Works by Liparulo, Irene


Results: 10
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    MiR-494 induces metabolic changes through G6pc targeting and modulates sorafenib response in hepatocellular carcinoma.

    Published in:
    Journal of Experimental & Clinical Cancer Research (17569966), 2023, v. 42, n. 1, p. 1, doi. 10.1186/s13046-023-02718-w
    By:
    • Bergamini, Christian;
    • Leoni, Ilaria;
    • Rizzardi, Nicola;
    • Melli, Mattia;
    • Galvani, Giuseppe;
    • Coada, Camelia Alexandra;
    • Giovannini, Catia;
    • Monti, Elisa;
    • Liparulo, Irene;
    • Valenti, Francesca;
    • Ferracin, Manuela;
    • Ravaioli, Matteo;
    • Cescon, Matteo;
    • Vasuri, Francesco;
    • Piscaglia, Fabio;
    • Negrini, Massimo;
    • Stefanelli, Claudio;
    • Fato, Romana;
    • Gramantieri, Laura;
    • Fornari, Francesca
    Publication type:
    Article
    3

    Coenzyme Q Depletion Reshapes MCF-7 Cells Metabolism.

    Published in:
    International Journal of Molecular Sciences, 2021, v. 22, n. 1, p. 198, doi. 10.3390/ijms22010198
    By:
    • Wang, Wenping;
    • Liparulo, Irene;
    • Rizzardi, Nicola;
    • Bolignano, Paola;
    • Calonghi, Natalia;
    • Bergamini, Christian;
    • Fato, Romana
    Publication type:
    Article
    4
    5

    A coordinated multiorgan metabolic response contributes to human mitochondrial myopathy.

    Published in:
    EMBO Molecular Medicine, 2023, v. 15, n. 7, p. 1, doi. 10.15252/emmm.202216951
    By:
    • Southwell, Nneka;
    • Primiano, Guido;
    • Nadkarni, Viraj;
    • Attarwala, Nabeel;
    • Beattie, Emelie;
    • Miller, Dawson;
    • Alam, Sumaitaah;
    • Liparulo, Irene;
    • Shurubor, Yevgeniya I;
    • Valentino, Maria Lucia;
    • Carelli, Valerio;
    • Servidei, Serenella;
    • Gross, Steven S;
    • Manfredi, Giovanni;
    • Chen, Qiuying;
    • D'Aurelio, Marilena
    Publication type:
    Article
    6
    7

    Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy.

    Published in:
    2021
    By:
    • Bonora, Elena;
    • Chakrabarty, Sanjiban;
    • Kellaris, Georgios;
    • Tsutsumi, Makiko;
    • Bianco, Francesca;
    • Bergamini, Christian;
    • Ullah, Farid;
    • Isidori, Federica;
    • Liparulo, Irene;
    • Diquigiovanni, Chiara;
    • Masin, Luca;
    • Rizzardi, Nicola;
    • Cratere, Mariapia Giuditta;
    • Boschetti, Elisa;
    • Papa, Valentina;
    • Maresca, Alessandra;
    • Cenacchi, Giovanna;
    • Casadio, Rita;
    • Martelli, Pierluigi;
    • Matera, Ivana
    Publication type:
    journal article
    8

    A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism.

    Published in:
    FASEB Journal, 2019, v. 33, n. 10, p. 1, doi. 10.1096/fj.201802722R
    By:
    • Diquigiovanni, Chiara;
    • Bergamini, Christian;
    • Diaz, Rebeca;
    • Liparulo, Irene;
    • Bianco, Francesca;
    • Masin, Luca;
    • Baldassarro, Vito Antonio;
    • Rizzardi, Nicola;
    • Tranchina, Antonia;
    • Buscherini, Francesco;
    • Wischmeijer, Anita;
    • Pippucci, Tommaso;
    • Scarano, Emanuela;
    • Cordelli, Duccio Maria;
    • Fato, Romana;
    • Seri, Marco;
    • Paracchini, Silvia;
    • Bonora, Elena
    Publication type:
    Article
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