Follow
Didem Torun Özkan
Didem Torun Özkan
Verified email at okan.edu.tr
Title
Cited by
Cited by
Year
The effects of Ankaferd Blood Stopper on transcription factors in HUVEC and the erythrocyte protein profile.
E Yılmaz, Ş Güleç, D Torun, İC Haznedaroğlu, N Akar
Turkish Journal of Hematology, 2011
532011
Novel mutations of integrin αIIb and β3 genes in Turkish children with Glanzmann’s thrombasthenia
H Tokgoz, D Torun Ozkan, U Caliskan, N Akar
Platelets 26 (8), 779-782, 2015
112015
Association of methylenetetrahydrofolate reductase C677T and cystathionine β-synthase polymorphisms in cardiovascular disease in the algerian population
B Houcher, Z Houcher, A Touabti, S Begag, D Torun, Y Eğin, N Akar, ...
Genetic Testing and Molecular Biomarkers 14 (6), 775-780, 2010
72010
Two new mutations at ERGIC-53 gene in a Turkish family
D Torun, E Yılmaz, A Atay, E Kürekçi, N Akar
Clinical and Applied Thrombosis/Hemostasis 17 (3), 248-250, 2011
42011
Pathogenic Ala303Val mutation in the PROS1 gene is associated with the pathogenesis of deep vein thrombosis.
DFA Bali, T Eroğlu, DT Özkan
32022
Identification of novel TUBB1 variants in patients with macrothrombocytopenia
ZO Çalişkaner, AA Waheed, MT Öztürk, Y Oymak, UH Tazebay, MN AKAR, ...
Turkish Journal of Medical Sciences 51 (2), 490-500, 2021
32021
Analysis of Protein C Inhibitor/ SERPINA5
D Torun Özkan, N Akar
Turkish Journal of Clinics and Laboratory 11 (1), 75-79, 2020
32020
Hemoglobin Lansing (Alpha)[HBA2 CD87 (HIS> GLU)(C> A)] in a Turkish Individual Resulting from Another Nucleotide Substitution/Bir Türk Bireyde Baska Bir Nükleotid Substitusyonu …
N Akar, D Torun, A Öztürk
Turkish Journal of Haematology 31 (3), 317, 2014
32014
Role of ZIP14 (SLC39A14) gene histidine rich regions in neural tube defects
D Torun, E Yılmaz, E Akar, N Akar
Egyptian Journal of Medical Human Genetics 12 (2), 135-137, 2011
32011
Molecular profiling of TAM tyrosine kinase receptors and ligands in endometrial carcinoma: An in silico-study
DF Akin, D Özkan
Taiwanese Journal of Obstetrics and Gynecology 62 (2), 311-324, 2023
22023
Genetic analysis of afibrinogenemia and hypofibrinogenemia: novel mutations in the FGB gene in the Turkish population
DT Özkan, N Sarper, N Akar
Acta Haematologica 143 (6), 529-532, 2020
22020
A novel protein C inhibitor gene mutation in pediatric stroke patients after bone marrow transplantation
D Torun, G Deda, M Ertem, Z Uysal, E Yılmaz, N Akar
Molecular biology reports 40, 5465-5468, 2013
22013
Identification of circadian-related gene mutation and expression patterns in skin cancer
DF AKIN, D Özkan
Sağlık Profesyonelleri Araştırma Dergisi 4 (3), 140-152, 2022
12022
A novel 110-bp insertion in a patient with homocysteinuria
D Torun, T İleri, K Gündüz, N Akar
Turk J Hematol 28, 354-6, 2011
12011
Angiotensinogen (AGT) gene screening and nutrigenetic approaches in patients diagnosed with hypertension
S Becer, D ÖZKAN
Turkish Journal of Clinics and Laboratory 13 (3), 316-321, 2022
2022
Beta-lactam antibiotic-induced thrombocytopenia: MYH9 & TUBB1 genes
NA Didem Özkan, Yasemin Ardıçoğlu Akışın, Dilara Fatma Akın Balı
Ann Clin Anal Med 13 (9), 973-977, 2022
2022
Case Report: A novel MYH9 mutation in a beta thalassemia major patient with thrombocytopenia
DT Özkan, N Akar
Egyptian Journal of Medical Human Genetics 19 (3), 271–272-271–272, 2018
2018
Screening of EPCR gene mutations in children with acute lymphoblastic leukemia
DFA Balı, DT Özkan, E Kürekçi, N Akar
The Egyptian Journal of Haematology 43 (3), 149-150, 2018
2018
Screening of single nucleotide polymorphism in CD95 (APO-1/FAS) promoter region (G-1377A) in children with acute leukemia
DF Akın, DT Özkan, E Kürekçi, N Akar
The Egyptian Journal of Haematology 43 (2), 45-48, 2018
2018
Investigation of SLC30A4 and SLC39A14 Zinc Transporter Gene’s Mutations in the Pathogenesis of Neural Tube Defects in Setif, Algeria
R Bourouba, D Torun, N Akar
Annual Research & Review in Biology 24 (6), 1-7, 2018
2018
The system can't perform the operation now. Try again later.
Articles 1–20