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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2007 1
2009 1
2010 1
2012 2
2013 2
2014 4
2015 1
2016 1
2017 3
2018 3
2019 2
2020 2
2021 0
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22 results
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Page 1
RNA-Mediated Disease Mechanisms in Neurodegenerative Disorders.
Neueder A. Neueder A. J Mol Biol. 2019 Apr 19;431(9):1780-1791. doi: 10.1016/j.jmb.2018.12.012. Epub 2018 Dec 29. J Mol Biol. 2019. PMID: 30597161 Review.
RNA Related Pathology in Huntington's Disease.
Neueder A, Bates GP. Neueder A, et al. Adv Exp Med Biol. 2018;1049:85-101. doi: 10.1007/978-3-319-71779-1_4. Adv Exp Med Biol. 2018. PMID: 29427099 Review.
Mitochondrial biology and the identification of biomarkers of Huntington's disease.
Neueder A, Orth M. Neueder A, et al. Neurodegener Dis Manag. 2020 Aug;10(4):243-255. doi: 10.2217/nmt-2019-0033. Epub 2020 Aug 4. Neurodegener Dis Manag. 2020. PMID: 32746707
Regulatory mechanisms of incomplete huntingtin mRNA splicing.
Neueder A, Dumas AA, Benjamin AC, Bates GP. Neueder A, et al. Nat Commun. 2018 Sep 27;9(1):3955. doi: 10.1038/s41467-018-06281-3. Nat Commun. 2018. PMID: 30262848 Free PMC article.
Silencing Srsf6 does not modulate incomplete splicing of the huntingtin gene in Huntington's disease models.
Mason MA, Gomez-Paredes C, Sathasivam K, Neueder A, Papadopoulou AS, Bates GP. Mason MA, et al. Among authors: neueder a. Sci Rep. 2020 Aug 20;10(1):14057. doi: 10.1038/s41598-020-71111-w. Sci Rep. 2020. PMID: 32820193 Free PMC article.
Phenotype onset in Huntington's disease knock-in mice is correlated with the incomplete splicing of the mutant huntingtin gene.
Franich NR, Hickey MA, Zhu C, Osborne GF, Ali N, Chu T, Bove NH, Lemesre V, Lerner RP, Zeitlin SO, Howland D, Neueder A, Landles C, Bates GP, Chesselet MF. Franich NR, et al. Among authors: neueder a. J Neurosci Res. 2019 Dec;97(12):1590-1605. doi: 10.1002/jnr.24493. Epub 2019 Jul 7. J Neurosci Res. 2019. PMID: 31282030 Free PMC article.
Myostatin inhibition prevents skeletal muscle pathophysiology in Huntington's disease mice.
Bondulich MK, Jolinon N, Osborne GF, Smith EJ, Rattray I, Neueder A, Sathasivam K, Ahmed M, Ali N, Benjamin AC, Chang X, Dick JRT, Ellis M, Franklin SA, Goodwin D, Inuabasi L, Lazell H, Lehar A, Richard-Londt A, Rosinski J, Smith DL, Wood T, Tabrizi SJ, Brandner S, Greensmith L, Howland D, Munoz-Sanjuan I, Lee SJ, Bates GP. Bondulich MK, et al. Among authors: neueder a. Sci Rep. 2017 Oct 27;7(1):14275. doi: 10.1038/s41598-017-14290-3. Sci Rep. 2017. PMID: 29079832 Free PMC article.
Aberrantly spliced HTT, a new player in Huntington's disease pathogenesis.
Gipson TA, Neueder A, Wexler NS, Bates GP, Housman D. Gipson TA, et al. Among authors: neueder a. RNA Biol. 2013 Nov;10(11):1647-52. doi: 10.4161/rna.26706. Epub 2013 Oct 11. RNA Biol. 2013. PMID: 24256709 Free PMC article.
Dysfunction of the CNS-heart axis in mouse models of Huntington's disease.
Mielcarek M, Inuabasi L, Bondulich MK, Muller T, Osborne GF, Franklin SA, Smith DL, Neueder A, Rosinski J, Rattray I, Protti A, Bates GP. Mielcarek M, et al. Among authors: neueder a. PLoS Genet. 2014 Aug 7;10(8):e1004550. doi: 10.1371/journal.pgen.1004550. eCollection 2014 Aug. PLoS Genet. 2014. PMID: 25101683 Free PMC article.
A common gene expression signature in Huntington's disease patient brain regions.
Neueder A, Bates GP. Neueder A, et al. BMC Med Genomics. 2014 Oct 30;7:60. doi: 10.1186/s12920-014-0060-2. BMC Med Genomics. 2014. PMID: 25358814 Free PMC article.
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