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Journal Abstract Search

91 related items for PubMed ID: 18336911

  • 1. 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
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  • 6. 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
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  • 8. Novel mutations within the RFX-B gene and partial rescue of MHC and related genes through exogenous class II transactivator in RFX-B-deficient cells.
    Nagarajan UM, Peijnenburg A, Gobin SJ, Boss JM, van den elsen PJ.
    J Immunol; 2000 Apr 01; 164(7):3666-74. PubMed ID: 10725724
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  • 10. Down-regulation of MHC class II expression through inhibition of CIITA transcription by lytic transactivator Zta during Epstein-Barr virus reactivation.
    Li D, Qian L, Chen C, Shi M, Yu M, Hu M, Song L, Shen B, Guo N.
    J Immunol; 2009 Feb 15; 182(4):1799-809. PubMed ID: 19201831
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  • 12. Molecular genetics of the Bare lymphocyte syndrome.
    Masternak K, Muhlethaler-Mottet A, Villard J, Peretti M, Reith W.
    Rev Immunogenet; 2000 Feb 15; 2(2):267-82. PubMed ID: 11258423
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  • 13. Mutation of RFXAP, a regulator of MHC class II genes, in primary MHC class II deficiency.
    Villard J, Lisowska-Grospierre B, van den Elsen P, Fischer A, Reith W, Mach B.
    N Engl J Med; 1997 Sep 11; 337(11):748-53. PubMed ID: 9287230
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  • 14. Type III bare lymphocyte syndrome associated with a novel RFXAP mutation: a case report.
    Gokturk B, Artac H, van Eggermond MJ, van den Elsen P, Reisli İ.
    Int J Immunogenet; 2012 Aug 11; 39(4):362-4. PubMed ID: 22390233
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  • 15. Detection of aberrant transcription of major histocompatibility complex class II antigen presentation genes in chronic lymphocytic leukaemia identifies HLA-DOA mRNA as a prognostic factor for survival.
    Souwer Y, Chamuleau ME, van de Loosdrecht AA, Tolosa E, Jorritsma T, Muris JJ, Dinnissen-van Poppel MJ, Snel SN, van de Corput L, Ossenkoppele GJ, Meijer CJ, Neefjes JJ, Marieke van Ham S.
    Br J Haematol; 2009 May 11; 145(3):334-43. PubMed ID: 19245431
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  • 16. Genetic and epigenetic control of the major histocompatibility complex class Ib gene HLA-G in trophoblast cell lines.
    Holling TM, Bergevoet MW, Wierda RJ, van Eggermond MC, van den Elsen PJ.
    Ann N Y Acad Sci; 2009 Sep 11; 1173():538-44. PubMed ID: 19758196
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  • 17. The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population.
    Naamane H, El Maataoui O, Ailal F, Barakat A, Bennani S, Najib J, Hassar M, Saile R, Bousfiha AA.
    Eur J Pediatr; 2010 Sep 11; 169(9):1069-74. PubMed ID: 20414676
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  • 18. MHC class II deficiency: definition of a new complementation group.
    Villard J, Mach B, Reith W.
    Immunobiology; 1997 Dec 11; 198(1-3):264-72. PubMed ID: 9442397
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