BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 11463838)

  • 1. Analysis of ankyrin repeats reveals how a single point mutation in RFXANK results in bare lymphocyte syndrome.
    Nekrep N; Geyer M; Jabrane-Ferrat N; Peterlin BM
    Mol Cell Biol; 2001 Aug; 21(16):5566-76. PubMed ID: 11463838
    [TBL] [Abstract][Full Text] [Related]  

  • 2. New functions of the major histocompatibility complex class II-specific transcription factor RFXANK revealed by a high-resolution mutagenesis study.
    Krawczyk M; Masternak K; Zufferey M; Barras E; Reith W
    Mol Cell Biol; 2005 Oct; 25(19):8607-18. PubMed ID: 16166641
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Conserved residues of the bare lymphocyte syndrome transcription factor RFXAP determine coordinate MHC class II expression.
    Long AB; Ferguson AM; Majumder P; Nagarajan UM; Boss JM
    Mol Immunol; 2006 Feb; 43(5):395-409. PubMed ID: 16337482
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel mutations in the RFXANK gene: RFX complex containing in-vitro-generated RFXANK mutant binds the promoter without transactivating MHC II.
    Wiszniewski W; Fondaneche MC; Louise-Plence P; Prochnicka-Chalufour A; Selz F; Picard C; Le Deist F; Eliaou JF; Fischer A; Lisowska-Grospierre B
    Immunogenetics; 2003 Feb; 54(11):747-55. PubMed ID: 12618906
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation and modeling analysis of the Saccharomyces cerevisiae Swi6 ankyrin repeats.
    Ewaskow SP; Sidorova JM; Hendle J; Emery JC; Lycan DE; Zhang KY; Breeden LL
    Biochemistry; 1998 Mar; 37(13):4437-50. PubMed ID: 9521763
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients.
    Masternak K; Barras E; Zufferey M; Conrad B; Corthals G; Aebersold R; Sanchez JC; Hochstrasser DF; Mach B; Reith W
    Nat Genet; 1998 Nov; 20(3):273-7. PubMed ID: 9806546
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in the bare lymphocyte syndrome define critical steps in the assembly of the regulatory factor X complex.
    Nekrep N; Jabrane-Ferrat N; Peterlin BM
    Mol Cell Biol; 2000 Jun; 20(12):4455-61. PubMed ID: 10825209
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Three novel mutations of the CIITA gene in MHC class II-deficient patients with a severe immunodeficiency.
    Dziembowska M; Fondaneche MC; Vedrenne J; Barbieri G; Wiszniewski W; Picard C; Cant AJ; Steimle V; Charron D; Alca-Loridan C; Fischer A; Lisowska-Grospierre B
    Immunogenetics; 2002 Feb; 53(10-11):821-9. PubMed ID: 11862382
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Transcriptional silencing of RFXAP in MHC class II-deficiency.
    van Eggermond MC; Tezcan I; Heemskerk MH; van den Elsen PJ
    Mol Immunol; 2008 May; 45(10):2920-8. PubMed ID: 18336911
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular genetics of the Bare lymphocyte syndrome.
    Masternak K; Muhlethaler-Mottet A; Villard J; Peretti M; Reith W
    Rev Immunogenet; 2000; 2(2):267-82. PubMed ID: 11258423
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of the ankyrin repeat proteins ANKRA and RFXANK as novel partners of class IIa histone deacetylases.
    Wang AH; Grégoire S; Zika E; Xiao L; Li CS; Li H; Wright KL; Ting JP; Yang XJ
    J Biol Chem; 2005 Aug; 280(32):29117-27. PubMed ID: 15964851
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Associations and interactions between bare lymphocyte syndrome factors.
    DeSandro AM; Nagarajan UM; Boss JM
    Mol Cell Biol; 2000 Sep; 20(17):6587-99. PubMed ID: 10938133
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Solution structure of the human oncogenic protein gankyrin containing seven ankyrin repeats and analysis of its structure--function relationship.
    Yuan C; Li J; Mahajan A; Poi MJ; Byeon IJ; Tsai MD
    Biochemistry; 2004 Sep; 43(38):12152-61. PubMed ID: 15379554
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hundreds of ankyrin-like repeats in functionally diverse proteins: mobile modules that cross phyla horizontally?
    Bork P
    Proteins; 1993 Dec; 17(4):363-74. PubMed ID: 8108379
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; Reith W
    EMBO J; 1997 Mar; 16(5):1045-55. PubMed ID: 9118943
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Novel RFXANK Mutation in a Chinese Child With MHC II Deficiency: Case Report and Literature Review.
    Cai YQ; Zhang H; Wang XZ; Xu C; Chao YQ; Shu Y; Tang LF
    Open Forum Infect Dis; 2020 Aug; 7(8):ofaa314. PubMed ID: 32875002
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Class II histone deacetylases confer signal responsiveness to the ankyrin-repeat proteins ANKRA2 and RFXANK.
    McKinsey TA; Kuwahara K; Bezprozvannaya S; Olson EN
    Mol Biol Cell; 2006 Jan; 17(1):438-47. PubMed ID: 16236793
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ankyrin repeat: a unique motif mediating protein-protein interactions.
    Li J; Mahajan A; Tsai MD
    Biochemistry; 2006 Dec; 45(51):15168-78. PubMed ID: 17176038
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lessons from the bare lymphocyte syndrome: molecular mechanisms regulating MHC class II expression.
    Waldburger JM; Masternak K; Muhlethaler-Mottet A; Villard J; Peretti M; Landmann S; Reith W
    Immunol Rev; 2000 Dec; 178():148-65. PubMed ID: 11213800
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Major histocompatibility complex class II transcriptional platform: assembly of nuclear factor Y and regulatory factor X (RFX) on DNA requires RFX5 dimers.
    Jabrane-Ferrat N; Nekrep N; Tosi G; Esserman LJ; Peterlin BM
    Mol Cell Biol; 2002 Aug; 22(15):5616-25. PubMed ID: 12101253
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.