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Frontiers in Molecular Biosciences|March 3, 2022
Modulation of miRISC-Mediated Gene Silencing in EukaryotesCourtney F Jungers, Sergej Djuranovic
Nature Communications|July 27, 2025
U-rich elements drive pervasive cryptic splicing in 3' UTR massively parallel reporter assaysKhoa Dao, Courtney F Jungers, Sergej Djuranovic, et al.
Biorxiv : the Preprint Server for Biology|August 16, 2024
U-rich elements drive pervasive cryptic splicing in 3' UTR massively parallel reporter assaysKhoa Dao, Courtney F Jungers, Sergej Djuranovic, et al.
The Journal of Biological Chemistry|July 25, 2020
Regulation of eukaryotic translation initiation factor 6 dynamics through multisite phosphorylation by GSK3Courtney F Jungers, Jonah M Elliff, Daniela S Masson-Meyers, et al.
Biorxiv : the Preprint Server for Biology|August 16, 2024
Role of U11/U12 minor spliceosome gene ZCRB1 in Ciliogenesis and WNT SignalingGeralle Powell-Rodgers, Mujeeb Ur Rehman Pirzada, Jahmiera Richee, et al.
Life Science Alliance|May 27, 2026
Loss of U11/U12 spliceosome gene ZCRB1 leads to aberrant ciliogenesis and WNT signalingMujeeb Ur Rehman Pirzada, Geralle Powell-Rodgers, Jahmiera Richee, et al.
Nature Communications|August 5, 2025
A rapid, simple, and economical method for the isolation of ribosomes and translational machinery for structural and functional studiesJessey Erath, Danielle Kemper, Elisha Mugo, et al.
Biorxiv : the Preprint Server for Biology|November 1, 2024
A rapid, facile, and economical method for the isolation of ribosomes and translational machinery for structural and functional studiesJessey Erath, Danielle Kemper, Elisha Mugo, et al.
Medrxiv : the Preprint Server for Health Sciences|November 14, 2023
A Massively Parallel Screen of 5'UTR Mutations Identifies Variants Impacting Translation and Protein Production in Neurodevelopmental Disorder GenesStephen P Plassmeyer, Colin P Florian, Michael J Kasper, et al.
Cell Reports Methods|December 4, 2025
Approaches for identification of 5' UTR mutations impacting translation and protein production from neurodevelopmental disorder genesStephen P Plassmeyer, Colin P Florian, Rebecca Chase, et al.
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