Search Results - "Caddeo, Andrea"

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  1. 1

    LPIAT1/MBOAT7 contains a catalytic dyad transferring polyunsaturated fatty acids to lysophosphatidylinositol by Caddeo, Andrea, Hedfalk, Kristina, Romeo, Stefano, Pingitore, Piero

    “…Human membrane bound O-acyltransferase domain-containing 7 (MBOAT7), also known as lysophosphatidylinositol acyltransferase 1 (LPIAT1), is an enzyme involved…”
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    TG68, a Novel Thyroid Hormone Receptor-β Agonist for the Treatment of NAFLD by Caddeo, Andrea, Kowalik, Marta Anna, Serra, Marina, Runfola, Massimiliano, Bacci, Andrea, Rapposelli, Simona, Columbano, Amedeo, Perra, Andrea

    “…Activation of thyroid hormone receptor β (THRβ) has shown beneficial effects on metabolic alterations, including non-alcoholic fatty liver disease (NAFLD)…”
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  3. 3

    Identification of novel loss of function variants in MBOAT7 resulting in intellectual disability by Heidari, Erfan, Caddeo, Andrea, Zarabadi, Kiana, Masoudi, Maryam, Tavasoli, Ali Reza, Romeo, Stefano, Garshasbi, Masoud

    Published in Genomics (San Diego, Calif.) (01-11-2020)
    “…The membrane bound O-acyltransferase domain-containing 7 (MBOAT7) gene codes for an enzyme involved in regulating arachidonic acid incorporation in…”
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    Potential use of TG68 - A novel thyromimetic - for the treatment of non-alcoholic fatty liver (NAFLD)-associated hepatocarcinogenesis by Caddeo, Andrea, Serra, Marina, Sedda, Francesca, Bacci, Andrea, Manera, Clementina, Rapposelli, Simona, Columbano, Amedeo, Perra, Andrea, Kowalik, Marta Anna

    Published in Frontiers in oncology (23-02-2023)
    “…Several lines of evidence suggest that the thyroid hormone signaling pathway is altered in patients with NAFLD and that pharmacological strategies to target…”
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    Precision medicine and nucleotide-based therapeutics to treat MASH by Caddeo, Andrea, Romeo, Stefano

    Published in Clinical and molecular hepatology (05-08-2024)
    “…Metabolic dysfunction-associated steatotic liver disease (MASLD) is a complex multifactorial disease and becoming the leading cause of liver-related morbidity…”
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    MBOAT7 in liver and extrahepatic diseases by Caddeo, Andrea, Spagnuolo, Rocco, Maurotti, Samantha

    Published in Liver international (01-11-2023)
    “…Abstract MBOAT7 is a protein anchored to endomembranes by several transmembrane domains. It has a catalytic dyad involved in remodelling of…”
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    3D culture models to study pathophysiology of steatotic liver disease by Caddeo, Andrea, Maurotti, Samantha, Kovooru, Lohitesh, Romeo, Stefano

    Published in Atherosclerosis (01-06-2024)
    “…Steatotic liver disease (SLD) refers to a spectrum of diseases caused by hepatic lipid accumulation. SLD has emerged as the leading cause of chronic liver…”
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    MBOAT7 is anchored to endomembranes by six transmembrane domains by Caddeo, Andrea, Jamialahmadi, Oveis, Solinas, Giovanni, Pujia, Arturo, Mancina, Rosellina Margherita, Pingitore, Piero, Romeo, Stefano

    Published in Journal of structural biology (01-06-2019)
    “…[Display omitted] •MBOAT7 is a protein strongly attached to endomembranes;•In silico analysis predicted a number of TMDs of MBOAT7 ranging from 5 to 12;•In…”
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    Metabolic reprogramming in Nrf2-driven proliferation of normal rat hepatocytes by Kowalik, Marta A, Taguchi, Keiko, Serra, Marina, Caddeo, Andrea, Puliga, Elisabetta, Bacci, Marina, Koshiba, Seizo, Inoue, Jin, Hishinuma, Eiji, Morandi, Andrea, Giordano, Silvia, Perra, Andrea, Yamamoto, Masayuki, Columbano, Amedeo

    Published in Hepatology (Baltimore, Md.) (01-04-2024)
    “…Cancer cells reprogram their metabolic pathways to support bioenergetic and biosynthetic needs and to maintain their redox balance. In several human tumors,…”
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    Molecular analysis of three known and one novel LPL variants in patients with type I hyperlipoproteinemia by Caddeo, A., Mancina, R.M., Pirazzi, C., Russo, C., Sasidharan, K., Sandstedt, J., Maurotti, S., Montalcini, T., Pujia, A., Leren, T.P., Romeo, S., Pingitore, P.

    “…Type I hyperlipoproteinemia, also known as familial chylomicronemia syndrome (FCS), is a rare autosomal recessive disorder caused by variants in LPL, APOC2,…”
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