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dc.contributor.authorKim, Do Eon-
dc.contributor.authorCho, Chang-Hoon-
dc.contributor.authorSim, Kyoung Mi-
dc.contributor.authorKwon, Osung-
dc.contributor.authorHwang, Eun Mi-
dc.contributor.authorKim, Hyung-Wook-
dc.contributor.authorPark, Jae-Yong-
dc.date.accessioned2024-01-19T21:00:46Z-
dc.date.available2024-01-19T21:00:46Z-
dc.date.created2021-09-02-
dc.date.issued2019-02-
dc.identifier.issn1226-2560-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/120393-
dc.description.abstract14-3-3 gamma plays diverse roles in different aspects of cellular processes. Especially in the brain where 14-3-3 gamma is enriched, it has been reported to be involved in neurological and psychiatric diseases (e.g. Williams-Beuren syndrome and Creutzfeldt-Jakob disease). However, behavioral abnormalities related to 14-3-3 gamma deficiency are largely unknown. Here, by using 14-3-3 gamma deficient mice, we found that homozygous knockout mice were prenatally lethal, and heterozygous mice showed developmental delay relative to wild-type littermate mice. In addition, in behavioral analyses, we found that 14-3-3 gamma heterozygote mice display hyperactive and depressive-like behavior along with more sensitive responses to acute stress than littermate control mice. These results suggest that 14-3-3 gamma levels may be involved in the developmental manifestation of related neuropsychiatric diseases. In addition, 14-3-3 gamma heterozygote mice may be a potential model to study the molecular pathophysiology of neuropsychiatric symptoms.-
dc.languageEnglish-
dc.publisherKOREAN SOC BRAIN & NEURAL SCIENCE, KOREAN SOC NEURODEGENERATIVE DISEASE-
dc.subjectNEURONAL MIGRATION DELAY-
dc.subject14-3-3GAMMA PROTEIN-
dc.subjectCEREBROSPINAL-FLUID-
dc.subjectDEFECTS-
dc.subjectEPILEPSY-
dc.subjectYWHAG-
dc.subjectEXPRESSION-
dc.subjectDELETIONS-
dc.subjectABLATION-
dc.subjectDISEASE-
dc.title14-3-3 gamma Haploinsufficient Mice Display Hyperactive and Stress-sensitive Behaviors-
dc.typeArticle-
dc.identifier.doi10.5607/en.2019.28.1.43-
dc.description.journalClass1-
dc.identifier.bibliographicCitationEXPERIMENTAL NEUROBIOLOGY, v.28, no.1, pp.43 - 53-
dc.citation.titleEXPERIMENTAL NEUROBIOLOGY-
dc.citation.volume28-
dc.citation.number1-
dc.citation.startPage43-
dc.citation.endPage53-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.identifier.kciidART002444446-
dc.identifier.wosid000460388900004-
dc.identifier.scopusid2-s2.0-85071836694-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.type.docTypeArticle-
dc.subject.keywordPlusNEURONAL MIGRATION DELAY-
dc.subject.keywordPlus14-3-3GAMMA PROTEIN-
dc.subject.keywordPlusCEREBROSPINAL-FLUID-
dc.subject.keywordPlusDEFECTS-
dc.subject.keywordPlusEPILEPSY-
dc.subject.keywordPlusYWHAG-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusDELETIONS-
dc.subject.keywordPlusABLATION-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordAuthor14-3-3 gamma-
dc.subject.keywordAuthorYwhag-
dc.subject.keywordAuthorHyperactivity-
dc.subject.keywordAuthorAnxiety-
dc.subject.keywordAuthorAcute stress-
dc.subject.keywordAuthorADHD-
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