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1دورية أكاديمية
المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Romatoloji Anabilim Dalı., orcid:0000-0002-0144-3263, Sarıcaoğlu, Hayriye, Yılmaz, Mediha, Karkucak, Mutlu, Öztürk, Hülya Z.Y., Yakut, Tahsin, Gülten, Tuna, Bülbül, Emel Başkan, Aydoğan, Kenan, Dilek, Kamil, AAH-1388-2021, 6603722836, 35148700000, 35388323500, 57197115377, 6602802424, 6505944216, 6602518817, 9739755800, 56005080200
مصطلحات موضوعية: Biochemistry & molecular biology, Genetics & heredity, Behcet's disease, Colchicine, ABCB1 gene, Polymorphism, Familial mediterranean fever, Multidrug-resistance gene, P-glycoprotein, Clinical-relevance, Mdr1, Association, Efficacy, Adult, Behcet syndrome, Case control studies, Female, Gene frequency, Genotype, Humans, Male, Middle aged, single nucleotide, MDR Gene, Multidrug Resistance Protein 1, Restriction Fragment Length Polymorphisms, Article, Behcet disease, Diarrhea, Drug withdrawal
وصف الملف: application/pdf
العلاقة: Makale - Uluslararası Hakemli Dergi; Genetics and Molecular Research; Sarıcaoğlu, H. vd. (2011). "Investigation of ABCB1 gene polymorphism with colchicine response in Behçet's disease". Genetics and Molecular Research, 10(1), 1-6.; https://doi.org/10.4238/vol10-1gmr824Test; http://www.funpecrp.com.br/gmr/year2011/vol10Test-1/pdf/gmr824.pdf; http://hdl.handle.net/11452/23737Test; 000286527300001; 2-s2.0-79251515771; 10
الإتاحة: https://doi.org/10.4238/vol10-1gmr824Test
http://hdl.handle.net/11452/23737Test
http://www.funpecrp.com.br/gmr/year2011/vol10Test-1/pdf/gmr824.pdf -
2دورية أكاديمية
المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Romatoloji Anabilim Dalı., orcid:0000-0002-0144-3263, Sarıcaoğlu, Hayriye, Yılmaz, Mediha, Karkucak, Mutlu, Öztürk, Hülya Z.Y., Yakut, Tahsin, Gülten, Tuna, Bülbül, Emel Başkan, Aydoğan, Kenan, Dilek, Kamil, AAH-1388-2021, 6603722836, 35148700000, 35388323500, 57197115377, 6602802424, 6505944216, 6602518817, 9739755800, 56005080200
مصطلحات موضوعية: Biochemistry & molecular biology, Genetics & heredity, Behcet's disease, Colchicine, ABCB1 gene, Polymorphism, Familial mediterranean fever, Multidrug-resistance gene, P-glycoprotein, Clinical-relevance, Mdr1, Association, Efficacy, Adult, Behcet syndrome, Case control studies, Female, Gene frequency, Genotype, Humans, Male, Middle aged, single nucleotide, MDR Gene, Multidrug Resistance Protein 1, Restriction Fragment Length Polymorphisms, Article, Behcet disease, Diarrhea, Drug withdrawal
وصف الملف: application/pdf
العلاقة: Makale - Uluslararası Hakemli Dergi; Genetics and Molecular Research; Sarıcaoğlu, H. vd. (2011). "Investigation of ABCB1 gene polymorphism with colchicine response in Behçet's disease". Genetics and Molecular Research, 10(1), 1-6.; https://doi.org/10.4238/vol10-1gmr824Test; http://www.funpecrp.com.br/gmr/year2011/vol10Test-1/pdf/gmr824.pdf; http://hdl.handle.net/11452/23737Test; 000286527300001; 2-s2.0-79251515771; 10
الإتاحة: https://doi.org/10.4238/vol10-1gmr824Test
http://hdl.handle.net/11452/23737Test
http://www.funpecrp.com.br/gmr/year2011/vol10Test-1/pdf/gmr824.pdf -
3دورية أكاديمية
المؤلفون: Gül, Cuma Bülent
المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Endokrinoloji ve Metabolizma Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/İmmünoloji Anabilim Dalı., orcid:0000-0001-7625-9148, orcid:0000-0003-0463-6818, Gül, Özen Öz, Cander, Soner, Budak, Ferah, Oral, Barbaros, Ersoy, Canan, AAI-1005-2021, F-4657-2014, K-7285-2012, AAH-8861-2021, 26040787100, 25027068600, 6701913697, 7004498001, 6701485882
مصطلحات موضوعية: Obstetrics & gynecology, Polycystic ovary syndrome, Cytokine signalling, SOCS1 polymorphism, Insulin resistance, Women, Prevalence, Expression, Variants, Proteins, Glucose, Obesity, Health, Adult, Body mass index, Case-control studie, Cholesterol, LDL, Female, Gene frequency, Humans, Logistic models, Middle aged, Polymerase chain reaction, Polymorphism, Genetic, Premenopause, Suppressor of cytokine signaling 1 protein, Triglycerides, Turkey
العلاقة: Makale - Uluslararası Hakemli Dergi; Journal of Obstetrics and Gynaecology; Sanayi; Gül, Ö. Ö. vd. (2017). ''Cytokine signal suppressor (SOCS) 1-1478 CA/del gene polymorphism in Turkish patients with polycystic ovary syndrome''. Journal of Obstetrics and Gynaecology, 37(7), 896-901.; https://doi.org/10.1080/01443615.2017.1309011Test; http://hdl.handle.net/11452/31884Test; 000411307000012; 2-s2.0-85020197942; 896; 901; 37
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4دورية أكاديمية
المؤلفون: Sarı, Esin Söğütlü, Yazıcı, Alper, Eser, Betül, Erol, Muhammet Kazım, Kılıç, Adil, Ermiş, Sıtkı Samet, Koytak, Arif, Akşıt, Hasan
المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., Yakut, Tahsin, 6602802424
مصطلحات موضوعية: 4G/5G polymorphism of PAI-1 gene, Central serous chorioretinopathy, Serum PAI-1 level, Promoter, Abnormalities, Risk, Ophthalmology, Toxicology, Adult, Female, Gene frequency, Genotype, Humans, Male, Middle aged, Plasminogen activator inhibitor 1, Polymorphism, genetic, Prevalence, Risk factors, Turkey, Central Serous Retinopathy, Fluorescence Angiography, Verteporfin, Genomic DNA, SERPINE1 protein, human, Article, Body mass, Clinical article
العلاقة: Makale - Uluslararası Hakemli Dergi; Cutaneous and Ocular Toxicology; Yurt içi; Sanayi; Sarı, E. S. vd. (2014). "The prevalence of 4G/5G polymorphism of plasminogen activator inhibitor-1 (PAI-1) gene in central serous chorioretinopathy and its association with plasma PAI-1 levels". Cutaneous and Ocular Toxicology, 33(4), 270-274.; 556-9535; https://doi.org/10.3109/15569527.2013.854372Test; http://hdl.handle.net/11452/27175Test; 000345498400002; 2-s2.0-84912100853; 270; 274; 33
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5دورية أكاديمية
المؤلفون: Sarı, Esin Söğütlü, Yazıcı, Alper, Eser, Betül, Erol, Muhammet Kazım, Kılıç, Adil, Ermiş, Sıtkı Samet, Koytak, Arif, Akşıt, Hasan
المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., Yakut, Tahsin, 6602802424
مصطلحات موضوعية: 4G/5G polymorphism of PAI-1 gene, Central serous chorioretinopathy, Serum PAI-1 level, Promoter, Abnormalities, Risk, Ophthalmology, Toxicology, Adult, Female, Gene frequency, Genotype, Humans, Male, Middle aged, Plasminogen activator inhibitor 1, Polymorphism, genetic, Prevalence, Risk factors, Turkey, Central Serous Retinopathy, Fluorescence Angiography, Verteporfin, Genomic DNA, SERPINE1 protein, human, Article, Body mass, Clinical article
العلاقة: Makale - Uluslararası Hakemli Dergi; Cutaneous and Ocular Toxicology; Yurt içi; Sanayi; Sarı, E. S. vd. (2014). "The prevalence of 4G/5G polymorphism of plasminogen activator inhibitor-1 (PAI-1) gene in central serous chorioretinopathy and its association with plasma PAI-1 levels". Cutaneous and Ocular Toxicology, 33(4), 270-274.; 556-9535; https://doi.org/10.3109/15569527.2013.854372Test; http://hdl.handle.net/11452/27175Test; 000345498400002; 2-s2.0-84912100853; 270; 274; 33
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6دورية أكاديمية
المؤلفون: Özçimen, Ahmet Ata
المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Mikrobiyoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Nefroloji ve Romatoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Fiziksel Tıp ve Rehabilitasyon Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Psikiyatri Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Nöroloji Anabilim Dalı., orcid:0000-0003-0463-6818, orcid:0000-0003-4436-3797, Dilek, Kamil, Bingöl, Ümit, Sarıcaoğlu, Hayriye, Sarandöl, Aslı, Taşkapılıoğlu, Özlem, Yurtkuran, Merih M., Yurtkuran, Mustafa Abbas, Oral, Haluk Barbaros, AAK-6623-2020, K-7285-2012, X-4479-2018, 56005080200, 6507727900, 6603722836, 14020405100, 23037226400, 55408539300, 7003389525, 7004498001
مصطلحات موضوعية: Genetics & heredity, Immunology, Interleukin-1 receptor antagonist, Inflammatory-bowel-disease, Ifn-gamma gene, In-vitro, Nucleotide-sequence, Cytokine production, Online databases, Long arm, Association, Risk, Adult, Behcet syndrome, Female, Gene frequency, Genetic predisposition to disease, Genotype, Humans, Interleukin-1, Male, Middle aged, Multigene Family, Polymorphism, genetic, single nucleotide, Turkey, Uveitis, Infliximab, Interleukin 1 receptor
العلاقة: Makale - Uluslararası Hakemli Dergi; T-2004/59; International Journal of Immunogenetics; Yurt içi; Özçimen, A. A. vd. (2011). "IL-1 cluster gene polymorphisms in Turkish patients with Behçet's disease". International Journal of Immunogenetics, 38(4), 295-301.; https://doi.org/10.1111/j.1744-313X.2011.01006.xTest; http://hdl.handle.net/11452/23505Test; 000292335800005; 2-s2.0-79959944004; 295; 301; 38
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7دورية أكاديمية
المؤلفون: Özçimen, Ahmet Ata
المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Mikrobiyoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Nefroloji ve Romatoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Fiziksel Tıp ve Rehabilitasyon Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Psikiyatri Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Nöroloji Anabilim Dalı., orcid:0000-0003-0463-6818, orcid:0000-0003-4436-3797, Dilek, Kamil, Bingöl, Ümit, Sarıcaoğlu, Hayriye, Sarandöl, Aslı, Taşkapılıoğlu, Özlem, Yurtkuran, Merih M., Yurtkuran, Mustafa Abbas, Oral, Haluk Barbaros, AAK-6623-2020, K-7285-2012, X-4479-2018, 56005080200, 6507727900, 6603722836, 14020405100, 23037226400, 55408539300, 7003389525, 7004498001
مصطلحات موضوعية: Genetics & heredity, Immunology, Interleukin-1 receptor antagonist, Inflammatory-bowel-disease, Ifn-gamma gene, In-vitro, Nucleotide-sequence, Cytokine production, Online databases, Long arm, Association, Risk, Adult, Behcet syndrome, Female, Gene frequency, Genetic predisposition to disease, Genotype, Humans, Interleukin-1, Male, Middle aged, Multigene Family, Polymorphism, genetic, single nucleotide, Turkey, Uveitis, Infliximab, Interleukin 1 receptor
العلاقة: Makale - Uluslararası Hakemli Dergi; T-2004/59; International Journal of Immunogenetics; Yurt içi; Özçimen, A. A. vd. (2011). "IL-1 cluster gene polymorphisms in Turkish patients with Behçet's disease". International Journal of Immunogenetics, 38(4), 295-301.; https://doi.org/10.1111/j.1744-313X.2011.01006.xTest; http://hdl.handle.net/11452/23505Test; 000292335800005; 2-s2.0-79959944004; 295; 301; 38
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