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Metabolic dysregulation in the Atp7b(−/−) Wilson’s disease mouse model
Inactivating mutations in the copper transporter Atp7b result in Wilson’s disease. The Atp7b(−/−) mouse develops hallmarks of Wilson’s disease. The activity of several nuclear receptors decreased in Atp7b(−/−) mice, and nuclear receptors are critical for maintaining metabolic homeostasis. Therefore,...
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Publicado no: | Proc Natl Acad Sci U S A |
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Main Authors: | , , , , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
National Academy of Sciences
2020
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6994990/ https://ncbi.nlm.nih.gov/pubmed/31924743 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1914267117 |
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