Common AAV gene therapy vectors show indiscriminate transduction of living human brain cell types.
McGinnis JP, Ortiz-Guzman J, Guevara MC, Mallannagari S, Belfort BDW, Bao S, Srivastava S, Morkas M, Ji E, Addison A, Tantry EK, Chen S, Wang Y, Chen Z, Katlowitz KA, Lange JJ, Blessing MM, Mohila CA, Ljungberg MC, Aldave G, Jalali A, Patel A, Sheth SA, Weiner HL, Gopinath S, Rao G, Harmanci AS, Curry D, Arenkiel BR.
McGinnis JP, et al. Among authors: weiner hl.
bioRxiv [Preprint]. 2024 Nov 15:2024.11.14.623624. doi: 10.1101/2024.11.14.623624.
bioRxiv. 2024.
PMID: 39605617
Free PMC article.
Preprint.