Original paper
MBNL1 overexpression is not sufficient to rescue the phenotypes in a mouse model of RNA toxicity
Abstract
Myotonic dystrophy type 1 (DM1) is caused by an expanded (CTG)n tract in the 3′UTR of the DM protein kinase (DMPK) gene. The RNA transcripts produced from the expanded allele sequester or alter the function of RNA-binding proteins (MBNL1, CUGBP1, etc.). The sequestration of MBNL1 results in RNA-splicing defects that contribute to disease. Overexpression of MBNL1 in skeletal muscle has been shown to rescue some of the DM1 features in a mouse...
Paper Details
Title
MBNL1 overexpression is not sufficient to rescue the phenotypes in a mouse model of RNA toxicity
Published Date
Apr 1, 2019
Journal
Volume
28
Issue
14
Pages
2330 - 2338
Citation AnalysisPro
You’ll need to upgrade your plan to Pro
Looking to understand the true influence of a researcher’s work across journals & affiliations?
- Scinapse’s Top 10 Citation Journals & Affiliations graph reveals the quality and authenticity of citations received by a paper.
- Discover whether citations have been inflated due to self-citations, or if citations include institutional bias.
Notes
History