Linear Skin Defects with Multiple Congenital Anomalies (LSDMCA): An Unconventional Mitochondrial Disorder by Alessia Indrieri, Brunella Franco

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Mutation-Independent Therapies for Retinal Diseases: Focus on Gene-Based Approaches by Sabrina Carrella, Sabrina Carrella, Alessia Indrieri, Alessia Indrieri, Brunella Franco, Brunella Franco, Sandro Banfi, Sandro Banfi

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Dopamine, Alpha-Synuclein, and Mitochondrial Dysfunctions in Parkinsonian Eyes by Alessia Indrieri, Alessia Indrieri, Rocco Pizzarelli, Brunella Franco, Brunella Franco, Elvira De Leonibus, Elvira De Leonibus

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COVID-19: High-JAKing of the Inflammatory “Flight” by Ruxolitinib to Avoid the Cytokine Storm by Cirino Botta, Alessia Indrieri, Alessia Indrieri, Eugenio Garofalo, Flavia Biamonte, Andrea Bruni, Pino Pasqua, Francesco Cesario, Francesco Saverio Costanzo, Federico Longhini, Francesco Mendicino

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The impairment of HCCS leads to MLS syndrome by activating a non‐canonical cell death pathway in the brain and eyes by Alessia Indrieri, Ivan Conte, Giancarlo Chesi, Alessia Romano, Jade Quartararo, Rosarita Tatè, Daniele Ghezzi, Massimo Zeviani, Paola Goffrini, Ileana Ferrero, Paola Bovolenta, Brunella Franco

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Microglia reactivity entails microtubule remodeling from acentrosomal to centrosomal arrays by Maria Rosito, Caterina Sanchini, Giorgio Gosti, Manuela Moreno, Simone De Panfilis, Maria Giubettini, Doriana Debellis, Federico Catalano, Giovanna Peruzzi, Roberto Marotta, Alessia Indrieri, Elvira De Leonibus, Maria Egle De Stefano, Davide Ragozzino, Giancarlo Ruocco, Silvia Di Angelantonio, Francesca Bartolini

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Integrated Genomics Identifies miR-181/TFAM Pathway as a Critical Driver of Drug Resistance in Melanoma by Anna Barbato, Antonella Iuliano, Mariagrazia Volpe, Romina D’Alterio, Simona Brillante, Filomena Massa, Rossella De Cegli, Sabrina Carrella, Massimiliano Salati, Annapina Russo, Giulia Russo, Sara Riccardo, Davide Cacchiarelli, Mariaelena Capone, Gabriele Madonna, Paolo A. Ascierto, Brunella Franco, Alessia Indrieri, Pietro Carotenuto

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miR‐181a/b downregulation: a mutation‐independent therapeutic approach for inherited retinal diseases by Sabrina Carrella, Martina Di Guida, Simona Brillante, Davide Piccolo, Ludovica Ciampi, Irene Guadagnino, Jorge Garcia Piqueras, Mariateresa Pizzo, Elena Marrocco, Marta Molinari, Georgios Petrogiannakis, Sara Barbato, Yulia Ezhova, Alberto Auricchio, Brunella Franco, Elvira De Leonibus, Enrico Maria Surace, Alessia Indrieri, Sandro Banfi

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Correction of oxidative stress enhances enzyme replacement therapy in Pompe disease by Antonietta Tarallo, Carla Damiano, Sandra Strollo, Nadia Minopoli, Alessia Indrieri, Elena Polishchuk, Francesca Zappa, Edoardo Nusco, Simona Fecarotta, Caterina Porto, Marcella Coletta, Roberta Iacono, Marco Moracci, Roman Polishchuk, Diego Luis Medina, Paola Imbimbo, Daria Maria Monti, Maria Antonietta De Matteis, Giancarlo Parenti

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