The bare lymphocyte syndrome: molecular clues to the transcriptional regulation of major histocompatibility complex class II genes.
暂无分享,去创建一个
[1] S. Westerheide,et al. Orientation and positional mapping of the subunits of the multicomponent transcription factors RFX and X2BP to the major histocompatibility complex class II transcriptional enhancer. , 1999, Nucleic acids research.
[2] P. J. van den Elsen,et al. Molecular analysis of an MHC class II deficiency patient reveals a novel mutation in the RFX5 gene , 1999, Immunogenetics.
[3] J. M. Boss,et al. RFX-B is the gene responsible for the most common cause of the bare lymphocyte syndrome, an MHC class II immunodeficiency. , 1999, Immunity.
[4] J. M. Boss,et al. CREB regulates MHC class II expression in a CIITA-dependent manner. , 1999, Immunity.
[5] J. Ting,et al. A defect in the nuclear translocation of CIITA causes a form of type II bare lymphocyte syndrome. , 1999, Immunity.
[6] B. Peterlin,et al. Interactions between the Class II Transactivator and CREB Binding Protein Increase Transcription of Major Histocompatibility Complex Class II Genes , 1999, Molecular and Cellular Biology.
[7] C. Benoist,et al. Mice lacking the transcription factor CIITA--a second look. , 1998, International immunology.
[8] R. Aebersold,et al. A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients , 1998, Nature Genetics.
[9] M. Merika,et al. Involvement of CREB Binding Protein in Expression of Major Histocompatibility Complex Class II Genes via Interaction with the Class II Transactivator , 1998, Molecular and Cellular Biology.
[10] P. J. van den Elsen,et al. The RFX complex is crucial for the constitutive and CIITA-mediated transactivation of MHC class I and beta2-microglobulin genes. , 1998, Immunity.
[11] P. J. van den Elsen,et al. Regulation of MHC class I and II gene transcription: differences and similarities , 1998, Immunogenetics.
[12] G. Stark,et al. CIITA stimulation of transcription factor binding to major histocompatibility complex class II and associated promoters in vivo. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[13] W. Reith,et al. Genetic and molecular definition of complementation group D in MHC class II deficiency. , 1998, Human molecular genetics.
[14] K. Rajewsky,et al. Residual MHC class II expression on mature dendritic cells and activated B cells in RFX5-deficient mice. , 1998, Immunity.
[15] C. S. Moreno,et al. Formation of a regulatory factor X/X2 box-binding protein/nuclear factor-Y multiprotein complex on the conserved regulatory regions of HLA class II genes. , 1997, Journal of immunology.
[16] W. Reith,et al. Mutation of RFXAP, a regulator of MHC class II genes, in primary MHC class II deficiency. , 1997, The New England journal of medicine.
[17] J. M. Boss,et al. Regulatory factor X, a bare lymphocyte syndrome transcription factor, is a multimeric phosphoprotein complex. , 1997, Journal of immunology.
[18] S. Westerheide,et al. HLA-DMA and HLA-DMB gene expression functions through the conserved S-X-Y region. , 1997, Journal of immunology.
[19] A. Peijnenburg,et al. Site α Is Crucial for Two Routes of IFNγ-Induced MHC Class I Transactivation: The ISRE-Mediated Route and a Novel Pathway Involving CIITA , 1997 .
[20] K. Ozato,et al. Induction of MHC class I expression by the MHC class II transactivator CIITA. , 1997, Immunity.
[21] C. Ucla,et al. Two novel mutations in the MHC class II transactivator CIITA in a second patient from MHC class II deficiency complementation group A , 1997, Human Genetics.
[22] P. Emery,et al. RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiency , 1997, The EMBO journal.
[23] R. Ransohoff,et al. TGF-beta suppresses IFN-gamma induction of class II MHC gene expression by inhibiting class II transactivator messenger RNA expression. , 1997, Journal of immunology.
[24] J. Boss. Regulation of transcription of MHC class II genes. , 1997, Current opinion in immunology.
[25] S. Antonarakis,et al. Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiency , 1997, Human mutation.
[26] R. Elhasid,et al. Major histocompatibility complex class II deficiency: a clinical review. , 1996, Blood reviews.
[27] Andrew J. Bannister,et al. The CBP co-activator is a histone acetyltransferase , 1996, Nature.
[28] J. M. Boss,et al. Complex architecture of major histocompatibility complex class II promoters: reiterated motifs and conserved protein-protein interactions , 1996, Molecular and cellular biology.
[29] R. Flavell,et al. Mice lacking the MHC class II transactivator (CIITA) show tissue-specific impairment of MHC class II expression. , 1996, Immunity.
[30] P. Cresswell,et al. HLA-DM induces clip dissociation from MHC class II αβ dimers and facilitates peptide loading , 1995, Cell.
[31] B. Durand,et al. A novel DNA-binding regulatory factor is mutated in primary MHC class II deficiency (bare lymphocyte syndrome). , 1995, Genes & development.
[32] S. Westerheide,et al. Activation of class II MHC genes requires both the X box region and the class II transactivator (CIITA). , 1995, Immunity.
[33] L. Glimcher,et al. Human MHC class II gene transcription directed by the carboxyl terminus of CIITA, one of the defective genes in type II MHC combined immune deficiency. , 1995, Immunity.
[34] S. Maity,et al. Recombinant rat CBF-C, the third subunit of CBF/NFY, allows formation of a protein-DNA complex with CBF-A and CBF-B and with yeast HAP2 and HAP3. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[35] G. Stark,et al. Molecular analysis of G1B and G3A IFN gamma mutants reveals that defects in CIITA or RFX result in defective class II MHC and Ii gene induction. , 1994, Immunity.
[36] R. Flavell,et al. Class II transactivator (CIITA) is sufficient for the inducible expression of major histocompatibility complex class II genes , 1994, The Journal of experimental medicine.
[37] B. Mach,et al. Regulation of MHC class II expression by interferon-gamma mediated by the transactivator gene CIITA. , 1994, Science.
[38] Eric O Long,et al. Two processing pathways for the MHC class II-restricted presentation of exogenous influenza virus antigen. , 1994, Journal of immunology.
[39] A. Fischer,et al. Major histocompatibility complex class II deficiency: clinical manifestations, immunologic features, and outcome. , 1993, The Journal of pediatrics.
[40] B. Mach,et al. Complementation cloning of an MHC class II transactivator mutated in hereditary MHC class II deficiency (or bare lymphocyte syndrome) , 1993, Cell.
[41] L. Glimcher,et al. Developmental and cytokine-mediated regulation of MHC class II gene promoter occupancy in vivo. , 1993, Journal of immunology.
[42] J. Riley,et al. Protease treatment of nuclear extracts distinguishes between class II MHC X1 box DNA-binding proteins in wild-type and class II-deficient B cells. , 1993, Journal of immunology.
[43] R. Flavell,et al. Reactivation of a major histocompatibility complex class II gene in mouse plasmacytoma cells and mouse T cells , 1992, The Journal of experimental medicine.
[44] W. Reith,et al. The DNA-binding defect observed in major histocompatibility complex class II regulatory mutants concerns only one member of a family of complexes binding to the X boxes of class II promoters , 1992, Molecular and cellular biology.
[45] J. M. Boss,et al. Single base pair substitutions within the HLA-DRA gene promoter separate the functions of the X1 and X2 boxes. , 1992, Journal of immunology.
[46] C. Seidl,et al. Genetic complexity of regulatory mutants defective for HLA class II gene expression. , 1992, Journal of immunology.
[47] J. M. Boss,et al. Two B cell factors bind the HLA-DRA X box region and recognize different subsets of HLA class II promoters. , 1991, Nucleic acids research.
[48] S. Urieli-Shoval,et al. Defective HLA DRA X box binding in the class II transactive transcription factor mutant 6.1.6 and in cell lines from class II immunodeficient patients. , 1991, Journal of immunology.
[49] J. Strominger,et al. Class II-antigen-negative patient and mutant B-cell lines represent at least three, and probably four, distinct genetic defects defined by complementation analysis. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[50] L. Glimcher,et al. In vivo footprinting of MHC class II genes: bare promoters in the bare lymphocyte syndrome. , 1991, Science.
[51] H. Geuze,et al. Segregation of MHC class II molecules from MHC class I molecules in the Golgi complex for transport to lysosomal compartments , 1991, Nature.
[52] B. Mach,et al. Combined immunodeficiency with defective expression in MHC class II genes. , 1989, Immunodeficiency reviews.
[53] J. M. Boss,et al. Conserved upstream sequences of human class II major histocompatibility genes enhance expression of class II genes in wild-type but not mutant B-cell lines. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[54] P. Jensen. Protein synthesis in antigen processing. , 1988, Journal of immunology.
[55] W. Reith,et al. Congenital immunodeficiency with a regulatory defect in MHC class II gene expression lacks a specific HLA-DR promoter binding protein, RF-X , 1988, Cell.
[56] J. Strominger,et al. Regulation of a transfected human class II major histocompatibility complex gene in human fibroblasts. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[57] B. Mach,et al. A trans-acting class II regulatory gene unlinked to the MHC controls expression of HLA class II genes , 1985, Nature.
[58] B. Mach,et al. Rapid A Defect in the Regulation of Major Histocompatibility Complex Class 11 Gene Expression in Human HLA-DR Negative Lymphocytes from Patients with Combined Immunodeficiency Syndrome , 2022 .
[59] P. Gladstone,et al. Identification of a trans-acting function regulating HLA-DR expression in a DR-negative B cell variant , 1980, Somatic cell genetics.
[60] P. Gladstone,et al. Stable variants affecting B cell alloantigens in human lymphoid cells , 1978, Nature.