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Alterations of presynaptic proteins in autism spectrum disorder

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dc.contributor.authorYeo, Xin Yi-
dc.contributor.authorLim, Yi Tang-
dc.contributor.authorChae, Woo Ri-
dc.contributor.authorPark, Chungwon-
dc.contributor.authorPark, Hyokeun-
dc.contributor.authorJung, Sangyong-
dc.date.accessioned2023-01-19T00:40:30Z-
dc.date.available2023-01-19T00:40:30Z-
dc.date.created2023-01-18-
dc.date.issued2022-11-
dc.identifier.issn1662-5099-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/86655-
dc.description.abstractThe expanded use of hypothesis-free gene analysis methods in autism research has significantly increased the number of genetic risk factors associated with the pathogenesis of autism. A further examination of the implicated genes directly revealed the involvement in processes pertinent to neuronal differentiation, development, and function, with a predominant contribution from the regulators of synaptic function. Despite the importance of presynaptic function in synaptic transmission, the regulation of neuronal network activity, and the final behavioral output, there is a relative lack of understanding of the presynaptic contribution to the pathology of autism. Here, we will review the close association among autism-related mutations, autism spectrum disorders (ASD) phenotypes, and the altered presynaptic protein functions through a systematic examination of the presynaptic risk genes relating to the critical stages of synaptogenesis and neurotransmission.-
dc.language영어-
dc.language.isoen-
dc.publisherFRONTIERS MEDIA SA-
dc.relation.isPartOfFRONTIERS IN MOLECULAR NEUROSCIENCE-
dc.titleAlterations of presynaptic proteins in autism spectrum disorder-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000892823800001-
dc.identifier.doi10.3389/fnmol.2022.1062878-
dc.identifier.bibliographicCitationFRONTIERS IN MOLECULAR NEUROSCIENCE, v.15-
dc.description.isOpenAccessY-
dc.identifier.scopusid2-s2.0-85143318666-
dc.citation.titleFRONTIERS IN MOLECULAR NEUROSCIENCE-
dc.citation.volume15-
dc.contributor.affiliatedAuthorChae, Woo Ri-
dc.type.docTypeReview-
dc.subject.keywordAuthorpresynaptic proteins-
dc.subject.keywordAuthorsynaptopathy-
dc.subject.keywordAuthorpresynaptic vesicle dynamics-
dc.subject.keywordAuthorvesicle release machinery-
dc.subject.keywordAuthorsynaptogenesis-
dc.subject.keywordAuthorautism spectrum disorders (ASD)-
dc.subject.keywordPlusSYNAPTIC VESICLE PROTEIN-
dc.subject.keywordPlusCELL-ADHESION MOLECULES-
dc.subject.keywordPlusOF-FUNCTION MUTATIONS-
dc.subject.keywordPlusSYNAPSIN-I-
dc.subject.keywordPlusDE-NOVO-
dc.subject.keywordPlusACTIVE ZONE-
dc.subject.keywordPlusMENTAL-RETARDATION-
dc.subject.keywordPlusDOWN-SYNDROME-
dc.subject.keywordPlusNEURONAL-ACTIVITY-
dc.subject.keywordPlusDROSOPHILA DSCAM-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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