Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/7780
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dc.contributor.authorKenar, A.N.I.-
dc.contributor.authorAy, Ö.I.-
dc.contributor.authorHerken, Hasan-
dc.contributor.authorErdal, M.E.-
dc.date.accessioned2019-08-16T12:32:03Z
dc.date.available2019-08-16T12:32:03Z
dc.date.issued2014-
dc.identifier.issn1738-3684-
dc.identifier.urihttps://hdl.handle.net/11499/7780-
dc.identifier.urihttps://doi.org/10.4306/pi.2014.11.1.76-
dc.description.abstractObjective The etiology of attention deficit hyperactivity disorder (ADHD) has not been entirely clarified yet. Structural and metabolic differences at the prefrontal striatal cerebellary system and the interaction of gene and environment are the main factors that thought to play roles in the etiology. Genetic investigations are performed especially about the dopamine pathways and receptors. In this study; it was aimed to investigate the association of the synaptobrevin-2 (VAMP-2) gene Ins/Del polymorphism and syntaxin 1A gene intron 7 polymorphism, which take place in encoding presynaptic protein, with adult ADHD. Methods One hundred thirty-nine patients, having ADHD aging between 18 and 60 years and 106 healthy people as controls were included into the study. DNA samples were extracted from whole blood and genetic analysis were performed. Results A significant difference was determined between ADHD and VAMP-2 Ins/Del polymorphism and syntaxin 1A intron 7 polymorphism according to the control group. These polymorphisms were found not to be associated with subtypes of ADHD. Conclusion It is supposed that synaptic protein genes together with dopaminergic genes might have roles in the etiology of ADHD. © 2014 Korean Neuropsychiatric Association.en_US
dc.language.isoenen_US
dc.relation.ispartofPsychiatry Investigationen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectADHDen_US
dc.subjectGeneticen_US
dc.subjectSynaptobrevin 2en_US
dc.subjectSyntaxin 1Aen_US
dc.subjectVAMP-2en_US
dc.subjectadulten_US
dc.subjectalleleen_US
dc.subjectarticleen_US
dc.subjectattention deficit disorderen_US
dc.subjectcontrolled studyen_US
dc.subjectDNA polymorphismen_US
dc.subjectdopaminergic systemen_US
dc.subjectfemaleen_US
dc.subjectgeneen_US
dc.subjectgene frequencyen_US
dc.subjectgenetic analysisen_US
dc.subjectgenetic associationen_US
dc.subjectgenotypeen_US
dc.subjectgenotype environment interactionen_US
dc.subjecthumanen_US
dc.subjectintronen_US
dc.subjectmajor clinical studyen_US
dc.subjectmaleen_US
dc.subjectmiddle ageden_US
dc.subjectpolymerase chain reactionen_US
dc.subjectrestriction fragment length polymorphismen_US
dc.subjectStructured Clinical Interview for DSM Disordersen_US
dc.subjectsynaptobrevin 2 geneen_US
dc.subjectsyntaxin 1A geneen_US
dc.subjectyoung adulten_US
dc.titleAssociation of VAMP-2 and syntaxin 1A genes with adult attention deficit hyperactivity disorderen_US
dc.typeArticleen_US
dc.identifier.volume11en_US
dc.identifier.issue1en_US
dc.identifier.startpage76
dc.identifier.startpage76en_US
dc.identifier.endpage83en_US
dc.identifier.doi10.4306/pi.2014.11.1.76-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid24605127en_US
dc.identifier.scopus2-s2.0-84893338563en_US
dc.identifier.wosWOS:000330682500011en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.openairetypeArticle-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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