Inmunología, Oftalmología y ORL
Fachbereich
Centro de Investigacion Biomedica en Red de Enfermedades Respiratorias
Madrid, EspañaPublikationen in Zusammenarbeit mit Forschern von Centro de Investigacion Biomedica en Red de Enfermedades Respiratorias (24)
2024
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Erratum: Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 (Genome medicine (2023) 15 1 (22))
Genome medicine
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MCJ: A mitochondrial target for cardiac intervention in pulmonary hypertension
Science advances, Vol. 10, Núm. 3, pp. eadk6524
2023
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A second update on mapping the human genetic architecture of COVID-19
Nature
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First Report of Neocucurbitaria unguis-hominis Keratitis
Journal of Fungi, Vol. 9, Núm. 1
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Inherited human ezrin deficiency impairs adaptive immunity
Journal of Allergy and Clinical Immunology, Vol. 152, Núm. 4, pp. 997-1009.e11
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Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
Genome Medicine, Vol. 15, Núm. 1
2022
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Human genetic and immunological determinants of critical COVID-19 pneumonia
Nature, Vol. 603, Núm. 7902, pp. 587-598
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Novel genes and sex differences in COVID-19 severity
Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806
2021
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Clinical and Immunological Features of Human BCL10 Deficiency
Frontiers in Immunology, Vol. 12
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Inter-hairpin linker sequences determine the structure of the ββ-solenoid fold: a “bottom-up” study of pneumococcal LytA choline-binding module
International Journal of Biological Macromolecules, Vol. 190, pp. 679-692
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Lymphocyte subsets early predict mortality in a large series of hospitalized COVID-19 patients in Spain
Clinical and Experimental Immunology, Vol. 203, Núm. 3, pp. 424-432
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Molecular bases for the association of FHR-1 with atypical hemolytic uremic syndrome and other diseases
Blood, Vol. 137, Núm. 25, pp. 3484-3494
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X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19
Science immunology, Vol. 6, Núm. 62
2020
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Autoantibodies against type I IFNs in patients with life-threatening COVID-19
Science, Vol. 370, Núm. 6515
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Human BCL10 Deficiency due to Homozygosity for a Rare Allele
Journal of Clinical Immunology, Vol. 40, Núm. 2, pp. 388-398
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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
Science, Vol. 370, Núm. 6515
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Long-term docosahexaenoic acid (DHA) supplementation in cystic fibrosis patients: a randomized, multi-center, double-blind, placebo-controlled trial
Prostaglandins Leukotrienes and Essential Fatty Acids, Vol. 162
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Turncoat Polypeptides: We Adapt to Our Environment
ChemBioChem, Vol. 21, Núm. 4, pp. 432-441
2019
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Double-strand break repair through homologous recombination in autosomal-recessive BCL10 deficiency
Journal of Allergy and Clinical Immunology, Vol. 143, Núm. 5, pp. 1931-1934.e1
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p38γ is essential for cell cycle progression and liver tumorigenesis
Nature