Assessing disease onset and progression in the SOD1 mouse model of ALS
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Neuroscience
Reference13 articles.
1. Pathways to motor neuron degeneration in transgenic mouse models
2. Motor Neuron Degeneration in Mice that Express a Human Cu,Zn Superoxide Dismutase Mutation
3. A low expressor line of transgenic mice carrying a mutant human Cu,Zn superoxide dismutase ( SOD1 ) gene develops pathological changes that most closely resemble those in human amyotrophic lateral sclerosis
4. Transgenic mouse model for familial amyotrophic lateral sclerosis with superoxide dismutase-1 mutation
5. Neuroprotective effects of creatine in a transgenic animal model of amyotrophic lateral sclerosis
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