NO |
NAME |
DATE |
1 | Evaluation of supervision systems by PhD students in Dokuz Eylul University Graduate School of Healt... | 12/05/2022 - 14/05/2022 |
2 | Autopsy and forensic sciences approach in COVID-19 caused deaths... | 15/01/2021 - 16/01/2021 |
3 | Immunonutritional therapy in COVID-19 pandemia... | 15/01/2021 - 16/01/2021 |
4 | Branchiootorenal sendromu (BOR); eya1, SIX1, SIX5 genleri mutasyon analizi ve ailesel segregasyon... | 27/10/2019 - 30/10/2019 |
5 | Fisetin ve Kanser... | 18/10/2019 - 19/10/2019 |
6 | Hypoxia-induced transcriptional regulation of the N-Myc down regulated gene 1 (NDRG1) in human brain... | 07/07/2018 - 12/07/2018 |
7 | The effects of curcumin on EPO, HIF1alpha, VEGF, and CRAF in breast cancer: in vitro research... | 26/10/2017 - 29/10/2017 |
8 | Modulation of the NDRG1 gene expression in a time and oxygen concentration dependent manner in human... | 05/10/2017 - 07/10/2017 |
9 | Modulation of Carbonic Anhydrase IX Expression by the Regulative Effect of Hypoxia and Cytokines in ... | 24/05/2017 - 27/05/2017 |
10 | Alternating oxygenation conditions don't modulate EGR-1 expression in human brain cancer cells in vi... | 22/05/2017 - 25/05/2017 |
11 | Anti-Migration Effects of Bevacizumab on the Breast Cancer Cell Lines... | 22/05/2017 - 25/05/2017 |
12 | Molecular validation analysis of GAPDH as a reference gene for tumour gene expression studies under ... | 10/05/2017 - 12/05/2017 |
13 | Molecular regulation of hypoxia ınduced genes related to human cancer... | 06/10/2016 - 08/10/2016 |
14 | Functional regulation of hypoxia induced genes in human brain cancer... | 03/08/2016 - 08/08/2016 |
15 | İnsan Beyin Kanserinde Hipoksi İndüklü Genlerin Fonksiyonel Olarak Düzenlenmesi... | 01/06/2016 - 03/06/2016 |
16 | N-Myc downregulated gene 1 (NDRG1) gen ekspresyonunun, NDRG1-siRNA'nın 'in vitro-kültüre edilmiş... | 27/10/2015 - 30/10/2015 |
17 | Carbonic anhydrase 9 modulation by the regulative effect of hypoxic oxygenation and cytokine express... | 08/10/2015 - 10/10/2015 |
18 | NDRG1 as a marker gene for accute hypoxic oxygenation conditions in the brain tumor environment... | 04/07/2015 - 09/07/2015 |
19 | Maintaining the quality of experimental results when analyzing the expression of gene expression in ... | 04/07/2015 - 09/07/2015 |
20 | Hypoxia induced CA9 targeting via different alternative approaches including sulfonamide derivative ... | 04/07/2015 - 09/07/2015 |
21 | Importance of volumetric data on brain in a PTEN mutation positive Bannayan-Riley-Ruvalcaba Syndrome... | 04/07/2015 - 09/07/2015 |
22 | Directed modulation of hypoxia induced carbonic anhydrase 9 (CA9) gene by various alternative approa... | 20/05/2015 - 22/05/2015 |
23 | Effects of Amygdalin on Apoptosis in Liver Cancer Cell Lines... | 20/05/2015 - 22/05/2015 |
24 | Recurrent pregnancy loss and familial marker chromosome: case report... | 31/05/2014 - 03/06/2014 |
25 | A patient with partial 12q dublication and 10q deletion... | 31/05/2014 - 03/06/2014 |
26 | A de nova marker chromosome derived from 15q in a patient with growth retardation: genotype-phenotyp... | 31/05/2014 - 03/06/2014 |
27 | Komplet gonadal disgenezi tanılı iki olgu... | 06/12/2013 - 07/12/2013 |
28 | İnfertil olguda saptanan 46,XY, inv(9)(p11q13)x2 karyotipinin değerlendirilmesi... | 06/12/2013 - 07/12/2013 |
29 | Tekrarlayan gebelik kaybı ve ailesel geçişli marker kromozom olgu sunumu... | 06/12/2013 - 07/12/2013 |
30 | 45,X/46,X,i(Xq) karyotipine sahip mozaik Turner sendromu olgusu... | 06/12/2013 - 07/12/2013 |
31 | Boraks paklitaksel'in MCF-7 meme kanseri hücre hattı üzerine olan sitotoksik etkisini potansiyeli... | 27/10/2013 - 30/10/2013 |
32 | Programlı hücre ölümü (PDCD1) geni polimorfizmleri ve Ankilozan Spondilit arasındaki ilişkini... | 27/10/2013 - 30/10/2013 |
33 | Age related macular degeneration and association of CFH Y402H, rs1410966, LOC387715 A69S, rs11200638... | 08/06/2013 - 11/06/2013 |
34 | Prothrombotic gene polymorphisms in young patients with cerebrovascular accident... | 08/06/2013 - 11/06/2013 |
35 | Diyabetik Ayak Sendromu ile takip edilen Tip 2 Diyabet Hastalarında Anjiotensin Dönüştürücü E... | 19/12/2012 - 23/12/2012 |
36 | Ensefalosel ve bilateral fibula agenezi bulunan 6p delesyon sendromlu 22 haftalık fetüs: Olgu Sunu... | 19/12/2012 - 23/12/2012 |
37 | Yaşa bağlı maküler dejenerasyon hastalığında complement factor H (Y402H), rs1410966, LOC38771... | 19/12/2012 - 23/12/2012 |
38 | Muscle hemangiomatosis presenting as a severe feature in a patient with the PTEN mutation: expanding... | 23/06/2012 - 26/06/2012 |
39 | Yaşlılık Biyolojisi... | 31/03/2012 - 01/04/2012 |
40 | WNT4 geninin gonadal gelişimdeki rolünün kriptorşidizm tanısı konan çocuklarda WNT4 geni muta... | 27/10/2011 - 30/10/2011 |
41 | Bannayan-Riley-Ruvalcaba sendromunda karaciger hemanjiyomu: PTEN geninin klinik fenotipte rolü... | 27/10/2011 - 30/10/2011 |
42 | Serebrovasküler Olay Geçiren Genç Hastalarda Trombotik Gen Polimorfizmlerinin Araştırılması... | 27/10/2011 - 30/10/2011 |
43 | A 10 46 Mb 12p11 1 12 1 interstitial deletion coincident with a 0 19 Mb NRXN1 deletion detected by a... | 28/05/2011 - 31/05/2015 |
44 | Modulator effects of the methylenetetrahydrofolate reductase 677C-T polymorphism on B12 vitamin and ... | 01/12/2010 - 05/12/2010 |
45 | Turner syndrome: approach to the patient in primary care and case report... | 01/12/2010 - 05/12/2010 |
46 | Investigation of PON polymorphism in the planned coronary by-pass surgery... | 01/12/2010 - 05/12/2010 |
47 | Age related macular degeneration and association of CFH Y402H and LOC387715 A69S polymorphisms in a ... | 01/12/2010 - 05/12/2010 |
48 | Yaşlanma Genleri... | 19/02/2010 - 19/02/2010 |
49 | 16p11 kromozom bölgesinde mikrodelesyon saptanan multiple konjenital anomalili olgu sunumu... | 19/02/2010 - 19/02/2010 |
50 | Tiroidektomi öyküsü olan bir graves hastasında tiroglobulin genine ait E33SNP C/C polimorfizmi... | 28/10/2009 - 31/10/2009 |
51 | Azospermili hastada saptanan 46, XY del(Yp) genotipi... | 20/05/2009 - 23/05/2009 |
52 | 46,XY[92]/47,XY,+mar[8] karyotipi saptanan, spina bifida ve meningomiyolosel fetal anomalili olgu su... | 21/11/2008 - 21/11/2008 |
53 | Yumuşak Doku Dolgu Maddesi Olarak Otolog Fibroblast ve Hyaluronik Asit Kullanımı: Deneysel Çalı... | 14/09/2005 - 17/05/2005 |
54 | İnmemiş Testisli Olgularda Y Kromozom Mikrodelesyon Analiz Sonuçları... | 21/04/2004 - 24/04/2004 |
55 | p210 BCR-ABL Füzyon Geni Saptanan Bir Akut Promyelositik Lösemi Olgu Sunumu... | 21/04/2004 - 24/04/2004 |
56 | FMF Ön Tanısı ile Başvuran 788 Hastanın Mutasyon Analiz Sonuçları... | 21/04/2004 - 24/04/2004 |
57 | Spontan Gebelik Kayıplarında Sitogenetik Sonuçlarımız... | 21/04/2004 - 24/04/2004 |
58 | Spinal Müsküler Atrofi Ön Tanısı Alan Olgularda Moleküler Analiz Sonuçları... | 21/04/2004 - 24/04/2004 |
59 | Gülhane Askeri Tıp Akademisi Tıbbi Genetik BD'nın 1999-2003 Yılları Arasındaki Amniosentez So... | 21/04/2004 - 24/04/2004 |
60 | 120 Oligospermik ve Azospermik Hastada Yq Mikrodelesyon Analiz Sonuçları... | 21/04/2004 - 24/04/2004 |
61 | Tissue engineered cartilage on collagen and PHBV8 Matrices... | 15/06/2002 - 18/06/2002 |
62 | Mitomisin C ile indüklenmiş lenfosit hücre kültürlerinde melatonin ve Beta-karotenin in vitro s... | 18/09/2001 - 21/09/2001 |
63 | The role of prenatally diagnosed bilateral choroid plexus cysts in double trisomy Klinefelter Edwar... | 07/07/2001 - 10/07/2001 |