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Mariarosa A  Melone
Mariarosa A Melone
Universitą degli Studi della Campania Luigi Vanvitelli
Verified email at unicampania.it
Title
Cited by
Cited by
Year
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
1992005
The carnitine system and cancer metabolic plasticity
MAB Melone, A Valentino, S Margarucci, U Galderisi, A Giordano, ...
Cell death & disease 9 (2), 228, 2018
1882018
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
1722019
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
1302016
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
1282001
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
1281998
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
1162005
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
1062015
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
1021996
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
992003
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
972018
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
972010
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
972004
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
902018
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
902013
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
892008
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
871999
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
782009
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
742009
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
732018
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