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Items: 1 to 20 of 26

1.

A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis.

Winn MP, Conlon PJ, Lynn KL, Farrington MK, Creazzo T, Hawkins AF, Daskalakis N, Kwan SY, Ebersviller S, Burchette JL, Pericak-Vance MA, Howell DN, Vance JM, Rosenberg PB.

Science. 2005 Jun 17;308(5729):1801-4. Epub 2005 May 5.

2.

The TRP superfamily of cation channels.

Montell C.

Sci STKE. 2005 Feb 22;2005(272):re3. Review.

PMID:
15728426
3.

Why is proteinuria an ominous biomarker of progressive kidney disease?

Zandi-Nejad K, Eddy AA, Glassock RJ, Brenner BM.

Kidney Int Suppl. 2004 Nov;(92):S76-89. Review.

4.

Induction of B7-1 in podocytes is associated with nephrotic syndrome.

Reiser J, von Gersdorff G, Loos M, Oh J, Asanuma K, Giardino L, Rastaldi MP, Calvaresi N, Watanabe H, Schwarz K, Faul C, Kretzler M, Davidson A, Sugimoto H, Kalluri R, Sharpe AH, Kreidberg JA, Mundel P.

J Clin Invest. 2004 May;113(10):1390-7.

5.

Regulation of TRPC6 channel activity by tyrosine phosphorylation.

Hisatsune C, Kuroda Y, Nakamura K, Inoue T, Nakamura T, Michikawa T, Mizutani A, Mikoshiba K.

J Biol Chem. 2004 Apr 30;279(18):18887-94. Epub 2004 Feb 3.

6.

Expression and relative abundance of short transient receptor potential channels in the rat renal microcirculation.

Facemire CS, Mohler PJ, Arendshorst WJ.

Am J Physiol Renal Physiol. 2004 Mar;286(3):F546-51. Epub 2003 Dec 16.

7.

TRP channels as cellular sensors.

Clapham DE.

Nature. 2003 Dec 4;426(6966):517-24. Review.

PMID:
14654832
8.

Gene expression profiles of podocyte-associated molecules as diagnostic markers in acquired proteinuric diseases.

Schmid H, Henger A, Cohen CD, Frach K, Gröne HJ, Schlöndorff D, Kretzler M.

J Am Soc Nephrol. 2003 Nov;14(11):2958-66.

9.

Nephrin and CD2AP associate with phosphoinositide 3-OH kinase and stimulate AKT-dependent signaling.

Huber TB, Hartleben B, Kim J, Schmidts M, Schermer B, Keil A, Egger L, Lecha RL, Borner C, Pavenstädt H, Shaw AS, Walz G, Benzing T.

Mol Cell Biol. 2003 Jul;23(14):4917-28.

10.

CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility.

Kim JM, Wu H, Green G, Winkler CA, Kopp JB, Miner JH, Unanue ER, Shaw AS.

Science. 2003 May 23;300(5623):1298-300.

11.

Fyn binds to and phosphorylates the kidney slit diaphragm component Nephrin.

Verma R, Wharram B, Kovari I, Kunkel R, Nihalani D, Wary KK, Wiggins RC, Killen P, Holzman LB.

J Biol Chem. 2003 Jun 6;278(23):20716-23. Epub 2003 Mar 31. Erratum in: J Biol Chem. 2005 Jul 15;280(28):26640.

12.

Cell biology of the glomerular podocyte.

Pavenstädt H, Kriz W, Kretzler M.

Physiol Rev. 2003 Jan;83(1):253-307. Review.

13.

Inherited podocytopathies: FSGS and nephrotic syndrome from a genetic viewpoint.

Pollak MR.

J Am Soc Nephrol. 2002 Dec;13(12):3016-23. Review. No abstract available.

14.

Determinants of vascular permeability in the kidney glomerulus.

Hamano Y, Grunkemeyer JA, Sudhakar A, Zeisberg M, Cosgrove D, Morello R, Lee B, Sugimoto H, Kalluri R.

J Biol Chem. 2002 Aug 23;277(34):31154-62. Epub 2002 May 30.

15.

Podocyte electrophysiology, in vivo and in vitro.

Pavenstädt H, Bek M.

Microsc Res Tech. 2002 May 15;57(4):224-7. Review.

PMID:
12012388
16.

The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death.

Putaala H, Soininen R, Kilpeläinen P, Wartiovaara J, Tryggvason K.

Hum Mol Genet. 2001 Jan 1;10(1):1-8.

PMID:
11136707
17.

T-Coffee: A novel method for fast and accurate multiple sequence alignment.

Notredame C, Higgins DG, Heringa J.

J Mol Biol. 2000 Sep 8;302(1):205-17.

PMID:
10964570
18.

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome.

Boute N, Gribouval O, Roselli S, Benessy F, Lee H, Fuchshuber A, Dahan K, Gubler MC, Niaudet P, Antignac C.

Nat Genet. 2000 Apr;24(4):349-54. Erratum in: Nat Genet 2000 May;25(1):125.

PMID:
10742096
19.

Getting a foothold in nephrotic syndrome.

Somlo S, Mundel P.

Nat Genet. 2000 Apr;24(4):333-5. No abstract available.

PMID:
10742089
20.

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis.

Kaplan JM, Kim SH, North KN, Rennke H, Correia LA, Tong HQ, Mathis BJ, Rodríguez-Pérez JC, Allen PG, Beggs AH, Pollak MR.

Nat Genet. 2000 Mar;24(3):251-6.

PMID:
10700177

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