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Molecular Therapy. Nucleic Acids|March 4, 2018
Transcriptome Profiling of Neovascularized Corneas Reveals miR-204 as a Multi-target Biotherapy Deliverable by rAAVsYi Lu, Phillip W L Tai, Jianzhong Ai, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|January 15, 2019
Evaluation of portable colposcopy and human papillomavirus testing for screening of cervical cancer in rural ChinaHaley Newman, Jilin Hu, Xiao Li, et al.
Iscience|May 11, 2026
An improved method for high-purity isolation of oligodendrocytes from neonatal and adult mouse brainPeiyi Guo, Elisabet Mandon, Jie Wang, et al.
Human Gene Therapy|May 16, 2009
Adeno-associated virus-mediated gene transfer to nonhuman primate liver can elicit destructive transgene-specific T cell responsesGuangping Gao, Qiang Wang, Roberto Calcedo, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 4, 2023
Schnurri-3 inhibition suppresses bone and joint damage in models of rheumatoid arthritisZheni Stavre, Jung-Min Kim, Yeon-Suk Yang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|November 2, 2005
High levels of persistent expression of alpha1-antitrypsin mediated by the nonhuman primate serotype rh.10 adeno-associated virus despite preexisting immunity to common human adeno-associated virusesBishnu P De, Adriana Heguy, Neil R Hackett, et al.
Human Gene Therapy|November 14, 2017
Delivery of Adeno-Associated Virus Vectors in Adult Mammalian Inner-Ear Cell Subtypes Without Auditory DysfunctionYong Tao, Mingqian Huang, Yilai Shu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 25, 2021
AAV5 delivery of CRISPR-Cas9 supports effective genome editing in mouse lung airwayShun-Qing Liang, Christopher J Walkey, Alexa E Martinez, et al.
International Journal of Medical Sciences|September 15, 2021
Cellular and Tissue Selectivity of AAV Serotypes for Gene Delivery to Chondrocytes and CartilageDong Suk Yoon, Kyoung-Mi Lee, Sehee Cho, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 26, 2011
Several rAAV vectors efficiently cross the blood-brain barrier and transduce neurons and astrocytes in the neonatal mouse central nervous systemHongwei Zhang, Bin Yang, Xin Mu, et al.
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