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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2021 | 1 |
2022 | 2 |
2023 | 1 |
2024 | 0 |
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4 results
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Page 1
TorsinA is essential for the timing and localization of neuronal nuclear pore complex biogenesis.
bioRxiv [Preprint]. 2023 Apr 27:2023.04.26.538491. doi: 10.1101/2023.04.26.538491.
bioRxiv. 2023.
PMID: 37162852
Free PMC article.
Preprint.
Genetic evidence of aberrant striatal synaptic maturation and secretory pathway alteration in a dystonia mouse model.
Yellajoshyula D, Opeyemi S, Dauer WT, Pappas SS.
Yellajoshyula D, et al.
Dystonia. 2022;1:10892. doi: 10.3389/dyst.2022.10892. Epub 2022 Dec 14.
Dystonia. 2022.
PMID: 36874764
Free PMC article.
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A pathogenic DYT-THAP1 dystonia mutation causes hypomyelination and loss of YY1 binding.
Yellajoshyula D, Rogers AE, Kim AJ, Kim S, Pappas SS, Dauer WT.
Yellajoshyula D, et al.
Hum Mol Genet. 2022 Mar 31;31(7):1096-1104. doi: 10.1093/hmg/ddab310.
Hum Mol Genet. 2022.
PMID: 34686877
Free PMC article.
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TorsinA restoration in a mouse model identifies a critical therapeutic window for DYT1 dystonia.
Li J, Levin DS, Kim AJ, Pappas SS, Dauer WT.
Li J, et al.
J Clin Invest. 2021 Mar 15;131(6):e139606. doi: 10.1172/JCI139606.
J Clin Invest. 2021.
PMID: 33529159
Free PMC article.
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