LRRK2 Modulates Vulnerability to Mitochondrial Dysfunction in Caenorhabditis elegans

Mutations in leucine-rich repeat kinase 2 (LRRK2) cause autosomal-dominant familial Parkinson's disease. We generated lines of Caenorhabditis elegans expressing neuronally directed human LRRK2. Expressing human LRRK2 increased nematode survival in response to rotenone or paraquat, which are age...

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Autori principali: Saha, Shamol, Guillily, Maria D., Ferree, Andrew, Lanceta, Joel, Chan, Diane, Ghosh, Joy, Hsu, Cindy H., Segal, Lilach, Raghavan, Kesav, Matsumoto, Kunihiro, Hisamoto, Naoki, Kuwahara, Tomoki, Iwatsubo, Takeshi, Moore, Landon, Goldstein, Lee, Cookson, Mark, Wolozin, Benjamin
Natura: Artigo
Lingua:Inglês
Pubblicazione: Society for Neuroscience 2009
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3127548/
https://ncbi.nlm.nih.gov/pubmed/19625511
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.2281-09.2009
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