Associated Papers
Prime editing-installed suppressor tRNAs for disease-agnostic genome editing.
Pierce SE et al.
Nature, 2025
41261131 (PubMed )
Supplement: 41586_2025_9732_MOESM17_ESM.xlsx › Sequence_Context_Screen
Loss-of-function mutations in KIF14 cause severe microcephaly and kidney development defects in humans and zebrafish.
Reilly ML et al.
Human Molecular Genetics, 2019
Mutations of KIF14 cause primary microcephaly by impairing cytokinesis.
Moawia A et al.
Annals of Neurology, 2017
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