Disruption of Mitochondrial Quality Control in Inherited Metabolic Disorders
Author:
Funder
National Institute of Brain Health, INSC
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s12035-024-04467-z.pdf
Reference71 articles.
1. Ferreira CR, Rahman S, Keller M et al (2021) An international classification of inherited metabolic disorders ( ICIMD ). J Inherit Metab Dis 44:164–177. https://doi.org/10.1002/jimd.12348
2. Saudubray J-M, Garcia-Cazorla À (2018) Inborn errors of metabolism overview. Pediatr Clin North Am 65:179–208. https://doi.org/10.1016/j.pcl.2017.11.002
3. Baker BM, Haynes CM (2011) Mitochondrial protein quality control during biogenesis and aging. Trends Biochem Sci 36:254–261. https://doi.org/10.1016/j.tibs.2011.01.004
4. Olichon A, Emorine LJ, Descoins E et al (2002) The human dynamin-related protein OPA1 is anchored to the mitochondrial inner membrane facing the inter-membrane space. FEBS Lett 523:171–176. https://doi.org/10.1016/s0014-5793(02)02985-x
5. Ishihara N, Fujita Y, Oka T, Mihara K (2006) Regulation of mitochondrial morphology through proteolytic cleavage of OPA1. EMBO J 25:2966–2977. https://doi.org/10.1038/sj.emboj.7601184
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