2022
DOI: 10.1080/01677063.2022.2144292
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Reduced branched-chain aminotransferase activity alleviates metabolic vulnerability caused by dim light exposure at night in Drosophila

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Cited by 6 publications
(2 citation statements)
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“…Altered circadian rhythm has been associated with SCA in several studies. (Kim, Lim, et al, 2021; Motolese et al, 2020; Petsakou et al, 2015; Pfeffer et al, 2017; Tsimpanouli, Ghimire, Barget, Weston, Costa, et al, 2022; Tsimpanouli, Ghimire, Barget, Weston, Paulson, et al, 2022). Type 3 SCA transgenic mice, show increased fragmentation in all sleep and wakefulness states, larger oscillations of beta power during REM and non‐REM sleep, indicating that common sleep‐related etiological factors may underlie the SCA3 phenotypes of mice (Tsimpanouli, Ghimire, Barget, Weston, Paulson, et al, 2022).…”
Section: Neurodegenerative Diseasesmentioning
confidence: 99%
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“…Altered circadian rhythm has been associated with SCA in several studies. (Kim, Lim, et al, 2021; Motolese et al, 2020; Petsakou et al, 2015; Pfeffer et al, 2017; Tsimpanouli, Ghimire, Barget, Weston, Costa, et al, 2022; Tsimpanouli, Ghimire, Barget, Weston, Paulson, et al, 2022). Type 3 SCA transgenic mice, show increased fragmentation in all sleep and wakefulness states, larger oscillations of beta power during REM and non‐REM sleep, indicating that common sleep‐related etiological factors may underlie the SCA3 phenotypes of mice (Tsimpanouli, Ghimire, Barget, Weston, Paulson, et al, 2022).…”
Section: Neurodegenerative Diseasesmentioning
confidence: 99%
“…Nevertheless, reduced CLOCK and BMAL1 expression levels were found in dermal fibroblasts derived from type 17 SCA patients (Motolese et al, 2020). Furthermore, a recent study by Kim, Lim, et al (2021)) showed that the expansion of polyglutamine repeats in Ataxin‐1, a gene linked to SCA type 1, leads to disrupted circadian rhythms in Drosophila, which may contribute to disease pathogenesis. These differences in gene expression found by the studies may be because SCA comprises a heterogeneous group of subtypes depending on the locus or causative gene.…”
Section: Neurodegenerative Diseasesmentioning
confidence: 99%