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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1991 1
1998 2
2001 1
2002 1
2003 1
2004 1
2005 2
2006 2
2007 4
2008 2
2009 3
2010 5
2011 7
2012 6
2013 10
2014 10
2015 10
2016 8
2017 16
2018 13
2019 15
2020 12
2021 10
2022 5
2023 5
2024 0

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134 results

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Page 1
Base-Edited CAR7 T Cells for Relapsed T-Cell Acute Lymphoblastic Leukemia.
Chiesa R, Georgiadis C, Syed F, Zhan H, Etuk A, Gkazi SA, Preece R, Ottaviano G, Braybrook T, Chu J, Kubat A, Adams S, Thomas R, Gilmour K, O'Connor D, Vora A, Qasim W; Base-Edited CAR T Group. Chiesa R, et al. Among authors: qasim w. N Engl J Med. 2023 Sep 7;389(10):899-910. doi: 10.1056/NEJMoa2300709. Epub 2023 Jun 14. N Engl J Med. 2023. PMID: 37314354 Clinical Trial.
Phase 1 clinical trial of CRISPR-engineered CAR19 universal T cells for treatment of children with refractory B cell leukemia.
Ottaviano G, Georgiadis C, Gkazi SA, Syed F, Zhan H, Etuk A, Preece R, Chu J, Kubat A, Adams S, Veys P, Vora A, Rao K, Qasim W; TT52 CRISPR-CAR group. Ottaviano G, et al. Among authors: qasim w. Sci Transl Med. 2022 Oct 26;14(668):eabq3010. doi: 10.1126/scitranslmed.abq3010. Epub 2022 Oct 26. Sci Transl Med. 2022. PMID: 36288281 Clinical Trial.
Genome-Edited T Cell Therapies.
Ottaviano G, Qasim W. Ottaviano G, et al. Among authors: qasim w. Hematol Oncol Clin North Am. 2022 Aug;36(4):729-744. doi: 10.1016/j.hoc.2022.03.006. Epub 2022 Jun 27. Hematol Oncol Clin North Am. 2022. PMID: 35773047 Review.
Genome-edited, donor-derived allogeneic anti-CD19 chimeric antigen receptor T cells in paediatric and adult B-cell acute lymphoblastic leukaemia: results of two phase 1 studies.
Benjamin R, Graham C, Yallop D, Jozwik A, Mirci-Danicar OC, Lucchini G, Pinner D, Jain N, Kantarjian H, Boissel N, Maus MV, Frigault MJ, Baruchel A, Mohty M, Gianella-Borradori A, Binlich F, Balandraud S, Vitry F, Thomas E, Philippe A, Fouliard S, Dupouy S, Marchiq I, Almena-Carrasco M, Ferry N, Arnould S, Konto C, Veys P, Qasim W; UCART19 Group. Benjamin R, et al. Among authors: qasim w. Lancet. 2020 Dec 12;396(10266):1885-1894. doi: 10.1016/S0140-6736(20)32334-5. Lancet. 2020. PMID: 33308471 Clinical Trial.
Genome Editing in Engineered T Cells for Cancer Immunotherapy.
Bonini C, Chapuis AG, Hudecek M, Guedan S, Magnani C, Qasim W. Bonini C, et al. Among authors: qasim w. Hum Gene Ther. 2023 Sep;34(17-18):853-869. doi: 10.1089/hum.2023.128. Hum Gene Ther. 2023. PMID: 37694593 Review.
Genome editing of therapeutic T cells.
Qasim W. Qasim W. Gene Genome Ed. 2021 Dec;2:None. doi: 10.1016/j.ggedit.2021.100010. Gene Genome Ed. 2021. PMID: 34977824 Free PMC article. Review.
Engineered T cell therapies.
Field AC, Qasim W. Field AC, et al. Among authors: qasim w. Expert Rev Mol Med. 2015 Nov 4;17:e19. doi: 10.1017/erm.2015.14. Expert Rev Mol Med. 2015. PMID: 26530808 Review.
Genome-Edited T Cell Therapies.
Delhove JMKM, Qasim W. Delhove JMKM, et al. Among authors: qasim w. Curr Stem Cell Rep. 2017;3(2):124-136. doi: 10.1007/s40778-017-0077-5. Epub 2017 Apr 18. Curr Stem Cell Rep. 2017. PMID: 28596938 Free PMC article. Review.
Hybrid lentiviral vectors.
Qasim W, Vink CA, Thrasher AJ. Qasim W, et al. Mol Ther. 2010 Jul;18(7):1263-7. doi: 10.1038/mt.2010.76. Epub 2010 Apr 20. Mol Ther. 2010. PMID: 20407425 Free PMC article. Review.
Allogeneic CAR T cell therapies for leukemia.
Qasim W. Qasim W. Am J Hematol. 2019 May;94(S1):S50-S54. doi: 10.1002/ajh.25399. Epub 2019 Feb 1. Am J Hematol. 2019. PMID: 30632623 Free article. Review.
134 results