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Results:
1-8
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Results: 8
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:
Lohi, H
Kujala, M
Kerkela, E
Saarialho-Kere, U
Kestila, M
Kere, J
Citation: H. Lohi et al., Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger, GENOMICS, 70(1), 2000, pp. 102-112
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:
Carrera, M
Kestila, M
de la Iglesia, C
Ruiz, J
Serra, B
Baraibar, R
Citation: M. Carrera et al., Maternal serum alpha-fetoprotein levels in congenital nephrotic syndrome carrier pregnancies, PRENAT DIAG, 19(5), 1999, pp. 489-490
Authors:
Ruotsalainen, V
Ljungberg, P
Wartiovaara, J
Lenkkeri, U
Kestila, M
Jalanko, H
Holmberg, C
Tryggvason, K
Citation: V. Ruotsalainen et al., Nephrin is specifically located at the slit diaphragm of glomerular podocytes, P NAS US, 96(14), 1999, pp. 7962-7967
Authors:
Lenkkeri, U
Mannikko, M
McCready, P
Lamerdin, J
Gribouval, O
Niaudet, P
Antignac, C
Kashtan, CE
Holmberg, C
Olsen, A
Kestila, M
Tryggvason, K
Citation: U. Lenkkeri et al., Structure of the gene for congenital nephrotic syndrome of the Finnish type (NPHS1) and characterization of mutations, AM J HU GEN, 64(1), 1999, pp. 51-61
Authors:
Pekkarinen, P
Kestila, M
Paloneva, J
Terwilliger, J
Varilo, T
Jarvi, O
Hakola, P
Peltonen, L
Citation: P. Pekkarinen et al., Fine-scale mapping of a novel dementia gene, PLOSL, by linkage disequilibrium, GENOMICS, 54(2), 1998, pp. 307-315
Risultati:
1-8
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