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Proceedings of the National Academy of Sciences of the United States of America|March 17, 2010
Restoration of visual function in P23H rhodopsin transgenic rats by gene delivery of BiP/Grp78Marina S Gorbatyuk, Tessa Knox, Matthew M LaVail, et al.
Plos One|October 22, 2013
Recombinant AAV-mediated BEST1 transfer to the retinal pigment epithelium: analysis of serotype-dependent retinal effectsKarina E Guziewicz, Barbara Zangerl, András M Komáromy, et al.
American Journal of Physiology. Renal Physiology|October 31, 2008
Angiostatin overexpression is associated with an improvement in chronic kidney injury by an anti-inflammatory mechanismWei Mu, David A Long, Xiaosen Ouyang, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|May 22, 2012
CCN2/CTGF regulates neovessel formation via targeting structurally conserved cystine knot motifs in multiple angiogenic regulatorsLiya Pi, Anitha K Shenoy, Jianwen Liu, et al.
Investigative Ophthalmology & Visual Science|February 22, 2014
AAV-mediated lysophosphatidylcholine acyltransferase 1 (Lpcat1) gene replacement therapy rescues retinal degeneration in rd11 miceXufeng Dai, Juanjuan Han, Yan Qi, et al.
International Journal of Immunopathology and Pharmacology|March 14, 2008
Recombinant allergens promote expression of aminopeptidase-n (CD13) on basophils in allergic patientsK Sonneck, C Baumgartner, L Rebuzzi, et al.
Gene Therapy|October 16, 2015
Photoreceptor-targeted gene delivery using intravitreally administered AAV vectors in dogsR F Boyd, D G Sledge, S L Boye, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 17, 2015
Targeted gene delivery to the enteric nervous system using AAV: a comparison across serotypes and capsid mutantsMatthew J Benskey, Nathan C Kuhn, James J Galligan, et al.
Investigative Ophthalmology & Visual Science|August 1, 2020
XIAP Protects Retinal Ganglion Cells in the Mutant ND4 Mouse Model of Leber Hereditary Optic NeuropathySarah J Wassmer, Yves De Repentigny, Derek Sheppard, et al.
Investigative Ophthalmology & Visual Science|May 21, 2010
Retinal disease in Rpe65-deficient mice: comparison to human leber congenital amaurosis due to RPE65 mutationsRafael C Caruso, Tomas S Aleman, Artur V Cideciyan, et al.
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