BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 12367583)

  • 1. A novel protocol to identify mutations in patients with wiskott-Aldrich syndrome.
    Jones LN; Lutskiy MI; Cooley J; Kenney DM; Rosen FS; Remold-O'Donnell E
    Blood Cells Mol Dis; 2002; 28(3):392-8. PubMed ID: 12367583
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Wiskott-Aldrich syndrome/X-linked thrombocytopenia: WASP gene mutations, protein expression, and phenotype.
    Zhu Q; Watanabe C; Liu T; Hollenbaugh D; Blaese RM; Kanner SB; Aruffo A; Ochs HD
    Blood; 1997 Oct; 90(7):2680-9. PubMed ID: 9326235
    [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. 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]  

  • 10. Identification of WASP mutations in 10 Australian families with Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
    Bourne HC; Weston S; Prasad M; Edkins E; Benson EM
    Pathology; 2004 Jun; 36(3):262-4. PubMed ID: 15203732
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR.
    Proust A; Guillet B; Picard C; de Saint Basile G; Pondarré C; Tamary H; Dreyfus M; Tchernia G; Fischer A; Delaunay J
    Blood Cells Mol Dis; 2007; 39(1):102-6. PubMed ID: 17400488
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations of the Wiskott-Aldrich Syndrome Protein (WASP): hotspots, effect on transcription, and translation and phenotype/genotype correlation.
    Jin Y; Mazza C; Christie JR; Giliani S; Fiorini M; Mella P; Gandellini F; Stewart DM; Zhu Q; Nelson DL; Notarangelo LD; Ochs HD
    Blood; 2004 Dec; 104(13):4010-9. PubMed ID: 15284122
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Identification of six novel WASP gene mutations in patients suffering from Wiskott-Aldrich syndrome.
    Brooimans RA; van den Berg AJ; Tamminga RY; Revesz T; Wulffraat NM; Zegers BJ
    Hum Mutat; 2000 Apr; 15(4):386-7. PubMed ID: 10737997
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Wiskott-Aldrich syndrome: no strict genotype-phenotype correlations but clustering of missense mutations in the amino-terminal part of the WASP gene product.
    Schindelhauer D; Weiss M; Hellebrand H; Golla A; Hergersberg M; Seger R; Belohradsky BH; Meindl A
    Hum Genet; 1996 Jul; 98(1):68-76. PubMed ID: 8682510
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Detection of a novel splice-site mutation that results in skipping exon 3 of the WASP gene in a patient with Wiskott-Aldrich syndrome.
    Ariga T; Yamada M; Pudua FR; Sakiyama Y
    Biochim Biophys Acta; 1996 Dec; 1317(3):158-60. PubMed ID: 8988230
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Wiskott-Aldrich syndrome in Argentina: 17 unique, including nine novel, mutations.
    El-Hakeh J; Rosenzweig S; Oleastro M; Basack N; Berozdnik L; Molina F; Rivas EM; Zelazko M; Danielian S
    Hum Mutat; 2002 Feb; 19(2):186-7. PubMed ID: 11793485
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.