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Protein Misfolding and Aggregation as a Therapeutic Target for Polyglutamine Diseases
The polyglutamine (polyQ) diseases, such as Huntington’s disease and several types of spinocerebellar ataxias, are a group of inherited neurodegenerative diseases that are caused by an abnormal expansion of the polyQ tract in disease-causative proteins. Proteins with an abnormally expanded polyQ str...
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| Vydáno v: | Brain Sci |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
MDPI
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5664055/ https://ncbi.nlm.nih.gov/pubmed/29019918 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/brainsci7100128 |
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