Versatile strategy for controlling the specificity and activity of engineered T cells.

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Published in Proc Natl Acad Sci U S A on January 12, 2016

Authors

Jennifer S Y Ma1, Ji Young Kim1, Stephanie A Kazane1, Sei-Hyun Choi2, Hwa Young Yun2, Min Soo Kim1, David T Rodgers1, Holly M Pugh1, Oded Singer1, Sophie B Sun1, Bryan R Fonslow3, James N Kochenderfer4, Timothy M Wright1, Peter G Schultz5, Travis S Young6, Chan Hyuk Kim6, Yu Cao2

Author Affiliations

1: Department of Biology, California Institute for Biomedical Research, La Jolla, CA 92037;
2: Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, La Jolla, CA 92037;
3: Department of Chemical Physiology, The Scripps Research Institute, La Jolla, CA 92037; SCIEX Separations, Brea, CA 92821;
4: Experimental Transplantation and Immunology Branch, National Institutes of Health, National Cancer Institute, Bethesda, MD 20892.
5: Department of Biology, California Institute for Biomedical Research, La Jolla, CA 92037; Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, La Jolla, CA 92037; schultz@scripps.edu tyoung@calibr.org chkim@calibr.org.
6: Department of Biology, California Institute for Biomedical Research, La Jolla, CA 92037; schultz@scripps.edu tyoung@calibr.org chkim@calibr.org.

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