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CRISPR-based isoform editing is a cutting-edge technology that could enable precise targeting of specific C/EBP isoforms, thereby reducing the risk of off-target effects (128130)
Despite effectively neutralizing TcdA in vitro across various clinical isolates when used alone, the transition of clinical trials from phase I to phase II was halted due to observed ineffectiveness
the pathological staging was pT3N0M0 (according to AJCC 8th TNM staging system)
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It continued at Newark eight years, and was then removed to Princeton
