IRAIDE
ALLOZA MORAL
INVESTIGADOR/A DOCTOR/A PERMANENTE
Ikerbasque, Fundación Vasca para la Ciencia
Bilbao, EspañaPublicaciones en colaboración con investigadoras/es de Ikerbasque, Fundación Vasca para la Ciencia (33)
2022
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Genomic Multiple Sclerosis Risk Variants Modulate the Expression of the ANKRD55–IL6ST Gene Region in Immature Dendritic Cells
Frontiers in Immunology, Vol. 12
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Pathophysiology of Atherosclerosis
International Journal of Molecular Sciences, Vol. 23, Núm. 6
2021
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Novel transcript discovery expands the repertoire of pathologically-associated, long non-coding rnas in vascular smooth muscle cells
International Journal of Molecular Sciences, Vol. 22, Núm. 3, pp. 1-16
2020
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Birc6 is associated with vulnerability of carotid atherosclerotic plaque
International Journal of Molecular Sciences, Vol. 21, Núm. 24, pp. 1-13
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Cholesterol efflux efficiency of reconstituted HDL is affected by nanoparticle lipid composition
Biomedicines, Vol. 8, Núm. 10
2019
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Interactome of the Autoimmune Risk Protein ANKRD55
Frontiers in Immunology, Vol. 10
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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
2018
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Characterization of carotid smooth muscle cells during phenotypic transition
Cells, Vol. 7, Núm. 3
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Inflammation in human carotid atheroma plaques
Cytokine and Growth Factor Reviews
2017
2016
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A role for autophagy in carotid atherosclerosis
European Stroke Journal, Vol. 1, Núm. 4, pp. 255-263
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Analysis of plasminogen genetic variants in multiple sclerosis patients
G3: Genes, Genomes, Genetics, Vol. 6, Núm. 7, pp. 2073-2079
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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Autophagy, Vol. 12, Núm. 1, pp. 1-222
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Novel insights into the multiple sclerosis risk gene ANKRD55
Journal of Immunology, Vol. 196, Núm. 11, pp. 4553-4565
2015
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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
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Cell-specific effects in different immune subsets associated with SOCS1 genotypes in multiple sclerosis
Multiple Sclerosis, Vol. 21, Núm. 12, pp. 1498-1512
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Genome-wide significant association with seven novel multiple sclerosis risk loci
Journal of Medical Genetics, Vol. 52, Núm. 12, pp. 848-855
2014
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Autophagic marker MAP1LC3B expression levels are associated with carotid atherosclerosis symptomatology
PLoS ONE, Vol. 9, Núm. 12
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Human endogenous retrovirus HERV-Fc1 association with multiple sclerosis susceptibility: A meta-analysis
PLoS ONE, Vol. 9, Núm. 3
2013
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A trifluoromethyl analogue of celecoxib exerts beneficial effects in neuroinflammation
PLoS ONE, Vol. 8, Núm. 12