ADOLFO JOSE
LOPEZ DE MUNAIN ARREGUI
IRAKASLE ELKARTUA
![Foto de David](/img/nophoto.png)
David
Otaegui Bichot
David Otaegui Bichot-rekin lankidetzan egindako argitalpenak (33)
2019
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T cells and immune functions of plasma extracellular vesicles are differentially modulated from adults to centenarians
Aging, Vol. 11, Núm. 22, pp. 10723-10741
2018
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Blood Markers in Healthy-Aged Nonagenarians: A Combination of High Telomere Length and Low Amyloidβ Are Strongly Associated With Healthy Aging in the Oldest Old
Frontiers in Aging Neuroscience, Vol. 10
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Expression profiling analysis reveals key Microrna-mRNA interactions in early retinal degeneration in retinitis pigmentosa
Investigative Ophthalmology and Visual Science, Vol. 59, Núm. 6, pp. 2381-2392
2017
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Progressive changes in non-coding RNA profile in leucocytes with age
Aging, Vol. 9, Núm. 4, pp. 1202-1218
2016
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Cancer risk in DM1 is sex-related and linked to miRNA-200/141 downregulation
Neurology, Vol. 87, Núm. 12, pp. 1250-1257
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SncRNA (microRNA &snoRNA) opposite expression pattern found in multiple sclerosis relapse and remission is sex dependent
Scientific Reports, Vol. 6
2015
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Age gene expression and coexpression progressive signatures in peripheral blood leukocytes
Experimental Gerontology, Vol. 72, pp. 50-56
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Identification of ncRNAs as potential therapeutic targets in multiple sclerosis through differential ncRNA - mRNA network analysis
BMC Genomics, Vol. 16, Núm. 1
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Neurogenetic Disorders in the Basque Population
Annals of Human Genetics, Vol. 79, Núm. 1, pp. 57-75
2014
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Blood miRNA expression pattern is a possible risk marker for natalizumab-associated progressive multifocal leukoencephalopathy in multiple sclerosis patients
Multiple Sclerosis Journal, Vol. 20, Núm. 14, pp. 1851-1859
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Circulating microparticles reflect treatment effects and clinical status in multiple sclerosis
Biomarkers in Medicine, Vol. 8, Núm. 5, pp. 653-661
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Transcriptomic profile reveals gender-specific molecular mechanisms driving multiple sclerosis progression
PLoS ONE, Vol. 9, Núm. 2
2012
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HLA-DRB1*15:01 and multiple sclerosis: A female association?
Multiple Sclerosis Journal, Vol. 18, Núm. 5, pp. 569-577
2010
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Cognitive/personality pattern and triplet expansion size in adult myotonic dystrophy type 1 (DM1): CTG repeats, cognition and personality in DM1
Psychological Medicine, Vol. 40, Núm. 3, pp. 487-495
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Penetrance in Parkinson's disease related to the LRRK2 R1441G mutation in the Basque country (Spain)
Movement Disorders, Vol. 25, Núm. 14, pp. 2340-2345
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Somatic mosaicism in a case of apparently sporadic Creutzfeldt-Jakob disease carrying a de novo D178N mutation in the PRNP gene
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 153, Núm. 7, pp. 1283-1291
2009
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Association between synapsin III gene promoter SNPs and multiple sclerosis in Basque patients
Multiple Sclerosis, Vol. 15, Núm. 1, pp. 124-128
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Cognitive function in facioscapulohumeral dystrophy correlates with the molecular defect
Genes, Brain and Behavior, Vol. 8, Núm. 1, pp. 53-59
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Differential micro RNA expression in PBMC from multiple sclerosis patients
PLoS ONE, Vol. 4, Núm. 7
2008
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Characterization of novel CAPN3 isoforms in white blood cells: An alternative approach for limb-girdle muscular dystrophy 2A diagnosis
Neurogenetics, Vol. 9, Núm. 3, pp. 173-182