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Recruitment of human eIF4G1 or DAP5 to the 5’ untranslated regions of a subset of cellular mRNAs drives cap-independent translation
Solomon A. Haizel, Usha Bhardwaj, View ORCID ProfileRuben L. Gonzalez Jr., Somdeb Mitra, View ORCID ProfileDixie J. Goss
doi: https://doi.org/10.1101/472498
Solomon A. Haizel
aPh.D. Program in Biochemistry, The Graduate Center of the City University of New York, New York, NY 10016
bDepartment of Chemistry, Hunter College, New York, NY 10065
Usha Bhardwaj
bDepartment of Chemistry, Hunter College, New York, NY 10065
Ruben L. Gonzalez Jr.
cDepartment of Chemistry, Columbia University, New York, NY 10027
Somdeb Mitra
cDepartment of Chemistry, Columbia University, New York, NY 10027
dDepartment of Chemistry, New York University, New York, NY 10003
Dixie J. Goss
aPh.D. Program in Biochemistry, The Graduate Center of the City University of New York, New York, NY 10016
bDepartment of Chemistry, Hunter College, New York, NY 10065
ePh.D. Program in Chemistry, The Graduate Center of the City University of New York, New York, NY 10016
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Posted November 16, 2018.
Recruitment of human eIF4G1 or DAP5 to the 5’ untranslated regions of a subset of cellular mRNAs drives cap-independent translation
Solomon A. Haizel, Usha Bhardwaj, Ruben L. Gonzalez Jr., Somdeb Mitra, Dixie J. Goss
bioRxiv 472498; doi: https://doi.org/10.1101/472498
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