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ALS-linked TDP-43(M337V) knock-in mice exhibit splicing deregulation without neurodegeneration
Abnormal accumulation of TAR DNA-binding protein 43 (TDP-43), a DNA/RNA binding protein, is a pathological signature of amyotrophic lateral sclerosis (ALS). Missense mutations in the TARDBP gene are also found in inherited and sporadic ALS, indicating that dysfunction in TDP-43 is causative for ALS....
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| Publicado no: | Mol Brain |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6971932/ https://ncbi.nlm.nih.gov/pubmed/31959210 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13041-020-0550-4 |
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