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

Myotonic dystrophy type 1 (DM1) is an autosomal-dominant multi-system disease caused by expanded CTG repeats in dystrophia myotonica protein kinase (DMPK). The expanded CTG repeats are unstable and can increase the length of the gene with age, which worsens the symptoms. In order to establish a huma...

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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2017
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5304155/
https://ncbi.nlm.nih.gov/pubmed/28211918
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep42522
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