Tryggvason K - Search Results

1

Pdlim2 is a novel actin-regulating protein of podocyte foot processes.

Sistani L, Dunér F, Udumala S, Hultenby K, Uhlen M, Betsholtz C, Tryggvason K, Wernerson A, Patrakka J. Sistani L, et al. Among authors: tryggvason k. Kidney Int. 2011 Nov;80(10):1045-54. doi: 10.1038/ki.2011.231. Epub 2011 Aug 3. Kidney Int. 2011. PMID: 21814175 Free article.

2

Can Alport syndrome be treated by gene therapy?

Tryggvason K, Heikkilä P, Pettersson E, Tibell A, Thorner P. Tryggvason K, et al. Kidney Int. 1997 May;51(5):1493-9. doi: 10.1038/ki.1997.205. Kidney Int. 1997. PMID: 9150464 Free article. Review. No abstract available.

3

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: tryggvason k. Kidney Int. 2000 Sep;58(3):972-80. doi: 10.1046/j.1523-1755.2000.00254.x. Kidney Int. 2000. PMID: 10972661 Free article.

4

Role of nephrin in cell junction formation in human nephrogenesis.

Ruotsalainen V, Patrakka J, Tissari P, Reponen P, Hess M, Kestilä M, Holmberg C, Salonen R, Heikinheimo M, Wartiovaara J, Tryggvason K, Jalanko H. Ruotsalainen V, et al. Among authors: tryggvason k. Am J Pathol. 2000 Dec;157(6):1905-16. doi: 10.1016/S0002-9440(10)64829-8. Am J Pathol. 2000. PMID: 11106563 Free PMC article.

5

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: tryggvason k. J Am Soc Nephrol. 2001 Feb;12(2):289-296. doi: 10.1681/ASN.V122289. J Am Soc Nephrol. 2001. PMID: 11158218

6

Unraveling the molecular make-up of the glomerular podocyte slit diaphragm.

Khoshnoodi J, Tryggvason K. Khoshnoodi J, et al. Among authors: tryggvason k. Exp Nephrol. 2001;9(6):355-9. doi: 10.1159/000052632. Exp Nephrol. 2001. PMID: 11701993 Review.

7

Genetic kidney diseases disclose the pathogenesis of proteinuria.

Jalanko H, Patrakka J, Tryggvason K, Holmberg C. Jalanko H, et al. Among authors: tryggvason k. Ann Med. 2001 Nov;33(8):526-33. doi: 10.3109/07853890108995962. Ann Med. 2001. PMID: 11730159 Review.

8

Recurrence of nephrotic syndrome in kidney grafts of patients with congenital nephrotic syndrome of the Finnish type: role of nephrin.

Patrakka J, Ruotsalainen V, Reponen P, Qvist E, Laine J, Holmberg C, Tryggvason K, Jalanko H. Patrakka J, et al. Among authors: tryggvason k. Transplantation. 2002 Feb 15;73(3):394-403. doi: 10.1097/00007890-200202150-00013. Transplantation. 2002. PMID: 11884936

9

Altered ultrastructural distribution of nephrin in minimal change nephrotic syndrome.

Wernerson A, Dunér F, Pettersson E, Widholm SM, Berg U, Ruotsalainen V, Tryggvason K, Hultenby K, Söderberg M. Wernerson A, et al. Among authors: tryggvason k. Nephrol Dial Transplant. 2003 Jan;18(1):70-6. doi: 10.1093/ndt/18.1.70. Nephrol Dial Transplant. 2003. PMID: 12480962

10

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: tryggvason k. Kidney Int. 2003 Aug;64(2):404-13. doi: 10.1046/j.1523-1755.2003.00097.x. Kidney Int. 2003. PMID: 12846735 Free article.

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