138 related articles for article (PubMed ID: 27814599)
1. The Bad, the Good and eIF3e/INT6.
Sesen J; Casaos J; Scotland SJ; Seva C; Eisinger-Mathason TS; Skuli N
Front Biosci (Landmark Ed); 2017 Jan; 22(1):1-20. PubMed ID: 27814599
[TBL] [Abstract][Full Text] [Related]
2. Int6/eIF3e silencing promotes functional blood vessel outgrowth and enhances wound healing by upregulating hypoxia-induced factor 2alpha expression.
Chen L; Endler A; Uchida K; Horiguchi S; Morizane Y; Iijima O; Toi M; Shibasaki F
Circulation; 2010 Aug; 122(9):910-9. PubMed ID: 20713899
[TBL] [Abstract][Full Text] [Related]
3. Decreased eIF3e/Int6 expression causes epithelial-to-mesenchymal transition in breast epithelial cells.
Gillis LD; Lewis SM
Oncogene; 2013 Aug; 32(31):3598-605. PubMed ID: 22907435
[TBL] [Abstract][Full Text] [Related]
4. Mammalian tumor suppressor Int6 specifically targets hypoxia inducible factor 2 alpha for degradation by hypoxia- and pVHL-independent regulation.
Chen L; Uchida K; Endler A; Shibasaki F
J Biol Chem; 2007 Apr; 282(17):12707-16. PubMed ID: 17324924
[TBL] [Abstract][Full Text] [Related]
5. Int6 silencing causes induction of angiogenic factors in neuronal cells via accumulation of hypoxia-inducible factor 2α and decreases brain damage in rats.
Miyashita R; Chen L; Oshiro H; Uchino H; Shibasaki F
Neurosci Lett; 2012 Oct; 528(1):83-8. PubMed ID: 22960363
[TBL] [Abstract][Full Text] [Related]
6. Int6/eIF3e is essential for proliferation and survival of human glioblastoma cells.
Sesen J; Cammas A; Scotland SJ; Elefterion B; Lemarié A; Millevoi S; Mathew LK; Seva C; Toulas C; Moyal EC; Skuli N
Int J Mol Sci; 2014 Jan; 15(2):2172-90. PubMed ID: 24481065
[TBL] [Abstract][Full Text] [Related]
7. Int6/eIF3e silenced HIF2α stabilization enhances migration and tube formation of HUVECs via IL-6 and IL-8 signaling.
Endler A; Chen L; Li Q; Uchida K; Hashimoto T; Lu L; Xu GT; Shibasaki F
Cytokine; 2013 Apr; 62(1):115-22. PubMed ID: 23478175
[TBL] [Abstract][Full Text] [Related]
8. Silencing of eIF3e promotes blood perfusion recovery after limb ischemia through stabilization of hypoxia-inducible factor 2α activity.
Hashimoto T; Chen L; Kimura H; Endler A; Koyama H; Miyata T; Shibasaki F; Watanabe T
J Vasc Surg; 2016 Jul; 64(1):219-226.e3. PubMed ID: 25758454
[TBL] [Abstract][Full Text] [Related]
9. INT6/eIF3e represses E-cadherin expression through HIF2α in lung carcinoma A549 cells.
Gotoh-Saito S; Sadato D; Shibasaki F
Genes Cells; 2022 Dec; 27(12):689-705. PubMed ID: 36116043
[TBL] [Abstract][Full Text] [Related]
10. Human INT6/eIF3e is required for nonsense-mediated mRNA decay.
Morris C; Wittmann J; Jäck HM; Jalinot P
EMBO Rep; 2007 Jun; 8(6):596-602. PubMed ID: 17468741
[TBL] [Abstract][Full Text] [Related]
11. Cell cycle-related variation in subcellular localization of eIF3e/INT6 in human fibroblasts.
Watkins SJ; Norbury CJ
Cell Prolif; 2004 Apr; 37(2):149-60. PubMed ID: 15030549
[TBL] [Abstract][Full Text] [Related]
12. An oncogenic role of eIF3e/INT6 in human breast cancer.
Grzmil M; Rzymski T; Milani M; Harris AL; Capper RG; Saunders NJ; Salhan A; Ragoussis J; Norbury CJ
Oncogene; 2010 Jul; 29(28):4080-9. PubMed ID: 20453879
[TBL] [Abstract][Full Text] [Related]
13. Int6 regulates both proteasomal degradation and translation initiation and is critical for proper formation of acini by human mammary epithelium.
Suo J; Snider SJ; Mills GB; Creighton CJ; Chen AC; Schiff R; Lloyd RE; Chang EC
Oncogene; 2011 Feb; 30(6):724-36. PubMed ID: 20890303
[TBL] [Abstract][Full Text] [Related]
14. Arabidopsis eIF3e is regulated by the COP9 signalosome and has an impact on development and protein translation.
Yahalom A; Kim TH; Roy B; Singer R; von Arnim AG; Chamovitz DA
Plant J; 2008 Jan; 53(2):300-11. PubMed ID: 18067529
[TBL] [Abstract][Full Text] [Related]
15. Expression of truncated eukaryotic initiation factor 3e (eIF3e) resulting from integration of mouse mammary tumor virus (MMTV) causes a shift from cap-dependent to cap-independent translation.
Chiluiza D; Bargo S; Callahan R; Rhoads RE
J Biol Chem; 2011 Sep; 286(36):31288-96. PubMed ID: 21737453
[TBL] [Abstract][Full Text] [Related]
16. INT6 interacts with MIF4GD/SLIP1 and is necessary for efficient histone mRNA translation.
Neusiedler J; Mocquet V; Limousin T; Ohlmann T; Morris C; Jalinot P
RNA; 2012 Jun; 18(6):1163-77. PubMed ID: 22532700
[TBL] [Abstract][Full Text] [Related]
17. Silencing of int6 gene restores function of the ischaemic hindlimb in a rat model of peripheral arterial disease.
Okamoto N; Tanaka A; Jung K; Karasawa K; Orito K; Matsuda A; Amagai Y; Oida K; Ohmori K; Matsuda H
Cardiovasc Res; 2011 Nov; 92(2):209-17. PubMed ID: 21771896
[TBL] [Abstract][Full Text] [Related]
18. INT6/EIF3E interacts with ATM and is required for proper execution of the DNA damage response in human cells.
Morris C; Tomimatsu N; Richard DJ; Cluet D; Burma S; Khanna KK; Jalinot P
Cancer Res; 2012 Apr; 72(8):2006-16. PubMed ID: 22508697
[TBL] [Abstract][Full Text] [Related]
19. The human T-lymphotropic virus type 1 tax protein inhibits nonsense-mediated mRNA decay by interacting with INT6/EIF3E and UPF1.
Mocquet V; Neusiedler J; Rende F; Cluet D; Robin JP; Terme JM; Duc Dodon M; Wittmann J; Morris C; Le Hir H; Ciminale V; Jalinot P
J Virol; 2012 Jul; 86(14):7530-43. PubMed ID: 22553336
[TBL] [Abstract][Full Text] [Related]
20. Eukaryotic translation initiation factor 3 (eIF3) subunit e is essential for embryonic development and cell proliferation.
Sadato D; Ono T; Gotoh-Saito S; Kajiwara N; Nomura N; Ukaji M; Yang L; Sakimura K; Tajima Y; Oboki K; Shibasaki F
FEBS Open Bio; 2018 Aug; 8(8):1188-1201. PubMed ID: 30087825
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]