Development of Novel Experimental Models to Study Flavoproteome Alterations in Human Neuromuscular Diseases: The Effect of Rf Therapy

por Tolomeo, Maria, Nisco, Alessia, Leone, Piero, Barile, Maria
Publicado 2020

Mutation of Aspartate 238 in FAD Synthase Isoform 6 Increases the Specific Activity by Weakening the FAD Binding

por Leone, Piero, Galluccio, Michele, Quarta, Stefano, Anoz-Carbonell, Ernesto, Medina, Milagros, Indiveri, Cesare, Barile, Maria
Publicado 2019

Subcellular Localization of Fad1p in Saccharomyces cerevisiae: A Choice at Post-Transcriptional Level?

por Bruni, Francesco, Giancaspero, Teresa Anna, Oreb, Mislav, Tolomeo, Maria, Leone, Piero, Boles, Eckhard, Roberti, Marina, Caselle, Michele, Barile, Maria
Publicado 2021

Mimicking human riboflavin responsive neuromuscular disorders by silencing flad‐1 gene in C. elegans : Alteration of vitamin transport and cholinergic transmission

por Leone, Piero, Tolomeo, Maria, Piancone, Elisabetta, Puzzovio, Pier Giorgio, De Giorgi, Carla, Indiveri, Cesare, Di Schiavi, Elia, Barile, Maria
Publicado 2021

Remaining challenges in cellular flavin cofactor homeostasis and flavoprotein biogenesis

por Giancaspero, Teresa A., Colella, Matilde, Brizio, Carmen, Difonzo, Graziana, Fiorino, Giuseppina M., Leone, Piero, Brandsch, Roderich, Bonomi, Francesco, Iametti, Stefania, Barile, Maria
Publicado 2015

Bacterial Production, Characterization and Protein Modeling of a Novel Monofuctional Isoform of FAD Synthase in Humans: An Emergency Protein?

por Leone, Piero, Galluccio, Michele, Barbiroli, Alberto, Eberini, Ivano, Tolomeo, Maria, Vrenna, Flavia, Gianazza, Elisabetta, Iametti, Stefania, Bonomi, Francesco, Indiveri, Cesare, Barile, Maria
Publicado 2018

Combined isobutyryl‐CoA and multiple acyl‐CoA dehydrogenase deficiency in a boy with altered riboflavin homeostasis

por Tummolo, Albina, Leone, Piero, Tolomeo, Maria, Solito, Rita, Mattiuzzo, Matteo, Lepri, Francesca Romana, Lorè, Tania, Cardinali, Roberta, De Giovanni, Donatella, Simonetti, Simonetta, Barile, Maria
Publicado 2022

Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency

por Olsen, Rikke K.J., Koňaříková, Eliška, Giancaspero, Teresa A., Mosegaard, Signe, Boczonadi, Veronika, Mataković, Lavinija, Veauville-Merllié, Alice, Terrile, Caterina, Schwarzmayr, Thomas, Haack, Tobias B., Auranen, Mari, Leone, Piero, Galluccio, Michele, Imbard, Apolline, Gutierrez-Rios, Purificacion, Palmfeldt, Johan, Graf, Elisabeth, Vianey-Saban, Christine, Oppenheim, Marcus, Schiff, Manuel, Pichard, Samia, Rigal, Odile, Pyle, Angela, Chinnery, Patrick F., Konstantopoulou, Vassiliki, Möslinger, Dorothea, Feichtinger, René G., Talim, Beril, Topaloglu, Haluk, Coskun, Turgay, Gucer, Safak, Botta, Annalisa, Pegoraro, Elena, Malena, Adriana, Vergani, Lodovica, Mazzà, Daniela, Zollino, Marcella, Ghezzi, Daniele, Acquaviva, Cecile, Tyni, Tiina, Boneh, Avihu, Meitinger, Thomas, Strom, Tim M., Gregersen, Niels, Mayr, Johannes A., Horvath, Rita, Barile, Maria, Prokisch, Holger
Publicado 2016