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Cited 11 time in webofscience Cited 20 time in scopus
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dc.contributor.authorKim, J-
dc.contributor.authorKim, HW-
dc.contributor.authorChang, S-
dc.contributor.authorKim, JW-
dc.contributor.authorJe, JH-
dc.contributor.authorRhyu, IJ-
dc.date.accessioned2015-06-25T03:33:11Z-
dc.date.available2015-06-25T03:33:11Z-
dc.date.created2013-03-06-
dc.date.issued2012-12-17-
dc.identifier.issn2045-2322-
dc.identifier.other2015-OAK-0000026699en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/12880-
dc.description.abstractAcervuli are calcified concretions in the pineal gland (PG). Particularly interesting are their incidence and size, which are believed to affect neurological disorders and many physiological functions of PG such as regulating circadian rhythm. Despite long investigations for a century, detailed growth mechanism of acervuli has yet to be studied. Here we study the growth morphology of acervuli in human PGs by a direct visualization in 3-dimension (3-D) using a synchrotron X-ray imaging method. For an entire PG, non-aggregated acervuli show Gaussian distribution in size with 47 +/- 28 mu m. The 3-D volume rendered images of acervuli reveal that the bumpy surfaces developed by lamination result in the mulberry-like structure. In addition, coalescence of multiple acervuli leads to large-scale lamination on the whole aggregate. We suggest a novel hypothesis on the growth patterns of acervuli by their nucleation density (N-d): i) mulberry-like structure at low N-d, and ii) large-scale lamination on an aggregate at high N-d.-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherNature Publishing Group-
dc.relation.isPartOfScientific Reports-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.titleGrowth patterns for acervuli in human pineal gland-
dc.typeArticle-
dc.contributor.college신소재공학과en_US
dc.identifier.doi10.1038/srep00984-
dc.author.googleKim, Jen_US
dc.author.googleKim, HWen_US
dc.author.googleRhyu, IJen_US
dc.author.googleJe, JHen_US
dc.author.googleKim, JWen_US
dc.author.googleChang, Sen_US
dc.relation.volume2en_US
dc.contributor.id10123980en_US
dc.relation.journalScientific Reportsen_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.relation.sciSCIen_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationScientific Reports, v.2-
dc.identifier.wosid000312383500002-
dc.date.tcdate2019-01-01-
dc.citation.titleScientific Reports-
dc.citation.volume2-
dc.contributor.affiliatedAuthorJe, JH-
dc.identifier.scopusid2-s2.0-84871887112-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc4-
dc.type.docTypeArticle-
dc.subject.keywordPlusELECTRON-PROBE MICROANALYSIS-
dc.subject.keywordPlusMELATONIN BIOSYNTHESIS-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.subject.keywordPlusMOUSE MODEL-
dc.subject.keywordPlusCALCIFICATION-
dc.subject.keywordPlusAGE-
dc.subject.keywordPlusCALCIUM-
dc.subject.keywordPlusMICROSCOPY-
dc.subject.keywordPlusCELLS-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-

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제정호JE, JUNG HO
Dept of Materials Science & Enginrg
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