Divergent Effects of G2019S and R1441C LRRK2 Mutations on LRRK2 and Rab10 Phosphorylations in Mouse Tissues

Mutations in LRRK2 cause familial Parkinson’s disease and common variants increase disease risk. LRRK2 kinase activity and cellular localization are tightly regulated by phosphorylation of key residues, primarily Ser1292 and Ser935, which impacts downstream phosphorylation of its substrates, among w...

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Detalles Bibliográficos
Autores principales: Iannotta, Lucia, Biosa, Alice, Kluss, Jillian H., Tombesi, Giulia, Kaganovich, Alice, Cogo, Susanna, Plotegher, Nicoletta, Civiero, Laura, Lobbestael, Evy, Baekelandt, Veerle, Cookson, Mark R., Greggio, Elisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690595/
https://www.ncbi.nlm.nih.gov/pubmed/33105882
http://dx.doi.org/10.3390/cells9112344

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690595/
https://www.ncbi.nlm.nih.gov/pubmed/33105882
http://dx.doi.org/10.3390/cells9112344

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