Casey A. Maguire

Affiliations: 
The Massachusetts General Hospital 
Area:
glioblastoma, gene therapy, genetic engineering
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"Casey Maguire"
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Publications

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Santoscoy MC, Espinoza P, De La Cruz D, et al. (2023) An AAV capsid increases transduction of striatum and a ChAT promoter allows selective cholinergic neuron transduction. Molecular Therapy. Methods & Clinical Development. 29: 532-540
Prabhakar S, Beauchamp RL, Cheah PS, et al. (2022) Gene replacement therapy in a schwannoma mouse model of neurofibromatosis type 2. Molecular Therapy. Methods & Clinical Development. 26: 169-180
Ahmed SG, Maguire CA, Cao SA, et al. (2022) Schwannoma Gene Therapy via Adeno-Associated Viral Vector Delivery of Apoptosis-Associated Speck-like Protein Containing CARD (ASC): Preclinical Efficacy and Safety. International Journal of Molecular Sciences. 23
Cheng M, Dietz L, Gong Y, et al. (2021) Neutralizing antibody evasion and transduction with purified extracellular vesicle-enveloped AAV vectors. Human Gene Therapy
Ivanchenko MV, Hanlon KS, Hathaway DM, et al. (2021) AAV-S: A versatile capsid variant for transduction of mouse and primate inner ear. Molecular Therapy. Methods & Clinical Development. 21: 382-398
Peters CW, Maguire CA, Hanlon KS. (2021) Delivering AAV to the Central Nervous and Sensory Systems. Trends in Pharmacological Sciences
Cheah PS, Prabhakar S, Yellen D, et al. (2021) Gene therapy for tuberous sclerosis complex type 2 in a mouse model by delivery of AAV9 encoding a condensed form of tuberin. Science Advances. 7
Xia Y, He J, Zhang H, et al. (2020) AAV-mediated gene transfer of DNase I in the liver of mice with colorectal cancer reduces liver metastasis and restores local innate and adaptive immune response. Molecular Oncology
Griciuc A, Federico AN, Natasan J, et al. (2020) Gene therapy for Alzheimer's Disease targeting CD33 reduces amyloid beta accumulation and neuroinflammation. Human Molecular Genetics
Maguire CA, Corey DP. (2020) Viral vectors for gene delivery to the inner ear. Hearing Research. 107927
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