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Cited 154 time in webofscience Cited 167 time in scopus
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Ceramide synthases as potential targets for therapeutic intervention in human diseases

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dc.contributor.authorPark, Joo-Won-
dc.contributor.authorPark, Woo-Jae-
dc.contributor.authorFuterman, Anthony H.-
dc.date.available2020-02-28T17:43:49Z-
dc.date.created2020-02-06-
dc.date.issued2014-05-
dc.identifier.issn1388-1981-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/12656-
dc.description.abstractCeramide is located at a key hub in the sphingolipid metabolic pathway and also acts as an important cellular signaling molecule. Ceramide contains one acyl chain which is attached to a sphingoid long chain base via an amide bond, with the acyl chain varying in length and degree of saturation. The identification of a family of six mammalian ceramide synthases (CerS) that synthesize ceramide with distinct acyl chains, has led to significant advances in our understanding of ceramide biology, including further delineation of the role of ceramide in various pathophysiologies in both mice and humans. Since ceramides, and the complex sphingolipids generated from ceramide, are implicated in disease, the CerS might potentially be novel targets for therapeutic intervention in the diseases in which the ceramide acyl chain length is altered. This article is part of a Special Issue entitled New Frontiers in Sphingolipid Biology. (C) 2013 Elsevier B.V. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE BV-
dc.relation.isPartOfBIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS-
dc.subjectSPHINGANINE N-ACYLTRANSFERASE-
dc.subjectLONGEVITY ASSURANCE GENE-1-
dc.subjectSPHINGOLIPID BIOSYNTHESIS-
dc.subjectINDUCED APOPTOSIS-
dc.subjectHUMAN HEAD-
dc.subjectFUMONISIN B1-
dc.subject(DIHYDRO)CERAMIDE SYNTHASE-
dc.subjectGLUCOSYLCERAMIDE SYNTHASE-
dc.subjectBIOPHYSICAL PROPERTIES-
dc.subjectINSULIN-RESISTANCE-
dc.titleCeramide synthases as potential targets for therapeutic intervention in human diseases-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000335706400005-
dc.identifier.doi10.1016/j.bbalip.2013.08.019-
dc.identifier.bibliographicCitationBIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, v.1841, no.5, pp.671 - 681-
dc.identifier.scopusid2-s2.0-84897954511-
dc.citation.endPage681-
dc.citation.startPage671-
dc.citation.titleBIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS-
dc.citation.volume1841-
dc.citation.number5-
dc.contributor.affiliatedAuthorPark, Woo-Jae-
dc.type.docTypeReview-
dc.subject.keywordAuthorSphingolipid-
dc.subject.keywordAuthorCeramide synthase-
dc.subject.keywordAuthorAcyl chain length-
dc.subject.keywordAuthorDisease-
dc.subject.keywordAuthorSpecificity-
dc.subject.keywordAuthorTherapeutic target-
dc.subject.keywordPlusSPHINGANINE N-ACYLTRANSFERASE-
dc.subject.keywordPlusLONGEVITY ASSURANCE GENE-1-
dc.subject.keywordPlusSPHINGOLIPID BIOSYNTHESIS-
dc.subject.keywordPlusINDUCED APOPTOSIS-
dc.subject.keywordPlusHUMAN HEAD-
dc.subject.keywordPlusFUMONISIN B1-
dc.subject.keywordPlus(DIHYDRO)CERAMIDE SYNTHASE-
dc.subject.keywordPlusGLUCOSYLCERAMIDE SYNTHASE-
dc.subject.keywordPlusBIOPHYSICAL PROPERTIES-
dc.subject.keywordPlusINSULIN-RESISTANCE-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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