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Methods in Molecular Biology (Clifton, N.J.)|March 22, 2021
Continuous and Discontinuous Approaches to Study FAD Synthesis and Degradation Catalyzed by Purified Recombinant FAD Synthase or Cellular FractionsPiero Leone, Maria Tolomeo, Maria Barile
Methods in Molecular Biology (Clifton, N.J.)|March 22, 2021
Purification of Recombinant Human 6His-FAD Synthase (Isoform 2) and Quantitation of FAD/Protein Monomer Ratio by UV-Vis SpectraPiero Leone, Stefano Quarta, Maria Tolomeo, et al.
International Journal of Molecular Sciences|July 30, 2020
Development of Novel Experimental Models to Study Flavoproteome Alterations in Human Neuromuscular Diseases: The Effect of Rf TherapyMaria Tolomeo, Alessia Nisco, Piero Leone, et al.
Journal of Inherited Metabolic Disease|June 9, 2016
Riboflavin transport and metabolism in humansMaria Barile, Teresa Anna Giancaspero, Piero Leone, et al.
International Journal of Biological Macromolecules|July 28, 2019
The hidden side of the human FAD synthase 2Piero Leone, Michele Galluccio, Carmen Brizio, et al.
International Journal of Molecular Sciences|December 15, 2019
Mutation of Aspartate 238 in FAD Synthase Isoform 6 Increases the Specific Activity by Weakening the FAD BindingPiero Leone, Michele Galluccio, Stefano Quarta, et al.
International Journal of Molecular Sciences|December 9, 2023
Micronutrient Deficiency in Inherited Metabolic Disorders Requiring Diet Regimen: A Brief Critical ReviewAlbina Tummolo, Rosa Carella, Donatella De Giovanni, et al.
Biochemical and Biophysical Research Communications|August 17, 2015
Human FAD synthase is a bi-functional enzyme with a FAD hydrolase activity in the molybdopterin binding domainTeresa Anna Giancaspero, Michele Galluccio, Angelica Miccolis, et al.
Structure (London, England : 1993)|April 30, 2024
Structural insights into the bifunctional enzyme human FAD synthaseGiulia Leo, Piero Leone, Elham Ataie Kachoie, et al.
IUBMB Life|September 24, 2021
Mimicking human riboflavin responsive neuromuscular disorders by silencing flad-1 gene in C. elegans: Alteration of vitamin transport and cholinergic transmissionPiero Leone, Maria Tolomeo, Elisabetta Piancone, et al.
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