BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

192 related articles for article (PubMed ID: 21559934)

  • 1. A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46,XY patient with Denys-Drash syndrome.
    da Silva TE; Nishi MY; Costa EM; Martin RM; Carvalho FM; Mendonca BB; Domenice S
    Pediatr Nephrol; 2011 Aug; 26(8):1311-5. PubMed ID: 21559934
    [TBL] [Abstract][Full Text] [Related]  

  • 2. WT1 Haploinsufficiency Supports Milder Renal Manifestation in Two Patients with Denys-Drash Syndrome.
    Guaragna MS; Ribeiro de Andrade JG; de Freitas Carli B; Belangero VM; Maciel-Guerra AT; Guerra-Júnior G; de Mello MP
    Sex Dev; 2017; 11(1):34-39. PubMed ID: 28081536
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Bilateral Wilms' tumor in a child with Denys-Drash syndrome: novel frameshift variant disrupts the WT1 nuclear location signaling region.
    Guaragna MS; Ledesma FL; Manzano VZ; Maciel-Guerra AT; Guerra-Júnior G; Silva MM; Luiz de Brito P; Palandi de Mello M
    J Pediatr Endocrinol Metab; 2022 Jun; 35(6):837-843. PubMed ID: 35304980
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel WT1 gene mutation in a newborn infant diagnosed with Denys-Drash syndrome.
    Hakan N; Aydin M; Erdogan O; Cavusoglu YH; Aycan Z; Ozaltin F; Zenciroglu A; Apaydin S; Gunes R; Sahin G; Cinar G; Okumus N
    Genet Couns; 2012; 23(2):255-61. PubMed ID: 22876585
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Case report: WT1 exon 6 truncation mutation and ambiguous genitalia in a patient with Denys-Drash syndrome.
    Chiang PW; Aliaga S; Travers S; Spector E; Tsai AC
    Curr Opin Pediatr; 2008 Feb; 20(1):103-6. PubMed ID: 18197048
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X.
    Heathcott RW; Morison IM; Gubler MC; Corbett R; Reeve AE
    Hum Mutat; 2002 Apr; 19(4):462. PubMed ID: 11933209
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel WT1 gene mutation in a chinese girl with denys-drash syndrome.
    Wang F; Cai J; Wang J; He M; Mao J; Zhu K; Zhao M; Guan Z; Li L; Jin H; Shu Q
    J Clin Lab Anal; 2021 May; 35(5):e23769. PubMed ID: 33942367
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Clinical and pathological features of Denys-Drash syndrome: report of 3 cases].
    Wang HY; Sun LZ; Yue ZH; Yang J; Jiang XY; Mo Y
    Zhonghua Er Ke Za Zhi; 2012 Nov; 50(11):855-8. PubMed ID: 23302619
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The novel WT1 gene mutation p.H377N associated to Denys-Drash syndrome.
    Guaragna MS; Soardi FC; Assumpção JG; Zambaldi Lde J; Cardinalli IA; Yunes JA; de Mello MP; Brandalise SR; Aguiar Sdos S
    J Pediatr Hematol Oncol; 2010 Aug; 32(6):486-8. PubMed ID: 20562648
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic analysis of two female patients with incomplete Denys-Drash syndrome.
    Ohta S; Ozawa T; Shiraga H; Fuse H
    Endocr J; 2000 Dec; 47(6):683-7. PubMed ID: 11228042
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel WT1 gene mutation in a patient with Wilms' tumor and 46, XY gonadal dysgenesis.
    Lee DG; Han DH; Park KH; Baek M
    Eur J Pediatr; 2011 Aug; 170(8):1079-82. PubMed ID: 21384108
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Focal Segmental Membranoproliferative Glomerulonephritis: A Histological Variant of Denys-Drash Syndrome.
    Karmila AB; Yap YC; Appadurai M; Oh L; Fazarina M; Abd Ghani F; Ariffin H
    Fetal Pediatr Pathol; 2021 Apr; 40(2):113-120. PubMed ID: 31707902
    [No Abstract]   [Full Text] [Related]  

  • 13. Clinical pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children.
    Yue Z; Pei Y; Sun L; Huang W; Huang H; Hu B; Yang J; Jiang X; Mo Y; Chen S; Lai KN; Wang Y
    Ren Fail; 2011; 33(9):910-4. PubMed ID: 21851196
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A familial WT1 mutation associated with incomplete Denys-Drash syndrome.
    Zhu C; Zhao F; Zhang W; Wu H; Chen Y; Ding G; Zhang A; Huang S
    Eur J Pediatr; 2013 Oct; 172(10):1357-62. PubMed ID: 23715653
    [TBL] [Abstract][Full Text] [Related]  

  • 15. New mutation in WT1 gene in a boy with an incomplete form of Denys-Drash syndrome: A CARE-compliant case report.
    Akramov NR; Shavaliev RF; Osipova IV
    Medicine (Baltimore); 2021 May; 100(19):e25864. PubMed ID: 34106634
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel WT1 mutation (C388Y) in a female child with Denys-Drash syndrome.
    Swiatecka-Urban A; Mokrzycki MH; Kaskel F; Da Silva F; Denamur E
    Pediatr Nephrol; 2001 Aug; 16(8):627-30. PubMed ID: 11519891
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Effects of Denys-Drash syndrome point mutations on the DNA binding activity of the Wilms' tumor suppressor protein WT1.
    Borel F; Barilla KC; Hamilton TB; Iskandar M; Romaniuk PJ
    Biochemistry; 1996 Sep; 35(37):12070-6. PubMed ID: 8810912
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A WT1 exon 1 mutation in a child diagnosed with Denys-Drash syndrome.
    Little S; Hanks S; King-Underwood L; Picton S; Cullinane C; Rapley E; Rahman N; Pritchard-Jones K
    Pediatr Nephrol; 2005 Jan; 20(1):81-5. PubMed ID: 15503171
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prophylactic bilateral nephrectomy and preemptive kidney transplantation for Denys-Drash syndrome prior to development of kidney failure.
    Hosokawa C; Hotta K; Okamoto T; Cho Y; Hirose T; Iwahara N; Manabe A; Shinohara N
    Pediatr Nephrol; 2024 Mar; 39(3):905-909. PubMed ID: 37572117
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.