CNR Institutional Research Information System

FERRI, ALBERTO
 Distribuzione geografica
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Continente #
NA - Nord America 423
AS - Asia 96
EU - Europa 83
Totale 602
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Nazione #
US - Stati Uniti d'America 423
SG - Singapore 94
IT - Italia 57
FI - Finlandia 16
DE - Germania 6
NL - Olanda 3
HK - Hong Kong 2
AT - Austria 1
Totale 602
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Città #
Santa Clara 399
Singapore 70
Rome 40
Helsinki 16
Falkenstein 6
Modena 4
Senago 3
Amsterdam 2
Giulianova 2
Hong Kong 2
Latina 2
Ashburn 1
Avellino 1
Bologna 1
Forest City 1
Parma 1
Pisa 1
Springfield 1
Vienna 1
Totale 554
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Nome #
Dysregulation of alternative splicing underlies synaptic defects in familial Amyotrophic Lateral Sclerosis 23
Caspase-3 triggers early synaptic dysfunction in a mouse model of Alzheimer's disease 22
Immunometabolic Signature and Tauopathy Markers in Blood Cells of Progressive Supranuclear Palsy 20
Mitochondrial redox signalling by p66Shc mediates ALS-like disease through Rac1 inactivation 20
An impaired splicing program underlies differentiation defects in hSOD1 G93A neural progenitor cells 16
CNF1 Increases Brain Energy Level, Counteracts Neuroinflammatory Markers and Rescues Cognitive Deficits in a Murine Model of Alzheimer's Disease 16
Endurance exercise has a negative impact on the onset of SOD1-G93A ALS in female mice and affects the entire skeletal muscle-motor neuron axis 14
Pattern of Mitochondrial Respiration in Peripheral Blood Cells of Patients with Parkinson's Disease 14
Physical exercise in amyotrophic lateral sclerosis: a potential co-adjuvant therapeutic option to counteract disease progression 13
Different Chronic Stress Paradigms Converge on Endogenous TDP43 Cleavage and Aggregation 12
Trimetazidine Improves Mitochondrial Dysfunction in SOD1G93A Cellular Models of Amyotrophic Lateral Sclerosis through Autophagy Activation 11
SerpinE1 drives a cell-autonomous pathogenic signaling in Hutchinson-Gilford progeria syndrome 11
Loss of homeostatic functions in microglia from a murine model of Friedreich's ataxia 11
Proteome data of neuroblastoma cells overexpressing Neuroglobin 10
Differential toxicity of TAR DNA-binding protein 43 isoforms depends on their submitochondrial localization in neuronal cells 10
Altered skeletal muscle glucose-fatty acid flux in amyotrophic lateral sclerosis 10
The proinflammatory action of microglial P2 receptors is enhanced in SOD1 models for amyotrophic lateral sclerosis. 10
Cysteine 111 affects aggregation and cytotoxicity of mutant Cu,Zn-superoxide dismutase associated with familial amyotrophic lateral sclerosis 9
Apaf1 mediates apoptosis and mitochondrial damage induced by mutant human SOD1s typical of familial amyotrophic lateral sclerosis 9
Histaminergic transmission slows progression of amyotrophic lateral sclerosis 9
Immune-mediated myogenesis and acetylcholine receptor clustering promote a slow disease progression in ALS mouse models 9
HIF1-positive and HIF1-negative glioblastoma cells compete in vitro but cooperate in tumor growth in vivo 9
Mechanistic Insights of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis: An Update on a Lasting Relationship 9
Resistance to striatal dopamine depletion induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine in mice expressing human mutant Cu,Zn superoxide dismutase 8
A study of the dual role of copper in superoxide dismutase as antioxidant and pro-oxidant in cellular models of amyotrophic lateral sclerosis 8
Overexpression of neuroglobin promotes energy metabolism and autophagy induction in human neuroblastoma SH-SY5Y cells 8
Protein aggregation landscape in neurodegenerative diseases: Clinical relevance and future applications 8
Mitochondria and ALS: Implications from novel genes and pathways 8
Neurodegeneration in amyotrophic lateral sclerosis : the role of oxidative stress and altered homeostasis of metals 8
Differences in CSF Biomarkers Profile of Patients with Parkinson's Disease Treated with MAO-B Inhibitors in Add-On 8
Glutaredoxin 2 prevents aggregation of mutant SOD1 in mitochondria and abolishes its toxicity. 8
Repurposing of Trimetazidine for Amyotrophic Lateral Sclerosis: a study in SOD1 G93A mice 8
Glutaredoxin 2 prevents aggregation of mutant SOD1 in mitochondria and abolishes its toxicity 8
SIRT3 and mitochondrial metabolism in neurodegenerative diseases 8
Mitochondrial dysfunction due to mutant copper/zinc superoxide dismutase associated with amyotrophic lateral sclerosis is reversed by N-acetylcysteine. 8
A multimolecular signaling complex including PrPC and LRP1 is strictly dependent on lipid rafts and is essential for the function of tissue plasminogen activator 8
What is "hyper" in the ALS Hypermetabolism? 8
HIF-1 positive and HIF-1 negative glioblastoma cells compete in vitro but coopoerate in tumor growth in vivo 8
Skeletal-Muscle Metabolic Reprogramming in ALS-SOD1(G93A) Mice Predates Disease Onset and Is A Promising Therapeutic Target 8
Neurodegeneration in amyotrophic lateral sclerosis: The role of oxidative stress and altered homeostasis of metals 8
Neuroglobin overexpression plays a pivotal role in neuroprotection through mitochondrial raft-like microdomains in neuroblastoma SK-N-BE2 cells 8
Role of mitochondrial raft-like microdomains in the regulation of cell apoptosis 7
Copper depletion increases the mitochondrial-associated SOD1 in neuronal cells. 7
Inflammatory cytokines increase mitochondrial damage in motoneuronal cells expressing mutant SOD1 7
Oxidative modulation of nuclear factor-?B in human cells expressing mutant fALS-typical superoxide dismutases 7
Skeletal muscle in als: An unappreciated therapeutic opportunity? 7
Oligomerization of mutant SOD1 in mitochondria of motoneuronal cells drives mitochondrial damage and cell toxicity 7
Oxidative modulation of nuclear factor-kappaB in human cells expressing mutant fALS-typical superoxide dismutases. 7
Expression of a Cu,Zn superoxide dismutase typical of familial amyotrophic lateral sclerosis induces mitochondrial alteration and increase of cytosolic Ca2+ concentration in transfected neuroblastoma SH-SY5Y cells. 7
Microglia morphological changes in the motor cortex of hsod1g93a transgenic als mice 7
Apoptosome inactivation rescues proneural end neural cells from neurodegeneration 7
Inactivation of cytochrome c oxidase by mutant SOD1s in mouse motoneuronal NSC-34 cells is independent from copper availability but is because of nitric oxide 7
Editorial: Mitochondrial Proteomics: Understanding Mitochondria Function and Dysfunction Through the Characterization of Their Proteome 7
Amyotrophic lateral sclerosis: from current developments in the laboratory to clinical implications 7
Familial ALS-superoxide dismutases associate with mitochondria and shift their redox potentials 7
Dynamic NAD(P)H post-synaptic autofluorescence signals for the assessment of mitochondrial function in a neurodegenerative disease: monitoring the primary motor cortex of G93A mice, an amyotrophic lateral sclerosis model. 7
Mitochondria and ALS: Implications from novel genes and pathways 7
Skeletal muscle metabolism: Origin or prognostic factor for amyotrophic lateral sclerosis (als) development? 7
Cell death in amyotrophic lateral sclerosis: interplay between neuronal and glial cells 7
Impairment of mitochondrial calcium handling in a mtSOD1 cell culture model of motoneuron disease 6
CNF1 enhances brain energy content and counteracts spontaneous epileptiform phenomena in aged DBA/2J Mice 6
Improvement of skeletal muscle performance in ageing by the metabolic modulator Trimetazidine 6
Calcineurin inhibition in sporadic and familial ALS patients 6
Superoxide dismutase 1 modulates expression of transferrin receptor 6
Voltage-activated sodium currents in a cell line expressing a Cu,Zn superoxide dismutase typical of familial ALS. 6
Neurochemistry of SOD1 and familial amyotrophic lateral sclerosis. 6
Copper-dependent oxidative stress, alteration of signal transduction and neurodegeneration in amyotrophic lateral sclerosis 6
Calcineurin activity is regulated both by redox compounds and by mutant familial amyotrophic lateral sclerosis-superoxide dismutase 6
CNF1 Increases Brain Energy Level, Counteracts Neuroinflammatory Markers and Rescues Cognitive Deficits in a Murine Model of Alzheimer's Disease 6
Impairment of glutamate transport and increased vulnerability to oxidative stress in neuroblastoma SH-SY5Y cells expressing a Cu,Zn superoxide dismutase typical of familial amyotrophic lateral sclerosis 6
Overexpression of superoxide dismutase 1 protects against beta-amyloid peptide toxicity: effect of estrogen and copper chelators 6
Oxidative inactivation of calcineurin by Cu,Zn superoxide dismutase G93A, a mutant typical of familial amyotrophic lateral sclerosis. 6
Acute focal brain damage alters mitochondrial dynamics and autophagy in axotomized neurons. 6
Aberrant copper chemistry as a major mediator of oxidative stress in a human cellular model of amyotrophic lateral sclerosis 6
Totale 657
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Categoria #
all - tutte 2.366
article - articoli 2.366
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 4.732
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/20246 0 0 0 0 0 0 0 0 2 0 0 4
2024/2025651 0 4 76 91 370 108 2 0 0 0 0 0
Totale 657