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References in periodicals archive ?
Recruitment of mRNA in eukaryotes is a multistep process involving initiation, elongation, and termination involving mature mRNA, free 40S ribosomal subunits, and many translation factors, including the eukaryotic translation initiation factors, eIF4E (in this study termed eIF4E1), eIF4A, and eIF4G (Merrick & Pavitt 2018).
Borden, "Phosphorylation of the eukaryotic translation initiation factor eIF4E contributes to its transformation and mRNA transport activities," Cancer Research, vol.
Chai, "Lentivirus-mediated knockdown of eukaryotic translation initiation factor 3 subunit D inhibits proliferation of HCT116 colon cancer cells," Bioscience Reports, vol.
Manaka et al., "Externalization and recognition by macrophages of large subunit of eukaryotic translation initiation factor 3 in apoptotic cells," Experimental Cell Research, vol.
Hekerman et al., "Selective inhibition of eukaryotic translation initiation factor 2[alpha] dephosphorylation potentiates fatty acid-induced endoplasmic reticulum stress and causes pancreatic [beta]-cell dysfunction and apoptosis," Journal of Biological Chemistry, vol.
ATF4, activating transcription factor 4; CHOP, C/EBP homolog protein; eIF2[alpha], eukaryotic translation initiation factor 2[alpha]; GADD34, growth arrest and DNA-damage inducible 34; GCN2, general control nonderepressible 2; HRI, haem-regulated inhibitor kinase; P, inorganic phosphate; PERK, protein kinase RNA-like endoplasmic reticulum kinase; PKR, double-stranded RNA-activated protein kinase; PP1, protein phosphatase 1.
The report provides comprehensive information on the Eukaryotic Translation Initiation Factor 4E (eIF-4E), targeted therapeutics, complete with analysis by indications, stage of development, mechanism of action (MoA), route of administration (RoA) and molecule type.
* The report provides a snapshot of the global therapeutic landscape for Eukaryotic Translation Initiation Factor 4E (eIF-4E)
Relationship between eukaryotic translation initiation factor 4E and malignant angiogenesis in non-Hodgkin lymphoma.
Upon activation, mTORC1 directly phosphorylates the eukaryotic translation initiation factor 4E (eIF4E) binding protein 1 (4E-BP1) and S6 kinase 1 (S6K1) to promote protein synthesis [30].
After the initiation of the ER stress response, it can mediate cellular apoptosis by phosphorylating the eukaryotic translation initiation factor 2a (eIF2a).
On close examination of the cell cycle regulatory proteins such as p27, Ki67 cyclin D1, and P53 and eukaryotic translation initiation factors 4E and 2 alpha expression, TCV exhibits a molecular profile which is comparable to thyroid tumours with an unfavourable prognosis [4,16-19].
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