[1]Hong T,Yan Y,Li J,et al.High prevalence of kras/braf somatic mutations in brain and spinal cord arteriovenous malformations[J].Brain,2019,142:23-34. [2]Huang J,Song J,Qu M,et al.MicroRNA-137 and microRNA-195* inhibit vasculogenesis in brain arteriovenous malformations[J].Ann Neurol,2017,82:371-384. [3]Yao J,Wu X,Zhang D,et al.Elevated endothelial Sox2 causes lumen disruption and cerebral arteriovenous malformations[J].J Clin Invest,2019,129:3121-3133. [4]Wang X,Hao Q,Zhao Y,et al.Dysregulation of cell-cell interactions in brain arteriovenous malformations:A quantitative proteomic study[J].Proteomics Clin Appl,2017,11.doi:10.1002/prca.201600093. [5]Guo Y,Xu B,Sun Z,et al.Quantitative protein profiling and pathway analysis of spinal arteriovenous malformations[J].Microvasc Res,2018,120:47-54. [6]Gao P,Chen Y,Lawton MT,et al.Evidence of endothelial progenitor cells in the human brain and spinal cord arteriovenous malformations[J].Neurosurgery,2010,67:1029-1035. [7]Nikolaev SI,Vetiska S,Bonilla X,et al.Somatic activating KRAS mutations in arteriovenous malformations of the brain[J].N Engl J Med,2018,378:250-261. [8]高鹏,杨明,孙林.线粒体相关内质网膜(mam)钙转运及调节蛋白介导线粒体钙稳态[J].中国细胞生物学学报,2018,40:585-593. [9]Mallilankaraman K,Cárdenas C,Doonan PJ,et al.MCUR1 is an essential component of mitochondrial Ca2+ uptake that regulates cellular metabolism[J].Nat Cell Biol,2012,14:1336-1343. [10]Li Y,Chen B,Yang X,et al.S100a8/a9 signaling causes mitochondrial dysfunction and cardiomyocyte death in response to ischemic/reperfusion injury[J].Circulation,2019,140:751-764. [11]Alabi RO,Farber G,Blobel CP.Intriguing roles for endothelial adam10/notch signaling in the development of organ-specific vascular beds[J].Physiol Rev,2018,98:2025-2061. [12]Chapados R,Abe K,Ihida-Stansbury K,et al.Rock controls matrix synthesis in vascular smooth muscle cells:Coupling vasoconstriction to vascular remodeling[J].Circ Res,2006,99:837-844. [13]王淳,李波,方文刚,等.PLGF通过激活Rho/ROCK信号通路介导人脑微血管内皮细胞间紧密连接开放[J].基础医学与临床,2013,33:960-965. [14]Parker DN,Tasneem S,Farndale RW,et al.The functions of the A1A2A3 domains in von willebrand factor include multimerin 1 binding[J].Thromb Haemost,2016,116:87-95. [15]Hong CC,Tang AT,Detter MR,et al.Cerebral cavernous malformations are driven by adamts5 proteolysis of versican[J].J Exp Med,2020,217,e20200140.doi:10.1084/jem.20200140. |