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Page 1
Mutations in ATP6AP2 cause autophagic liver disease in humans.
Autophagy. 2018;14(6):1088-1089. doi: 10.1080/15548627.2018.1434370. Epub 2018 May 10.
Autophagy. 2018.
PMID: 29388887
Free PMC article.
A polarized cell system amenable to subcellular resolution imaging of influenza virus infection.
Brault JB, Thouvenot C, Cannata Serio M, Paisant S, Fernandes J, Gény D, Danglot L, Mallet A, Naffakh N.
Brault JB, et al. Among authors: cannata serio m.
PLoS One. 2024 Jan 25;19(1):e0292977. doi: 10.1371/journal.pone.0292977. eCollection 2024.
PLoS One. 2024.
PMID: 38271396
Free PMC article.
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De novo SCAMP5 mutation causes a neurodevelopmental disorder with autistic features and seizures.
Hubert L, Cannata Serio M, Villoing-Gaudé L, Boddaert N, Kaminska A, Rio M, Lyonnet S, Munnich A, Poirier K, Simons M, Besmond C.
Hubert L, et al. Among authors: cannata serio m.
J Med Genet. 2020 Feb;57(2):138-144. doi: 10.1136/jmedgenet-2018-105927. Epub 2019 Aug 22.
J Med Genet. 2020.
PMID: 31439720
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Unconventional secretion of α-Crystallin B requires the Autophagic pathway and is controlled by phosphorylation of its serine 59 residue.
D'Agostino M, Scerra G, Cannata Serio M, Caporaso MG, Bonatti S, Renna M.
D'Agostino M, et al. Among authors: cannata serio m.
Sci Rep. 2019 Nov 15;9(1):16892. doi: 10.1038/s41598-019-53226-x.
Sci Rep. 2019.
PMID: 31729431
Free PMC article.
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Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects.
Rujano MA, Cannata Serio M, Panasyuk G, Péanne R, Reunert J, Rymen D, Hauser V, Park JH, Freisinger P, Souche E, Guida MC, Maier EM, Wada Y, Jäger S, Krogan NJ, Kretz O, Nobre S, Garcia P, Quelhas D, Bird TD, Raskind WH, Schwake M, Duvet S, Foulquier F, Matthijs G, Marquardt T, Simons M.
Rujano MA, et al. Among authors: cannata serio m.
J Exp Med. 2017 Dec 4;214(12):3707-3729. doi: 10.1084/jem.20170453. Epub 2017 Nov 10.
J Exp Med. 2017.
PMID: 29127204
Free PMC article.
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Mutations in the V-ATPase Assembly Factor VMA21 Cause a Congenital Disorder of Glycosylation With Autophagic Liver Disease.
Cannata Serio M, Graham LA, Ashikov A, Larsen LE, Raymond K, Timal S, Le Meur G, Ryan M, Czarnowska E, Jansen JC, He M, Ficicioglu C, Pichurin P, Hasadsri L, Minassian B, Rugierri A, Kalimo H, Ríos-Ocampo WA, Gilissen C, Rodenburg R, Jonker JW, Holleboom AG, Morava E, Veltman JA, Socha P, Stevens TH, Simons M, Lefeber DJ.
Cannata Serio M, et al.
Hepatology. 2020 Dec;72(6):1968-1986. doi: 10.1002/hep.31218.
Hepatology. 2020.
PMID: 32145091
Free PMC article.
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The cytosolic chaperone α-crystallin B rescues folding and compartmentalization of misfolded multispan transmembrane proteins.
D'Agostino M, Lemma V, Chesi G, Stornaiuolo M, Cannata Serio M, D'Ambrosio C, Scaloni A, Polishchuk R, Bonatti S.
D'Agostino M, et al. Among authors: cannata serio m.
J Cell Sci. 2013 Sep 15;126(Pt 18):4160-72. doi: 10.1242/jcs.125443. Epub 2013 Jul 10.
J Cell Sci. 2013.
PMID: 23843626
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