24307138 22819011 25666058 25136055 28484853 30820866 23443018 23500957 29325610 35563872 23953108 31721251 25201111 27625393 23813740 31445906 35053321 23843646 32086717 24176420 28542277 24318420 28855740 23063563 30284037 26295943 29987489 3132354 - Search Results

Year	Number of Results
2012	3
2013	7
2014	4
2015	4
2016	1
2017	3
2018	2
2019	7
2020	2
2021	1
2022	4
2023	0

1

Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias.

Matilla-Dueñas A, Ashizawa T, Brice A, Magri S, McFarland KN, Pandolfo M, Pulst SM, Riess O, Rubinsztein DC, Schmidt J, Schmidt T, Scoles DR, Stevanin G, Taroni F, Underwood BR, Sánchez I. Matilla-Dueñas A, et al. Cerebellum. 2014 Apr;13(2):269-302. doi: 10.1007/s12311-013-0539-y. Cerebellum. 2014. PMID: 24307138 Free PMC article.

2

Pre-mRNA splicing in disease and therapeutics.

Singh RK, Cooper TA. Singh RK, et al. Trends Mol Med. 2012 Aug;18(8):472-82. doi: 10.1016/j.molmed.2012.06.006. Epub 2012 Jul 18. Trends Mol Med. 2012. PMID: 22819011 Free PMC article. Review.

3

Aurora B-dependent phosphorylation of Ataxin-10 promotes the interaction between Ataxin-10 and Plk1 in cytokinesis.

Tian J, Tian C, Ding Y, Li Z, Geng Q, Xiahou Z, Wang J, Hou W, Liao J, Dong MQ, Xu X, Li J. Tian J, et al. Sci Rep. 2015 Feb 10;5:8360. doi: 10.1038/srep08360. Sci Rep. 2015. PMID: 25666058 Free PMC article.

4

The autosomal dominant spinocerebellar ataxias: emerging mechanistic themes suggest pervasive Purkinje cell vulnerability.

Hekman KE, Gomez CM. Hekman KE, et al. J Neurol Neurosurg Psychiatry. 2015 May;86(5):554-61. doi: 10.1136/jnnp-2014-308421. Epub 2014 Aug 18. J Neurol Neurosurg Psychiatry. 2015. PMID: 25136055 Free PMC article. Review.

5

Protein sequestration as a normal function of long noncoding RNAs and a pathogenic mechanism of RNAs containing nucleotide repeat expansions.

Morriss GR, Cooper TA. Morriss GR, et al. Hum Genet. 2017 Sep;136(9):1247-1263. doi: 10.1007/s00439-017-1807-6. Epub 2017 May 8. Hum Genet. 2017. PMID: 28484853 Free PMC article. Review.

6

Motor Performances of Spontaneous and Genetically Modified Mutants with Cerebellar Atrophy.

Lalonde R, Strazielle C. Lalonde R, et al. Cerebellum. 2019 Jun;18(3):615-634. doi: 10.1007/s12311-019-01017-5. Cerebellum. 2019. PMID: 30820866 Free article. Review.

7

Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability.

McFarland KN, Liu J, Landrian I, Gao R, Sarkar PS, Raskin S, Moscovich M, Gatto EM, Teive HA, Ochoa A, Rasmussen A, Ashizawa T. McFarland KN, et al. Eur J Hum Genet. 2013 Nov;21(11):1272-6. doi: 10.1038/ejhg.2013.32. Epub 2013 Feb 27. Eur J Hum Genet. 2013. PMID: 23443018 Free PMC article.

8

RNA toxicity in human disease and animal models: from the uncovering of a new mechanism to the development of promising therapies.

Sicot G, Gomes-Pereira M. Sicot G, et al. Biochim Biophys Acta. 2013 Sep;1832(9):1390-409. doi: 10.1016/j.bbadis.2013.03.002. Epub 2013 Mar 15. Biochim Biophys Acta. 2013. PMID: 23500957 Free article. Review.

9

Autosomal-dominant cerebellar ataxias.

Mundwiler A, Shakkottai VG. Mundwiler A, et al. Handb Clin Neurol. 2018;147:173-185. doi: 10.1016/B978-0-444-63233-3.00012-9. Handb Clin Neurol. 2018. PMID: 29325610 Review.

10

Mechanistic and Therapeutic Insights into Ataxic Disorders with Pentanucleotide Expansions.

Zhang N, Ashizawa T. Zhang N, et al. Cells. 2022 May 6;11(9):1567. doi: 10.3390/cells11091567. Cells. 2022. PMID: 35563872 Free PMC article. Review.

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