Population
Poliovirus genome manipulated by replacing its 2A-encoding sequence with the corresponding sequence of…
Comparison
Chimeric PV genomes and introduction of specific… vs Wild-type PV genome (implied)
Design
Preclinical
Authors
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CBV4 2A(pro) functionally substitutes for PV in chimeras with targeted mutations; extends enterovirus compatibility data but leaves open any translational applications.
The 2A(pro) protein of the closely related enterovirus CBV4 can functionally substitute for that of PV in vivo, and specific genetic modifications can drastically improve the growth of the chimeric virus.
Lu et al. (1995) studied this question.
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