載入...
Heterochromatin loss as a determinant of progerin‐induced DNA damage in Hutchinson–Gilford Progeria
Hutchinson–Gilford progeria is a premature aging syndrome caused by a truncated form of lamin A called progerin. Progerin expression results in a variety of cellular defects including heterochromatin loss, DNA damage, impaired proliferation and premature senescence. It remains unclear how these diff...
Na minha lista:
| 發表在: | Aging Cell |
|---|---|
| Main Authors: | , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
John Wiley and Sons Inc.
2020
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7059134/ https://ncbi.nlm.nih.gov/pubmed/32087607 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/acel.13108 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|