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Prostaglandins & Other Lipid Mediators|April 1, 2019
Neutral sphingomyelinase increases and delocalizes in the absence of Toll-Like Receptor 4: A new insight for MPTP neurotoxicityElisabetta Albi, Samuela Cataldi, Michela Codini, et al.
Frontiers in Physiology|January 24, 2022
LY294002 Inhibits Intermediate Conductance Calcium-Activated Potassium (KCa3.1) Current in Human Glioblastoma CellsConcetta Caglioti, Federico Palazzetti, Lorenzo Monarca, et al.
The International Journal of Biochemistry & Cell Biology|April 1, 2017
Origin of α-mannosidase activity in CSFAnna Tasegian, Silvia Paciotti, Maria Rachele Ceccarini, et al.
Biochimie|November 22, 2017
VDR independent induction of acid-sphingomyelinase by 1,23(OH)2 D3 in gastric cancer cells: Impact on apoptosis and cell morphologyElisabetta Albi, Samuela Cataldi, Ivana Ferri, et al.
International Journal of Biological Macromolecules|February 6, 2025
Protective effects of silk fibroin against 6-OHDA in SH-SY5Y human neuroblastoma cells and comparative study with its release from gelatin filmsMaria Rachele Ceccarini, Martina Alunni Cardinali, Rocco Malaspina, et al.
Nutrients|December 20, 2018
Solid Dispersion of Resveratrol Supported on Magnesium DiHydroxide (Resv@MDH) Microparticles Improves Oral BioavailabilityRoberto Spogli, Maria Bastianini, Francesco Ragonese, et al.
Mediators of Inflammation|January 30, 2018
Mouse Thyroid Gland Changes in Aging: Implication of Galectin-3 and SphingomyelinaseGiovanna Traina, Samuela Cataldi, Paola Siccu, et al.
Molecular Biology of the Cell|July 1, 2015
Very-long-chain fatty acid sphingomyelin in nuclear lipid microdomains of hepatocytes and hepatoma cells: can the exchange from C24:0 to C16:0 affect signal proteins and vitamin D receptor?Andrea Lazzarini, Antonio Macchiarulo, Alessandro Floridi, et al.
International Journal of Molecular Sciences|November 4, 2018
Nuclear Lipid Microdomains Regulate Daunorubicin Resistance in Hepatoma CellsMichela Codini, Carmela Conte, Samuela Cataldi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 24, 2012
First pilot newborn screening for four lysosomal storage diseases in an Italian region: identification and analysis of a putative causative mutation in the GBA geneSilvia Paciotti, Emanuele Persichetti, Severo Pagliardini, et al.
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