HNRNPA1-induced spliceopathy in a transgenic mouse model of myotonic dystrophy

Studies on myotonic dystrophy type 1 (DM1) have led to the RNA-mediated disease model for hereditary disorders caused by noncoding microsatellite expansions. This model proposes that DM1 disease manifestations are caused by a reversion to fetal RNA processing patterns in adult tissues due to the exp...

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Detalles Bibliográficos
Autores principales: Li, Moyi, Zhuang, Yan, Batra, Ranjan, Thomas, James D., Li, Mao, Nutter, Curtis A., Scotti, Marina M., Carter, Helmut A., Wang, Zhan Jun, Huang, Xu-Sheng, Pu, Chuan Qiang, Swanson, Maurice S., Xie, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Biological Sciences
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7071875/
https://www.ncbi.nlm.nih.gov/pubmed/32086392
http://dx.doi.org/10.1073/pnas.1907297117

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7071875/
https://www.ncbi.nlm.nih.gov/pubmed/32086392
http://dx.doi.org/10.1073/pnas.1907297117

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