Steven J. Gray

Affiliations: 
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 
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"Steven Gray"
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Cross-listing: Cell & Gene Therapy Tree

Parents

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

Collaborators

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Inseyah Bagasrawala collaborator (FlyTree)
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Publications

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Presa M, Bailey RM, Ray S, et al. (2025) Preclinical use of a clinically-relevant scAAV9/SUMF1 vector for the treatment of multiple sulfatase deficiency. Communications Medicine. 5: 29
Bharucha-Goebel DX, Todd JJ, Saade D, et al. (2024) Intrathecal Gene Therapy for Giant Axonal Neuropathy. The New England Journal of Medicine. 390: 1092-1104
Gumusgoz E, Kasiri S, Verma M, et al. (2023) CSTB gene replacement improves neuroinflammation, neurodegeneration and ataxia in murine type 1 progressive myoclonus epilepsy. Gene Therapy
Vyas M, Deschenes NM, Osmon KJL, et al. (2023) Efficacy of Adeno-Associated Virus Serotype 9-Mediated Gene Therapy for AB-Variant GM2 Gangliosidosis. International Journal of Molecular Sciences. 24
Ling Q, Herstine JA, Bradbury A, et al. (2023) AAV-based in vivo gene therapy for neurological disorders. Nature Reviews. Drug Discovery
Casy W, Garza IT, Chen X, et al. (2023) SMRT Sequencing Enables High-Throughput Identification of Novel AAVs from Capsid Shuffling and Directed Evolution. Genes. 14
Wong H, Hooper AW, Kang HR, et al. (2023) CNS-dominant human FMRP isoform rescues seizures, fear, and sleep abnormalities in Fmr1-KO mice. Jci Insight. 8
Chen X, Lim DA, Lawlor MW, et al. (2023) Biodistribution of adeno-associated virus gene therapy following CSF-directed administration. Human Gene Therapy
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
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