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| Issue Date | Title | Author(s) |
| 2019 | Altered microRNA 5692b and microRNA let-7d expression levels in children and adolescents with attention deficit hyperactivity disorder | Aydin, S.U.; Kabukçu Başay, Bürge ; Çetin, Gökhan Ozan ; Güngör Aydın, Ayşegül ; Tepeli, E. |
| 2018 | Association of synaptosomal-associated protein 25 (SNAP-25) gene polymorphism with temperament and character traits in women with fibromyalgia syndrome | Dogru, A.; Balkarli, A.; Tepeli, Emre ; Aydin, E.; Cobankara, V. |
| 2009 | A case of schizophrenia accompanying velocardiofacial syndrome | Şengül, Cem ; Efe, Muharrem ; Tepeli, Emre ; Çetin, Gökhan Ozan ; Düzcan, Füsun ; Herken, Hasan |
| 2015 | Comparison of IL-23 receptor gene polymorphisms in patients with primary sjogren syndrome, ankylosing spondylitis, and ankylosing spondylitis with sjogren's syndrome [Conference Object] | Temel, S; Balkarli, A; Tepeli, Emre ; Çobankara, Veli |
| 2016 | Comparison of IL-23 receptor gene polymorphisms in patients with primary sjögren syndrome, ankylosing spondylitis. and ankylosing spondylitis with sjögren’s syndrome [Article] | Temel, Şahin ; Balkarlı, Ayşe; Elmas, Levent ; Tepeli, Emre ; Çobankara, Veli |
| 2014 | Contribution of MLPA to routine testing to detect the prognostic chromosomal abnormalities in chronic lymphocytic leukemia | Ayaz, A.; Tepeli, Emre ; Sari, Hakan İsmail ; Cetin, O.; Eser, M.; Dogu, H.; Bağcı, Gülseren |
| 2015 | Could serum pentraxin 3 levels and IgM deposition in skin biopsies predict subsequent renal involvement in children with Henoch–Schönlein purpura? | Yüksel, Selçuk ; Çağlar, Murat ; Evrengül, Havva; Becerir, Tülay ; Tepeli, Emre ; Ergin, Ahmet ; Avcı Çiçek, Esin |
| 2011 | Determination of O-6-Methylguanine DNA Methyltransferase Promoter Methylation in Non-Small Cell Lung Cancer [Article] | Ekim, M.; Caner, Vildan ; Büyükpinarbaşili, N.; Tepeli, E. ; Elmas, L.; Bagcı, Gülseren |
| 2011 | Determination of O6-methylguanine DNA methyltransferase promoter methylation in non-small cell lung cancer [Conference Object] | Ekim, M; Caner, Vildan ; Buyukpinarbasili, N; Tepeli, E ; Elmas, L; Bağcı, Gülseren |
| 2012 | The determination of relationship between "excision repair cross-complementing group 1" (ERCC1) gene T19007C and C8092A single nucleotide polymorphisms and clinicopathological parameters in non-small cell lung cancer | Koç, Esin; Caner, Vildan ; Büyükpınarbaşılı, N.; Tepeli, Emre ; Türk, Nilay Şen ; Çetin, Gökhan Ozan ; Bağcı, Gülseren |
| 2018 | Diffüz Büyük B-hücreli Lenfoma Patogenezinde Tümör-kökenli Ekzozomların Fonksiyonal Önemi | Bağcı, Gülseren ; Çetin, Gökhan Ozan ; Tepeli, Emre ; Türk, Nilay Şen ; Caner, Vildan |
| 2015 | Esansiyel hipertansiyonlu olgularda CHGA geni promotor bölge polimorfizmlerinin araştırılması | Eser, Metin ; Şanlıalp, Musa ; Tepeli, Emre ; Tufan, Lale Şatıroğlu ; Kaftan, Havane Asuman ; Semerci, Cavidan Nur |
| 2012 | Expression of ERCC1 and its clinicopathological correlations in non-small cell lung cancer | Tepeli, Emre ; Caner, Vildan ; Büyükpınarbaşılı, N.; Çetin, Gökhan Ozan ; Düzcan, Füsun ; Elmas, Levent ; Bağcı, Gülseren |
| 2017 | Familial mutation in caffey disease with reduced penetrance: A case report | Özdemir, Özmert Muhammet Ali ; Tancer-Elçi, Hazal ; Polat, Aziz ; Güçtürk, İnci ; Tepeli, Emre ; Zeybek, Selcan; Ayaz, Akif |
| 2010 | Familial translocation (2;18) ascertained through recurrent spontaneous abortions [Article] | Bağcı, Gülseren ; Tepeli, Emre ; Düzcan, Füsun ; Çetin, G. Ozan ; Alataş, Erkan |
| 2007 | Familial translocation (2;18) ascertained through recurrent spontaneous abortions [Conference Object] | Bağcı, Gülseren ; Düzcan, Füsun ; Alatas, E ; Tepeli, Emre ; Çetin, G. Ozan |
| 2003 | Family history, clinical features, and molecular characterization of a patient with autosomal recessive non-syndromic hearing loss | Düzcan, F.; Wollnik, B.; Tepeli, E. ; Ardıç, Fazıl Necdet ; Uyguner, O.; Bağcı, Hüseyin. |
| 2004 | Femoral-facial syndrome with hemifacial microsomia and hypoglossia | Düzcan, F.; Ergin, H. ; Perçin, E.F.; Tepeli, E. ; Erkula, G. |
| 2014 | Frequency of mefv gene mutation and correlatin of mevf gene mutation with clinical symptoms in patients with gout | Balkarli, A; Tepeli, E ; Çobankara, Veli |
| 2014 | GADD45? methylation is more common in benign prostatic hyperplasia than in prostate cancer | Can, O.; Caner, Vildan ; Türk, Nilay Şen ; Tuncay, Ömer Levent ; Eskicorapci, S.Y. ; Tepeli, Emre ; Çetin, Ozan |
