Human DJ-1-specific Transcriptional Activation of Tyrosine Hydroxylase Gene

Loss-of-function mutation in the DJ-1 gene causes a subset of familial Parkinson disease. The mechanism underlying DJ-1-related selective vulnerability in the dopaminergic pathway is, however, not known. DJ-1 has multiple functions, including transcriptional regulation, and one of transcriptional ta...

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Detalles Bibliográficos
Autores principales: Ishikawa, Shizuma, Taira, Takahiro, Takahashi-Niki, Kazuko, Niki, Takeshi, Ariga, Hiroyoshi, Iguchi-Ariga, Sanae M. M.
Formato: Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2010
Materias:
Gene Regulation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000953/
https://www.ncbi.nlm.nih.gov/pubmed/20938049
http://dx.doi.org/10.1074/jbc.M110.137034

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000953/
https://www.ncbi.nlm.nih.gov/pubmed/20938049
http://dx.doi.org/10.1074/jbc.M110.137034

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