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Mitochondrial diseases and the role of the yeast models

Published:2010-10-14 Issue:8 Volume:10 Page:1006-1022
ISSN:1567-1356
Container-title:FEMS Yeast Research
language:en
Short-container-title:

Author:

Rinaldi Teresa,Dallabona Cristina,Ferrero Ileana,Frontali Laura,Bolotin-Fukuhara Monique

Publisher

Oxford University Press (OUP)

Subject

Applied Microbiology and Biotechnology,General Medicine,Microbiology

Link

http://academic.oup.com/femsyr/article-pdf/10/8/1006/17939362/10-8-1006.pdf

Reference172 articles.

1. Expanding insights of mitochondrial dysfunction in Parkinson's disease;Abou-Sleiman;Nat Rev Neurosci,2006

2. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28;Alexander;Nat Genet,2000

3. OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes;Amati-Bonneau;Brain,2008

4. Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma;Astuti;Am J Hum Genet,2001

5. Isolation of drugs active against mammalian prions using a yeast-based screening assay;Bach;Nat Biotechnol,2003

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