Publicaciones en las que colabora con ANTONIO ARNAIZ VILLENA (35)

2001

  1. A point mutation in a domain of IFN gamma receptor 1 provokes severe immunodeficiency

    European Journal of Immunogenetics, Vol. 28, Núm. 2, pp. 201

  2. 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

  3. Both morphological and molecular characters support speciation of South American siskins by sexual selection

    Cellular and Molecular Life Sciences, Vol. 58, Núm. 14, pp. 2117-2128

  4. 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

  5. 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

  6. HLA alleles and haplotypes in the Turkish population: Relatedness to Kurds, Armenians and other Mediterraneans

    Tissue Antigens, Vol. 57, Núm. 4, pp. 308-317

  7. HLA molecular markers in Tuvinians: A population with both Oriental and Caucasoid characteristics

    Annals of Human Genetics, Vol. 65, Núm. 3, pp. 245-261

  8. Lack of MHC-G4 and soluble (G5, G6) isoforms in the higher primates, Pongidae

    European Journal of Immunogenetics, Vol. 28, Núm. 2, pp. 271

  9. 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

  10. 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

  11. Phylogeography of crossbills, bullfinches, grosbeaks, and rosefinches

    Cellular and Molecular Life Sciences, Vol. 58, Núm. 8, pp. 1159-1166

  12. Role of Nijmegen breakage syndrome protein in specific T-lymphocyte activation pathways

    Clinical and Diagnostic Laboratory Immunology, Vol. 8, Núm. 4, pp. 757-761

  13. The evolution of MHC-G in humans and primates based on three new 3'UT polymorphisms

    European Journal of Immunogenetics, Vol. 28, Núm. 2, pp. 272

  14. The evolution of the MHC-G gene does not support a functional role for the complete protein

    Immunological Reviews, Vol. 183, pp. 65-75

  15. The old world sparrows (genus passer) phylogeography and their relative abundance of nuclear mtDNA pseudogenes

    Journal of Molecular Evolution, Vol. 53, Núm. 2, pp. 144-154

  16. The origin of Palestinians and their genetic relatedness with other Mediterranean populations

    Human Immunology

2000

  1. A novel CD18 genomic deletion in a patient with severe leucocyte adhesion deficiency: A possible CD2/lymphocyte function-associated antigen-1 functional association in humans

    Immunology, Vol. 99, Núm. 3, pp. 440-450

  2. Evolution of MHC-G in humans and primates based on three new 3′UT polymorphisms

    Human Immunology

  3. Fourteen years' follow-up of an autoimmune patient lacking the CD3γ subunit of the T-lymphocyte receptor [8]

    Blood

  4. HLA genes in Arabic-speaking Moroccans: Close relatedness to Berbers and Iberians

    Tissue Antigens, Vol. 55, Núm. 3, pp. 239-249