Cytotoxic T lymphocyte antigen-4 (CTLA-4) A49G polymorphism and autoimmune blood diseases by Faruk Aktürk, Veysel Sabri Hançer, Reyhan Küçükkaya

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Two Rare Pathogenic HBB Variants in a Patient with β-Thalassemia Intermedia by Veysel Sabri Hançer, Tunç Fışgın, Murat Büyükdoğan

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Cytotoxic T lymphocyte antigen-4 (CTLA-4) A49G polymorphism and autoimmune blood diseases by Faruk Aktürk, Veysel Sabri Hançer, Reyhan Küçükkaya

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Three Factor 11 Mutations Associated with Factor XI Deficiency in a Turkish Family by Veysel Sabri Hançer, Zafer Gökgöz, Murat Büyükdoğan

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ADAMTS-13 gene expression in antiphospholipid syndrome by Veysel Sabri Hançer, Reyhan Diz Küçükkaya, Ayşegül Topal-Sarıkaya

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ADAMTS-13 gene expression in antiphospholipid syndrome by Veysel Sabri Hançer, Reyhan Diz Küçükkaya, Ayşegül Topal Sarıkaya

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MPL W515L/K Mutations in Chronic Myeloproliferative Neoplasms by Timur Selçuk Akpınar, Veysel Sabri Hançer, Meliha Nalçacı, Reyhan Diz- Küçükkaya

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New indicator of cellular ischemia in coronary slow-flow phenomenon: Cell-free DNA by Mustafa Yolcu, Ali Dogan, Nuri Kurtoglu, Veysel Sabri Hancer, Mehmet Gürbüzel

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Three Novel Calreticulin Mutations in Two Turkish Patients by Veysel Sabri Hançer, Hüseyin Tokgöz, Serkan Güvenç, Ümran Çalışkan, Murat Büyükdoğan

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β globin mutations in Turkish, Northern Iraqi and Albanian patients with β thalassemia major by Veysel Sabri Hancer, Tunc Fisgin, Murat Buyukdogan, Ceyhun Bozkurt, Sotiraq Lako

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The Relationship between P-Selectin Polymorphisms and Thrombosis in Antiphospholipid Syndrome: A Pilot Case-Control Study by Nilüfer Alpay, Veysel Sabri Hançer, Burak Erer, Murat İnanç, Reyhan Diz Küçükkaya

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The relationship between clinical parameters and hepatocyte growth factor/c-Met levels in the sperm of infertile males by Basak Ozge Kayan, Veysel Sabri Hancer, Uzay Gormus, Cenk Ozcan, Faruk Abike, Cem Murat Baykal

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A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing by İlker Karacan, Reyhan Diz Küçükkaya, Fatma Nur Karakuş, Seyhun Solakoğlu, Aslıhan Tolun, Veysel Sabri Hancer, Eda Tahir Turanlı

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NOVEL RUNX1 VARIATION IN B-CELL ACUTE LYMPHOBLASTIC LEUKEMIA by Egzona Qipa, Muradiye Acar, Sureyya Bozkurt, Murat Buyukdogan, Hazal Berivan Sonmez, Muge Sayitoglu, Yucel Erbilgin, Zeynep Karakas, Veysel Sabri Hancer

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Aberrant Activation-Induced Cytidine Deaminase Gene Expression Links BCR/ABL1-Negative Classical Myeloproliferative Neoplasms by Hasan Dermenci, Aynur Daglar Aday, Aysegul Basak Akadam Teker, Veysel Sabri Hancer, Metin Yusuf Gelmez, Meliha Nalcaci, Akif Selim Yavuz

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INVESTIGATION OF PTGS2, MAGE-A3, CALR, KRT19 AND TMPRSS4 EXPRESSIONS IN HCT116 COLON CANCER AND PC3 PROSTATE CANCER CELL LINES by Süreyya Bozkurt, Filiz Yarımcan, Hüseyin Ayhan, Hacer Kotan, Hüma Tuğçe Sezgin, Elif Çınar, Ceren Aynacı, Remzi Okan Akar, Veysel Sabri Hançer

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Polymorphisms of the angiotensin-converting enzyme and angiotensinogen gene in patients with atrial fibrillation by Nurdan Papila Topal, Beste Ozben, Veysel Sabri Hancer, Azra Meryem Tanrikulu, Reyhan Diz-Kucukkaya, Ali Serdar Fak, Yelda Basaran, Osman Yesildag

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Angiotensin-converting enzyme gene polymorphism in arrhythmogenic right ventricular dysplasia: is DD genotype helpful in predicting syncope risk? by Beste Ozben, Ibrahim Altun, Veysel Sabri Hancer, Ahmet Kaya Bilge, Azra Meryem Tanrikulu, Reyhan Diz-Kucukkaya, Ali Serdar Fak, Ercument Yilmaz, Kamil Adalet

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