Transcriptional responses to loss or gain of function of the leucine-rich repeat kinase 2 (LRRK2) gene uncover biological processes modulated by LRRK2 activity

Mutations in the leucine-rich repeat kinase 2 gene (LRRK2) are the most common genetic cause of Parkinson's disease (PD) and cause both autosomal dominant familial and sporadic PD. Currently, the physiological and pathogenic activities of LRRK2 are poorly understood. To decipher the biological...

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Detaylı Bibliyografya
Asıl Yazarlar: Nikonova, Elena V., Xiong, Yulan, Tanis, Keith Q., Dawson, Valina L., Vogel, Robert L., Finney, Eva M., Stone, David J., Reynolds, Ian J., Kern, Jonathan T., Dawson, Ted M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2012
Konular:
Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3235012/
https://ncbi.nlm.nih.gov/pubmed/21972245
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr451
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