期刊文献+

膜周部室间隔缺损患者内皮素1多态性的研究 被引量:1

原文传递
导出
摘要 内皮素1(ET1)在正常胚胎发育过程中起重要作用,与神经嵴细胞的发生有关,ET1基因敲除老鼠表现出主动脉弓畸形和室间隔缺损。ET1 TaqI单核苷酸多态性为内含子4的8000位点T/C的转换,可能引起ET1表达的差异,因此可能与先天性心脏病的易感性有关。我们运用PCR—RFLP的方法,以医院为基础的病例对照研究,探讨ET1 TaqI多态性与膜周部室缺发生的易感性。
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2010年第7期963-963,共1页 Chinese Journal of Experimental Surgery
  • 相关文献

参考文献4

  • 1Kurihara Y,KuriharaH,OdaH,et al.Aortic arch malformations and ventricular septa] defect in mice deficient in endothelin-1.J Clin Invest,1995,96:293-300. 被引量:1
  • 2金树琦,郭晓玲,王蒙琴,纪晓玲.内皮素-1基因Taq I多态性与冠心病的关系[J].中国分子心脏病学杂志,2007,7(4):208-213. 被引量:2
  • 3Marino B,Digilio MC.Congenital heart disease and genetic syndromes:specific correlation between cardiac phenotype and genotype.Cardiovasc Pathol,2000,9:303-315. 被引量:1
  • 4Fu YC,Bass J,Amin Z,et al.Transcathe-ter closure of perimembranous ventricular septal defects using the new Amplatzer membranous VSD occluder:results of the U.S.phase I trial.J Am Coll Cardiol,2006,47:319-325. 被引量:1

二级参考文献13

  • 1[1]Yanagisawa M,Tomizawa T.A novel potent vasoconstrictor peptide produced by vascular endothelial cells[J].Nature,1988,332:411 -415. 被引量:1
  • 2[2]Berge K,Berg K.A Taq Ⅰ RFLP at the EDN1 gene locus[J].Nucleic Acids Res,1990,18:6176. 被引量:1
  • 3[3]Gurmukh S Sainani,Vibhuti G Maru,Arun P Mehra.Role of Endothelin-1 in Genesis of Coronary Artery Disease[J].Indian Heart,2005,57:121-127. 被引量:1
  • 4[4]Taylor AJ,Bobik A,Richards M,et al.Myocardial endothelin-1 release and indices of inflammation during angioplasty for acute myocardial infarction and stabal coronary artery disease[J].Am heart J,2004 Aug,148(2):e10. 被引量:1
  • 5[5]Tadao A,Mikiyo I,Akihiro I,et al.Chromosormal assignments of the human endothelia family genes:the endothelia-1 gene to 6p23-24,the endothelia-2 gene to 1p34,and the endothelia-3 gene to 20q132-q133[J].Am,l Hum Genet,1991,48:990-996. 被引量:1
  • 6[6]Konstanze D,Farhas AN,Christian M,et al.Identification of twelve polymorphisma in the endothelin-1 gene by use of fluorescently labeled oligonucleotides and PCR with restriction fragment polymorphism analysis[J].Clinical Chemistry,2004,50(2):448-451. 被引量:1
  • 7[7]Kozak M,Holla LI,Krivan L,Vasku A,Sepsi M,Borivoj S,et al.Endothelin-1 gene polymorphism in the identification of patients at risk for malignant ventricular arrhythmia[J].Med Sci Monit,2002,8:BR164-167. 被引量:1
  • 8[8]Lydie H,Mudr,Anna Y.Association of 3 gene polymorphisms with atopic disease[J].J Allergy Clin Immunol,1999,103(4):702-708. 被引量:1
  • 9[11]Vicky C,Vanessa T,et al.ET-1 and ecNOS gene polymorphisms and susceptibility to acute chest syndrome and painful vaso-occlusive crises in chidren with sickle cell anemia[J].Haematologica,2006,91(9):1277-1278. 被引量:1
  • 10[12]Berge K,Gerg K,No effect of Taq Ⅰ polymorphisms in DNA at blood pressure level or variability[J].Clin Genet,1992,41:90. 被引量:1

共引文献1

同被引文献6

  • 1崔华,封志纯,孙强.血浆和心肌组织血管紧张素Ⅱ水平对肺动脉高压患者左室心肌细胞凋亡和间质纤维化程度的不同影响[J].中国组织工程研究与临床康复,2007,11(8):1457-1460. 被引量:1
  • 2Bakshi KD,Vaidyanathan B,Sundaram KR,et al.Determinants of early outcome after neonatal cardiac surgery in a developing country[J].Thorac Cardiovasc Surg,2007,134(3):765-771. 被引量:1
  • 3徐志伟.室间隔缺损.见:徐志伟.小儿心脏手术学[M].北京:人民军医出版社,2006:337-350. 被引量:2
  • 4Borg KT,Caulfield JB.The collage matrix of the heart[J].Fed Proc,1981,40(7):2037-2041. 被引量:1
  • 5Piper C,Schultheiss HP,Akdemir D,et al.Remodeling of the cardiac extracellular matix differs between volume-and pressure-overloaded ventricles and is specific for each heart valve lesion[J].Heart value Dis,2003,12(5):592-600. 被引量:1
  • 6Gardi C, Calzoni P, Marcolongo P, et al. Collagen breakdown products and lung collagen metabolism:an in vitro study on fibroblast culrures[J]. Thorax,1994,49(4):312 318. 被引量:1

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部