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Journal Abstract Search

204 related items for PubMed ID: 33621527

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  • 23. ApoM/HDL-C and apoM/apoA-I ratios are indicators of diabetic nephropathy in healthy controls and type 2 diabetes mellitus.
    Zhang P, Gao J, Pu C, Feng G, Wang L, Huang L, Zhang Y.
    Clin Chim Acta; 2017 Mar; 466():31-37. PubMed ID: 28073663
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  • 24. BSMI single nucleotide polymorphism in vitamin D receptor gene is associated with decreased circulatory levels of serum 25-hydroxyvitamin D among micro and macrovascular complications of type 2 diabetes mellitus.
    Ezhilarasi K, Dhamodharan U, Vijay V.
    Int J Biol Macromol; 2018 Sep; 116():346-353. PubMed ID: 29738868
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  • 25. Apolipoprotein M promoter polymorphisms alter promoter activity and confer the susceptibility to the development of type 1 diabetes.
    Wu X, Niu N, Brismar K, Zhu X, Wang X, Efendic S, Du T, Liu Y, Gu HF, Liu Y.
    Clin Biochem; 2009 Jan; 42(1-2):17-21. PubMed ID: 19007767
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  • 26. The association of interieukin-6 polymorphism (rs1800795) with microvascular complications in Type 2 diabetes mellitus.
    Cui J, Zhang X, Guo C, Zhang L.
    Biosci Rep; 2020 Oct 30; 40(10):. PubMed ID: 33016995
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  • 27. The APOE4 allele is associated with a decreased risk of retinopathy in type 2 diabetics.
    Dlouha L, Pelikanova T, Veleba J, Adamkova V, Lanska V, Sosna T, Pacal L, Kankova K, Hubacek JA.
    Mol Biol Rep; 2021 Aug 30; 48(8):5873-5879. PubMed ID: 34328600
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  • 29. Effects of hyperlipidaemia on plasma apolipoprotein M levels in patients with type 2 diabetes mellitus: an independent case-control study.
    Zhang P, Gao J, Pu C, Feng G, Wang L, Huang L, Tao Q, Zhang Y.
    Lipids Health Dis; 2016 Sep 15; 15(1):158. PubMed ID: 27633510
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  • 30. Variants of the adiponectin gene and diabetic microvascular complications in patients with type 2 diabetes.
    Choe EY, Wang HJ, Kwon O, Kim KJ, Kim BS, Lee BW, Ahn CW, Cha BS, Lee HC, Kang ES, Mantzoros CS.
    Metabolism; 2013 May 15; 62(5):677-85. PubMed ID: 23260797
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  • 31. Regulation of apolipoprotein M gene expression by MODY3 gene hepatocyte nuclear factor-1alpha: haploinsufficiency is associated with reduced serum apolipoprotein M levels.
    Richter S, Shih DQ, Pearson ER, Wolfrum C, Fajans SS, Hattersley AT, Stoffel M.
    Diabetes; 2003 Dec 15; 52(12):2989-95. PubMed ID: 14633861
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  • 32. Association of resistin (rs3745367) and urotensin II (rs228648 and rs2890565) gene polymorphisms with risk of type 2 diabetes mellitus in Indian population.
    Kumar V, Singh J, Bala K, Singh J.
    Mol Biol Rep; 2020 Dec 15; 47(12):9489-9497. PubMed ID: 33269434
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  • 33. Association of HaeIII single nucleotide polymorphisms in the SLC2A1 gene with risk of diabetic nephropathy; evidence from Kurdish patients with type 2 diabetes mellitus.
    Amini S, Javanmardi M, Mokarizadeh A, Maroofi F, Jalali C, Azadi NA, Mohammadi H, Abdi M.
    QJM; 2016 Jun 15; 109(6):399-404. PubMed ID: 26337659
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  • 36. Determination of single-nucleotide polymorphism in the proximal promoter region of apolipoprotein M gene in coronary artery diseases.
    Zheng L, Luo G, Zhang X, Zhang J, Zhu J, Wei J, Mu Q, Chen L, Nilsson-Ehle P, Xu N.
    Int J Gen Med; 2009 Dec 29; 2():177-82. PubMed ID: 20360902
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  • 37. The association between apolipoprotein M and insulin resistance varies with country of birth.
    Memon AA, Bennet L, Zöller B, Wang X, Palmér K, Dahlbäck B, Sundquist J, Sundquist K.
    Nutr Metab Cardiovasc Dis; 2014 Nov 29; 24(11):1174-80. PubMed ID: 24984825
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  • 38. Common polymorphism in the cannabinoid type 1 receptor gene (CNR1) is associated with microvascular complications in type 2 diabetes.
    Buraczynska M, Wacinski P, Zukowski P, Dragan M, Ksiazek A.
    J Diabetes Complications; 2014 Nov 29; 28(1):35-9. PubMed ID: 24075694
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  • 39. A prospective evaluation of apolipoprotein M gene T-778C polymorphism in relation to coronary artery disease in Han Chinese.
    Jiao GQ, Yuan ZX, Xue YS, Yang CJ, Lu CB, Lu ZQ, Xiao MD.
    Clin Biochem; 2007 Oct 29; 40(15):1108-12. PubMed ID: 17674965
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  • 40. Association of rs7903146, rs12255372, and rs290487 polymorphisms in TCF7L2 gene with type 2 diabetes in an Iranian Kurdish ethnic group.
    Shokouhi S, Delpisheh A, Haghani K, Mahdizadeh M, Bakhtiyari S.
    Clin Lab; 2014 Oct 29; 60(8):1269-76. PubMed ID: 25185411
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