GTP binding regulates cellular localization of Parkinson's disease-associated LRRK2

Mutations in leucine-rich repeat kinase 2 (LRRK2) comprise the most common cause of familial Parkinson's disease (PD), and sequence variants modify risk for sporadic PD. Previous studies indicate that LRRK2 interacts with microtubules (MTs) and alters MT-mediated vesicular transport processes....

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Hum Mol Genet
Autors principals: Blanca Ramírez, Marian, Ordóñez, Antonio Jesús Lara, Fdez, Elena, Madero-Pérez, Jesús, Gonnelli, Adriano, Drouyer, Matthieu, Chartier-Harlin, Marie-Christine, Taymans, Jean-Marc, Bubacco, Luigi, Greggio, Elisa, Hilfiker, Sabine
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2017
Matèries:
Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5886193/
https://ncbi.nlm.nih.gov/pubmed/28453723
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddx161
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars