Yazar "Hancer, Veysel Sabri" için listeleme
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Activation-induced cytidine deaminase mRNA levels in chronic lymphocytic leukemia
Hancer, Veysel Sabri; Kose, Murat; Diz-Kucukkaya, Reyhan; Yavuz, Akif Selim; Aktan, Melih (INFORMA HEALTHCARE, 2011)The Rai and Binet staging systems, which are used as standard methods for evaluating the prognosis of chronic lymphocytic leukemia (CLL), have some restrictions in identifying patients with early-stage CLL who will progress ... -
The Clinical Significance of JAK2V617F Mutation for Philadelphia-Negative Chronic Myeloproliferative Neoplasms in Patients with Splanchic Vein Thrombosis
Hindilerden, Fehmi; Hindilerden, Ipek Yonal; Pinarbasi, Binnur; Hancer, Veysel Sabri; Kaymakoglu, Sabahattin; Kucukkaya, Reyhan Diz; Nalcaci, Meliha (Cig Media Group, Lp, 2019)[No abstract available] -
The clinical significance of JAK2V617F mutation for Philadelphia-negative chronic myeloproliferative neoplasms in patients with splanchnic vein thrombosis
Yonal, Ipek; Pinarbasi, Binnur; Hindilerden, Fehmi; Hancer, Veysel Sabri; Nalcaci, Meliha; Kaymakoglu, Sabahattin; Diz-Kucukkaya, Reyhan (SPRINGER, 2012)Polycythemia vera (PV), essential thrombocythemia (ET) and idiopathic myelofibrosis (IMF), collectively known as Philadelphia-negative (Ph-negative) chronic myeloproliferative neoplasms (MPNs), MPNs represent the most ... -
Comparison of KRAS Mutation Tests in Colorectal Cancer Patients
Hancer, Veysel Sabri; Buyukdogan, Murat; Turkmen, Ilknur; Bassullu, Nuray; Altug, Tuncay; Diz-Kucukkaya, Reyhan; Demir, Gokhan (MARY ANN LIEBERT INC, 2011)The KRAS pathway and studies evaluating KRAS as a prognostic marker in colorectal cancer are discussed along with advances in KRAS gene mutation testing. Highly sensitive real-time polymerase chain reaction (PCR) methods ... -
Eculizumab therapy in a child with hemolytic uremic syndrome and CFI mutation
Cayci, F. Semsa; Cakar, Nilgun; Hancer, Veysel Sabri; Uncu, Nermin; Acar, Banu; Gur, Gokce (SPRINGER, 2012)Background Hemolytic uremic syndrome (HUS) is the most common cause of acute renal failure in childhood. It usually occurs after a prodromal episode of diarrhea and it leads to significant morbidity and mortality during ... -
Glycoprotein Ib alpha Kozak polymorphism in patients presenting with early-onset acute coronary syndrome
Golcuk, Ebru; Yalin, Kivanc; Akdeniz, Cansu Selcan; Teker, Erhan; Teker, Basak; Hancer, Veysel Sabri; Oncul, Aytac (TERMEDIA PUBLISHING HOUSE LTD, 2018)Introduction: Glycoprotein Ib alpha (GPIb alpha) receptor is the chief molecule responsible for initial platelet adhesion to the subendothelium. A thymidine to cytosine single nucleotide substitution at position -5 from ... -
Glycoprotein Ib-alpha Kozak polymorphism in ischemic stroke
Esen, Fatma Inci; Hancer, Veysel Sabri; Kucukkaya, Reyhan Diz; Yesilot, Nilufer; Coban, Oguzhan; Bahar, Sara; Tuncay, Rezzan (MANEY PUBLISHING, 2012)Background: Recently, a T/C polymorphism in the Kozak sequence of glycoprotein Ib-alpha (GPIb-alpha) gene at position 25 from the initiator ATG codons, has been identified. The presence of -5C allele increases the surface ... -
The impact of platelet membrane glycoprotein Ib alpha and Ia/IIa polymorphisms on the risk of thrombosis in the antiphospholipid syndrome
Yonal, Ipek; Hindilerden, Fehmi; Hancer, Veysel Sabri; Artim-Esen, Bahar; Daglar, Aynur; Akadam, Basak; Diz-Kucukkaya, Reyhan (PERGAMON-ELSEVIER SCIENCE LTD, 2012)Background: Pathogenesis of thrombus formation in antiphospholipid syndrome (APS) is not clear. Platelet membrane glycoprotein (GP) receptors play important roles in development of thrombosis. Objectives: We investigated ... -
A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing
Karacan, Ilker; Kucukkaya, Reyhan Diz; Karakus, Fatma Nur; Solakoglu, Seyhun; Tolun, Aslihan; Hancer, Veysel Sabri; Turanli, Eda Tahir (GALENOS YAYINCILIK, 2019)Objective: Autosomal recessive cutis laxa type IIA (ARCL2A) is a rare congenital disorder characterized by loose arid elastic skin, growth and developmental delay, and skeletal anomalies. It is caused by biallelic mutations ... -
Overexpression of Fc mu receptor (FCMR, TOSO) gene in chronic lymphocytic leukemia patients
Hancer, Veysel Sabri; Diz-Kucukkaya, Reyhan; Aktan, Melih (HUMANA PRESS INC, 2012)Rai and Binet staging systems that have been used as a standard method for evaluating the prognosis of chronic lymphocytic leukemia (CLL) have some restrictions in distinguishing the early stage CLL patients that will ... -
Pharmacogenetic Aspect of Intravitreal Ranibizumab Treatment in Neovascular Age-Related Macular Degeneration: A Five-Year Follow-Up
Sengul, Elvan Alper; Artunay, Ozgur; Rasier, Rifat; Kockar, Alev; Afacan, Ceyda; Hancer, Veysel Sabri; Yuzbasioglu, Erdal (TAYLOR & FRANCIS INC, 2018)Purpose: This study aims to evaluate the role of complement factor H (CFH) in response to intravitreal ranibizumab (IVR) treatment, which is administered to patients with neovascular age-related macular degeneration ...