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陈晨
Life Science
中国医科大学
辽宁
Language: 中文, 英语
罕见病
致病机理
遗传调控
表观遗传调控
生殖障碍
基因组学
表观基因组学
疾病机制
遗传病
生殖健康
Areas of Focus
- 罕见病的致病机理
- 生殖障碍疾病的遗传与表观遗传调控
Publications
- 卵泡体外激活在早发性卵巢功能不全患者辅助生殖中的研究进展, 刘湛傲，陈晨, 2023
- CRISPR-Cas9基因编辑技术在肿瘤治疗中的研究进展, 丁弈丹，陈晨, 2022
- Recurrent Stroke-Like Symptoms After Cesarean Section Deliveries in a Female Patient With X-Linked Charcot-Marie-Tooth Type 1, Qu Li, Chen Chen, Yan Ren, Xu Liu, 2020
- Novel homozygous nonsense mutations in LHCGR lead to empty follicle syndrome and 46, XY disorder of sex development, Chen C, Xu X, Kong L, Li P, Zhou F, Zhao S, Xin X, Tan J, Zhang X, 2018
- A Novel Splicing Mutation Identified in a Chinese Family with X-linked Alport Syndrome Using Targeted Next-Generation Sequencing, Chen C, Lu CX, Wang Q, Cao LH, Luo Y, Zhang X, 2016
- Screening of Duchenne Muscular Dystrophy (DMD) Mutations and Investigating Its Mutational Mechanism in Chinese Patients, Chen C, Ma H, Zhang F, Chen L, Xing X, Wang S, Zhang X, Luo Y, 2014
- TERT Promoter Mutations Lead to High Transcriptional Activity under Hypoxia and Temozolomide Treatment and Predict Poor Prognosis in Gliomas, Chen C, Han S, Meng L, Li Z, Zhang X, Wu A, 2014
