Загрузка...

RAB7L1-Mediated Relocalization of LRRK2 to the Golgi Complex Causes Centrosomal Deficits via RAB8A

Mutations in the LRRK2 gene cause autosomal-dominant Parkinson’s disease (PD), and both LRRK2 as well as RAB7L1 have been implicated in increased susceptibility to idiopathic PD. RAB7L1 has been shown to increase membrane-association and kinase activity of LRRK2, and both seem to be mechanistically...

Полное описание

Сохранить в:
Библиографические подробности
Опубликовано в: :Front Mol Neurosci
Главные авторы: Madero-Pérez, Jesús, Fernández, Belén, Lara Ordóñez, Antonio Jesús, Fdez, Elena, Lobbestael, Evy, Baekelandt, Veerle, Hilfiker, Sabine
Формат: Artigo
Язык:Inglês
Опубликовано: Frontiers Media S.A. 2018
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC6243087/
https://ncbi.nlm.nih.gov/pubmed/30483055
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnmol.2018.00417
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!