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2014 | 1 |
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TDP-43 proteinopathy alters the ribosome association of multiple mRNAs including the glypican Dally-like protein (Dlp)/GPC6.
Acta Neuropathol Commun. 2021 Mar 24;9(1):52. doi: 10.1186/s40478-021-01148-z.
Acta Neuropathol Commun. 2021.
PMID: 33762006
Free PMC article.
Fragile X protein mitigates TDP-43 toxicity by remodeling RNA granules and restoring translation.
Coyne AN, Yamada SB, Siddegowda BB, Estes PS, Zaepfel BL, Johannesmeyer JS, Lockwood DB, Pham LT, Hart MP, Cassel JA, Freibaum B, Boehringer AV, Taylor JP, Reitz AB, Gitler AD, Zarnescu DC.
Coyne AN, et al.
Hum Mol Genet. 2015 Dec 15;24(24):6886-98. doi: 10.1093/hmg/ddv389. Epub 2015 Sep 18.
Hum Mol Genet. 2015.
PMID: 26385636
Free PMC article.
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Futsch/MAP1B mRNA is a translational target of TDP-43 and is neuroprotective in a Drosophila model of amyotrophic lateral sclerosis.
Coyne AN, Siddegowda BB, Estes PS, Johannesmeyer J, Kovalik T, Daniel SG, Pearson A, Bowser R, Zarnescu DC.
Coyne AN, et al.
J Neurosci. 2014 Nov 26;34(48):15962-74. doi: 10.1523/JNEUROSCI.2526-14.2014.
J Neurosci. 2014.
PMID: 25429138
Free PMC article.
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Motor neurons and glia exhibit specific individualized responses to TDP-43 expression in a Drosophila model of amyotrophic lateral sclerosis.
Estes PS, Daniel SG, McCallum AP, Boehringer AV, Sukhina AS, Zwick RA, Zarnescu DC.
Estes PS, et al.
Dis Model Mech. 2013 May;6(3):721-33. doi: 10.1242/dmm.010710. Epub 2013 Feb 1.
Dis Model Mech. 2013.
PMID: 23471911
Free PMC article.
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