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Additional file 4 of The enhanced association between mutant CHMP2B and spastin is a novel pathological link between frontotemporal dementia and hereditary spastic paraplegias

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Additional file 1 of The enhanced association between mutant CHMP2B and spastin is a novel pathological link between frontotemporal dementia and hereditary spastic paraplegias

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Additional file 3 of The enhanced association between mutant CHMP2B and spastin is a novel pathological link between frontotemporal dementia and hereditary spastic paraplegias

Chen, Y., Krishnan, G., Parsi, S., Pons, M. C., Nikolaki, V., Cao, L., Xu, Z., & Gao, F. (2022) · Figshare · doi:10.6084/m9.figshare.21621920

Additional file 2 of The enhanced association between mutant CHMP2B and spastin is a novel pathological link between frontotemporal dementia and hereditary spastic paraplegias

Chen, Y., Krishnan, G., Parsi, S., Pons, M. C., Nikolaki, V., Cao, L., Xu, Z., & Gao, F. (2022) · Figshare · doi:10.6084/m9.figshare.21621917

Additional file 1 of Quantitative patterns of motor cortex proteinopathy across ALS genotypes

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Mutations in CHMP2B in Lower Motor Neuron Predominant Amyotrophic Lateral Sclerosis (ALS)

Cox, L. E., Ferraiuolo, L., Goodall, E. F., Heath, P. R., Higginbottom, A., Mortiboys, H., Hollinger, H. C., Hartley, J. A., Brockington, A., Burness, C. E., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009872 · Cited by 262

Defective neuronal and oligodendroglial differentiation by FTD3- and ALS17-associated Ile29-to-Val mutation of CHMP2B

Yamawaki, M., Akiba, M., Matsumoto, N., Watanabe, N., Hattori, K., Takeuchi, Y., Morimoto, T., Oizumi, H., Ohbuchi, K., Miyamoto, Y., et al. (2019) · Molecular Genetics and Metabolism Reports · doi:10.1016/j.ymgmr.2019.100458 · Cited by 2

A transgenic mouse expressing CHMP2Bintron5mutant in neurons develops histological and behavioural features of amyotrophic lateral sclerosis and frontotemporal dementia

Vernay, A., Therreau, L., Blot, B., Risson, V., Dirrig‐Grosch, S., Waegaert, R., Lequeu, T., Sellal, F., Schaeffer, L., Sadoul, R., et al. (2016) · Human Molecular Genetics · doi:10.1093/hmg/ddw182 · Cited by 35

Lessons learned from CHMP2B, implications for frontotemporal dementia and amyotrophic lateral sclerosis

Ugbode, C., & West, R. J. H. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.105144 · Cited by 55

Longitudinal transcriptomic analysis of altered pathways in a CHMP2Bintron5-based model of ALS-FTD

Waegaert, R., Dirrig‐Grosch, S., Parisot, F., Keime, C., Henriques, A., Loeffler, J., & René, F. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.104710 · Cited by 8