These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

215 related articles for article (PubMed ID: 16264326)

  • 41. 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]  

  • 42. 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]  

  • 43. Wiskott-Aldrich Syndrome: a model for defective actin reorganization, cell trafficking and synapse formation.
    Notarangelo LD; Ochs HD
    Curr Opin Immunol; 2003 Oct; 15(5):585-91. PubMed ID: 14499269
    [TBL] [Abstract][Full Text] [Related]  

  • 44. 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]  

  • 45. 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]  

  • 46. Wiskott-Aldrich Syndrome in four male siblings from a consanguineous family from Lebanon.
    Mansour R; El-Orfali Y; Saber A; Noun D; Youssef N; Youssef Y; Hanna-Wakim R; Dbaibo G; Abboud M; Massaad MJ
    Clin Immunol; 2020 Oct; 219():108573. PubMed ID: 32814211
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndrome.
    Aiuti A; Biasco L; Scaramuzza S; Ferrua F; Cicalese MP; Baricordi C; Dionisio F; Calabria A; Giannelli S; Castiello MC; Bosticardo M; Evangelio C; Assanelli A; Casiraghi M; Di Nunzio S; Callegaro L; Benati C; Rizzardi P; Pellin D; Di Serio C; Schmidt M; Von Kalle C; Gardner J; Mehta N; Neduva V; Dow DJ; Galy A; Miniero R; Finocchi A; Metin A; Banerjee PP; Orange JS; Galimberti S; Valsecchi MG; Biffi A; Montini E; Villa A; Ciceri F; Roncarolo MG; Naldini L
    Science; 2013 Aug; 341(6148):1233151. PubMed ID: 23845947
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Wiskott-Aldrich Syndrome causing mutation, Pro373Ser restricts conformational changes essential for WASP activity in T-cells.
    Jain N; George B; Thanabalu T
    Biochim Biophys Acta; 2014 Apr; 1842(4):623-34. PubMed ID: 24440360
    [TBL] [Abstract][Full Text] [Related]  

  • 49. 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]  

  • 50. Evolution of highly polymorphic T cell populations in siblings with the Wiskott-Aldrich Syndrome.
    Lutskiy MI; Park JY; Remold SK; Remold-O'Donnell E
    PLoS One; 2008; 3(10):e3444. PubMed ID: 18941616
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Lentiviral-mediated gene therapy leads to improvement of B-cell functionality in a murine model of Wiskott-Aldrich syndrome.
    Bosticardo M; Draghici E; Schena F; Sauer AV; Fontana E; Castiello MC; Catucci M; Locci M; Naldini L; Aiuti A; Roncarolo MG; Poliani PL; Traggiai E; Villa A
    J Allergy Clin Immunol; 2011 Jun; 127(6):1376-84.e5. PubMed ID: 21531013
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A partial down-regulation of WASP is sufficient to inhibit podosome formation in dendritic cells.
    Olivier A; Jeanson-Leh L; Bouma G; Compagno D; Blondeau J; Seye K; Charrier S; Burns S; Thrasher AJ; Danos O; Vainchenker W; Galy A
    Mol Ther; 2006 Apr; 13(4):729-37. PubMed ID: 16360341
    [TBL] [Abstract][Full Text] [Related]  

  • 53. 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]  

  • 54. Role of Wiskott Aldrich syndrome protein in haematological malignancies: genetics, molecular mechanisms and therapeutic strategies.
    R P; Shanmugam G; Rakshit S; Sarkar K
    Pathol Res Pract; 2024 Jan; 253():155026. PubMed ID: 38118219
    [TBL] [Abstract][Full Text] [Related]  

  • 55. The Wiskott-Aldrich syndrome protein (WASP): roles in signaling and cytoskeletal organization.
    Snapper SB; Rosen FS
    Annu Rev Immunol; 1999; 17():905-29. PubMed ID: 10358777
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Wiskott-Aldrich syndrome: a comprehensive review.
    Massaad MJ; Ramesh N; Geha RS
    Ann N Y Acad Sci; 2013 May; 1285():26-43. PubMed ID: 23527602
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. Revertant T lymphocytes in a patient with Wiskott-Aldrich syndrome: analysis of function and distribution in lymphoid organs.
    Trifari S; Scaramuzza S; Catucci M; Ponzoni M; Mollica L; Chiesa R; Cattaneo F; Lafouresse F; Calvez R; Vermi W; Medicina D; Castiello MC; Marangoni F; Bosticardo M; Doglioni C; Caniglia M; Aiuti A; Villa A; Roncarolo MG; Dupré L
    J Allergy Clin Immunol; 2010 Feb; 125(2):439-448.e8. PubMed ID: 20159256
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Use of zinc-finger nucleases to knock out the WAS gene in K562 cells: a human cellular model for Wiskott-Aldrich syndrome.
    Toscano MG; Anderson P; Muñoz P; Lucena G; Cobo M; Benabdellah K; Gregory PD; Holmes MC; Martin F
    Dis Model Mech; 2013 Mar; 6(2):544-54. PubMed ID: 23324327
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Clinical course of patients with WASP gene mutations.
    Imai K; Morio T; Zhu Y; Jin Y; Itoh S; Kajiwara M; Yata J; Mizutani S; Ochs HD; Nonoyama S
    Blood; 2004 Jan; 103(2):456-64. PubMed ID: 12969986
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.