Comparative study of behavioural tests in the SOD1G93A mouse model of amyotrophic lateral sclerosis
Author:
Affiliation:
1. LAGENBIO-I3A, Facultad de Veterinaria, IIS Aragón, Universidad de Zaragoza, Miguel Servet 177, 50013 Zaragoza, Spain
Publisher
Japanese Association for Laboratory Animal Science
Subject
General Veterinary,General Biochemistry, Genetics and Molecular Biology,Animal Science and Zoology,General Medicine
Link
https://www.jstage.jst.go.jp/article/expanim/64/2/64_14-0077/_pdf
Reference24 articles.
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2. 2. Aartsma-Rus A. and van Putten M. 2014. Assessing functional performance in the mdx mouse model. J. Vis. Exp.e51303.
3. 3. Azari M.F., Lopes E.C., Stubna C., Turner B.J., Zang D., Nicola N.A., Kurek J.B., and Cheema S.S. 2003. Behavioural and anatomical effects of systemically administered leukemia inhibitory factor in the SOD1(G93A G1H) mouse model of familial amyotrophic lateral sclerosis. Brain Res. 982: 92–97.
4. 4. Azzouz M., Leclerc N., Gurney M., Warter J.M., Poindron P., and Borg J. 1997. Progressive motor neuron impairment in an animal model of familial amyotrophic lateral sclerosis. Muscle Nerve 20: 45–51.
5. 5. Brooks S.P. and Dunnett S.B. 2009. Tests to assess motor phenotype in mice: a user’s guide. Nat. Rev. Neurosci. 10: 519–529Review.
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