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Sphingosine-1-phosphate receptors: Biology and therapeutic potential in kidney disease

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dc.contributor.authorJo, S-K-
dc.contributor.authorBajwa, A.-
dc.contributor.authorAwad, A. S.-
dc.contributor.authorLynch, K. R.-
dc.contributor.authorOkusa, M. D.-
dc.date.accessioned2021-09-09T07:42:13Z-
dc.date.available2021-09-09T07:42:13Z-
dc.date.created2021-06-10-
dc.date.issued2008-06-
dc.identifier.issn0085-2538-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/123412-
dc.description.abstractThe major sphingolipid metabolite, sphingosine-1-phosphate (S1P), has important biological functions. S1P is the ligand for a family of five G-protein-coupled receptors with distinct signaling pathways that regulate angiogenesis, vascular maturation, immunity, chemotaxis, and other important biological pathways. Recently, clinical trials have targeted S1P receptors (S1PRs) for autoimmune diseases and transplantation and have generated considerable interest in developing additional, more selective compounds. This review summarizes current knowledge on the biology of S1P and S1PRs that forms the basis for future drug development and the treatment of kidney disease.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE INC-
dc.subjectPROTEIN-COUPLED RECEPTOR-
dc.subjectACUTE-RENAL-FAILURE-
dc.subjectSPHINGOSINE 1-PHOSPHATE RECEPTORS-
dc.subjectISCHEMIA-REPERFUSION INJURY-
dc.subjectSMOOTH-MUSCLE-CELLS-
dc.subjectMULTIPLE SIGNALING PATHWAYS-
dc.subjectMEDIATED TISSUE PROTECTION-
dc.subjectHUMAN ENDOTHELIAL-CELLS-
dc.subjectMATURE DENDRITIC CELLS-
dc.subjectT-CELL-
dc.titleSphingosine-1-phosphate receptors: Biology and therapeutic potential in kidney disease-
dc.typeArticle-
dc.contributor.affiliatedAuthorJo, S-K-
dc.identifier.doi10.1038/ki.2008.34-
dc.identifier.scopusid2-s2.0-43749098568-
dc.identifier.wosid000255897400005-
dc.identifier.bibliographicCitationKIDNEY INTERNATIONAL, v.73, no.11, pp.1220 - 1230-
dc.relation.isPartOfKIDNEY INTERNATIONAL-
dc.citation.titleKIDNEY INTERNATIONAL-
dc.citation.volume73-
dc.citation.number11-
dc.citation.startPage1220-
dc.citation.endPage1230-
dc.type.rimsART-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaUrology & Nephrology-
dc.relation.journalWebOfScienceCategoryUrology & Nephrology-
dc.subject.keywordPlusPROTEIN-COUPLED RECEPTOR-
dc.subject.keywordPlusACUTE-RENAL-FAILURE-
dc.subject.keywordPlusSPHINGOSINE 1-PHOSPHATE RECEPTORS-
dc.subject.keywordPlusISCHEMIA-REPERFUSION INJURY-
dc.subject.keywordPlusSMOOTH-MUSCLE-CELLS-
dc.subject.keywordPlusMULTIPLE SIGNALING PATHWAYS-
dc.subject.keywordPlusMEDIATED TISSUE PROTECTION-
dc.subject.keywordPlusHUMAN ENDOTHELIAL-CELLS-
dc.subject.keywordPlusMATURE DENDRITIC CELLS-
dc.subject.keywordPlusT-CELL-
dc.subject.keywordAuthorFTY720-
dc.subject.keywordAuthorSEW2871-
dc.subject.keywordAuthorischemia-reperfusion injury-
dc.subject.keywordAuthoracute kidney injury-
dc.subject.keywordAuthorsphingolipid-
dc.subject.keywordAuthorS1P-
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