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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/13529
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dc.contributor.authorGaikwad, Anil Bhanudas-
dc.date.accessioned2023-12-27T06:58:56Z-
dc.date.available2023-12-27T06:58:56Z-
dc.date.issued2023-08-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S1359644623001654-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13529-
dc.description.abstractAcute kidney injury (AKI)-to-chronic kidney disease (CKD) transition is a slow but persistent progression toward end-stage kidney disease. Earlier reports have shown that Hippo components, such as Yes-associated protein (YAP) and its homolog Transcriptional coactivator with PDZ-binding motif (TAZ), regulate inflammation and fibrogenesis during the AKI-to-CKD transition. Notably, the roles and mechanisms of Hippo components vary during AKI, AKI-to-CKD transition, and CKD. Hence, it is important to understand these roles in detail. This review addresses the potential of Hippo regulators or components as future therapeutic targets for halting the AKI-to-CKD transition.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectPharmacyen_US
dc.subjectHippo signalingen_US
dc.subjectYAP/TAZen_US
dc.subjectAcute Kidney Injury (AKI)en_US
dc.subjectChronic kidney diseases (CKD)en_US
dc.subjectAKI-to-CKD transitionen_US
dc.titleHippo signaling in acute kidney injury to chronic kidney disease transition: Current understandings and future targetsen_US
dc.typeArticleen_US
Appears in Collections:Department of Pharmacy

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