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Compensation for chronic oxidative stress in ALADIN null mice
Mutations in the AAAS gene coding for the nuclear pore complex protein ALADIN lead to the autosomal recessive disorder triple A syndrome. Triple A patients present with a characteristic phenotype including alacrima, achalasia and adrenal insufficiency. Patient fibroblasts show increased levels of ox...
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| Publicat a: | Biol Open |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Company of Biologists Ltd
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5829508/ https://ncbi.nlm.nih.gov/pubmed/29362278 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/bio.030742 |
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