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Immunotherapy of HCC metastases with autologous T cell receptor redirected T cells, targeting HBsAg in a liver transplant patient.
Qasim W, Brunetto M, Gehring AJ, Xue SA, Schurich A, Khakpoor A, Zhan H, Ciccorossi P, Gilmour K, Cavallone D, Moriconi F, Farzhenah F, Mazzoni A, Chan L, Morris E, Thrasher A, Maini MK, Bonino F, Stauss H, Bertoletti A. Qasim W, et al. J Hepatol. 2015 Feb;62(2):486-91. doi: 10.1016/j.jhep.2014.10.001. Epub 2014 Oct 13. J Hepatol. 2015. PMID: 25308176
Gene therapy for severe combined immune deficiency.
Qasim W, Gaspar HB, Thrasher AJ. Qasim W, et al. Expert Rev Mol Med. 2004 Jul 2;6(13):1-15. doi: 10.1017/S1462399404007884. Expert Rev Mol Med. 2004. PMID: 15236670 Review.
RISC control for gene therapy.
Qasim W, Thrasher AJ. Qasim W, et al. Nat Biotechnol. 2006 Jun;24(6):661-2. doi: 10.1038/nbt0606-661. Nat Biotechnol. 2006. PMID: 16763596 No abstract available.
Capture and generation of adenovirus specific T cells for adoptive immunotherapy.
Chatziandreou I, Gilmour KC, McNicol AM, Costabile M, Sinclair J, Cubitt D, Campbell JD, Kinnon C, Qasim W, Gaspar HB. Chatziandreou I, et al. Among authors: qasim w. Br J Haematol. 2007 Jan;136(1):117-26. doi: 10.1111/j.1365-2141.2006.06386.x. Epub 2006 Nov 8. Br J Haematol. 2007. PMID: 17092305 Free article.
152 results