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The stained cells were measured at 515 nm fluorescence emission using FACSverse flow cytometer (BD) and the data were processed by FACSverse software

Twenty thousand cells per well were processed in a BD Accuri C6 flow cytometer (BD Biosciences, San Jose, CA, United States) and analyzed by FlowJo v

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doi: 10.1056/NEJMoa1910434 6 SmithTJKahalyGJEzraDGFlemingJCDaileyRATangRAet al