İstanbul Üniversitesi
Akademik Veri Yönetim Sistemi
Yayınlar & Eserler
SCI,SSCI,AHCI İNDEKSLERİNE GİREN DERGİLERDE YAYINLANAN MAKALELER
Gündüz M.C., Evkuran Dal G., Kurban İ., Turna Ö., Günay Uçmak Z., Uçmak M., et al., "Uterine Immune Response After Single and Double Fresh Sperm Insemination in Mares", KAFKAS UNİVERSİTESİ VETERİNER FAKULTESİ DERGİSİ, vol.23, pp.879-886, 2017
Selçuk B.Ş., Bayrak A.E., Ünaltuna N., "Higher expression level of Bat3 is associated with silencing of the Midn gene in primary mouse cardiomyocytes", TURKISH JOURNAL OF BIOLOGY, vol.40, pp.1295-1302, 2016 (Link)
Peeters U., Scornik F., Riuro H., Perez G., Bayrak A.E., Van Malderen S., et al., "Contribution of Cardiac Sodium Channel beta-Subunit Variants to Brugada Syndrome", CIRCULATION JOURNAL, vol.79, pp.2118-+, 2015 (Abstract)
Çoban N., Onat A., Guclu-Geyik F., Bayrak A.E., Can G., Erginel-Unaltuna N., "Gender-specific associations of the APOA1-75G > A polymorphism with several metabolic syndrome components in Turkish adults", CLINICA CHIMICA ACTA, vol.431, pp.244-249, 2014 (Abstract)
Güleç Ç., Abaci N., Bayrak F., Bayrak A.E., Kahveci G., Guven C., et al., "Association between non-coding polymorphisms of HOPX gene and syncope in hypertrophic cardiomyopathy", ANADOLU KARDIYOLOJI DERGISI-THE ANATOLIAN JOURNAL OF CARDIOLOGY, vol.14, pp.617-624, 2014
Çoban N., Onat A., Guclu-Geyik F., Bayrak A.E., Sansoy V., Hergenc G., et al., "Gender- and obesity-specific effect of apolipoprotein C3 gene (APOC3)-482C > T polymorphism on triglyceride concentration in Turkish adults", CLINICAL CHEMISTRY AND LABORATORY MEDICINE, vol.50, pp.285-292, 2012
Guclu-Geyik F., Onat A., Çoban N., Bayrak A.E., Sansoy V., Can G., et al., "Minor allele of the APOA4 gene T347S polymorphism predisposes to obesity in postmenopausal Turkish women", MOLECULAR BIOLOGY REPORTS, vol.39, pp.10907-10914, 2012 (Abstract)
Bayrak A.E., Ozsait B., Erginel-Unaltuna N., "Isolation and analysis of genes mainly expressed in adult mouse heart using subtractive hybridization cDNA library", MOLECULAR BIOLOGY REPORTS, vol.39, pp.8065-8074, 2012
Bayrak A.E., Onat A., Yuzbasiogullari B., Mononen N., Laaksonen R., Kahonen M., et al., "The APOE -219G/T and +113G/C polymorphisms affect insulin resistance among Turks", METABOLISM-CLINICAL AND EXPERIMENTAL, vol.60, pp.655-663, 2011
Onat A., Bayrak A.E., Can G., Kucukdurmaz Z., Hergenc G., Erginel-Unaltuna N., "Apolipoprotein A-I positively associated with diabetes in women independently of apolipoprotein E genotype and apolipoprotein B levels", NUTRITION, vol.26, pp.975-980, 2010
Abaci N., Güleç Ç., Bayrak F., Bayrak A.E., Kahveci G., Erginel-Unaltuna N., "The variations of BOP gene in hypertrophic cardiomyopathy", ANADOLU KARDIYOLOJI DERGISI-THE ANATOLIAN JOURNAL OF CARDIOLOGY, vol.10, pp.303-309, 2010
Ozsait B., Bayrak A.E., Levula M., Erginel-Unaltuna N., Kahonen M., Rai M., et al., "Niemann-Pick type C fibroblasts have a distinct microRNA profile related to lipid metabolism and certain cellular components", BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, vol.403, pp.316-321, 2010
Sarwar N., Sandhu M.S., Ricketts S.L., Butterworth A.S., Di Angelantonio E., Boelcholdt S.M., et al.,"Triglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studies", LANCET, vol.375, pp.1634-1639, 2010 (Group Author(s): Triglyceride Coronary Dis Genetics )
Oksala N., Levula M., Airla N., Pelto-Huikko M., Ortiz R.M., Jarvinen O., et al., "ADAM-9, ADAM-15, and ADAM-17 are upregulated in macrophages in advanced human atherosclerotic plaques in aorta and carotid and femoral arteriesTampere vascular study", ANNALS OF MEDICINE, vol.41, pp.279-290, 2009 (Abstract)
Bayrak A.E., Erginel-Unaltuna N., Onat A., Ozsait B., Eklund C., Hurme M., et al., "Association of C-reactive protein (CRP) gene allelic variants with serum CRP levels and hypertension in Turkish adults", ATHEROSCLEROSIS, vol.206, pp.474-479, 2009
Bayrak A.E., Onat A., Poda M., Humphries S.E., Palmen J., Guclu F., et al., "Gender-modulated impact of apolipoprotein A5 gene (APOA5)-1131T > C and c.56C > G polymorphisms on lipids, dyslipidernia and metabolic syndrome in Turkish adults", CLINICAL CHEMISTRY AND LABORATORY MEDICINE, vol.46, pp.778-784, 2008
Okumus G., Kiyan E., Arseven O., Tabak L., Bayrak A.E., Unaltuna N.E., et al., "Platelet glycoprotein Ia 807c/T and 873g/A polymorphisms in patients with venous thromboembolism", CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, vol.13, pp.101-103, 2007
Bayrak A.E., Onat A., Poda M., Humphries S.E., Acharya J., Hergenc G., et al., "The S447X variant of lipoprotein lipase gene is associated with metabolic syndrome and lipid levels among Turks", CLINICA CHIMICA ACTA, vol.383, pp.110-115, 2007
Bayrak F., Bayrak A.E., Mutlu B., Kahveci G., Basaran Y., Erginel-Unaltuna N., "Ventricular pre-excitation and cardiac hypertrophy mimicking hypertrophic cardiomyopathy in a Turkish family with a novel PRKAG2 mutation", EUROPEAN JOURNAL OF HEART FAILURE, vol.8, pp.712-715, 2006
Bayrak A.E., Erginel-Unaltuna N., "Platelet glycoprotein Ia 807C/T (Phe224) and 873G/A (Thr246) dimorphism in Turkey", AMERICAN JOURNAL OF HEMATOLOGY, vol.69, pp.83-84, 2002
Erginel-Unaltuna N., Peoc'H K., Bayrak A.E., Acuner T., Issever H., Laplanche J., "Distribution of the M129V polymorphism of the prion protein gene in a Turkish population suggests a high risk for Creutzfeldt-Jakob disease", EUROPEAN JOURNAL OF HUMAN GENETICS, vol.9, pp.965-968, 2001
DİĞER DERGİLERDE YAYINLANAN MAKALELER
Selçuk B.Ş., Kömürcü Bayrak E., Kalkan M.A., Çelebi G., Ünaltuna N., "Kalbe özgü “subtractive” hibridizasyon cDNA kütüphanesinden elde edilen Mfn2, mt-Atp6, Midn ve Kpnb1 genlerinin yetişkin, neonatal ve embriyonik dokulardaki ekspresyon analizi", Deneysel Tıp Dergisi, cilt.7, ss.21-33, 2017
Poda M., Geyik F., Çoban N., Tüysüz B., Güven Z.G., Bayrak A.E., et al., "Evaluation of Dystrophin Gene Deletion Patterns in a Large Duchene/Becker Muscular Dystrophy Patient Sample; 17 Years Experience from one Turkish Diagnostic Center", Deneysel Tıp Dergisi, cilt.7, ss.50-61, 2017
Geyik F., Bayrak A.E., Bayrak F. , Çoban N., Öztunç E.F., Ünaltuna N., "Kardiyomiyopatiye Neden Olna Kardiyak Troponin T Gne Mutasyonlarının Araştırılması", Deneysel Tıp Araştırma Enstitüsü Dergisi, cilt.4, ss.17-24, 2016
Bayrak A.E., Poda M., Güven Z.G., Geyik F., Çoban N., Güleç Ç., et al., "15 Yıllık Huntington Hastalığı Genetik Test Sonuçları ve Literatürdeki HH Test Kılavuzları", Deneysel Tıp Araştırma Enstitüsü Dergisi, cilt.4, ss.10-16, 2016
Bayrak A.E., Erginel-Unaltuna N., "Gen anlatımı analiz yöntemlerine genel bakış", Deneysel Tıp Araştırma Enstitüsü Dergisi, cilt.1, ss.28-35, 2011
Ozsait B., Bayrak A.E., Poda M., Can G., Onat A., Hergenc G., et al., "CETP TaqIB polymorphism in Turkish adults: association with dyslipidemia and metabolic syndrome", Anadolu Kardiyoloji Dergisi, cilt.8, ss.324-330, 2008
Bayrak F., Bayrak A.E., Mutlu B., Kahveci G., Erginel-Unaltuna N., "Genetic analysis of the Irx4 gene in hypertrophic cardiomyopathy", Türk Kardiyoloji Derneği Arşivi, cilt.36, ss.90-95, 2008
Bayrak A.E., Issever H., Unaltuna N.E., "Glycoprotein Ia 807TT/873AA Genotype is not Associated With Myocardial Infarction", Anadolu Kardiyoloji Dergisi, cilt.5, ss.182-186, 2005
Bayrak A.E., Koç-Bebek A., Tüysüz B., Bebek N., Poda M., Özdemir C., et al., "Spinal Müsküler Atrofi (SMA) Hastalığının Prenatal Dönemde Moleküler Tanısı", Moleküler Tanı Dergisi, cilt.1, ss.9-12, 2004
HAKEMLİ KONGRE / SEMPOZYUMLARIN BİLDİRİ KİTAPLARINDA YER ALAN YAYINLAR
Bayrak A.E., Bayrak F., Kahveci G., Guclu-Geyik F., Erginel-Unaltuna N., "Sarcomeric gene mutations in Turkish families with hypertrophic cardiomyopathy", European Human Genetics Conference 2015, Glasgow, INGILTERE, 8-11 Haziran 2015, vol.23, no.1, pp.50-50
Ozsait B., Bayrak A.E., Jylha M., Perola M., Kristiansson K., Mononen N., et al., "USF1 GENE IS INVOLVED IN THE REGULATION OF HUMAN LONGEVITY", 77th Congress of the European Atherosclerosis Society, İSTANBUL, TÜRKIYE, 26-29 Temmuz 2008, vol.9, no.1, pp.103-103
Bayrak A.E., Ozsait B., Mononen N., Laaksonen R., Onat A., Hergenc G., et al., "CRP GENE POLYMORPHISMS ARE INVOLVED IN THE REGULATION OF PLASMA CRP CONCENTRATIONS IN TURKISH POPULATION: TURKISH ADULT RISK FACTOR STUDY", 77th Congress of the European Atherosclerosis Society, İSTANBUL, TÜRKIYE, 26-29 Temmuz 2008, vol.9, no.1, pp.104-104
Hergenc G., Onat A., Bayrak A.E., Erginel-Unaltuna N., Karabulut A., Can G., "Interrelation between apolipoprotein (apo) E genotype, serum levels of apo E and apo B: Association of uncommon genotypes with diabetes favor men", AACC Annual Meeting, Washington, ABD, 27-31 Temmuz 2008, vol.54, pp.A149-A149
Bayrak A.E., Ozsait B., Poda M., Onat A., Can G., Humphries S.E., et al., "Genes and HDL-C association in the adult Turkish population", 76th Congress of the European Atherosclerosis Society, Helsinki, FINLANDIYA, 10-13 Haziran 2007, vol.8, pp.52-52
Yuzbasiogullari B., Bayrak A.E., Onat A., Hergenc G., Erginel-Unaltuna N., "Effects of ACE insertion/deletion polymorphism on TARF study population", 32nd FEBS Congress, Vienna, AVUSTURYA, 7-12 Temmuz 2007, vol.274, pp.370-370
Poda M., Bayrak A.E., Sansoy V., Onat A., Can G., Hergenc G., et al., "The UCP3-55C/T polymorphism effects blood pressure levels in the Turkish adult risk factor (TARF) study", 76th Congress of the European Atherosclerosis Society, Helsinki, FINLANDIYA, 10-13 Haziran 2007, vol.8, pp.52-52
Ozsait B., Bayrak A.E., Onat A., Sansoy V., Hergenc G., Humphries S., et al., "CETP Taq1B-B2 allele is protective for dyslipidemia and not predictive for metabolic syndrome in Turkish adults", 76th Congress of the European Atherosclerosis Society, Helsinki, FINLANDIYA, 10-13 Haziran 2007, vol.8, pp.53-53
Horgusluoglu-Guner E., Bayrak A.E., Onat A., Hergenc G., Erginel-Unaltuna N., "Association between the PPAR-alpha L162V variant and components of the metabolic syndrome", 32nd FEBS Congress, Vienna, AVUSTURYA, 7-12 Temmuz 2007, vol.274, pp.371-371
Poda M., Bayrak A.E., Sansoy V., Onat A., Hergenc G., Humphries S.E., et al.,"", , Helsinki, , 10-13 Haziran 2007
Bayrak A.E., Sansoy V., Onat A., Erginel-Unaltuna N., "Relationship of the Prol2Ala PPAR-gamma 2 polymorphism with obesity in the adult Turkish population", 31st FEBS Congress, İSTANBUL, TÜRKIYE, 24-29 Haziran 2006, vol.273, pp.195-195
Mutlu B., Bayrak A.E., Bayrak F., Kahveci G., Basaran Y., Unaltuna N.E., "A novel mutation in PRKAG2 responsible for familial Wolff-Parkinson-White syndrome and severe cardiac hypertrophy", European Society of Cardiology Congress, Stockholm, ISVEÇ, 3-7 Eylül 2005, vol.26, pp.198-198
KİTAP ve KİTAP BÖLÜMLERİ
Ünaltuna N., Bayrak A.E., Çoban N., Geyik F., Poda M., Selçuk B.Ş., et al.,"TEKHARF Genetik Kanadı: Koroner Kalp Hastalığı ve Metabolik Sendrom Genetik Risk Faktörleri", TEKHARF ÇALIŞMASI 2015, Yetişkinlerimizin Sağlığı ve Kronik Hastalıklara Tıbbın Yaklaşımına Öncülük, Onat A., Ed., Logos Yayınevi, İstanbul, ss.240-252, 2015
Bayrak A.E., "Impact of genetic polymorphisms on insulin resistance", in: Insulin Resistance, Arora S. , Eds., InTech d.o.o., Rijeka, Croatia , pp.49-72, 2012
Unaltuna N.E., Poda M., Bayrak A.E., Ozsait B., Guclu-Geyik F., Çoban N., et al., "TEKHARF 2011, Halkımızın Kusurlu Kalp Sağlığına Işık Yoluyla, Tıbba Büyük Katkı", TEKHARF Genetik Kanadı Koroner Kalp Hastalığı ve Metabolik Sendrom Genetik Risk Faktörleri, Onat A., Ed., Logos Yayıncılık Tic. A.Ş., İstanbul, ss.209-219, 2011
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