33 results on '"Bayoglu, Burcu"'
Search Results
2. Downregulation of MMP-2 and MMP-9 genes in obesity patients and their relation with obesity-related phenotypes
3. The effects of 5-HTTLPR/rs25531 serotonin transporter gene polymorphisms on antisocial personality disorder among criminals in a sample of the Turkish population
4. AGT rs699 and AGTR1 rs5186 gene variants are associated with cardiovascular-related phenotypes in atherosclerotic peripheral arterial obstructive disease
5. Contributors
6. Glucose and connections with OLR1 and IL17A genes
7. Polymorphisms in the long non-coding RNA CDKN2B-AS1 may contribute to higher systolic blood pressure levels in hypertensive patients
8. Genetic variants rs1994016 and rs3825807 in ADAMTS7 affect its mRNA expression in atherosclerotic occlusive peripheral arterial disease
9. Increased IL18 mRNA levels in peripheral artery disease and its association with triglyceride and LDL cholesterol levels: a pilot study
10. Review for "Molecular genetic associations between a prominent serotonin transporter gene polymorphism (5‐HTTLPR/rs25531) and individual differences in tendencies toward autistic traits and generalized internet use disorder in China and Germany"
11. Serotonin-2a receptor and catechol-O-methyltransferase polymorphisms in panic disorder
12. Roles of OLR1 and IL17A variants on clinical phenotypes of Turkish patients undergoing coronary artery bypass surgery.
13. Chromosome 9p21 rs10757278 polymorphism is associated with the risk of metabolic syndrome
14. Downregulation of MMP-2 and MMP-9 genes in obesity patients and their relation with obesity-related phenotypes.
15. Roles of OLR1and IL17Avariants on clinical phenotypes of Turkish patients undergoing coronary artery bypass surgery
16. Genetic polymorphism of angiotensin I-converting enzyme (ACE), but not angiotensin II type I receptor (ATr1), has a gender-specific role in panic disorder
17. AGT rs699 and AGTR1 rs5186 gene variants are associated with cardiovascular-related phenotypes in atherosclerotic peripheral arterial obstructive disease
18. Evaluation of effects of melatonin and caffeic acid phenethyl ester on acute potassium dichromate toxicity and genotoxicity in rats
19. Catechol-O-Methyltransferase Val158Met and brain-derived neurotrophic factor Val66Met gene polymorphisms in paraphilic sexual offenders
20. Orexin/hypocretin receptor, Orx1, gene variants are associated with major depressive disorder
21. Downregulation of MMP-2 and MMP-9 genes in obesity patients and their relation with obesity-related phenotypes
22. The Roles of the Long Non-Coding RNA Transcripts in Cardiovascular Diseases
23. Genetic variants rs1994016 and rs3825807 in ADAMTS7 affect its mRNA expression in atherosclerotic occlusive peripheral arterial disease
24. Upregulation of OLR1 and IL17A genes and their association with blood glucose and lipid levels in femoropopliteal artery disease
25. Orexin/hypocretin receptor, Orx1, gene variants are associated with major depressive disorder.
26. Evaluation of effects of melatonin and caffeic acid phenethyl ester on acute potassium dichromate toxicity and genotoxicity in rats
27. Increased IL18 mRNA levels in peripheral artery disease and its association with triglyceride and LDL cholesterol levels: a pilot study
28. Genetic Polymorphism of the Serotonin Transporter Gene, SLC6A4 rs16965628, Is Associated with Obsessive Compulsive Disorder
29. Evaluation of association between common genetic variants on chromosome 9p21 and coronary artery disease in Turkish population
30. Pro198Leu polymorphism in the oxidative stress gene, glutathione peroxidase-1, is associated with a gender-specific risk for panic disorder
31. Lack of association between endothelial nitric oxide synthase glu298Asp variation, visceral obesity and insulin related phenotypes in Turkish type 2 diabetic patients
32. The Severity of Internal Carotid Artery Stenosis is Associated with the Cyclin-Dependent Kinase Inhibitor 2A Gene Expression
33. Orexin/hypocretin receptor, Orx 1 , gene variants are associated with major depressive disorder.
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