Ruotsalainen V - Search Results

1

Disease-causing missense mutations in NPHS2 gene alter normal nephrin trafficking to the plasma membrane.

Nishibori Y, Liu L, Hosoyamada M, Endou H, Kudo A, Takenaka H, Higashihara E, Bessho F, Takahashi S, Kershaw D, Ruotsalainen V, Tryggvason K, Khoshnoodi J, Yan K. Nishibori Y, et al. Among authors: ruotsalainen v. Kidney Int. 2004 Nov;66(5):1755-65. doi: 10.1111/j.1523-1755.2004.00898.x. Kidney Int. 2004. PMID: 15496146 Free article.

2

The effect of dexamethasone on defective nephrin transport caused by ER stress: a potential mechanism for the therapeutic action of glucocorticoids in the acquired glomerular diseases.

Fujii Y, Khoshnoodi J, Takenaka H, Hosoyamada M, Nakajo A, Bessho F, Kudo A, Takahashi S, Arimura Y, Yamada A, Nagasawa T, Ruotsalainen V, Tryggvason K, Lee AS, Yan K. Fujii Y, et al. Among authors: ruotsalainen v. Kidney Int. 2006 Apr;69(8):1350-9. doi: 10.1038/sj.ki.5000317. Kidney Int. 2006. PMID: 16531978 Free article.

3

N-linked glycosylation is critical for the plasma membrane localization of nephrin.

Yan K, Khoshnoodi J, Ruotsalainen V, Tryggvason K. Yan K, et al. Among authors: ruotsalainen v. J Am Soc Nephrol. 2002 May;13(5):1385-9. doi: 10.1097/01.asn.0000013297.11876.5b. J Am Soc Nephrol. 2002. PMID: 11961028

4

Clustering-induced tyrosine phosphorylation of nephrin by Src family kinases.

Lahdenperä J, Kilpeläinen P, Liu XL, Pikkarainen T, Reponen P, Ruotsalainen V, Tryggvason K. Lahdenperä J, et al. Among authors: ruotsalainen v. Kidney Int. 2003 Aug;64(2):404-13. doi: 10.1046/j.1523-1755.2003.00097.x. Kidney Int. 2003. PMID: 12846735 Free article.

5

Discovery of the congenital nephrotic syndrome gene discloses the structure of the mysterious molecular sieve of the kidney.

Tryggvason K, Ruotsalainen V, Wartiovaara J. Tryggvason K, et al. Among authors: ruotsalainen v. Int J Dev Biol. 1999;43(5):445-51. Int J Dev Biol. 1999. PMID: 10535322 Review.

6

Monoclonal antibodies to human nephrin.

Ruotsalainen V, Reponen P, Khoshnoodi J, Kilpeläinen P, Tryggvason K. Ruotsalainen V, et al. Hybrid Hybridomics. 2004 Feb;23(1):55-63. doi: 10.1089/153685904322772033. Hybrid Hybridomics. 2004. PMID: 15000849

7

Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients.

Patrakka J, Kestilä M, Wartiovaara J, Ruotsalainen V, Tissari P, Lenkkeri U, Männikkö M, Visapää I, Holmberg C, Rapola J, Tryggvason K, Jalanko H. Patrakka J, et al. Among authors: ruotsalainen v. Kidney Int. 2000 Sep;58(3):972-80. doi: 10.1046/j.1523-1755.2000.00254.x. Kidney Int. 2000. PMID: 10972661 Free article.

8

Expression of nephrin in pediatric kidney diseases.

Patrakka J, Ruotsalainen V, Ketola I, Holmberg C, Heikinheimo M, Tryggvason K, Jalanko H. Patrakka J, et al. Among authors: ruotsalainen v. J Am Soc Nephrol. 2001 Feb;12(2):289-296. doi: 10.1681/ASN.V122289. J Am Soc Nephrol. 2001. PMID: 11158218

9

Expression of nephrin in acquired human glomerular disease.

Huh W, Kim DJ, Kim MK, Kim YG, Oh HY, Ruotsalainen V, Tryggvason K. Huh W, et al. Among authors: ruotsalainen v. Nephrol Dial Transplant. 2002 Mar;17(3):478-84. doi: 10.1093/ndt/17.3.478. Nephrol Dial Transplant. 2002. PMID: 11865096

10

Co-localization of nephrin, podocin, and the actin cytoskeleton: evidence for a role in podocyte foot process formation.

Saleem MA, Ni L, Witherden I, Tryggvason K, Ruotsalainen V, Mundel P, Mathieson PW. Saleem MA, et al. Among authors: ruotsalainen v. Am J Pathol. 2002 Oct;161(4):1459-66. doi: 10.1016/S0002-9440(10)64421-5. Am J Pathol. 2002. PMID: 12368218 Free PMC article.

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