scholarly article | Q13442814 |
P356 | DOI | 10.1261/RNA.032631.112 |
P8608 | Fatcat ID | release_bhw7s6jfifaanptvryc7wwubdi |
P932 | PMC publication ID | 3358639 |
P698 | PubMed publication ID | 22532700 |
P5875 | ResearchGate publication ID | 224836336 |
P2093 | author name string | Taran Limousin | |
Theophile Ohlmann | |||
Pierre Jalinot | |||
Christelle Morris | |||
Julia Neusiedler | |||
Vincent Mocquet | |||
P2860 | cites work | Interaction between the Ret finger protein and the Int-6 gene product and co-localisation into nuclear bodies | Q22010587 |
Human INT6 interacts with MCM7 and regulates its stability during S phase of the cell cycle | Q24297698 | ||
Mammalian tumor suppressor Int6 specifically targets hypoxia inducible factor 2 alpha for degradation by hypoxia- and pVHL-independent regulation | Q24298432 | ||
Human INT6/eIF3e is required for nonsense-mediated mRNA decay | Q24304228 | ||
Mass spectrometry reveals modularity and a complete subunit interaction map of the eukaryotic translation factor eIF3 | Q24309617 | ||
The translation initiation factor eIF3-p48 subunit is encoded by int-6, a site of frequent integration by the mouse mammary tumor virus genome | Q24311711 | ||
PCI complexes: Beyond the proteasome, CSN, and eIF3 Troika. | Q37580456 | ||
Regulation of protein synthesis and the role of eIF3 in cancer | Q37797917 | ||
Int6 regulates both proteasomal degradation and translation initiation and is critical for proper formation of acini by human mammary epithelium | Q39648518 | ||
Evidence for the transforming activity of a truncated Int6 gene, in vitro | Q40782244 | ||
A core complex of CPSF73, CPSF100, and Symplekin may form two different cleavage factors for processing of poly(A) and histone mRNAs | Q41656652 | ||
SLIP1, a factor required for activation of histone mRNA translation by the stem-loop binding protein | Q41911054 | ||
Orientation and expression of methicillin-resistant Staphylococcus aureus small RNAs by direct multiplexed measurements using the nCounter of NanoString technology | Q42684914 | ||
Int6/eIF3e silencing promotes functional blood vessel outgrowth and enhances wound healing by upregulating hypoxia-induced factor 2alpha expression | Q42823549 | ||
An oncogenic role of eIF3e/INT6 in human breast cancer | Q45384502 | ||
Fission yeast homolog of murine Int-6 protein, encoded by mouse mammary tumor virus integration site, is associated with the conserved core subunits of eukaryotic translation initiation factor 3. | Q45739186 | ||
Arabidopsis eIF3e (INT-6) associates with both eIF3c and the COP9 signalosome subunit CSN7. | Q47822595 | ||
The Arabidopsis homologue of an eIF3 complex subunit associates with the COP9 complex | Q48002052 | ||
ESTablishing a human transcript map | Q72048152 | ||
Silencing of human Int-6 impairs mitosis progression and inhibits cyclin B-Cdk1 activation | Q81042711 | ||
The polyadenylation factor CPSF-73 is involved in histone-pre-mRNA processing | Q81327465 | ||
Reconstitution reveals the functional core of mammalian eIF3 | Q24312641 | ||
Regulated degradation of replication-dependent histone mRNAs requires both ATR and Upf1 | Q24313451 | ||
Knockdown of SLBP results in nuclear retention of histone mRNA | Q24318762 | ||
Conserved motifs in both CPSF73 and CPSF100 are required to assemble the active endonuclease for histone mRNA 3'-end maturation | Q24321829 | ||
Characterization of the interaction between the interferon-induced protein P56 and the Int6 protein encoded by a locus of insertion of the mouse mammary tumor virus | Q24524346 | ||
Symplekin and multiple other polyadenylation factors participate in 3'-end maturation of histone mRNAs | Q24537115 | ||
Yin6, a fission yeast Int6 homolog, complexes with Moe1 and plays a role in chromosome segregation | Q24672269 | ||
Genome-wide analysis of mRNAs bound to the histone stem-loop binding protein | Q24674162 | ||
Int-6, a highly conserved, widely expressed gene, is mutated by mouse mammary tumor virus in mammary preneoplasia | Q24676100 | ||
PCI proteins eIF3e and eIF3m define distinct translation initiation factor 3 complexes | Q24815484 | ||
The retinoblastoma protein associates with the protein phosphatase type 1 catalytic subunit | Q27860669 | ||
Complex formation by all five homologues of mammalian translation initiation factor 3 subunits from yeast Saccharomyces cerevisiae | Q27931017 | ||
Identification of a translation initiation factor 3 (eIF3) core complex, conserved in yeast and mammals, that interacts with eIF5 | Q27937750 | ||
Association of the mammalian proto-oncoprotein Int-6 with the three protein complexes eIF3, COP9 signalosome and 26S proteasome | Q28200835 | ||
The human histone gene expression regulator HBP/SLBP is required for histone and DNA synthesis, cell cycle progression and cell proliferation in mitotic cells | Q28293702 | ||
Formation of the 3' end of histone mRNA: getting closer to the end | Q28751417 | ||
Direct multiplexed measurement of gene expression with color-coded probe pairs | Q29614417 | ||
A versatile in vivo and in vitro eukaryotic expression vector for protein engineering | Q29620181 | ||
Translation initiation factor eIF4G-1 binds to eIF3 through the eIF3e subunit | Q33246406 | ||
Schizosaccharomyces pombe Int6 and Ras homologs regulate cell division and mitotic fidelity via the proteasome | Q34173343 | ||
The histone 3'-terminal stem-loop-binding protein enhances translation through a functional and physical interaction with eukaryotic initiation factor 4G (eIF4G) and eIF3 | Q34303822 | ||
Cell cycle-related variation in subcellular localization of eIF3e/INT6 in human fibroblasts | Q34306923 | ||
The stem-loop binding protein stimulates histone translation at an early step in the initiation pathway | Q34366460 | ||
Exclusion of Int-6 from PML nuclear bodies by binding to the HTLV-I Tax oncoprotein. | Q34387191 | ||
Structural roles for human translation factor eIF3 in initiation of protein synthesis | Q34472092 | ||
eIF3: a versatile scaffold for translation initiation complexes | Q34558903 | ||
A fission yeast homolog of Int-6, the mammalian oncoprotein and eIF3 subunit, induces drug resistance when overexpressed | Q34778925 | ||
Fission yeast Int6 is not essential for global translation initiation, but deletion of int6(+) causes hypersensitivity to caffeine and affects spore formation | Q34779158 | ||
Expression of truncated Int6/eIF3e in mammary alveolar epithelium leads to persistent hyperplasia and tumorigenesis | Q36393252 | ||
Poly(A)-binding protein-interacting protein 1 binds to eukaryotic translation initiation factor 3 to stimulate translation | Q36949719 | ||
Staged assembly of histone gene expression machinery at subnuclear foci in the abbreviated cell cycle of human embryonic stem cells | Q36964278 | ||
Translation factors promote the formation of two states of the closed-loop mRNP. | Q36984169 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1163-1177 | |
P577 | publication date | 2012-04-24 | |
P1433 | published in | RNA | Q7277164 |
P1476 | title | INT6 interacts with MIF4GD/SLIP1 and is necessary for efficient histone mRNA translation | |
P478 | volume | 18 |