Motor Neuron Disease: The Contribution of TAR-43 Gene in Amyotrophic Lateral Sclerosis
Author:
Publisher
Jaypee Brothers Medical Publishing
Subject
General Medicine
Link
https://www.apibpj.com/doi/pdf/10.5005/jp-journals-10070-8009
Reference13 articles.
1. 1. Xu L, Liu T, Liu L, et al. Global variation in prevalence and incidence of amyotrophic lateral sclerosis: A systematic review and meta-analysis. Journal of neurology 2020;267(4):944–953. DOI: 10.1007/s00415-019-09652-y.
2. 2. Mancuso R, Navarro X. Amyotrophic lateral sclerosis: Current perspectives from basic research to the clinic. Prog Neurobiol 2015; 133:1–26. DOI: 10.1016/j.pneurobio.2015.07.004.
3. 3. François-Moutal L, Perez-Miller S, Scott DD, et al. Structural insights into TDP-43 and effects of post-translational modifications. Front Mol Neurosci 2019;12:301. DOI: 10.3389/fnmol.2019.00301.
4. 4. Maria Johanna de Boer E, K OrieV, Williams T, et al. TDP-43 proteinopathies: A new wave of neurodegenerative diseases. J Neurol Neurosurg Psychiatry 2020;92(1):86–95. DOI: 10.1136/jnnp-2020-322983.
5. 5. Peng AYT, Agrawal I, Ho YW, et al. Loss of TDP-43 in astrocytes leads to motor deficits by triggering A1-like reactive phenotype and triglial dysfunction. Proc Natl Acad Sci U S A 2020;117(46):29101–29112. DOI: 10.1073/pnas.2007806117.
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