索引超出了数组界限。
[1] 中华医学会心血管病学分会. 中国部分地区1980、1990、2000年慢性心力衰竭住院病例回顾性调查[J]. 中华心血管病杂志, 2002, 30(8):450-454.
[2] Kelwick R, Desanlis I, Wheeler GN, et al. The ADAMTS(a disintegrin and metalloproteinase with thrombospondin motifs)family[J]. Genome Biol, 2015, 16:113.
[3] 刘瑜婷, 高艳香, 郑金刚. ADAMTSs 家族与心血管疾病关系的研究进展[J]. 心血管病学进展, 2016, 37(6):611-614.
[4] Lin EA, Liu CJ. The role of ADAMTSs in arthritis[J]. Protein Cell, 2010, 1(1):33-47.
[5] Sun Y, Huang J, Yang Z. The roles of ADAMTS in angiogenesis and cancer[J]. Tumour Biol, 2015, 36(6):4039-4051.
[6] Wu W, Wang H, Yu C, et al. Association of ADAMTS-7 levels with cardiac function in a rat model of acute myocardial infarction[J]. Cell Physiol Biochem, 2016, 38(3):950-958.
[7] Kessler T, Zhang L, Liu Z, et al. ADAMTS-7 inhibits re-endothelialization of injured arteries and promotes vascular remodeling through cleavage of thrombospondin-1[J]. Circulation, 2015, 131(13):1191-1201.
[8] Wu W, Zhou Y, Li Y, et al. Association between plasma ADAMTS-7 levels and ventricular remodeling in patients with acute myocardial infarction[J]. Eur J Med Res, 2015, 20:27.
[9] Reilly MP, Li M, He J, et al. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies[J]. Lancet, 2011, 377(9763):383-392.
[10] Valiente-Alandi I, Schafer AE, Blaxall BC. Extracellular matrix-mediated cellular communication in the heart[J]. J Mol Cell Cardiol, 2016, 91:228-237.
[11] Zhang Y, Lin J, Wei F. The function and roles of ADAMTS-7 in inflammatory diseases[J]. Mediators Inflamm, 2015, 2015:801546.
[12] Wang L, Zheng J, Bai X, et al. ADAMTS-7 mediates vascular smooth muscle cell migration and neointima formation in balloon-injured rat arteries[J]. Circ Res, 2009, 104(5):688-698.
[13] Bauer RC, Tohyama J, Cui J, et al. Knockout of Adamts7, a novel coronary artery disease locus in humans, reduces atherosclerosis in mice[J]. Circulation, 2015, 131(13):1202-1213.