BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

276 related articles for article (PubMed ID: 10792605)

  • 1. WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis.
    Denamur E; Bocquet N; Baudouin V; Da Silva F; Veitia R; Peuchmaur M; Elion J; Gubler MC; Fellous M; Niaudet P; Loirat C
    Kidney Int; 2000 May; 57(5):1868-72. PubMed ID: 10792605
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 10(10):2219-23. PubMed ID: 10505700
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Donor splice-site mutations in WT1 are responsible for Frasier syndrome.
    Barbaux S; Niaudet P; Gubler MC; Grünfeld JP; Jaubert F; Kuttenn F; Fékété CN; Souleyreau-Therville N; Thibaud E; Fellous M; McElreavey K
    Nat Genet; 1997 Dec; 17(4):467-70. PubMed ID: 9398852
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 10(10):2215-8. PubMed ID: 10505699
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 7(4):709-14. PubMed ID: 9499425
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 73(6):487-91. PubMed ID: 20497763
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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(2):89-93. PubMed ID: 24856380
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Exon 9 mutations in the WT1 gene, without influencing KTS splice isoforms, are also responsible for Frasier syndrome.
    Kohsaka T; Tagawa M; Takekoshi Y; Yanagisawa H; Tadokoro K; Yamada M
    Hum Mutat; 1999; 14(6):466-70. PubMed ID: 10571943
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genotype-phenotype associations in WT1 glomerulopathy.
    Lipska BS; Ranchin B; Iatropoulos P; Gellermann J; Melk A; Ozaltin F; Caridi G; Seeman T; Tory K; Jankauskiene A; Zurowska A; Szczepanska M; Wasilewska A; Harambat J; Trautmann A; Peco-Antic A; Borzecka H; Moczulska A; Saeed B; Bogdanovic R; Kalyoncu M; Simkova E; Erdogan O; Vrljicak K; Teixeira A; Azocar M; Schaefer F;
    Kidney Int; 2014 May; 85(5):1169-78. PubMed ID: 24402088
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 46,XY phenotypic male with focal segmental glomerulosclerosis caused by the WT1 splice site mutation.
    Tajima T; Sasaki S; Tanaka Y; Kusunoki H; Nagashima T; Nonomura K; Fujieda K
    Horm Res; 2003; 60(6):302-5. PubMed ID: 14646409
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The ratio of +/-KTS splice variants of the Wilms' tumour suppressor protein WT1 mRNA is determined by an intronic enhancer.
    Yang C; Romaniuk PJ
    Biochem Cell Biol; 2008 Aug; 86(4):312-21. PubMed ID: 18756326
    [TBL] [Abstract][Full Text] [Related]  

  • 12. WT1 intron 9 splice acceptor site mutation in a 46,XY male with focal segmental glomerulosclerosis.
    Kanemoto K; Ishikura K; Ariyasu D; Hamasaki Y; Hataya H; Hasegawa Y; Ikeda M
    Pediatr Nephrol; 2007 Mar; 22(3):454-8. PubMed ID: 17061122
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical characteristics and WT1 genetic analysis of patients with steroid resistant nephrotic syndrome accompanied with genitourinary malformations.
    Li JG; Zhao D; Ding J; Xiao HJ; Guan N; Fan QF; Zhang HW
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Dec; 32(6):949-57. PubMed ID: 18182709
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An unusual phenotype of Frasier syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis.
    Melo KF; Martin RM; Costa EM; Carvalho FM; Jorge AA; Arnhold IJ; Mendonca BB
    J Clin Endocrinol Metab; 2002 Jun; 87(6):2500-5. PubMed ID: 12050205
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Do intronic mutations affecting splicing of WT1 exon 9 cause Frasier syndrome?
    Kikuchi H; Takata A; Akasaka Y; Fukuzawa R; Yoneyama H; Kurosawa Y; Honda M; Kamiyama Y; Hata J
    J Med Genet; 1998 Jan; 35(1):45-8. PubMed ID: 9475094
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Wilms' tumour 1 gene mutations in south Indian children with steroid-resistant nephrotic syndrome.
    Kumar AS; Srilakshmi R; Karthickeyan S; Balakrishnan K; Padmaraj R; Senguttuvan P
    Indian J Med Res; 2016 Aug; 144(2):276-280. PubMed ID: 27934809
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in WT1 in boys with sporadic isolated steroid-resistant nephrotic syndrome.
    Yang Y; Zhao F; Tu X; Yu Z
    Genet Mol Res; 2016 Mar; 15(1):15017559. PubMed ID: 26985958
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Expression in Xenopus oocytes shows that WT1 binds transcripts in vivo, with a central role for zinc finger one.
    Ladomery M; Sommerville J; Woolner S; Slight J; Hastie N
    J Cell Sci; 2003 Apr; 116(Pt 8):1539-49. PubMed ID: 12640038
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Clinical characteristics and WT1 genetic analysis of patients with steroid-resistant nephrotic syndrome accompanied with genitourinary malformations].
    Li JG; Zhao D; Ding J; Xiao HJ; Fan QF; Guan N; Chen Y; Zhang HW
    Zhonghua Er Ke Za Zhi; 2008 Sep; 46(9):692-7. PubMed ID: 19099861
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 25(10):2171-4. PubMed ID: 20419325
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.