Population
Patients or experimental models with neurological diseases affecting the central nervous system or…
Design
Review
Authors
Loading...
HSV-1 vectors merit expanded preclinical optimization for CNS gene therapy; leaves open clinical translation pending safety and efficacy trials.
HSV-1-derived vectors represent a promising approach for gene therapy in neurological diseases and brain tumors, with ongoing research focusing on targeted and transcriptionally regulatable transgene expression.
Breakefield et al. (1999) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: