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Repression of the antioxidant NRF2 pathway in premature aging
Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare, invariably fatal premature aging disorder. The disease is caused by constitutive production of progerin, a mutant form of the nuclear architectural protein lamin A, leading, through unknown mechanisms, to diverse morphological, epigenetic and ge...
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| Published in: | Cell |
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| Main Authors: | , , , , , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
2016
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4893198/ https://ncbi.nlm.nih.gov/pubmed/27259148 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2016.05.017 |
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