Effect of 3-nitropropionic acid on sirtuin gene expression in Sirt3 deficient mice
Huntington's disease (HD) is an autosomal inherited progressive neurodegenerative disorder which is caused by the CAG trinucleotide repeat in the huntingtin gene. The mutation induces mitochondrial dysfunction in neurons, which leads to striatal neuronal loss. The efficacy of the available ther...
Elmentve itt :
| Szerzők: | |
|---|---|
| Dokumentumtípus: | Cikk |
| Megjelent: |
2024
|
| Sorozat: | NEUROSCIENCE LETTERS
836 |
| Tárgyszavak: | |
| doi: | 10.1016/j.neulet.2024.137882 |
| mtmt: | 35068067 |
| Online Access: | http://publicatio.bibl.u-szeged.hu/33512 |