Pearson CE - Search Results

1

CAG repeat-binding small molecule improves motor coordination impairment in a mouse model of Dentatorubral-pallidoluysian atrophy.

Hasuike Y, Tanaka H, Gall-Duncan T, Mehkary M, Nakatani K, Pearson CE, Tsuji S, Mochizuki H, Nakamori M. Hasuike Y, et al. Among authors: pearson ce. Neurobiol Dis. 2022 Feb;163:105604. doi: 10.1016/j.nbd.2021.105604. Epub 2021 Dec 28. Neurobiol Dis. 2022. PMID: 34968706 Free article.

2

Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues.

López Castel A, Nakamori M, Tomé S, Chitayat D, Gourdon G, Thornton CA, Pearson CE. López Castel A, et al. Among authors: pearson ce. Hum Mol Genet. 2011 Jan 1;20(1):1-15. doi: 10.1093/hmg/ddq427. Epub 2010 Nov 1. Hum Mol Genet. 2011. PMID: 21044947 Free PMC article.

3

Bidirectional transcription stimulates expansion and contraction of expanded (CTG)*(CAG) repeats.

Nakamori M, Pearson CE, Thornton CA. Nakamori M, et al. Among authors: pearson ce. Hum Mol Genet. 2011 Feb 1;20(3):580-8. doi: 10.1093/hmg/ddq501. Epub 2010 Nov 18. Hum Mol Genet. 2011. PMID: 21088112 Free PMC article.

4

Identification of restriction endonucleases sensitive to 5-cytosine methylation at non-CpG sites, including expanded (CAG)n/(CTG)n repeats.

López Castel A, Nakamori M, Thornton CA, Pearson CE. López Castel A, et al. Among authors: pearson ce. Epigenetics. 2011 Apr;6(4):416-20. doi: 10.4161/epi.6.4.14953. Epub 2011 Apr 1. Epigenetics. 2011. PMID: 21364324 Free PMC article.

5

Replacement of the myotonic dystrophy type 1 CTG repeat with 'non-CTG repeat' insertions in specific tissues.

Axford MM, López-Castel A, Nakamori M, Thornton CA, Pearson CE. Axford MM, et al. Among authors: pearson ce. J Med Genet. 2011 Jul;48(7):438-43. doi: 10.1136/jmg.2010.085944. Epub 2011 May 27. J Med Genet. 2011. PMID: 21622935 Free PMC article.

6

MSH3 polymorphisms and protein levels affect CAG repeat instability in Huntington's disease mice.

Tomé S, Manley K, Simard JP, Clark GW, Slean MM, Swami M, Shelbourne PF, Tillier ER, Monckton DG, Messer A, Pearson CE. Tomé S, et al. Among authors: pearson ce. PLoS Genet. 2013;9(2):e1003280. doi: 10.1371/journal.pgen.1003280. Epub 2013 Feb 28. PLoS Genet. 2013. PMID: 23468640 Free PMC article.

7

Detection of slipped-DNAs at the trinucleotide repeats of the myotonic dystrophy type I disease locus in patient tissues.

Axford MM, Wang YH, Nakamori M, Zannis-Hadjopoulos M, Thornton CA, Pearson CE. Axford MM, et al. Among authors: pearson ce. PLoS Genet. 2013;9(12):e1003866. doi: 10.1371/journal.pgen.1003866. Epub 2013 Dec 19. PLoS Genet. 2013. PMID: 24367268 Free PMC article.

8

Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31.

Ishiguro T, Sato N, Ueyama M, Fujikake N, Sellier C, Kanegami A, Tokuda E, Zamiri B, Gall-Duncan T, Mirceta M, Furukawa Y, Yokota T, Wada K, Taylor JP, Pearson CE, Charlet-Berguerand N, Mizusawa H, Nagai Y, Ishikawa K. Ishiguro T, et al. Among authors: pearson ce. Neuron. 2017 Apr 5;94(1):108-124.e7. doi: 10.1016/j.neuron.2017.02.046. Epub 2017 Mar 23. Neuron. 2017. PMID: 28343865 Free PMC article.

9

Molecular genetics of congenital myotonic dystrophy.

Lanni S, Pearson CE. Lanni S, et al. Among authors: pearson ce. Neurobiol Dis. 2019 Dec;132:104533. doi: 10.1016/j.nbd.2019.104533. Epub 2019 Jul 19. Neurobiol Dis. 2019. PMID: 31326502 Free article. Review.

10

A slipped-CAG DNA-binding small molecule induces trinucleotide-repeat contractions in vivo.

Nakamori M, Panigrahi GB, Lanni S, Gall-Duncan T, Hayakawa H, Tanaka H, Luo J, Otabe T, Li J, Sakata A, Caron MC, Joshi N, Prasolava T, Chiang K, Masson JY, Wold MS, Wang X, Lee MYWT, Huddleston J, Munson KM, Davidson S, Layeghifard M, Edward LM, Gallon R, Santibanez-Koref M, Murata A, Takahashi MP, Eichler EE, Shlien A, Nakatani K, Mochizuki H, Pearson CE. Nakamori M, et al. Among authors: pearson ce. Nat Genet. 2020 Feb;52(2):146-159. doi: 10.1038/s41588-019-0575-8. Epub 2020 Feb 14. Nat Genet. 2020. PMID: 32060489 Free PMC article.

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