Search Results - "Ataç, F. Belgin"

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    Uncoupling protein gene UCP1-3826A/G, UCP2 Ins/Del and UCP3-55C/T polymorphisms in obese Turkish children by Verdi, Hasibe, Kınık, Sibel Tulgar, Baysan-Çebi, H Pınar, Yalçın, Yaprak Yılmaz, Yazıcı-Güvercin, Ayşe Canan, Aydın, Beril, Tütüncü, Neslihan Başcıl, Ataç, F Belgin

    Published in The Turkish journal of pediatrics (2020)
    “…Mitochondrial uncoupling proteins (UCP) 1, 2 and 3 are members of the anion carrier protein family located in the inner mitochondrial membrane. There are…”
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    Journal Article
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    Aspirin resistance in cerebrovascular disease and the role of glycoprotein IIIa polymorphism in Turkish stroke patients by Derle, Eda, Öcal, Ruhsen, Kibaroğlu, Seda, Çelikkol, Ceyda, Bayraktar, Nilüfer, Verdi, Hasibe, Ataç, Belgin F, Can, Ufuk

    Published in Blood coagulation & fibrinolysis (01-03-2016)
    “…Aspirin resistance occurs in 5–45% of high-risk patients, with various mechanisms proposed for its development. This study aimed to determine the relationships…”
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    PAI-1 gene 4G/5G polymorphism, cytokine levels and their relations with metabolic parameters in obese children by Kinik, Sibel Tulgar, Ozbek, Namik, Yuce, Muammer, Yazici, Ayse Canan, Verdi, Hasibe, Ataç, F Belgin

    Published in Thrombosis and haemostasis (01-02-2008)
    “…Obesity is associated with the changes of plasminogen activator inhibitor-1 (PAI-1), tumor necrosis factor-alpha (TNFalpha) and transforming growth factor beta…”
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    Methylenetetrahydrofolate reductase C677T mutation and nonalcoholic fatty liver disease by SERIN, Ender, GÜCLÜ, Mustafa, ATAC, F. Belgin, VERDI, Hasibe, KAYASELCUK, Fazilet, OZER, Birol, BILEZIKCI, Banu, YILMAZ, Ugur

    Published in Digestive diseases and sciences (01-05-2007)
    “…A mutation in the methylenetetrahydrofolate reductase (MTHFR) gene is known as one of the causes of hyperhomocyteinemia. The oxidation products of homocysteine…”
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    Angiotensin I-Converting Enzyme Gene (I/D) Polymorphism in Patients With Migraine by Horasanlı, Bahriye, Ataç, F. Belgin, Çöven, İlker, Karakurum Goksel, Basak, Benli, Sibel

    Published in Headache (01-01-2013)
    “…In addition to the wide expression in many tissues including vascular endothelial cells, production of angiotensin II and degradation of bradykinin may…”
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    β-3AR W64R Polymorphism and 30-Minute Post-Challenge Plasma Glucose Levels in Obese Children by Verdi, Hasibe, Tulgar Kınık, Sibel, Yılmaz Yalçın, Yaprak, Muratoğlu Şahin, Nursel, Yazıcı, Ayşe Canan, Ataç, F Belgin

    “…In this study, we aimed to investigate the association of W64R polymorphism of the β3-adrenergic receptor gene (β-3AR) with childhood obesity and related…”
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    Atypical phenotypes of DYT1 dystonia in three children by Yilmaz, Unsal, Yüksel, Deniz, Atac, F.Belgin, Yilmaz, Deniz, Verdi, Hasibe, Senbil, Nesrin

    Published in Brain & development (Tokyo. 1979) (01-04-2013)
    “…Abstract DYT-1 dystonia is the most common primary dystonia seen in childhood. It is an autosomal dominantly inherited disorder caused by deletion of a GAG…”
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    Plasminogen activator inhibitor-1 gene 4G/5G polymorphism in Turkish children with asthma and allergic rhinitis by Ozbek, Ozlem Yilmaz, Ataç, F Belgin, Ogus, Ersin, Ozbek, Namik

    Published in Allergy and asthma proceedings (01-01-2009)
    “…Plasminogen activator inhibitor (PAI-1) has an essential role in tissue remodeling after inflammation. Recent literature revealed only one study evaluating…”
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    Transforming growth factor-beta1 (509 C/T, 915 G/C, 869 T/C) polymorphisms are not related to obesity in Turkish children by Kanra, Ali Riza, Tulgar-Kinik, Sibel, Verdi, Hasibe, Ataç, F Belgin, Yazici, Ayse Canan, Ozbek, Namik

    Published in Turkish journal of pediatrics (01-11-2011)
    “…Increasing expression of transforming growth factor-beta 1 (TGF-beta1) from fatty tissue affects the serum level and hence may stimulate expression of the…”
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    Journal Article
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    Heterozygous methylenetetrahydrofolate reductase 677C-T gene mutation with mild hyperhomocysteinemia associated with intrauterine iliofemoral artery thrombosis by Alioglu, Bulent, Ozyurek, Emel, Tarcan, Aylin, Atac, F Belgin, Gurakan, Berkan, Ozbek, Namik

    Published in Blood coagulation & fibrinolysis (01-09-2006)
    “…Neonatal thrombosis is a serious event that can cause mortality or severe morbidity. Newborn-related factors, including genetic prothrombotic risk factors, may…”
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    The Frequency of Factor V Leiden, Prothrombin G20210A and Methylenetetrahydrofolate Reductase C677T Mutations in Migraine Patients by Ruhsen Öcal, Ufuk Can, Hasibe Verdi, F. Belgin Ataç, Namık Özbek, Yıldız Kaya, Ü. Sibel Benli

    Published in Türk nöroloji dergisi (01-12-2010)
    “…OBJECTIVE: Migraine is an independent risk factor for ischemic stroke, but its pathophysiology is still unclear. Genetic factors that predispose patients to…”
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    Cardiac transplant in a child with recurrent thrombosis due to congenital thrombophilic mutations by Ozkan, Suleyman, Atac, F Belgin, Ozcobanoglu, Salih, Uguz, Emrah, Sezgin, Atilla, Verdi, Hasibe, Ozbek, Namik, Aslamaci, Sait

    “…A modified Blalock-Taussig shunt had been implanted 3 times to treat cyanosis to a patient who has uncorrectable congenital cardiac deformity. We repaired the…”
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    Proinflammatory Cytokine Single Nucleotide Polymorphisms in Nasal Polyposis by Erbek, Selim S, Yurtcu, Erkan, Erbek, Seyra, Atac, F. Belgin, Sahin, Feride I, Cakmak, Ozcan

    “…OBJECTIVE To investigate the association between nasal polyposis (NP) and single nucleotide polymorphisms of the proinflammatory cytokines IL (interleukin) 1α…”
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    The Role of miRNA in Endometriosis by Bilgili,Gamze, Verdi,Hasibe, Zeyneloğlu,B. Hulusi, Tohma,Yusuf Aytaç, Ataç,Fatma Belgin

    Published in Gazi tıp dergisi (05-11-2021)
    “…Endometriosis is characterized by the presence of endometrial gland and stroma outside of the endometrial cavity. Not only the complex nature of disease limits…”
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    The effect of plasminogen activator inhibitor-1 gene 4G/5G polymorphism on glucose and lipid metabolisms in Turkish obese children by Kınık, Sibel Tulgar, Ataç, F. Belgin, Verdi, Hasibe, Çetintaş, Sedat, Şahin, Feride İ., Özbek, Namık

    Published in Clinical endocrinology (Oxford) (01-05-2005)
    “…Summary Objective Obesity is a metabolic disorder that is associated with increased plasminogen activator inhibitor‐1 (PAI‐1) concentration in the circulation…”
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    Analysis of prothrombotic mutations and polymorphisms in children who developed thrombosis in the perioperative period of congenital cardiac surgery by Ozbek, Namik, Ataç, F Belgin, Yildirim, Selman V, Verdi, Hasibe, Yazici, Canan, Yilmaz, Başak T, Tokel, N Kürşat

    Published in Cardiology in the young (01-02-2005)
    “…In this study, we investigated some of the prothrombothic mutations and polymorphisms in 15 children with congenital cardiac malformations who developed severe…”
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    Thrombosis in children with cardiac pathology: analysis of acquired and inherited risk factors by Alioglu, Bulent, Avci, Zekai, Tokel, Kursat, Atac, F Belgin, Ozbek, Namik

    Published in Blood coagulation & fibrinolysis (01-06-2008)
    “…The present study was conducted to analyze the features and risk factors of childhood thrombotic events in patients with cardiac defect followed-up at our…”
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    Transforming growth factor-betal (509 C/T, 915 G/C, 869 T/C) polymorphisms are not related to obesity in Turkish children by Kanra, Ali Riza, Tulgar-Kinik, Sibel, Verdi, Hasibe, Ataç, F Belgin, Yazici, Ayse Canan

    Published in Turkish journal of pediatrics (01-11-2011)
    “…Increasing expression of transforming growth factor-beta 1 (TGF-beta1) from fatty tissue affects the serum level and hence may stimulate expression of the…”
    Get full text
    Journal Article