Andrea Caricasole
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Explore the profile of Andrea Caricasole including associated specialties, affiliations and a list of published articles.
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53
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2060
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Recent Articles
1.
Ziliotto N, Lencioni S, Cirinciani M, Zanardi A, Alessio M, Solda G, et al.
EBioMedicine
. 2025 Mar;
113:105625.
PMID: 40043514
Background: Aceruloplasminemia (ACP) is a rare recessive disease caused by loss of ceruloplasmin activity due to pathogenic variants in the ceruloplasmin (CP) gene. ACP causes iron accumulation in various organs,...
2.
Belloli S, Monterisi C, Rainone P, Coliva A, Zanardi A, Conti A, et al.
Commun Biol
. 2025 Feb;
8(1):264.
PMID: 39972187
Mutations in the ceruloplasmin (CP) gene are responsible for the rare genetic disease aceruloplasminemia characterized by iron accumulation in different organs, including the brain. We previously reported that administration of...
3.
Zanardi A, Nardini I, Raia S, Conti A, Ferrini B, DAdamo P, et al.
Commun Biol
. 2024 Jan;
7(1):140.
PMID: 38291108
Plasma-derived therapeutic proteins are produced through an industrial fractionation process where proteins are purified from individual intermediates, some of which remain unused and are discarded. Relatively few plasma-derived proteins are...
4.
Mannella V, Chaabane L, Canu T, Zanardi A, Raia S, Conti A, et al.
FEBS Open Bio
. 2023 Nov;
14(2):258-275.
PMID: 37986139
Ceruloplasmin (Cp) is a ferroxidase that plays a role in cellular iron homeostasis and is mainly expressed in the liver and secreted into the blood. Cp is also produced by...
5.
Cariulo C, Martufi P, Verani M, Toledo-Sherman L, Lee R, Dominguez C, et al.
Life Sci Alliance
. 2023 Aug;
6(10).
PMID: 37553253
N-terminal phosphorylation at residues T3 and S13 is believed to have important beneficial implications for the biological and pathological properties of mutant huntingtin, where inhibitor of nuclear factor kappa B...
6.
Migazzi A, Scaramuzzino C, Anderson E, Tripathy D, Hernandez I, Grant R, et al.
Cell Rep
. 2021 Apr;
35(2):108980.
PMID: 33852844
The huntingtin (HTT) protein transports various organelles, including vesicles containing neurotrophic factors, from embryonic development throughout life. To better understand how HTT mediates axonal transport and why this function is...
7.
Mori F, Nardini I, Caricasole A, Amega N, Farina C
Haemophilia
. 2021 Feb;
27(3):e409-e411.
PMID: 33529361
No abstract available.
8.
Birolini G, Valenza M, Di Paolo E, Vezzoli E, Talpo F, Maniezzi C, et al.
EMBO Mol Med
. 2020 Sep;
12(10):e12519.
PMID: 32959531
A variety of pathophysiological mechanisms are implicated in Huntington's disease (HD). Among them, reduced cholesterol biosynthesis has been detected in the HD mouse brain from pre-symptomatic stages, leading to diminished...
9.
Hegde R, Chiki A, Petricca L, Martufi P, Arbez N, Mouchiroud L, et al.
EMBO J
. 2020 Aug;
39(17):e104671.
PMID: 32757223
Phosphorylation of the N-terminal domain of the huntingtin (HTT) protein has emerged as an important regulator of its localization, structure, aggregation, clearance and toxicity. However, validation of the effect of...
10.
Cariulo C, Verani M, Martufi P, Ingenito R, Finotto M, DeGuire S, et al.
Biochem Biophys Res Commun
. 2019 Nov;
521(3):549-554.
PMID: 31677786
Huntington's disease (HD) is a progressive neurodegenerative disorder caused by an expansion of a CAG triplet repeat (encoding for a polyglutamine tract) within the first exon of the huntingtin gene....