Hospital Universitario 12 de Octubre-ko ikertzaileekin lankidetzan egindako argitalpenak (8)

2019

  1. Extreme phenotypes with identical mutations: Two patients with same non-sense NHEJ1 homozygous mutation

    Frontiers in Immunology, Vol. 10, Núm. JAN

2013

  1. Congenital T-cell receptor immunodeficiencies

    Inmunologia

  2. Human CD3γ, but not CD3δ, haploinsufficiency differentially impairs γδ versus αβ surface TCR expression

    BMC Immunology, Vol. 14, Núm. 1

2011

  1. CD3γ-independent pathways in TCR-mediated signaling in mature T and iNKT lymphocytes

    Cellular Immunology, Vol. 271, Núm. 1, pp. 62-66

  2. Possible role of Artemis c.512C>G polymorphic variant in Omenn syndrome

    DNA Repair

2007

  1. Differential biological role of CD3 chains revealed by human immunodeficiencies

    Journal of Immunology, Vol. 178, Núm. 4, pp. 2556-2564

1998

  1. Transcription and weak expression of HLA-DRB6: A gene with anomalies in exon 1 and other regions

    Immunogenetics, Vol. 48, Núm. 1, pp. 16-21

1996

  1. Allelic diversity at the primate Mhc-G locus: Exon 3 bears stop codons in all Cercophitecinae sequences

    Immunogenetics, Vol. 43, Núm. 6, pp. 327-336