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Natural and pathogenic protein sequence variation affecting prion-like domains within and across human proteomes
BACKGROUND: Impaired proteostatic regulation of proteins with prion-like domains (PrLDs) is associated with a variety of human diseases including neurodegenerative disorders, myopathies, and certain forms of cancer. For many of these disorders, current models suggest a prion-like molecular mechanism...
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| Publicat a: | BMC Genomics |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6947906/ https://ncbi.nlm.nih.gov/pubmed/31914925 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-019-6425-3 |
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