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Autophagy|February 2, 2018
Mutations in ATP6AP2 cause autophagic liver disease in humansMagda Cannata Serio, Maria A Rujano, Matias SimonsJournal of Cell Science|July 12, 2013
The cytosolic chaperone α-crystallin B rescues folding and compartmentalization of misfolded multispan transmembrane proteinsMassimo D'Agostino, Valentina Lemma, Giancarlo Chesi, et al.Plos One|January 25, 2024
A polarized cell system amenable to subcellular resolution imaging of influenza virus infectionJean-Baptiste Brault, Catherine Thouvenot, Magda Cannata Serio, et al.Journal of Medical Genetics|August 24, 2019
De novo SCAMP5 mutation causes a neurodevelopmental disorder with autistic features and seizuresLaurence Hubert, Magda Cannata Serio, Laure Villoing-Gaudé, et al.Nature Communications|April 11, 2026
A delayed translocation into the endoplasmic reticulum controls the post-translational modifications of PD-L1Magda Cannata Serio, Fulvia Vitale, Gianluca Scerra, et al.Nature Communications|August 6, 2025
A light-resuming strategy as a screening method for selecting Sec61 inhibitors down-modulating PD-L1 expressionFulvia Vitale, Gianluca Scerra, Laura Marrone, et al.Cell Reports|December 5, 2024
Myosin 1b regulates intestinal epithelial morphogenesis via interaction with UNC45ACéline Revenu, Corinne Lebreton, Magda Cannata Serio, et al.The Journal of Experimental Medicine|November 12, 2017
Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defectsMaria A Rujano, Magda Cannata Serio, Ganna Panasyuk, et al.Hepatology (Baltimore, Md.)|March 8, 2020
Mutations in the V-ATPase Assembly Factor VMA21 Cause a Congenital Disorder of Glycosylation With Autophagic Liver DiseaseMagda Cannata Serio, Laurie A Graham, Angel Ashikov, et al.Pageof 1