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导致家族性局灶节段性肾小球硬化新基因——TRPC6 被引量:2

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出处 《肾脏病与透析肾移植杂志》 CAS CSCD 2006年第2期140-143,共4页 Chinese Journal of Nephrology,Dialysis & Transplantation
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参考文献30

  • 1Guan N,Ding J,Zhang J,et al.Expression of nephrin,podocin,alpha-actinin,and WT1 in children with nephrotic syndrome.Pediatr Nephrol,2003,18 (11):1122-1127.
  • 2Guan N,Ding J,Deng J,et al.Key molecular events in puromycin aminonucleoside nephrosis rats.Pathol Int,2004,54 (9):703-711.
  • 3Fan Q,Ding J,Zhang J,et al.Effect of the knockdown of podocin mRNA on nephrin and alpha-actinin in mouse podocyte.Exp Biol Med (Maywood),2004,229(9):964 -970.
  • 4邓江红,丁洁,管娜,范青锋,张敬京.嘌呤霉素肾病大鼠肾小球足细胞相关分子表达的共定位分布[J].肾脏病与透析肾移植杂志,2004,13(3):205-210. 被引量:5
  • 5李玲,邹万忠,张波,王盛兰,侯琳.病理性因素对体外肾小管上皮细胞表型转化的影响[J].中华肾脏病杂志,2003,19(1):1-5. 被引量:21
  • 6Winn MP,Conlon PJ,Lynn KL,et al.A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis.Science,2005,308 (5729):1801 -1804.
  • 7Reiser J,Polu KR,Moller CC,et al.TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function.Nat Genet,2005,37 (7):739-744.
  • 8D Esposito M,Strazzullo M,Cuccurese M.Identification and assignment of the human transient receptor potential channel 6 gene TRPC6to chromosome 1 1q21-> q22.Cytogenet Cell Genet,1998,83 (1-2):46 -47.
  • 9Estacion M,Li S,Sinkins WG,et al.Activation of human TRPC6channels by receptor stimulation.J Biol Chem,2004,279 (21):22047-22056.
  • 10Montell C.The TRP superfamily of cation channels.Sci STKE,2005,2005 (272):re3.

二级参考文献25

  • 1Kestila M, Lenkkeri U, Mannikko M, et al. Positionally cloned gene for a novel glomerular protein nephrin is nutated in congenital nephrotic syndrome. J Mol Cell, 1998, 1 (4): 575
  • 2Tryggvason K. Unraveling the mechanisms of glomerular ultrafiltration:nephrin, a key component of the slit diaphragm J An Soc Nephrol,1999, 10(11): 2440
  • 3Luinula P, Sandstrom N, Novikov D, et al. Podocyte-associated molecules in puromycin aminonucleoside nephrosis of the rat. Lab Invest,2002, 82 (6): 713
  • 4Boute N, Gribouval O, Roselli S, et al. NPHS2, encoding the glomerular protein podocin, is mutated in antosomal recessive steroid-resistant nephrotic syndrome. Nat Genet, 2000, 24 (4): 349
  • 5Kaplan JM, Kim SH, North KN, et al. Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis. Nat Genet,2000, 24 (3): 251
  • 6Shih NY, Li J, Karpitskii V, et al. Congenital nephritic sydrome in mice lacking CD2-associated protein. Science, 1999, 286 (10): 312
  • 7Tryggvason K, Wartiovaara J. Molecular basis of glomerular permselectivity. Curr Opin Nephrol Hypertens , 2001 , 10(4) :543
  • 8Khoshnoodi J, Tryggvason K. Unraveling the molecular make-up of the glomerular podocyte slit diaphragm Exp Nephrol, 2001, 9 (6): 355
  • 9Mundel P, Shankland S. Podicyte biology and response to injury. J Am Soc Nephrol, 2002, 13:3005
  • 10Guan N, Ding J, Zhang JJ, et al. Expression of nephrin, podocin, a-actinin and WT1 in children with nephrotic syndrome. Pediatr Nephrol,2003, 18:1122

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