Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Kim, Do Eon | - |
dc.contributor.author | Cho, Chang-Hoon | - |
dc.contributor.author | Sim, Kyoung Mi | - |
dc.contributor.author | Kwon, Osung | - |
dc.contributor.author | Hwang, Eun Mi | - |
dc.contributor.author | Kim, Hyung-Wook | - |
dc.contributor.author | Park, Jae-Yong | - |
dc.date.accessioned | 2024-01-19T21:00:46Z | - |
dc.date.available | 2024-01-19T21:00:46Z | - |
dc.date.created | 2021-09-02 | - |
dc.date.issued | 2019-02 | - |
dc.identifier.issn | 1226-2560 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/120393 | - |
dc.description.abstract | 14-3-3 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.language | English | - |
dc.publisher | KOREAN SOC BRAIN & NEURAL SCIENCE, KOREAN SOC NEURODEGENERATIVE DISEASE | - |
dc.subject | NEURONAL MIGRATION DELAY | - |
dc.subject | 14-3-3GAMMA PROTEIN | - |
dc.subject | CEREBROSPINAL-FLUID | - |
dc.subject | DEFECTS | - |
dc.subject | EPILEPSY | - |
dc.subject | YWHAG | - |
dc.subject | EXPRESSION | - |
dc.subject | DELETIONS | - |
dc.subject | ABLATION | - |
dc.subject | DISEASE | - |
dc.title | 14-3-3 gamma Haploinsufficient Mice Display Hyperactive and Stress-sensitive Behaviors | - |
dc.type | Article | - |
dc.identifier.doi | 10.5607/en.2019.28.1.43 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | EXPERIMENTAL NEUROBIOLOGY, v.28, no.1, pp.43 - 53 | - |
dc.citation.title | EXPERIMENTAL NEUROBIOLOGY | - |
dc.citation.volume | 28 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 43 | - |
dc.citation.endPage | 53 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.description.journalRegisteredClass | kci | - |
dc.identifier.kciid | ART002444446 | - |
dc.identifier.wosid | 000460388900004 | - |
dc.identifier.scopusid | 2-s2.0-85071836694 | - |
dc.relation.journalWebOfScienceCategory | Medicine, Research & Experimental | - |
dc.relation.journalWebOfScienceCategory | Neurosciences | - |
dc.relation.journalResearchArea | Research & Experimental Medicine | - |
dc.relation.journalResearchArea | Neurosciences & Neurology | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | NEURONAL MIGRATION DELAY | - |
dc.subject.keywordPlus | 14-3-3GAMMA PROTEIN | - |
dc.subject.keywordPlus | CEREBROSPINAL-FLUID | - |
dc.subject.keywordPlus | DEFECTS | - |
dc.subject.keywordPlus | EPILEPSY | - |
dc.subject.keywordPlus | YWHAG | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordPlus | DELETIONS | - |
dc.subject.keywordPlus | ABLATION | - |
dc.subject.keywordPlus | DISEASE | - |
dc.subject.keywordAuthor | 14-3-3 gamma | - |
dc.subject.keywordAuthor | Ywhag | - |
dc.subject.keywordAuthor | Hyperactivity | - |
dc.subject.keywordAuthor | Anxiety | - |
dc.subject.keywordAuthor | Acute stress | - |
dc.subject.keywordAuthor | ADHD | - |
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