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Gene Delivery to Human Limbal Stem Cells Using Viral Vectors.
Song L, Song Z, Fry NJ, Conatser L, Llanga T, Mei H, Kafri T, Hirsch ML. Song L, et al. Among authors: kafri t. Hum Gene Ther. 2019 Nov;30(11):1336-1348. doi: 10.1089/hum.2019.071. Epub 2019 Sep 25. Hum Gene Ther. 2019. PMID: 31392914 Free PMC article.
Employing a gain-of-function factor IX variant R338L to advance the efficacy and safety of hemophilia B human gene therapy: preclinical evaluation supporting an ongoing adeno-associated virus clinical trial.
Monahan PE, Sun J, Gui T, Hu G, Hannah WB, Wichlan DG, Wu Z, Grieger JC, Li C, Suwanmanee T, Stafford DW, Booth CJ, Samulski JJ, Kafri T, McPhee SW, Samulski RJ. Monahan PE, et al. Among authors: kafri t. Hum Gene Ther. 2015 Feb;26(2):69-81. doi: 10.1089/hum.2014.106. Epub 2015 Jan 21. Hum Gene Ther. 2015. PMID: 25419787 Free PMC article.
Gene delivery by lentivirus vectors.
Cockrell AS, Kafri T. Cockrell AS, et al. Among authors: kafri t. Mol Biotechnol. 2007 Jul;36(3):184-204. doi: 10.1007/s12033-007-0010-8. Mol Biotechnol. 2007. PMID: 17873406 Review.
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