Characterization of Protease-Activated Receptor (PAR) ligands: Parmodulins are reversible allosteric inhibitors of PAR1-driven calcium mobilization in endothelial cells

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DOI:10.1016/j.bmc.2018.04.016
文献类型：期刊论文
补充材料：仅需补充材料
文献链接：https://doi.org/10.1016/j.bmc.2018.04.016

Elsevier

Abstract：Several classes of ligands for Protease-Activated Receptors (PARs) have shown impressive anti-inflammatory and cytoprotective activities, including PAR2 antagonists and the PAR1-targeting pa

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