Molecular Genetics of Spinocerebellar Ataxia Type 8 (SCA8)
Author:
Publisher
Informa UK Limited
Subject
Cell Biology,Molecular Biology
Link
http://www.tandfonline.com/doi/pdf/10.4161/rna.2.2.1682
Cited by 20 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Unveiling RNA Dysfunction: A Key Player in Neurodegeneration;Altered Metabolism: A Major Contributor of Comorbidities in Neurodegenerative Diseases;2024
2. Spastic paraplegia is the main manifestation of a spinocerebellar ataxia type 8 lineage in China: a case report and review of literature;Frontiers in Human Neuroscience;2023-07-17
3. Understanding the Pathogenicity of Noncoding RNA Expansion-Associated Neurodegenerative Disorders;Insights into Human Neurodegeneration: Lessons Learnt from Drosophila;2019
4. Computational models for lncRNA function prediction and functional similarity calculation;Briefings in Functional Genomics;2018-09-21
5. The RNA binding KH domain of Spoonbill depletes pathogenic non-coding spinocerebellar ataxia 8 transcripts and suppresses neurodegeneration in Drosophila;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2016-09
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