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AAV-Mediated Gene Delivery to the Mouse Liver.
Cunningham SC, Alexander IE. Cunningham SC, et al. Among authors: alexander ie. Methods Mol Biol. 2019;1937:213-219. doi: 10.1007/978-1-4939-9065-8_12. Methods Mol Biol. 2019. PMID: 30706398
Gene delivery to the juvenile mouse liver using AAV2/8 vectors.
Cunningham SC, Dane AP, Spinoulas A, Logan GJ, Alexander IE. Cunningham SC, et al. Among authors: alexander ie. Mol Ther. 2008 Jun;16(6):1081-8. doi: 10.1038/mt.2008.72. Epub 2008 Apr 15. Mol Ther. 2008. PMID: 18414478 Free article.
Gene therapy: progress in childhood disease.
Ginn SL, Alexander IE. Ginn SL, et al. Among authors: alexander ie. J Paediatr Child Health. 2012 Jun;48(6):466-71. doi: 10.1111/j.1440-1754.2011.02204.x. Epub 2011 Oct 21. J Paediatr Child Health. 2012. PMID: 22017270 Review.
Conversion of the Liver into a Biofactory for DNaseI Using Adeno-Associated Virus Vector Gene Transfer Reduces Neutrophil Extracellular Traps in a Model of Systemic Lupus Erythematosus.
Ahmad A, Mandwie M, O'Sullivan KM, Smyth C, York J, Doyle H, Holdsworth SR, Pickering MC, Lachmann PJ, Alexander IE, Logan GJ. Ahmad A, et al. Among authors: alexander ie. Hum Gene Ther. 2022 May;33(9-10):560-571. doi: 10.1089/hum.2021.264. Hum Gene Ther. 2022. PMID: 35293226
179 results