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Effects of uncoupling protein 2 -866G/A polymorphism on platelet reactivity and prognosis in Chinese patients with type 2 diabetes and ischemic stroke.

Chai Y, Gu B, Qiu JR, Yi HG, Zhu Q, Zhang L, Hu G.

Int J Neurosci. 2013 Nov;123(11):752-8. doi: 10.3109/00207454.2013.798733. Epub 2013 Aug 1.


The uncoupling protein 2 -866G > a polymorphism is associated with the risk of ischemic stroke in Chinese type 2 diabetic patients.

Chai Y, Gu B, Qiu JR, Yi HG, Zhu Q, Zhang L, Hu G.

CNS Neurosci Ther. 2012 Aug;18(8):636-40. doi: 10.1111/j.1755-5949.2012.00333.x. Epub 2012 May 22.


The common -866G/A polymorphism in the promoter region of the UCP-2 gene is associated with reduced risk of type 2 diabetes in Caucasians from Italy.

Bulotta A, Ludovico O, Coco A, Di Paola R, Quattrone A, Carella M, Pellegrini F, Prudente S, Trischitta V.

J Clin Endocrinol Metab. 2005 Feb;90(2):1176-80. Epub 2004 Nov 23.


Associations between UCP1 -3826A/G, UCP2 -866G/A, Ala55Val and Ins/Del, and UCP3 -55C/T polymorphisms and susceptibility to type 2 diabetes mellitus: case-control study and meta-analysis.

de Souza BM, Brondani LA, Bouças AP, Sortica DA, Kramer CK, Canani LH, Leitão CB, Crispim D.

PLoS One. 2013;8(1):e54259. doi: 10.1371/journal.pone.0054259. Epub 2013 Jan 24.


The frequent UCP2 -866G>A polymorphism protects against insulin resistance and is associated with obesity: a study of obesity and related metabolic traits among 17 636 Danes.

Andersen G, Dalgaard LT, Justesen JM, Anthonsen S, Nielsen T, Thørner LW, Witte D, Jørgensen T, Clausen JO, Lauritzen T, Holmkvist J, Hansen T, Pedersen O.

Int J Obes (Lond). 2013 Feb;37(2):175-81. doi: 10.1038/ijo.2012.22. Epub 2012 Feb 21.


Association of the UCP polymorphisms with susceptibility to obesity: case-control study and meta-analysis.

Brondani LA, de Souza BM, Assmann TS, Bouças AP, Bauer AC, Canani LH, Crispim D.

Mol Biol Rep. 2014 Aug;41(8):5053-67. doi: 10.1007/s11033-014-3371-7. Epub 2014 Apr 22. Erratum in: Mol Biol Rep. 2014 Sep;41(9):6325. de Almeida Brondani, Letícia [corrected to Brondani, Leticia de Almeida].


UCP2 -866G/A and Ala55Val, and UCP3 -55C/T polymorphisms in association with type 2 diabetes susceptibility: a meta-analysis study.

Xu K, Zhang M, Cui D, Fu Y, Qian L, Gu R, Wang M, Shen C, Yu R, Yang T.

Diabetologia. 2011 Sep;54(9):2315-24. doi: 10.1007/s00125-011-2245-y. Epub 2011 Jul 13.


Uncoupling protein 2 and 3 gene polymorphisms and their association with type 2 diabetes in asian indians.

Vimaleswaran KS, Radha V, Ghosh S, Majumder PP, Sathyanarayana Rao MR, Mohan V.

Diabetes Technol Ther. 2011 Jan;13(1):19-25. doi: 10.1089/dia.2010.0091.


Role of functional polymorphisms of the IL-10 gene promoter in the risk of ischemic stroke in Chinese Uyghur population: One case-control study.

Tong Y, Cai L, Zhang YW, Lin L, Liu S, Hou S, Wu Y, Han S, Lu Q, Liu J.

Int J Cardiol. 2016 May 15;211:58-60. doi: 10.1016/j.ijcard.2016.02.151. Epub 2016 Mar 2. No abstract available.


Uncoupling protein 2 promoter polymorphism -866G/A, central adiposity, and metabolic syndrome in Asians.

Shen H, Qi L, Tai ES, Chew SK, Tan CE, Ordovas JM.

Obesity (Silver Spring). 2006 Apr;14(4):656-61.


CYP2C19 polymorphisms and antiplatelet effects of clopidogrel in acute ischemic stroke in China.

Jia DM, Chen ZB, Zhang MJ, Yang WJ, Jin JL, Xia YQ, Zhang CL, Shao Y, Chen C, Xu Y.

Stroke. 2013 Jun;44(6):1717-9. doi: 10.1161/STROKEAHA.113.000823. Epub 2013 May 2.


Association of the UCP-1 single nucleotide polymorphism A-3826G with the dampness-phlegm pattern among Korean stroke patients.

Lim JH, Ko MM, Moon TW, Cha MH, Lee MS.

BMC Complement Altern Med. 2012 Oct 9;12:180. doi: 10.1186/1472-6882-12-180.


[Association between polymorphism in uncoupling proteins and type 2 diabetes in a northwestern Colombian population].

Franco-Hincapié L, Duque CE, Parra MV, Gallego N, Villegas A, Ruiz-Linares A, Bedoya G.

Biomedica. 2009 Mar;29(1):108-18. Spanish.


Interaction between the UCP2 -866 G>A polymorphism, diabetes, and beta-blocker use among patients with acute coronary syndromes.

Beitelshees AL, Finck BN, Leone TC, Cresci S, Wu J, Province MA, Fabbrini E, Kirk E, Zineh I, Klein S, Spertus JA, Kelly DP.

Pharmacogenet Genomics. 2010 Apr;20(4):231-8. doi: 10.1097/FPC.0b013e3283377abc. Erratum in: Pharmacogenet Genomics. 2012 May;22(5):396.


The gene polymorphisms of UCP1 but not PPAR γ and TCF7L2 are associated with diabetic retinopathy in Chinese type 2 diabetes mellitus cases.

Zhang Y, Meng N, Lv Z, Li H, Qu Y.

Acta Ophthalmol. 2015 May;93(3):e223-9. doi: 10.1111/aos.12542. Epub 2014 Oct 1.


Lack of association between family history of stroke and 1-year outcomes after acute ischemic stroke in Chinese.

Wang XG, Wang CX, Yang HJ, Wang AX, Li D, Zheng HG, Wang YL, Liu GF, Zhao XQ, Wang YJ.

CNS Neurosci Ther. 2013 Oct;19(10):845-6. doi: 10.1111/cns.12164. Epub 2013 Aug 30. No abstract available.


Influence of C3435T multidrug resistance gene-1 (MDR-1) polymorphism on platelet reactivity and prognosis in patients with acute coronary syndromes.

Spiewak M, Małek ŁA, Kostrzewa G, Kisiel B, Serafin A, Filipiak KJ, Płoski R, Opolski G.

Kardiol Pol. 2009 Aug;67(8):827-34.


NINJ2 polymorphism is associated with ischemic stroke in Chinese Han population.

Wan XH, Li SJ, Cheng P, Zhang Q, Yang XC, Zhong GZ, Hu WL, Jin L, Wang XF.

J Neurol Sci. 2011 Sep 15;308(1-2):67-71. doi: 10.1016/j.jns.2011.06.011. Epub 2011 Jun 30.


Uncoupling protein 2 -866G/A and uncoupling protein 3 -55C/T polymorphisms in young South African Indian coronary artery disease patients.

Phulukdaree A, Moodley D, Khan S, Chuturgoon AA.

Gene. 2013 Jul 25;524(2):79-83. doi: 10.1016/j.gene.2013.04.048. Epub 2013 Apr 29. Review.


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