Neurociencias
Département
Instituto de Parasitología y Biomedicina López Neyra
Armilla, EspañaPublications en collaboration avec des chercheurs de Instituto de Parasitología y Biomedicina López Neyra (20)
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
2022
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Pathogenic LRRK2 regulates centrosome cohesion via Rab10/RILPL1-mediated CDK5RAP2 displacement
iScience, Vol. 25, Núm. 6
2020
2019
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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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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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Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation
Molecular Neurodegeneration, Vol. 13, Núm. 1
2017
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Dynamic properties of calcium-activated chloride currents in Xenopus laevis oocytes
Scientific Reports, Vol. 7
2016
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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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Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356
Autophagy
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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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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Human endogenous retrovirus HERV-Fc1 association with multiple sclerosis susceptibility: A meta-analysis
PLoS ONE, Vol. 9, Núm. 3
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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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TNFRSF1A polymorphisms rs1800693 and rs4l49584 in patients with multiple sclerosis
Neurology, Vol. 80, Núm. 22, pp. 2010-2016
2012
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A cytokine gene screen uncovers SOCS1 as genetic risk factor for multiple sclerosis
Genes and Immunity, Vol. 13, Núm. 1, pp. 21-28
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Chitinase 3-like 1 plasma levels are increased in patients with progressive forms of multiple sclerosis
Multiple Sclerosis Journal, Vol. 18, Núm. 7, pp. 983-990