Instituto Universitario de Investigación en Neuroquímica
Centro/Instituto
King's College London
Londres, Reino UnidoPublicaciones en colaboración con investigadores/as de King's College London (23)
2023
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Editorial: Molecular signalling and pathways contributing to neurodevelopmental disorders: insights into potential therapeutic avenues
Frontiers in Molecular Neuroscience
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Programming of neural progenitors of the adult subependymal zone towards a glutamatergic neuron lineage by neurogenin 2
Stem Cell Reports, Vol. 18, Núm. 12, pp. 2418-2433
2022
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Clinical trials in pediatric ALS: a TRICALS feasibility study
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Vol. 23, Núm. 7-8, pp. 481-488
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Examining the immune signatures of SARS-CoV-2 infection in pregnancy and the impact on neurodevelopment: Protocol of the SIGNATURE longitudinal study
Frontiers in Pediatrics, Vol. 10
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Preclinical animal models of mental illnesses to translate findings from the bench to the bedside: Molecular brain mechanisms and peripheral biomarkers associated to early life stress or immune challenges
European Neuropsychopharmacology, Vol. 58, pp. 55-79
2021
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Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis
JAMA Neurology, Vol. 78, Núm. 10, pp. 1236-1248
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
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Severe mental illness and European COVID-19 vaccination strategies
The Lancet Psychiatry
2018
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Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
Neuron, Vol. 97, Núm. 6, pp. 1268-1283.e6
2017
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Loss of Cannabinoid CB1 Receptors Induces Cortical Migration Malformations and Increases Seizure Susceptibility
Cerebral Cortex, Vol. 27, Núm. 11, pp. 5303-5317
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Specific Features of SVZ Neurogenesis after Cortical Ischemia: A Longitudinal Study
Scientific Reports, Vol. 7, Núm. 1
2016
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CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia
Nature Communications, Vol. 7
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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
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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Autophagy, Vol. 12, Núm. 1, pp. 1-222
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NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
Nature Genetics, Vol. 48, Núm. 9, pp. 1037-1042
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The metabolic co-regulator PGC1α suppresses prostate cancer metastasis
Nature Cell Biology, Vol. 18, Núm. 6, pp. 645-656
2015
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Complexity of the cell-cell interactions in the innate immune response after cerebral ischemia
Brain Research, Vol. 1623, pp. 53-62
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Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
Science, Vol. 347, Núm. 6229, pp. 1436-1441
2014
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Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS
Neuron, Vol. 84, Núm. 2, pp. 324-331
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Programming of neural cells by (endo)cannabinoids: From physiological rules to emerging therapies
Nature Reviews Neuroscience, Vol. 15, Núm. 12, pp. 786-801