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Mitochondrial energy metabolism is required for lifespan extension by the spastic paraplegia-associated protein spartin
Hereditary spastic paraplegias, a group of neurodegenerative disorders, can be caused by loss-of-function mutations in the protein spartin. However, the physiological role of spartin remains largely elusive. Here we show that heterologous expression of human or Drosophila spartin extends chronologic...
Autores principales: | Ring, Julia, Rockenfeller, Patrick, Abraham, Claudia, Tadic, Jelena, Poglitsch, Michael, Schimmel, Katherina, Westermayer, Julia, Schauer, Simon, Achleitner, Bettina, Schimpel, Christa, Moitzi, Barbara, Rechberger, Gerald N., Sigrist, Stephan J., Carmona-Gutierrez, Didac, Kroemer, Guido, Büttner, Sabrina, Eisenberg, Tobias, Madeo, Frank |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shared Science Publishers OG
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722644/ https://www.ncbi.nlm.nih.gov/pubmed/29234670 http://dx.doi.org/10.15698/mic2017.12.603 |
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