Zobrazeno 1 - 10
of 100
pro vyhledávání: '"A. Nur Buyru"'
Autor:
M. Cem Ar, Deram Büyüktaş, A. Emre Eşkazan, Şeniz Öngören, Eda Tanrıkulu, Zafer Başlar, A. Nur Buyru, Burhan Ferhanoğlu, Yıldız Aydın, Nükhet Tüzüner, Teoman Soysal
Publikováno v:
Turkish Journal of Hematology, Vol 29, Iss 3, Pp 242-247 (2012)
OBJECTIVE: Bone marrow fibrosis is the second most common complication causing morbidity and mortality in patients with Philadelphia negative myeloproliferative neoplasms (MPNs). The aim of this study was to investigate the association of JAK2V617F m
Externí odkaz:
https://doaj.org/article/154967967e834a20a495f8b200b43a2e
Publikováno v:
BMC Cancer, Vol 18, Iss 1, Pp 1-7 (2018)
Abstract Background Laryngeal squamous cell carcinoma (LSCC) is the second most common cancer of the head and neck. In order to identify differentially expressed genes which may have a role in LSCC carcinogenesis, we performed GeneFishing Assay. One
Externí odkaz:
https://doaj.org/article/0cb05dda5ad940cc9e95904eebd52129
Publikováno v:
DNA and Cell Biology. 40:1222-1229
To elucidate the pathogenesis of prostate diseases, following in silico analysis, the LKB1 gene was selected for further investigation. The LKB1 gene has been associated with poor prognosis and is ...
Publikováno v:
Medicine Science, Vol 2, Iss 1, Pp 403-13 (2013)
Chronic obstructive pulmonary disease (COPD) is a disease which genetic and environmental factors play an important role in COPD development. VDBP (Vitamin D Binding Protein ) gene might be responsible for COPD development. The purpose of this study
Externí odkaz:
https://doaj.org/article/01ef9fd7168849639d157275f44eac99
Publikováno v:
Molecular Biology Reports. 47:1605-1612
Breast cancer, which is the most common type of cancer among women, is a heterogenous disease. It results from progressive accumulation of genetic and epigenetic alterations in different genes. The Dok1 protein has been identified as the major substr
Publikováno v:
PLoS ONE, Vol 10, Iss 1, p e0115353 (2015)
Different types of genetic and epigenetic changes are associated with HNSCC. The molecular mechanisms of HNSCC carcinogenesis are still undergoing intensive investigation. WWOX gene expression is altered in many cancers and in a recent work reduced W
Externí odkaz:
https://doaj.org/article/9220452b298e4f64a6fc902ef209e449
Autor:
Hikmet, Koseoglu, Asuman, Celebi, Gunay, Galamiyeva, Nejat, Dalay, Hakan, Ozkardes, Nur, Buyru
Publikováno v:
DNA and cell biology. 40(9)
To elucidate the pathogenesis of prostate diseases, following
Publikováno v:
Journal of Pediatric Hematology/Oncology. 41:519-524
The aim of this study was to evaluate the clinical characteristics, risk factors, treatment, and outcomes of pediatric stroke cases. A total of 118 patients diagnosed with arterial ischemic stroke (AIS), hemorrhagic stroke, and sinovenous thrombosis
Publikováno v:
Clinical Otolaryngology. 44:914-918
OBJECTIVE The purpose of this study was to investigate the hyaluronic acid (HA) and hyaluronidase-1 (HYAL-1) levels in laryngeal cancer patients. STUDY DESIGN Prospective, controlled clinical trial. SETTING University Medical Center. PARTICIPANTS Fif
Publikováno v:
Cancer Research. 82:776-776
Although thyroid cancer (TC) is a rare cancer with a rate of 2.1%, it is the most common cancer type among endocrine tumors. The molecular mechanisms of thyroid cancer, which develops as a result of environmental and genetic factors, are still unclea