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ER strikes again: Proteostasis Dysfunction In ALS
The precise contribution of endoplasmic reticulum (ER) chaperone protein disulfide isomerase (PDI) variants in human amyotrophic lateral sclerosis (ALS) patients to the pathogenesis of ALS remained unclear. In the present study, Woehlbier et al (2016) demonstrated that these PDI variants are capable...
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| Publicado no: | EMBO J |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4972132/ https://ncbi.nlm.nih.gov/pubmed/26968985 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/embj.201694117 |
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