BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

565 related articles for article (PubMed ID: 25931402)

  • 21. [WASP gene mutation analysis of a family of X-linked thrombocytopenia].
    Shi RM; Liu ZG; Yang YH
    Zhongguo Dang Dai Er Ke Za Zhi; 2010 Oct; 12(10):784-7. PubMed ID: 20959042
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Disruption of hSWI/SNF complexes in T cells by WAS mutations distinguishes X-linked thrombocytopenia from Wiskott-Aldrich syndrome.
    Sarkar K; Sadhukhan S; Han SS; Vyas YM
    Blood; 2014 Nov; 124(23):3409-19. PubMed ID: 25253772
    [TBL] [Abstract][Full Text] [Related]  

  • 23. WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
    Derry JM; Kerns JA; Weinberg KI; Ochs HD; Volpini V; Estivill X; Walker AP; Francke U
    Hum Mol Genet; 1995 Jul; 4(7):1127-35. PubMed ID: 8528199
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Hematopoietic Stem Cell Transplantation for X-Linked Thrombocytopenia With Mutations in the WAS gene.
    Oshima K; Imai K; Albert MH; Bittner TC; Strauss G; Filipovich AH; Morio T; Kapoor N; Dalal J; Schultz KR; Casper JT; Notarangelo LD; Ochs HD; Nonoyama S
    J Clin Immunol; 2015 Jan; 35(1):15-21. PubMed ID: 25388447
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Identification of WASP mutations, mutation hotspots and genotype-phenotype disparities in 24 patients with the Wiskott-Aldrich syndrome.
    Greer WL; Shehabeldin A; Schulman J; Junker A; Siminovitch KA
    Hum Genet; 1996 Dec; 98(6):685-90. PubMed ID: 8931701
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical, Laboratory Features and Clinical Courses of Patients with Wiskott Aldrich Syndrome and X-linked Thrombocytopenia-A single center study.
    Bildik HN; Cagdas D; Ozturk Kura A; Oskay Halacli S; Sanal O; Tezcan I
    Immunol Invest; 2022 Jul; 51(5):1272-1283. PubMed ID: 34098853
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The Wiskott-Aldrich syndrome.
    Ochs HD; Thrasher AJ
    J Allergy Clin Immunol; 2006 Apr; 117(4):725-38; quiz 739. PubMed ID: 16630926
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genetic characteristics of eighty-seven patients with the Wiskott-Aldrich syndrome.
    Gulácsy V; Freiberger T; Shcherbina A; Pac M; Chernyshova L; Avcin T; Kondratenko I; Kostyuchenko L; Prokofjeva T; Pasic S; Bernatowska E; Kutukculer N; Rascon J; Iagaru N; Mazza C; Tóth B; Erdos M; van der Burg M; Maródi L;
    Mol Immunol; 2011 Feb; 48(5):788-92. PubMed ID: 21185603
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [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]  

  • 30. Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndrome.
    Facchetti F; Blanzuoli L; Vermi W; Notarangelo LD; Giliani S; Fiorini M; Fasth A; Stewart DM; Nelson DL
    J Pathol; 1998 May; 185(1):99-107. PubMed ID: 9713366
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus.
    Kolluri R; Shehabeldin A; Peacocke M; Lamhonwah AM; Teichert-Kuliszewska K; Weissman SM; Siminovitch KA
    Hum Mol Genet; 1995 Jul; 4(7):1119-26. PubMed ID: 8528198
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Intermittent low platelet counts hampering diagnosis of X-linked thrombocytopenia in children: report of two unrelated cases and a novel mutation in the gene coding for the Wiskott-Aldrich syndrome protein.
    Medina SS; Siqueira LH; Colella MP; Yamaguti-Hayakawa GG; Duarte BKL; Dos Santos Vilela MM; Ozelo MC
    BMC Pediatr; 2017 Jun; 17(1):151. PubMed ID: 28641574
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutations of the same gene.
    Zhu Q; Zhang M; Blaese RM; Derry JM; Junker A; Francke U; Chen SH; Ochs HD
    Blood; 1995 Nov; 86(10):3797-804. PubMed ID: 7579347
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Report of clinical presentations and two novel mutations in patients with Wiskott-Aldrich syndrome/X-linked Thrombocytopenia.
    Udomkittivorakul N; Wattanasirichaigoon D; Manuyakorn W; Pongphitcha P; Khongkraparn A; Tunlayadechanont P; Sirachainan N
    Platelets; 2022 Jul; 33(5):792-796. PubMed ID: 34705590
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Wiskott-Aldrich syndrome protein and platelets.
    Oda A; Ochs HD
    Immunol Rev; 2000 Dec; 178():111-7. PubMed ID: 11213795
    [TBL] [Abstract][Full Text] [Related]  

  • 38. X-linked thrombocytopenia in a female with a complex familial pattern of X-chromosome inactivation.
    Daza-Cajigal V; Martínez-Pomar N; Garcia-Alonso A; Heine-Suñer D; Torres S; Vega AK; Molina IJ; Matamoros N
    Blood Cells Mol Dis; 2013 Aug; 51(2):125-9. PubMed ID: 23689198
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of a Novel Gene Mutation in a Chinese Pedigree with X-linked Thrombocytopenia.
    Zhang JW; Luo YX; Yang YL; Long B; Lu Y; Zhang XZ
    Clin Lab; 2018 Oct; 64(11):. PubMed ID: 30549999
    [TBL] [Abstract][Full Text] [Related]  

  • 40. New insights into the biology of Wiskott-Aldrich syndrome (WAS).
    Thrasher AJ
    Hematology Am Soc Hematol Educ Program; 2009; ():132-8. PubMed ID: 20008191
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 29.