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Sato, S., Fujita, N
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PARs are seven-transmembrane domain receptors that are activated by the specific proteolytic cleavage of the N-terminal extracellular domain by endogenous serine proteases, such as thrombin (which acts on PAR-1, -3, and -4) and trypsin, tryptase, factor VIIa, and FXa (which act on PAR-2), and the released N-terminal tail binds the receptor itself and induces intracellular signaling [2]
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