Concepedia

M Serio

MS

8

Publications

271

Citations

8

H-Index

1968

Active since

Affiliations

Institut des Maladies Génétiques Imagine(Current)

Sorbonne Paris Cité

Délégation Paris 5

Université Paris Cité

Institut Necker Enfants Malades

M Serio is an author at Institut des Maladies Génétiques Imagine specializing in diabetes, metabolic syndrome, and endocrinology.

ORCID

Top concepts

Publications per year

1968–2020

8

Publications

8

Mutations in the X-linked <i>ATP6AP2</i> cause a glycosylation disorder with autophagic defects

Maria A. Rujano, M Serio, Ganna Panasyuk et al. · The Journal of Experimental Medicine · 2017 · 84 citations · Full text

Mutations in the V‐ATPase Assembly Factor VMA21 Cause a Congenital Disorder of Glycosylation With Autophagic Liver Disease

M Serio, Laurie A. Graham, Angel Ashikov et al. · Hepatology · 2020 · 50 citations · Full text

Unconventional secretion of α-Crystallin B requires the Autophagic pathway and is controlled by phosphorylation of its serine 59 residue

M. D’Agostino, Gianluca Scerra, M Serio et al. · Scientific Reports · 2019 · 35 citations · Full text

The cytosolic chaperone α-Crystallin B rescues appropriate folding and compartmentalization of misfolded multispan transmembrane proteins

M. D’Agostino, Valentina Lemma, Giancarlo Chesi et al. · Journal of Cell Science · 2013 · 32 citations

Identification of a novel mutation in the arginine vasopressin-neurophysin II gene affecting the sixth intrachain disulfide bridge of the neurophysin II moiety

Silvana Baglioni, Giovanni Corona, Mario Maggi et al. · European Journal of Endocrinology · 2004 · 22 citations · Full text

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