Additional file 1: Figure S1. of Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation

Madero-Pérez, Jesús; Fdez, Elena; Fernández, Belén; Lara Ordóñez, Antonio; Blanca Ramírez, Marian; Gómez-Suaga, Patricia; Waschbüsch, Dieter; Lobbestael, Evy; Baekelandt, Veerle; Nairn, Angus; 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; Greggio, Elisa; Hilfiker, Sabine

doi:10.6084/m9.figshare.5811912.v1

13024_2018_235_MOESM1_ESM.docx (1.13 MB)

Additional file 1: Figure S1. of Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation

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posted on 2018-01-23, 05:00 authored by Jesús Madero-Pérez, Elena Fdez, Belén Fernández, Antonio Lara Ordóñez, Marian Blanca Ramírez, Patricia Gómez-Suaga, Dieter Waschbüsch, Evy Lobbestael, Veerle Baekelandt, Angus Nairn, Javier Ruiz-Martínez, Ana Aiastui, Adolfo López de Munain, Pawel Lis, Thomas Comptdaer, Jean-Marc Taymans, Marie-Christine Chartier-Harlin, Alexandria Beilina, Adriano Gonnelli, Mark Cookson, Elisa Greggio, Sabine Hilfiker

Distinct pathogenic LRRK2 mutants cause deficits in centrosome cohesion in transfected HEK293T cells. (DOCX 1160 kb)

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Michael J. Fox Foundation for Parkinson's Research

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Centrosome LRRK2 Parkinson’s disease Phosphorylation Rab8a

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Additional file 1: Figure S1. of Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation

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Michael J. Fox Foundation for Parkinson's Research

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