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SMN Protein Contributes to Skeletal Muscle Cell Maturation Via Caspase-3 and Akt Activation
Background/Aim: In spinal muscular atrophy (SMA), systemic deficiency of survival motor neurons (SMN) caused by loss or mutation of SMN1 leads to SMA symptoms. SMA was, for a long time, considered as a selective motor-neuron disease. However, accumulated evidence suggests that skeletal muscle cells...
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| Yayımlandı: | In Vivo |
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| Asıl Yazarlar: | , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
International Institute of Anticancer Research
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7811598/ https://ncbi.nlm.nih.gov/pubmed/33144430 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21873/invivo.12161 |
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