Search Results - "Yegin, O"

The Arg753Gln polymorphism of the human Toll-like receptor 2 gene in tuberculosis disease by Ogus, A.C, Yoldas, B, Ozdemir, T, Uguz, A, Olcen, S, Keser, I, Coskun, M, Cilli, A, Yegin, O

“…Toll-like receptor 2 (TLR2), a member of the Toll-like receptor family, plays an important role in recognition of, and subsequent immune response activation…”
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TNF-α gene 1031 T/C polymorphism in Turkish patients with Behçet's disease by Akman, A., Sallakci, N., Coskun, M., Bacanli, A., Yavuzer, U., Alpsoy, E., Yegin, O.

“…Summary Background  Genetic factors that predispose individuals to Behçet's disease (BD) are considered to play an important role in development of the…”
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Selective IgM deficiency in a boy with ring chromosome 18 by Celmeli, F, Turkkahraman, D, Cetin, Z, Mihci, E, Yegin, O

“…The incidence of chromosome 18 deletion syndrome is about 1 per 40 000 live births, and 18q- is one of the most common autosomal deletion syndromes in humans…”
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Relationship between periodontal findings and the TNF-α Gene 1031T/C polymorphism in Turkish patients with Behçet's disease by Akman, A, Sallakci, N, Kacaroglu, H, Tosun, O, Yavuzer, U, Alpsoy, E, Yegin, O

“…Background  Genetic factors that predispose individuals to Behçet's disease (BD) and periodontal disease. Tumour necrosis factor‐alpha (TNF‐α) has been…”
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Jessner lymphocytic infiltrate as a side effect of bee venom immunotherapy by Yalcin, A D, Bisgin, A, Akman, A, Erdogan, G, Ciftcioglu, M A, Yegin, O

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CTLA-4 gene polymorphism of exon 1(+49 A/G) in Turkish systemic lupus erythematosus patients by Ulker, M., Yazisiz, V., Sallakci, N., Avci, A. B., Sanlioglu, S., Yegin, O., Terzioglu, E.

“…Summary Cytotoxic T lymphocyte‐associated antigen‐4 is a cell‐surface molecule providing a negative signal for T cell activation. CTLA‐4 gene polymorphisms are…”
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Toll-like receptor 2 Arg753Gln gene polymorphism in Turkish patients with Behçet's disease by Bacanli, A., Sallakci, N., Yavuzer, U., Alpsoy, E., Yegin, O.

“…Summary Having considered the impact of the function of TLR2 in the recognition of several microorganisms that are thought to have an association with Behçet's…”
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CTLA-4 gene 49A/G polymorphism in Turkish patients with Behçet's disease by Sallakci, N., Bacanli, A., Coskun, M., Yavuzer, U., Alpsoy, E., Yegin, O.

“…Summary Genetic factors predisposing individuals to Behçet's disease (BD) are considered to play important roles in the development of the disease. Patients…”
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Predictive value of plasma and cerebrospinal fluid tumour necrosis factor-α and interleukin-1β concentrations on outcome of full term infants with hypoxic–ischaemic encephalopathy by Oygür, Nihal, Sönmez, Özlem, Saka, Osman, Yeǧin, Olcay

“…AIM To determine the predictive value of plasma and cerebrospinal fluid (CSF) tumour necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) concentrations on the…”
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Cytokines in acute rheumatic fever by YEGIN, O, COSKUN, M, ERTUG, H

“…Plasma concentrations of inflammatory cytokines (IL-1 alpha, IL-1 beta, IL-6, IL-8 and TNF alpha) were determined by ELISA in 27 patients with acute rheumatic…”
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Transferrin receptor in proliferation of T lymphocytes in infants with iron deficiency by ARTAC, H., COSKUN, M., KARADOGAN, I., YEGIN, O., YESILIPEK, A.

“…Summary The aim of this study was to contribute to clarify the mechanism of cellular immune insufficiency occurring during iron deficiency. We studied the…”
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Peripheral stem cell transplantation in a child with amegakaryocytic thrombocytopenia by YESILIPEK, M. A, HAZAR, V, KÜPESIZ, A, YEGIN, O

“…Congenital amegakaryocytic thrombocytopenia (CAMT) is an unusual cause of thrombocytopenia without radial or other congenital anomalies in the newborn…”
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Peripheral blood stem cell transplantation in children with beta-thalassemia by YESILIPEK, M. A, HAZAR, V, KÜPESIZ, A, KIZILÖRS, A, UGUZ, A, YEGIN, O

“…Fifteen patients with beta-thalassemia received an allogeneic peripheral blood stem cell transplant. Median age was 3.5 years (1-15 years). Six were class I,…”
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Simvastatin Therapy in Lymphocyte Cross-Match–Positive Kidney Transplantation Candidates by Yakupoglu, U., Kocak, H., Karatas, G.U., Yakupoglu, Y.K., Dinckan, A., Kececioglu, N., Gurkan, A., Demirbas, A., Yegin, O., Tuncer, M.

“…Recent identification of several mechanisms by which statins decrease recruitment of monocytes and T cells into the arterial wall and inhibit both T-cell and…”
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On Smith predictor based controllers for plants with time delay and multiple unstable modes by Yeg̃in, M.O., Özbay, H.

“…This work proposes an extension of the Smith predictor to design stabilizing controllers for linear time-invariant (LTI) time-delay single-input single-output…”
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An Unusual Presentation of Immunodeficiency with Hyper‐IgM by Uğuz, Ayşen, Yilmaz, Ertan, Çiftçioğlu, M. Akif, Yeğin, Olcay

“…: Hyper‐IgM syndrome is a rare immunodeficiency disease characterized by markedly decreased serum IgG, IgA, and IgE levels but normal or elevated IgM levels…”
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European internet-based patient and research database for primary immunodeficiencies: results 2006-2008 by Gathmann, B, Grimbacher, B, Beauté, J, Dudoit, Y, Mahlaoui, N, Fischer, A, Knerr, V, Kindle, G

“…Primary immunodeficiencies (PID) are rare diseases; therefore transnational studies are essential to maximize the scientific outcome and to improve diagnosis…”
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Relationship between hepatitis C virus infection and human leucocyte antigens in renal transplant patients by Tuncer, M, Sarikaya, M, Yegin, O, Süleymanlar, G, Ersoy, F, Yakupoglu, G

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Interferon-alpha therapy for refractory idiopathic thrombocytopenic purpura in children by Yeşilipek, M A, Yeğin, O

“…Interferon (IFN)-alpha therapy was presented as a possible treatment for refractory immune thrombocytopenic purpura (ITP). We used 3 x 10(6) U recombinant IFN…”
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Failure of granulocyte colony-stimulating factor and granulocyte-macrophage colony-stimulating factor in a patient with Kostmann syndrome by Hazar, V, Ongun, H, Yeşilipek, M A, Yeğin, O

“…We present a seven-month-old boy referred to our hospital with a history of recurrent suppurative infections starting in his neonatal period. Anemia, absolute…”
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