The identification of ‘boosters’ that drive gene overexpression directly in a CAR construct provides a simple and scalable strategy for developing effective CAR-NK cell therapies for solid tumours.
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The model must be autoregressive. It receives a token sequence as input and predicts the next token. Output digits are generated one at a time, with each new token fed back as input for predicting the next. The carry propagation must emerge from this autoregressive process — not from explicit state variables passed between steps in Python.