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Analysis of genetics and risk factors of Alzheimer’s Disease
MP Ates, Y Karaman, S Guntekin, MA Ergun
Neuroscience 325, 124-131, 2016
502016
Thiopurine methyltransferase polymorphisms and mercaptopurine tolerance in Turkish children with acute lymphoblastic leukemia
M Albayrak, U Konyssova, Z Kaya, T Gursel, S Guntekin, EF Percin, ...
Cancer chemotherapy and pharmacology 68, 1155-1159, 2011
312011
CFH Y402H and VEGF polymorphisms and anti-VEGF treatment response in exudative age-related macular degeneration
B Kepez Yildiz, S Ozdek, MA Ergun, S Ergun, F Yaylacioglu Tuncay, ...
Ophthalmic Research 56 (3), 132-138, 2016
282016
Influence of folate-related gene polymorphisms on high-dose methotrexate-related toxicity and prognosis in Turkish children with acute lymphoblastic leukemia
B Yazıcıoğlu, Z Kaya, SG Ergun, F Perçin, Ü Koçak, İ Yenicesu, T Gürsel
Turkish Journal of Hematology 34 (2), 143, 2017
252017
Synthesis of novel indole-isoxazole hybrids and evaluation of their cytotoxic activities on hepatocellular carcinoma cell lines
M Hawash, DC Kahraman, SG Ergun, R Cetin-Atalay, SN Baytas
BMC chemistry 15, 1-14, 2021
232021
Pharmacophore modeling and virtual screening studies to identify novel selective SIRT2 inhibitors
G Eren, A Bruno, S Guntekin-Ergun, R Cetin-Atalay, F Ozgencil, Y Ozkan, ...
Journal of Molecular Graphics and Modelling 89, 60-73, 2019
212019
Design and synthesis of novel substituted indole-acrylamide derivatives and evaluation of their anti-cancer activity as potential tubulin-targeting agents
M Hawash, DC Kahraman, A Olgac, SG Ergun, E Hamel, R Cetin-Atalay, ...
Journal of Molecular Structure 1254, 132345, 2022
182022
Twenty-four genes are upregulated in patients with hypospadias
R Karabulut, Z Turkyilmaz, K Sonmez, G Kumas, SG Ergun, MA Ergun, ...
Balkan Journal of Medical Genetics 16 (2), 39-43, 2013
182013
Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6
FY Tuncay, GK Kurekci, SG Ergun, OT Pasaoglu, RF Akata, PR Dincer
Molecular Vision 22, 1267, 2016
172016
Evaluation of GenoFlow Thrombophilia Array Test Kit in Its Detection of Mutations in Factor V Leiden (G1691A), Prothrombin G20210A, MTHFR C677T and …
E Aytekin, SG Ergun, MA Ergun, FE Percin
Genetic testing and molecular biomarkers 18 (11), 717-721, 2014
112014
The evaluation of long-term effects of ionizing radiation through measurement of current sister chromatid exchange (SCE) rates in radiology technologists, compared with …
E Tug, G Kayhan, D Kan, S Guntekin, MA Ergun
Mutation Research/Genetic Toxicology and Environmental Mutagenesis 757 (1 …, 2013
112013
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium
M Dundar, U Fahrioglu, SH Yildiz, B Bakir-Gungor, SG Temel, H Akin, ...
Functional & integrative genomics 22 (3), 291-315, 2022
102022
The correlation of attention deficit hyperactivity disorder with DRD4 gene polymorphism in Turkey
E Guney, E Iseri, SG Ergun, EF Percin, MA Ergun, O Yalcin, S Sener
International Journal of Human Genetics 13 (3), 145-152, 2013
102013
Novel indole-pyrazole hybrids as potential tubulin-targeting agents; Synthesis, antiproliferative evaluation, and molecular modeling studies
M Hawash, SG Ergun, DC Kahraman, A Olgac, E Hamel, R Cetin-Atalay, ...
Journal of Molecular Structure 1285, 135477, 2023
92023
Identification of Three Novel FBN1 Mutations and Their Phenotypic Relationship of Marfan Syndrome
G Kayhan, MA Ergun, SG Ergun, S Kula, FE Percin
Genetic Testing and Molecular Biomarkers 22 (8), 474-480, 2018
92018
Association of polymorphisms in APOE and LOXL1 with pseudoexfoliation syndrome and pseudoexfoliation glaucoma in a Turkish population
F Yaylacioğlu Tuncay, Z Aktaş, MA Ergün, SG Ergün, M Hasanreisoğlu, ...
Ophthalmic Genetics 38 (1), 95-97, 2017
92017
Single-nucleotide polymorphisms in IL23R-IL12RB2 (rs1495965) are highly prevalent in patients with Behcet’s uveitis and vary between populations
M Kramer, M Hasanreisoglu, S Weiss, D Kumova, M Schaap-Fogler, ...
Ocular Immunology and Inflammation, 2018
82018
LRP5-linked osteoporosis-pseudoglioma syndrome mimicking isolated microphthalmia
SG Ergun, GG Akay, MA Ergun, EF Perçin
European Journal of Medical Genetics 60 (3), 200-204, 2017
82017
EGF-SNX3-EGFR axis drives tumor progression and metastasis in triple-negative breast cancers
E Cicek, A Circir, M Oyken, O Akbulut Caliskan, DN Dioken, ...
Oncogene 41 (2), 220-232, 2022
62022
Identification of an mRNA isoform switch for HNRNPA1 in breast cancers
M Erdem, İ Ozgul, DN Dioken, I Gurcuoglu, S Guntekin Ergun, ...
Scientific Reports 11 (1), 24444, 2021
62021
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Artiklar 1–20