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Journal Abstract Search

300 related items for PubMed ID: 11213795

  • 21. 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 15; 104(13):4010-9. PubMed ID: 15284122
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  • 23. Wiskott-Aldrich syndrome in a female.
    Lutskiy MI, Sasahara Y, Kenney DM, Rosen FS, Remold-O'Donnell E.
    Blood; 2002 Oct 15; 100(8):2763-8. PubMed ID: 12351383
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  • 26. Absence of expression of the Wiskott-Aldrich syndrome protein in peripheral blood cells of Wiskott-Aldrich syndrome patients.
    MacCarthy-Morrogh L, Gaspar HB, Wang YC, Katz F, Thompson L, Layton M, Jones AM, Kinnon C.
    Clin Immunol Immunopathol; 1998 Jul 15; 88(1):22-7. PubMed ID: 9683546
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  • 27. 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 Jul 15; 14(1):54-66. PubMed ID: 10447259
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  • 28. 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 Jul 15; 31(3):332-7. PubMed ID: 14636648
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  • 29. 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 04; 33(5):792-796. PubMed ID: 34705590
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  • 30. Wiskott-Aldrich syndrome.
    Notarangelo LD, Miao CH, Ochs HD.
    Curr Opin Hematol; 2008 Jan 04; 15(1):30-6. PubMed ID: 18043243
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  • 32. 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 04; 185(1):99-107. PubMed ID: 9713366
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  • 33. Protein assays for diagnosis of Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
    Qasim W, Gilmour KC, Heath S, Ashton E, Cranston T, Thomas A, Finn A, Davies EG, Thrasher AJ, Kinnon C, Jones A, Gaspar HB.
    Br J Haematol; 2001 Jun 04; 113(4):861-5. PubMed ID: 11442475
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  • 35. 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 04; 58(2):297-9. PubMed ID: 22038941
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  • 37. The Wiskott-Aldrich syndrome.
    Orange JS, Stone KD, Turvey SE, Krzewski K.
    Cell Mol Life Sci; 2004 Sep 04; 61(18):2361-85. PubMed ID: 15378206
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  • 38. Wiskott-Aldrich syndrome iPS cells produce megakaryocytes with defects in cytoskeletal rearrangement and proplatelet formation.
    Ingrungruanglert P, Amarinthnukrowh P, Rungsiwiwut R, Maneesri-le Grand S, Sosothikul D, Suphapeetiporn K, Israsena N, Shotelersuk V.
    Thromb Haemost; 2015 Apr 04; 113(4):792-805. PubMed ID: 25518736
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  • 39. 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 04; 11(4):345-8. PubMed ID: 23264413
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