Recent advances and new perspectives in mitochondrial dysfunction
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
https://www.nature.com/articles/s41598-023-34624-8.pdf
Reference17 articles.
1. Ardissone, A. et al. Clinical, imaging, biochemical and molecular features in Leigh syndrome: A study from the Italian network of mitochondrial diseases. Orphanet. J. Rare Dis. 16, 413 (2021).
2. Johnston, D. S., Su, Y. A. & Alesci, S. Mitochondrial gene profiling: Translational perspectives. Pharmacogenomics 10, 1645–1655 (2009).
3. Mey, G. M., Mahajan, K. R. & DeSilva, T. M. Neurodegeneration in multiple sclerosis. WIREs Mech. Dis. 15, e1583 (2023).
4. Nolin, S. L., Napoli, E., Flores, A., Hagerman, R. J. & Giulivi, C. Deficits in prenatal serine biosynthesis underlie the mitochondrial dysfunction associated with the Autism-linked FMR1 gene. Int. J. Mol. Sci. 22, 5886 (2021).
5. Schmidt, R. J., Liang, D., Busgang, S. A., Curtin, P. & Giulivi, C. Maternal plasma metabolic profile demarcates a role for neuroinflammation in non-typical development of children. Metabolites 11, 545 (2021).
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