Antonio
Arnáiz Villena
Publicaciones en las que colabora con Antonio Arnáiz Villena (10)
2001
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A point mutation in a domain of IFN gamma receptor 1 provokes severe immunodeficiency
European Journal of Immunogenetics, Vol. 28, Núm. 2, pp. 201
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A point mutation in a domain of gamma interferon receptor 1 provokes severe immunodeficiency
Clinical and Diagnostic Laboratory Immunology, Vol. 8, Núm. 1, pp. 133-137
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Cathepsin C gene: First compound heterozygous patient with Papillon-Lefèvre syndrome and a novel symptomless mutation
Human mutation, Vol. 17, Núm. 2, pp. 152-153
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Cathepsin C gene: First compound heterozygous patient with papillon-lefevre syndrome, a new symptomless mutation and its possible regulation by retinoids
European Journal of Immunogenetics, Vol. 28, Núm. 2, pp. 330
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Cell surface phenotype and cytokine secretion in Caco-2 cell cultures: Lack of HLA class II molecules and increased RANTES production and IL-2 transcription upon stimulation with IL-1β
European Journal of Immunogenetics, Vol. 28, Núm. 2, pp. 332
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New mutations and defective phorbol myristate acetate activation of T-lvmphocytes in ataxia telangiectasia patients
European Journal of Immunogenetics, Vol. 28, Núm. 2, pp. 330
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Novel mutations and defective protein kinase C activation of T-lymphocytes in ataxia telangiectasia
Clinical and Experimental Immunology, Vol. 123, Núm. 3, pp. 472-480
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Role of Nijmegen breakage syndrome protein in specific T-lymphocyte activation pathways
Clinical and Diagnostic Laboratory Immunology, Vol. 8, Núm. 4, pp. 757-761
2000
1999
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Higher incidence of autoantibodies in X-linked chronic granulomatous disease carriers: Random X-chromosome inactivation may be related to autoimmunity
Autoimmunity, Vol. 31, Núm. 4, pp. 261-264