BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 26277674)

  • 1. 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]  

  • 2. Identification of five novel WASP mutations in Chinese families with Wiskott-Aldrich syndrome.
    Chan KW; Lee TL; Chung BH; Yang X; Lau YL
    Hum Mutat; 2002 Aug; 20(2):151-2. PubMed ID: 12124997
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 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. [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]  

  • 6. [Mutation analysis of WASP gene and prenatal diagnosis of Wiskott-Aldrich syndrome].
    Liu N; Shi H; Kong X; Wu Q; Xu X; Bai Q; Feng Y; Zhao Z
    Zhonghua Er Ke Za Zhi; 2014 Sep; 52(9):662-6. PubMed ID: 25476427
    [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. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Detection of six novel mutations in WASP gene in fifteen Iranian Wiskott-Aldrich patients.
    Safaei S; Fazlollahi MR; Houshmand M; Hamidieh AA; Bemanian MH; Alavi S; Mousavi F; Pourpak Z; Moin M
    Iran J Allergy Asthma Immunol; 2012 Dec; 11(4):345-8. PubMed ID: 23264413
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Analysis of clinical and molecular characteristics of Wiskott-Aldrich syndrome in 24 patients from 23 unrelated Chinese families.
    Zhang ZY; Xiao HQ; Jiang LP; Zhou Y; Zhao Q; Yu J; Liu W; Yang XQ; Zhao XD
    Pediatr Allergy Immunol; 2010 May; 21(3):522-32. PubMed ID: 20546529
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 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. Multiple independent second-site mutations in two siblings with somatic mosaicism for Wiskott-Aldrich syndrome.
    Boztug K; Germeshausen M; Avedillo Díez I; Gulacsy V; Diestelhorst J; Ballmaier M; Welte K; Maródi L; Chernyshova L; Klein C
    Clin Genet; 2008 Jul; 74(1):68-74. PubMed ID: 18479478
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Clinical and molecular characterization of Thai patients with Wiskott-Aldrich syndrome.
    Amarinthnukrowh P; Ittiporn S; Tongkobpetch S; Chatchatee P; Sosothikul D; Shotelersuk V; Suphapeetiporn K
    Scand J Immunol; 2013 Jan; 77(1):69-74. PubMed ID: 23033889
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.