Reprogramming human T cell function and specificity with non-viral genome targeting-Reference-Cited by-同舟云学术

Reprogramming human T cell function and specificity with non-viral genome targeting

Published:2018-07 Issue:7714 Volume:559 Page:405-409
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Roth Theodore L.,Puig-Saus Cristina,Yu Ruby,Shifrut Eric,Carnevale Julia,Li P. Jonathan,Hiatt Joseph,Saco Justin,Krystofinski Paige,Li Han,Tobin Victoria,Nguyen David N.,Lee Michael R.,Putnam Amy L.,Ferris Andrea L.,Chen Jeff W.,Schickel Jean-Nicolas,Pellerin Laurence,Carmody David,Alkorta-Aranburu Gorka,del Gaudio Daniela,Matsumoto Hiroyuki,Morell Montse,Mao Ying,Cho Min,Quadros Rolen M.,Gurumurthy Channabasavaiah B.,Smith Baz,Haugwitz Michael,Hughes Stephen H.,Weissman Jonathan S.,Schumann Kathrin,Esensten Jonathan H.,May Andrew P.,Ashworth Alan,Kupfer Gary M.,Greeley Siri Atma W.,Bacchetta Rosa,Meffre Eric,Roncarolo Maria Grazia,Romberg Neil,Herold Kevan C.,Ribas Antoni,Leonetti Manuel D.,Marson Alexander

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41586-018-0326-5.pdf

Reference29 articles.

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4. Verhoeyen, E., Costa, C. & Cosset, F.-L. Lentiviral vector gene transfer into human T cells. Methods Mol. Biol. 506, 97–114 (2009).

5. Eyquem, J. et al. Targeting a CAR to the TRAC locus with CRISPR/Cas9 enhances tumour rejection. Nature 543, 113–117 (2017).

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