E. Bote

Widespread gene transfer in the central nervous system of cynomolgus macaques following delivery of AAV9 into the cisterna magna

B. Pukenas, C. Vite, James M. Wilson, 2014, Molecular therapy. Methods & clinical development.

Evaluation of Intrathecal Routes of Administration for Adeno-Associated Viral Vectors in Large Animals.

C. Vite, James M. Wilson, Nathan Katz, 2018, Human gene therapy.

AAV8 Gene Therapy for Crigler-Najjar Syndrome in Macaques Elicited Transgene T Cell Responses That Are Resident to the Liver

M. Betts, James M. Wilson, R. Calcedo, 2018, Molecular therapy. Methods & clinical development.

Optimized Adeno-Associated Viral-Mediated Human Factor VIII Gene Therapy in Cynomolgus Macaques.

Lili Wang, James M. Wilson, S. Wadsworth, 2018, Human gene therapy.

Safety and Efficacy of Subretinal Readministration of a Viral Vector in Large Animals to Treat Congenital Blindness

J. Golden, J. Bennett, K. High, 2010, Science Translational Medicine.

Impact of intravenous infusion time on AAV8 vector pharmacokinetics, safety, and liver transduction in cynomolgus macaques

James M. Wilson, L. Kattenhorn, P. Bell, 2016, Molecular therapy. Methods & clinical development.

Safety and Efficacy of Subretinal Readministration of a Viral Vector in Large Animals to Treat Congenital Blindness

J. Golden, J. Bennett, K. High, 2010, Science Translational Medicine.