FACULTAD DE CIENCIAS BIOMÉDICAS Y DE LA SALUD
Facultad
Instituto de Parasitología y Biomedicina López Neyra
Armilla, EspañaPublicaciones en colaboración con investigadores/as de Instituto de Parasitología y Biomedicina López Neyra (26)
2020
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Predictive factors and early biomarkers of response in multiple sclerosis patients treated with natalizumab
Scientific Reports, Vol. 10, Núm. 1
2018
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Enzymatic production of fully deacetylated chitooligosaccharides and their neuroprotective and anti-inflammatory properties
Biocatalysis and Biotransformation, Vol. 36, Núm. 1, pp. 57-67
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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
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
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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A new risk variant for multiple sclerosis at the immunoglobulin heavy chain locus associates with intrathecal IgG, IgM index and oligoclonal bands
Multiple Sclerosis, Vol. 21, Núm. 9, pp. 1104-1111
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Functional consequences for apoptosis by transcription elongation regulator 1 (TCERG1)-Mediated Bcl-x and Fas/CD95 Alternative Splicing
PLoS ONE, Vol. 10, Núm. 10
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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
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Influence of the LILRA3 deletion on multiple sclerosis risk: Original data and meta-analysis
PLoS ONE, Vol. 10, Núm. 8
2014
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HERV-W polymorphism in chromosome X is associated with multiple sclerosis risk and with differential expression of MSRV
Retrovirology, Vol. 11, Núm. 1
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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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Fine Mapping and Functional Analysis of the Multiple Sclerosis Risk Gene CD6
PLoS ONE, Vol. 8, Núm. 4
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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
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MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis
Brain, Vol. 136, Núm. 6, pp. 1778-1782
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Transcription elongation regulator 1 (TCERG1) regulates competent RNA polymerase II-mediated elongation of HIV-1 transcription and facilitates efficient viral replication
Retrovirology, Vol. 10, Núm. 1
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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ANKRD55 and DHCR7 are novel multiple sclerosis risk loci
Genes and Immunity, Vol. 13, Núm. 3, pp. 253-257
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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
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Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1
PLoS ONE, Vol. 7, Núm. 5
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Replication study of 10 genes showing evidence for association with multiple sclerosis: Validation of TMEM39A, IL12B and CLBL genes
Multiple Sclerosis Journal, Vol. 18, Núm. 7, pp. 959-965