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Year | Number of Results |
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2007 | 1 |
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Hematopoietic stem cell gene transfer in a tumor-prone mouse model uncovers low genotoxicity of lentiviral vector integration.
Nat Biotechnol. 2006 Jun;24(6):687-96. doi: 10.1038/nbt1216. Epub 2006 May 28.
Nat Biotechnol. 2006.
PMID: 16732270
Is the post-transplantation treatment with AMD beneficial?
Jiang Y, Ulyanova T, Papayannopoulou T.
Jiang Y, et al.
Blood Cells Mol Dis. 2012 Jun 15;49(1):29-31. doi: 10.1016/j.bcmd.2012.03.005. Epub 2012 Apr 5.
Blood Cells Mol Dis. 2012.
PMID: 22483574
Free PMC article.
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Gene editing in human stem cells using zinc finger nucleases and integrase-defective lentiviral vector delivery.
Lombardo A, Genovese P, Beausejour CM, Colleoni S, Lee YL, Kim KA, Ando D, Urnov FD, Galli C, Gregory PD, Holmes MC, Naldini L.
Lombardo A, et al.
Nat Biotechnol. 2007 Nov;25(11):1298-306. doi: 10.1038/nbt1353. Epub 2007 Oct 28.
Nat Biotechnol. 2007.
PMID: 17965707
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Lentiviral vector gene transfer is limited by the proteasome at postentry steps in various types of stem cells.
Santoni de Sio FR, Gritti A, Cascio P, Neri M, Sampaolesi M, Galli C, Luban J, Naldini L.
Santoni de Sio FR, et al.
Stem Cells. 2008 Aug;26(8):2142-52. doi: 10.1634/stemcells.2007-0705. Epub 2008 May 15.
Stem Cells. 2008.
PMID: 18483423
Free article.
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The genotoxic potential of retroviral vectors is strongly modulated by vector design and integration site selection in a mouse model of HSC gene therapy.
Montini E, Cesana D, Schmidt M, Sanvito F, Bartholomae CC, Ranzani M, Benedicenti F, Sergi LS, Ambrosi A, Ponzoni M, Doglioni C, Di Serio C, von Kalle C, Naldini L.
Montini E, et al.
J Clin Invest. 2009 Apr;119(4):964-75. doi: 10.1172/JCI37630. Epub 2009 Mar 23.
J Clin Invest. 2009.
PMID: 19307726
Free PMC article.
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