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新疆哈、汉族原发性高血压与Cx43基因多态性的相关性 被引量:2

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摘要 目的:探讨新疆哈萨克族、汉族人群缝隙连接蛋白43(connexin43,Cx43)基因多态性与原发性高血压(essential hypertension,EH)的关联性。方法:应用飞行时间质谱(time of flight mass spectrum)芯片技术,检测EH组(n=250)和对照组(n=250)Cx43基因3个SNP位点(rs1925223、rs2071165、rs3805787)多态性。结果:rs1925223位点在汉族人群中EH组的CC、CG和GG基因型频率分别为6.4%、35.6%和58%,与对照组相比差异具有统计学意义(P=0.048)。结论:Cx43基因rs1925223位点多态性可能与新疆汉族EH相关。
出处 《实用医学杂志》 CAS 北大核心 2014年第23期3785-3787,共3页 The Journal of Practical Medicine
基金 国家重点基础研究发展计划(973计划)项目(编号:2012CB26600) 兵团博士基金项目(编号:2010JC16) 兵团医药专项(编号:2012BA021,2010GG34)
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参考文献15

  • 1Cong MH. Molecular genetics of human hypertension[J]. Clin Sci (Lond) , 2006,110(3) :315-326.
  • 2Dhein S, Duerrschmidt N, Scholl A, et al. A new role for extracellular Ca2 + in gap-junction remodeling I studies in humans and rats[J]. Naunyn Schmiedebergs Arch Pharmacol, 2008, 377 (2) : 125-138.
  • 3Ram R, Wescott AP, Varandas K, et al. Mena associates and modulates connexin 43 remodeling in cardiomyocytes[I]. Am I Physiol Heart Circ Physiol, 2014,306(1): 154-159.
  • 4LinJ, Keener IP. Micridimain effects on transverse cardiac propagetion[J]. IophysJ, 2014, 106 ( 4) : 925-931.
  • 5SmythJW, Shaw RM. Autoregulation of connexin43 gap junction formation by internally translated isoforms[J] . Cell Rep, 2013,5(3) :611-618.
  • 6Zhang SS, Haw RM. Trafficking highways to the intercalated disc: new insights unlocking the specificity of connexin43 localization[J]. Cell Commun Adhes, 2014,21(1):43-54.
  • 7Laird DW. Life cycle of connexins in health and disease[J]. BiochemJ, 2006,394(3) :527-543.
  • 8王恩帮,何芳.缝隙连接与高血压的研究进展[J].中国现代医药杂志,2010,12(9):122-124. 被引量:8
  • 9李环,胡殿兴,陈威,张燚,靳曙光.Connexin 43介导细胞缝隙连接的研究进展[J].北华大学学报(自然科学版),2014,15(1):43-48. 被引量:9
  • 10Fava C, Danese E, Monlagnana M, et al. Serine/threonine kinase 39 is a candidate gene for primary hypertension especially in women: results from two cohort studies in Swedes[J].J Hypertens, 2011,29 (3) : 484-491.

二级参考文献92

  • 1严继承,郑一凡,曾群力,祝慧娟,朱心强.玉米赤霉烯酮对细胞间隙连接通讯的影响[J].卫生毒理学杂志,2004,18(3):160-162. 被引量:9
  • 2程蕾,李静,耿美玉.细胞间隙连接通讯与肿瘤[J].现代生物医学进展,2007,7(4):626-628. 被引量:13
  • 3[1]Azzam EI,de Toledo SM,Little JB,et al.Evidence for the participation of gap junction mediated intercellular communication in the transmission of damage singals from irradiated to nonirradiated cells[J].Proc Natl Acad Sci USA,2001,98:247-248.
  • 4[2]Yao J,Hiramatsu N,Zhu Y,et al.Nitric oxide-mediated regulation of connexin43 expression and gap junctional intercellular com munication in mesangial cells[J].J Am Soc Nephrol,2005,16:58-67.
  • 5[3]Kson BE,Ramos SI,Duling BR.Ca2+ and inositol 1,4,5-trisphosphate mediated signaling across the myoendothelial junction[J].Circ Res,2007,100:246-254.
  • 6[4]Kruger O,Beny JL,Chabaud F,et al.Altered dye diffusion and upregulation of connexin37 in mouse aortic endothelium deficient in eonnexin40[J].J Vasc Res,2002,39:160-172.
  • 7[5]Watts SW,Webb RC.Vascular gap junctional communication is increased in mineralocoriocoid-salt[J].Hypertention,1996,28:888-893.
  • 8[6]Haefliger JA,Meda P.Chronic hypertension alters the expression of cx43 in cardiovascular muscle cells[J].Braz J Med Biol Res,2000,33:431-438.
  • 9[7]Yeh HI,Lee PY,Su CH,et al.Reduced expression of endothelial connexins 43 and 47 in hypertensive rats is rectified after 7-day carvedilol treatment[J].Am J Hypertens,2006,19:129-135.
  • 10[8]Goto K,Rummery NM,Grayson TH,et al.Attenuation of conducted vasodilatation in rat mesenteric arteries during hypertension:role of inwardly rectifying potassium channels[J].J Physiol,2004,561:215-231.

共引文献31

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  • 1陈卓,单可人,任锡麟.胱硫醚合酶基因及其在人群中的多态性[J].中国优生与遗传杂志,2005,13(7):4-6. 被引量:5
  • 2August P. Initial treatment of hypertension [J]. N EngI J Med, 2003,348(7) : 610-617.
  • 3Lucock M, Yates Z, Martin C, et al. Hydrogen sulphide-related thiol metabolism and nutrigenetics in relation to hypertension in an elderly population [J]. Genes Nutr, 2013,8(2) : 221-229.
  • 4T sai MY, Hanson NQ, Schwieh tenberg, et al. AmPlification Refraetory mutation system to Identify mutations in cystathionine-beta-synthase defieieney [J]. Clin Chem, 1995, 41 (12) : 1775-1777.
  • 5Fava C, Danese E, Monlagnana M, et al. Serine/threonine kinase 39 is a candidate gene for primary hypertension especially in women:results from two cohort studies in Swedes [J]. J Hypertens, 2011,29(3) :484-491.
  • 6Meier M, Oliveriusova J, Kraus JP, et al. Structural insights into mutaoons of cystathfenine beta-synthase [J]. Biochim Biophys Acta, 2003,1647 (1-2) : 206-213.
  • 7Mendes CC, Raimundo AM, Oliveria LD, et al. DHFR 19-bp deletion and SHMT C1420T polymorphisms and metabolite concentrations of the folate pathway in individuals with Down syndrome [J]. Genet Test Med Mol Biomarkers, 2013,17 (4) : 274-277.
  • 8Sarov M, Not A, de Baulny HO, et al. A case of bomocystinuria due to CBS gene mutations revealed by cerebral venous thrombosis [J]. J Neurol Sci, 2014,336( 1 ) : 257-259.
  • 9Zhao R, Zhu H, Dao J, et al. Study on genotyPes of cystathionine betaSynthase in netiral Tubede feets [J]. Wei Sheng Yan Jiu, 2000,29(1) :50-51.
  • 10Fava C, Danese E, Monlagnana M, et al. Serine/threonine kinase 39 is a candidate gene for primaPy hypertension espeeially in women:results from two cohort studies in Swedes [J ]. J Hypertens,201 1,29(3) :484-491.

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