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Cited 4 time in webofscience Cited 5 time in scopus
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dc.contributor.authorKim, J-
dc.contributor.authorPark, TJ-
dc.contributor.authorKwon, N-
dc.contributor.authorLee, D-
dc.contributor.authorKim, S-
dc.contributor.authorKohmura, Y-
dc.contributor.authorIshikawa, T-
dc.contributor.authorKim, KT-
dc.contributor.authorCurran, T-
dc.contributor.authorJe, JH-
dc.date.accessioned2017-07-19T11:40:12Z-
dc.date.available2017-07-19T11:40:12Z-
dc.date.created2015-03-03-
dc.date.issued2015-07-
dc.identifier.issn1863-2653-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/35291-
dc.description.abstractThe dendritic planarity of Purkinje cells is critical for cerebellar circuit formation. In the absence of Crk and CrkL, the Reelin pathway does not function resulting in partial Purkinje cell migration and defective dendritogenesis. However, the relationships among Purkinje cell migration, dendritic development and Reelin signaling have not been clearly delineated. Here, we use synchrotron X-ray microscopy to obtain 3-D images of Golgi-stained Purkinje cell dendrites. Purkinje cells that failed to migrate completely exhibited conical dendrites with abnormal 3-D arborization and reduced dendritic complexity. Furthermore, their spines were fewer in number with a distorted morphology. In contrast, Purkinje cells that migrated successfully displayed planar dendritic and spine morphologies similar to normal cells, despite reduced dendritic complexity. These results indicate that, during cerebellar formation, Purkinje cells migrate into an environment that supports development of dendritic planarity and spine formation. While Reelin signaling is important for the migration process, it does not make a direct major contribution to dendrite formation.-
dc.languageEnglish-
dc.publisherSpringer Verlag-
dc.relation.isPartOfBrain Structure and Function-
dc.titleDendritic planarity of Purkinje cells is independent of Reelin signaling-
dc.typeArticle-
dc.identifier.doi10.1007/S00429-014-0780-2-
dc.type.rimsART-
dc.identifier.bibliographicCitationBrain Structure and Function, v.220, no.4, pp.2263 - 2273-
dc.identifier.wosid000356874700028-
dc.date.tcdate2019-03-01-
dc.citation.endPage2273-
dc.citation.number4-
dc.citation.startPage2263-
dc.citation.titleBrain Structure and Function-
dc.citation.volume220-
dc.contributor.affiliatedAuthorKim, S-
dc.contributor.affiliatedAuthorKim, KT-
dc.contributor.affiliatedAuthorJe, JH-
dc.identifier.scopusid2-s2.0-84933183081-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc1-
dc.description.scptc1*
dc.date.scptcdate2018-05-121*
dc.description.isOpenAccessY-
dc.type.docTypeArticle-
dc.subject.keywordPlusNEURONAL MIGRATION-
dc.subject.keywordPlusMICE LACKING-
dc.subject.keywordPlusMUTANT MICE-
dc.subject.keywordPlusCRK-
dc.subject.keywordPlusPATHWAY-
dc.subject.keywordPlusROLES-
dc.subject.keywordPlusMOUSE-
dc.subject.keywordPlusDISABLED-1-
dc.subject.keywordPlusMORPHOLOGY-
dc.subject.keywordPlusRADIOLOGY-
dc.subject.keywordAuthorDendritic planarity-
dc.subject.keywordAuthorPurkinje cell-
dc.subject.keywordAuthorReelin signaling-
dc.subject.keywordAuthorMigration-
dc.subject.keywordAuthorSynchrotron X-ray imaging-
dc.relation.journalWebOfScienceCategoryAnatomy & Morphology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaAnatomy & Morphology-
dc.relation.journalResearchAreaNeurosciences & Neurology-

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김경태KIM, KYONG TAI
Dept of Life Sciences
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