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PRIMARY T-CELL IMMUNODEFICIENCIES

被引：23
作者：
FISCHER, A
机构：
[1] INSERM U 132, Hôpital des Enfants-Malades, Paris
来源：
CURRENT OPINION IN IMMUNOLOGY | 1993年 / 5卷 / 04期
关键词：
D O I：
10.1016/0952-7915(93)90040-Y
中图分类号：
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号：
100102 ;
摘要：
The phenotypes of many primary T-cell immunodeficiencies have been described, including diseases associated with defective T-cell differentiation and/or activation. Recently, genotypes have been defined for some of them, such as X-linked severe combined immunodeficiency and CD3 deficiencies (or hyper IgM syndrome). Phenotype/genotype correlation studies open a fruitful way to a better understanding of primary T-cell immunodeficiencies.
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页码：569 / 578
页数：10
相关论文
共 91 条
  • [1] ABBPLEBY MW, 1992, CELL, V70, P751
  • [2] SEQUENCE REQUIREMENTS FOR SPLICING OF HIGHER EUKARYOTIC NUCLEAR PRE-MESSENGER-RNA
    AEBI, M
    HORNIG, H
    PADGETT, RA
    REISER, J
    WEISSMANN, C
    [J]. CELL, 1986, 47 (04) : 555 - 565
  • [3] CD40 LIGAND GENE DEFECTS RESPONSIBLE FOR X-LINKED HYPER-IGM SYNDROME
    ALLEN, RC
    ARMITAGE, RJ
    CONLEY, ME
    ROSENBLATT, H
    JENKINS, NA
    COPELAND, NG
    BEDELL, MA
    EDELHOFF, S
    DISTECHE, CM
    SIMONEAUX, DK
    FANSLOW, WC
    BELMONT, J
    SPRIGGS, MK
    [J]. SCIENCE, 1993, 259 (5097) : 990 - 993
  • [4] PRIMARY IMMUNODEFICIENCY CAUSED BY MUTATIONS IN THE GENE ENCODING THE CD3-GAMMA SUBUNIT OF THE LYMPHOCYTE-T RECEPTOR
    ARNAIZVILLENA, A
    TIMON, M
    CORELL, A
    PEREZACIEGO, P
    MARTINVILLA, JM
    REGUEIRO, JR
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (08) : 529 - 533
  • [5] THE CD40 LIGAND, GP39, IS DEFECTIVE IN ACTIVATED T-CELLS FROM PATIENTS WITH X-LINKED HYPER-IGM SYNDROME
    ARUFFO, A
    FARRINGTON, M
    HOLLENBAUGH, D
    LI, X
    MILATOVICH, A
    NONOYAMA, S
    BAJORATH, J
    GROSMAIRE, LS
    STENKAMP, R
    NEUBAUER, M
    ROBERTS, RL
    NOELLE, RJ
    LEDBETTER, JA
    FRANCKE, U
    OCHS, HD
    [J]. CELL, 1993, 72 (02) : 291 - 300
  • [6] AUST MR, 1992, AM J HUM GENET, V51, P763
  • [7] MUTATIONS IN THE DNA LIGASE-I GENE OF AN INDIVIDUAL WITH IMMUNODEFICIENCIES AND CELLULAR-HYPERSENSITIVITY TO DNA-DAMAGING AGENTS
    BARNES, DE
    TOMKINSON, AE
    LEHMANN, AR
    WEBSTER, ADB
    LINDAHL, T
    [J]. CELL, 1992, 69 (03) : 495 - 503
  • [8] CLASS-II-ANTIGEN-NEGATIVE PATIENT AND MUTANT B-CELL LINES REPRESENT AT LEAST 3, AND PROBABLY 4, DISTINCT GENETIC-DEFECTS DEFINED BY COMPLEMENTATION ANALYSIS
    BENICHOU, B
    STROMINGER, JL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (10) : 4285 - 4288
  • [9] BLAESE RM, 1993, PEDIATR RES, V33, P549
  • [10] Bosma M J, 1992, Immunodefic Rev, V3, P261
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