姓 名: |
李静宜 |
学 科: |
衰老生物学 |
电话/传真: |
+86-10-64807583 / |
电子邮件: |
lijingyi@ioz.ac.cn |
通讯地址: |
北京市朝阳区大屯路甲3号院干细胞与再生医学研究院大楼 膜生物学国家重点实验室 100101 |
更多信息: |
衰老与再生研究组
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简历介绍:
1.教育经历:
2008-2012年 河北农业大学 生物技术 学士学位
2012-2017年 北京大学 细胞生物学 博士学位
2.工作经历:
2017年7月-2020年8月 中国科学院生物物理研究所,副研究员
2020年9月至今 中国科学院动物研究所,副研究员
研究领域:
综合运用多组学手段多层次解析衰老及相关疾病的发生发展机制,探究新型干预靶标。
社会任职:
获奖及荣誉:
承担科研项目情况:
代表论著:
(#共同第一作者)
- S. Wang#, Y. Zheng#, J. Li#, Y Yang#, W. Zhang#, M. Song, Z. Liu, Z. Min, H. Hu, Y. Jing, X. He, L. Sun, L. Ma, C. R. Esteban, P. Chan, J. Qiao, Q. Zhou, J. C. I. Belmonte, J. Qu, F. Tang, and G.-H. Liu, “Single-cell transcriptomic atlas of primate ovarian aging,” Cell, vol. 180, no. 3, pp. 585-600, 2020. (Cover story)
- W. Zhang#, J. Li#, K. Suzuki#, J. Qu#, P. Wang, J. Zhou, X. Liu, R. Ren, X. Xu, A. Ocampo, T. Yuan, J. Yang, Y. Li, L. Shi, D. Guan, H. Pan, S. Duan, Z. Ding, M. Li, F. Yi, R. Bai, Y. Wang, C. Chen, F. Yang, X. Li, Z. Wang, E. Aizawa, A. Goebl, R. D. Soligalla, P. Reddy, C. R. Esteban, F. Tang, G.-H. Liu, and J. C. I. Belmonte, “A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging,” Science, vol. 348, no. 6239, pp. 1160–1163, 2015.
- J. Li#, Y. Zheng#, P. Yan#, M. Song#, S. Wang#, L. Sun, Z. Liu, S. Ma, P. Chan, Q. Zhou, J. C. I. Belmonte, W. Zhang, G.-H. Liu, F. Tang, J. Qu, “A Single-cell Transcriptomic Atlas of Primate Pancreatic Islet Aging,” National Science Review, vol. 8, no. 2, 2021. DOI: 10.1093/nsr/nwaa127.
- J. Li#, X. Zhou#, X. Liu#, J. Ren#, J. Wang, W. Wang, Y. Zheng, X. Shi, T. Sun, Z. Li, A. Kang, F. Tang, L. Wen, and W. Fu, “Detection of Colorectal Cancer in Circulating Cell-Free DNA by Methylated CpG Tandem Amplification and Sequencing,” Clinical Chemistry, vol. 65, no. 7, pp. 916-926, 2019.
- J. Yang#, J. Li#, K. Suzuki#, X. Liu, J. Wu, W. Zhang, R. Ren, W. Zhang, P. Chan, J. C. I. Belmonte, J. Qu, F. Tang, and G.-H. Liu, “Genetic enhancement in cultured human adult stem cells conferred by a single nucleotide recoding,” Cell Research, vol. 27, no. 9, pp. 1178–1181, 2017.
- L. Wen#, J. Li#, H. Guo#, X. Liu#, S. Zheng, D. Zhang, W. Zhu, J. Qu, L. Guo, D. Du, X. Jin, Y. Zhang, Y. Gao, J. Shen, H. Ge, F. Tang, Y. Huang, and J. Peng, “Genome-scale detection of hypermethylated CpG islands in circulating cell-free DNA of hepatocellular carcinoma patients,” Cell Research, vol. 25, no. 11, pp. 1250–1264, 2015.
- W.Wang, Y. Zheng, S. Sun, W. Li, M. Song, Q. Ji, Z. Wu, Z. Liu, Y. Fan, F. Liu, J. Li, C. R. Esteban, Si Wang, Qi Zhou, J. C. I. Belmonte, W. Zhang, J. Qu, F. Tang, G.-H. Liu, “A genome-wide crispr-based screen identifies kat7 as a driver of cellular senescence,” Science Translational Medicine, vol. 13, pp. 2655, 2021.
- L. Deng, R. Ren, Z. Liu, M. Song, J. Li, Z. Wu, X. Ren, L. Fu, W. Li, W. Zhang, P. Guillen, J. C. I. Belmonte, P. Chan, J. Qu & G.-H. Liu, “Stabilizing heterochromatin by DGCR8 alleviates senescence and osteoarthritis,” Nature Communications, vol. 10, no. 1, pp. 3329, 2019.
- X. Liu, J. Ren, N. Luo, H. Guo, Y. Zheng, J. Li, F. Tang, L. Wen, J. Peng, “Comprehensive DNA methylation analysis of tissue of origin of plasma cell-free DNA by methylated CpG tandem amplification and sequencing (MCTA-Seq),” Clinical Epigenetics, vol. 11, no. 1, pp. 93, 2019.
- P. Wang, Z. Liu, X. Zhang, J. Li, L. Sun, Z. Ju, J. Li, P. Chan, G.-H. Liu, W. Zhang, M. Song, and J. Qu, “CRISPR/Cas9-mediated gene knockout reveals a guardian role of NF-κB/RelA in maintaining the homeostasis of human vascular cells,” Protein & Cell, vol. 9, no. 11, pp. 945-965, 2018.
- H. Pan, D. Guan, X. Liu, J. Li, L. Wang, J. Wu, and J. Zhou, “SIRT6 safeguards human mesenchymal stem cells from oxidative stress by coactivating NRF2,” Cell Research, vol. 26, no. 2, pp. 190–205, 2016.
- S. Duan, G. Yuan, X. Liu, R. Ren, J. Li, W. Zhang, J. Wu, X. Xu, L. Fu, Y. Li, J. Yang, W. Zhang, R. Bai, F. Yi, K. Suzuki, H. Gao, C. R. Esteban, C. Zhang, J. C. Izpisua Belmonte, Z. Chen, X. Wang, T. Jiang, J. Qu, F. Tang, and G.-H. Liu, “PTEN deficiency reprogrammes human neural stem cells towards a glioblastoma stem cell-like phenotype.,” Nature Communications, vol. 6, pp. 10068, 2015.
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