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NEUROBIOLOGY OF DISEASE
Rivista
Codice:
E117221
ISSN:
0969-9961
Dati Generali
Dati Generali
Pubblicazioni (93)
Pulisci
Ordina Pubblicazioni:
ascendente
decrescente
1-(2',4'-dichlorophenyl)-6-methyl-N-cyclohexylamine-1,4-dihydroindeno[1,2-c]pyrazole-3-carboxamide, a novel CB2 agonist, alleviates neuropathic pain through functional microglial changes in mice.
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17beta-estradiol rescues spinal motoneurons from AMPA-induced toxicity: A role for glial cells.
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A WNT1-regulated developmental gene cascade prevents dopaminergic neurodegeneration in adult En1+/- mice.
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A prolonged pharmacological blockade of type-5 metabotropic glutamate receptors protects cultured spinal cord motor neurons against excitotoxic death
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A voxel-based PET study of dopamine transporters in Parkinson's disease: relevance of age at onset.
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Activation of PPAR gamma receptors reduces levodopa-induced dyskinesias in 6-OHDA-lesioned rats
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Acute restraint stress impairs histamine type 2 receptor ability to increase the excitability of medium spiny neurons in the nucleus accumbens
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Adolescent exposure to THC in female rats disrupts developmental changes in the prefrontal cortex
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Adolescent exposure to THC in female rats disrupts developmental changes in the prefrontal cortex
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Altered calcium homeostasis in motor neurons following AMPA receptor but not voltage-dependent calcium channels' activation in a genetic model of amyotrophic lateral sclerosis
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Altered responses of dopamine D3 receptor null mice to excitotoxic or anxiogenic stimuli: Possible involvement of the endocannabinoid and endovanilloid systems
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An animal model of Miller Fisher syndrome: Mitochondrial hydrogen peroxide is produced by the autoimmune attack of nerve terminals and activates Schwann cells
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An endocannabinoid tone limits excitotoxicity in vitro and in a model of multiple sclerosis
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Apaf1 mediates apoptosis and mitochondrial damage induced by mutant human SOD1s typical of familial amyotrophic lateral sclerosis
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Brain-derived neurotrophic factor (BDNF) overexpression in the forebrain results in learning and memory impairments
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CXCR2 increases in ALS cortical neurons and its inhibition prevents motor neurons degeneration in vitro and improves neuromuscular function in SOD1G93A mice
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Cannabidiol inhibits microglia activation and mitigates neuronal damage induced by kainate in an in-vitro seizure model
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Cathepsin D: Analysis of its potential role as an amyloid beta degrading protease
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Cell-specific expression of the epm1 (cystatin B) gene in developing rat cerebellum
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Cerebellar granule cells transplanted in vivo can follow physiological and unusual migratory routes to integrate into the recipient cortex.
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Cerebral collateral flow defines topography and evolution of molecular penumbra in experimental ischemic stroke
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Changes in the expression of extracellular regulated kinase (ERK 1/2) in the R6/2 mouse model of Huntington's disease after phosphodiesterase IV inhibition
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Corrigendum to AD-linked, toxic NH2 human tau affects the quality control of mitochondria in neurons, [Neurobioly of Disease (2014) 62, 489-507] DOI: 10.1016/j.nbd.2013.10.018
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Decreased endocannabinoid levels in the brain and beneficial effects of agents activating cannabinoid and/or vanilloid receptors in a rat model of multiple sclerosis
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Differential regulation of transcripts for dystrophin Isoforms, dystroglycan, and alpha3AChR subunit in mouse sympathetic ganglia following postganglionic nerve crush.
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Dopamine D2 receptor dysfunction is rescued by adenosine A2A receptor antagonism in a model of DYT1 dystonia
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Dynamic changes in pro- and anti-inflammatory cytokines in microglia after PPAR-gamma agonist neuroprotective treatment in the MPTPp mouse model of progressive Parkinson's disease
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Dynamic changes in pro-and anti-inflammatory cytokines in microglia after PPAR-g agonist neuroprotective treatment in the MPTPp mouse model of progressive Parkinson's disease.
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Dysregulated autophagy as a new aspect of the molecular pathogenesis of Krabbe disease
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Dystrophin stabilizes ?3- but not ?7-containing nicotinic acetylcholine receptor subtypes at the postsynaptic apparatus in the mouse superior cervical ganglion
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Dystrophin stabilizes alpha 3- but not alpha 7-containing nicotinic acetylcholine receptor subtypes at the postsynaptic apparatus in the mouse superior cervical ganglion.
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Early environmental therapy rescues brain development in a mouse model of Down syndrome
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Evidence for chronic mitochondrial impairment in the cervical spinal cord of a murine model of motor neuron disease.
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Exocytosis regulates trafficking of GABA and glycine heterotransporters in spinal cord glutamatergic synapses: A mechanism for the excessive heterotransporter-induced release of glutamate in experimental amyotrophic lateral sclerosis
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Fluoxetine in adulthood normalizes GABA release and rescues hippocampal synaptic Plasticity and spatial memory in a mouse model of Down Syndrome
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Fragile X mental retardation protein (FMRP) and metabotropic glutamate receptor subtype 5 (mGlu5) control stress granule formation in astrocytes
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Functional and structural correlates of magnetic resonance patterns in a new in vitro model of cerebral ischemia by transient occlusion of the medial cerebral artery
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Gene co-expression networks shed light into diseases of brain iron accumulation
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Gene expression profiles in a transgenic animal model of fragile X syndrome
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Gene expression profiles in a transgenic animal model of fragile x syndrome
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Genes and pathways differentially expressed in the brains of Fxr2 knockout mice
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Impairment of PMP22 transgenig Schwann cells differentiatic in culture: implications for Charcot-Marie-Tooth type 1A disease
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In vitro drug treatments reduce the deleterious effects of aggregates containing polyAla expanded PHOX2B proteins.
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Increased transcription of transglutaminase 1 mediates neuronal death in in vitro models of neuronal stress and A beta 1-42-mediated toxicity
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Inflammatory cytokines increase mitochondrial damage in motoneuronal cells expressing mutant SOD1
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Integrative human and murine multi-omics: Highlighting shared biomarkers in the neuronal ceroid lipofuscinoses
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Interaction of Tau with Fe65 links tau to APP.
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Interactions of dopamine, iron, and alpha-synuclein linked to dopaminergic neuron vulnerability in Parkinson's disease and Neurodegeneration with Brain Iron Accumulation disorders
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Interferon-gamma causes mood abnormalities by altering cannabinoid CB1 receptor function in the mouse striatum
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Intravitreal gene therapy restores the autophagy-lysosomal pathway and attenuates retinal degeneration in cathepsin D-deficient mice
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Lack of dystrophin functionally affects alpha 3 beta 2/beta 4-nicotinic acethylcholine receptors in sympathetic neurons of dystrophic mdx mice
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Lack of dystrophin functionally affects alpha3beta2/beta4-nicotinic acethylcholine receptors in sympathetic neurons of dystrophic mdx mice.
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Lamotrigine rescues neuronal alterations and prevents seizure-induced memory decline in an Alzheimer's disease mouse mode
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Lateral habenula dysfunctions in Tm4sf2(-/y) mice model for neurodevelopmental disorder
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Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in Ca(V)2.1 knockin migraine mice
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Megalencephalic leukoencephalopathy with subcortical cysts protein-1 modulates endosomal pH and protein trafficking in astrocytes: Relevance to MLC disease pathogenesis
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Mislocalised FUS mutants stall spliceosomal snRNPs in the cytoplasm
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Mitochondrial dysfunction due to mutant copper/zinc superoxide dismutase associated with amyotrophic lateral sclerosis is reversed by N-acetylcysteine.
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Mitochondrial dysfunction due to mutant copper/zinc superoxide dismutase associated with familial amyotrophic lateral sclerosis is reversed by n-acetyl-cysteine
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Mitochondrial iron and energetic dysfunction distinguish fibroblasts and induced neurons from pantothenate kinase-associated neurodegeneration patients
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Molecular classification of amyotrophic lateral sclerosis by unsupervised clustering of gene expression in motor cortex
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Monitoring disease evolution and treatment response in lysosomal disorders by the peripheral benzodiazepine receptor ligand PK11195.
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Motor neuron degeneration, severe myopathy and TDP-43 increase in a transgenic pig model of SOD1-linked familiar ALS
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N-Palmitoylethanolamine-oxazoline (PEA-OXA): A new therapeutic strategy to reduce neuroinflammation, oxidative stress associated to vascular dementia in an experimental model of repeated bilateral common carotid arteries occlusion
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Neuroferritinopathy: From ferritin structure modification to pathogenetic mechanism
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Neutralization of a unique, negatively-charged residue in the voltage sensor of K V 7.2 subunits in a sporadic case of benign familial neonatal seizures.
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Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome
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Pharmacological rescue of adult hippocampal neurogenesis in a mouse model of X-linked intellectual disability
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Phosphodiesterase 10 inhibition reduces striatal excitotoxicity in the quinolinic acid model of Huntington's disease
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Plastic and behavioral abnormalities in experimental Huntington's disease: a crucial role for cholinergic interneurons
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Protective activation of the endocannabinoid system during ischemia in dopamine neurons.
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Reactive astrocytosis-induced perturbation of synaptic homeostasis is restored by nerve growth factor
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Reduced GABAB receptor subunit expression and paired-pulse depression in a genetic model of absence seizures
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Regionalized neurofilament accumulation and motoneuron degeneration are linked phenotypes in wobbler neuromuscular disease.
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Retrovirus mediated gene transfer and cross-correction of galactocerebrosidase in twitcher glial cells results in appropriate localization and phenotype correction
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Selective defects in channel permeability associated with Cx32 mutations causing X-linked Charcot-Marie-Tooth disease
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Selective nicotinic acetylcholine receptor subunit deficits identified in Alzheimer's disease, Parkinson's disease and dementia with Lewy bodies by immunoprecipitation
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Structural insights into the multi-determinant aggregation of TDP-43 in motor neuron-like cells
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Substance P receptor activation induces downregulation of the AMPA receptor functionality in cortical neurons from a genetic model of Amyotrophic Lateral Sclerosis.
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Synaptic alterations as a neurodevelopmental trait of Duchenne muscular dystrophy
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T 1 AM-TAAR1 signalling protects against OGD-induced synaptic dysfunction in the entorhinal cortex
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TGF-beta 1 protects against Abeta-neurotoxicity via the phosphatidylinositol-3-kinase pathway
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TGF-ß1 protects against Aß-neurotoxicity via the phosphatidylinositol-3-kinase pathway.
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The endocannabinoid system is modulated in response to spinal cord injury in rats.
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The first reported generation of several induced pluripotent stem cell line from homozygous and heterozygous Huntington's disease patients demonstrates mutation related enhanced lysosomal activity
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The metabotropic P2Y4 receptor participates in the commitment to differentiation and cell death of human neuroblastoma SH-SY5Y cells.
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Transcriptional dysregulation and impairment of PHOX2B auto-regulatory mechanism induced by polyalanine expansion mutations associated with congenital central hypoventilation syndrome
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Transient upregulation of translational efficiency in prodromal and early symptomatic Tg2576 mice contributes to Abeta pathology
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Ultra-micronized palmitoylethanolamide ...
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Ultra-micronized palmitoylethanolamide rescues the cognitive decline-associated loss of neural plasticity in the neuropathic mouse entorhinal cortex-dentate gyrus pathway
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UsnRNP trafficking is regulated by stress granules and compromised by mutant ALS proteins.
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WDR79/TCAB1 plays a conserved role in the control of locomotion and ameliorates phenotypic defects in SMA models
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h channel-dependent deficit of theta oscillation resonance and phase shift in temporal lobe epilepsy
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