In: PLOS ONE
5(7), e11783
[PDF, 3MB]
Abstract
Mutations in the gene encoding the E3 ubiquitin ligase parkin (PARK2) are responsible for the majority of autosomal recessive parkinsonism. Similarly to other knockout mouse models of PD-associated genes, parkin knockout mice do not show a substantial neuropathological or behavioral phenotype, while loss of parkin in Drosophila melanogaster leads to a severe phenotype, including reduced lifespan, apoptotic flight muscle degeneration and male sterility. In order to study the function of parkin in more detail and to address possible differences in its role in different species, we chose Danio rerio as a different vertebrate model system.
Dokumententyp: | Zeitschriftenartikel |
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Publikationsform: | Publisher's Version |
Fakultät: | Medizin |
Themengebiete: | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit |
URN: | urn:nbn:de:bvb:19-epub-15060-3 |
ISSN: | 1932-6203 |
Sprache: | Englisch |
Dokumenten ID: | 15060 |
Datum der Veröffentlichung auf Open Access LMU: | 03. Mai 2013, 07:38 |
Letzte Änderungen: | 04. Nov. 2020, 12:55 |