Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/93595
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dc.contributor.authorMcGuane, J.T.-
dc.contributor.authorConrad, K.P.-
dc.date.issued2012-
dc.identifier.citationDrug Discovery Today: Disease Models, 2012; 9(3):e119-e127-
dc.identifier.issn1740-6757-
dc.identifier.issn1740-6757-
dc.identifier.urihttp://hdl.handle.net/2440/93595-
dc.description.abstractPreeclampsia is an important obstetric complication that arises in 5% of women after the 20th week of gestation, for which there is no specific therapy and no cure. Although much of the recent investigation in this field has focused on soluble forms of the angiogenic membrane receptor tyrosine kinase Flt1 and the transforming growth factor β co-receptor Endoglin, there is significant clinical potential for several GPCR targets and their agonists or antagonists in preeclampsia. In this review, we discuss several of the most promising candidates in this category, including calcitonin receptor-like receptor/receptor activity modifying protein 1 complexes, the angiotensin AT1, 2 and Mas receptors, and the relaxin receptor RXFP1. We also address some of the controversies surrounding the roles and therapeutic potential of these GPCRs and their (ant)agonists in preeclampsia.-
dc.description.statementofresponsibilityJ.T. McGuane, K.P. Conrad-
dc.language.isoen-
dc.publisherElsevier-
dc.rights© 2012 Elsevier Ltd. All rights reserved.-
dc.source.urihttp://dx.doi.org/10.1016/j.ddmod.2012.05.001-
dc.titleGPCRs as potential therapeutic targets in preeclampsia-
dc.typeJournal article-
dc.identifier.doi10.1016/j.ddmod.2012.05.001-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 2
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