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NEUROBIOLOGY OF DISEASE
Rivista
Codice:
E117221
ISSN:
0969-9961
Dati Generali
Dati Generali
Pubblicazioni (30)
Pulisci
Ordina Pubblicazioni:
ascendente
decrescente
A novel neuroferritinopathy mouse model (FTL 498InsTC) shows progressive brain iron dysregulation, morphological signs of early neurodegeneration and motor coordination deficits
Articolo
A voxel-based PET study of dopamine transporters in Parkinson's disease: Relevance of age at onset
Articolo
Astrocyte TrkB promotes brain injury and edema formation in ischemic stroke
Articolo
Both Schwann cell and axonal defects cause motor peripheral neuropathy in Ebf2-/- mice
Articolo
C. elegans detects toxicity of traumatic brain injury generated tau
Articolo
CHARACTERIZATION OF THE L-FERRITIN VARIANT 460INSA RESPONSIBLE OF A HEREDITARY FERRITINOPATHY DISORDER
Articolo
Disorganization of anatomical connectivity in obsessive compulsive disorder: A multi-parameter diffusion tensor imaging study in a subpopulation of patients
Articolo
Dopamine D2 receptor activation potently inhibits striatal glutamatergic transmission in a G2019S LRRK2 genetic model of Parkinson's disease
Articolo
Enhanced SPARCL1 expression in cancer stem cells improves preclinical modeling of glioblastoma by promoting both tumor infiltration and angiogenesis
Articolo
Exercise attenuates the clinical, synaptic and dendritic abnormalities of experimental autoimmune encephalomyelitis
Articolo
Fibroblasts from FAD-linked presenilin 1 mutations display a normal unfolded protein response but overproduce Ab42 in response to tunicamycin
Articolo
Gender differences in dopaminergic system dysfunction in de novo Parkinson's disease clinical subtypes
Articolo
High frequency stimulation of the anterior vermis modulates behavioural response to chronic stress: involvement of the prefrontal cortex and dorsal raphe?
Articolo
In vivo susceptibility to energy failure parkinsonism and LRRK2 kinase activity
Articolo
Late onset motoneuron disorder caused by mitochondrial Hsp60 chaperone deficiency in mice
Articolo
Mice harbouring a SCA28 patient mutation in AFG3L2 develop late-onset ataxia associated with enhanced mitochondrial proteotoxicity
Articolo
Mitochondrial iron and energetic dysfunction distinguish fibroblasts and induced neurons from pantothenate kinase-associated neurodegeneration patients.
Articolo
Monitoring disease evolution and treatment response in lysosomal disorders by the peripheral benzodiazepine receptor ligand PK11195
Articolo
Neurobiology of disease
Articolo
Neuroferritinopathy: From ferritin structure modification to pathogenetic mechanism.
Articolo
Oxidative stress and cell death in cells expressing L-ferritin variants causing neuroferritinopathy
Articolo
Pantothenate kinase-2 (Pank2) silencing causes cell growth reduction, cell-specific ferroportin upregulation and iron deregulation
Articolo
Preventive exercise attenuates IL-2-driven mood disorders in multiple sclerosis
Articolo
Reactive astrocytes and Wnt/beta-catenin signaling link nigrostriatal injury to repair in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson's disease
Articolo
Receptor for Advanced Glycation Endproducts is upregulated in temporal lobe epilepsy and contributes to experimental seizures
Articolo
The PRRT2 knockout mouse recapitulates the neurological diseases associated with PRRT2 mutations
Articolo
The first reported generation of several induced pluripotent stem cell lines from homozygous and heterozygous Huntington's disease patients demonstrates mutation related enhanced lysosomal activity
Articolo
The gut-brain axis: Correlation of choroid plexus volume and permeability with inflammatory biomarkers in Crohn's disease
Articolo
The role of dopaminergic signalling from physiology to neuroprotection in acute and chronic disorders
Articolo
The therapeutic potential of neural stem/progenitor cells in murine globoid cell leukodystrophy is conditioned by macrophage/microglia activation
Articolo
No Results Found
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