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Results: 1-25/50
Authors:
Patton, BL
Cunningham, JM
Thyboll, J
Kortesmaa, J
Westerblad, H
Edstrom, L
Tryggvason, K
Sanes, JR
Citation: Bl. Patton et al., Properly formed but improperly localized synaptic specializations in the absence of laminin alpha 4, NAT NEUROSC, 4(6), 2001, pp. 597-604
Authors:
Tryggvason, K
Wartiovaara, J
Citation: K. Tryggvason et J. Wartiovaara, Molecular basis of glomerular permselectivity, CURR OP NEP, 10(4), 2001, pp. 543-549
Authors:
Beltcheva, O
Martin, P
Lenkkeri, U
Tryggvason, K
Citation: O. Beltcheva et al., Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome, HUM MUTAT, 17(5), 2001, pp. 368-373
Authors:
Patrakka, J
Ruotsalainen, V
Ketola, I
Holmberg, C
Heikinheimo, M
Tryggvason, K
Jalanko, H
Citation: J. Patrakka et al., Expression of nephrin in pediatric kidney diseases, J AM S NEPH, 12(2), 2001, pp. 289-296
Authors:
Khoshnoodi, J
Tryggvason, K
Citation: J. Khoshnoodi et K. Tryggvason, Unraveling the molecular make-up of the glomerular podocyte slit diaphragm, EXP NEPHROL, 9(6), 2001, pp. 355-359
Authors:
Heikkila, P
Tibell, A
Morita, T
Chen, Y
Wu, G
Sado, Y
Ninomiya, Y
Pettersson, E
Tryggvason, K
Citation: P. Heikkila et al., Adenovirus-mediated transfer of type IV collagen alpha 5 chain cDNA into swine kidney in vivo: deposition of the protein into the glomerular basementmembrane, GENE THER, 8(11), 2001, pp. 882-890
Authors:
Liu, L
Done, SC
Khoshnoodi, J
Bertorello, A
Wartiovaara, J
Berggren, PO
Tryggvason, K
Citation: L. Liu et al., Defective nephrin trafficking caused by missense mutations in the NPHS1 gene: insight into the mechanisms of congenital nephrotic syndrome, HUM MOL GEN, 10(23), 2001, pp. 2637-2644
Authors:
Putaala, H
Soininen, R
Kilpelainen, P
Wartiovaara, J
Tryggvason, K
Citation: H. Putaala et al., The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death, HUM MOL GEN, 10(1), 2001, pp. 1-8
Authors:
Khoshnoodi, J
Tryggvason, K
Citation: J. Khoshnoodi et K. Tryggvason, Congenital nephrotic syndromes, CUR OP GEN, 11(3), 2001, pp. 322-327
Authors:
Martin, PH
Tryggvason, K
Citation: Ph. Martin et K. Tryggvason, Two novel alternatively spliced 9-bp exons in the COL4A5 gene, PED NEPHROL, 16(1), 2001, pp. 41-44
Authors:
Lenander, C
Habermann, J
Ost, A
Nilsson, B
Schimmelpenning, H
Tryggvason, K
Auer, G
Citation: C. Lenander et al., Laminin-5 gamma 2 chain expression correlates with unfavorable prognosis in colon carcinomas, ANAL CELL P, 22(4), 2001, pp. 201-209
Authors:
Jalanko, H
Patrakka, J
Tryggvason, K
Holmberg, C
Citation: H. Jalanko et al., Genetic kidney diseases disclose the pathogenesis of proteinuria, ANN MED, 33(8), 2001, pp. 526-533
Authors:
Habermann, J
Lenander, C
Roblick, UJ
Kruger, S
Ludwig, D
Alaiya, A
Freitag, S
Dumbgen, L
Bruch, HP
Stange, E
Salo, S
Tryggvason, K
Auer, G
Schimmelpenning, H
Citation: J. Habermann et al., Ulcerative colitis and colorectal carcinoma - DNA-profile, laminin-5 gamma2 chain and cyclin A expression as early markers for risk assessment, SC J GASTR, 36(7), 2001, pp. 751-758
Authors:
Geberhiwot, T
Assefa, D
Kortesmaa, J
Ingerpuu, S
Pedraza, C
Wondimu, Z
Charo, J
Kiessling, R
Virtanen, I
Tryggvason, K
Patarroyo, M
Citation: T. Geberhiwot et al., Laminin-8 (alpha 4 beta 1 gamma 1) is synthesized by lymphoid cells, promotes lymphocyte migration and costimulates T cell proliferation, J CELL SCI, 114(2), 2001, pp. 423-433
Authors:
Tryggvason, K
Romert, A
Eriksson, U
Citation: K. Tryggvason et al., Biosynthesis of 9-cis-retinoic acid in vivo - The roles of different retinol dehydrogenases and a structure-activity analysis of microsomal retinol dehydrogenases, J BIOL CHEM, 276(22), 2001, pp. 19253-19258
Authors:
Parpala-Sparman, T
Paakko, P
Kortteinen, P
Salonurmi, T
Lukkarinen, O
Tryggvason, K
Citation: T. Parpala-sparman et al., Closed-circuit organ perfusion technique for gene transfer into the lungs.An experimental trial on farm pigs, EUR J CL IN, 31(3), 2001, pp. 264-271
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:
Kraal, G
van der Laan, LJW
Elomaa, O
Tryggvason, K
Citation: G. Kraal et al., The macrophage receptor MARCO, MICROBES IN, 2(3), 2000, pp. 313-316
Authors:
Putaala, H
Sainio, K
Sariola, H
Tryggvason, K
Citation: H. Putaala et al., Primary structure of mouse and rat nephrin cDNA and structure and expression of the mouse gene, J AM S NEPH, 11(6), 2000, pp. 991-1001
Authors:
Jais, JP
Knebelmann, B
Giatras, I
De Marchi, M
Rizzoni, G
Renieri, A
Weber, M
Gross, O
Netzer, KO
Flinter, F
Pirson, Y
Verellen, C
Wieslander, J
Persson, U
Tryggvason, K
Martin, P
Hertz, JM
Schroder, C
Sanak, M
Krejcova, S
Carvalho, MF
Saus, J
Antignac, C
Smeets, H
Gubler, MC
Citation: Jp. Jais et al., X-linked Alport syndrome: Natural history in 195 families and genotype-phenotype correlations in males, J AM S NEPH, 11(4), 2000, pp. 649-657
Authors:
Heikkila, P
Tryggvason, K
Thorner, P
Citation: P. Heikkila et al., Animal models of Alport syndrome: Advancing the prospects for effective human gene therapy, EXP NEPHROL, 8(1), 2000, pp. 1-7
Authors:
Geberhiwot, T
Wondimu, Z
Salo, S
Pikkarainen, T
Kortesmaa, J
Tryggvason, K
Virtanen, I
Patarroyo, M
Citation: T. Geberhiwot et al., Chain specificity assignment of monoclonal antibodies to human laminins byusing recombinant laminin beta 1 and gamma 1 chains, MATRIX BIOL, 19(2), 2000, pp. 163-167
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:
Airenne, T
Lin, YF
Olsson, M
Ekblom, P
Vainio, S
Tryggvason, K
Citation: T. Airenne et al., Differential expression of mouse laminin gamma 2 and gamma 2chain transcripts, CELL TIS RE, 300(1), 2000, pp. 129-137
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