引用本文: 王秉林,戈小虎. FⅤ Leiden 與FⅡG20210A 突變在不同種族人群易栓癥中表達(dá)的研究現(xiàn)狀. 中國普外基礎(chǔ)與臨床雜志, 2012, 19(7): 793-795. doi: 復(fù)制
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1. | 趙永強(qiáng). 易栓癥的研究概況 [J]. 中國實(shí)用內(nèi)科雜志, 2007,1(27):49-51. |
2. | 閨振宇, 華寶來, 馬西虎, 等. 672 例靜脈血栓栓塞癥相關(guān)危險(xiǎn)因素分析 [J]. 中國血液學(xué)雜志, 2007, 28(9):579-581. |
3. | De Stefano Ⅴ, Martinelli I, Leone G, et al. The risk of recurrent deep venous thrombosis among heterozygous carriers of both factorⅤ Leiden and the G20210A prothrombin mutation [J]. N Engl J Med, 1999, 341(11):801-806. |
4. | Gerhardt A, Scharf RE, Beckmann MW,et al. Prothrombin and factor Ⅴ mutations in women with a history of thrombosis during pregnancy and the puerperium [J]. N Engl J Med, 2000,342(6): 374-380. |
5. | Bertina RM, Koelemen BP, Koster T, et al. Mutation in blood coagulation factor Ⅴ associated with resistance to activated protein C [J]. Nature, 1994, 369(6475): 64-67. |
6. | Rees DC, Cox M, Clegg JB, et al. World distribution of factor Ⅴ Leiden [J]. Lancet, 1995, 346(8983):1133-1134. |
7. | 畢云天, 胡玉紅, 梁萬東, 等. 凝血因子Ⅴ基因突變(1691G/A)與腦血栓、深靜脈血栓相關(guān)性的研究 [J]. 中國優(yōu)生與遺傳學(xué)雜志, 2000, 8(5):17-19. |
8. | Mazoyer E, Ripoll L, Gueguen R, et al. Prevalence of factor Ⅴ Leiden and prothrombin G20210A mutation in a large French population selected for nonthrombotic history:geographical and age distribution [J]. Blood Coagul Fibrinolysis, 2009, 20(7):503-510. |
9. | Agrawal N, Kumar S, Puneet, et al. Activated protein C resistance in deep venous thrombosis [J]. Ann Vasc Surg, 2009,23(3):364-366. |
10. | 鄭紅, 連建華, 賀穎, 等. 中國人群凝血酶原FⅡ G20210A 和FⅤ Leiden 的分布 [J]. 鄭州大學(xué)學(xué)報(bào)( 醫(yī)學(xué)版), 2006,1(41):103-106. |
11. | 郭辰虹, 郭瓊行, 龔瑤琴, 等. 凝血因子Ⅴ基因Leiden 突變和凝血酶原基因G20210A 突變與下肢深靜脈血栓形成關(guān)系的探討 [J]. 山東大學(xué)學(xué)報(bào)( 醫(yī)學(xué)版), 2002, 40(3): 235-237. |
12. | 李鳳芹, 楊志剛, 劉國勛, 等. 粵西籍人群FⅤ Leiden 基因突變的初步調(diào)查 [J]. 廣東醫(yī)學(xué)院學(xué)報(bào), 2000, 6(2):122-124. |
13. | 楊忠偉, 馮秀麗, 肖白, 等. 新疆蒙古族冠心病人群中FⅤLeiden 基因突變的研究——附41 例報(bào)告 [J]. 新醫(yī)學(xué), 2009,7(40):445-447. |
14. | 高麗霞, 哈力達(dá)? 亞森, 許風(fēng)雷,等. 新疆地區(qū)動脈血栓形成患者抗活化蛋白C 及FⅤ Leiden 突變的調(diào)查 [J]. 血栓與止血,2007, 4(13):161-163. |
15. | 羅佳濱, 關(guān)月, 馬洪星, 等. 凝血因子Ⅴ基因點(diǎn)突變1691A 在不同種族人群中的分布 [J]. 中華遺傳學(xué)雜志, 1996, 13(4):219-220. |
16. | Wu J, Gu J, Xu J, et al. Factor Ⅴ Leiden mutation in one family of Chinese orign [J]. Chin Med J (Engl), 2001, 114(4):379-381. |
17. | 邢顏超, 馬愛華, 程維興, 等. 凝血因子1691G→A 基因突變的研究分析 [J]. 中國微循環(huán)雜志, 2003, 6(3):140-142.. |
18. | Poort SR, Rosendaal FR, Reitsma PH, et al. A common genetic variation in the 3’-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis [J]. Blood, 1996, 88(10):3698-3703. |
19. | Margaglione M, Brancaccio V, De lucia D, et al. Inherited thrombophilic risk factors and venous thromboembolism:distinct role in peripheral deep venous thrombosis and pulmonary embolism [J]. Chest, 2000, 118(5): 1405-1411. |
20. | Zalavras CG, Giotopoulou S, Dokou E, et al. Prevalence of the G20210A prothrombin gene mutation in Northwestern Greece and association with venous thromboembolism [J]. Int Angiol,2003, 22(1): 55-57. |
21. | Zivelin A, Rosenberg N, Faier S, et al. A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin gene [J]. Blood, 1998, 92(4): 119-124. |
22. | Rosendaal FR, Doggen CJM, Zivelin A, et al. Geographic distribution of the 20210 G to A prothrombin variant [J]. Thromb Haemost, 1998, 79(4): 706-708. |
23. | Dowling NF, Austin H, Dilley A, et al. The epidemiology of venous thromboembolism in Caucasians and African-Americans:the GATE study [J]. Thromb Haemost, 2003, 1(1):80-87. |
24. | Angchaisuksiri P, Pingsuthiwong S, Aryuchai K, et al. Prevalence of the G1691A mutation in the factor Ⅴ gene (factor Ⅴ Leiden) and the G20210A prothrombin gene mutation in the Thai population [J]. Hematol, 2000, 65(2):119-122. |
25. | Arruda VR, Siquiera LH, Chiaparini LC, et al. Prevalence of the prothrombin gene variant 20210 G→A among patients with myocardial infarction [J]. Canliovasc, 1998, 37(1):42-45. |
26. | Lu Y, Zhao Y, Liu G, et al. Factor Ⅴ gene G1691A mutation,prothrombin gene G20210A mutation, and MTHFR gene C677T mutation are not risk factors for pulmonary thromboembolism in Chinese population [J]. Thromb Res, 2002, 106(1):7-12. |
27. | Jun ZJ, Ping T, Lei Y, et al. Prevalence of factor Ⅴ Leiden and prothrombin G20210A mutations in Chinese patients with deep venous thrombosis and pulmonary embolism [J]. Clin Lab Haematol,2006, 28(2):111-116. |
28. | 賀穎, 齊華, 連建華, 等. 凝血酶原基因G20210A 變異與深靜脈血栓關(guān)系的研究 [J]. 中國優(yōu)生與遺傳雜志, 2002, 6(10):19-21. |
29. | 常建華, 馬越, 張廣森, 等. 中國壯族人群凝血酶原基因G20210A 突變頻率研究 [J]. 中華醫(yī)學(xué)遺傳學(xué)雜志, 2005,6(22):341-343. |
30. | 金國棟, 徐耕, 傅國勝, 等. 凝血酶原基因G20210A 和凝血因子Ⅴ Leiden 突變與冠心病的相關(guān)性探討 [J]. 中國病理生理雜志, 2003, 19(7):969-971. |
- 1. 趙永強(qiáng). 易栓癥的研究概況 [J]. 中國實(shí)用內(nèi)科雜志, 2007,1(27):49-51.
- 2. 閨振宇, 華寶來, 馬西虎, 等. 672 例靜脈血栓栓塞癥相關(guān)危險(xiǎn)因素分析 [J]. 中國血液學(xué)雜志, 2007, 28(9):579-581.
- 3. De Stefano Ⅴ, Martinelli I, Leone G, et al. The risk of recurrent deep venous thrombosis among heterozygous carriers of both factorⅤ Leiden and the G20210A prothrombin mutation [J]. N Engl J Med, 1999, 341(11):801-806.
- 4. Gerhardt A, Scharf RE, Beckmann MW,et al. Prothrombin and factor Ⅴ mutations in women with a history of thrombosis during pregnancy and the puerperium [J]. N Engl J Med, 2000,342(6): 374-380.
- 5. Bertina RM, Koelemen BP, Koster T, et al. Mutation in blood coagulation factor Ⅴ associated with resistance to activated protein C [J]. Nature, 1994, 369(6475): 64-67.
- 6. Rees DC, Cox M, Clegg JB, et al. World distribution of factor Ⅴ Leiden [J]. Lancet, 1995, 346(8983):1133-1134.
- 7. 畢云天, 胡玉紅, 梁萬東, 等. 凝血因子Ⅴ基因突變(1691G/A)與腦血栓、深靜脈血栓相關(guān)性的研究 [J]. 中國優(yōu)生與遺傳學(xué)雜志, 2000, 8(5):17-19.
- 8. Mazoyer E, Ripoll L, Gueguen R, et al. Prevalence of factor Ⅴ Leiden and prothrombin G20210A mutation in a large French population selected for nonthrombotic history:geographical and age distribution [J]. Blood Coagul Fibrinolysis, 2009, 20(7):503-510.
- 9. Agrawal N, Kumar S, Puneet, et al. Activated protein C resistance in deep venous thrombosis [J]. Ann Vasc Surg, 2009,23(3):364-366.
- 10. 鄭紅, 連建華, 賀穎, 等. 中國人群凝血酶原FⅡ G20210A 和FⅤ Leiden 的分布 [J]. 鄭州大學(xué)學(xué)報(bào)( 醫(yī)學(xué)版), 2006,1(41):103-106.
- 11. 郭辰虹, 郭瓊行, 龔瑤琴, 等. 凝血因子Ⅴ基因Leiden 突變和凝血酶原基因G20210A 突變與下肢深靜脈血栓形成關(guān)系的探討 [J]. 山東大學(xué)學(xué)報(bào)( 醫(yī)學(xué)版), 2002, 40(3): 235-237.
- 12. 李鳳芹, 楊志剛, 劉國勛, 等. 粵西籍人群FⅤ Leiden 基因突變的初步調(diào)查 [J]. 廣東醫(yī)學(xué)院學(xué)報(bào), 2000, 6(2):122-124.
- 13. 楊忠偉, 馮秀麗, 肖白, 等. 新疆蒙古族冠心病人群中FⅤLeiden 基因突變的研究——附41 例報(bào)告 [J]. 新醫(yī)學(xué), 2009,7(40):445-447.
- 14. 高麗霞, 哈力達(dá)? 亞森, 許風(fēng)雷,等. 新疆地區(qū)動脈血栓形成患者抗活化蛋白C 及FⅤ Leiden 突變的調(diào)查 [J]. 血栓與止血,2007, 4(13):161-163.
- 15. 羅佳濱, 關(guān)月, 馬洪星, 等. 凝血因子Ⅴ基因點(diǎn)突變1691A 在不同種族人群中的分布 [J]. 中華遺傳學(xué)雜志, 1996, 13(4):219-220.
- 16. Wu J, Gu J, Xu J, et al. Factor Ⅴ Leiden mutation in one family of Chinese orign [J]. Chin Med J (Engl), 2001, 114(4):379-381.
- 17. 邢顏超, 馬愛華, 程維興, 等. 凝血因子1691G→A 基因突變的研究分析 [J]. 中國微循環(huán)雜志, 2003, 6(3):140-142..
- 18. Poort SR, Rosendaal FR, Reitsma PH, et al. A common genetic variation in the 3’-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis [J]. Blood, 1996, 88(10):3698-3703.
- 19. Margaglione M, Brancaccio V, De lucia D, et al. Inherited thrombophilic risk factors and venous thromboembolism:distinct role in peripheral deep venous thrombosis and pulmonary embolism [J]. Chest, 2000, 118(5): 1405-1411.
- 20. Zalavras CG, Giotopoulou S, Dokou E, et al. Prevalence of the G20210A prothrombin gene mutation in Northwestern Greece and association with venous thromboembolism [J]. Int Angiol,2003, 22(1): 55-57.
- 21. Zivelin A, Rosenberg N, Faier S, et al. A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin gene [J]. Blood, 1998, 92(4): 119-124.
- 22. Rosendaal FR, Doggen CJM, Zivelin A, et al. Geographic distribution of the 20210 G to A prothrombin variant [J]. Thromb Haemost, 1998, 79(4): 706-708.
- 23. Dowling NF, Austin H, Dilley A, et al. The epidemiology of venous thromboembolism in Caucasians and African-Americans:the GATE study [J]. Thromb Haemost, 2003, 1(1):80-87.
- 24. Angchaisuksiri P, Pingsuthiwong S, Aryuchai K, et al. Prevalence of the G1691A mutation in the factor Ⅴ gene (factor Ⅴ Leiden) and the G20210A prothrombin gene mutation in the Thai population [J]. Hematol, 2000, 65(2):119-122.
- 25. Arruda VR, Siquiera LH, Chiaparini LC, et al. Prevalence of the prothrombin gene variant 20210 G→A among patients with myocardial infarction [J]. Canliovasc, 1998, 37(1):42-45.
- 26. Lu Y, Zhao Y, Liu G, et al. Factor Ⅴ gene G1691A mutation,prothrombin gene G20210A mutation, and MTHFR gene C677T mutation are not risk factors for pulmonary thromboembolism in Chinese population [J]. Thromb Res, 2002, 106(1):7-12.
- 27. Jun ZJ, Ping T, Lei Y, et al. Prevalence of factor Ⅴ Leiden and prothrombin G20210A mutations in Chinese patients with deep venous thrombosis and pulmonary embolism [J]. Clin Lab Haematol,2006, 28(2):111-116.
- 28. 賀穎, 齊華, 連建華, 等. 凝血酶原基因G20210A 變異與深靜脈血栓關(guān)系的研究 [J]. 中國優(yōu)生與遺傳雜志, 2002, 6(10):19-21.
- 29. 常建華, 馬越, 張廣森, 等. 中國壯族人群凝血酶原基因G20210A 突變頻率研究 [J]. 中華醫(yī)學(xué)遺傳學(xué)雜志, 2005,6(22):341-343.
- 30. 金國棟, 徐耕, 傅國勝, 等. 凝血酶原基因G20210A 和凝血因子Ⅴ Leiden 突變與冠心病的相關(guān)性探討 [J]. 中國病理生理雜志, 2003, 19(7):969-971.