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Progressive Impairment of Lactate-based Gluconeogenesis in the Huntington’s Disease Mouse Model R6/2
Huntington’s disease (HD) is a neurodegenerative illness, where selective neuronal loss in the brain caused by expression of mutant huntingtin protein leads to motor dysfunction and cognitive decline in addition to peripheral metabolic changes. In this study we confirm our previous observation of im...
Tallennettuna:
| Julkaisussa: | PLoS Curr |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Public Library of Science
2015
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4447482/ https://ncbi.nlm.nih.gov/pubmed/26064782 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/currents.hd.019b33aae1c519e6e8b68e7cf3e7818e |
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