Suppr超能文献

CRISPR 碱基编辑器筛选可大规模鉴定变异功能。

CRISPR base editor screens identify variant function at scale.

机构信息

Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA; Computational Biology Program, Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA; Department of Genome Sciences, University of Washington, Seattle, WA, USA.

Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA; Computational Biology Program, Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA; Department of Genome Sciences, University of Washington, Seattle, WA, USA.

出版信息

Mol Cell. 2021 Feb 18;81(4):647-648. doi: 10.1016/j.molcel.2021.01.036.

Abstract

Cuella-Martin et al. (2021) and Hanna et al. (2021) showcase CRISPR base editing in large-scale pooled screens in human cells to discover both loss- and gain-of-function variants, enabling protein structure/function insights and clinical variant interpretation.

摘要

Cuella-Martin 等人(2021 年)和 Hanna 等人(2021 年)展示了在人类细胞中的大规模 pooled 筛选中使用 CRISPR 碱基编辑技术来发现功能丧失和获得性功能变异体,从而能够深入了解蛋白质结构/功能,并进行临床变异体解释。

相似文献

3
Directed Evolution of CRISPR-Cas9 Base Editors.CRISPR-Cas9 碱基编辑器的定向进化。
Trends Biotechnol. 2019 Nov;37(11):1151-1153. doi: 10.1016/j.tibtech.2019.09.005. Epub 2019 Oct 14.
6
The current CRISPR methods.当前的CRISPR方法。
Methods. 2021 Oct;194:1-2. doi: 10.1016/j.ymeth.2021.08.002. Epub 2021 Aug 10.

引用本文的文献

本文引用的文献

6
Accurate classification of BRCA1 variants with saturation genome editing.饱和基因组编辑精准分类 BRCA1 变异。
Nature. 2018 Oct;562(7726):217-222. doi: 10.1038/s41586-018-0461-z. Epub 2018 Sep 12.
9
High-throughput Phenotyping of Lung Cancer Somatic Mutations.肺癌体细胞突变的高通量表型分析
Cancer Cell. 2016 Aug 8;30(2):214-228. doi: 10.1016/j.ccell.2016.06.022. Epub 2016 Jul 28.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验