j integr plant biol, 2024, https:// doi: 10.1111/jipb.13729
abstract
two guanine base editors created using an engineered n-methylpurine dna glycosylase with crispr systems achieved targeted g-to-t editing with 4.94-12.50% efficiency in rice (oryza sativa). the combined use of the dna glycosylase and deaminases enabled co-editing of target guanines with adenines or cytosines.
j integr plant biol,if=9.3
