Zobrazeno 1 - 10 of 42 pro vyhledávání: '"Vito, Porcelli"'
1
Akademický článek
Lipidomics reveals the reshaping of the mitochondrial phospholipid profile in cells lacking OPA1 and mitofusins
Autor: Andrea Castellaneta, Ilario Losito, Vito Porcelli, Serena Barile, Alessandra Maresca, Valentina Del Dotto, Valentina Losacco, Ludovica Sofia Guadalupi, Cosima Damiana Calvano, David C. Chan, Valerio Carelli, Luigi Palmieri, Tommaso R.I. Cataldi
Publikováno v: Journal of Lipid Research, Vol 65, Iss 6, Pp 100563- (2024)
Depletion or mutations of key proteins for mitochondrial fusion, like optic atrophy 1 (OPA1) and mitofusins 1 and 2 (Mfn 1 and 2), are known to significantly impact the mitochondrial ultrastructure, suggesting alterations of their membranes’ lipid
Externí odkaz: https://doaj.org/article/6589c03608d146cbb7ee3463e3fa33a0
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2
Akademický článek
Dopamine and Citicoline-Co-Loaded Solid Lipid Nanoparticles as Multifunctional Nanomedicines for Parkinson’s Disease Treatment by Intranasal Administration
Autor: Stefano Castellani, Giorgia Natalia Iaconisi, Francesca Tripaldi, Vito Porcelli, Adriana Trapani, Eugenia Messina, Lorenzo Guerra, Cinzia Di Franco, Giuseppe Maruccio, Anna Grazia Monteduro, Filomena Corbo, Sante Di Gioia, Giuseppe Trapani, Massimo Conese
Publikováno v: Pharmaceutics, Vol 16, Iss 8, p 1048 (2024)
This work aimed to evaluate the potential of the nanosystems constituted by dopamine (DA) and the antioxidant Citicoline (CIT) co-loaded in solid lipid nanoparticles (SLNs) for intranasal administration in the treatment of Parkinson disease (PD). Suc
Externí odkaz: https://doaj.org/article/1f1ab735209c4911b1f6e1e0eb162bb7
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3
Akademický článek
Methyl carbamates of phosphatidylethanolamines and phosphatidylserines reveal bacterial contamination in mitochondrial lipid extracts of mouse embryonic fibroblasts
Autor: Andrea Castellaneta, Vito Porcelli, Ilario Losito, Serena Barile, Alessandra Maresca, Valentina Del Dotto, Ludovica Sofia Guadalupi, Cosima Damiana Calvano, Valerio Carelli, Luigi Palmieri, Tommaso R. I. Cataldi
Publikováno v: Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract The occurrence of methyl carbamates of phosphatidylethanolamines and phosphatidylserines in the lipid extract of mitochondria obtained from mouse embryonic fibroblasts was ascertained by hydrophilic interaction liquid chromatography with ele
Externí odkaz: https://doaj.org/article/90836e2c7f57433ab8dac88e080a1b39
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4
Akademický článek
An Overview of Mitochondrial Protein Defects in Neuromuscular Diseases
Autor: Federica Marra, Paola Lunetti, Rosita Curcio, Francesco Massimo Lasorsa, Loredana Capobianco, Vito Porcelli, Vincenza Dolce, Giuseppe Fiermonte, Pasquale Scarcia
Publikováno v: Biomolecules, Vol 11, Iss 11, p 1633 (2021)
Neuromuscular diseases (NMDs) are dysfunctions that involve skeletal muscle and cause incorrect communication between the nerves and muscles. The specific causes of NMDs are not well known, but most of them are caused by genetic mutations. NMDs are g
Externí odkaz: https://doaj.org/article/32d8e5b4944a4c479666fbc332831895
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8
Phospholipidomics of peripheral blood mononuclear cells (PBMCs): the tricky case of children with autism spectrum disorder (ASD) and their healthy siblings
Autor: Royston Goodacre, Yun Xu, Cosima Damiana Calvano, Andrea De Giacomo, Francesco Palmisano, Luigi Palmieri, Giovanni Ventura, Vito Porcelli, Tommaso R. I. Cataldi
Publikováno v: ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Autism spectrum disorder (ASD) is a broad and heterogeneous group of neurological developmental disorders characterized by impaired social interaction and communication, restricted and repetitive behavioural patterns, and altered sensory processing.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18dee51532371960dc612ff359391fef
https://pubmed.ncbi.nlm.nih.gov/32737553
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10
An Overview of Mitochondrial Protein Defects in Neuromuscular Diseases
Autor: Vito Porcelli, Loredana Capobianco, Giuseppe Fiermonte, Vincenza Dolce, Francesco Massimo Lasorsa, Federica Marra, Rosita Curcio, Paola Lunetti, Pasquale Scarcia
Publikováno v: Biomolecules, Vol 11, Iss 1633, p 1633 (2021)
Biomolecules
Neuromuscular diseases (NMDs) are dysfunctions that involve skeletal muscle and cause incorrect communication between the nerves and muscles. The specific causes of NMDs are not well known, but most of them are caused by genetic mutations. NMDs are g
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5e4abc6e04d0db1658ac63e297a4557
https://doi.org/10.3390/biom11111633
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