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시냅스뇌질환연구단
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Slc6a20a Heterozygous and Homozygous Mutant Mice Display Differential Behavioral and Transcriptomic Changes

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dc.contributor.authorKim, Junhyung-
dc.contributor.authorJunyeop Daniel Roh-
dc.contributor.authorKim, Seongbin-
dc.contributor.authorKang, Hyojin-
dc.contributor.authorMihyun Bae-
dc.contributor.authorEunjoon Kim-
dc.date.accessioned2022-07-29T07:19:43Z-
dc.date.available2022-07-29T07:19:43Z-
dc.date.created2022-04-12-
dc.date.issued2022-03-
dc.identifier.issn1662-5099-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/11985-
dc.description.abstractCopyright © 2022 Kim, Roh, Kim, Kang, Bae and Kim.SLC6A20A is a proline and glycine transporter known to regulate glycine homeostasis and NMDA receptor (NMDAR) function in the brain. A previous study found increases in ambient glycine levels and NMDA receptor-mediated synaptic transmission in the brains of Slc6a20a-haploinsufficient mice, but it remained unknown whether Slc6a20a deficiency leads to disease-related behavioral deficits in mice. Here, we report that Slc6a20a heterozygous and homozygous mutant mice display differential behavioral phenotypes in locomotor, repetitive behavioral, and spatial and fear memory domains. In addition, these mice show differential transcriptomic changes in synapse, ribosome, mitochondria, autism, epilepsy, and neuron-related genes. These results suggest that heterozygous and homozygous Slc6a20a deletions in mice lead to differential changes in behaviors and transcriptomes.-
dc.language영어-
dc.publisherFrontiers Media S.A.-
dc.titleSlc6a20a Heterozygous and Homozygous Mutant Mice Display Differential Behavioral and Transcriptomic Changes-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000773606700001-
dc.identifier.scopusid2-s2.0-85127153480-
dc.identifier.rimsid78001-
dc.contributor.affiliatedAuthorJunyeop Daniel Roh-
dc.contributor.affiliatedAuthorMihyun Bae-
dc.contributor.affiliatedAuthorEunjoon Kim-
dc.identifier.doi10.3389/fnmol.2022.857820-
dc.identifier.bibliographicCitationFrontiers in Molecular Neuroscience, v.15-
dc.relation.isPartOfFrontiers in Molecular Neuroscience-
dc.citation.titleFrontiers in Molecular Neuroscience-
dc.citation.volume15-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusN-METHYLGLYCINE SARCOSINE-
dc.subject.keywordPlusTRANSPORTER-I INHIBITOR-
dc.subject.keywordPlusGLYCINE TRANSPORTER-
dc.subject.keywordPlusSYNAPTIC PLASTICITY-
dc.subject.keywordPlusORPHAN TRANSPORTER-
dc.subject.keywordPlusCLIMBING BEHAVIOR-
dc.subject.keywordPlusMOLECULAR-CLONING-
dc.subject.keywordPlusNMDA RECEPTORS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusMUTATIONS-
dc.subject.keywordAuthorsynapse-
dc.subject.keywordAuthorautism spectrum disorders-
dc.subject.keywordAuthorepilepsy-
dc.subject.keywordAuthorglycine and proline transport-
dc.subject.keywordAuthorlearning and memory-
dc.subject.keywordAuthormitochondria-
dc.subject.keywordAuthorNMDA receptors-
dc.subject.keywordAuthorribosomes-
Appears in Collections:
Center for Synaptic Brain Dysfunctions(시냅스 뇌질환 연구단) > 1. Journal Papers (저널논문)
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