SMAD4 mutations and cross-talk between TGF-β/IFNγ signaling accelerate rates of DNA damage and cellular senescence, resulting in a segmental progeroid syndrome-the Myhre syndrome.
第一作者:
Renuka,Kandhaya-Pillai
第一单位:
Department of Pathology, University of Washington, Box 357470, HSB, Seattle, WA, K-543, USA.
作者:
主题词
隐睾(Cryptorchidism);DNA损伤(DNA Damage);面容(Facies);生长障碍(Growth Disorders);手畸形, 先天性(Hand Deformities, Congenital);人类(Humans);突变(Mutation);Smad4蛋白质(Smad4 Protein);转化生长因子β(Transforming Growth Factor beta)
DOI
10.1007/s11357-020-00318-6
PMID
33428109
发布时间
2022-12-08
- 浏览4
GeroScience
2021年43卷3期
1481-1496页
相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文


换一批



