A serine protease-mediated fragment generated after cleavage and release from the N-terminal of PAR2, enabling non-invasive monitoring of PAR2 activation and associated inflammatory processes in rheumatic diseases.
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A serine protease-mediated fragment generated after cleavage and release from the N-terminal of PAR2, enabling non-invasive monitoring of PAR2 activation and associated inflammatory processes in rheumatic diseases.
A citrullinated and matrix metalloproteinase-degraded fragment of vimentin, enabling non-invasive monitoring of macrophage-driven inflammation and tissue remodeling across autoimmune and fibrotic diseases.
