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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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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
American Society for Biochemistry and Molecular Biology
2010
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3000953/ https://ncbi.nlm.nih.gov/pubmed/20938049 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M110.137034 |
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