants
inferred← citeshttps://doi.org/10.2139/ssrn.4871974openalex-extracted
Modulation of Stress Granule Dynamics by Phosphorylation and Ubiquitination in Plants
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The translational regulation of maternal mRNA s in time and space
inferred← citeshttps://doi.org/10.1002/1873-3468.14787openalex-snapshot
The autophagy of stress granules
inferred← citeshttps://doi.org/10.1002/9781119860914.ch28openalex-snapshot
Posttranscriptional Control of Brain Development
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inferred← citeshttps://doi.org/10.1002/advs.202404822openalex-snapshot
FUS Selectively Facilitates circRNAs Packing into Small Extracellular Vesicles within Hypoxia Neuron
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tRNA modifications: Necessary for correct tRNA‐derived fragments during the recovery from stress?
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Experience and the ever‐changing brain: What the transcriptome can reveal
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mRNPs : Structure and role in development
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mRNA Fate in Human Cells; Degradation and Subcellular Localisation
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FIT for Purpose: PNA‐Based Probes Enable mRNA Imaging in Living Cells
inferred← citeshttps://doi.org/10.1002/cm.21294openalex-snapshot
Translational control by eIF2α in neurons: Beyond the stress response
inferred← citeshttps://doi.org/10.1002/hlca.201900255openalex-snapshot
Caprin‐1 Promotes Cellular Uptake of Nucleic Acids with Backbone and Sequence Discrimination
inferred← citeshttps://doi.org/10.1002/ijc.30833openalex-snapshot
The role of cold‐inducible RNA binding protein in cell stress response
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Intrinsic factors behind long COVID: IV. Hypothetical roles of the SARS‐CoV‐2 nucleocapsid protein and its liquid–liquid phase separation
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RNA N6‐methyladenosine in nonocular and ocular disease
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ORF57/MTA in KSHV Biology and Pathogenesis: Update From 2015
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Host Translational Control by Stress Granules Promotes Mycobacterium tuberculosis Pathogenesis
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Proteomics elucidating physiological and pathological functions of TDP‐43
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In vitro labeling strategies for in cellulo fluorescence microscopy of single ribonucleoprotein machines
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Temporal Control Over Complex, Simple, and Multiphase Coacervates Using Ureolysis and Ammonium Carbonate Decomposition
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Inflammation: cytokines and RNA‐based regulation
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Functional interactions between mRNA turnover and surveillance and the ubiquitin proteasome system
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Control of cytoplasmic translation in plants
inferred← citeshttps://doi.org/10.1002/wrna.1135openalex-snapshot
Long non‐coding RNAs coordinate cellular responses to stress
inferred← citeshttps://doi.org/10.1002/wrna.1165openalex-snapshot
The role of the DEAD‐box RNA helicase DDX3 in mRNA metabolism
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YB ‐1 protein: functions and regulation
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Effects of stress and aging on ribonucleoprotein assembly and function in the germ line
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RNA in development: how ribonucleoprotein granules regulate the life cycles of pathogenic protozoa
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DDX6 and its orthologs as modulators of cellular and viral RNA expression
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RNA ‐binding proteins in eye development and disease: implication of conserved RNA granule components
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Germ cell ribonucleoprotein granules in different clades of life: From insects to mammals
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The RNA regulatory programs that govern lymphocyte development and function
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A little less aggregation a little more replication: Viral manipulation of stress granules
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The role of posttranslational modifications in the assembly of stress granules
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Turnover of AU‐rich‐containing mRNAs during stress: a matter of survival
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Decoding the functions of post‐transcriptional regulators in the determination of inflammatory states: focus on macrophage activation
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Severe ethanol stress induces assembly of stress granules in Saccharomyces cerevisiae
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Aggregation of FET Proteins as a Pathological Change in Amyotrophic Lateral Sclerosis
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APEX Proximity Labeling of Stress Granule Proteins
inferred← citeshttps://doi.org/10.1007/978-1-0716-2597-2_33openalex-snapshot
An Optimized Stress Granule Detection Method: Investigation of UBQLN2 Effect on Stress Granule Formation
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Is Transcription the Dominant Force During Dynamic Changes in Gene Expression?
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The Exosomes of Trypanosomes and Other Protists
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Spatiotemporal Aspects of MicroRNA-Mediated Gene Regulation
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Safe Keeping the Message: mRNP Complexes Tweaking after Transcription
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Relationship of Other Cytoplasmic Ribonucleoprotein Bodies (cRNPB) to GW/P Bodies
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Function of GW182 and GW Bodies in siRNA and miRNA Pathways
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Isolation of Chromatoid Bodies from Mouse Testis as a Rich Source of Short RNAs
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In Vitro Synthesis, Delivery, and Bioavailability of Exogenous mRNA in Gene Transfer Mediated by PiggyBac Transposition
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Analysis of the Cellular Stress Response During Ebola Virus Infection by Immunofluorescence
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Plant Oxidative Stress Associated with Flood Stress
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Post-transcriptional Regulation of Glucocorticoid Function
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RNA Granules and Diseases: A Case Study of Stress Granules in ALS and FTLD
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Diverse Mechanisms of Translation Regulation and Their Role in Cancer
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Harnessing Stress Granule Formation by Small Molecules to Inhibit the Cellular Replication of SARS-CoV-2
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The function of RNA-binding proteins at the synapse: implications for neurodegeneration
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Stress-induced changes in miRNA biogenesis and functioning
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Deubiquitination and the regulation of stress granule assembly
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It is all about the process(ing): P-body granules and the regulation of signal transduction
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Reversible protein aggregation as cytoprotective mechanism against heat stress
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Stress granules safeguard against MAPK signaling hyperactivation by sequestering PKC/Pck2: new findings and perspectives
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Protein aggregation in amyotrophic lateral sclerosis
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Pur-alpha regulates cytoplasmic stress granule dynamics and ameliorates FUS toxicity
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Stem cell systems and regeneration in planaria
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Dysregulated expression of lipid storage and membrane dynamics factors in Tia1 knockout mouse nervous tissue
inferred← citeshttps://doi.org/10.1007/s10048-015-0441-5openalex-snapshot
Genetic ablation of ataxin-2 increases several global translation factors in their transcript abundance but decreases translation rate
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MicroRNA Alternations in the Testes Related to the Sterility of Triploid Fish
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METTL1 promotes cadmium-induced stress granules formation via enhancing translation of G3BP1 and expression of m7G- 3' tiRNA MetCAT
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CREB2 Functions as a Central Mediator of Oxidative Neuronal Death Triggered by Microglial Glutamate Release Under Neuroinflammatory Conditions
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TOB1 and TOB2 mark distinct RNA processing granules in differentiating lens fiber cells
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Impairment of stress granule assembly via inhibition of the eIF2alpha phosphorylation sensitizes glioma cells to chemotherapeutic agents
inferred← citeshttps://doi.org/10.1007/s11064-019-02763-yopenalex-snapshot
Missing in Action: Dysfunctional RNA Metabolism in Oligodendroglial Cells as a Contributor to Neurodegenerative Diseases?
inferred← citeshttps://doi.org/10.1007/s11357-009-9126-zopenalex-snapshot
Expression levels of TRPC1 and TRPC6 ion channels are reciprocally altered in aging rat aorta: implications for age-related vasospastic disorders
inferred← citeshttps://doi.org/10.1007/s12017-013-8221-6openalex-snapshot
AMPA Receptor Properties are Modulated in the Early Stages Following Pilocarpine-induced Status Epilepticus
inferred← citeshttps://doi.org/10.1007/s12250-019-00122-3openalex-snapshot
Viral Regulation of RNA Granules in Infected Cells
inferred← citeshttps://doi.org/10.1007/s12265-025-10619-wopenalex-snapshot
Connecting the Dots: Stress Granule and Cardiovascular Diseases
inferred← citeshttps://doi.org/10.1007/s12640-023-00669-wopenalex-snapshot
RNA-Binding Proteins: A Role in Neurotoxicity?
inferred← citeshttps://doi.org/10.1007/s13238-017-0430-6openalex-snapshot
Screening novel stress granule regulators from a natural compound library
inferred← citeshttps://doi.org/10.1007/s13311-016-0503-xopenalex-snapshot
Fluid-Based Biomarkers for Amyotrophic Lateral Sclerosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-380860-8.00003-3openalex-snapshot
RNA Editing by Mammalian ADARs
inferred← citeshttps://doi.org/10.1016/b978-0-12-381462-3.00057-4openalex-snapshot
Renal Ammonium Ion Production and Excretion
inferred← citeshttps://doi.org/10.1016/b978-0-12-385863-4.00013-7openalex-snapshot
Aspects of Trypanosoma cruzi Stage Differentiation
inferred← citeshttps://doi.org/10.1016/b978-0-12-388448-0.00028-0openalex-snapshot
Probes for Intracellular RNA Imaging in Live Cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-394299-9.00006-0openalex-snapshot
An Emerging Role of RNA-Binding Proteins as Multifunctional Regulators of Lymphocyte Development and Function
inferred← citeshttps://doi.org/10.1016/b978-0-12-394306-4.00013-7openalex-snapshot
New Insights into the Regulation of RNP Granule Assembly in Oocytes
inferred← citeshttps://doi.org/10.1016/b978-0-12-404740-2.00008-2openalex-snapshot
Normal and Aberrantly Capped mRNA Decapping
inferred← citeshttps://doi.org/10.1016/bs.aambs.2019.08.001openalex-snapshot
Application of model systems to study adaptive responses of Mycobacterium tuberculosis during infection and disease
inferred← citeshttps://doi.org/10.1016/bs.aivir.2016.08.001openalex-snapshot
Viral and Cellular mRNA Translation in Coronavirus-Infected Cells
inferred← citeshttps://doi.org/10.1016/bs.aivir.2023.07.001openalex-snapshot
How do they do it? The infection biology of potyviruses
inferred← citeshttps://doi.org/10.1016/bs.mie.2019.02.035openalex-snapshot
Targeted m6A reader proteins to study the epitranscriptome
inferred← citeshttps://doi.org/10.1016/bs.mie.2024.11.018openalex-snapshot
A general framework to analyze potential roles of tDRs in mammalian protein synthesis
inferred← citeshttps://doi.org/10.1016/j.abb.2019.108185openalex-snapshot
CO ameliorates endothelial senescence induced by 5-fluorouracil through SIRT1 activation
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2024.107474openalex-snapshot
Changes on corpus luteum structure and progesterone synthesis pathway after hCG or GnRH treatment during the early luteal phase in sheep
inferred← citeshttps://doi.org/10.1016/j.arr.2019.02.001openalex-snapshot
Unravelling protein aggregation as an ageing related process or a neuropathological response
inferred← citeshttps://doi.org/10.1016/j.bbadis.2013.04.011openalex-snapshot
Functional diversity of protein fibrillar aggregates from physiology to RNA granules to neurodegenerative diseases
inferred← citeshttps://doi.org/10.1016/j.bbadis.2020.165939openalex-snapshot
Hypusination of Eif5a regulates cytoplasmic TDP-43 aggregation and accumulation in a stress-induced cellular model
inferred← citeshttps://doi.org/10.1016/j.bbagen.2021.129996openalex-snapshot
What's new about CNBP? Divergent functions and activities for a conserved nucleic acid binding protein
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2013.02.003openalex-snapshot
Tristetraprolin (TTP): Interactions with mRNA and proteins, and current thoughts on mechanisms of action
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2014.11.009openalex-snapshot
Stress granules, P-bodies and cancer
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2019.194474openalex-snapshot
DEKTV and YVG motifs in the Lsm domain are important for the activity of Scd6, a conserved translation repressor protein
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2026.195184openalex-snapshot
Short-lived lncRNAs as candidate kinetic sensors of cellular stress
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2014.08.016openalex-snapshot
Ki-1/57 and CGI-55 ectopic expression impact cellular pathways involved in proliferation and stress response regulation
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2015.03.015openalex-snapshot
5′-AMP-activated protein kinase alpha regulates stress granule biogenesis
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2020.118876openalex-snapshot
Molecular mechanisms of stress granule assembly and disassembly
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2021.119209openalex-snapshot
Heat stress regulates the expression of TPK1 gene at transcriptional and post-transcriptional levels in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.bbapap.2013.01.003openalex-snapshot
Protein disorder, prion propensities, and self-organizing macromolecular collectives
inferred← citeshttps://doi.org/10.1016/j.bbcan.2009.11.001openalex-snapshot
A new generation of proto-oncogenes: Cold-inducible RNA binding proteins
inferred← citeshttps://doi.org/10.1016/j.bbcan.2023.188871openalex-snapshot
The role of the NDRG1 in the pathogenesis and treatment of breast cancer
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.03.088openalex-snapshot
Hsp90 is involved in the formation of P-bodies and stress granules
inferred← citeshttps://doi.org/10.1016/j.bbrc.2014.08.115openalex-snapshot
Aggregation of ALS-linked FUS mutant sequesters RNA binding proteins and impairs RNA granules formation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.03.017openalex-snapshot
Carbon monoxide induces the assembly of stress granule through the integrated stress response
inferred← citeshttps://doi.org/10.1016/j.biocel.2009.11.018openalex-snapshot
Cytoplasmic ribonucleoprotein (RNP) bodies and their relationship to GW/P bodies
inferred← citeshttps://doi.org/10.1016/j.biocel.2013.03.017openalex-snapshot
Calreticulin-dimerization induced by post-translational arginylation is critical for stress granules scaffolding
inferred← citeshttps://doi.org/10.1016/j.brainres.2011.12.053openalex-snapshot
Cold-inducible RNA binding protein inhibits H2O2-induced apoptosis in rat cortical neurons
inferred← citeshttps://doi.org/10.1016/j.canlet.2017.02.031openalex-snapshot
Roles of cancer/testis antigens (CTAs) in breast cancer
inferred← citeshttps://doi.org/10.1016/j.cbpa.2013.07.009openalex-snapshot
Stress granules form in Brachionus manjavacas (Rotifera) in response to a variety of stressors
inferred← citeshttps://doi.org/10.1016/j.cbpa.2022.102149openalex-snapshot
Small-molecule modulators of protein–RNA interactions
inferred← citeshttps://doi.org/10.1016/j.cbpa.2026.102695openalex-snapshot
Always on the move: Mapping spatiotemporal interactome with proximity labeling in mammalian cells
inferred← citeshttps://doi.org/10.1016/j.ceb.2012.03.011openalex-snapshot
Subcellular specialization of multifaceted 3′end modifying nucleotidyltransferases
inferred← citeshttps://doi.org/10.1016/j.ceb.2018.03.001openalex-snapshot
Close encounters of the RNAi kind: the silencing life of the adherens junctions
inferred← citeshttps://doi.org/10.1016/j.cej.2025.168568openalex-snapshot
ISRIB-loaded nanoplatform disrupts cellular homeostasis by depleting glutathione and inhibiting stress granules formation to drive immunosuppressive reprogramming
inferred← citeshttps://doi.org/10.1016/j.cell.2011.10.011openalex-snapshot
The Seeds of Neurodegeneration: Prion-like Spreading in ALS
inferred← citeshttps://doi.org/10.1016/j.cell.2012.04.016openalex-snapshot
Cell-free Formation of RNA Granules: Bound RNAs Identify Features and Components of Cellular Assemblies
inferred← citeshttps://doi.org/10.1016/j.cell.2013.01.033openalex-snapshot
Dual Specificity Kinase DYRK3 Couples Stress Granule Condensation/Dissolution to mTORC1 Signaling
inferred← citeshttps://doi.org/10.1016/j.cell.2013.05.037openalex-snapshot
Eukaryotic Stress Granules Are Cleared by Autophagy and Cdc48/VCP Function
inferred← citeshttps://doi.org/10.1016/j.cell.2013.07.031openalex-snapshot
Inhibition of mTORC1 by Astrin and Stress Granules Prevents Apoptosis in Cancer Cells
inferred← citeshttps://doi.org/10.1016/j.cell.2015.04.029openalex-snapshot
Regnase-1 and Roquin Regulate a Common Element in Inflammatory mRNAs by Spatiotemporally Distinct Mechanisms
inferred← citeshttps://doi.org/10.1016/j.cell.2015.09.041openalex-snapshot
Pausing on Polyribosomes: Make Way for Elongation in Translational Control
inferred← citeshttps://doi.org/10.1016/j.cell.2015.10.040openalex-snapshot
The LC Domain of hnRNPA2 Adopts Similar Conformations in Hydrogel Polymers, Liquid-like Droplets, and Nuclei
inferred← citeshttps://doi.org/10.1016/j.cell.2016.10.002openalex-snapshot
C9orf72 Dipeptide Repeats Impair the Assembly, Dynamics, and Function of Membrane-Less Organelles
inferred← citeshttps://doi.org/10.1016/j.cell.2016.11.054openalex-snapshot
Spatiotemporal Control of Intracellular Phase Transitions Using Light-Activated optoDroplets
inferred← citeshttps://doi.org/10.1016/j.cell.2018.11.004openalex-snapshot
The Human RNA-Binding Proteome and Its Dynamics during Translational Arrest
inferred← citeshttps://doi.org/10.1016/j.cell.2020.11.010openalex-snapshot
Single-Molecule Imaging Reveals Translation of mRNAs Localized to Stress Granules
inferred← citeshttps://doi.org/10.1016/j.cell.2023.05.047openalex-snapshot
QKI shuttles internal m7G-modified transcripts into stress granules and modulates mRNA metabolism
inferred← citeshttps://doi.org/10.1016/j.cell.2024.05.058openalex-snapshot
Microglial-derived C1q integrates into neuronal ribonucleoprotein complexes and impacts protein homeostasis in the aging brain
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.01.030openalex-snapshot
Mitochondrial RNA Granules Are Centers for Posttranscriptional RNA Processing and Ribosome Biogenesis
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.01.063openalex-snapshot
A Mitochondria-Specific Isoform of FASTK Is Present In Mitochondrial RNA Granules and Regulates Gene Expression and Function
inferred← citeshttps://doi.org/10.1016/j.celrep.2017.06.082openalex-snapshot
Glycolytic Enzymes Coalesce in G Bodies under Hypoxic Stress
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.05.041openalex-snapshot
Different Material States of Pub1 Condensates Define Distinct Modes of Stress Adaptation and Recovery
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.06.094openalex-snapshot
Hypertonic Stress Causes Cytoplasmic Translocation of Neuronal, but Not Astrocytic, FUS due to Impaired Transportin Function
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.05.085openalex-snapshot
Mutant FUS and ELAVL4 (HuD) Aberrant Crosstalk in Amyotrophic Lateral Sclerosis
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.02.066openalex-snapshot
The RNA-Binding Protein Rasputin/G3BP Enhances the Stability and Translation of Its Target mRNAs
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.03.084openalex-snapshot
Pan-retroviral Nucleocapsid-Mediated Phase Separation Regulates Genomic RNA Positioning and Trafficking
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111086openalex-snapshot
Hyperosmotic-stress-induced liquid-liquid phase separation of ALS-related proteins in the nucleus
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111879openalex-snapshot
A circadian clock translational control mechanism targets specific mRNAs to cytoplasmic messenger ribonucleoprotein granules
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111968openalex-snapshot
Liquid-liquid phase separation of nucleocapsid proteins during SARS-CoV-2 and HIV-1 replication
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.113769openalex-snapshot
hnRNPA2B1 represses the disassembly of arsenite-induced stress granules and is essential for male fertility
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114360openalex-snapshot
Isoform-specific sequestration of protein kinase A fine-tunes intracellular signaling during heat stress
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116493openalex-snapshot
DDX3X acts as a selective dual switch regulator of mRNA translation in acute ER stress
inferred← citeshttps://doi.org/10.1016/j.chembiol.2024.09.009openalex-snapshot
RNA infrastructure profiling illuminates transcriptome structure in crowded spaces
inferred← citeshttps://doi.org/10.1016/j.cis.2016.05.012openalex-snapshot
Protein intrinsic disorder-based liquid–liquid phase transitions in biological systems: Complex coacervates and membrane-less organelles
inferred← citeshttps://doi.org/10.1016/j.cmet.2013.02.006openalex-snapshot
The Mitochondrial RNA-Binding Protein GRSF1 Localizes to RNA Granules and Is Required for Posttranscriptional Mitochondrial Gene Expression
inferred← citeshttps://doi.org/10.1016/j.coi.2011.08.009openalex-snapshot
Protein kinase PKR and RNA adenosine deaminase ADAR1: new roles for old players as modulators of the interferon response
inferred← citeshttps://doi.org/10.1016/j.crcbio.2021.100009openalex-snapshot
Tdrd3 regulates the progression of meiosis II through translational control of Emi2 mRNA in mouse oocytes
inferred← citeshttps://doi.org/10.1016/j.cryobiol.2019.03.011openalex-snapshot
Transcriptome and proteome analyses to investigate the molecular underpinnings of cold response in the Colorado potato beetle, Leptinotarsa decemlineata
inferred← citeshttps://doi.org/10.1016/j.cub.2013.09.058openalex-snapshot
Coordination of Translational Control and Protein Homeostasis during Severe Heat Stress
inferred← citeshttps://doi.org/10.1016/j.dci.2013.05.004openalex-snapshot
RNAi and antiviral defense in Drosophila: Setting up a systemic immune response
inferred← citeshttps://doi.org/10.1016/j.devcel.2009.10.017openalex-snapshot
Nuclear Bodies: Random Aggregates of Sticky Proteins or Crucibles of Macromolecular Assembly?
inferred← citeshttps://doi.org/10.1016/j.devcel.2010.03.003openalex-snapshot
trans Regulation: Do mRNAs Have a Herd Mentality?
inferred← citeshttps://doi.org/10.1016/j.devcel.2013.09.024openalex-snapshot
Translation Repressors, an RNA Helicase, and Developmental Cues Control RNP Phase Transitions during Early Development
inferred← citeshttps://doi.org/10.1016/j.devcel.2015.05.014openalex-snapshot
RNA Binding Protein Nanos2 Organizes Post-transcriptional Buffering System to Retain Primitive State of Mouse Spermatogonial Stem Cells
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.10.005openalex-snapshot
RNA-Seeded Functional Amyloids Balance Growth and Survival
inferred← citeshttps://doi.org/10.1016/j.exer.2014.12.011openalex-snapshot
Molecular characterization of mouse lens epithelial cell lines and their suitability to study RNA granules and cataract associated genes
inferred← citeshttps://doi.org/10.1016/j.exphem.2024.104279openalex-snapshot
Role of RNA modifications in blood development and regeneration
inferred← citeshttps://doi.org/10.1016/j.expneurol.2024.114678openalex-snapshot
Muscone alleviates neuronal injury via increasing stress granules formation and reducing apoptosis in acute ischemic stroke
inferred← citeshttps://doi.org/10.1016/j.expneurol.2026.115885openalex-snapshot
Modulating inflammasome (NLRP3) activation and stress granule (SG) formation: Insight of neuroprotection by Normobaric oxygen (NBO) in ischemic stroke
inferred← citeshttps://doi.org/10.1016/j.febslet.2014.04.023openalex-snapshot
Transportin‐1 and Transportin‐2: Protein nuclear import and beyond
inferred← citeshttps://doi.org/10.1016/j.febslet.2014.04.045openalex-snapshot
Human Tudor staphylococcal nuclease (Tudor‐SN) protein modulates the kinetics of AGTR1‐3′UTR granule formation
inferred← citeshttps://doi.org/10.1016/j.febslet.2015.03.013openalex-snapshot
Dimerization model of the C‐terminal RNA Recognition Motif of HuR
inferred← citeshttps://doi.org/10.1016/j.febslet.2015.06.009openalex-snapshot
TDP‐35 sequesters TDP‐43 into cytoplasmic inclusions through binding with RNA
inferred← citeshttps://doi.org/10.1016/j.fgb.2019.01.010openalex-snapshot
Transcriptional profiling and localization of GUL-1, a COT-1 pathway component, in Neurospora crassa
inferred← citeshttps://doi.org/10.1016/j.gde.2011.04.005openalex-snapshot
mRNA localization: assembly of transport complexes and their incorporation into particles
inferred← citeshttps://doi.org/10.1016/j.gene.2025.149776openalex-snapshot
The important role of stress granules in prostate cancer development, progression, and drug resistance
inferred← citeshttps://doi.org/10.1016/j.gpb.2022.01.003openalex-snapshot
Screening Linear and Circular RNA Transcripts from Stress Granules
inferred← citeshttps://doi.org/10.1016/j.heares.2022.108634openalex-snapshot
An emerging role for stress granules in neurodegenerative disease and hearing loss
inferred← citeshttps://doi.org/10.1016/j.ibmb.2013.04.004openalex-snapshot
Characterization of Tudor-sn-containing granules in the silkworm, Bombyx mori
inferred← citeshttps://doi.org/10.1016/j.ibmb.2015.07.011openalex-snapshot
Loqs depends on R2D2 to localize in D2 body-like granules and functions in RNAi pathways in silkworm cells
inferred← citeshttps://doi.org/10.1016/j.ijrobp.2023.08.045openalex-snapshot
Differential Formation of Stress Granules in Radiosensitive and Radioresistant Head and Neck Squamous Cell Carcinoma Cells
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110359openalex-snapshot
Stress granules in cancer: Adaptive dynamics and therapeutic implications
inferred← citeshttps://doi.org/10.1016/j.isci.2024.111162openalex-snapshot
Modulation of stress granule dynamics by phosphorylation and ubiquitination in plants
inferred← citeshttps://doi.org/10.1016/j.isci.2025.112578openalex-snapshot
Assembly and disassembly of stress granules in kidney diseases
inferred← citeshttps://doi.org/10.1016/j.it.2014.07.006openalex-snapshot
Antiviral innate immunity and stress granule responses
inferred← citeshttps://doi.org/10.1016/j.jbc.2024.107413openalex-snapshot
PolyQ-expanded ataxin-2 aggregation impairs cellular processing-body homeostasis via sequestering the RNA helicase DDX6
inferred← citeshttps://doi.org/10.1016/j.jbc.2025.110738openalex-snapshot
The ubiquitin ligase Nedd4-2 promotes localization of DNMBP/Tuba to P-bodies under hyperosmotic stress
inferred← citeshttps://doi.org/10.1016/j.jbiosc.2014.02.025openalex-snapshot
Importance of glucose-6-phosphate dehydrogenase (G6PDH) for vanillin tolerance in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.jbiosc.2019.05.016openalex-snapshot
Xylene causes oxidative stress and pronounced translation repression in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.jhep.2014.11.018openalex-snapshot
Hepatitis C virus infection inhibits P-body granule formation in human livers
inferred← citeshttps://doi.org/10.1016/j.jmb.2011.03.064openalex-snapshot
Interplay between Posttranscriptional and Posttranslational Interactions of RNA-Binding Proteins
inferred← citeshttps://doi.org/10.1016/j.jmb.2011.11.040openalex-snapshot
Three RNA Recognition Motifs Participate in RNA Recognition and Structural Organization by the Pro-Apoptotic Factor TIA-1
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