Sfoglia per Autore
FAD forming and destroying via human FAD synthase: a puzzle of modulated and modulating activities
2019-01-01 Leone, Piero; Quarta, Stefano; Galluccio, Michele; Indiveri, Cesare; Barile, Maria
Mutation of aspartate 238 in FAD synthase isoform 6 increases the specific activity by weakening the FAD binding
2019-01-01 Leone, P.; Galluccio, M.; Quarta, S.; Anoz-Carbonell, E.; Medina, M.; Indiveri, C.; Barile, M.
hFADS6 and its “supermutant”: a possible therapeutic target?
2019-01-01 Leone, Piero; Quarta, S.; Galluccio, M.; Indiveri, C.; Barile, M.
Alteration of flavin homeostasis in neuromuscular disorders and cancer
2019-01-01 Tolomeo, Maria; Leone, Piero; Barile, Maria
Development of Novel Experimental Models to Study Flavoproteome Alterations in Human Neuromuscular Diseases: The Effect of Rf Therapy
2020-01-01 Tolomeo, M.; Nisco, A.; Leone, P.; Barile, M.
FAD synthase deficiency: a severe mitochondrial myopathy searching for novel therapeutic strategies
2020-01-01 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.
Subcellular localization of fad1p in saccharomyces cerevisiae: A choice at post-transcriptional level?
2021-01-01 Bruni, F.; Giancaspero, T. A.; Oreb, M.; Tolomeo, M.; Leone, P.; Boles, E.; Roberti, M.; Caselle, M.; Barile, M.
Mimicking human riboflavin responsive neuromuscular disorders by silencing flad-1 gene in C. elegans: Alteration of vitamin transport and cholinergic transmission
2021-01-01 Leone, P.; Tolomeo, M.; Piancone, E.; Puzzovio, P. G.; De Giorgi, C.; Indiveri, C.; Di Schiavi, E.; Barile, M.
Continuous and Discontinuous Approaches to Study FAD Synthesis and Degradation Catalyzed by Purified Recombinant FAD Synthase or Cellular Fractions
2021-01-01 Leone, Piero; Tolomeo, Maria; Barile, Maria
Purification of Recombinant Human 6His-FAD Synthase (Isoform 2) and Quantitation of FAD/Protein Monomer Ratio by UV-Vis Spectra
2021-01-01 Leone, Piero; Quarta, Stefano; Tolomeo, Maria; Barile, Maria
FAD synthase deficiency: a severe mitochondrial myopathy involving a secondary reduction of RFVT2 expression
2022-01-01 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
2022-01-01 Tummolo, Albina; Leone, Piero; Tolomeo, Maria; Solito, Rita; Mattiuzzo, Matteo; Lepri, Francesca Romana; Lorè, Tania; Cardinali, Roberta; De Giovanni, Donatella; Simonetti, Simonetta; Barile, Maria
Retrograde response to mitochondrial dysfunctions associated to LOF variations in FLAD1 exon 2: unraveling the importance of RFVT2
2022-01-01 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
2023-01-01 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
2023-01-01 Tummolo, Albina; Carella, Rosa; De Giovanni, Donatella; Paterno, Giulia; Simonetti, Simonetta; Tolomeo, Maria; Leone, Piero; Barile, Maria
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| FAD forming and destroying via human FAD synthase: a puzzle of modulated and modulating activities | 1-gen-2019 | Leone, Piero; Quarta, Stefano; Galluccio, Michele; Indiveri, Cesare; Barile, Maria | |
| Mutation of aspartate 238 in FAD synthase isoform 6 increases the specific activity by weakening the FAD binding | 1-gen-2019 | Leone, P.; Galluccio, M.; Quarta, S.; Anoz-Carbonell, E.; Medina, M.; Indiveri, C.; Barile, M. | |
| hFADS6 and its “supermutant”: a possible therapeutic target? | 1-gen-2019 | Leone, Piero; Quarta, S.; Galluccio, M.; Indiveri, C.; Barile, M. | |
| Alteration of flavin homeostasis in neuromuscular disorders and cancer | 1-gen-2019 | Tolomeo, Maria; Leone, Piero; Barile, Maria | |
| 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. | |
| 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. | |
| 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. | |
| 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. | |
| 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 | |
| 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 | |
| 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 | |
| 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 |
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