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Journal Abstract Search

445 related items for PubMed ID: 29973202

  • 1. Interaction between endothelial nitric oxide synthase rs1799983, cholesteryl ester-transfer protein rs708272 and angiopoietin-like protein 8 rs2278426 gene variants highly elevates the risk of type 2 diabetes mellitus and cardiovascular disease.
    El-Lebedy D.
    Cardiovasc Diabetol; 2018 Jul 04; 17(1):97. PubMed ID: 29973202
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  • 3. The minor allele of ANGPTL8 rs2278426 has a protective effect against CAD in T2DM patients.
    Bilgin AG, Ekici B, Ozuynuk-Ertugrul AS, Erkan AF, Coban N.
    Gene; 2024 Jul 01; 914():148418. PubMed ID: 38552749
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  • 4. Association between rs2278426 (C/T) and rs892066 (C/G) variants of ANGPTL8 (betatrophin) and susceptibility to type2 diabetes mellitus.
    Ghasemi H, Karimi J, Khodadadi I, Saidijam M, Tavilani H.
    J Clin Lab Anal; 2019 Jan 01; 33(1):e22649. PubMed ID: 30191588
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  • 5. The relationship of ACE and CETP gene polymorphisms with cardiovascular disease in a cohort of Asian Indian patients with and those without type 2 diabetes.
    Ganesan M, Bhaskar S, Mani R, Idris MM, Khaja N, Gulla S, Kumar U, Moova S, Vattam KK, Eppa K, Hasan Q, Pulakurthy UR.
    J Diabetes Complications; 2011 Jan 01; 25(5):303-8. PubMed ID: 21185205
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  • 6. Apolipoprotein E gene polymorphism and risk of type 2 diabetes and cardiovascular disease.
    El-Lebedy D, Raslan HM, Mohammed AM.
    Cardiovasc Diabetol; 2016 Jan 22; 15():12. PubMed ID: 26800892
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  • 8. Association between CETP gene polymorphism, insulin resistance and risk of diabetes mellitus in patients with vascular disease.
    Koopal C, van der Graaf Y, Asselbergs FW, Westerink J, Visseren FL, SMART study group.
    Atherosclerosis; 2015 Oct 22; 242(2):605-10. PubMed ID: 26318399
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  • 9. Association of ANGPTL8 (Betatrophin) Gene Variants with Components of Metabolic Syndrome in Arab Adults.
    Alenad A, Alenezi MM, Alokail MS, Wani K, Mohammed AK, Alnaami AM, Sulimani M, Zargar S, Clerici M, Al-Daghri NM.
    Sci Rep; 2020 Apr 21; 10(1):6764. PubMed ID: 32317770
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  • 11. The joint effect of the endothelin receptor B gene (EDNRB) polymorphism rs10507875 and nitric oxide synthase 3 gene (NOS3) polymorphism rs869109213 in Slovenian patients with type 2 diabetes mellitus and diabetic retinopathy.
    Bregar D, Cilenšek I, Mankoč S, Reschner A, Petrovič D, Globočnik Petrovič M.
    Bosn J Basic Med Sci; 2018 Feb 20; 18(1):80-86. PubMed ID: 28817788
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  • 13. Association of endothelial nitric oxide synthase gene polymorphisms with type 2 diabetes mellitus: a meta-analysis.
    Jia Z, Zhang X, Kang S, Wu Y.
    Endocr J; 2013 Feb 20; 60(7):893-901. PubMed ID: 23563728
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  • 14. The Arg59Trp variant in ANGPTL8 (betatrophin) is associated with total and HDL-cholesterol in American Indians and Mexican Americans and differentially affects cleavage of ANGPTL3.
    Hanson RL, Leti F, Tsinajinnie D, Kobes S, Puppala S, Curran JE, Almasy L, Lehman DM, Blangero J, Duggirala R, DiStefano JK.
    Mol Genet Metab; 2016 Jun 20; 118(2):128-37. PubMed ID: 27117576
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  • 15. Functional G894T (rs1799983) polymorphism and intron-4 VNTR variant of nitric oxide synthase (NOS3) gene are susceptibility biomarkers of obesity among Tunisians.
    Nasr HB, Dimassi S, M'hadhbi R, Debbabi H, Kortas M, Tabka Z, Chahed K.
    Obes Res Clin Pract; 2016 Jun 20; 10(4):465-75. PubMed ID: 25956856
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  • 18. Association of NOS3 gene polymorphisms with essential hypertension in Sudanese patients: a case control study.
    Gamil S, Erdmann J, Abdalrahman IB, Mohamed AO.
    BMC Med Genet; 2017 Nov 13; 18(1):128. PubMed ID: 29132319
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  • 19. Associations of cholesteryl ester transfer protein (CETP) gene variants with predisposition to age-related macular degeneration.
    Liutkeviciene R, Vilkeviciute A, Streleckiene G, Kriauciuniene L, Chaleckis R, Deltuva VP.
    Gene; 2017 Dec 15; 636():30-35. PubMed ID: 28918250
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  • 20. Association of endothelial nitric oxide synthase (NOS3) gene polymorphisms with primary open-angle glaucoma in a Saudi cohort.
    Kondkar AA, Azad TA, Sultan T, Osman EA, Almobarak FA, Al-Obeidan SA.
    PLoS One; 2020 Dec 15; 15(1):e0227417. PubMed ID: 31914149
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