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Page 1
Creation of a mouse expressing defective human factor IX.
Jin DY, Zhang TP, Gui T, Stafford DW, Monahan PE. Jin DY, et al. Among authors: gui t. Blood. 2004 Sep 15;104(6):1733-9. doi: 10.1182/blood-2004-01-0138. Epub 2004 Jun 3. Blood. 2004. PMID: 15178576 Free 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: gui 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.
Correction of factor IX deficiency in mice by embryonic stem cells differentiated in vitro.
Fair JH, Cairns BA, Lapaglia MA, Caballero M, Pleasant WA, Hatada S, Kim HS, Gui T, Pevny L, Meyer AA, Stafford DW, Smithies O, Frelinger JA. Fair JH, et al. Among authors: gui t. Proc Natl Acad Sci U S A. 2005 Feb 22;102(8):2958-63. doi: 10.1073/pnas.0409840102. Epub 2005 Feb 7. Proc Natl Acad Sci U S A. 2005. PMID: 15699326 Free PMC article.
Inadvertent Transfer of Murine VL30 Retrotransposons to CAR-T Cells.
Lee SH, Hao Y, Gui T, Dotti G, Savoldo B, Zou F, Kafri T. Lee SH, et al. Among authors: gui t. Adv Cell Gene Ther. 2022;2022:6435077. doi: 10.1155/2022/6435077. Epub 2022 May 31. Adv Cell Gene Ther. 2022. PMID: 36081760 Free PMC article.
211 results