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 TitleAuthors / EditorsDate
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Molecular genetics of the Bare lymphocyte syndrome Masternak, Krzysztof; Muhlethaler-Mottet, Annick; Villard, Jean; Peretti, M.; Reith, Walter 2000
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RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiency Durand, Bénédicte; Sperisen, P.; Emery, P.; Barras, Emmanuele; ... Reith, Walter 1997
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Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiency Villard, Jean; Reith, Walter; Barras, Emmanuele; Gos, A.; ... Mach, Bernard 1997
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Regulation of MHC class II genes: lessons from a disease Mach, Bernard; Steimle, Viktor; Martinez-Soria, Eduardo; Reith, Walter 1996
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Molecular defects in the bare lymphocyte syndrome and regulation of MHC class II genes Reith, Walter; Steimle, Viktor; Mach, Bernard 1995
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A novel DNA-binding regulatory factor is mutated in primary MHC class II deficiency (bare lymphocyte syndrome) Steimle, Viktor; Durand, Bénédicte; Barras, Emmanuele; Zufferey, Madeleine; ... Reith, Walter 1995
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MHC class II-deficient combined immunodeficiency: a disease of gene regulation Mach, Bernard; Steimle, Viktor; Reith, Walter 1994