Ciencias de la Salud
Wissensbereich
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Instituto de Parasitología y Biomedicina López Neyra
Armilla, EspañaPublikationen in Zusammenarbeit mit Forschern von Instituto de Parasitología y Biomedicina López Neyra (51)
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
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Systemic cellular migration: The forces driving the directed locomotion movement of cells
PNAS Nexus, Vol. 3, Núm. 5
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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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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HLA association with the susceptibility to anti-synthetase syndrome
Joint Bone Spine, Vol. 88, Núm. 3
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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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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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Magnetic and Photoluminescent Sensors Based on Metal-Organic Frameworks Built up from 2-aminoisonicotinate
Scientific Reports, Vol. 10, Núm. 1
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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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Dopaminergic control of ADAMTS2 expression through cAMP/CREB and ERK: molecular effects of antipsychotics
Translational Psychiatry, Vol. 9, Núm. 1
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Evidence of conditioned behavior in amoebae
Nature Communications, Vol. 10, Núm. 1
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Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease
PLoS Genetics, Vol. 15, Núm. 6
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Identification of a 3′-Untranslated Genetic Variant of RARB Associated With Carotid Intima-Media Thickness in Rheumatoid Arthritis: A Genome-Wide Association Study
Arthritis and Rheumatology, Vol. 71, Núm. 3, pp. 351-360
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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
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The nucleus does not significantly affect the migratory trajectories of amoeba in two-dimensional environments
Scientific Reports, Vol. 9, Núm. 1
2018
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Exome sequencing study in patients with multiple sclerosis reveals variants associated with disease course 06 Biological Sciences 0604 Genetics 11 Medical and Health Sciences 1109 Neurosciences
Journal of Neuroinflammation, Vol. 15, Núm. 1
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Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis
Human molecular genetics, Vol. 27, Núm. 24, pp. 4333-4343