Gene therapy for human severe combined immunodeficiencies

被引:12
作者
Fischer, A [1 ]
Hacein-Bey, S [1 ]
Le Deist, F [1 ]
de Saint Basile, G [1 ]
Cavazzana-Calvo, M [1 ]
机构
[1] Hop Necker Enfants Malad, INSERM U429, F-75015 Paris, France
关键词
D O I
10.1016/S1074-7613(01)00175-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
[No abstract available]
引用
收藏
页码:1 / 4
页数:4
相关论文
共 25 条
  • [21] Thymic function after hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency.
    Patel, DD
    Gooding, ME
    Parrott, RE
    Curtis, KM
    Haynes, BF
    Buckley, RH
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (18) : 1325 - 1332
  • [22] ROBERTS JL, 1989, NEW ENGL J MED, V340, P508
  • [23] Issues in the manufacture and transplantation of genetically modified hematopoietic stem cells
    Sadelain, M
    Frassoni, F
    Rivière, I
    [J]. CURRENT OPINION IN HEMATOLOGY, 2000, 7 (06) : 364 - 377
  • [24] Stable and functional lymphoid reconstitution of common cytokine receptor γ chain deficient mice by retroviral-mediated gene transfer
    Soudais, C
    Shiho, T
    Sharara, LI
    Guy-Grand, D
    Taniguchi, T
    Fischer, A
    Di Santo, JP
    [J]. BLOOD, 2000, 95 (10) : 3071 - 3077
  • [25] Progress in the use of gene transfer methods to treat genetic blood diseases
    Williams, DA
    Smith, FO
    [J]. HUMAN GENE THERAPY, 2000, 11 (15) : 2059 - 2066