The death domain protein p84N5, but not the short isoform p84N5s, is cell cycle-regulated and shuttles between the nucleus and the cytoplasm (Q24303509)

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English	The death domain protein p84N5, but not the short isoform p84N5s, is cell cycle-regulated and shuttles between the nucleus and the cytoplasm	scientific article

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The death domain protein p84N5, but not the short isoform p84N5s, is cell cycle-regulated and shuttles between the nucleus and the cytoplasm (English)

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GOA release 2020-03-11

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Marta Muzio

4

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Fabio Gasparri

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Francesco Sola

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Giuseppe Locatelli

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language of work or name

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publication date

10 September 2004

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574

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1-3

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13-9

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Live or let die: the cell's response to p53

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The role of p53 and pRB in apoptosis and cancer

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Rb function in cell-cycle regulation and apoptosis

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E2F-1-mediated transactivation is inhibited by complex formation with the retinoblastoma susceptibility gene product

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The amino-terminal region of the retinoblastoma gene product binds a novel nuclear matrix protein that co-localizes to centers for RNA processing

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TREX is a conserved complex coupling transcription with messenger RNA export

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Nuclear localization is required for induction of apoptotic cell death by the Rb-associated p84N5 death domain protein

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The death domain: a module shared by proteins with diverse cellular functions.

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IRAK (Pelle) family member IRAK-2 and MyD88 as proximal mediators of IL-1 signaling

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FLICE, a novel FADD-homologous ICE/CED-3-like protease, is recruited to the CD95 (Fas/APO-1) death--inducing signaling complex

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Analysis of canonical and non-canonical splice sites in mammalian genomes

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Recycling the Cell Cycle

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Trichostatin and leptomycin. Inhibition of histone deacetylation and signal-dependent nuclear export

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Mutation of E2f-1 suppresses apoptosis and inappropriate S phase entry and extends survival of Rb-deficient mouse embryos

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Apoptosis induced by the nuclear death domain protein p84N5 is inhibited by association with Rb protein

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.07.074

7 January 2021

based on heuristic

inferred from DOI database lookup

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