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dc.contributor.authorBireller, Elif Sinem
dc.contributor.authorKucukali, Cem İsmail
dc.contributor.authorGULEC, Huseyin
dc.contributor.authorTuzun, Erdem
dc.contributor.authorCakmakoglu, Bedia
dc.contributor.authorTOPALOGLU, Muruvvet
dc.date.accessioned2021-03-03T17:25:21Z
dc.date.available2021-03-03T17:25:21Z
dc.date.issued2017
dc.identifier.citationTOPALOGLU M., Tuzun E., GULEC H., Bireller E. S. , Cakmakoglu B., Kucukali C. İ. , "Neuronal nitric oxide synthase polymorphisms in obsessive-compulsive disorder", NORDIC JOURNAL OF PSYCHIATRY, cilt.71, sa.2, ss.115-119, 2017
dc.identifier.issn0803-9488
dc.identifier.otherav_499d8ce6-cf97-456d-817d-8a90453b489c
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/52929
dc.identifier.urihttps://doi.org/10.1080/08039488.2016.1240230
dc.description.abstractBackground: Obsessive-compulsive disorder (OCD) is a mental disease characterized by recurrent and intrusive thoughts and repetitive behaviours that negatively affect the quality-of-life of the patients. Recent studies have implicated the participation of neuronal nitric oxide in OCD pathogenesis as a neurotransmitter modulator.Aims: To identify whether variations in neuronal nitric oxide synthase (nNOS) genes may render individuals susceptible to OCD development.Methods: This study examined nNOS polymorphisms in 100 OCD patients and 121 unrelated healthy controls by polymerase chain reaction and restriction enzyme digestion methods.Results: nNOS 276 C+genotype incidence was significantly higher in OCD patients than controls and conferred a 2-fold increased risk for OCD. No significant differences were observed in frequencies of nNOS 84 genotypes between patients and controls.Conclusion: This study shows an association between nNOS gene polymorphism and OCD. Exact mechanisms by which nNOS gene variants contribute to OCD pathogenesis need to be further investigated.
dc.language.isoeng
dc.subjectPsikiyatri
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.titleNeuronal nitric oxide synthase polymorphisms in obsessive-compulsive disorder
dc.typeMakale
dc.relation.journalNORDIC JOURNAL OF PSYCHIATRY
dc.contributor.departmentErenkoy Mental & Neurological Disorders Education & Research Hospital , ,
dc.identifier.volume71
dc.identifier.issue2
dc.identifier.startpage115
dc.identifier.endpage119
dc.contributor.firstauthorID69368


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