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  • PARKINSON’S DISEASE-ASSOCIATED MUTATIONS IN LRRK2 CAUSE CENTROSOMAL DEFECTS VIA RAB8A PHOSPHORYLATION.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P1501, doi. 10.1016/j.jalz.2017.07.604
    By:
    • Madero-Pérez, Jesús;
    • Fdez, Elena;
    • Fernández, Belén;
    • Lara Ordóñez, Antonio J.;
    • Ramírez, Marian Blanca;
    • Gómez-Suaga, Patricia;
    • Waschbüsch, Dieter;
    • Lobbestael, Evy;
    • Baekelandt, Veerle;
    • Nairn, Angus C.;
    • Ruiz-Martínez, Javier;
    • Aiastui, Ana;
    • de Munaín, Adolfo López;
    • Lis, Pawel;
    • Comptdaer, Thomas;
    • Taymans, Jean-Marc;
    • Chartier-Harlin, Marie-Christine;
    • Beilina, Alexandra;
    • Gonnelli, Adriano;
    • Cookson, Mark R.
    Publication type:
    Article

  • Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation.

    Published in:
    Molecular Neurodegeneration, 2018, v. 13, p. 1, doi. 10.1186/s13024-018-0235-y
    By:
    • Madero-Pérez, Jesús;
    • Fdez, Elena;
    • Fernández, Belén;
    • Lara Ordóñez, Antonio J.;
    • Blanca Ramírez, Marian;
    • Gómez-Suaga, Patricia;
    • Waschbüsch, Dieter;
    • Lobbestael, Evy;
    • Baekelandt, Veerle;
    • Nairn, Angus C.;
    • Ruiz-Martínez, Javier;
    • Aiastui, Ana;
    • López de Munain, Adolfo;
    • Lis, Pawel;
    • Comptdaer, Thomas;
    • Taymans, Jean-Marc;
    • Chartier-Harlin, Marie-Christine;
    • Beilina, Alexandria;
    • Gonnelli, Adriano;
    • Cookson, Mark R.
    Publication type:
    Article