Design of a Novel Gene Therapy Construct to Achieve Sustained Brain-Derived Neurotrophic Factor Signaling in Neurons

por Osborne, Andrew, Wang, Aiden X.Z., Tassoni, Alessia, Widdowson, Peter S., Martin, Keith R.
Publicado 2018

Angiopoietins in Diabetic Retinopathy: Current Understanding and Therapeutic Potential

por Whitehead, Michael, Osborne, Andrew, Widdowson, Peter S., Yu-Wai-Man, Patrick, Martin, Keith R.
Publicado 2019

Neuroprotection of retinal ganglion cells by a novel gene therapy construct that achieves sustained enhancement of brain-derived neurotrophic factor/tropomyosin-related kinase rece...

por Osborne, Andrew, Khatib, Tasneem Z., Songra, Lalana, Barber, Amanda C., Hall, Katie, Kong, George Y. X., Widdowson, Peter S., Martin, Keith R.
Publicado 2018

Receptor-ligand supplementation via a self-cleaving 2A peptide–based gene therapy promotes CNS axonal transport with functional recovery

por Khatib, Tasneem Z., Osborne, Andrew, Yang, Sujeong, Ali, Zara, Jia, Wanyi, Manyakin, Ilya, Hall, Katie, Watt, Robert, Widdowson, Peter S., Martin, Keith R.
Publicado 2021

EIAV-Based Retinal Gene Therapy in the shaker1 Mouse Model for Usher Syndrome Type 1B: Development of UshStat

por Zallocchi, Marisa, Binley, Katie, Lad, Yatish, Ellis, Scott, Widdowson, Peter, Iqball, Sharifah, Scripps, Vicky, Kelleher, Michelle, Loader, Julie, Miskin, James, Peng, You-Wei, Wang, Wei-Min, Cheung, Linda, Delimont, Duane, Mitrophanous, Kyriacos A., Cosgrove, Dominic
Publicado 2014