Faculty of Medicine

Academic Members

Süreyya  Bozkurt

Süreyya Bozkurt,  Dr.

CV
Faculty Member

She had her Bachelor’s degree from Biology department at Hacettepe University in 1991. She earned her Master’s degree from Ankara University Biotechnology Institute, Basic Biotechnology in 2005. She studied at Montpellier University Department of Medical Genetics- France as a researcher in 2005 and she received European Molecular Cytogenetics Diploma from Montpellier University. She earned her PhD degree from Ankara University Faculty of Medicine, Department of Medical Biology in 2011. She studied at Imperial Collage of London- England in Molecular Patology Laboratory Cancer Cytogenetics Unit as visiting researcher in 2013. She was assistant professor in Oncology Institute Department of Basic Oncology at Hacettepe University between 2015-2016. She has been assistant professor at Istinye University, Faculty of Medicine Department of Medical Biology since 2016. Her research areas are cancer cytogenetics, molecular cytogenetics and cancer epigenetics.

Research Areas: Kanser genetiği, Lösemi sitogenetiği ve Kanser epigenetiği

Main Areas: Tıbbi Biyoloji, 

2020 - New mutations in KCNT2 gene causing early infantile epileptic encephalopathy type 57: Case study and literature review
ALAGÖZ MERYEM,KHERAD NASIM,BOZKURT SÜREYYA,YÜKSEL ADNAN. Acta Biochimica Polonica, 67(3), 431-434.
2020 - Investigation of PTGS2, MAGE-A3, CALR, KRT19 and TMPRSS4 expressions in HCT116 colon cancer and PC3 prostate cancer cell lines
BOZKURT SÜREYYA,YARIMCAN FİLİZ,AYHAN HÜSEYİN,KOTAN HACER,SEZGİN HÜMA TUĞÇE,ÇINAR ELİF,AYNACI CEREN,AKAR REMZİ OKAN,HANÇER VEYSEL SABRİ. Genetics Applications, 4(2), 37-42.
2020 - Rare Cytogenetic Anomalies in Two Pediatric Patients with Acute Leukemia
BOZKURT SÜREYYA,ÜNAL CANGÜL ŞULE,BAYHAN TURAN,GÜMRÜK FATMA,ÇETİN MUALLA. Turkish Journal of Hematology,
2020 - MDA-MB-231 Meme Kanseri Hücre Dizisinde Prostoglandin Endoperoksid H Sentaz 2 (PTGS2), Kalretikulin (CALR) ve Keratin-19 (KRT19) Genlerinin Transkripsiyon Aşamasında Anlatımlarının Araştırılması
KAYA YİĞİT DUYGU,BOZKURT SÜREYYA. Harran Üniversitesi Tıp Fakültesi Dergisi, 17(3), 397-400.
2020 - Expression Analysis in the Transcription Level of PTGS2, CALR, MAGE-A3 Genes in Non-Small Cell Lung Cancer
KÖSE BÜŞRA,BOZKURT SÜREYYA. Harran Üniversitesi Tıp Fakültesi Dergisi, 17(1), 108-112.
2019 - Çocukluk Çağı Lösemi Tanılı Hastalarda Sitogenetik Anomaliler
BOZKURT SÜREYYA,ÜNAL CANGÜL ŞULE,BAYHAN TURAN,GÜMRÜK FATMA,ÇETİN MUALLA. Acta Oncologica Turcica, 52(3), 424-431.
2019 - Retrospective evaluation of chromosome 1 anomalies in hematologic malignancies: A single center study
BOZKURT SÜREYYA,OKAY MÜFİDE,SAĞLAM FİLİZ,HAZNEDAROĞLU İBRAHİM CELALETTİN. Genetics Applications, 3(3), 17-24.
2019 - Cytogenetic anomalies in Multiple Myeloma patients:A single center study.
BOZKURT SÜREYYA,BÜYÜKAŞIK YAHYA,DEMİROĞLU HALUK,ALADAĞ KARAKULAK ELİFCAN,OKAY MÜFİDE,KARATAŞ AYŞE,AKSU SALİH,HAZNEDAROĞLU İBRAHİM CELALETTİN,SAYINALP NİLGÜN,ÖZCEBE OSMAN İLHAMİ,GÖKER HAKAN. Genetics Applications, 3(1), 51-56.
2019 - Hematological Neoplastic Disorders With Chromosome 3 Abnormalities
BOZKURT SÜREYYA,OKAY MÜFİDE,SAĞLAM FİLİZ,HAZNEDAROĞLU İBRAHİM CELALETTİN. Acta Medica Mediterranea, 35(5), 2703-2707.
2019 - Aggressive Clinicopathological Course of Myeloma with t(3;16) (q21;q22) Cytogenetic Abnormality
BOZKURT SÜREYYA,OKAY MÜFİDE,HAZNEDAROĞLU İBRAHİM CELALETTİN. Turkish Journal of Hematology, 36(1), 62-63.
2019 - Determining the frequency of iron overload at diagnosis in de novo acute myeloid leukemia patients with multilineage dysplasia or myelodysplasia-related changes: a case control study
YAVUZ BORAN,AYDIN MÜRÜVVET SEDA,BOZKURT SÜREYYA,ÜNER AYŞEGÜL,BÜYÜKAŞIK YAHYA. Journal of Hematopathology, 12(3), 135-141.
2018 - Characterization of imatinib-resistant K562 cell line displaying resistance mechanisms. Cell Mol Biol (Noisy-le-grand).
HEKMATSHOAR YALDA,ÖZKAN TÜLİN,ALTINOK GÜNEŞ BUKET,BOZKURT SÜREYYA,KARADAĞ GÜREL AYNUR,KARABAY ARZU ZEYNEP,SUNGUROĞLU ASUMAN. Cellular and Molecular Biology, 64(6), 23-30.
2017 - Sole Infrequent Karyotypic Aberration Trisomy 6 in a Patient with Acute Myeloid Leukemia and Breast Cancer in Remission
AYDIN MÜRÜVVET SEDA,BOZKURT SÜREYYA,GÜNEŞ GÜRSEL,MALKAN ÜMİT YAVUZ,ETGÜL SEZGİN,BÜYÜKAŞIK YAHYA,HAZNEDAROĞLU İBRAHİM CELALETTİN,SAYINALP NİLGÜN,GÖKER HAKAN,DEMİROĞLU HALUK,ÖZCEBE OSMAN İLHAMİ,AKSU SALİH. Turkish Journal of Hematology, 34(1), 103-104.
2016 - The Impact of Variant Philadelphia Chromosome Translocations on the Clinical Course of Chronic Myeloid Leukemia
EYÜPOĞLU NESRİN DAMLA,BOZKURT SÜREYYA,HAZNEDAROĞLU İBRAHİM CELALETTİN,BÜYÜKAŞIK YAHYA,GÜVEN DENİZ CAN. Turkish Journal of Hematology, 33(1), 60-65.
2016 - Comparison of Myelodysplastic Syndrome Prognostic Scoring Systems
BEKTAŞ ÖZLEN,ÜNER AYŞEGÜL,ELİAÇIK EYLEM,UZ BURAK,IŞIK AYŞE,ETGÜL SEZGİN,BOZKURT SÜREYYA,HAZNEDAROĞLU İBRAHİM CELALETTİN,GÖKER HAKAN,SAYINALP NİLGÜN,AKSU SALİH,DEMİROĞLU HALUK,ÖZCEBE OSMAN İLHAMİ,BÜYÜKAŞIK YAHYA. Turkish Journal of Hematology, 33(2), 119-126.
2015 - Clinical and pathological correlations of marrow PUMA and P53 expressions in myelodysplastic syndromes
BEKTAŞ ÖZLEN,ÜNER AYŞEGÜL,BÜYÜKAŞIK YAHYA,UZ BURAK,BOZKURT SÜREYYA,ELİAÇIK EYLEM,IŞIK AYŞE,HAZNEDAROĞLU İBRAHİM CELALETTİN,GÖKER HAKAN,DEMİROĞLU HALUK,AKSU SALİH,ÖZCEBE OSMAN İLHAMİ,SAYINALP NİLGÜN. APMIS, 123(5), 445-451.
2013 - Prognostic importance of additional cytogenetic anomalies in chronic myeloid leukemia
BOZKURT SÜREYYA,UZ BURAK,BÜYÜKAŞIK YAHYA,BEKTAŞ ÖZLEN,İNANÇ AYTEN,GÖKER HAKAN,KANSU EMİN. Medical Oncology, 30(1), 443-.
2013 - The roles of epigenetic modifications of proapoptotic BID and BIM genes in imatinib-resistant chronic myeloid leukemia cells
BOZKURT SÜREYYA,ÖZKAN TÜLİN,ÖZMEN FÜSUN,BARAN YUSUF,SUNGUROĞLU ASUMAN,KANSU EMİN. Hematology, 18(4), 217-223.
2011 - P16 and p27 tumor suppressor gene methylation status in childhood Wilms tumor cases
BOZKURT CEYHUN,BOZKURT SÜREYYA,ARDA NİLÜFER,ULYA ERTEM AYŞE,ŞAHİN GÜRSES,YÜKSEK NAZMİYE,GÜÇ DİCLE,KANSU EMİN. Turkish Journal Of Medical Sciences, 41(4), 633-638.
2011 - Secondary childhood acute myeloid leukemia with complex karyotypic anomalies including monosomy 7, monosomy 5 and translocation (110) after 131I-metaiodobenzylguanidine therapy for relapsed neuroblastoma
İNCESOY ÖZDEMİR SONAY,BOZKURT CEYHUN,YÜKSEK NAZMİYE,ÖREN AYŞE CEYDA,ŞAHİN GÜRSES,BOZKURT SÜREYYA,ERTEM ULYA. Turkish Journal of Pedıatrics, 53(1), 83-86.