Unveiling RNA Dysfunction: A Key Player in Neurodegeneration
Author:
Publisher
Springer Nature Singapore
Link
https://link.springer.com/content/pdf/10.1007/978-981-97-4288-2_10
Reference140 articles.
1. Adie W (1923) Dystrophia myotonica (myotonia atrophica), an heredo-familial disease with cataract. Proc R Soc Med 16:36–44
2. Alves CN, Braga TKK, Somensi DN, Nascimento B, Lima JAS, Fujihara S (2018) X-linked spinal and bulbar muscular atrophy (Kennedy’s disease): the first case described in the Brazilian Amazon. Einstein 16:eRC4011
3. Arber C, Toombs J, Lovejoy C, Ryan NS, Paterson RW, Willumsen N, Gkanatsiou E, Portelius E, Blennow K, Heslegrave A (2020) Familial Alzheimer’s disease patient-derived neurons reveal distinct mutation-specific effects on amyloid beta. Mol Psychiatry 25:2919–2931
4. Barker H, Niblock M, Lee Y (2017) RNA misprocessing in C9orf72-linked neurodegeneration. Front Cell Neurosci 11:195
5. Baud A, Derbis M, Tutak K, Sobczak K (2022) Partners in crime: proteins implicated in RNA repeat expansion diseases. Wiley Interdiscip Rev 13:e1709
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