Nancy Kedersha

Evidence that ternary complex (eIF2-GTP-tRNA(i)(Met))-deficient preinitiation complexes are core constituents of mammalian stress granules.

Stressful initiations.

Sendai virus trailer RNA binds TIAR, a cellular protein involved in virus-induced apoptosis.

Visibly stressed: the role of eIF2, TIA-1, and stress granules in protein translation.

Regulation of cyclooxygenase-2 expression by the translational silencer TIA-1.

U1 snRNP-dependent function of TIAR in the regulation of alternative RNA processing of the human calcitonin/CGRP pre-mRNA.

Vaults bind directly to microtubules via their caps and not their barrels.

Granzyme B leakage-induced cell death: a new type of activation-induced natural killer cell death.

Arthritis suppressor genes TIA-1 and TTP dampen the expression of tumor necrosis factor alpha, cyclooxygenase 2, and inflammatory arthritis.

MK2-induced tristetraprolin:14-3-3 complexes prevent stress granule association and ARE-mRNA decay.

Post-transcriptional regulation of proinflammatory proteins.

FAST is a BCL-X(L)-associated mitochondrial protein.

Stress granule assembly is mediated by prion-like aggregation of TIA-1.

FAST is a survival protein that senses mitochondrial stress and modulates TIA-1-regulated changes in protein expression.

Mystique is a new insulin-like growth factor-I-regulated PDZ-LIM domain protein that promotes cell attachment and migration and suppresses Anchorage-independent growth.

Heme-regulated inhibitor kinase-mediated phosphorylation of eukaryotic translation initiation factor 2 inhibits translation, induces stress granule formation, and mediates survival upon arsenite exposure.

Importance of eIF2alpha phosphorylation and stress granule assembly in alphavirus translation regulation.

Stress granules and processing bodies are dynamically linked sites of mRNP remodeling.

RNA granules.

Eukaryotic initiation factor 2alpha-independent pathway of stress granule induction by the natural product pateamine A.

Polysome-bound endonuclease PMR1 is targeted to stress granules via stress-specific binding to TIA-1.

On again, off again: the SRC-3 transcriptional coactivator moonlights as a translational corepressor.

Fas-activated serine/threonine phosphoprotein (FAST) is a regulator of alternative splicing.

Ribosomal slowdown mediates translational arrest during cellular division.

Elucidation of a C-rich signature motif in target mRNAs of RNA-binding protein TIAR.

T-cell intracellular antigen-1 (TIA-1)-induced translational silencing promotes the decay of selected mRNAs.

Mammalian stress granules and processing bodies.

Stress granules: the Tao of RNA triage.

Autoantibodies to the translational suppressors T cell intracytoplasmic antigen 1 and T cell intracytoplasmic antigen 1-related protein in patients with rheumatic diseases: increased prevalence in systemic lupus erythematosus and systemic sclerosis and correlation with clinical features.

A functional RNAi screen links O-GlcNAc modification of ribosomal proteins to stress granule and processing body assembly.

Real-time and quantitative imaging of mammalian stress granules and processing bodies.

Identification of a cytoplasmic complex that adds a cap onto 5'-monophosphate RNA.

RNA granules: post-transcriptional and epigenetic modulators of gene expression.

Stress granules.

Metazoan stress granule assembly is mediated by P-eIF2alpha-dependent and -independent mechanisms.

Angiogenin-induced tRNA-derived stress-induced RNAs promote stress-induced stress granule assembly.

Regulation of translation by stress granules and processing bodies.

Fast kinase domain-containing protein 3 is a mitochondrial protein essential for cellular respiration.

Visualization of single mRNAs reveals temporal association of proteins with microRNA-regulated mRNA.

Stress puts TIA on TOP.

Relationship of GW/P-bodies with stress granules.

Stress granules and cell signaling: more than just a passing phase?

Dysregulated expression of lipid storage and membrane dynamics factors in Tia1 knockout mouse nervous tissue.

Activation of stress response pathways promotes formation of antiviral granules and restricts virus replication.

Stress granules, P-bodies and cancer.

Viral and cellular proteins containing FGDF motifs bind G3BP to block stress granule formation.

Stress granules regulate double-stranded RNA-dependent protein kinase activation through a complex containing G3BP1 and Caprin1.

Methods for the characterization of stress granules in virus infected cells.

G3BP-Caprin1-USP10 complexes mediate stress granule condensation and associate with 40S subunits.

Vinca alkaloid drugs promote stress-induced translational repression and stress granule formation.

YB-1 regulates tiRNA-induced Stress Granule formation but not translational repression.

Mammalian ataxin-2 modulates translation control at the pre-initiation complex via PI3K/mTOR and is induced by starvation.

Ebola Virus Does Not Induce Stress Granule Formation during Infection and Sequesters Stress Granule Proteins within Viral Inclusions.

Stress-specific differences in assembly and composition of stress granules and related foci.

Phase Separation of C9orf72 Dipeptide Repeats Perturbs Stress Granule Dynamics.