Authors:
Doublier, S
Ruotsalainen, V
Salvidio, G
Lupia, E
Biancone, L
Conaldi, PG
Reponen, P
Tryggvason, K
Camussi, G
Citation: S. Doublier et al., Nephrin redistribution on podocytes is a potential mechanism for proteinuria in patients with primary acquired nephrotic syndrome, AM J PATH, 158(5), 2001, pp. 1723-1731
Authors:
Paloneva, J
Kestila, M
Wu, J
Salminen, A
Bohling, T
Ruotsalainen, V
Hakola, P
Bakker, ABH
Phillips, JH
Pekkarinen, P
Lanier, LL
Timonen, T
Peltonen, L
Citation: J. Paloneva et al., Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts, NAT GENET, 25(3), 2000, pp. 357-361
Authors:
Li, C
Ruotsalainen, V
Tryggvason, K
Shaw, AS
Miner, JH
Citation: C. Li et al., CD2AP is expressed with nephrin in developing podocytes and is found widely in mature kidney and elsewhere, AM J P-REN, 279(4), 2000, pp. F785-F792
Authors:
Patrakka, J
Kestila, M
Wartiovaara, J
Ruotsalainen, V
Tissari, P
Lenkkeri, U
Mannikko, M
Visapaa, I
Holmberg, C
Rapola, J
Tryggvason, K
Jalanko, H
Citation: J. Patrakka et al., Congenital nephrotic syndrome (NPHS1): Features resulting from different mutations in Finnish patients, KIDNEY INT, 58(3), 2000, pp. 972-980
Authors:
Ruotsalainen, V
Patrakka, J
Tissari, P
Reponen, P
Hess, M
Kestila, M
Holmberg, C
Salonen, R
Heikinheimo, M
Wartiovaara, J
Tryggvason, K
Jalanko, H
Citation: V. Ruotsalainen et al., Role of nephrin in cell junction formation in human nephrogenesis, AM J PATH, 157(6), 2000, pp. 1905-1916
Authors:
Tryggvason, K
Ruotsalainen, V
Wartiovaara, J
Citation: K. Tryggvason et al., Discovery of the congenital nephrotic syndrome gene discloses the structure of the mysterious molecular sieve of the kidney, INT J DEV B, 43(5), 1999, pp. 445-451