Linear Skin Defects with Multiple Congenital Anomalies (LSDMCA): An Unconventional Mitochondrial Disorder

le Indrieri, Alessia, Franco, Brunella
Foilsithe in Genes (Basel) (2021)

The Role of MicroRNAs in Mitochondria-Mediated Eye Diseases

le Carrella, Sabrina, Massa, Filomena, Indrieri, Alessia
Foilsithe in Front Cell Dev Biol (2021)

Mutation-Independent Therapies for Retinal Diseases: Focus on Gene-Based Approaches

le Carrella, Sabrina, Indrieri, Alessia, Franco, Brunella, Banfi, Sandro
Foilsithe in Front Neurosci (2020)

Dopamine, Alpha-Synuclein, and Mitochondrial Dysfunctions in Parkinsonian Eyes

le Indrieri, Alessia, Pizzarelli, Rocco, Franco, Brunella, De Leonibus, Elvira
Foilsithe in Front Neurosci (2020)

The Pervasive Role of the miR-181 Family in Development, Neurodegeneration, and Cancer

le Indrieri, Alessia, Carrella, Sabrina, Carotenuto, Pietro, Banfi, Sandro, Franco, Brunella
Foilsithe in Int J Mol Sci (2020)

Synthetic long non-coding RNAs [SINEUPs] rescue defective gene expression in vivo

le Indrieri, Alessia, Grimaldi, Claudia, Zucchelli, Silvia, Tammaro, Roberta, Gustincich, Stefano, Franco, Brunella
Foilsithe in Sci Rep (2016)

The HOPS complex subunit VPS39 controls ciliogenesis through autophagy

le Iaconis, Daniela, Crina, Claudia, Brillante, Simona, Indrieri, Alessia, Morleo, Manuela, Franco, Brunella
Foilsithe in Hum Mol Genet (2020)

COVID-19: High-JAKing of the Inflammatory “Flight” by Ruxolitinib to Avoid the Cytokine Storm

le Botta, Cirino, Indrieri, Alessia, Garofalo, Eugenio, Biamonte, Flavia, Bruni, Andrea, Pasqua, Pino, Cesario, Francesco, Costanzo, Francesco Saverio, Longhini, Federico, Mendicino, Francesco
Foilsithe in Front Oncol (2021)

The impairment of HCCS leads to MLS syndrome by activating a non-canonical cell death pathway in the brain and eyes

le Indrieri, Alessia, Conte, Ivan, Chesi, Giancarlo, Romano, Alessia, Quartararo, Jade, Tatè, Rosarita, Ghezzi, Daniele, Zeviani, Massimo, Goffrini, Paola, Ferrero, Ileana, Bovolenta, Paola, Franco, Brunella
Foilsithe 2013

The impairment of HCCS leads to MLS syndrome by activating a non-canonical cell death pathway in the brain and eyes

le Indrieri, Alessia, Conte, Ivan, Chesi, Giancarlo, Romano, Alessia, Quartararo, Jade, Tatè, Rosarita, Ghezzi, Daniele, Zeviani, Massimo, Goffrini, Paola, Ferrero, Ileana, Bovolenta, Paola, Franco, Brunella
Foilsithe 2014

α-synuclein overexpression in the retina leads to vision impairment and degeneration of dopaminergic amacrine cells

le Marrocco, Elena, Indrieri, Alessia, Esposito, Federica, Tarallo, Valeria, Carboncino, Anna, Alvino, Filomena Grazia, De Falco, Sandro, Franco, Brunella, De Risi, Maria, De Leonibus, Elvira
Foilsithe in Sci Rep (2020)

Mutations in COX7B Cause Microphthalmia with Linear Skin Lesions, an Unconventional Mitochondrial Disease

le Indrieri, Alessia, van Rahden, Vanessa Alexandra, Tiranti, Valeria, Morleo, Manuela, Iaconis, Daniela, Tammaro, Roberta, D’Amato, Ilaria, Conte, Ivan, Maystadt, Isabelle, Demuth, Stephanie, Zvulunov, Alex, Kutsche, Kerstin, Zeviani, Massimo, Franco, Brunella
Foilsithe 2012

Integrated Genomics Identifies miR-181/TFAM Pathway as a Critical Driver of Drug Resistance in Melanoma

le Barbato, Anna, Iuliano, Antonella, Volpe, Mariagrazia, D’Alterio, Romina, Brillante, Simona, Massa, Filomena, De Cegli, Rossella, Carrella, Sabrina, Salati, Massimiliano, Russo, Annapina, Russo, Giulia, Riccardo, Sara, Cacchiarelli, Davide, Capone, Mariaelena, Madonna, Gabriele, Ascierto, Paolo A., Franco, Brunella, Indrieri, Alessia, Carotenuto, Pietro
Foilsithe in Int J Mol Sci (2021)

miR‐181a/b downregulation exerts a protective action on mitochondrial disease models

le Indrieri, Alessia, Carrella, Sabrina, Romano, Alessia, Spaziano, Alessandra, Marrocco, Elena, Fernandez‐Vizarra, Erika, Barbato, Sara, Pizzo, Mariateresa, Ezhova, Yulia, Golia, Francesca M, Ciampi, Ludovica, Tammaro, Roberta, Henao‐Mejia, Jorge, Williams, Adam, Flavell, Richard A, De Leonibus, Elvira, Zeviani, Massimo, Surace, Enrico M, Banfi, Sandro, Franco, Brunella
Foilsithe in EMBO Mol Med (2019)