可能因为您的浏览器不支持样式,您可以更新您的浏览器到最新版本,以获取对此功能的支持,访问下面的网站,获取关于浏览器的信息:
[1] Blankenberg S, Barbaux S, Tiret L. Adhesion molecules and atherosclerosis[J]. Atherosclerosis, 2003, 170(2):191-203.
[2] Ye SQ, Usher D, Virgil D, et al. A PstI polymorphism detects the mutation of Serine128 to Arginine in CD 62E genea risk factor for coronary artery disease[J]. J Biomed Sci, 1999, 6(1):18-21.
[3] Ross R. Atherosclerosisan inflammatory disease[J]. New Engl J Med, 1999, 340(2): 115-126.
[4] O′Brien KD, McDonald TO, Chait A, et al. Neovascular expression of Eselectin, intercellular adhesion moleculE1, and vascular cell adhesion moleculE1 in human atherosclerosis and their relation to intimal leukocyte content[J]. Circulation,1996, 93(4):672-682.
[5] Nooteboom A, van der Linden CJ, Hendriks T. Modulation of adhesion molecule expression on endothelial cells after induction by lipopolysaccharidEstimulated whole blood[J]. Scand J Immunol, 2004, 59(5):440-448.
[6] Alonso R, Mata P, De Andres R, et al. Sustained longterm improvement of arterial endothelial function in heterozygous familial hypercholesterolemia patients treated with simvastatin[J]. Atherosclerosis, 2001, 157(2):423-429.
[7] Rauchhaus M, Gross M, Schulz S, et al. The Eselectin SER128ARG gene polymorphism and restenosis after successful coronary angioplasty[J]. Int J Cardiol, 2002, 83(3): 249-257.
[8] Kilickap M, Tutar E, Aydintug O, et al. Increase in soluble Eselectin level after PTCA and stent implantation: a potential marker of restenosis[J] . Int J Cardiol, 2004,93(1):13-18.