Works by Davidson, Mercy M.


Results: 15
    1
    2

    Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene.

    Published in:
    Nature Genetics, 1999, v. 23, n. 3, p. 333, doi. 10.1038/15513
    By:
    • Papadopoulou, Lefkothea C.;
    • Sue, Carolyn M.;
    • Davidson, Mercy M.;
    • Tanji, Kurenai;
    • Nishino, Ichizo;
    • Sadlock, James E.;
    • Krishna, Sindu;
    • Walker, Winsome;
    • Selby, Jeanette;
    • Glerum, D. Moira;
    • Coster, Rudy Van;
    • Lyon, Gilles;
    • Scalais, Emmanuel;
    • Lebel, Roger;
    • Kaplan, Paige;
    • Shanske, Sara;
    • De Vivo, Darryl C.;
    • Bonilla, Eduardo;
    • Hirano, Michio
    Publication type:
    Article
    3

    Sex-specific pathways in early cardiac response to pressure overload in mice.

    Published in:
    Journal of Molecular Medicine, 2008, v. 86, n. 9, p. 1013, doi. 10.1007/s00109-008-0385-4
    By:
    • Witt, Henning;
    • Schubert, Carola;
    • Jaekel, Juliane;
    • Fliegner, Daniela;
    • Penkalla, Adam;
    • Tiemann, Klaus;
    • Stypmann, Joerg;
    • Roepcke, Stefan;
    • Brokat, Sebastian;
    • Mahmoodzadeh, Shokoufeh;
    • Brozova, Eva;
    • Davidson, Mercy M.;
    • Ruiz Noppinger, Patricia;
    • Grohé, Christian;
    • Regitz-Zagrosek, Vera
    Publication type:
    Article
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    9

    SIRT3-mediated inhibition of FOS through histone H3 deacetylation prevents cardiac fibrosis and inflammation.

    Published in:
    Signal Transduction & Targeted Therapy, 2020, v. 5, n. 1, p. 1, doi. 10.1038/s41392-020-0114-1
    By:
    • Palomer, Xavier;
    • Román-Azcona, M. Silvia;
    • Pizarro-Delgado, Javier;
    • Planavila, Ana;
    • Villarroya, Francesc;
    • Valenzuela-Alcaraz, Brenda;
    • Crispi, Fátima;
    • Sepúlveda-Martínez, Álvaro;
    • Miguel-Escalada, Irene;
    • Ferrer, Jorge;
    • Nistal, J. Francisco;
    • García, Raquel;
    • Davidson, Mercy M.;
    • Barroso, Emma;
    • Vázquez-Carrera, Manuel
    Publication type:
    Article
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    12

    A functionally dominant mitochondrial DNA mutation.

    Published in:
    Human Molecular Genetics, 2008, v. 17, n. 12, p. 1814, doi. 10.1093/hmg/ddn073
    By:
    • Sacconi, Sabrina;
    • Salviati, Leonardo;
    • Nishigaki, Yutaka;
    • Walker, Winsome F.;
    • Hernandez-Rosa, Evelyn;
    • Trevisson, Eva;
    • Delplace, Severine;
    • Desnuelle, Claude;
    • Shanske, Sara;
    • Hirano, Michio;
    • Schon, Eric A.;
    • Bonilla, Eduardo;
    • De Vivo, Darryl C.;
    • DiMauro, Salvatore;
    • Davidson, Mercy M.
    Publication type:
    Article
    13
    14
    15

    Copper and bezafibrate cooperate to rescue cytochrome c oxidase deficiency in cells of patients with sco2 mutations.

    Published in:
    Orphanet Journal of Rare Diseases, 2012, v. 7, n. 1, p. 21, doi. 10.1186/1750-1172-7-21
    By:
    • Casarin, Alberto;
    • Giorgi, Gianpietro;
    • Pertegato, Vanessa;
    • Siviero, Roberta;
    • Cerqua, Cristina;
    • Doimo, Mara;
    • Basso, Giuseppe;
    • Sacconi, Sabrina;
    • Cassina, Matteo;
    • Rizzuto, Rosario;
    • Brosel, Sonja;
    • Davidson, Mercy M.;
    • DiMauro, Salvatore;
    • Schon, Eric A.;
    • Clementi, Maurizio;
    • Trevisson, Eva;
    • Salviati, Leonardo
    Publication type:
    Article