Steven J. Gray

2008-2018 Gene Therapy Center University of North Carolina, Chapel Hill, Chapel Hill, NC 
 2017- Neurology and Pediatrics University of Texas Southwestern Medical Center, Dallas, TX, United States 
"Steven Gray"
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Cross-listing: Cell & Gene Therapy Tree


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Ellen Fanning grad student 2000-2006 Vanderbilt University (Chemistry Tree)
Jude Samulski post-doc 2006-2008 UNC Chapel Hill (Cell & Gene Therapy Tree)


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Inseyah Bagasrawala collaborator (FlyTree)
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Chen X, Dong T, Hu Y, et al. (2022) AAV9/MFSD8 gene therapy is effective in preclinical models of neuronal ceroid lipofuscinosis type 7 disease. The Journal of Clinical Investigation
Ling Q, Rioux M, Hu Y, et al. (2021) Adeno-associated viral vector serotype 9-based gene replacement therapy for -related Leigh syndrome. Molecular Therapy. Methods & Clinical Development. 23: 158-168
Judson MC, Shyng C, Simon JM, et al. (2021) Dual-isoform hUBE3A gene transfer improves behavioral and seizure outcomes in Angelman syndrome model mice. Jci Insight. 6
Kot S, Karumuthil-Melethil S, Woodley E, et al. (2021) Investigating Immune Responses to the scAAV9- Gene Therapy Treatment in Tay-Sachs Disease and Sandhoff Disease Mouse Models. International Journal of Molecular Sciences. 22
Armao D, Bouldin TW, Bailey RM, et al. (2021) Extensive rod and cone photoreceptor-cell degeneration in rat models of giant axonal neuropathy: implications for gene therapy of human disease. Ophthalmic Genetics. 1-4
Sinnett SE, Boyle E, Lyons C, et al. (2021) Engineered microRNA-based regulatory element permits safe high-dose miniMECP2 gene therapy in Rett mice. Brain : a Journal of Neurology
Presa M, Bailey RM, Davis C, et al. (2021) AAV9-mediated FIG4 delivery prolongs life span in Charcot Marie Tooth disease type 4J mouse model. The Journal of Clinical Investigation
Francis JS, Markov V, Wojtas ID, et al. (2021) Preclinical biodistribution, tropism, and efficacy of oligotropic AAV/Olig001 in a mouse model of congenital white matter disease. Molecular Therapy. Methods & Clinical Development. 20: 520-534
Mendell JR, Al-Zaidy SA, Rodino-Klapac LR, et al. (2020) Current Clinical Applications of in vivo Gene Therapy with AAVs. Molecular Therapy : the Journal of the American Society of Gene Therapy
Chen X, Snanoudj-Verber S, Pollard L, et al. (2020) Preclinical Gene Therapy with AAV9/AGA in Aspartylglucosaminuria Mice Provides Evidence for Clinical Translation. Molecular Therapy : the Journal of the American Society of Gene Therapy
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