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Targeting the phospholipase A2 receptor ameliorates premature aging phenotypes
Hutchinson–Gilford progeria syndrome (HGPS) is a lethal premature aging that recapitulates many normal aging characteristics. This disorder is caused by mutation in the LMNA gene leading to the production of progerin which induces misshapen nuclei, cellular senescence, and aging. We previously showe...
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| Yayımlandı: | Aging Cell |
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| Asıl Yazarlar: | , , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
John Wiley and Sons Inc.
2018
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6260922/ https://ncbi.nlm.nih.gov/pubmed/30216637 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/acel.12835 |
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