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Lamin Mutations Cause Increased YAP Nuclear Entry in Muscle Stem Cells
Mutations in the LMNA gene, encoding the nuclear envelope A-type lamins, are responsible for muscular dystrophies, the most severe form being the LMNA-related congenital muscular dystrophy (L-CMD), with severe defects in myonucleus integrity. We previously reported that L-CMD mutations compromise th...
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| 出版年: | Cells |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
MDPI
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7226749/ https://ncbi.nlm.nih.gov/pubmed/32231000 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cells9040816 |
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