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  • Author: Walker SE
  • References

Author: Walker SE


References 11 references


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  • Liu X, et al. (2021) Deletion of the N-Terminal Domain of Yeast Eukaryotic Initiation Factor 4B Reprograms Translation and Reduces Growth in Urea. Front Mol Biosci 8:787781 PMID:35047555
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  • Liu X, et al. (2019) Reconstitution and analyses of RNA interactions with eukaryotic translation initiation factors and ribosomal preinitiation complexes. Methods 162-163:42-53 PMID:30926531
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  • Sehgal N, et al. (2018) CRISPR Gene Editing in Yeast: An Experimental Protocol for an Upper-Division Undergraduate Laboratory Course. Biochem Mol Biol Educ 46(6):592-601 PMID:30311729
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  • Munoz AM, et al. (2017) Active yeast ribosome preparation using monolithic anion exchange chromatography. RNA Biol 14(2):188-196 PMID:27981882
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  • Zhou F, et al. (2014) Identification and characterization of functionally critical, conserved motifs in the internal repeats and N-terminal domain of yeast translation initiation factor 4B (yeIF4B). J Biol Chem 289(17):11860
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  • Zhou F, et al. (2014) Identification and characterization of functionally critical, conserved motifs in the internal repeats and N-terminal domain of yeast translation initiation factor 4B (yeIF4B). J Biol Chem 289(3):1704-22 PMID:24285537
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  • Park EH, et al. (2013) Yeast eukaryotic initiation factor 4B (eIF4B) enhances complex assembly between eIF4A and eIF4G in vivo. J Biol Chem 288(4):2340-54 PMID:23184954
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  • Walker SE, et al. (2013) Yeast eIF4B binds to the head of the 40S ribosomal subunit and promotes mRNA recruitment through its N-terminal and internal repeat domains. RNA 19(2):191-207 PMID:23236192
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  • Park EH, et al. (2011) Multiple elements in the eIF4G1 N-terminus promote assembly of eIF4G1•PABP mRNPs in vivo. EMBO J 30(2):302-16 PMID:21139564
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  • Shin BS, et al. (2011) Initiation factor eIF2γ promotes eIF2-GTP-Met-tRNAi(Met) ternary complex binding to the 40S ribosome. Nat Struct Mol Biol 18(11):1227-34 PMID:22002225
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  • Mitchell SF, et al. (2010) The 5'-7-methylguanosine cap on eukaryotic mRNAs serves both to stimulate canonical translation initiation and to block an alternative pathway. Mol Cell 39(6):950-62 PMID:20864040
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