Combining comparative proteomics and molecular genetics uncovers regulators of synaptic and axonal stability and degeneration in vivo.
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Authors
Rooney, Timothy M
Lamont, Douglas J
Wright, Ann K
Jackson, Mandy
Publication Date
2012-01Journal Title
PLoS genetics
ISSN
1553-7390
Volume
8
Issue
8
Pages
e1002936
Language
eng
Type
Article
This Version
VoR
Physical Medium
Print-Electronic
Metadata
Show full item recordCitation
Wishart, T. M., Rooney, T. M., Lamont, D. J., Wright, A. K., Morton, J., Jackson, M., Freeman, M. R., & et al. (2012). Combining comparative proteomics and molecular genetics uncovers regulators of synaptic and axonal stability and degeneration in vivo.. PLoS genetics, 8 (8), e1002936. https://doi.org/10.1371/journal.pgen.1002936
Keywords
Axons, Synapses, Animals, Mice, Drosophila, Huntington Disease, Brain Injuries, Spinocerebellar Ataxias, Nerve Degeneration, Wallerian Degeneration, Thiolester Hydrolases, Aldehyde Dehydrogenase, Drosophila Proteins, Molecular Chaperones, Proteomics, Mutation, HSP40 Heat-Shock Proteins, rho-Associated Kinases, S100 Calcium Binding Protein G, Calbindin 2
Identifiers
External DOI: https://doi.org/10.1371/journal.pgen.1002936
This record's URL: https://www.repository.cam.ac.uk/handle/1810/302160