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Cells were washed three times with standard saline (138 buffer) containing 0.1% BSA in the presence or absence of ectonucleotidase inhibitors as indicated, for 30 min at 37 C

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AST and ALT were measured using enzymatic UV kinetic methods in accordance with International Federation of Clinical Chemistry (IFCC) standards, with NADH consumption monitored at 340 nm

I would say for some, the downside risk is higher