Mariarosa A  Melone
Mariarosa A Melone
Universitą degli Studi della Campania Luigi Vanvitelli
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Cited by
Molecular pathways involved in neural in vitro differentiation of marrow stromal stem cells
FP Jori, MA Napolitano, MAB Melone, M Cipollaro, A Cascino, L Altucci, ...
Journal of cellular biochemistry 94 (4), 645-655, 2005
The carnitine system and cancer metabolic plasticity
MAB Melone, A Valentino, S Margarucci, U Galderisi, A Giordano, ...
Cell death & disease 9 (2), 228, 2018
Metabolic syndrome, Mediterranean diet, and polyphenols: Evidence and perspectives
M Finicelli, T Squillaro, F Di Cristo, A Di Salle, MAB Melone, U Galderisi, ...
Journal of Cellular Physiology 234 (5), 5807-5826, 2019
The role of cathepsin D in the pathogenesis of human neurodegenerative disorders
C Vidoni, C Follo, M Savino, MAB Melone, C Isidoro
Medicinal research reviews 36 (5), 845-870, 2016
17‐B estradiol elicits an autocrine leiomyoma cell proliferation: Evidence for a stimulation of protein kinase‐dependent pathway
A Barbarisi, O Petillo, A Di Lieto, MAB Melone, S Margarucci, M Cannas, ...
Journal of cellular physiology 186 (3), 414-424, 2001
Tissue Transglutaminase-Catalyzed Formation of High-Molecular-Weight Aggregatesin VitroIs Favored with Long Polyglutamine Domains: A Possible Mechanism Contributing to CAG …
V Gentile, C Sepe, M Calvani, MAB Melone, R Cotrufo, AJL Cooper, ...
Archives of Biochemistry and Biophysics 352 (2), 314-321, 1998
Neuroacanthocytosis: new developments in a neglected group of dementing disorders
A Danek, HH Jung, MAB Melone, L Rampoldi, V Broccoli, RH Walker
Journal of the Neurological Sciences 229, 171-186, 2005
Changes in autophagy, proteasome activity and metabolism to determine a specific signature for acute and chronic senescent mesenchymal stromal cells
S Capasso, N Alessio, T Squillaro, G Di Bernardo, MA Melone, ...
Oncotarget 6 (37), 39457, 2015
Modulation of cytokine production in activated human monocytes by somatostatin
G Peluso, O Petillo, MAB Melone, G Mazzarella, M Ranieri, GF Tajana
Neuropeptides 30 (5), 443-451, 1996
Skeletal muscle metabolism in physiology and in cancer disease
A Giordano, M Calvani, O Petillo, M Carteni', MRAB Melone, G Peluso
Journal of cellular biochemistry 90 (1), 170-186, 2003
Nano-delivery systems for encapsulation of dietary polyphenols: An experimental approach for neurodegenerative diseases and brain tumors
T Squillaro, A Cimini, G Peluso, A Giordano, MAB Melone
Biochemical pharmacology 154, 303-317, 2018
RAGE–TXNIP axis is required for S100B-promoted Schwann cell migration, fibronectin expression and cytokine secretion
O Sbai, TS Devi, MAB Melone, F Feron, M Khrestchatisky, LP Singh, ...
Journal of cell science 123 (24), 4332-4339, 2010
Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype
MAB Melone, A Tessa, S Petrini, G Lus, S Sampaolo, G di Fede, ...
Archives of neurology 61 (2), 269-272, 2004
Resveratrol protects neuronal-like cells expressing mutant Huntingtin from dopamine toxicity by rescuing ATG4-mediated autophagosome formation
C Vidoni, E Secomandi, A Castiglioni, MAB Melone, C Isidoro
Neurochemistry international 117, 174-187, 2018
Systemic delivery of recombinant brain derived neurotrophic factor (BDNF) in the R6/2 mouse model of Huntington’s disease
C Giampa, E Montagna, C Dato, MAB Melone, G Bernardi, FR Fusco
PloS one 8 (5), e64037, 2013
RAGE recycles at the plasma membrane in S100B secretory vesicles and promotes Schwann cells morphological changes
L Perrone, G Peluso, MAB Melone
Journal of cellular physiology 217 (1), 60-71, 2008
Differentiation and apoptosis of neuroblastoma cells: role of N‐myc gene product
U Galderisi, G Di Bernardo, M Cipollaro, G Peluso, A Cascino, R Cotrufo, ...
Journal of cellular biochemistry 73 (1), 97-105, 1999
Identification of novel mutations in the SLC25A15 gene in hyperornithinemia‐hyperammonemia‐homocitrullinuria (HHH) syndrome: A clinical, molecular, and …
A Tessa, G Fiermonte, C Dionisi‐Vici, E Paradies, MR Baumgartner, ...
Human mutation 30 (5), 741-748, 2009
Screening of ARHSP‐TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion
PS Denora, D Schlesinger, C Casali, F Kok, A Tessa, A Boukhris, ...
Human mutation 30 (3), E500-E519, 2009
Next generation molecular diagnosis of hereditary spastic paraplegias: an Italian cross-sectional study
A D'Amore, A Tessa, C Casali, MT Dotti, A Filla, G Silvestri, A Antenora, ...
Frontiers in Neurology 9, 981, 2018
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