Bioquímica y Biología Molecular
Departamento
Achucarro Basque Center for Neuroscience
Leioa, EspañaPublicaciones en colaboración con investigadoras/es de Achucarro Basque Center for Neuroscience (26)
2024
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Neddylation orchestrates the complex transcriptional and posttranscriptional program that drives Schwann cell myelination
Science Advances, Vol. 10, Núm. 15
2023
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Functional evolutionary convergence of long noncoding RNAs involved in embryonic development
Communications Biology, Vol. 6, Núm. 1
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P-Rex1 is a novel substrate of the E3 ubiquitin ligase Malin associated with Lafora disease
Neurobiology of Disease, Vol. 177
2021
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Fluorine Labeling of Nanoparticles and in Vivo 19F Magnetic Resonance Imaging
ACS Applied Materials and Interfaces, Vol. 13, Núm. 11, pp. 12941-12949
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
2020
2019
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Interactome of the Autoimmune Risk Protein ANKRD55
Frontiers in Immunology, Vol. 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
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Long Interleukin-22 Binding Protein Isoform-1 Is an Intracellular Activator of the Unfolded Protein Response
Frontiers in immunology, Vol. 9, pp. 2934
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The era of GWAS is over – Yes
Multiple Sclerosis Journal
2017
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RNAseq based transcriptomics study of SMCs from carotid atherosclerotic plaque: BMP2 and IDs proteins are crucial regulators of plaque stability
Scientific Reports, Vol. 7, Núm. 1
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Response to interferon-beta treatment in multiple sclerosis patients: A genome-wide association study
Pharmacogenomics Journal, Vol. 17, Núm. 4, pp. 312-318
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Role of antioxidants in neonatal hypoxic–ischemic brain injury: New therapeutic approaches
International Journal of Molecular Sciences, Vol. 18, Núm. 2
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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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