| Activation of autophagy, observed in liver tissues from patients with Wilson disease and from ATP7B-deficient animals, protects hepatocytes from copper-induced apoptosis EV Polishchuk, A Merolla, J Lichtmannegger, A Romano, A Indrieri, ... Gastroenterology 156 (4), 1173-1189. e5, 2019 | 185 | 2019 |
| Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial disease A Indrieri, VA Van Rahden, V Tiranti, M Morleo, D Iaconis, R Tammaro, ... The American Journal of Human Genetics 91 (5), 942-949, 2012 | 140 | 2012 |
| The pervasive role of the miR-181 family in development, neurodegeneration, and cancer A Indrieri, S Carrella, P Carotenuto, S Banfi, B Franco International journal of molecular sciences 21 (6), 2092, 2020 | 115 | 2020 |
| miR‐181a/b downregulation exerts a protective action on mitochondrial disease models A Indrieri, S Carrella, A Romano, A Spaziano, E Marrocco, ... EMBO molecular medicine 11 (5), e8734, 2019 | 63 | 2019 |
| Synthetic long non-coding RNAs [SINEUPs] rescue defective gene expression in vivo A Indrieri, C Grimaldi, S Zucchelli, R Tammaro, S Gustincich, B Franco Scientific reports 6 (1), 27315, 2016 | 48 | 2016 |
| The impairment of HCCS leads to MLS syndrome by activating a non‐canonical cell death pathway in the brain and eyes A Indrieri, I Conte, G Chesi, A Romano, J Quartararo, R Tate, D Ghezzi, ... EMBO molecular medicine 5 (2), 280-293, 2013 | 47 | 2013 |
| Dopamine, alpha-synuclein, and mitochondrial dysfunctions in parkinsonian eyes A Indrieri, R Pizzarelli, B Franco, E De Leonibus Frontiers in Neuroscience 14, 567129, 2020 | 41 | 2020 |
| α-synuclein overexpression in the retina leads to vision impairment and degeneration of dopaminergic amacrine cells E Marrocco, A Indrieri, F Esposito, V Tarallo, A Carboncino, FG Alvino, ... Scientific Reports 10 (1), 9619, 2020 | 31 | 2020 |
| Integrated genomics identifies miR-181/TFAM pathway as a critical driver of drug resistance in melanoma A Barbato, A Iuliano, M Volpe, R D’alterio, S Brillante, F Massa, ... International journal of molecular sciences 22 (4), 1801, 2021 | 21 | 2021 |
| Correction of oxidative stress enhances enzyme replacement therapy in Pompe disease A Tarallo, C Damiano, S Strollo, N Minopoli, A Indrieri, E Polishchuk, ... EMBO molecular medicine 13 (11), e14434, 2021 | 18 | 2021 |
| The HOPS complex subunit VPS39 controls ciliogenesis through autophagy D Iaconis, C Crina, S Brillante, A Indrieri, M Morleo, B Franco Human molecular genetics 29 (6), 1018-1029, 2020 | 16 | 2020 |
| Metabolic Regulation of the Ultradian Oscillator Hes1 by Reactive Oxygen Species S Ventre, A Indrieri, C Fracassi, B Franco, I Conte, L Cardone, ... Journal of molecular biology 427 (10), 1887-1902, 2015 | 14 | 2015 |
| Microglia Reactivity Entails Microtubule Remodeling From Acentrosomal to Centrosomal Arrays M Rosito, C Sanchini, G Gosti, M Moreno, S De Panfilis, M Giubettini, ... Cell Reports 42 (2), 112104, 2023 | 13 | 2023 |
| The role of MicroRNAs in mitochondria-mediated eye diseases S Carrella, F Massa, A Indrieri Frontiers in Cell and Developmental Biology 9, 653522, 2021 | 11 | 2021 |
| Mutation-independent therapies for retinal diseases: focus on gene-based approaches S Carrella, A Indrieri, B Franco, S Banfi Frontiers in Neuroscience 14, 588234, 2020 | 10 | 2020 |
| COVID-19: high-JAKing of the inflammatory “flight” by ruxolitinib to avoid the cytokine storm C Botta, A Indrieri, E Garofalo, F Biamonte, A Bruni, P Pasqua, F Cesario, ... Frontiers in oncology 10, 599502, 2021 | 9 | 2021 |
| Linear skin defects with multiple congenital anomalies (LSDMCA): An unconventional mitochondrial disorder A Indrieri, B Franco Genes 12 (2), 263, 2021 | 8 | 2021 |
| miR‐181a/b downregulation: a mutation‐independent therapeutic approach for inherited retinal diseases S Carrella, M Di Guida, S Brillante, D Piccolo, L Ciampi, I Guadagnino, ... EMBO Molecular Medicine 14 (11), e15941, 2022 | 4 | 2022 |
| Targeting the MITF/APAF-1 axis as salvage therapy for MAPK inhibitors in resistant melanoma P Carotenuto, A Romano, A Barbato, P Quadrano, S Brillante, M Volpe, ... Cell Reports 41 (6), 2022 | 3 | 2022 |
| Microphthalmia With Linear Skin Lesions (MLS) Syndrome: An Unconventional Mitochondrial Disorder A Indrieri, B Franco Epstein's Inborn Errors of Development: The Molecular Basis of Clinical …, 2016 | 2 | 2016 |
Brunella Franco, MDFederico II University and Telethon Institute of Genetics and Medicine TIGEM, Naples ItalyEmail verificata su tigem.it
