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Volumn 19, Issue 3, 2004, Pages 154-158

Cellular and gene therapy for major histocompatibility complex class II deficiency

Author keywords

[No Author keywords available]

Indexed keywords

MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 2; HLA ANTIGEN CLASS 2;

EID: 3042721509     PISSN: 08861714     EISSN: None     Source Type: Journal    
DOI: 10.1152/nips.01462.2003     Document Type: Review
Times cited : (17)

References (18)
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  • 4
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    • RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiency
    • Durand B, Sperisen P, Emery P, Barras E, Zufferey M, Mach B, and Reith W. RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiency. EMBO J 16: 1045-1055, 1997.
    • (1997) EMBO J , vol.16 , pp. 1045-1055
    • Durand, B.1    Sperisen, P.2    Emery, P.3    Barras, E.4    Zufferey, M.5    Mach, B.6    Reith, W.7
  • 5
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    • Primary immunodeficiency diseases: An experimental model for molecular medicine
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    • Fischer, A.1
  • 10
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    • Expression of the three human major histocompatibility complex class II isotypes exhibits a differential dependence on the transcription factor RFXAP
    • Peretti M, Villard J, Barras E, Zufferey M, and Reith W. Expression of the three human major histocompatibility complex class II isotypes exhibits a differential dependence on the transcription factor RFXAP. Mol Cell Biol 21: 5699-5709, 2001.
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    • The bare lymphocyte syndrome and the regulation of MHC expression
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    • Reith, W.1    Mach, B.2
  • 12
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    • High-level transgene expression in human hematopoietic progenitors and differentiated blood lineages after transduction with improved lentiviral vectors
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    • Salmon, P.1    Kindler, V.2    Ducrey, O.3    Chapuis, B.4    Zubler, R.H.5    Trono, D.6
  • 13
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    • A novel DNA binding regulatory factor is mutated in primary MHC class II deficiency (bare lymphocyte syndrome)
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  • 14
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    • Complementation cloning of an MHC class II transactivator mutated in hereditary MHC class II deficiency (or bare lymphocyte syndrome)
    • Steimle V, Otten LA, Zufferey M, and Mach B. Complementation cloning of an MHC class II transactivator mutated in hereditary MHC class II deficiency (or bare lymphocyte syndrome). Cell 75: 135-146, 1993.
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  • 18
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    • A functionally essential domain of RFX5 mediates activation of major histocompatibility complex class II promoters by promoting cooperative binding between RFX and NF-Y
    • Villard J, Peretti M, Masternak K, Barras E, Caretti G, Mantovani R, and Reith W. A functionally essential domain of RFX5 mediates activation of major histocompatibility complex class II promoters by promoting cooperative binding between RFX and NF-Y. Mol Cell Biol 20: 3364-3376, 2001.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.