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FAD synthase deficiency: a severe mitochondrial myopathy searching for novel therapeutic strategies 1-gen-2020 Barile, M.; Tolomeo, M.; Latronico, T.; Chimenti, G.; Leone, P.; Nisco, A.; Dipace, G.; Cardinale, M.; Lanza, M.; Barbaro, R.; Petrosillo, G.; Lezza, A. M. S.; Liuzzi, G. M.; Colella, M.; Olsen, R.
Development of Novel Experimental Models to Study Flavoproteome Alterations in Human Neuromuscular Diseases: The Effect of Rf Therapy 1-gen-2020 Tolomeo, M.; Nisco, A.; Leone, P.; Barile, M.
Functional Study of the Human Riboflavin Transporter 2 Using Proteoliposomes System 1-gen-2021 Console, Lara; Tolomeo, Maria; Indiveri, Cesare
Subcellular localization of fad1p in saccharomyces cerevisiae: A choice at post-transcriptional level? 1-gen-2021 Bruni, F.; Giancaspero, T. A.; Oreb, M.; Tolomeo, M.; Leone, P.; Boles, E.; Roberti, M.; Caselle, M.; Barile, M.
Purification of Recombinant Human 6His-FAD Synthase (Isoform 2) and Quantitation of FAD/Protein Monomer Ratio by UV-Vis Spectra 1-gen-2021 Leone, Piero; Quarta, Stefano; Tolomeo, Maria; Barile, Maria
Alteration of Flavin Cofactor Homeostasis in Human Neuromuscular Pathologies 1-gen-2021 Tolomeo, Maria; Nisco, Alessia; Barile, Maria
Continuous and Discontinuous Approaches to Study FAD Synthesis and Degradation Catalyzed by Purified Recombinant FAD Synthase or Cellular Fractions 1-gen-2021 Leone, Piero; Tolomeo, Maria; Barile, Maria
Impact of natural mutations on the riboflavin transporter 2 and their relevance to human riboflavin transporter deficiency 2 1-gen-2021 Console, L.; Tolomeo, M.; Cosco, J.; Massey, K.; Barile, M.; Indiveri, C.
Mimicking human riboflavin responsive neuromuscular disorders by silencing flad-1 gene in C. elegans: Alteration of vitamin transport and cholinergic transmission 1-gen-2021 Leone, P.; Tolomeo, M.; Piancone, E.; Puzzovio, P. G.; De Giorgi, C.; Indiveri, C.; Di Schiavi, E.; Barile, M.
Alteration of Riboflavin transporter expression in human cancer 1-gen-2022 Nisco, Alessia; Tolomeo, Maria; Tiago, Carvalho; DI MOLFETTA, Daria; Barile, Maria
FAD synthase deficiency: a severe mitochondrial myopathy involving a secondary reduction of RFVT2 expression 1-gen-2022 Barile, Maria; Tolomeo, Maria; Chimienti, Guglielmina; Lanza, Martina; Barbaro, Roberto; Latronico, Tiziana; Nisco, Alessia; Leone, Piero; Petrosillo, Giuseppe; Liuzzi, Grazia M.; Lezza, Angela M. S.; Colella, Matilde; Olsen, Rikke K.
Combined isobutyryl‐CoA and multiple acyl‐CoA dehydrogenase deficiency in a boy with altered riboflavin homeostasis 1-gen-2022 Tummolo, Albina; Leone, Piero; Tolomeo, Maria; Solito, Rita; Mattiuzzo, Matteo; Lepri, Francesca Romana; Lorè, Tania; Cardinali, Roberta; De Giovanni, Donatella; Simonetti, Simonetta; Barile, Maria
Adapting cellular riboflavin transport and metabolism in pancreatic ductal adenocarcinoma 1-gen-2022 Nisco, Alessia; Squicciarino, Maria; Tolomeo, Maria; Carvalho, Tiago; DI MOLFETTA, Daria; Barile, Maria
Retrograde response to mitochondrial dysfunctions associated to LOF variations in FLAD1 exon 2: unraveling the importance of RFVT2 1-gen-2022 Tolomeo, Maria; Chimienti, Guglielmina Alessandra; Lanza, Martina; Barbaro, Roberto; Nisco, Alessia; Latronico, Tiziana; Leone, Piero; Petrosillo, Giuseppe; Liuzzi, Grazia Maria; Ryder, Bryony; Inbar-Feigenberg, Michal; Colella, Matilde; Lezza, Angela M. S.; Olsen, Rikke K. J.; Barile, Maria
Increased demand for FAD synthesis in differentiated and stem pancreatic cancer cells is accomplished by modulating FLAD1 gene expression: the inhibitory effect of Chicago Sky Blue 1-gen-2023 Nisco, Alessia; Carvalho, Tiago M A; Tolomeo, Maria; Di Molfetta, Daria; Leone, Piero; Galluccio, Michele; Medina, Milagros; Indiveri, Cesare; Reshkin, Stephan Joel; Cardone, Rosa Angela; Barile, Maria
Micronutrient Deficiency in Inherited Metabolic Disorders Requiring Diet Regimen: A Brief Critical Review 1-gen-2023 Tummolo, Albina; Carella, Rosa; De Giovanni, Donatella; Paterno, Giulia; Simonetti, Simonetta; Tolomeo, Maria; Leone, Piero; Barile, Maria
Mostrati risultati da 21 a 36 di 36
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