Ana
Bernal Chico
Senior researcher
Publikationen (14) Publikationen von Ana Bernal Chico
2024
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Autoimmune inflammation triggers aberrant astrocytic calcium signaling to impair synaptic plasticity
Brain, Behavior, and Immunity, Vol. 121, pp. 192-210
2023
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Endocannabinoid signaling in brain diseases: Emerging relevance of glial cells
GLIA, Vol. 71, Núm. 1, pp. 103-126
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The endocannabinoid system and autoimmune demyelination: A focus on multiple sclerosis
Neurobiology and Physiology of the Endocannabinoid System (Elsevier), pp. 229-240
2021
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CB1 Hartzaile kanabinoidearen azalpena saguaren garuneko zelula oligodendroglialetan
Osasun zientzak: IV. Ikergazte Nazioarteko Ikerteta Euskaraz. 2021eko ekainaren 9, 10 eta . Gasteiz, Euskal Herria.
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Δ9-Tetrahydrocannabinol promotes oligodendrocyte development and CNS myelination in vivo
GLIA, Vol. 69, Núm. 3, pp. 532-545
2020
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ABHD6-aren inhibizioaren azterketa birmielinizazioa bultzatzeko kuprizonaren desmielinizazio primarioaren aniamalia-ereduan.
Ekaia: Euskal Herriko Unibertsitateko zientzi eta teknologi aldizkaria, Núm. 38, pp. 241-257
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Gene expression analysis of astrocyte and microglia endocannabinoid signaling during autoimmune demyelination
Biomolecules, Vol. 10, Núm. 9, pp. 1-19
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P2x7 receptors control demyelination and inflammation in the cuprizone model
Brain, Behavior, and Immunity - Health, Vol. 4
2018
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Deregulation of the endocannabinoid system and therapeutic potential of ABHD6 blockade in the cuprizone model of demyelination
Biochemical Pharmacology, Vol. 157, pp. 189-201
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Re-examining the potential of targeting ABHD6 in multiple sclerosis: Efficacy of systemic and peripherally restricted inhibitors in experimental autoimmune encephalomyelitis
Neuropharmacology, Vol. 141, pp. 181-191
2015
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Blockade of monoacylglycerol lipase inhibits oligodendrocyte excitotoxicity and prevents demyelination in vivo
GLIA, Vol. 63, Núm. 1, pp. 163-176
2013
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Cytosolic zinc accumulation contributes to excitotoxic oligodendroglial death
GLIA, Vol. 61, Núm. 5, pp. 750-764
2010
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Coexistence of two different pseudohypoparathyroidism subtypes (Ia and Ib) in the same kindred with independent Gsα coding mutations and GNAS imprinting defects
Journal of Medical Genetics, Vol. 47, Núm. 4, pp. 276-280
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New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism
European Journal of Endocrinology, Vol. 163, Núm. 6, pp. 953-962