BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 10733494)

  • 1. Mapping of a syndrome of X-linked thrombocytopenia with Thalassemia to band Xp11-12: further evidence of genetic heterogeneity of X-linked thrombocytopenia.
    Raskind WH; Niakan KK; Wolff J; Matsushita M; Vaughan T; Stamatoyannopoulos G; Watanabe C; Rios J; Ochs HD
    Blood; 2000 Apr; 95(7):2262-8. PubMed ID: 10733494
    [TBL] [Abstract][Full Text] [Related]  

  • 2. X-linked thrombocytopenia and Wiskott-Aldrich syndrome: similar regional assignment but distinct X-inactivation pattern in carriers.
    De Saint-Basile G; Schlegel N; Caniglia M; Le Deist F; Kaplan C; Lecompte T; Piller F; Fischer A; Griscelli C
    Ann Hematol; 1991 Aug; 63(2):107-10. PubMed ID: 1912030
    [TBL] [Abstract][Full Text] [Related]  

  • 3. X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP gene.
    Villa A; Notarangelo L; Macchi P; Mantuano E; Cavagni G; Brugnoni D; Strina D; Patrosso MC; Ramenghi U; Sacco MG
    Nat Genet; 1995 Apr; 9(4):414-7. PubMed ID: 7795648
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Platelet proteome and function in X-linked thrombocytopenia with thalassemia and
    Bergemalm D; Ramström S; Kardeby C; Hultenby K; Eremo AG; Sihlbom C; Bergström J; Palmblad J; Åström M
    Haematologica; 2021 Nov; 106(11):2947-2959. PubMed ID: 33054111
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Isolated X-linked thrombocytopenia in two unrelated families is associated with point mutations in the Wiskott-Aldrich syndrome protein gene.
    de Saint Basile G; Lagelouse RD; Lambert N; Schwarz K; Le Mareck B; Odent S; Schlegel N; Fischer A
    J Pediatr; 1996 Jul; 129(1):56-62. PubMed ID: 8757563
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Wiskott-Aldrich syndrome in a female with skewed X-chromosome inactivation.
    Andreu N; Pujol-Moix N; Martinez-Lostao L; Oset M; Muñiz-Diaz E; Estivill X; Volpini V; Fillat C
    Blood Cells Mol Dis; 2003; 31(3):332-7. PubMed ID: 14636648
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. X-linked thrombocytopenia with thalassemia displays bone marrow reticulin fibrosis and enhanced angiogenesis: comparisons with primary myelofibrosis.
    Åström M; Hahn-Strömberg V; Zetterberg E; Vedin I; Merup M; Palmblad J
    Am J Hematol; 2015 Mar; 90(3):E44-8. PubMed ID: 25421114
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. X-linked gray platelet syndrome due to a GATA1 Arg216Gln mutation.
    Tubman VN; Levine JE; Campagna DR; Monahan-Earley R; Dvorak AM; Neufeld EJ; Fleming MD
    Blood; 2007 Apr; 109(8):3297-9. PubMed ID: 17209061
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of X-chromosome inactivation and presumptive expression of the Wiskott-Aldrich syndrome (WAS) gene in hematopoietic cell lineages of a thrombocytopenic carrier female of WAS.
    Notarangelo LD; Parolini O; Porta F; Locatelli F; Lanfranchi A; Marconi M; Nespoli L; Albertini A; Craig IW; Ugazio AG
    Hum Genet; 1991 Dec; 88(2):237-41. PubMed ID: 1684569
    [TBL] [Abstract][Full Text] [Related]  

  • 15. X-linked thrombocytopenia in a girl.
    Inoue H; Kurosawa H; Nonoyama S; Imai K; Kumazaki H; Matsunaga T; Sato Y; Sugita K; Eguchi M
    Br J Haematol; 2002 Sep; 118(4):1163-5. PubMed ID: 12199801
    [TBL] [Abstract][Full Text] [Related]  

  • 16. IVS6+5G>A found in Wiskott-Aldrich syndrome and X-linked thrombocytopenia in a Korean family.
    Yoon SH; Cho T; Kim HJ; Kim SY; Ko JH; Baek HS; Lee HJ; Lee CH
    Pediatr Blood Cancer; 2012 Feb; 58(2):297-9. PubMed ID: 22038941
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Missense mutations of the WASP gene cause intermittent X-linked thrombocytopenia.
    Notarangelo LD; Mazza C; Giliani S; D'Aria C; Gandellini F; Ravelli C; Locatelli MG; Nelson DL; Ochs HD; Notarangelo LD
    Blood; 2002 Mar; 99(6):2268-9. PubMed ID: 11877312
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Missense C168T in the Wiskott--Aldrich Syndrome protein gene is a common mutation in X-linked thrombocytopenia.
    Ho LL; Ayling J; Prosser I; Kronenberg H; Iland H; Joshua D
    Br J Haematol; 2001 Jan; 112(1):76-80. PubMed ID: 11167787
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The Wiskott-Aldrich syndrome.
    Peacocke M; Siminovitch KA
    Semin Dermatol; 1993 Sep; 12(3):247-54. PubMed ID: 8105860
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.