Showing results 11 to 30 of 42
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Issue Date | Title | Author(s) |
2016 | Detection of TET2, KRAS and CBL variants by Next Generation Sequencing and analysis of their correlation with JAK2 and FLT3 in childhood AML | Akın, D. F.; Öner D. A.; Mumcuoğlu M.; Ezer, U.; Bahce M.; Kurekci E.; Akar, Mehmet Nejat |
2015 | DETECTION OF TET2, KRAS, AND CBL VARIANTS BY NEXT GENERATION SEQUENCING IN CHILDHOOD ACUTE MYELOID LEUKEMIA | Akın, D. F.; Aslar, D.; Mumcuoğlu, M.; Ezer, U.; Bahce, M.; Kürekci, E.; Akar, Mehmet Nejat |
2016 | Distribution Of Platelet And Platelet Indices Due To Age | Ardıçoğlu Akışın, Nazife Yasemin ; Akar, Mehmet Nejat |
2018 | Enlarging the gene-geography of Europe and the Mediterranean area to STR loci of common forensic use: longitudinal and latitudinal frequency gradients | Messina, Francesco; Finocchio, Andrea ; Akar, Mehmet Nejat ; Loutradis, Aphrodite; Michalodimitrakis, Emmanuel I.; Brdicka, Radim; Jodice, Carla; Novelletto, Andrea |
2011 | Factor V Leiden and Natural Selection | Akar, Mehmet Nejat |
2012 | Factor V leiden and prothrombin 20210A mutations among turkish pediatric leukemia patients | Akın, Dilara Fatma; Sipahi, Kadir; Kayaalp, Tugba; Eğin, Yonca; Tasdelen, Serpil; Kurekci, Emin; Akar, Mehmet Nejat |
10-May-2018 | A finely resolved phylogeny of Y chromosome Hg J illuminates the processes of Phoenician and Greek colonizations in the Mediterranean | Finocchio, Andrea ; Trombetta, Beniamino ; Messina, Francesco ; D'Atanasio, Eugenia; Akar, Mehmet Nejat ; Loutradis, Aphrodite; Michalodimitrakis, Emmanuel I.; Cruciani, Fulvio ; Novelletto, Andrea |
2014 | FIRST OBSERVATION OF DE NOVO MYH9 GENE MUTATION IN A PATIENT WITH MACROTHROMBOCYTOPENIA | Torun, Didem; Duman, T.; Akar, Mehmet Nejat |
2016 | FIRST OBSERVATION OF TUBB1 GENE MUTATIONS IN TURKISH PATIENTS WITH MACROTHROMBOCYTOPENIA | Özkan, D. T.; Waheed, A. A.; Kandilci, A.; Akar, Mehmet Nejat |
2018 | Frequency of thiopurine S-methyltransferase gene variations in Turkish children with acute leukemia | Akın, Dilara Fatma; Aşlar-Öner, Deniz; Kürekçi, Emin; Akar, Mehmet Nejat |
Sep-2018 | Frequency of vitamin K oxidoreductase complex subunit-1 (VKORC1) polymorphisms and warfarin dose management in patients with venous thromboembolism | Kabalak, Pınar Akın; Savaş, İsmail; Akar, Mehmet Nejat ; Demir, Nalan; Eğin, Yonca |
Sep-2020 | Further note on Hemoglobin Fontainebleau (a21(B2) Ala-Pro) | Akar, Mehmet Nejat ; Ardıçoğlu Akışın, Nazife Yasemin |
2013 | High resolution transcriptomic analysis of trousseau syndrome | Dalkılıç, S.; Özkeserli, Z.; İlk, O.; Oğuzülgen, I. K.; Akar, Mehmet Nejat ; Özdağ, H. |
Jan-2019 | A Human Mission: Dumlupinar | Akar, Mehmet Nejat |
2011 | Kikuchi-fujimoto disease associated with aseptic meningitis: A case report | Arslan Z. ; Uysal O.; Özön A.; Rad A.; Atacanli A.; Akar, Mehmet Nejat ; Sümer M. |
2014 | NOVEL MUTATIONS AT GPIIB/GPIIIA GENES FROM TURKISH PATIENTS WITH GLANZMANN THROMBASTHENIA SYNDROME | Özkan, D. T.; Çalışkan, U.; Akar, Mehmet Nejat |
Jul-2018 | A novel MYH9 mutation in a beta thalassemia major patient with thrombocytopenia. | Özkan, Didem Torun; Akar, Mehmet Nejat |
2016 | Novel TUBB1 gene mutations in Turkish patients with macrothrombocytopenia | Özkan, D. T.; Waheed, A. A.; Kandilci, A.; Akar, Mehmet Nejat |
2020 | Platelet Satellitism | Ardıçoğlu Akışın, Nazife Yasemin ; Akar, Mehmet Nejat |
2015 | Radioactive fallout and neural tube defects | Akar, Nejat |