CRISPR-Cas9 mediated efficient PD-1 disruption on human primary T cells for adoptive therapy
利用 CRISPR-Cas9 介导的高效 PD-1 基因敲除技术对人原代 T 细胞进行过继治疗
期刊:British Journal of Cancer
影响因子:6.8
doi:10.1038/bjc.2014.592
Rakha, E A; Tan, P H; Varga, Z; Tse, G M; Shaaban, A M; Climent, F; van Deurzen, C H M; Purnell, D; Dodwell, D; Chan, T; Ellis, I O; Daniele, Bruno; Sangro, Bruno; Petrylak, Daniel; Calabrò, Fabio; Cartenì, Giacomo; Montesarchio, Vincenzo; De Placido, Sabino; Ascierto, Paolo A; Su, Shu; Liu, Baorui; Zou, Zhengyun