A Single Injection of Recombinant Adeno-Associated Virus into the Lumbar Cistern Delivers Transgene Expression Throughout the Whole Spinal Cord.

Guo Y, Wang D, Qiao T, Yang C, Su Q, Gao G, Xu Z. Mol Neurobiol. 2016 Jul;53(5):3235-48.

Axonal transport of AAV9 in nonhuman primate brain.

Green F, Samaranch L, Zhang HS, Manning-Bog A, Meyer K, Forsayeth J, Bankiewicz KS. Gene Ther. 2016 Jun;23(6):520-6.

AAV viral vector delivery to the brain by shape-conforming MR-guided infusions.

Bankiewicz KS, Sudhakar V, Samaranch L, San Sebastian W, Bringas J, Forsayeth J. J Control Release. 2016 Feb 27.

MRI-Guided Delivery of Viral Vectors.

Salegio EA, Bringas J, Bankiewicz KS. Methods Mol Biol. 2016;1382:217-30.

State-of-the-art human gene therapy: part II. Gene therapy strategies and clinical applications.

Wang D, Gao G. Discov Med. 2014 Sep;18(98):151-61.

State-of-the-art human gene therapy: part I. Gene delivery technologies.

Wang D, Gao G. Discov Med. 2014 Jul-Aug;18(97):67-77.

The potential of adeno-associated viral vectors for gene delivery to muscle tissue.

Wang D, Zhong L, Nahid MA, Gao G. Expert Opin Drug Deliv. 2014 Mar;11(3):345-64.

AAV9-mediated expression of a non-self protein in nonhuman primate central nervous system triggers widespread neuroinflammation driven by antigen-presenting cell transduction.

Samaranch L, San Sebastian W, Kells AP, Salegio EA, Heller G, Bringas JR, Pivirotto P, DeArmond S, Forsayeth J, Bankiewicz KS. Mol Ther. 2014 Feb;22(2):329-37.

Adeno-associated virus type 6 is retrogradely transported in the non-human primate brain.

San Sebastian W, Samaranch L, Heller G, Kells AP, Bringas J, Pivirotto P, Forsayeth J, Bankiewicz KS. Gene Ther. 2013 Dec;20(12):1178-83.

Gene therapy for misfolding protein diseases of the central nervous system.

San Sebastian W, Samaranch L, Kells AP, Forsayeth J, Bankiewicz KS. Neurotherapeutics. 2013 Jul;10(3):498-510.

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