Stress granules and processing bodies are dynamically linked sites of mRNP remodeling (Q24678779)

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Language	Label	Description	Also known as
English	Stress granules and processing bodies are dynamically linked sites of mRNP remodeling	scientific article

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scholarly article

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Stress granules and processing bodies are dynamically linked sites of mRNP remodeling (English)

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author name string

Nancy Kedersha

1

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Georg Stoecklin

2

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Maranatha Ayodele

3

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Patrick Yacono

4

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Jens Lykke-Andersen

5

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Marvin J Fritzler

6

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Donalyn Scheuner

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Randal J Kaufman

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David E Golan

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Paul Anderson

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original language of film or TV show

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publication date

20 June 2005

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Journal of Cell Biology

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169

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6

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871-84

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

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GW182 is critical for the stability of GW bodies expressed during the cell cycle and cell proliferation

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

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Functional analysis of mRNA scavenger decapping enzymes

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

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Cytoplasmic foci are sites of mRNA decay in human cells

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Nonsense-mediated mRNA decay: from vacuum cleaner to Swiss army knife

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

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The GW182 protein colocalizes with mRNA degradation associated proteins hDcp1 and hLSm4 in cytoplasmic GW bodies

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The RasGAP-associated endoribonuclease G3BP assembles stress granules

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The human LSm1-7 proteins colocalize with the mRNA-degrading enzymes Dcp1/2 and Xrnl in distinct cytoplasmic foci

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Functional cloning of BRF1, a regulator of ARE-dependent mRNA turnover

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A phosphorylated cytoplasmic autoantigen, GW182, associates with a unique population of human mRNAs within novel cytoplasmic speckles

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The mammalian exosome mediates the efficient degradation of mRNAs that contain AU-rich elements

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AU binding proteins recruit the exosome to degrade ARE-containing mRNAs

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Control of mRNA decay by heat shock-ubiquitin-proteasome pathway

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Decapping and Decay of Messenger RNA Occur in Cytoplasmic Processing Bodies

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Targeting an mRNA for decapping: displacement of translation factors and association of the Lsm1p-7p complex on deadenylated yeast mRNAs

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The 3' to 5' degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 3' to 5' exonucleases of the exosome complex

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Recruitment and activation of mRNA decay enzymes by two ARE-mediated decay activation domains in the proteins TTP and BRF-1

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A monomeric red fluorescent protein

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