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The Biology of Prostaglandins and Their Role as a Target for Allergic Airway Disease Therapy

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dc.contributor.authorLee, Kijeong-
dc.contributor.authorLee, Sang Hag-
dc.contributor.authorKim, Tae Hoon-
dc.date.accessioned2021-08-31T08:48:16Z-
dc.date.available2021-08-31T08:48:16Z-
dc.date.created2021-06-18-
dc.date.issued2020-03-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/57477-
dc.description.abstractProstaglandins (PGs) are a family of lipid compounds that are derived from arachidonic acid via the cyclooxygenase pathway, and consist of PGD(2), PGI(2), PGE(2), PGF(2), and thromboxane B-2. PGs signal through G-protein coupled receptors, and individual PGs affect allergic inflammation through different mechanisms according to the receptors with which they are associated. In this review article, we have focused on the metabolism of the cyclooxygenase pathway, and the distinct biological effect of each PG type on various cell types involved in allergic airway diseases, including asthma, allergic rhinitis, nasal polyposis, and aspirin-exacerbated respiratory disease.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherMDPI-
dc.subjectEXACERBATED RESPIRATORY-DISEASE-
dc.subjectORAL CRTH2 ANTAGONIST-
dc.subjectA(2) RECEPTOR ANTAGONIST-
dc.subjectDENDRITIC CELL-FUNCTION-
dc.subjectINNATE LYMPHOID-CELLS-
dc.subjectNECROSIS-FACTOR-ALPHA-
dc.subjectEXHALED NITRIC-OXIDE-
dc.subjectSMOOTH-MUSCLE-CELLS-
dc.subjectHUMAN MAST-CELLS-
dc.subjectTHROMBOXANE A(2)-
dc.titleThe Biology of Prostaglandins and Their Role as a Target for Allergic Airway Disease Therapy-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Tae Hoon-
dc.identifier.doi10.3390/ijms21051851-
dc.identifier.scopusid2-s2.0-85081259292-
dc.identifier.wosid000524908500302-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.21, no.5-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES-
dc.citation.titleINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES-
dc.citation.volume21-
dc.citation.number5-
dc.type.rimsART-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusEXACERBATED RESPIRATORY-DISEASE-
dc.subject.keywordPlusORAL CRTH2 ANTAGONIST-
dc.subject.keywordPlusA(2) RECEPTOR ANTAGONIST-
dc.subject.keywordPlusDENDRITIC CELL-FUNCTION-
dc.subject.keywordPlusINNATE LYMPHOID-CELLS-
dc.subject.keywordPlusNECROSIS-FACTOR-ALPHA-
dc.subject.keywordPlusEXHALED NITRIC-OXIDE-
dc.subject.keywordPlusSMOOTH-MUSCLE-CELLS-
dc.subject.keywordPlusHUMAN MAST-CELLS-
dc.subject.keywordPlusTHROMBOXANE A(2)-
dc.subject.keywordAuthorprostaglandins-
dc.subject.keywordAuthorallergy-
dc.subject.keywordAuthorasthma-
dc.subject.keywordAuthorallergic rhinitis-
dc.subject.keywordAuthorAERD-
dc.subject.keywordAuthorPGD(2)-
dc.subject.keywordAuthorPGE(2)-
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