| 1 | IDMS, WT1
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| Focal segmental glomerulosclerosis in patients with complete deletion of one WT1 allele.
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| Iijima K, Someya T, Ito S, Nozu K, Nakanishi K, Matsuoka K, Ohashi H, Nagata M, Kamei K, Sasaki S.
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| Pediatrics 129(6):e1621-5. doi: 10.1542/peds.2011-1323. Epub 2012 May 14.
2012
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| 2 | IDMS, WT1
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| A murine model of Denys-Drash syndrome reveals novel transcriptional targets of WT1 in podocytes.
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| Ratelade J, Arrondel C, Hamard G, Garbay S, Harvey S, Biebuyck N, Schulz H, Hastie N, Pontoglio M, Gubler MC, Antignac C, Heidet L.
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| Hum Mol Genet 19(1):1-15. Epub .PMID: 19797313 2010
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| 3 | IDMS, WT1
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| Membranoproliferative glomerulonephritis associated with a mutation in Wilms' tumour suppressor gene 1.
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| Bockenhauer D, van't Hoff W, Chernin G, Heeringa SF, Sebire NJ.
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| Pediatr Nephrol 24(7):1399-401. Epub 2009 Feb 11.PMID: 19205749 2009
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| 4 | IDMS, WT1
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| Constitutional WT1 correlate with clinical features in children with progressive nephropathy.
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| Takata A, Kikuchi H, Fukuzawa R, Ito S, Honda M, Hata J.
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| J Med Genet 37(9):698-701. No abstract available. 2000
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| 5 | IDMS, WT1
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| Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database.
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| Jeanpierre C, et al.
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| Am J Hum Genet 62 : 824-833. 1998
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| 6 | IDMS, WT1
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| Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations.
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| Schumacher V, et al.
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| Kidney Int 53 : 1594-1600. 1998
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