High LRRK2 Levels Fail to Induce or Exacerbate Neuronal Alpha-Synucleinopathy in Mouse Brain

The G2019S mutation in the multidomain protein leucine-rich repeat kinase 2 (LRRK2) is one of the most frequently identified genetic causes of Parkinson’s disease (PD). Clinically, LRRK2(G2019S) carriers with PD and idiopathic PD patients have a very similar disease with brainstem and cortical Lewy...

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Detalles Bibliográficos
Autores principales: Herzig, Martin C., Bidinosti, Michael, Schweizer, Tatjana, Hafner, Thomas, Stemmelen, Christine, Weiss, Andreas, Danner, Simone, Vidotto, Nella, Stauffer, Daniela, Barske, Carmen, Mayer, Franziska, Schmid, Peter, Rovelli, Giorgio, van der Putten, P. Herman, Shimshek, Derya R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352901/
https://www.ncbi.nlm.nih.gov/pubmed/22615783
http://dx.doi.org/10.1371/journal.pone.0036581

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352901/
https://www.ncbi.nlm.nih.gov/pubmed/22615783
http://dx.doi.org/10.1371/journal.pone.0036581

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