Myotonic dystrophy type 1 patient-derived iPSCs for the investigation of CTG repeat instability-Reference-Cited by-同舟云学术

Myotonic dystrophy type 1 patient-derived iPSCs for the investigation of CTG repeat instability

Published:2017-02-13 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Ueki Junko,Nakamori Masayuki,Nakamura Masahiro,Nishikawa Misato,Yoshida Yoshinori,Tanaka Azusa,Morizane Asuka,Kamon Masayoshi,Araki Toshiyuki,Takahashi Masanori P.,Watanabe Akira,Inagaki Nobuya,Sakurai Hidetoshi

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep42522.pdf

Reference38 articles.

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2. Lee, J. E. & Cooper, T. A. Pathogenic mechanisms of myotonic dystrophy. Biochem Soc Trans 37, 1281–1286, doi: 10.1042/BST0371281 (2009).

3. Nakamori, M. & Thornton, C. Epigenetic changes and non-coding expanded repeats. Neurobiol Dis 39, 21–27, doi: 10.1016/j.nbd.2010.02.004 (2010).

4. Lopez Castel, A. et al. Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues. Hum Mol Genet 20, 1–15, doi: 10.1093/hmg/ddq427 (2011).

5. Thornton, C. A., Johnson, K. & Moxley, R. T. 3rd . Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes. Ann Neurol 35, 104–107, doi: 10.1002/ana.410350116 (1994).

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