Mitigating Motor Neuronal Loss in C. elegans Model of ALS8
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-017-11798-6.pdf
Reference41 articles.
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3. Millecamps, S. et al. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations. Journal of medical genetics 47, 554–560, doi: https://doi.org/10.1136/jmg.2010.077180 (2010).
4. Kanekura, K., Nishimoto, I., Aiso, S. & Matsuoka, M. Characterization of amyotrophic lateral sclerosis-linked P56S mutation of vesicle-associated membrane protein-associated protein B (VAPB/ALS8). The Journal of biological chemistry 281, 30223–30233, doi: https://doi.org/10.1074/jbc.M605049200 (2006).
5. Tran, D., Chalhoub, A., Schooley, A., Zhang, W. & Ngsee, J. K. A mutation in VAPB that causes amyotrophic lateral sclerosis also causes a nuclear envelope defect. Journal of cell science 125, 2831–2836, doi: https://doi.org/10.1242/jcs.102111 (2012).
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