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A subset of SMN complex members have a specific role in tissue regeneration via ERBB pathway-mediated proliferation
Spinal muscular atrophy (SMA) is the most common genetic disease in children. SMA is generally caused by mutations in the gene SMN1. The survival of motor neurons (SMN) complex consists of SMN1, Gemins (2–8), and Strap/Unrip. We previously demonstrated smn1 and gemin5 inhibited tissue regeneration i...
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| Publicado no: | NPJ Regen Med |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group UK
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7096462/ https://ncbi.nlm.nih.gov/pubmed/32218991 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41536-020-0089-0 |
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