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Highly efficient therapeutic gene editing of human hematopoietic stem cells.
Wu Y, Zeng J, Roscoe BP, Liu P, Yao Q, Lazzarotto CR, Clement K, Cole MA, Luk K, Baricordi C, Shen AH, Ren C, Esrick EB, Manis JP, Dorfman DM, Williams DA, Biffi A, Brugnara C, Biasco L, Brendel C, Pinello L, Tsai SQ, Wolfe SA, Bauer DE. Wu Y, et al. Among authors: williams da. Nat Med. 2019 May;25(5):776-783. doi: 10.1038/s41591-019-0401-y. Epub 2019 Mar 25. Nat Med. 2019. PMID: 30911135 Free PMC article.
Efficient retrovirus-mediated transfer of the multidrug resistance 1 gene into autologous human long-term repopulating hematopoietic stem cells.
Abonour R, Williams DA, Einhorn L, Hall KM, Chen J, Coffman J, Traycoff CM, Bank A, Kato I, Ward M, Williams SD, Hromas R, Robertson MJ, Smith FO, Woo D, Mills B, Srour EF, Cornetta K. Abonour R, et al. Among authors: williams sd, williams da. Nat Med. 2000 Jun;6(6):652-8. doi: 10.1038/76225. Nat Med. 2000. PMID: 10835681 Clinical Trial.
Side effects of retroviral gene transfer into hematopoietic stem cells.
Baum C, Düllmann J, Li Z, Fehse B, Meyer J, Williams DA, von Kalle C. Baum C, et al. Among authors: williams da. Blood. 2003 Mar 15;101(6):2099-114. doi: 10.1182/blood-2002-07-2314. Epub 2003 Jan 2. Blood. 2003. PMID: 12511419 Free article. Review.
1,228 results