BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

188 related articles for article (PubMed ID: 20683686)

  • 1. A novel WASP gene mutation in a Chinese boy with Wiskott-Aldrich syndrome.
    Yu H; Liu T; Meng W; Hou L
    Int J Hematol; 2010 Sep; 92(2):271-5. PubMed ID: 20683686
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Identification of two novel WASP gene mutations in 3 boys with Wiskott-Aldrich syndrome].
    Jiang LP; Xu YH; Yang XQ; Liu EM; Wang LJ; Lau YL; Chan KW
    Zhonghua Er Ke Za Zhi; 2003 Aug; 41(8):590-3. PubMed ID: 14744380
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The genotype of the original Wiskott phenotype.
    Binder V; Albert MH; Kabus M; Bertone M; Meindl A; Belohradsky BH
    N Engl J Med; 2006 Oct; 355(17):1790-3. PubMed ID: 17065640
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel WASP mutation in a patient with Wiskott-Aldrich syndrome: Case report and review of the literature.
    Eghbali M; Sadeghi-Shabestari M; Najmi Varzaneh F; Zare Bidoki A; Rezaei N
    Allergol Immunopathol (Madr); 2016; 44(5):450-4. PubMed ID: 26993433
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel mutation W252X in the WAS gene in a Korean patient with Wiskott-Aldrich syndrome.
    Kim HJ; Yoo EH; Ki CS; Yoo GH; Koo HH; Kim JW; Kim SH
    Int J Hematol; 2006 Jun; 83(5):426-8. PubMed ID: 16787874
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel termination codon mutation of the WAS gene in a Thai family with Wiskott-Aldrich syndrome.
    Chatchatee P; Srichomthong C; Chewatavorn A; Shotelersuk V
    Int J Mol Med; 2003 Dec; 12(6):939-41. PubMed ID: 14612970
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Two novel mutations identified in the Wiskott-Aldrich syndrome protein gene cause Wiskott-Aldrich syndrome and thrombocytopenia.
    Andreu N; Matamoros N; Escudero A; Fillat C
    Int J Mol Med; 2007 May; 19(5):777-82. PubMed ID: 17390083
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical aspects and genetic analysis of taiwanese patients with wiskott-Aldrich syndrome protein mutation: the first identification of x-linked thrombocytopenia in the chinese with novel mutations.
    Lee WI; Huang JL; Jaing TH; Wu KH; Chien YH; Chang KW
    J Clin Immunol; 2010 Jul; 30(4):593-601. PubMed ID: 20232122
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular characterization of two Malaysian patients with Wiskott-Aldrich syndrome.
    Baharin MF; Kader Ibrahim SB; Yap SH; Abdul Manaf AM; Mat Ripen A; Dhaliwal JS
    Malays J Pathol; 2015 Aug; 37(2):153-8. PubMed ID: 26277674
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A familial case of Wiskott-Aldrich Syndrome with a hotspot mutation in exon 2 of the WAS Gene.
    Park SK; Kim CS; Song DK; Kim JY; Choi IJ; Kim DK
    J Korean Med Sci; 2007 Dec; 22(6):998-1001. PubMed ID: 18162713
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A case of Wiskott-Aldrich syndrome with de novo mutation at exon 4.
    Doğu F; Ariga T; Ikincioğullari A; Bozdoğan G; Aytekin C; Metin A; Babacan E
    Turk J Pediatr; 2006; 48(1):66-8. PubMed ID: 16562789
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Wiskott-Aldrich syndrome in a girl caused by heterozygous WASP mutation and extremely skewed X-chromosome inactivation: a novel association with maternal uniparental isodisomy 6.
    Takimoto T; Takada H; Ishimura M; Kirino M; Hata K; Ohara O; Morio T; Hara T
    Neonatology; 2015; 107(3):185-90. PubMed ID: 25633059
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and molecular characteristics of Wiskott-Aldrich Syndrome in five unrelated Chinese families.
    Jiang J; Zhou J; Wei M; Singh S; Nikuze L; Huang L; Li Y; Jiang J; Wei H
    Scand J Immunol; 2022 Jan; 95(1):e13115. PubMed ID: 34758123
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of a novel WAS mutation in a South African patient presenting with atypical Wiskott-Aldrich syndrome: a case report.
    Glanzmann B; Möller M; Schoeman M; Urban M; van Helden PD; Frigati L; Grewal R; Pieters H; Loos B; Hoal EG; Glashoff RH; Cornelissen H; Rabie H; Esser MM; Kinnear CJ
    BMC Med Genet; 2020 Jun; 21(1):124. PubMed ID: 32503528
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and genetic analysis of 2 rare cases of Wiskott-Aldrich syndrome from Chinese minorities: Two case reports.
    Liu H; Wang Y; Li Y; Tao L; Zhang Y; He X; Zhou Y; Liu X; Wang Y; Li L
    Medicine (Baltimore); 2021 Apr; 100(16):e25527. PubMed ID: 33879693
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations of the WASP gene in 10 Japanese patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
    Itoh S; Nonoyama S; Morio T; Imai K; Okawa H; Ochs HD; Shimadzu M; Yata J
    Int J Hematol; 2000 Jan; 71(1):79-83. PubMed ID: 10729999
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel mutations in the Wiskott-Aldrich syndrome protein gene and their effects on transcriptional, translational, and clinical phenotypes.
    Lemahieu V; Gastier JM; Francke U
    Hum Mutat; 1999; 14(1):54-66. PubMed ID: 10447259
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of WASP mutations in 14 Spanish families with Wiskott-Aldrich syndrome.
    Fillat C; Español T; Oset M; Ferrando M; Estivill X; Volpini V
    Am J Med Genet; 2001 Apr; 100(2):116-21. PubMed ID: 11298372
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical aspects and molecular analysis of Chinese patients with Wiskott-Aldrich syndrome in Taiwan.
    Lee WI; Yang CY; Jaing TH; Huang JL; Chien YH; Chang KW
    Int Arch Allergy Immunol; 2008; 145(1):15-23. PubMed ID: 17703096
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Wiskott-Aldrich syndrome/X-linked thrombocytopenia in China: Clinical characteristic and genotype-phenotype correlation.
    Liu DW; Zhang ZY; Zhao Q; Jiang LP; Liu W; Tu WW; Song WX; Zhao XD
    Pediatr Blood Cancer; 2015 Sep; 62(9):1601-8. PubMed ID: 25931402
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.