BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

204 related articles for article (PubMed ID: 16544979)

  • 41. Lentiviral vectors for the treatment of Wiskott-Aldrich syndrome.
    Nienhuis AW
    Gene Ther; 2005 Apr; 12(7):555-6. PubMed ID: 18360950
    [No Abstract]   [Full Text] [Related]  

  • 42. Ten years of gene therapy for primary immune deficiencies.
    Aiuti A; Roncarolo MG
    Hematology Am Soc Hematol Educ Program; 2009; ():682-9. PubMed ID: 20008254
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Gene therapy for Wiskott-Aldrich Syndrome.
    Bosticardo M; Ferrua F; Cavazzana M; Aiuti A
    Curr Gene Ther; 2014; 14(6):413-21. PubMed ID: 25245089
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Improvement of migratory defects in a murine model of Wiskott-Aldrich syndrome gene therapy.
    Blundell MP; Bouma G; Calle Y; Jones GE; Kinnon C; Thrasher AJ
    Mol Ther; 2008 May; 16(5):836-44. PubMed ID: 18388921
    [TBL] [Abstract][Full Text] [Related]  

  • 45. The genotype of the original Wiskott phenotype.
    Binder V; Albert MH; Kabus M; Bertone M; Meindl A; Belohradsky BH
    N Engl J Med; 2006 Oct; 355(17):1790-3. PubMed ID: 17065640
    [TBL] [Abstract][Full Text] [Related]  

  • 46. 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]  

  • 47. 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]  

  • 48. Stem-cell gene therapy for the Wiskott-Aldrich syndrome.
    Boztug K; Schmidt M; Schwarzer A; Banerjee PP; Díez IA; Dewey RA; Böhm M; Nowrouzi A; Ball CR; Glimm H; Naundorf S; Kühlcke K; Blasczyk R; Kondratenko I; Maródi L; Orange JS; von Kalle C; Klein C
    N Engl J Med; 2010 Nov; 363(20):1918-27. PubMed ID: 21067383
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Retroviral WASP gene transfer into human hematopoietic stem cells reconstitutes the actin cytoskeleton in myeloid progeny cells differentiated in vitro.
    Dewey RA; Avedillo Díez I; Ballmaier M; Filipovich A; Greil J; Güngör T; Happel C; Maschan A; Noyan F; Pannicke U; Schwarz K; Snapper S; Welte K; Klein C
    Exp Hematol; 2006 Sep; 34(9):1161-9. PubMed ID: 16939809
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Antigen receptor-induced activation and cytoskeletal rearrangement are impaired in Wiskott-Aldrich syndrome protein-deficient lymphocytes.
    Zhang J; Shehabeldin A; da Cruz LA; Butler J; Somani AK; McGavin M; Kozieradzki I; dos Santos AO; Nagy A; Grinstein S; Penninger JM; Siminovitch KA
    J Exp Med; 1999 Nov; 190(9):1329-42. PubMed ID: 10544204
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Genome editing for primary immunodeficiencies: A therapeutic perspective on Wiskott-Aldrich syndrome.
    Naseem A; Steinberg Z; Cavazza A
    Front Immunol; 2022; 13():966084. PubMed ID: 36059471
    [TBL] [Abstract][Full Text] [Related]  

  • 52. WASP (Wiskott-Aldrich syndrome protein) gene mutations and phenotype.
    Imai K; Nonoyama S; Ochs HD
    Curr Opin Allergy Clin Immunol; 2003 Dec; 3(6):427-36. PubMed ID: 14612666
    [TBL] [Abstract][Full Text] [Related]  

  • 53. WASP-WIP complex in the molecular pathogenesis of Wiskott-Aldrich syndrome.
    Sasahara Y
    Pediatr Int; 2016 Jan; 58(1):4-7. PubMed ID: 26331277
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Stable and functional lymphoid reconstitution in artemis-deficient mice following lentiviral artemis gene transfer into hematopoietic stem cells.
    Benjelloun F; Garrigue A; Demerens-de Chappedelaine C; Soulas-Sprauel P; Malassis-Séris M; Stockholm D; Hauer J; Blondeau J; Rivière J; Lim A; Le Lorc'h M; Romana S; Brousse N; Pâques F; Galy A; Charneau P; Fischer A; de Villartay JP; Cavazzana-Calvo M
    Mol Ther; 2008 Aug; 16(8):1490-9. PubMed ID: 18560421
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Wiskott-Aldrich syndrome.
    Notarangelo LD; Miao CH; Ochs HD
    Curr Opin Hematol; 2008 Jan; 15(1):30-6. PubMed ID: 18043243
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Clinical aspects and molecular analysis of Chinese patients with Wiskott-Aldrich syndrome in Taiwan.
    Lee WI; Yang CY; Jaing TH; Huang JL; Chien YH; Chang KW
    Int Arch Allergy Immunol; 2008; 145(1):15-23. PubMed ID: 17703096
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Clinical Manifestations and Pathophysiological Mechanisms of the Wiskott-Aldrich Syndrome.
    Candotti F
    J Clin Immunol; 2018 Jan; 38(1):13-27. PubMed ID: 29086100
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Diverse genomic integration of a lentiviral vector developed for the treatment of Wiskott-Aldrich syndrome.
    Mantovani J; Charrier S; Eckenberg R; Saurin W; Danos O; Perea J; Galy A
    J Gene Med; 2009 Aug; 11(8):645-54. PubMed ID: 19455589
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Gene therapy for Wiskott-Aldrich syndrome: History, new vectors, future directions.
    Ferrua F; Marangoni F; Aiuti A; Roncarolo MG
    J Allergy Clin Immunol; 2020 Aug; 146(2):262-265. PubMed ID: 32623069
    [No Abstract]   [Full Text] [Related]  

  • 60. Phenotypic and genotypic correction of WASP gene mutation in Wiskott-Aldrich syndrome by unrelated cord blood stem cell transplantation.
    Lee YH; Lim YJ; Shin SA; Song CH; Jo EK; Jung JA; Lee HB
    J Korean Med Sci; 2009 Aug; 24(4):751-4. PubMed ID: 19654965
    [TBL] [Abstract][Full Text] [Related]  

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