The role of mRNA turnover in the regulation of tristetraprolin expression: evidence for an extracellular signal-regulated kinase-specific, AU-rich element-dependent, autoregulatory pathway
about
CARHSP1 is required for effective tumor necrosis factor alpha mRNA stabilization and localizes to processing bodies and exosomesThe roles of TTP and BRF proteins in regulated mRNA decayCompetitive regulation of nucleolin expression by HuR and miR-494Hallmarks of cancer and AU-rich elementsInterleukin-1-inducible MCPIP protein has structural and functional properties of RNase and participates in degradation of IL-1beta mRNAmiR-29a suppresses tristetraprolin, which is a regulator of epithelial polarity and metastasisDifferential expression and functional analysis of the tristetraprolin family during early differentiation of 3T3-L1 preadipocytesFunctional analysis of KSRP interaction with the AU-rich element of interleukin-8 and identification of inflammatory mRNA targets.RhoA activation participates in rearrangement of processing bodies and release of nucleated AU-rich mRNAs.Phosphorylation site analysis of the anti-inflammatory and mRNA-destabilizing protein tristetraprolin.The UL41 protein of herpes simplex virus mediates selective stabilization or degradation of cellular mRNAs.Role of herpes simplex virus ICP27 in the degradation of mRNA by virion host shutoff RNaseEGF activates TTP expression by activation of ELK-1 and EGR-1 transcription factorsExpression, purification, and biochemical characterization of the antiinflammatory tristetraprolin: a zinc-dependent mRNA binding protein affected by posttranslational modifications.Mitogen-activated protein kinase-activated protein kinase 2 regulates tumor necrosis factor mRNA stability and translation mainly by altering tristetraprolin expression, stability, and binding to adenine/uridine-rich elementRNase L attenuates mitogen-stimulated gene expression via transcriptional and post-transcriptional mechanisms to limit the proliferative responseNitric oxide activation of Erk1/2 regulates the stability and translation of mRNA transcripts containing CU-rich elementsA masked PY-NLS in Drosophila TIS11 and its mammalian homolog tristetraprolinGlucocorticoids regulate tristetraprolin synthesis and posttranscriptionally regulate tumor necrosis factor alpha inflammatory signaling.Dominant Suppression of Inflammation via Targeted Mutation of the mRNA Destabilizing Protein Tristetraprolin.Aging impairs murine B cell differentiation and function in primary and secondary lymphoid tissuesComputational Model of MicroRNA Control of HIF-VEGF Pathway: Insights into the Pathophysiology of Ischemic Vascular Disease and CancerTristetraprolin Down-Regulation Contributes to Persistent TNF-Alpha Expression Induced by Cigarette Smoke Extract through a Post-Transcriptional MechanismRegulation of p21/CIP1/WAF-1 mediated cell-cycle arrest by RNase L and tristetraprolin, and involvement of AU-rich elements.Genome-wide map of RNA degradation kinetics patterns in dendritic cells after LPS stimulation facilitates identification of primary sequence and secondary structure motifs in mRNAs.The role of tristetraprolin in cancer and inflammation.Genome-wide analysis identifies interleukin-10 mRNA as target of tristetraprolinNegative feedback regulation of the yeast CTH1 and CTH2 mRNA binding proteins is required for adaptation to iron deficiency and iron supplementation.Cellular responses to HSV-1 infection are linked to specific types of alterations in the host transcriptome.Tristetraprolin (TTP): interactions with mRNA and proteins, and current thoughts on mechanisms of action.Post-transcriptional regulation of iron homeostasis in Saccharomyces cerevisiae.A flexible approach to studying post-transcriptional gene regulation in stably transfected mammalian cells.TIS11 family proteins and their roles in posttranscriptional gene regulation.Posttranscriptional regulation by RNA-binding proteins during epithelial-to-mesenchymal transition.MAPK signal transduction underlying brain inflammation and gliosis as therapeutic target.Interferons limit inflammatory responses by induction of tristetraprolin.RNase-L control of cellular mRNAs: roles in biologic functions and mechanisms of substrate targeting.Tristetraprolin: roles in cancer and senescence.Identification of TTP mRNA targets in human dendritic cells reveals TTP as a critical regulator of dendritic cell maturation.Transcriptional regulation of tristetraprolin by NF-κB signaling in LPS-stimulated macrophages.
P2860
Q24307398-9B2270A1-DF21-465A-B38A-78B8CFE8A2F0Q24633013-6F245B45-CD0B-4873-AA00-CF8A3B36EDAFQ24635240-A2F20A99-5E75-447A-A605-F9EBD570EC9DQ26744134-4056E2ED-B55D-4904-9F86-7977F77774D1Q28118792-123E6EB6-D334-4D9D-872F-C3839859EAC9Q28236600-AF543E10-4415-47DB-A3A3-520A18871903Q28505723-D7F1E8E2-699C-484A-BA73-4B5927FAD43CQ30480964-1FFFF0FD-E75D-4F1F-9EA6-4B391B55DA7DQ30499882-97B893AA-BC74-4ABB-9825-2E65E83B0222Q33309340-63DDB46B-A9E7-499C-A9A3-CDFAE01C0F2BQ33583191-87213E97-744F-4277-8B48-508546165139Q34120868-0EC3B06A-B014-4BE5-B429-9E8694EA169AQ34203752-88798897-AC65-4DF1-A492-704B598778D7Q34314339-26826D16-D6B5-4346-819F-44EF7E31C926Q34519852-CE3D61CD-2A6C-47E7-9CA1-E58B8C5422ACQ34580412-AE8DE59D-1C4B-4F64-99E1-6FCAB97008E7Q34666775-55F05E1B-9BAC-465A-A020-D8ECC050FAE9Q34950313-B2C07E7E-28F3-4ACE-A6EB-A5910EFD2307Q35131624-3CF7D980-3D74-4E0C-A14A-6CC23E900833Q35757055-C7A94857-618C-4E9E-8834-1BD3AA8D5FA3Q35806803-4996D8C5-1839-4417-B9C3-E86EF7014458Q35847324-F06C0B5F-84E9-4365-BEDD-E54C7A72E129Q36212077-D40D13FE-F5DC-4371-B42C-1FCBD07AA997Q36228609-35FC81B1-801B-4669-9ED1-ABC5FC04FDA7Q36268817-F0233A07-FD48-4303-A242-08B211E12EA4Q36290434-0E04A752-44E5-4D91-9F94-1185F4C5B8A0Q36727319-EFBED7B7-35BB-4B72-9CB2-CEC8F4B685DFQ36827099-BE837EEF-4EB8-4F97-B677-34AD4B3A7385Q37050034-0F20039E-1399-40D5-AFE5-AA5D4F0C9FEBQ37119721-2976369D-27B7-4484-8AB5-A2FED22B32F1Q37139091-2121A9D9-57F9-42DA-8783-788FFAAC015FQ37205768-A3EA4CBC-CBA7-4F30-89D3-A8471E5B62EAQ37292351-CF79059D-94E7-45C5-9004-FBD183BCFE50Q37308115-5F093ED5-2128-41AF-85D8-7EC53A87C186Q37640015-E650B137-0109-4D1F-9599-DCAFCA1A91A1Q37659150-C2F91CBE-8F4C-45DB-B2CD-3491204095DDQ37686220-C25D15EB-E276-4296-8C34-DF45A1E18289Q37990333-A7D3B92E-8EE2-4F93-9341-1FE42E8618E5Q38292350-9D92F3C7-5E92-4092-B109-D2E3D6CD802FQ38319526-33EE42BA-44B6-44DC-B0F3-CCED59010360
P2860
The role of mRNA turnover in the regulation of tristetraprolin expression: evidence for an extracellular signal-regulated kinase-specific, AU-rich element-dependent, autoregulatory pathway
description
2004 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հունիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2004
@ast
im Juni 2004 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2004/06/15)
@sk
vědecký článek publikovaný v roce 2004
@cs
wetenschappelijk artikel (gepubliceerd op 2004/06/15)
@nl
наукова стаття, опублікована в червні 2004
@uk
مقالة علمية (نشرت في 15-6-2004)
@ar
name
The role of mRNA turnover in t ...... endent, autoregulatory pathway
@ast
The role of mRNA turnover in t ...... endent, autoregulatory pathway
@en
The role of mRNA turnover in t ...... endent, autoregulatory pathway
@nl
type
label
The role of mRNA turnover in t ...... endent, autoregulatory pathway
@ast
The role of mRNA turnover in t ...... endent, autoregulatory pathway
@en
The role of mRNA turnover in t ...... endent, autoregulatory pathway
@nl
prefLabel
The role of mRNA turnover in t ...... endent, autoregulatory pathway
@ast
The role of mRNA turnover in t ...... endent, autoregulatory pathway
@en
The role of mRNA turnover in t ...... endent, autoregulatory pathway
@nl
P2093
P3181
P1476
The role of mRNA turnover in t ...... endent, autoregulatory pathway
@en
P2093
John E. Connolly
Seth A. Brooks
William F. C. Rigby
P304
P3181
P356
10.4049/JIMMUNOL.172.12.7263
P407
P577
2004-06-15T00:00:00Z