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Page 1
Loss of the batten disease protein CLN3 leads to mis-trafficking of M6PR and defective autophagic-lysosomal reformation.
Nat Commun. 2023 Jul 3;14(1):3911. doi: 10.1038/s41467-023-39643-7.
Nat Commun. 2023.
PMID: 37400440
Free PMC article.
Pathogenesis of Mucopolysaccharidoses, an Update.
Fecarotta S, Tarallo A, Damiano C, Minopoli N, Parenti G.
Fecarotta S, et al. Among authors: minopoli n.
Int J Mol Sci. 2020 Apr 4;21(7):2515. doi: 10.3390/ijms21072515.
Int J Mol Sci. 2020.
PMID: 32260444
Free PMC article.
Review.
Item in Clipboard
microRNAs as biomarkers in Pompe disease.
Tarallo A, Carissimo A, Gatto F, Nusco E, Toscano A, Musumeci O, Coletta M, Karali M, Acampora E, Damiano C, Minopoli N, Fecarotta S, Della Casa R, Mongini T, Vercelli L, Santoro L, Ruggiero L, Deodato F, Taurisano R, Bembi B, Dardis A, Banfi S, Pijnappel WWP, van der Ploeg AT, Parenti G.
Tarallo A, et al. Among authors: minopoli n.
Genet Med. 2019 Mar;21(3):591-600. doi: 10.1038/s41436-018-0103-8. Epub 2018 Jul 12.
Genet Med. 2019.
PMID: 29997386
Free article.
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Correction of oxidative stress enhances enzyme replacement therapy in Pompe disease.
Tarallo A, Damiano C, Strollo S, Minopoli N, Indrieri A, Polishchuk E, Zappa F, Nusco E, Fecarotta S, Porto C, Coletta M, Iacono R, Moracci M, Polishchuk R, Medina DL, Imbimbo P, Monti DM, De Matteis MA, Parenti G.
Tarallo A, et al. Among authors: minopoli n.
EMBO Mol Med. 2021 Nov 8;13(11):e14434. doi: 10.15252/emmm.202114434. Epub 2021 Oct 4.
EMBO Mol Med. 2021.
PMID: 34606154
Free PMC article.
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Carnitine is a pharmacological allosteric chaperone of the human lysosomal α-glucosidase.
Iacono R, Minopoli N, Ferrara MC, Tarallo A, Damiano C, Porto C, Strollo S, Roig-Zamboni V, Peluso G, Sulzenbacher G, Cobucci-Ponzano B, Parenti G, Moracci M.
Iacono R, et al. Among authors: minopoli n.
J Enzyme Inhib Med Chem. 2021 Dec;36(1):2068-2079. doi: 10.1080/14756366.2021.1975694.
J Enzyme Inhib Med Chem. 2021.
PMID: 34565280
Free PMC article.
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