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DJ1 represses glycolysis and cell proliferation by transcriptionally upregulating pink1
DJ1 is a multifunctional protein whose mutations cause autosomal recessive early-onset Parkinson disease (PD). DJ1 loss of function disrupts mitochondrial function, but the signaling pathway whereby it interferes with energy metabolism is unknown. Here, we found that mouse embryonic fibroblasts obta...
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| Publicado no: | Biochem J |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4385472/ https://ncbi.nlm.nih.gov/pubmed/25670069 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BJ20141025 |
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