DK 54724/DK/NIDDK NIH HHS/United States[Grant Number] - Search Results

Year	Number of Results
1999	1
2000	1
2001	4
2002	3
2003	2
2004	1
2021	0

1

Genetic kidney diseases disclose the pathogenesis of proteinuria.

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

2

Unraveling the mechanisms of glomerular ultrafiltration: nephrin, a key component of the slit diaphragm.

Tryggvason K. Tryggvason K. J Am Soc Nephrol. 1999 Nov;10(11):2440-5. J Am Soc Nephrol. 1999. PMID: 10541305 Free article. Review. No abstract available.

3

Nephrin promotes cell-cell adhesion through homophilic interactions.

Khoshnoodi J, Sigmundsson K, Ofverstedt LG, Skoglund U, Obrink B, Wartiovaara J, Tryggvason K. Khoshnoodi J, et al. Am J Pathol. 2003 Dec;163(6):2337-46. doi: 10.1016/S0002-9440(10)63590-0. Am J Pathol. 2003. PMID: 14633607 Free PMC article.

4

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. Nephrol Dial Transplant. 2003 Jan;18(1):70-6. doi: 10.1093/ndt/18.1.70. Nephrol Dial Transplant. 2003. PMID: 12480962

5

Proteinuria and prenatal diagnosis of congenital nephrosis in fetal carriers of nephrin gene mutations.

Patrakka J, Martin P, Salonen R, Kestilä M, Ruotsalainen V, Männikkö M, Ryynänen M, Rapola J, Holmberg C, Tryggvason K, Jalanko H. Patrakka J, et al. Lancet. 2002 May 4;359(9317):1575-7. doi: 10.1016/S0140-6736(02)08504-5. Lancet. 2002. PMID: 12047969

6

Nephrin strands contribute to a porous slit diaphragm scaffold as revealed by electron tomography.

Wartiovaara J, Ofverstedt LG, Khoshnoodi J, Zhang J, Mäkelä E, Sandin S, Ruotsalainen V, Cheng RH, Jalanko H, Skoglund U, Tryggvason K. Wartiovaara J, et al. J Clin Invest. 2004 Nov;114(10):1475-83. doi: 10.1172/JCI22562. J Clin Invest. 2004. PMID: 15545998 Free PMC article.

7

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

Yan K, Khoshnoodi J, Ruotsalainen V, Tryggvason K. Yan K, et al. 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 Free article.

8

Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome.

Beltcheva O, Martin P, Lenkkeri U, Tryggvason K. Beltcheva O, et al. Hum Mutat. 2001 May;17(5):368-73. doi: 10.1002/humu.1111. Hum Mutat. 2001. PMID: 11317351

9

Defective nephrin trafficking caused by missense mutations in the NPHS1 gene: insight into the mechanisms of congenital nephrotic syndrome.

Liu L, Doné SC, Khoshnoodi J, Bertorello A, Wartiovaara J, Berggren PO, Tryggvason K. Liu L, et al. Hum Mol Genet. 2001 Nov 1;10(23):2637-44. doi: 10.1093/hmg/10.23.2637. Hum Mol Genet. 2001. PMID: 11726550

10

Primary structure of mouse and rat nephrin cDNA and structure and expression of the mouse gene.

Putaala H, Sainio K, Sariola H, Tryggvason K. Putaala H, et al. J Am Soc Nephrol. 2000 Jun;11(6):991-1001. J Am Soc Nephrol. 2000. PMID: 10820162 Free article.

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