Parkin is a disease modifier in the mutant SOD1 mouse model of ALS.
- Published in:
- EMBO Molecular Medicine, 2018, v. 10, n. 10, p. N.PAG, doi. 10.15252/emmm.201808888
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- Publication type:
- Article
Works matching AU Palomo, Gloria M.
Results: 5
1
2
Sex specific activation of the ERα axis of the mitochondrial UPR (UPR<sup>mt</sup>) in the G93A-SOD1 mouse model of familial ALS.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1318, doi. 10.1093/hmg/ddx049
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- Publication type:
- Article
3
Silencing of frataxin gene expression triggers p53-dependent apoptosis in human neuron-like cells.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2807, doi. 10.1093/hmg/ddr187
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- Publication type:
- Article
4
ALS-FTLD-linked mutations of SQSTM1/p62 disrupt selective autophagy and NFE2L2/NRF2 anti-oxidative stress pathway.
- Published in:
- Autophagy, 2020, v. 16, n. 5, p. 917, doi. 10.1080/15548627.2019.1644076
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- Publication type:
- Article
5
Functional Recovery in a Friedreich's Ataxia Mouse Model by Frataxin Gene Transfer Using an HSV-1 Amplicon Vector.
- Published in:
- Molecular Therapy, 2007, v. 15, n. 6, p. 1072, doi. 10.1038/sj.mt.6300143
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- Publication type:
- Article