Magda Serio-Cannata
Paris, France
Last Updated: 09/26/2026
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Found 10 publications
A delayed translocation into the endoplasmic reticulum controls the post-translational modifications of PD-L1.
Journal: Nature communications
Published: October 29, 2024
A polarized cell system amenable to subcellular resolution imaging of influenza virus infection.
Journal: PloS one
Published: September 21, 2023
Myosin 1b regulates intestinal epithelial morphogenesis via interaction with UNC45A.
Journal: Cell reports
Published: March 20, 2023
Mutations in the V-ATPase Assembly Factor VMA21 Cause a Congenital Disorder of Glycosylation With Autophagic Liver Disease.
Journal: Hepatology (Baltimore, Md.)
Published: July 16, 2019
Unconventional secretion of α-Crystallin B requires the Autophagic pathway and is controlled by phosphorylation of its serine 59 residue.
Journal: Scientific reports
Published: January 24, 2019
De novo SCAMP5 mutation causes a neurodevelopmental disorder with autistic features and seizures.
Journal: Journal of medical genetics
Published: December 10, 2018
Mutations in ATP6AP2 cause autophagic liver disease in humans.
Journal: Autophagy
Published: February 02, 2018
Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects.
Journal: The Journal of experimental medicine
Published: March 10, 2017
The cytosolic chaperone α-crystallin B rescues folding and compartmentalization of misfolded multispan transmembrane proteins.
Journal: Journal of cell science
Published: July 12, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026