Search Results - "Pehlivan, S"

The circadian systems genes and their importance of human health by Pehlivan, S

“…The circadian rhythm is the timing mechanism that creates approximately 24-hour rhythms in cellular and bodily functions in almost all living species. These…”
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Monte Carlo simulation of reasons for early failure of implants: effects of two risk factors by Buhara, O., Pehlivan, S.

“…We have estimated the joint effects of two important risk factors on early failure of implants and then ranked all quoted risks by importance. We made a…”
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Quantitative detection of methylated SOCS-1 in schizophrenia and bipolar disorder considering SOCS-1 -1478 CA/del polymorphism and clinical parameters by Aytac, H.M., Pehlivan, S., Pehlivan, M., Oyaci, Y.

“…Introduction Suppressor of cytokine signaling (SOCS) proteins are the critical negative regulators of immune responses that exert their effects by inhibiting…”
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Effectiveness of erector spinae plane block in patients with percutaneous nephrolithotomy by Pehlivan, S, Gergin, O, Baydilli, N, Ulgey, A, Erkan, I, Bayram, A

“…Background: Percutaneous nephrolithotomy operation is a minimally invasive surgical procedure for the treatment of kidney stones. Aim: This study aimed to…”
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A New Clock is Running for Multiple Myeloma: Circadian Clock Protein-Period 3 (PER-3) Polymorphism by Serin, I., Pehlivan, S., Demir, I., Oyacı, Y., Pehlivan, M.

“…Circadian Clock Protein PERIOD 3 ( ) is situated on chromosome 1p36.23 and has a polymorphic domain that expresses 4 or 5 copies of the 54-bp tandem repeat…”
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PB1967: ROLE OF CYTOKINES IN MULTIPLE MYELOMA: IL‐1RN AND IL‐4 VNTR POLYMORPHISMS by Serin, I., OYACI, Y., PEHLIVAN, M., PEHLIVAN, S.

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The effect of hereditary thrombotic factors and comorbidities on the severity of COVID-19 disease by Kose, M, Senkal, N, Konyaoglu, H, Emet, A, Oyaci, Y, Pehlivan, S, Sayin, G Y

“…Coronavirus disease 2019 (COVID-19) has rapidly spread worldwide and presents critical challenges for public health. Due to its chronic and systemic course,…”
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PB1968: EPIGENETIC AND GENETIC INVESTIGATION OF SOCS‐1 GENE IN PATIENTS WITH MULTIPLE MYELOMA by Serin, I., TUNCEL, F. C., PEHLIVAN, S., OYACI, Y., PEHLIVAN, M.

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Statistical convergence in fuzzy normed linear spaces by SENCIMEN, C, PEHLIVAN, S

“…In this paper we introduce the notions of statistically convergent sequence and statistically Cauchy sequence in a fuzzy normed linear space ( FNS) and…”
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The functional variants of endothelial nitric oxide synthase gene associated with rheumatoid arthritis in Turkish adults by Pehlivan, S., Aydeniz, A., Sever, T., Altindag, O., Pehlivan, M., Gursoy, S., Oguzkan-Balci, S.

“…This study aimed to investigate whether functional variants of endothelial nitric oxide synthase (eNOS) gene play any role in rheumatoid arthritis (RA)…”
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Effects of TNFalpha, NOS3, MDR1 Gene Polymorphisms on Clinical Parameters, Prognosis and Survival of Multiple Myeloma Cases by Basmaci, C, Pehlivan, M, Tomatir, AG, Sever, T, Okan, V, Yilmaz, M, Oguzkan-Balci, S, Pehlivan, S

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Distribution of CXCR4 and tumour-infiltrating lymphocytes in breast cancer subtypes; their relationship with each other, axillary lymph node involvement, and other prognostic indicators by Pehlivan, Fatma S, Sivrikoz, Oya N, Dag, Filiz, Kececi, Sibel D, Sanal, Salahattin M

“…We have investigated the distribution of chemokine receptor 4 (CXCR4) and CD8-positive, tumour-infiltrating T lymphocytes (CD8+ TILs) in breast cancer subtypes…”
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Setleis syndrome: clinical, molecular and structural studies of the first TWIST2 missense mutation by Rosti, R.O., Uyguner, Z.O., Nazarenko, I., Bekerecioglu, M., Cadilla, C.L., Ozgur, H., Lee, B.H., Aggarwal, A.K., Pehlivan, S., Desnick, R.J.

“…Setleis syndrome is characterized by bitemporal scar‐like lesions and other characteristic facial features. It results from recessive mutations that truncate…”
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Association of XRCC1 and XPD functional gene variants with nicotine dependence and/or schizophrenia: a case-control study and in silico analysis by Pehlivan, S., Aydin, N., Nursal, A. F., Uysal, M. A., Pehlivan, M., Tekcan, A., Yavuz, F. K., Sever, U., Yavuzlar, H., Kurnaz, S., Uysal, S., Aydin, P. C.

“…OBJECTIVE: The role of DNA repair mechanisms has received attention recently in schizophrenia (Sch). Sch patients show an increased prevalence of nicotine…”
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Association of Macrophage Migration Inhibitory Factor Gene Promoter Polymorphisms with Multiple Sclerosis in Turkish Patients by Akcali, A, Pehlivan, S, Pehlivan, M, Sever, T, Neyal, M

“…Elevated levels of macrophage migration inhibitory factor (MIF) have been observed in the cerebrospinal fluid of patients with multiple sclerosis. This study…”
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eNOS and XRCC4 VNTR variants contribute to formation of nicotine dependence and/or schizophrenia by Pehlivan, S, Uysal, M A, Aydin, P C, Pehlivan, M, Nursal, A F, Yavuzlar, H, Kurnaz, S, Sever, U, Yavuz, F K, Uysal, S, Aydin, N

“…This study aimed to evaluate whether VNTR variants in the Endothelial Nitric Oxide Synthase (eNOS) and the XRCC4 gene play any role in nicotine dependence (ND)…”
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Conversion to Sirolimus for Chronic Allograft Nephropathy and Calcineurin Inhibitor Toxicity and the Adverse Effects of Sirolimus After Conversion by Sayin, B, Karakayali, H, Colak, T, Sevmis, S, Pehlivan, S, Demirhan, B, Haberal, M

“…Abstract Background Chronic allograft nephropathy and calcineurin inhibitor toxicity may cause graft loss. After kidney transplantation, especially among those…”
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Changes of tumor necrosis factor-α, interleukin-10, and tartrate-resistant acid phosphatase5b in the crevicular fluid in relation to orthodontic movement by Karaduman, B, Uraz, A, Altan, GN, Baloş Tuncer, B, Alkan, Ö, Gönen, S, Pehlivan, S, Çetiner, D

“…The aim of this study was to determine gingival crevicular fluid (GCF) expressions of tumor necrosis factor-α (TNF-α), interleukin-10 (IL-10), and…”
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DNA repair genes polymorphisms in multiple myeloma: no association with XRCC1 (Arg399Gln) polymorphism, but the XRCC4 (VNTR in intron 3 and G-1394T) and XPD (Lys751Gln) polymorphisms is associated with the disease in Turkish patients by Cifci, S, Yilmaz, M, Pehlivan, M, Sever, T, Okan, V, Pehlivan, S

“…This study aims to investigate the association between the polymorphisms in DNA repair genes (XPD, XRCC1, and XRCC4) and clinical parameters in patients with…”
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Multigene methylation analysis of conventional renal cell carcinoma by Onay, H, Pehlivan, S, Koyuncuoglu, M, Kirkali, Z, Ozkinay, F

“…Renal cell carcinoma (RCC) is the most common malignancy of the kidney. Since RCC is curable when it is confined to the renal capsule, early diagnosis is…”
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