Unravelling the enigma of selective vulnerability in neurodegeneration: motor neurons resistant to degeneration in ALS show distinct gene expression characteristics and decreased susceptibility to excitotoxicity.

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Authors
Brockington, Alice
  Ning, Ke
Heath, Paul R
Wood, Elizabeth
  Kirby, Janine
Fusi, Nicolò
  Lawrence, Neil
Publication Date
2013-01
Journal Title
Acta neuropathologica
ISSN
0001-6322
Publisher
Springer Science and Business Media LLC
Volume
125
Issue
1
Pages
95-109
Language
eng
Type
Article
This Version
VoR
Physical Medium
Print-Electronic
Metadata
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Citation
Brockington, A., Ning, K., Heath, P. R., Wood, E., Kirby, J., Fusi, N., Lawrence, N., et al. (2013). Unravelling the enigma of selective vulnerability in neurodegeneration: motor neurons resistant to degeneration in ALS show distinct gene expression characteristics and decreased susceptibility to excitotoxicity.. Acta neuropathologica, 125 (1), 95-109. https://doi.org/10.1007/s00401-012-1058-5
Keywords
Spinal Cord, Motor Neurons, Humans, Amyotrophic Lateral Sclerosis, Genetic Predisposition to Disease, Nerve Degeneration, gamma-Aminobutyric Acid, Receptors, AMPA, Synaptic Transmission, Gene Expression Regulation, Aged, Middle Aged, Female, Male
Identifiers
External DOI: https://doi.org/10.1007/s00401-012-1058-5
This record's URL: https://www.repository.cam.ac.uk/handle/1810/300878

Rights
Attribution 4.0 International
Licence URL: https://creativecommons.org/licenses/by/4.0/

Attribution 4.0 International
Except where otherwise noted, this item's licence is described as Attribution 4.0 International