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Akademický článek

Microribonucleic acid dysregulations in children and adolescents with obsessive–compulsive disorder

Autor: Kandemir H, Erdal ME, Selek S, İzci Ay Ö, Karababa İF, Ay ME, Kandemir SB, Yılmaz ŞG, Ekinci S, Taşdelen B, Bayazit H

Publikováno v: Neuropsychiatric Disease and Treatment, Vol 2015, Iss default, Pp 1695-1701 (2015)

Hasan Kandemir,1 Mehmet Emin Erdal,2 Salih Selek,3 Özlem İzci Ay,2 İbrahim Fatih Karababa,4 Mustafa Ertan Ay,2 Sultan Basmaci Kandemir,5 Şenay Görücü Yılmaz,2 Suat Ekinci,6 Bahar Taşdelen,7 Hüseyin Bayazit41Department of Child and Adolescen

Externí odkaz: https://doaj.org/article/2a816db69f794ade88c91495ae38e9cf

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Are brain derived neurotrophic factor, neurotrophin-3 and neurotrophin-4 gene expression changes effective in the pathogenesis of major depression?

Autor: Yüksel Balim, D., İzci Ay, Ö., Ay, M.E., Karakaş, Ü., İnci Kenar, Ayşenur., Erdal, M.E.

Objective: Brain-derived neurotrophic factor (BDNF), neurotrophin-3 (NT-3) and neurotrophin-4 (NT-4) are neuro-trophins and they are critical regulators of the survival, differentiation, growth and plasticity of neuronal networks. There is plenty of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6e05915de23ce4cf227198c173717cfe

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Akademický článek

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Akademický článek

P-07 - Association of the DRD2 TaqIA, 5-HT1B A-161T and CNR1 1359 G/A polymorphisms with alcohol dependence: a single center experience in denizli province of turkey

Autor: Balci Sengul, C., Erdal, M.E., Sengul, C., İzci Ay, Ö., Efe, M., Ay, M.E., Herken, H.

Publikováno v: In European Psychiatry 2012 27 Supplement 1:1-1

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Akademický článek

White matter alterations related to attention-deficit hyperactivity disorder and COMT val158met polymorphism: children with valine homozygote attention-deficit hyperactivity disorder have altered white matter connectivity in the right cingulum (cingulate gyrus)

Autor: Kabukcu Basay B, Buber A, Basay O, Alacam H, Ozturk O, Suren S, Izci Ay O, Acikel C, Agladıoglu K, Erdal ME, Ercan ES, Herken H

Publikováno v: Neuropsychiatric Disease and Treatment, Vol 2016, Iss Issue 1, Pp 969-981 (2016)

Burge Kabukcu Basay,1 Ahmet Buber,1 Omer Basay,1 Huseyin Alacam,2 Onder Ozturk,1 Serkan Suren,3 Ozlem Izci Ay,4 Cengizhan Acikel,5 Kadir Agladioglu,6 Mehmet Emin Erdal,4 Eyup Sabri Ercan,7 Hasan Herken21Child and Adolescent Psychiatry Department, Pam

Externí odkaz: https://doaj.org/article/0ae40d004b334ee7b02017ee2b3186fb

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Akademický článek

Lack of association of DRD3 and CNR1 polymorphisms with premenstrual dysphoric disorders.

Autor: Yıldız M; Department of Psychiatry, Faculty of Medicine, Gaziosmanpaşa University, Tokat, Turkey., Vural M; Department of Obstetrics and Gynecology, Faculty of Medicine, Harran University, Sanliurfa, Turkey., Erdal ME; Department of Medical Biology and Genetics, Faculty of Medicine, Mersin University, Mersin, Turkey., İzci Ay Ö; Department of Medical Biology and Genetics, Faculty of Medicine, Mersin University, Mersin, Turkey., Yılmaz ŞG; Department of Medical Biology and Genetics, Faculty of Medicine, Mersin University, Mersin, Turkey., Karababa İF; Department of Psychiatry, Faculty of Medicine, Harran University, Sanliurfa, Turkey., Selek S; Department of Psychiatry &Behavıoral Sciences, University of Texas Health Science Center at Houston, Houston, Texas, USA.

Publikováno v: Iranian journal of reproductive medicine [Iran J Reprod Med] 2015 Apr; Vol. 13 (4), pp. 221-6.

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