期刊文献+

可溶性尿激酶型纤溶酶原激活物受体与足细胞病 被引量:1

原文传递
导出
摘要 足细胞病是对病变主要累及肾小球足细胞的一类肾脏疾病的统称.1995年,Floege等[1]在对小鼠的肾小球硬化症研究中首次采用了"podocyte disease"的表述形式.Pollak[2]在2002年首次将涉及足细胞损伤的一系列肾小球疾病称为足细胞病(Podocytopathies),病理表现为足细胞数量的减少,以足突融合为主要形式的形态学变化,以及作为足细胞结构蛋白分子的表达变化等特征.
出处 《中华儿科杂志》 CAS CSCD 北大核心 2015年第2期146-148,共3页 Chinese Journal of Pediatrics
基金 国家自然科学基金(81270792、81470939、81170664) 高等学校博士学科点专项科研基金(20120101110018) 浙江省卫生高层次创新人才培养对象及卫生部科学研究基金-浙江省医药卫生重大科技计划(WK,J2010-2-14) 浙江省医药卫生科技计划(2014KYA123,2014KYB148) 浙江省人口计划生育科研项目(2014KYA261)
  • 相关文献

参考文献33

  • 1Floege J, Hackmann B, Kliem V, et al. Spontaneous glomerulosclerosis in milan normotensive rats - a podocyte disease [J]. J Am Soc Nephrol, 1995, 6(3) :864-864.
  • 2Pollak MR. Inherited podocytopathies: FSGS and nephroticsyndrome from a genetic viewpoint[ J]. J Am Soc Nephrol, 2002, 13 (12) :3016-3023.
  • 3Reiser J, Gupta V, Kistler AD. Toward the development of podocyte-speciflc drugs[ J]. Kidney Int, 2010, 77 (8) :6624568.
  • 4Faul C, Donnelly M, Merscher-Gomez S, et al. The actin cytoskeleton of kidney podocytes is a direct target of the antiproteinuric effect of cyclosporine A [ J ]. Nat Med, 2008, 14 (9) :931-938.
  • 5Patrakka J,Tryggvason K. New insights into the role of podocytes in proteinuria [ J ]. Nat Rev Nephrol. 2009. 5 (8) ,463-468.
  • 6陈意志,赵学智,吴俊.从局灶节段性肾小球硬化的哥伦比亚病理分型到足细胞病的分类[J].中华肾脏病杂志,2009(9):734-738. 被引量:11
  • 7Barisoni L, Mundel P. Podocyte biology and the emerging understanding of podocyte diseases[J]. Am J Nephrel, 2003, 23 (5) :353-360.
  • 8Thun M, Macho B,Eugen-Olsen J. suPAR : the molecular crystal ball [ J ]. Dis Markers, 2009, 27 (3-4) : 157-172.
  • 9Ostergaard C, Benfleld T, Lundgren JD, et al. Soluble urokinase receptor is elevated in eerebrospinal fluid from patients with purulent meningitis and is associated with fatal outcome [ J ]. Seand J Infect Dis, 2004, 36( 1 ) :14-19.
  • 10Gustafsson A, Ajeti V, Ljunggren L. Detection of suPAR in the saliva of healthy young adults:comparison with plasma levels[ J ]. Biomark insights, 2011,6:119-125.

二级参考文献35

  • 1潘晓霞,陈楠,周伟,王朝晖,张文,王伟铭,陈晓农,巫永睿,陆颖.原发性局灶节段性肾小球硬化患者CD2AP基因突变的研究[J].中华肾脏病杂志,2006,22(1):13-18. 被引量:24
  • 2师素芳,王素霞,章友康,赵明辉,邹万忠.不同病理类型局灶节段性肾小球硬化症的临床病理分析[J].中华病理学杂志,2007,36(1):11-14. 被引量:5
  • 3Schnaper HW, Robson AM, Kopp JB. Nephrotic syndrome: minimal change disease, focal segmental glomerulosclerosis, and collapsing glomerulopathy //Schrier RW. Diseases of the Kidney and Urinary Tract. 8th. Philadelphia: Lippincott Williams & Wilkins, 2006: 1585-1672.
  • 4Pollak MR. Inherited podocytopathies: FSGS and nephrotic syndrome from a genetic viewpoint. J Am Soc Nephrol, 2002, 13: 3016-3023.
  • 5D'Agati V. Pathologic classification of focal segmental glomerulosclerosis. Semin Nephrol, 2003, 23: 117-134.
  • 6D'Agati VD, Fogo AB, Bruijn JA, et al. Pathologic classification of focal segmental glomerulosclerosis: a working proposal. Am J Kidney Dis, 2004, 43: 368-382.
  • 7Barisoni L, Schnaper HW, Kopp JB. A proposed taxonomy for the podocytopathies: a reassessment of the primary nephrotic diseases. Clin J Am Soc Nephrol, 2007, 2: 529-542.
  • 8Barisoni L, Schnaper HW, Kopp JB. Advances in the biology and genetics of the podocytopathies: implications for diagnosis and therapy. Arch Pathol Lab Med, 2009, 133: 201-216.
  • 9Gipson DS, Chin H, Presler TP, et al. Differential risk of remission and ESRD in childhood FSGS. Pediatr Nephrol, 2006, 21: 344-349.
  • 10Stokes MB, Valeri AM, Markowitz GS, et al. Cellular focal segmental glomerulosclerosis: Clinical and pathologic features. Kidney Int, 2006, 70: 1783-1792.

共引文献10

同被引文献2

引证文献1

二级引证文献2

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