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肾病综合征患者肾小球中Nephrin的表达意义

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出处 《中国中西医结合肾病杂志》 2005年第8期490-491,共2页 Chinese Journal of Integrated Traditional and Western Nephrology
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参考文献5

  • 1Patrakka J, Kestila M, Wartiovaara J, et al. Congenital nephrotic syndrome (NPHS1): Features resulting from different mutations in Finnish patients. Kidney Int, 2000, 58(3) :972 - 980.
  • 2Ruotsalainen V, Patrakka J, Tissari P, et al. Role of nephrin in cell junction formation in human nephrogenesis. American Journal of Pathology,Am J Pathol,2000,157(6): 1905 - 1916.
  • 3Patrakka J, Martin P, Salonen R, et al. Proteinuria and prenatal diagnosis of congenital nephrosis in fetal carriers of nephrin gene mutations. Lancet, 2002,359 (9317): 1575 -1577.
  • 4Putaala H, Soininen R, Kilpelainen P, et al. The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death. Human Mol Gene, 2001,10(1):1-8.
  • 5Doublier S,Salvidio G, Lupia E, et al. Nephrin expression is reduced in human diabetic nephropathy: evidence for a distinct role for glycated albumin and angiotensin Ⅱ. Diabetes,2003,52(4):1023-1030.

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