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Standard immunosuppressants reduce overall immune function, increasing infection risk
Given the expression of St14 (matriptase) in the intestinal crypt cells, we next determined the role of matriptase-PAR2 signaling for postprandial GIP regulation by using PAR2-K36E mutant mice

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Abstract Metabolic-dysfunction-associated fatty liver disease (MAFLD) or metabolic-dysfunction-associated steatotic liver disease (MASLD) has been recognised as one of the most important aetiologies of chronic liver disease and also a marker of high risk for atherosclerotic cardiovascular disease (ASCVD) in patients with or without diabetes