Design of a Novel Gene Therapy Construct to Achieve Sustained Brain-Derived Neurotrophic Factor Signaling in NeuronsAndrew Osborne(University of Cambridge), Keith R. Martin(University of Cambridge)Human Gene TherapyFebruary 22, 201810.1089/hum.2017.069Cited by 43SaveCiteExport RISWatch citationsRelated PapersReceptor-ligand supplementation via a self-cleaving 2A peptide–based gene therapy promotes CNS axonal transport with functional recovery|Science Advances|2021|34Hydrostatic Pressure Does Not Cause Detectable Changes in Survival of Human Retinal Ganglion Cells|PLoS ONE|2015|23