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Cited 174 times in

Inflammation-associated lymphangiogenesis: A double-edged sword?

DC Field Value Language
dc.contributor.author김한솔-
dc.date.accessioned2015-01-06T16:35:02Z-
dc.date.available2015-01-06T16:35:02Z-
dc.date.issued2014-
dc.identifier.issn0021-9738-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/98377-
dc.description.abstractLymphangiogenesis and lymphatic vessel remodeling are complex biological processes frequently observed during inflammation. Accumulating evidence indicates that inflammation-associated lymphangiogenesis (IAL) is not merely an endpoint event, but actually a phenomenon actively involved in the pathophysiology of various inflammatory disorders. The VEGF-C/VEGFR-3 and VEGF-A/VEGF-R2 signaling pathways are two of the best-studied pathways in IAL. Methods targeting these molecules, such as prolymphangiogenic or antilymphatic treatments, were found to be beneficial in various preclinical and/or clinical studies. This Review focuses on the most recent achievements in the fields of lymphatic biology relevant to inflammatory conditions. Additionally, preclinical and clinical therapies that modulate IAL are summarized.-
dc.description.statementOfResponsibilityopen-
dc.format.extent936~942-
dc.relation.isPartOfJOURNAL OF CLINICAL INVESTIGATION-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAngiogenic Proteins/physiology-
dc.subject.MESHAnimals-
dc.subject.MESHDiabetes Mellitus/immunology-
dc.subject.MESHDiabetes Mellitus/physiopathology-
dc.subject.MESHGraft Rejection/immunology-
dc.subject.MESHGraft Rejection/physiopathology-
dc.subject.MESHHumans-
dc.subject.MESHInflammation/physiopathology-
dc.subject.MESHInflammatory Bowel Diseases/immunology-
dc.subject.MESHInflammatory Bowel Diseases/physiopathology-
dc.subject.MESHLymphangiogenesis*-
dc.subject.MESHRespiratory System/immunology-
dc.subject.MESHRespiratory System/physiopathology-
dc.subject.MESHSignal Transduction-
dc.titleInflammation-associated lymphangiogenesis: A double-edged sword?-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Radiology (영상의학)-
dc.contributor.googleauthorHonsoul Kim-
dc.contributor.googleauthorRaghu P. Kataru-
dc.contributor.googleauthorGou Young Koh-
dc.identifier.doi10.1172/JCI71607-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01099-
dc.relation.journalcodeJ01322-
dc.identifier.eissn1558-8238-
dc.identifier.pmid24590279-
dc.identifier.urlhttp://www.jci.org/articles/view/71607-
dc.contributor.alternativeNameKim, Hon Soul-
dc.contributor.affiliatedAuthorKim, Hon Soul-
dc.rights.accessRightsfree-
dc.citation.volume124-
dc.citation.number3-
dc.citation.startPage936-
dc.citation.endPage942-
dc.identifier.bibliographicCitationJOURNAL OF CLINICAL INVESTIGATION, Vol.124(3) : 936-942, 2014-
dc.identifier.rimsid56562-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Radiology (영상의학교실) > 1. Journal Papers

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