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164 related items for PubMed ID: 15687485

  • 1. Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population.
    Orloff MS, Iyengar SK, Winkler CA, Goddard KA, Dart RA, Ahuja TS, Mokrzycki M, Briggs WA, Korbet SM, Kimmel PL, Simon EE, Trachtman H, Vlahov D, Michel DM, Berns JS, Smith MC, Schelling JR, Sedor JR, Kopp JB.
    Physiol Genomics; 2005 Apr 14; 21(2):212-21. PubMed ID: 15687485
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  • 2. Surgical management and genotype/phenotype correlations in WT1 gene-related diseases (Drash, Frasier syndromes).
    Auber F, Lortat-Jacob S, Sarnacki S, Jaubert F, Salomon R, Thibaud E, Jeanpierre C, Nihoul-Fékété C.
    J Pediatr Surg; 2003 Jan 14; 38(1):124-9; discussion 124-9. PubMed ID: 12592634
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  • 5. A female infant with Frasier syndrome showing splice site mutation in Wilms' tumor gene (WT1) intron 9.
    Fujita S, Sugimoto K, Miyazawa T, Yanagida H, Tabata N, Okada M, Takemura T.
    Clin Nephrol; 2010 Jun 14; 73(6):487-91. PubMed ID: 20497763
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  • 7. Frasier syndrome: a cause of focal segmental glomerulosclerosis in a 46,XX female.
    Demmer L, Primack W, Loik V, Brown R, Therville N, McElreavey K.
    J Am Soc Nephrol; 1999 Oct 14; 10(10):2215-8. PubMed ID: 10505699
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  • 10. Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases.
    Denamur E, Bocquet N, Mougenot B, Da Silva F, Martinat L, Loirat C, Elion J, Bensman A, Ronco PM.
    J Am Soc Nephrol; 1999 Oct 14; 10(10):2219-23. PubMed ID: 10505700
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  • 11. [WT1 mutation as a cause of progressive nephropathy in Frasier syndrome--case report].
    Wasilewska A, Zoch-Zwierz W, Tenderenda E, Rybi-Szumińska A, Kołodziejczyk Z.
    Pol Merkur Lekarski; 2009 Jun 14; 26(156):642-4. PubMed ID: 19711733
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  • 13. The Wt1+/R394W mouse displays glomerulosclerosis and early-onset renal failure characteristic of human Denys-Drash syndrome.
    Gao F, Maiti S, Sun G, Ordonez NG, Udtha M, Deng JM, Behringer RR, Huff V.
    Mol Cell Biol; 2004 Nov 14; 24(22):9899-910. PubMed ID: 15509792
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  • 14. WT1 microdeletion and slowly progressing focal glomerulosclerosis in a patient with male pseudohermaphroditism, childhood leukemia, Wilms tumor and cerebellar angioblastoma.
    Buglyó G, Méhes G, Vargha G, Biró S, Mátyus J.
    Clin Nephrol; 2013 May 14; 79(5):414-8. PubMed ID: 23618379
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  • 15. [Frasier syndrome: a rare syndrome with WT1 gene mutation in pediatric urology].
    Zugor V, Zenker M, Schrott KM, Schott GE.
    Aktuelle Urol; 2006 Jan 14; 37(1):64-6. PubMed ID: 16440249
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  • 16. Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms.
    Klamt B, Koziell A, Poulat F, Wieacker P, Scambler P, Berta P, Gessler M.
    Hum Mol Genet; 1998 Apr 14; 7(4):709-14. PubMed ID: 9499425
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  • 18. Frasier syndrome: early gonadoblastoma and cyclosporine responsiveness.
    Sinha A, Sharma S, Gulati A, Sharma A, Agarwala S, Hari P, Bagga A.
    Pediatr Nephrol; 2010 Oct 14; 25(10):2171-4. PubMed ID: 20419325
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  • 19. Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis - a single-centre experience.
    Bińczak-Kuleta A, Rubik J, Litwin M, Ryder M, Lewandowska K, Taryma-Leśniak O, Clark JS, Grenda R, Ciechanowicz A.
    Bosn J Basic Med Sci; 2014 May 14; 14(2):89-93. PubMed ID: 24856380
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  • 20. Gonadal mosaicism of Frasier syndrome in 3 Chinese siblings with donor splice site mutation of Wilms' tumour gene.
    Chak WL, To KF, Cheng YL, Tsui KM, Lo KL, Tong HM, Lai FM, Wong FK, Choi KS, Chau KF, Li CS.
    Nephron; 2002 Jul 14; 91(3):526-9. PubMed ID: 12119492
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