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Factor V Leiden, prothrombin G20210A and methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms and the risk of tamoxifen-associated thromboembolism in breast cancer patients.

作者信息

Eroğlu Aydan, Akar Nejat

出版信息

Thromb Res. 2011 Apr;127(4):384-5. doi: 10.1016/j.thromres.2010.10.025. Epub 2010 Nov 19.

DOI:10.1016/j.thromres.2010.10.025
PMID:21093891
Abstract
摘要

相似文献

1
Factor V Leiden, prothrombin G20210A and methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms and the risk of tamoxifen-associated thromboembolism in breast cancer patients.
Thromb Res. 2011 Apr;127(4):384-5. doi: 10.1016/j.thromres.2010.10.025. Epub 2010 Nov 19.
2
The 19-bp deletion of dihydrofolate reductase (DHFR), methylenetetrahydrofolate reductase (MTHFR) C677T, Factor V Leiden, prothrombin G20210A polymorphisms in cancer patients with and without thrombosis.有血栓形成和无血栓形成的癌症患者中二氢叶酸还原酶（DHFR）19碱基对缺失、亚甲基四氢叶酸还原酶（MTHFR）C677T、凝血因子V莱顿突变、凝血酶原G20210A多态性
Ann Hematol. 2009 Jan;88(1):73-6. doi: 10.1007/s00277-008-0569-6. Epub 2008 Aug 6.
3
Factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations are not associated with chronic limb ischemia: the Linz Peripheral Arterial Disease (LIPAD) study.因子V莱顿突变、凝血酶原G20210A突变和亚甲基四氢叶酸还原酶C677T突变与慢性肢体缺血无关：林茨外周动脉疾病（LIPAD）研究。
J Vasc Surg. 2005 May;41(5):808-15. doi: 10.1016/j.jvs.2005.01.039.
4
Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran.凝血因子V G1691A、凝血酶原G20210A及亚甲基四氢叶酸还原酶基因多态性C677T与伊朗西部的冠状动脉疾病和2型糖尿病无关。
Blood Coagul Fibrinolysis. 2009 Jun;20(4):252-6. doi: 10.1097/MBC.0b013e3283255487.
5
Factor V Leiden G1691A, prothrombin G20210A, and MTHFR C677T mutations in Turkish inflammatory bowel disease patients.土耳其炎症性肠病患者中的凝血因子V Leiden G1691A、凝血酶原G20210A和亚甲基四氢叶酸还原酶C677T突变
Hepatogastroenterology. 2007 Jul-Aug;54(77):1438-42.
6
Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians.200名健康约旦人凝血因子V莱顿突变、凝血酶原G20210A突变和亚甲基四氢叶酸还原酶C677T突变的患病率
Clin Lab Sci. 2004 Fall;17(4):200-2.
7
Thrombophilic polymorphisms - factor V Leiden G1691A, prothrombin G20210A and MTHFR C677T - in Tunisian patients with cerebral venous thrombosis.血栓形成倾向的多态性 - 因子 V 莱顿 G1691A、凝血酶原 G20210A 和 MTHFR C677T - 在突尼斯脑静脉血栓形成患者中。
J Clin Neurosci. 2012 Sep;19(9):1326-7. doi: 10.1016/j.jocn.2011.11.029. Epub 2012 Jun 20.
8
Effect of Factor V Leiden and prothrombin G20210-->A mutations on thromboembolic risk in the national surgical adjuvant breast and bowel project breast cancer prevention trial.在国家外科辅助乳腺和肠道项目乳腺癌预防试验中，凝血因子V莱顿突变和凝血酶原G20210A突变对血栓栓塞风险的影响。
J Natl Cancer Inst. 2006 Jul 5;98(13):904-10. doi: 10.1093/jnci/djj262.
9
Prothrombin and factor V mutations in women with a history of thrombosis during pregnancy and the puerperium.有妊娠和产褥期血栓形成病史女性的凝血酶原和因子V突变
N Engl J Med. 2000 Feb 10;342(6):374-80. doi: 10.1056/NEJM200002103420602.
10
PLA2 polymorphism of platelet glycoprotein IIb/IIIa but not Factor V Leiden and prothrombin G20210A polymorphisms is associated with venous thromboembolism and more recurrent events in central Iran.血小板糖蛋白IIb/IIIa的磷脂酶A2多态性而非因子V莱顿和凝血酶原G20210A多态性与伊朗中部的静脉血栓栓塞及更多复发事件相关。
Blood Coagul Fibrinolysis. 2013 Jul;24(5):471-6. doi: 10.1097/MBC.0b013e32835e4260.

引用本文的文献

1
MTHFR 677C>T polymorphism and the risk of breast cancer: evidence from an original study and pooled data for 28031 cases and 31880 controls.亚甲基四氢叶酸还原酶（MTHFR）677C>T基因多态性与乳腺癌风险：一项原始研究及28031例病例和31880例对照的汇总数据的证据
PLoS One. 2015 Mar 24;10(3):e0120654. doi: 10.1371/journal.pone.0120654. eCollection 2015.