by Institution Author "Hancer, Veysel Sabri"
Now showing items 1-17 of 17
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Aberrant activation-induced cytidine deaminase gene expression links BCR/ABL1-negative classical myeloproliferative neoplasms
Dermenci, Hasan; Daglar Aday, Aynur; Akadam Teker, Aysegul Basak; Hancer, Veysel; Gelmez, Metin Yusuf; Nalcaci, Meliha; Yavuz, Akif Selim (TR- Dizin, 2022)Aim: Activation-induced cytidine deaminase (AID) has been associated with tumor initiation and development because of its ability to generate DNA damage and somatic mutations that cause genomic instability. This study ... -
A case mimicking chronic myeloid leukemia with t(8;22)(p11;q11)/BCR-FGFR1 and sequential transformation to B-acute lymphoblastic leukemia and acute myeloid leukemia
Bayrak, Ayse Gul; Ucur, Ali; Daglar-Aday, Aynur; Bagatır, Gulcin; Erdem, Simge; Hancer, Veysel Sabri; Nalcacı, Meliha; Ozturk, Sukru; Cefle, Kivanc; Palanduz, Sukru; Yavuz, Akif Selim (Springer Science and Business Media Deutschland GmbH, 2021)Myeloid/lymphoid neoplasm is a rare malignancy with an aggressive course and rapid transformation to acute myeloid leukemia (AML), or less frequently to acute lymphoblastic leukemia (ALL). Cases with t(8;22)(p11;q11) ... -
Case report of a young patient with transthyretin amyloidosis associated with Gly67Ala mutation
Salihoglu, Ayse; Yildirim, Suleyman; Ar, Muhlis Cem; Hancer, Veysel Sabri; Bozcan, Selma; Yilmaz, Umut; Serin, Nergis; Tuzuner, Nukhet; Celik, Aykut Ferhat (Taylor & Francis Ltd, 2019)Hereditary transthyretin-mediated amyloidosis (hATTR) is a rare, systemic and progressive autosomal dominant disease caused by mutations in the TTR gene. Systemic deposition of amyloidogenic mutant transthyretin results ... -
Cholangitis, döhle bodies, may-hegglin anomaly
Cholangitis, Döhle bodies, May-Hegglin anomaly -
The clinical significance of jak2v617f mutation for philadelphia-negative chronic myeloproliferative neoplasms in patients with splanchic vein thrombosis
Hindilerden, Fehmi; Hindilerden, Ipek Yonal; Pinarbasi Simsek, Binnur; Hancer, Veysel Sabri; Kaymakoglu, Sabahattin; Kucukkaya, Reyhan Diz; Nalcaci, Meliha (Cig Media Group, Lp, 2019)Context: High prevalence of JAK2V617F mutation in splanchic vein thrombosis (SVT), including Budd-Chiari syndrome (BCS) and portal vein thrombosis (PVT) raised suspicion of an underlying Philadelphiaenegative chronic ... -
Kruppel-Like transcription factor-4 gene expression and DNA methylation status in type 2 diabetes and diabetic nephropathy patients
Coskun, Zeynep Mine; Ersoz, Melike; Adas, Mine; Hancer, Veysel Sabri; Boysan, Serife Nur; Gonen, Mustafa Sait; Acar, Aynur (Elsevier Science Inc, 2019)Background/Aim. Diabetic nephropathy (DN) is one of the most serious microvascular complications in diabetic patients. The kruppel-like transcription factor-4 (KLF-4) affects the expression of genes involved in the ... -
New indicator of cellular ischemia in coronary slow-flow phenomenon: cell-free DNA
Yolcu, M.; Dogan, A.; Kurtoglu, N.; Hancer, V.S.; Gürbüzel, M (Turkish Society of Cardiology, 2020)Objective: Coronary slow-flow phenomenon (CSFP) is defined as the delayed arrival of coronary blood flow to the distal vascular bed in at least 1 major epicardial coronary artery. Cell-free DNA (cfDNA) is a type of DNA ... -
A novel COL3A1c.2644G > T; p.(Gly882Cys) variant in a Turkish family with vascular ehlers-danlos syndrome
Aydiner, Omer; Hancer, Veysel Sabri (Karger, 2020)Vascular Ehlers-Danlos syndrome (vEDS) is an autosomal dominant disease, also known as EDS type IV. The estimated prevalence for all EDS varies between 1/10,000 and 1/25,000 with EDS type IV representing approximately 5-10% ... -
A novel ganciclovir resistance mutation in the UL97 gene of the HHV-5 in an adult hematopoietic stem cell transplant recipient
Hancer, Veysel Sabri; Saglam Yarimcan, Filiz; Buyukdogan, Murat; Aki, Sahika Zeynep; Oksuz, Burcu; Acar, Kadir; Acar, Muradiye; Bulut, Pelin (Future Medicine Ltd, 2017)Therapeutic management of cytomegalovirus (CMV) disease in hematopoietic stem cell transplantation patients can become a challenge because of the emergence of anti-CMV drug resistance. This case report presents a patient ... -
A novel pathological arsb mutation (c.870G>A; p.Trp290stop) in mucopolysaccharidosis type VI patients
Hancer, Veysel Sabri; Buyukdogan, Murat; Babameto-Laku, Anila (Karger, 2019)Mucopolysaccharidosis (MPS) type VI, also known as Maroteaux-Lamy syndrome, is a lysosomal storage disorder, characterized by the deficiency of the arylsulfatase B enzyme. The clinical phenotype and severity of the illness ... -
Pharmacogenetic aspect of intravitreal ranibizumab treatment in neovascular age-related macular degeneration: a five-year follow-up
Şengül, 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 ... -
Prevalence of human papilloma virus types in Turkish and Albanian women
Hancer, Veysel Sabri; Buyukdogan, Murat; Bylykbashi, Ilta; Oksuz, Burcu; Acar, Muradiye (Wolters Kluwer Medknow Publications, 2018)Background: Human papilloma virus (HPV) infection is the major etiologic agent of cervical carcinoma. The aim of this study was to determine the prevalence of HPV infection and genotype distribution in cervical swabs from ... -
Prognostic significance of carbonic anhydrase IX overexpression in stage III non-small cell lung cancer patients after neoadjuvant treatment
Ibis, Kamuran; Saglam, Sezer; Saglam, Esra Kaytan; Firat, Pinar; Yilmazbayhan, Dilek; Toker, Alper; Ozkan, Berker; Hancer, Veysel Sabri; Buyukdogan, Murat; Disci, Rian; Pilanci, Kezban Nur (Elsevier Gmbh, Urban & Fischer Verlag, 2018)Background: To assess the prognostic importance of carbonic anhydrase IX (CA IX), a hypoxic biomarker, after neoadjuvant treatment in Stage III non-small cell lung cancer (NSCLC) patients. Methods: Tissue CA IX expression ... -
The relationship between clinical parameters and hepatocyte growth factor/c-Met levels in the sperm of infertile males
Kayan, Basak Ozge; Hancer, Veysel Sabri; Gormus, Uzay; Ozcan, Cenk; Abike, Faruk; Baykal, Cem Murat (IMR PRESS, 2022)Objective: Hepatocyte growth factor is a pleiotropic cytokine with potent mitogenic activity in many organs and tissues. The receptor for hepatocyte growth factor is c-Met, a transmembrane glycoprotein with tyrosine kinase ... -
Three factor 11 mutations associated with factor XI deficiency in a Turkish family
Hancer, Veysel Sabri; Gokgoz, Zafer; Buyukdogan, Murat (Galenos Yayincilik, 2018)Factor XI (FXI) is a homodimeric serine protease, which is produced in the liver and circulates in the plasma complexed with high-molecular-weight kininogen. FXI plays an important role in the amplification of the initial ... -
Three novel calreticulin mutations in two Turkish patients
Hancer, Veysel Sabri; Tokgoz, Huseyin; Guvenc, Serkan; Caliskan, Umran; Buyukdogan, Murat (Galenos Yayincilik, 2017)Calreticulin (CALR) mutations were first identified exclusively in JAK2-MPL-negative essential thrombocythemia (ET) and primary myelofibrosis (PMF) at a rate of 60%-88%, accounting for 1/4 to 1/3 of all patients with ... -
Two rare pathogenic HBB variants in a patient with beta-thalassemia intermedia
Hancer, Veysel Sabri; Fisgin, Tunc; Buyukdogan, Murat (Galenos Yayincilik, 2020)The β-thalassemias are a group of hereditary disorders with autosomal recessive inheritance characterized by the presence of defective synthesis of the β-globin chain, an integral component of the hemoglobin molecule, ...
