Population
Cells infected with dicistronic retroviral vectors designed to express human placental alkaline phosphatase…
Design
Preclinical
Follow-up
prolonged culture
Authors
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Advances dicistronic vector feasibility in preclinical models; leaves open translation to human gene therapy.
The use of VL30 and MoMLV 5' leader sequences with IRES and packaging functions enables the creation of stable, high-titer dicistronic retroviral vectors for efficient coexpression of two exogenous genes.
Torrent et al. (1996) studied this question.
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