Publikationen in Zusammenarbeit mit Forschern von Universitat Pompeu Fabra (13)

2023

  1. A second update on mapping the human genetic architecture of COVID-19

    Nature

2021

  1. Huntington's disease-specific mis-splicing unveils key effector genes and altered splicing factors

    Brain, Vol. 144, Núm. 7, pp. 2009-2023

2020

  1. Autoantibodies against type I IFNs in patients with life-threatening COVID-19

    Science, Vol. 370, Núm. 6515

  2. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

    Science, Vol. 370, Núm. 6515

2019

  1. Multi-centre validation of a flow cytometry method to identify optimal responders to interferon-beta in multiple sclerosis

    Clinica Chimica Acta, Vol. 488, pp. 135-142

  2. Unexpected relevant role of gene mosaicism in patients with primary immunodeficiency diseases

    Journal of Allergy and Clinical Immunology, Vol. 143, Núm. 1, pp. 359-368

2018

  1. Anti-CD69 therapy induces rapid mobilization and high proliferation of HSPCs through S1P and mTOR

    Leukemia, Vol. 32, Núm. 6, pp. 1445-1457

2017

  1. Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development

    Scientific Reports, Vol. 7

2015

  1. Structural Dissection of Crotalicidin, a Rattlesnake Venom Cathelicidin, Retrieves a Fragment with Antimicrobial and Antitumor Activity

    Journal of Medicinal Chemistry, Vol. 58, Núm. 21, pp. 8553-8563

2014

  1. The leukocyte activation receptor CD69 controls T cell differentiation through its interaction with galectin-1

    Molecular and Cellular Biology, Vol. 34, Núm. 13, pp. 2479-2487

2012

  1. DNA Vaccination Partially Protects against African Swine Fever Virus Lethal Challenge in the Absence of Antibodies

    PLoS ONE, Vol. 7, Núm. 9

  2. Gene expression induced by Toll-like receptors in macrophages requires the transcription factor NFAT5

    Journal of Experimental Medicine, Vol. 209, Núm. 2, pp. 379-393

2008

  1. Gly111Ser mutation in CD8A gene causing CD8 immunodeficiency is found in Spanish Gypsies

    Molecular Immunology, Vol. 45, Núm. 2, pp. 479-484