| Title | Authors / Editors | Date |
unige:10941 |
MHC class II-deficient combined immunodeficiency: a disease of gene regulation |
Mach, Bernard; Steimle, Viktor; Reith, Walter |
1994 |
unige:11542 |
Molecular defects in the bare lymphocyte syndrome and regulation of MHC class II genes |
Reith, Walter; Steimle, Viktor; Mach, Bernard |
1995 |
unige:11592 |
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 |
unige:11437 |
Regulation of MHC class II genes: lessons from a disease |
Mach, Bernard; Steimle, Viktor; Martinez-Soria, Eduardo; Reith, Walter |
1996 |
unige:11231 |
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 |
unige:9076 |
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 |
unige:10942 |
Molecular genetics of the Bare lymphocyte syndrome |
Masternak, Krzysztof; Muhlethaler-Mottet, Annick; Villard, Jean; Peretti, M.; Reith, Walter |
2000 |