Ianire Astobiza Pérez-rekin lankidetzan egindako argitalpenak (8)

2020

  1. The Rare IL22RA2 Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1, -2 and -3 and Is Associated with Risk for Multiple Sclerosis

    Cells, Vol. 9, Núm. 1

2019

  1. Pharmacological targeting of the er-resident chaperones GRP94 or cyclophilin b induces secretion of IL-22 binding protein isoform-1 (IL-22bpi1)

    International Journal of Molecular Sciences, Vol. 20, Núm. 10

2016

  1. Analysis of plasminogen genetic variants in multiple sclerosis patients

    G3: Genes, Genomes, Genetics, Vol. 6, Núm. 7, pp. 2073-2079

  2. Novel insights into the multiple sclerosis risk gene ANKRD55

    Journal of Immunology, Vol. 196, Núm. 11, pp. 4553-4565

2015

  1. A functional variant that affects exon-skipping and protein expression of SP140 as genetic mechanism predisposing to multiple sclerosis

    Human Molecular Genetics, Vol. 24, Núm. 19, pp. 5619-5627

  2. Cell-specific effects in different immune subsets associated with SOCS1 genotypes in multiple sclerosis

    Multiple Sclerosis, Vol. 21, Núm. 12, pp. 1498-1512

  3. Genome-wide significant association with seven novel multiple sclerosis risk loci

    Journal of Medical Genetics, Vol. 52, Núm. 12, pp. 848-855

2014

  1. Human endogenous retrovirus HERV-Fc1 association with multiple sclerosis susceptibility: A meta-analysis

    PLoS ONE, Vol. 9, Núm. 3