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Volumn 115, Issue 1 SPEC. ISS., 2005, Pages 70-73

Evolution of a T-B- SCID into an Omenn syndrome phenotype following parainfluenza 3 virus infection

Author keywords

Exoantigen; Genotype phenotype correlation; Omenn syndrome; Parainfluenza virus infection; RAG mutation; T cell rearrangement; T B SCID

Indexed keywords

RAG1 PROTEIN; RAG2 PROTEIN;

EID: 18144365147     PISSN: 15216616     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.clim.2004.08.016     Document Type: Conference Paper
Times cited : (38)

References (9)
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    • M.R. Lieber, J.E. Hesse, S. Lewis, G.C. Bosma, N. Rosenberg, K. Mizuuchi, M.L. Bosma, and M. Gellert The defect in murine severe combined immunodeficiency: joining of signal sequences but not coding segments in V(D)J recombination Cell 55 1988 7 16
    • (1988) Cell , vol.55 , pp. 7-16
    • Lieber, M.R.1    Hesse, J.E.2    Lewis, S.3    Bosma, G.C.4    Rosenberg, N.5    Mizuuchi, K.6    Bosma, M.L.7    Gellert, M.8
  • 5
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    • V(D)J recombination defects in lymphocytes due to RAG mutations: Severe immunodeficiency with a spectrum of clinical presentations
    • A. Villa, C. Sobacchi, and D. Luigi V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations Blood 97 2001 81 88
    • (2001) Blood , vol.97 , pp. 81-88
    • Villa, A.1    Sobacchi, C.2    Luigi, D.3
  • 6
    • 0035353213 scopus 로고    scopus 로고
    • Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B-severe combined immune deficiency or Omenn syndrome
    • B. Corneo, D. Moshous, T. Gungor, N. Wulffraat, P. Philippet, F.L. Le Deist, A. Fischer, and J.P. de Villartay Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B-severe combined immune deficiency or Omenn syndrome Blood 97 2001 2772 2776
    • (2001) Blood , vol.97 , pp. 2772-2776
    • Corneo, B.1    Moshous, D.2    Gungor, T.3    Wulffraat, N.4    Philippet, P.5    Le Deist, F.L.6    Fischer, A.7    De Villartay, J.P.8
  • 7
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    • Detection of RAG mutations and prenatal diagnosis in families presenting with either T-B-severe combined immunodeficiency or Omenn syndrome
    • U. Tabori, Z. Mark, N. Amariglio, A. Etzioni, H. Golan, B. Biloray, A. Toren, G. Rechavi, and I. Dalal Detection of RAG mutations and prenatal diagnosis in families presenting with either T-B-severe combined immunodeficiency or Omenn syndrome Clin. Genet. 65 2004 322 326
    • (2004) Clin. Genet. , vol.65 , pp. 322-326
    • Tabori, U.1    Mark, Z.2    Amariglio, N.3    Etzioni, A.4    Golan, H.5    Biloray, B.6    Toren, A.7    Rechavi, G.8    Dalal, I.9
  • 9
    • 0029948541 scopus 로고    scopus 로고
    • The role of interleukin-10 in the inhibition of T-cell proliferation and apoptosis mediated by parainfluenza virus type 3
    • S. Sieg, C. King, Y. Huang, and D. Kaplan The role of interleukin-10 in the inhibition of T-cell proliferation and apoptosis mediated by parainfluenza virus type 3 J. Virol. 70 1996 4845 4848
    • (1996) J. Virol. , vol.70 , pp. 4845-4848
    • Sieg, S.1    King, C.2    Huang, Y.3    Kaplan, D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.