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Resulting variants, X(PC4)aX(PC4)d, were less active on procaspase-1 than X(PC2) and X(PC3) proteases, but were highly selective for procaspase-1 cleavage (Fig
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Funding This work was supported by the Ministry of Education (MOE) Fundamental Research Grant Scheme (FRGS/1/2015/SKK08/TAYLOR/03/1) awarded to WY
Reference ranges vary slightly between laboratories, but the general framework used by most U.S
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