Search Results - "D’Agostino, Massimo"

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    PD-L1 Expression Fluctuates Concurrently with Cyclin D in Glioblastoma Cells by Tufano, Martina, D’Arrigo, Paolo, D’Agostino, Massimo, Giordano, Carolina, Marrone, Laura, Cesaro, Elena, Romano, Maria Fiammetta, Romano, Simona

    Published in Cells (Basel, Switzerland) (09-09-2021)
    “…Despite Glioblastoma (GBM) frequently expressing programmed cell death ligand-1 (PD-L1), treatment with anti-programmed cell death-1 (PD1) has not yielded…”
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    Lysosomal positioning diseases: beyond substrate storage by Scerra, Gianluca, De Pasquale, Valeria, Scarcella, Melania, Caporaso, Maria Gabriella, Pavone, Luigi Michele, D'Agostino, Massimo

    Published in Open biology (26-10-2022)
    “…Lysosomal storage diseases (LSDs) comprise a group of inherited monogenic disorders characterized by lysosomal dysfunctions due to undegraded substrate…”
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    Early onset effects of single substrate accumulation recapitulate major features of LSD in patient-derived lysosomes by Scerra, Gianluca, De Pasquale, Valeria, Pavone, Luigi Michele, Caporaso, Maria Gabriella, Mayer, Andreas, Renna, Maurizio, D'Agostino, Massimo

    Published in iScience (23-07-2021)
    “…Lysosome functions mainly rely on their ability to either degrade substrates or release them into the extracellular space. Lysosomal storage disorders (LSDs)…”
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    A tethering complex drives the terminal stage of SNARE-dependent membrane fusion by D’Agostino, Massimo, Risselada, Herre Jelger, Lürick, Anna, Ungermann, Christian, Mayer, Andreas

    Published in Nature (London) (30-11-2017)
    “…Tethering proteins, known to mediate initial recognition and attachment during membrane fusion, are essential for driving the transition from the hemifused…”
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    Assay of Lipid Mixing and Fusion Pore Formation in the Fusion of Yeast Vacuoles by D'Agostino, Massimo, Mayer, Andreas

    “…Fluorescence de-quenching can be used to analyze membrane lipid mixing during an in vitro fusion reaction. Here we describe a method to measure lipid mixing…”
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    N‑Substituted l‑Iminosugars for the Treatment of Sanfilippo Type B Syndrome by De Pasquale, Valeria, Esposito, Anna, Scerra, Gianluca, Scarcella, Melania, Ciampa, Mariangela, Luongo, Antonietta, D’Alonzo, Daniele, Guaragna, Annalisa, D’Agostino, Massimo, Pavone, Luigi Michele

    Published in Journal of medicinal chemistry (09-02-2023)
    “…Sanfilippo syndrome comprises a group of four genetic diseases due to the lack or decreased activity of enzymes involved in heparan sulfate (HS) catabolism. HS…”
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    The Lack of STING Impairs the MHC-I Dependent Antigen Presentation and JAK/STAT Signaling in Murine Macrophages by Caiazza, Carmen, Brusco, Teresa, D'Alessio, Federica, D'Agostino, Massimo, Avagliano, Angelica, Arcucci, Alessandro, Ambrosino, Concetta, Fiume, Giuseppe, Mallardo, Massimo

    “…STING is a transmembrane ER resident protein that was initially described as a regulator of innate immune response triggered by viral DNA and later found to be…”
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    Effects of Long-Term Citrate Treatment in the PC3 Prostate Cancer Cell Line by Caiazza, Carmen, D'Agostino, Massimo, Passaro, Fabiana, Faicchia, Deriggio, Mallardo, Massimo, Paladino, Simona, Pierantoni, Giovanna Maria, Tramontano, Donatella

    “…Acute administration of a high level of extracellular citrate displays an anti-proliferative effect on both in vitro and in vivo models. However, the long-term…”
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    Fusion Pores Live on the Edge by Blokhuis, Edgar M, D’Agostino, Massimo, Mayer, Andreas, Risselada, H. Jelger

    Published in The journal of physical chemistry letters (20-02-2020)
    “…Biological transmission of vesicular content occurs by opening of a fusion pore. Recent experimental observations have illustrated that fusion pores between…”
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    Protocol for labeling and fixation of intact lysosomes with esterified amino acid analogs to assess lysosomal expansion in living eukaryotic cells by Scerra, Gianluca, Caporaso, Maria Gabriella, Renna, Maurizio, D’Agostino, Massimo

    Published in STAR protocols (17-12-2021)
    “…The lysosomal compartment is a key hub for cell metabolism, and morphological alterations have been described in several pathological conditions. Here, we…”
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    Methylmalonic acidemia triggers lysosomal-autophagy dysfunctions by Costanzo, Michele, Cevenini, Armando, Kollipara, Laxmikanth, Caterino, Marianna, Bianco, Sabrina, Pirozzi, Francesca, Scerra, Gianluca, D'Agostino, Massimo, Pavone, Luigi Michele, Sickmann, Albert, Ruoppolo, Margherita

    Published in Cell & bioscience (17-05-2024)
    “…Methylmalonic acidemia (MMA) is a rare inborn error of propionate metabolism caused by deficiency of the mitochondrial methylmalonyl-CoA mutase (MUT) enzyme…”
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    Steric hindrance of SNARE transmembrane domain organization impairs the hemifusion-to-fusion transition by D'Agostino, Massimo, Risselada, Herre Jelger, Mayer, Andreas

    Published in EMBO reports (01-11-2016)
    “…SNAREs fuse membranes in several steps. Trans ‐SNARE complexes juxtapose membranes, induce hemifused stalk structures, and open the fusion pore. A recent…”
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    ER Reorganization is Remarkably Induced in COS-7 Cells Accumulating Transmembrane Protein Receptors Not Competent for Export from the Endoplasmic Reticulum by D’Agostino, Massimo, Crespi, Arianna, Polishchuk, Elena, Generoso, Serena, Martire, Gianluca, Colombo, Sara Francesca, Bonatti, Stefano

    Published in The Journal of membrane biology (01-11-2014)
    “…The newly synthesized mutant L501fsX533 Frizzled-4 form and the alpha3beta4 nicotinic acetylcholine receptor expressed in the absence of nicotine accumulate in…”
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