Functional genomics and the future of iPSCs in disease modeling
Imogen R. Brooks, Cristina Maria Garrone, Caoimhe Kerins, Cher Shen Kiar, Sofia Syntaka, Jessie Z. Xu, Francesca Maria Spagnoli, Fiona M. Watt
King's College London European Molecular Biology Laboratory
阅读操作
确认中在文库中上传 PDF 后可生成中文音频讲解。
摘要与影响
Induced pluripotent stem cells (iPSCs) are valuable in disease modeling because of their potential to expand and differentiate into virtually any cell type and recapitulate key aspects of human biology. Functional genomics are genome-wide studies that aim to discover genotype-phenotype relationships, thereby revealing the impact of human genetic diversity on normal and pathophysiology. In this review, we make the case that human iPSCs (hiPSCs) are a powerful tool for functional genomics, since they provide an in vitro platform for the study of population genetics. We describe cutting-edge tools and strategies now available to researchers, including multi-omics technologies, advances in hiPSC culture techniques, and innovations in drug development. Functional genomics approaches based on hiPSCs hold great promise for advancing drug discovery, disease etiology, and the impact of genetic variation on human biology.
逐年被引趋势
关键指标
同类平均 = 1
同领域 · 同年份 · 同类型
Google Scholar 与 OpenAlex 的被引统计范围不同,数值存在差异属正常。
AI 辅助阅读
依据:摘要
可就本文提问;依据不足时会说明。
学术脉络
学科主题
生物医学Pluripotent Stem Cells Research
CRISPR and Genetic Engineering · Genetic Associations and Epidemiology
参考文献 113
此处列出前 3 条
引用本文 53
按被引量排序,此处列出前 3 条