Nakamori M - Search Results

1

Straightjacket/α2δ3 deregulation is associated with cardiac conduction defects in myotonic dystrophy type 1.

Auxerre-Plantié E, Nakamori M, Renaud Y, Huguet A, Choquet C, Dondi C, Miquerol L, Takahashi MP, Gourdon G, Junion G, Jagla T, Zmojdzian M, Jagla K. Auxerre-Plantié E, et al. Among authors: nakamori m. Elife. 2019 Dec 12;8:e51114. doi: 10.7554/eLife.51114. Elife. 2019. PMID: 31829940 Free PMC article.

2

[Erythrocyte from Duchenne muscular dystrophy is fragile].

Matsumura T, Takahashi M, Nakamori M, Saito T, Nozaki S, Fujimura H, Shinno S. Matsumura T, et al. Among authors: nakamori m. Rinsho Shinkeigaku. 2004 Oct;44(10):695-8. Rinsho Shinkeigaku. 2004. PMID: 15568487 Japanese.

3

Altered mRNA splicing of the skeletal muscle ryanodine receptor and sarcoplasmic/endoplasmic reticulum Ca2+-ATPase in myotonic dystrophy type 1.

Kimura T, Nakamori M, Lueck JD, Pouliquin P, Aoike F, Fujimura H, Dirksen RT, Takahashi MP, Dulhunty AF, Sakoda S. Kimura T, et al. Among authors: nakamori m. Hum Mol Genet. 2005 Aug 1;14(15):2189-200. doi: 10.1093/hmg/ddi223. Epub 2005 Jun 22. Hum Mol Genet. 2005. PMID: 15972723

4

Altered mRNA splicing of dystrophin in type 1 myotonic dystrophy.

Nakamori M, Kimura T, Fujimura H, Takahashi MP, Sakoda S. Nakamori M, et al. Muscle Nerve. 2007 Aug;36(2):251-7. doi: 10.1002/mus.20809. Muscle Nerve. 2007. PMID: 17487865

5

Endoplasmic reticulum stress in myotonic dystrophy type 1 muscle.

Ikezoe K, Nakamori M, Furuya H, Arahata H, Kanemoto S, Kimura T, Imaizumi K, Takahashi MP, Sakoda S, Fujii N, Kira J. Ikezoe K, et al. Among authors: nakamori m. Acta Neuropathol. 2007 Nov;114(5):527-35. doi: 10.1007/s00401-007-0267-9. Epub 2007 Jul 28. Acta Neuropathol. 2007. PMID: 17661063

6

Molecular mechanisms responsible for aberrant splicing of SERCA1 in myotonic dystrophy type 1.

Hino S, Kondo S, Sekiya H, Saito A, Kanemoto S, Murakami T, Chihara K, Aoki Y, Nakamori M, Takahashi MP, Imaizumi K. Hino S, et al. Among authors: nakamori m. Hum Mol Genet. 2007 Dec 1;16(23):2834-43. doi: 10.1093/hmg/ddm239. Epub 2007 Aug 29. Hum Mol Genet. 2007. PMID: 17728322

7

Aberrantly spliced alpha-dystrobrevin alters alpha-syntrophin binding in myotonic dystrophy type 1.

Nakamori M, Kimura T, Kubota T, Matsumura T, Sumi H, Fujimura H, Takahashi MP, Sakoda S. Nakamori M, et al. Neurology. 2008 Feb 26;70(9):677-85. doi: 10.1212/01.wnl.0000302174.08951.cf. Neurology. 2008. PMID: 18299519

8

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: nakamori m. 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.

9

The role of α-dystrobrevin in striated muscle.

Nakamori M, Takahashi MP. Nakamori M, et al. Int J Mol Sci. 2011;12(3):1660-71. doi: 10.3390/ijms12031660. Epub 2011 Mar 4. Int J Mol Sci. 2011. PMID: 21673914 Free PMC article. Review.

10

Stabilization of expanded (CTG)•(CAG) repeats by antisense oligonucleotides.

Nakamori M, Gourdon G, Thornton CA. Nakamori M, et al. Mol Ther. 2011 Dec;19(12):2222-7. doi: 10.1038/mt.2011.191. Epub 2011 Oct 4. Mol Ther. 2011. PMID: 21971425 Free PMC article.

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