scholarly article | Q13442814 |
P50 | author | Jens Lykke-Andersen | Q55154882 |
P2093 | author name string | Tobias M Franks | |
P2860 | cites work | A role for the eIF4E-binding protein 4E-T in P-body formation and mRNA decay | Q24679242 |
MicroRNA-dependent localization of targeted mRNAs to mammalian P-bodies | Q24681266 | ||
RNA granules | Q24683783 | ||
Decapping and Decay of Messenger RNA Occur in Cytoplasmic Processing Bodies | Q27931286 | ||
Yeast Sm-like proteins function in mRNA decapping and decay | Q27936322 | ||
Targeting an mRNA for decapping: displacement of translation factors and association of the Lsm1p-7p complex on deadenylated yeast mRNAs | Q27936762 | ||
Targeting of aberrant mRNAs to cytoplasmic processing bodies | Q27939158 | ||
Involvement of microRNA in AU-rich element-mediated mRNA instability | Q28118466 | ||
Recruitment and activation of mRNA decay enzymes by two ARE-mediated decay activation domains in the proteins TTP and BRF-1 | Q28118675 | ||
Tristetraprolin and other CCCH tandem zinc-finger proteins in the regulation of mRNA turnover | Q28215400 | ||
Relief of microRNA-mediated translational repression in human cells subjected to stress | Q28246349 | ||
Argonaute 2/RISC resides in sites of mammalian mRNA decay known as cytoplasmic bodies | Q28252216 | ||
A KH domain RNA binding protein, KSRP, promotes ARE-directed mRNA turnover by recruiting the degradation machinery | Q28264688 | ||
Inhibition of translational initiation by Let-7 MicroRNA in human cells | Q28265842 | ||
Movement of eukaryotic mRNAs between polysomes and cytoplasmic processing bodies | Q28270553 | ||
Individual RNA recognition motifs of TIA-1 and TIAR have different RNA binding specificities | Q28274328 | ||
Concerted action of poly(A) nucleases and decapping enzyme in mammalian mRNA turnover | Q28281490 | ||
Disruption of GW bodies impairs mammalian RNA interference | Q28281500 | ||
Chorioallantoic fusion defects and embryonic lethality resulting from disruption of Zfp36L1, a gene encoding a CCCH tandem zinc finger protein of the Tristetraprolin family | Q28585872 | ||
A pathogenetic role for TNF alpha in the syndrome of cachexia, arthritis, and autoimmunity resulting from tristetraprolin (TTP) deficiency | Q28589649 | ||
TIA-1 is a translational silencer that selectively regulates the expression of TNF-alpha | Q28594475 | ||
AU-rich elements: characterization and importance in mRNA degradation | Q29547896 | ||
General translational repression by activators of mRNA decapping | Q29614567 | ||
RNA stabilization by the AU-rich element binding protein, HuR, an ELAV protein | Q29615186 | ||
Processing bodies require RNA for assembly and contain nontranslating mRNAs | Q29615264 | ||
The cap-to-tail guide to mRNA turnover | Q29619835 | ||
Premature translational termination triggers mRNA decapping | Q29620198 | ||
Overexpression of HuR, a nuclear-cytoplasmic shuttling protein, increases the in vivo stability of ARE-containing mRNAs | Q29620269 | ||
Differential distribution of exosome subunits at the nuclear lamina and in cytoplasmic foci. | Q30476869 | ||
Cap-independent polysomal association of natural mRNAs encoding c-myc, BiP, and eIF4G conferred by internal ribosome entry sites | Q31957370 | ||
A resource for large-scale RNA-interference-based screens in mammals. | Q33200135 | ||
Versatile role for hnRNP D isoforms in the differential regulation of cytoplasmic mRNA turnover | Q33954794 | ||
Identification and functional outcome of mRNAs associated with RNA-binding protein TIA-1. | Q34097417 | ||
ARE-mRNA degradation requires the 5'-3' decay pathway. | Q34360717 | ||
SMG7 acts as a molecular link between mRNA surveillance and mRNA decay | Q34368226 | ||
Translational repression by RNA-binding protein TIAR | Q34520016 | ||
The tandem CCCH zinc finger protein tristetraprolin and its relevance to cytokine mRNA turnover and arthritis | Q21195674 | ||
Evidence that tristetraprolin binds to AU-rich elements and promotes the deadenylation and destabilization of tumor necrosis factor alpha mRNA. | Q22010036 | ||
Interactions of CCCH zinc finger proteins with mRNA. Binding of tristetraprolin-related zinc finger proteins to Au-rich elements and destabilization of mRNA | Q22253466 | ||
Human Upf proteins target an mRNA for nonsense-mediated decay when bound downstream of a termination codon | Q24290775 | ||
AU binding proteins recruit the exosome to degrade ARE-containing mRNAs | Q24291926 | ||
The mammalian exosome mediates the efficient degradation of mRNAs that contain AU-rich elements | Q24292126 | ||
Interactions of CCCH zinc finger proteins with mRNA: non-binding tristetraprolin mutants exert an inhibitory effect on degradation of AU-rich element-containing mRNAs | Q24292131 | ||
Multiple processing body factors and the ARE binding protein TTP activate mRNA decapping | Q24299303 | ||
GW182 is critical for the stability of GW bodies expressed during the cell cycle and cell proliferation | Q24307714 | ||
Feedback inhibition of macrophage tumor necrosis factor-alpha production by tristetraprolin | Q24323168 | ||
An unconventional human Ccr4-Caf1 deadenylase complex in nuclear cajal bodies | Q24337378 | ||
Functional cloning of BRF1, a regulator of ARE-dependent mRNA turnover | Q24534314 | ||
A role for eIF4E and eIF4E-transporter in targeting mRNPs to mammalian processing bodies | Q24537397 | ||
A crucial role for GW182 and the DCP1:DCP2 decapping complex in miRNA-mediated gene silencing | Q24537488 | ||
The human LSm1-7 proteins colocalize with the mRNA-degrading enzymes Dcp1/2 and Xrnl in distinct cytoplasmic foci | Q24540163 | ||
The GW182 protein colocalizes with mRNA degradation associated proteins hDcp1 and hLSm4 in cytoplasmic GW bodies | Q24540223 | ||
Human Dcp2: a catalytically active mRNA decapping enzyme located in specific cytoplasmic structures | Q24543188 | ||
Tethering KSRP, a decay-promoting AU-rich element-binding protein, to mRNAs elicits mRNA decay | Q24548948 | ||
A role for the P-body component GW182 in microRNA function | Q24669847 | ||
Cytoplasmic foci are sites of mRNA decay in human cells | Q24677437 | ||
Stress granules and processing bodies are dynamically linked sites of mRNP remodeling | Q24678779 | ||
AU-rich element-mediated translational control: complexity and multiple activities of trans-activating factors | Q35003442 | ||
Formation of GW bodies is a consequence of microRNA genesis | Q35016215 | ||
The control of mRNA stability in response to extracellular stimuli. | Q35042665 | ||
Novel mRNA targets for tristetraprolin (TTP) identified by global analysis of stabilized transcripts in TTP-deficient fibroblasts | Q35221409 | ||
RNA decapping inside and outside of processing bodies. | Q36131538 | ||
Circumstances and mechanisms of inhibition of translation by secondary structure in eucaryotic mRNAs | Q36796132 | ||
Somatic mRNA turnover mutants implicate tristetraprolin in the interleukin-3 mRNA degradation pathway. | Q39453060 | ||
Identification of TIAR as a protein binding to the translational regulatory AU-rich element of tumor necrosis factor alpha mRNA. | Q40980265 | ||
The developmental timing regulator AIN-1 interacts with miRISCs and may target the argonaute protein ALG-1 to cytoplasmic P bodies in C. elegans | Q47068671 | ||
The CCCH tandem zinc-finger protein Zfp36l2 is crucial for female fertility and early embryonic development. | Q52559820 | ||
AUF1 binding affinity to A+U-rich elements correlates with rapid mRNA degradation | Q71119789 | ||
Evidence that tristetraprolin is a physiological regulator of granulocyte-macrophage colony-stimulating factor messenger RNA deadenylation and stability | Q73520889 | ||
P433 | issue | 6 | |
P921 | main subject | ZFP36 ring finger protein | Q21110024 |
ZFP36 ring finger protein like 1 | Q21120026 | ||
positive regulation of intracellular mRNA localization | Q22301073 | ||
P304 | page(s) | 719-735 | |
P577 | publication date | 2007-03-01 | |
P1433 | published in | Genes & Development | Q1524533 |
P1476 | title | TTP and BRF proteins nucleate processing body formation to silence mRNAs with AU-rich elements | |
P478 | volume | 21 |
Q42501988 | A crossroad of microRNAs and immediate early genes (IEGs) encoding oncogenic transcription factors in breast cancer |
Q28294112 | A functional RNAi screen links O-GlcNAc modification of ribosomal proteins to stress granule and processing body assembly |
Q33923637 | A molecular profile of cocaine abuse includes the differential expression of genes that regulate transcription, chromatin, and dopamine cell phenotype |
Q37406103 | A role for transportin in deposition of TTP to cytoplasmic RNA granules and mRNA decay |
Q40675814 | A versatile ribosomal protein promoter-based reporter system for selective assessment of RNA stability and post-transcriptional control |
Q61795967 | AU-rich element-binding proteins in colorectal cancer |
Q35807264 | AU-rich-element-dependent translation repression requires the cooperation of tristetraprolin and RCK/P54. |
Q85195043 | Analyzing P-bodies and stress granules in Saccharomyces cerevisiae |
Q37219994 | Analyzing P-bodies in Saccharomyces cerevisiae |
Q39765724 | Anthrax lethal toxin promotes dephosphorylation of TTP and formation of processing bodies |
Q33907851 | AtTZF gene family localizes to cytoplasmic foci. |
Q50295838 | BRF1 Complex recruits RNA degradation activities |
Q57497767 | BRF1 ameliorates LPS-induced inflammation through autophagy crosstalking with MAPK/ERK signaling |
Q24649055 | C. elegans La-related protein, LARP-1, localizes to germline P bodies and attenuates Ras-MAPK signaling during oogenesis |
Q48133543 | Cell type-specific suppression of mechanosensitive genes by audible sound stimulation. |
Q27342467 | Characterizing mRNA interactions with RNA granules during translation initiation inhibition |
Q35823712 | Chemical structure requirements and cellular targeting of microRNA-122 by peptide nucleic acids anti-miRs |
Q43086956 | Complementarity of end regions increases the lifetime of small RNAs in mammalian cells |
Q26864862 | Composition and function of P bodies in Arabidopsis thaliana |
Q34307730 | Comprehensive analysis of CCCH zinc finger family in poplar (Populus trichocarpa). |
Q36994939 | Coordinated changes in mRNA turnover, translation, and RNA processing bodies in bronchial epithelial cells following inflammatory stimulation |
Q34193713 | Coordinated expression of tristetraprolin post-transcriptionally attenuates mitogenic induction of the oncogenic Ser/Thr kinase Pim-1. |
Q37208192 | Cyclin B1 mRNA translation is temporally controlled through formation and disassembly of RNA granules |
Q34496106 | Cytoplasmic mRNP granules at a glance |
Q41002587 | DDX6 regulates sequestered nuclear CUG-expanded DMPK-mRNA in dystrophia myotonica type 1. |
Q28508125 | Deadenylation is prerequisite for P-body formation and mRNA decay in mammalian cells |
Q34769859 | Decoding ARE-mediated decay: is microRNA part of the equation? |
Q47071694 | Degradation of hsp70 and other mRNAs in Drosophila via the 5' 3' pathway and its regulation by heat shock |
Q34574859 | Differential utilization of decapping enzymes in mammalian mRNA decay pathways |
Q50447198 | Diffuse decapping enzyme DCP2 accumulates in DCP1 foci under heat stress in Arabidopsis thaliana |
Q36084105 | Dis3- and exosome subunit-responsive 3' mRNA instability elements |
Q35926324 | Drosophila eyes absent is a novel mRNA target of the tristetraprolin (TTP) protein DTIS11 |
Q38646470 | Dual RNA Processing Roles of Pat1b via Cytoplasmic Lsm1-7 and Nuclear Lsm2-8 Complexes |
Q45080818 | Dynamic interaction between P-bodies and transport ribonucleoprotein particles in dendrites of mature hippocampal neurons |
Q34793205 | ELAVL1 regulates alternative splicing of eIF4E transporter to promote postnatal angiogenesis |
Q24294915 | Exonuclease hDIS3L2 specifies an exosome-independent 3'-5' degradation pathway of human cytoplasmic mRNA |
Q40044648 | Fas-activated Ser/Thr phosphoprotein (FAST) is a eukaryotic initiation factor 4E-binding protein that regulates mRNA stability and cell survival |
Q26773059 | Feedback Regulation of Kinase Signaling Pathways by AREs and GREs |
Q47155013 | Fine regulation of ARF17 for anther development and pollen formation |
Q33669936 | Formation of GW/P bodies as marker for microRNA-mediated regulation of innate immune signaling in THP-1 cells |
Q83225154 | GC content shapes mRNA storage and decay in human cells |
Q36172058 | Hepatitis C virus infection alters P-body composition but is independent of P-body granules |
Q38256804 | Human 4E-T represses translation of bound mRNAs and enhances microRNA-mediated silencing |
Q24336741 | Human Pat1b connects deadenylation with mRNA decapping and controls the assembly of processing bodies |
Q33694001 | IL-17 regulates CXCL1 mRNA stability via an AUUUA/tristetraprolin-independent sequence |
Q39908800 | Identification of GW182 and its novel isoform TNGW1 as translational repressors in Ago2-mediated silencing |
Q37560020 | Inflammation: cytokines and RNA-based regulation |
Q36119318 | Inhibition of nonsense-mediated mRNA decay (NMD) by a new chemical molecule reveals the dynamic of NMD factors in P-bodies |
Q30438742 | Inhibition of tristetraprolin deadenylation by poly(A) binding protein |
Q42070135 | Kaposi's sarcoma-associated herpesvirus G-protein-coupled receptor prevents AU-rich-element-mediated mRNA decay |
Q36668282 | LPS-induced production of TNF-α and IL-6 in mast cells is dependent on p38 but independent of TTP |
Q28300045 | Localization of AU-rich element-containing mRNA in cytoplasmic granules containing exosome subunits |
Q36336831 | Mechanistic aspects of COX-2 expression in colorectal neoplasia |
Q36249379 | MicroRNA and AU-rich element regulation of prostaglandin synthesis |
Q38042546 | Multiple functions of tristetraprolin/TIS11 RNA-binding proteins in the regulation of mRNA biogenesis and degradation |
Q36920373 | Mutant tristetraprolin: a potent inhibitor of malignant glioma cell growth. |
Q40786966 | NB-LRR signaling induces translational repression of viral transcripts and the formation of RNA processing bodies through mechanisms differing from those activated by UV stress and RNAi |
Q30498700 | Novel mRNA-containing cytoplasmic granules in ALK-transformed cells |
Q35230739 | Overexpression of AtTTP affects ARF17 expression and leads to male sterility in Arabidopsis |
Q37976384 | P-bodies and their functions during mRNA cell cycle: mini-review. |
Q52695010 | P38 activation induces the dissociation of tristetraprolin from Argonaute 2 to increase ARE-mRNA stabilization. |
Q33309340 | Phosphorylation site analysis of the anti-inflammatory and mRNA-destabilizing protein tristetraprolin |
Q28818470 | Pigmy MicroRNA: surveillance cops in Therapies kingdom |
Q35957603 | Plant Tandem CCCH Zinc Finger Proteins Interact with ABA, Drought, and Stress Response Regulators in Processing-Bodies and Stress Granules |
Q30155985 | Poliovirus-mediated disruption of cytoplasmic processing bodies |
Q37338867 | Polysomes, P bodies and stress granules: states and fates of eukaryotic mRNAs |
Q24654207 | Post-transcriptional Regulation of Genes Encoding Anti-microbial Peptides in Drosophila |
Q26747406 | Post-transcriptional Regulation of Immunological Responses through Riboclustering |
Q37113415 | Post-transcriptional control of cytokine production |
Q37661362 | Post-transcriptional regulons coordinate the initiation and resolution of inflammation |
Q34232095 | Post-transcriptional up-regulation of Tsc-22 by Ybx1, a target of miR-216a, mediates TGF-{beta}-induced collagen expression in kidney cells. |
Q33924658 | Posttranscriptional Regulation of Cyclooxygenase 2 Expression in Colorectal Cancer |
Q36817904 | Protection of specific maternal messenger RNAs by the P body protein CGH-1 (Dhh1/RCK) during Caenorhabditis elegans oogenesis |
Q35212469 | Putative molecular mechanisms underlying tandem CCCH zinc finger protein mediated plant growth, stress, and gene expression responses. |
Q38552147 | RNA binding proteins as regulators of immune cell biology. |
Q38238681 | RNA granules and cytoskeletal links. |
Q37784866 | RNA granules: the good, the bad and the ugly |
Q39042850 | RNA-binding proteins in immune regulation: a focus on CCCH zinc finger proteins |
Q48330341 | Rapidly induced gene networks following induction of long-term potentiation at perforant path synapses in vivo |
Q35001141 | Re-capping the message |
Q37769284 | Regulation of cytokines by small RNAs during skin inflammation. |
Q37694319 | Regulation of mRNA decay in plant responses to salt and osmotic stress. |
Q39215435 | Regulation of mRNA stability by CCCH-type zinc-finger proteins in immune cells |
Q39013191 | Regulation of mRNA turnover in cystic fibrosis lung disease |
Q35049975 | Relationship of GW/P-bodies with stress granules. |
Q30499882 | RhoA activation participates in rearrangement of processing bodies and release of nucleated AU-rich mRNAs |
Q36826366 | Role of the RNA-binding protein tristetraprolin in glucocorticoid-mediated gene regulation. |
Q35949029 | Small interfering RNA-mediated silencing induces target-dependent assembly of GW/P bodies |
Q38136844 | Stress granules and cell signaling: more than just a passing phase? |
Q35689148 | Stress granules, P-bodies and cancer. |
Q38071446 | Structural and functional control of the eukaryotic mRNA decapping machinery. |
Q37292351 | TIS11 family proteins and their roles in posttranscriptional gene regulation |
Q38213696 | Tandem CCCH zinc finger proteins in plant growth, development and stress response |
Q36358461 | Target Discrimination in Nonsense-Mediated mRNA Decay Requires Upf1 ATPase Activity |
Q33424478 | Temporally regulated traffic of HuR and its associated ARE-containing mRNAs from the chromatoid body to polysomes during mouse spermatogenesis |
Q37058523 | Tethering of proteins to RNAs by bacteriophage proteins |
Q37989882 | The 5' → 3' exoribonuclease XRN1/Pacman and its functions in cellular processes and development |
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Q39181215 | The Arabidopsis tandem zinc finger protein AtTZF1 affects ABA- and GA-mediated growth, stress and gene expression responses |
Q51922916 | The Arabidopsis tandem zinc finger protein AtTZF1 traffics between the nucleus and cytoplasmic foci and binds both DNA and RNA. |
Q34536989 | The Biosynthesis Characteristics of TTP and TNF Can Be Regulated through a Posttranscriptional Molecular Loop |
Q37177771 | The C-Terminal RGG Domain of Human Lsm4 Promotes Processing Body Formation Stimulated by Arginine Dimethylation. |
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