TOLOMEO, MARIA
TOLOMEO, MARIA
Istituto di Biomembrane, Bioenergetica e Biotecnologie Molecolari (IBIOM)
Altered dimerization of certain riboflavin transporter 2 mutants: a possible source of UPR, altered calcium signalling and mitochondrial derangements in RTD2
2025 Tolomeo, Maria; Magliocca, Valentina; Petrini, Stefania; Nisco, Alessia; Barbaro, Roberto; Lanza, Martina; Piccione, Michela; Giudetti, Anna Maria; Massey, Keith; Console, Lara; Indiveri, Cesare; Zanier, Katia; Bertini, Enrico; Persichini, Tiziana; Compagnucci, Claudia; Colella, Matilde; Barile, Maria
Identification and Characterization of a Novel Biallelic SLC12A2 Variant Associated With Kilquist Syndrome ( OMIM #619080)
2025 Leone, Piero; Nisco, Alessia; De Gennaro, Luciana; Tolomeo, Maria; Lorefice, Elisa; Petrosillo, Giuseppe; Russo, Silvia; De Giovanni, Donatella; Catacchio, Claudia Rita; Lepri, Francesca Romana; Ventura, Mario; Simonetti, Simonetta; Tummolo, Albina; Barile, Maria
Production of the recombinant human riboflavin transporters SLC52A1, 3 and functional assay in proteoliposomes
2025 Console, Lara; Tolomeo, Maria; Travo, Luciana; Giudice, Deborah; Nisco, Alessia; Barile, Maria; Indiveri, Cesare
Exploring the impact of flavin homeostasis on cancer cell metabolism
2024 Nisco, Alessia; Tolomeo, Maria; Scalise, Mariafrancesca; Zanier, Katia; Barile, Maria
Over-Production of the Human SLC7A10 in E. coli and Functional Assay in Proteoliposomes
2024 Galluccio, Michele; Mazza, Tiziano; Scalise, Mariafrancesca; Tripicchio, Martina; Scarpelli, Martina; Tolomeo, Maria; Pochini, Lorena; Indiveri, Cesare
Structural insights into the bifunctional enzyme human FAD synthase
2024 Leo, Giulia; Leone, Piero; Ataie Kachoie, Elham; Tolomeo, Maria; Galluccio, Michele; Indiveri, Cesare; Barile, Maria; Capaldi, Stefano
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 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 Tummolo, Albina; Carella, Rosa; De Giovanni, Donatella; Paterno, Giulia; Simonetti, Simonetta; Tolomeo, Maria; Leone, Piero; Barile, Maria
Combined isobutyryl-CoA and multiple acyl-CoA dehydrogenase deficiency in a boy with altered riboflavin homeostasis
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
Impact of natural mutations on the riboflavin transporter 2 and their relevance to human riboflavin transporter deficiency 2
2022 Console, Lara; Tolomeo, Maria; Cosco, Jessica; Massey, Keith; Barile, Maria; Indiveri, Cesare
Retrograde response to mitochondrial dysfunctions associated to LOF variations in FLAD1 exon 2: unraveling the importance of RFVT2
2022 Tolomeo, M; Chimienti, G; Lanza, M; Barbaro, R; Nisco, A; Latronico, T; Leone, P; Petrosillo, G; Liuzzi, Gm; Ryder, B; Inbarfeigenberg, M; Colella, M; Lezza, Ams; Olsen, Rkj; Barile, M
Alteration of Flavin Cofactor Homeostasis in Human Neuromuscular Pathologies
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
2021 Leone, Piero; Tolomeo, Maria; Barile, Maria
Functional Study of the Human Riboflavin Transporter 2 Using Proteoliposomes System
2021 Console, Lara; Tolomeo, Maria; Indiveri, Cesare
Mimicking human riboflavin responsive neuromuscular disorders by silencing flad-1 gene in C. elegans: Alteration of vitamin transport and cholinergic transmission
2021 Leone, Piero; Tolomeo, Maria; Piancone, Elisabetta; Puzzovio Pier, Giorgio; De Giorgi, Carla; Indiveri, Cesare; DI SCHIAVI, Elia; Barile, Maria
Purification of Recombinant Human 6His-FAD Synthase (Isoform 2) and Quantitation of FAD/Protein Monomer Ratio by UV-Vis Spectra
2021 Leone, Piero; Quarta, Stefano; Tolomeo, Maria; Barile, Maria
Subcellular Localization of Fad1p in Saccharomyces cerevisiae: A Choice at Post-Transcriptional Level?
2021 Bruni, Francesco; Giancaspero, Teresa Anna; Oreb, Mislav; Tolomeo, Maria; Leone, Piero; Boles, Eckhard; Roberti, Marina; Caselle, Michele; Barile, Maria
Development of Novel Experimental Models to Study Flavoproteome Alterations in Human Neuromuscular Diseases: The Effect of Rf Therapy
2020 Tolomeo, Maria; Nisco, Alessia; Leone, Piero; Barile, Maria
Reconstitution in Proteoliposomes of the Recombinant Human Riboflavin Transporter 2 (SLC52A2) Overexpressed in E. coli
2019 Console, Lara; Tolomeo, Maria; Colella, Matilde; Barile, Maria; Indiveri, Cesare
A Novel Truncating FLAD1 Variant, Causing Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in an 8-Year-Old Boy
2018 Ryder, B.; Tolomeo, M.; Nochi, Z.; Colella, M.; Barile, M.; Olsen, R. K.; Inbar-Feigenberg, M.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Altered dimerization of certain riboflavin transporter 2 mutants: a possible source of UPR, altered calcium signalling and mitochondrial derangements in RTD2 | 1-gen-2025 | Tolomeo, Maria; Magliocca, Valentina; Petrini, Stefania; Nisco, Alessia; Barbaro, Roberto; Lanza, Martina; Piccione, Michela; Giudetti, Anna Maria; Massey, Keith; Console, Lara; Indiveri, Cesare; Zanier, Katia; Bertini, Enrico; Persichini, Tiziana; Compagnucci, Claudia; Colella, Matilde; Barile, Maria | |
| Identification and Characterization of a Novel Biallelic SLC12A2 Variant Associated With Kilquist Syndrome ( OMIM #619080) | 1-gen-2025 | Leone, Piero; Nisco, Alessia; De Gennaro, Luciana; Tolomeo, Maria; Lorefice, Elisa; Petrosillo, Giuseppe; Russo, Silvia; De Giovanni, Donatella; Catacchio, Claudia Rita; Lepri, Francesca Romana; Ventura, Mario; Simonetti, Simonetta; Tummolo, Albina; Barile, Maria | |
| Production of the recombinant human riboflavin transporters SLC52A1, 3 and functional assay in proteoliposomes | 1-gen-2025 | Console, Lara; Tolomeo, Maria; Travo, Luciana; Giudice, Deborah; Nisco, Alessia; Barile, Maria; Indiveri, Cesare | |
| Exploring the impact of flavin homeostasis on cancer cell metabolism | 1-gen-2024 | Nisco, Alessia; Tolomeo, Maria; Scalise, Mariafrancesca; Zanier, Katia; Barile, Maria | |
| Over-Production of the Human SLC7A10 in E. coli and Functional Assay in Proteoliposomes | 1-gen-2024 | Galluccio, Michele; Mazza, Tiziano; Scalise, Mariafrancesca; Tripicchio, Martina; Scarpelli, Martina; Tolomeo, Maria; Pochini, Lorena; Indiveri, Cesare | |
| Structural insights into the bifunctional enzyme human FAD synthase | 1-gen-2024 | Leo, Giulia; Leone, Piero; Ataie Kachoie, Elham; Tolomeo, Maria; Galluccio, Michele; Indiveri, Cesare; Barile, Maria; Capaldi, Stefano | |
| 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 | |
| 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 | |
| Impact of natural mutations on the riboflavin transporter 2 and their relevance to human riboflavin transporter deficiency 2 | 1-gen-2022 | Console, Lara; Tolomeo, Maria; Cosco, Jessica; Massey, Keith; Barile, Maria; Indiveri, Cesare | |
| Retrograde response to mitochondrial dysfunctions associated to LOF variations in FLAD1 exon 2: unraveling the importance of RFVT2 | 1-gen-2022 | Tolomeo, M; Chimienti, G; Lanza, M; Barbaro, R; Nisco, A; Latronico, T; Leone, P; Petrosillo, G; Liuzzi, Gm; Ryder, B; Inbarfeigenberg, M; Colella, M; Lezza, Ams; Olsen, Rkj; Barile, M | |
| 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 | |
| Functional Study of the Human Riboflavin Transporter 2 Using Proteoliposomes System | 1-gen-2021 | Console, Lara; Tolomeo, Maria; Indiveri, Cesare | |
| 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, Piero; Tolomeo, Maria; Piancone, Elisabetta; Puzzovio Pier, Giorgio; De Giorgi, Carla; Indiveri, Cesare; DI SCHIAVI, Elia; 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 | |
| Subcellular Localization of Fad1p in Saccharomyces cerevisiae: A Choice at Post-Transcriptional Level? | 1-gen-2021 | Bruni, Francesco; Giancaspero, Teresa Anna; Oreb, Mislav; Tolomeo, Maria; Leone, Piero; Boles, Eckhard; Roberti, Marina; Caselle, Michele; Barile, Maria | |
| Development of Novel Experimental Models to Study Flavoproteome Alterations in Human Neuromuscular Diseases: The Effect of Rf Therapy | 1-gen-2020 | Tolomeo, Maria; Nisco, Alessia; Leone, Piero; Barile, Maria | |
| Reconstitution in Proteoliposomes of the Recombinant Human Riboflavin Transporter 2 (SLC52A2) Overexpressed in E. coli | 1-gen-2019 | Console, Lara; Tolomeo, Maria; Colella, Matilde; Barile, Maria; Indiveri, Cesare | |
| A Novel Truncating FLAD1 Variant, Causing Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in an 8-Year-Old Boy | 1-gen-2018 | Ryder, B.; Tolomeo, M.; Nochi, Z.; Colella, M.; Barile, M.; Olsen, R. K.; Inbar-Feigenberg, M. |