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Leukemia & Lymphoma|June 7, 2006
Evaluation of biologic activity of tryptase secreted from blast cells in acute myeloid leukemiaKaroline Sonneck, Stefan Florian, Alexandra Böhm, et al.
Gene Therapy|March 19, 2010
Self-complementary AAV-mediated gene therapy restores cone function and prevents cone degeneration in two models of Rpe65 deficiencyJ Pang, S E Boye, B Lei, et al.
Investigative Ophthalmology & Visual Science|February 5, 2016
Targeting the Nrf2 Signaling Pathway in the Retina With a Gene-Delivered Secretable and Cell-Penetrating PeptideCristhian J Ildefonso, Henrique Jaime, Emily E Brown, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 18, 2005
Long-term restoration of rod and cone vision by single dose rAAV-mediated gene transfer to the retina in a canine model of childhood blindnessGregory M Acland, Gustavo D Aguirre, Jean Bennett, et al.
The American Journal of Pathology|February 28, 2009
Lowering blood pressure blocks mesangiolysis and mesangial nodules, but not tubulointerstitial injury, in diabetic eNOS knockout miceTomoki Kosugi, Marcelo Heinig, Takahiro Nakayama, et al.
Gene Therapy|June 28, 2019
Effects of a combinatorial treatment with gene and cell therapy on retinal ganglion cell survival and axonal outgrowth after optic nerve injuryGabriel Nascimento-Dos-Santos, Leandro Coelho Teixeira-Pinheiro, Almir Jordão da Silva-Júnior, et al.
Gene Therapy|April 8, 2016
Reduced retinal transduction and enhanced transgene-directed immunogenicity with intravitreal delivery of rAAV following posterior vitrectomy in dogsR F Boyd, S L Boye, T J Conlon, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 9, 2010
Long-term retinal function and structure rescue using capsid mutant AAV8 vector in the rd10 mouse, a model of recessive retinitis pigmentosaJi-jing Pang, Xufeng Dai, Shannon E Boye, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 10, 2013
Transient photoreceptor deconstruction by CNTF enhances rAAV-mediated cone functional rescue in late stage CNGB3-achromatopsiaAndrás M Komáromy, Jessica S Rowlan, Amanda T Parton Corr, et al.
JAMA Ophthalmology|January 25, 2014
Safety and effects of the vector for the Leber hereditary optic neuropathy gene therapy clinical trialRajeshwari D Koilkonda, Hong Yu, Tsung-Han Chou, et al.
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