about
Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotypeRAGE-TXNIP axis is required for S100B-promoted Schwann cell migration, fibronectin expression and cytokine secretionHigh grade glioblastoma is associated with aberrant expression of ZFP57, a protein involved in gene imprinting, and of CPT1A and CPT1C that regulate fatty acid metabolismCharcot-Marie-Tooth disease with giant axons: a clinicopathological and genetic entity.Foix-Chavany-Marie syndrome in a 17-year-old female with congenital cytomegalovirus infection.Ruta graveolens L. induces death of glioblastoma cells and neural progenitors, but not of neurons, via ERK 1/2 and AKT activation.Unusual Stüve-Wiedemann syndrome with complete maternal chromosome 5 isodisomyHuntington's disease: new frontiers for molecular and cell therapy.Acetylcholinesterase in neuroblastoma and neuroblastoma x glioma hybrid cells: cellular localization and molecular forms.Giant thrombosed intracavernous carotid artery aneurysm presenting as Tolosa-Hunt syndrome in a patient harboring a new pathogenic neurofibromatosis type 1 mutation: a case report and review of the literature.Alterations in the carnitine cycle in a mouse model of Rett syndrome.Silencing of RB1 and RB2/P130 during adipogenesis of bone marrow stromal cells results in dysregulated differentiation.Changes in autophagy, proteasome activity and metabolism to determine a specific signature for acute and chronic senescent mesenchymal stromal cells.Controlled delivery of the heparan sulfate/FGF-2 complex by a polyelectrolyte scaffold promotes maximal hMSC proliferation and differentiation.First study on the peptidergic innervation of the brain superior sagittal sinus in humans.The Role of Cathepsin D in the Pathogenesis of Human Neurodegenerative Disorders.Impact of lysosomal storage disorders on biology of mesenchymal stem cells: Evidences from in vitro silencing of glucocerebrosidase (GBA) and alpha-galactosidase A (GLA) enzymes.Huntingtin polyQ Mutation Impairs the 17β-Estradiol/Neuroglobin Pathway Devoted to Neuron Survival.Dopamine exacerbates mutant Huntingtin toxicity via oxidative-mediated inhibition of autophagy in SH-SY5Y neuroblastoma cells: Beneficial effects of anti-oxidant therapeutics.Differential carnitine/acylcarnitine translocase expression defines distinct metabolic signatures in skeletal muscle cells.RB2/p130 ectopic gene expression in neuroblastoma stem cells: evidence of cell-fate restriction and induction of differentiationTissue transglutaminase-catalyzed formation of high-molecular-weight aggregates in vitro is favored with long polyglutamine domains: a possible mechanism contributing to CAG-triplet diseases.Antisense oligonucleotides and myotonin gene expression in C2 mouse cells.The differential effects of poly(2-hydroxyethyl methacrylate) and poly(2-hydroxyethyl methacrylate)/poly(caprolactone) polymers on cell proliferation and collagen synthesis by human lung fibroblasts.Rasagiline for sleep disorders in patients with Parkinson's disease: a prospective observational study.Synergistic Interplay between Curcumin and Polyphenol-Rich Foods in the Mediterranean Diet: Therapeutic Prospects for Neurofibromatosis 1 Patients.Correction: Systemic Delivery of Recombinant Brain Derived Neurotrophic Factor (BDNF) in the R6/2 Mouse Model of Huntington's Disease.Mutant huntingtin regulates EGF receptor fate in non-neuronal cells lacking wild-type protein.Phosphodiesterase 10A (PDE10A) localization in the R6/2 mouse model of Huntington's disease.Resveratrol protects neuronal-like cells expressing mutant Huntingtin from dopamine toxicity by rescuing ATG4-mediated autophagosome formation.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.Diffuse glioblastoma resembling acute hemorrhagic leukoencephalitis.RAGE recycles at the plasma membrane in S100B secretory vesicles and promotes Schwann cells morphological changes.Role of RB and RB2/P130 genes in marrow stromal stem cells plasticity.Efficient cultivation of neural stem cells with controlled delivery of FGF-2.Vacuolated PAS-positive lymphocytes as an hallmark of Pompe disease and other myopathies related to impaired autophagy.Targeted therapy of human glioblastoma via delivery of a toxin through a peptide directed to cell surface nucleolin.Localization of neuroglobin in the brain of R6/2 mouse model of Huntington's disease.Verapamil Inhibits Ser202/Thr205 Phosphorylation of Tau by Blocking TXNIP/ROS/p38 MAPK Pathway.Adult-onset brain tumors and neurodegeneration: Are polyphenols protective?
P50
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P50
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researcher ORCID ID = 0000-0002-7213-9277
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wetenschapper
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Mariarosa Ab Melone
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Mariarosa Ab Melone
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Mariarosa Ab Melone
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Mariarosa Ab Melone
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Mariarosa Ab Melone
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Mariarosa Ab Melone
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Mariarosa Ab Melone
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Mariarosa Ab Melone
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Mariarosa Ab Melone
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Mariarosa Ab Melone
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Mariarosa Ab Melone
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Mariarosa Ab Melone
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0000-0002-7213-9277