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Gene Expression Profiling in Melasma in Korean Women

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dc.contributor.authorChung, Bo Young-
dc.contributor.authorNoh, Tai Kyung-
dc.contributor.authorYang, Sang Hwa-
dc.contributor.authorKim, Il Hwan-
dc.contributor.authorLee, Mi Woo-
dc.contributor.authorYoon, Tae Jin-
dc.contributor.authorChang, Sung Eun-
dc.date.available2020-11-02T19:44:40Z-
dc.date.created2020-10-16-
dc.date.issued2014-
dc.identifier.issn1018-8665-
dc.identifier.urihttps://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/10033-
dc.description.abstractBackground: There has been a paucity of data about the difference in gene expression between melasma lesional skin and normal adjacent one. Objective: Our aim was to identify novel genes involved in the pathogenesis of melasma. Methods: We performed a microarray analysis and confirmed the results on quantitative real-time polymerase chain reaction (qRT-PCR) in Korean women with melasma. Results: There were 334 genes whose degree of expression showed a significant difference between melasma lesional skin and normal adjacent one. Of these, five were confirmed on qRT-PCR. In melasma lesional skin, there were down-regulation of genes involved in the PPAR signaling pathway and up-regulation of genes involved in neuronal component and the functions of stratum corneum barrier. Conclusion: This result suggests that the pathogenesis of melasma might be associated with novel genes involved in the above signaling pathway in Korean women. (C) 2014 S. Karger AG, Basel-
dc.language영어-
dc.language.isoen-
dc.publisherKARGER-
dc.subjectMELANOCYTE-STIMULATING HORMONE-
dc.subjectLESCH-NYHAN-DISEASE-
dc.subjectATOPIC-DERMATITIS-
dc.subjectULTRAVIOLET-RADIATION-
dc.subjectSIGNALING PATHWAY-
dc.subjectMOLECULAR-CLONING-
dc.subjectARACHIDONIC-ACID-
dc.subjectBINDING-PROTEINS-
dc.subjectLESIONAL SKIN-
dc.subjectDT-DIAPHORASE-
dc.titleGene Expression Profiling in Melasma in Korean Women-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Il Hwan-
dc.identifier.doi10.1159/000365080-
dc.identifier.scopusid2-s2.0-84917739603-
dc.identifier.wosid000347451000010-
dc.identifier.bibliographicCitationDERMATOLOGY, v.229, no.4, pp.333 - 342-
dc.relation.isPartOfDERMATOLOGY-
dc.citation.titleDERMATOLOGY-
dc.citation.volume229-
dc.citation.number4-
dc.citation.startPage333-
dc.citation.endPage342-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaDermatology-
dc.relation.journalWebOfScienceCategoryDermatology-
dc.subject.keywordPlusMELANOCYTE-STIMULATING HORMONE-
dc.subject.keywordPlusLESCH-NYHAN-DISEASE-
dc.subject.keywordPlusATOPIC-DERMATITIS-
dc.subject.keywordPlusULTRAVIOLET-RADIATION-
dc.subject.keywordPlusSIGNALING PATHWAY-
dc.subject.keywordPlusMOLECULAR-CLONING-
dc.subject.keywordPlusARACHIDONIC-ACID-
dc.subject.keywordPlusBINDING-PROTEINS-
dc.subject.keywordPlusLESIONAL SKIN-
dc.subject.keywordPlusDT-DIAPHORASE-
dc.subject.keywordAuthorMelasma-
dc.subject.keywordAuthorMicroarray analysis-
dc.subject.keywordAuthorPathogenesis-
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Kim, Il Hwan or Il-Hwan
Ansan Hospital (Department of Dermatology, Ansan Hospital)
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