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- W1542387560 endingPage "400" @default.
- W1542387560 startingPage "392" @default.
- W1542387560 abstract "Upon infection, antigen-specific T lymphocytes become activated, proliferate, differentiate, and acquire various effector functions. Much of our understanding of the molecular mechanisms underlying these processes derives from studies leveraging gene deletion, RNAi, and overexpression approaches. However, these perturbations do not inform on the regulation of gene activity under physiological conditions. Genetic reporter systems that couple biological events to detectable output signals are capable of providing this information. Here, we review the reporter approaches being currently used to investigate various aspects of T cell behavior, and discuss advantages and disadvantages inherent to different designs. We outline emerging applications based on recent advances in other fields, and highlight the potential of synthetic biology and genome engineering to address open questions in the field." @default.
- W1542387560 created "2016-06-24" @default.
- W1542387560 creator A5001016649 @default.
- W1542387560 creator A5016128619 @default.
- W1542387560 creator A5062019804 @default.
- W1542387560 creator A5073287402 @default.
- W1542387560 date "2015-07-01" @default.
- W1542387560 modified "2023-10-18" @default.
- W1542387560 title "Assessing T lymphocyte function and differentiation by genetically encoded reporter systems" @default.
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