Biogipuzkoa
Centro de investigación
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Instituto de Parasitología y Biomedicina López Neyra
Armilla, EspañaPublicaciones en colaboración con investigadores/as de Instituto de Parasitología y Biomedicina López Neyra (26)
2024
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A potential patient stratification biomarker for Parkinson´s disease based on LRRK2 kinase-mediated centrosomal alterations in peripheral blood-derived cells
npj Parkinson's Disease, Vol. 10, Núm. 1
2023
2022
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Detailed stratified GWAS analysis for severe COVID-19 in four European populations
Human Molecular Genetics, Vol. 31, Núm. 23, pp. 3945-3966
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Identification of the genetic mechanism that associates L3MBTL3 to multiple sclerosis
Human Molecular Genetics, Vol. 31, Núm. 13, pp. 2155-2163
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Pathogenic LRRK2 regulates centrosome cohesion via Rab10/RILPL1-mediated CDK5RAP2 displacement
iScience, Vol. 25, Núm. 6
2021
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Associative Conditioning Is a Robust Systemic Behavior in Unicellular Organisms: An Interspecies Comparison
Frontiers in Microbiology, Vol. 12
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Mapping the human genetic architecture of COVID-19
Nature, Vol. 600, Núm. 7889, pp. 472-477
2020
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A new risk variant for multiple sclerosis at 11q23.3 locus is associated with expansion of CXCR5+ circulating regulatory T cells
Journal of Clinical Medicine, Vol. 9, Núm. 3
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Genomewide association study of severe covid-19 with respiratory failure
New England Journal of Medicine, Vol. 383, Núm. 16, pp. 1522-1534
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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
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Evidence of conditioned behavior in amoebae
Nature Communications, Vol. 10, Núm. 1
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RAB8, RAB10 and RILPL1 contribute to both LRRK2 kinase-mediated centrosomal cohesion and ciliogenesis deficits
Human Molecular Genetics, Vol. 28, Núm. 21, pp. 3552-3568
2018
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Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation
Molecular Neurodegeneration, Vol. 13, Núm. 1
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
2014
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Human bone marrow stromal cells lose immunosuppressive and anti-inflammatory properties upon oncogenic transformation
Stem Cell Reports, Vol. 3, Núm. 4, pp. 606-619
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LRRK2 delays degradative receptor trafficking by impeding late endosomal budding through decreasing Rab7 activity
Human Molecular Genetics, Vol. 23, Núm. 25, pp. 1-18
2013
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Fine Mapping and Functional Analysis of the Multiple Sclerosis Risk Gene CD6
PLoS ONE, Vol. 8, Núm. 4
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Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk
Journal of Medical Genetics, Vol. 50, Núm. 3, pp. 140-143
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Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis
Journal of Medical Genetics, Vol. 50, Núm. 1, pp. 25-33