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RasmussenLBSchomburgLKhrleJPedersenIBHollenbachBHgAet al

Abnormal NLRP3 inflammasome activation and excessive IL-1 secretion is the major reason of CAPS, and has been demonstrated in three clinical subtypes: neonatal-onset multisystem inflammatory disease (NOMID), Muckle-Wells syndrome (MWS), and familial cold autoinflammatory syndrome (FCAS)

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Similar content being viewed by others Background Mechanistic studies of tumor progression are increasingly focusing on protein modification in which lipidation plays an important role