• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

RAB4A纯合敲除诱导多能干细胞(iPSC)系的产生。

Generation of RAB4A homozygous knockout induced pluripotent stem cell (iPSC) line.

作者信息

Wang Rui, Shen Qing

机构信息

CAS Key Laboratory of Regenerative Biology, Joint School of Life Sciences, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou Medical University, Guangzhou, China; Centre for Regenerative Medicine and Health, Hong Kong Institute of Science & Innovation, Chinese Academy of Sciences, Hong Kong Special Administrative Region; Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, China-New Zealand Joint Laboratory on Biomedicine and Health, CUHK-GIBH Joint Research Laboratory on Stem Cells and Regenerative Medicine, Institute for Stem Cell and Regeneration, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China; University of Chinese Academy of Sciences, Beijing, China.

Guangzhou Baikang Cell Life Science and Technology Company Limited, Guangzhou, China.

出版信息

Stem Cell Res. 2024 Dec;81:103556. doi: 10.1016/j.scr.2024.103556. Epub 2024 Sep 14.

DOI:10.1016/j.scr.2024.103556
PMID:39299131
Abstract

The RAB4A gene is a member of the largest group in the Ras superfamily of small GTPases, which regulate membrane trafficking. The encoded protein is associated with early endosomes and is involved in sorting and recycling. In this study, we generated induced pluripotent stem cells (iPSC) from a healthy individual by electroporation of peripheral blood mononuclear cells. We generated a RAB4A homozygous knockout human iPSC line via CRISPR/Cas9 gene editing. The iPSCs-RAB4A had a normal karyotype, expressed pluripotency markers, and maintained trilineage differentiation potential.

摘要

RAB4A基因是小GTP酶Ras超家族中最大的一组成员,该家族调节膜运输。编码的蛋白质与早期内体相关,参与分选和再循环。在本研究中,我们通过电穿孔外周血单个核细胞从一名健康个体中生成了诱导多能干细胞(iPSC)。我们通过CRISPR/Cas9基因编辑生成了RAB4A纯合敲除的人类iPSC系。iPSCs-RAB4A具有正常的核型,表达多能性标志物,并保持三系分化潜能。

相似文献

1
Generation of RAB4A homozygous knockout induced pluripotent stem cell (iPSC) line.RAB4A纯合敲除诱导多能干细胞(iPSC)系的产生。
Stem Cell Res. 2024 Dec;81:103556. doi: 10.1016/j.scr.2024.103556. Epub 2024 Sep 14.
2
Generation of a homozygous (MCRIi031-A-3) WT1 knockout human iPSC line.生成一个纯合的(MCRIi031-A-3)WT1 敲除的人诱导多能干细胞系。
Stem Cell Res. 2024 Sep;79:103494. doi: 10.1016/j.scr.2024.103494. Epub 2024 Jul 10.
3
Generation of KCNH2 heterozygous knockout induced pluripotent stem cell (iPSC) line (Long and Short QT Syndrome).KCNH2 杂合型基因敲除诱导多能干细胞(iPSC)系的建立(长 QT 综合征和短 QT 综合征)。
Stem Cell Res. 2024 Jun;77:103400. doi: 10.1016/j.scr.2024.103400. Epub 2024 Mar 26.
4
Generation of heterozygous (MCRIi031-A-1) and homozygous (MCRIi031-A-2) SOX9 knockout human iPSC lines.生成杂合子(MCRIi031-A-1)和纯合子(MCRIi031-A-2)SOX9 敲除人 iPSC 系。
Stem Cell Res. 2024 Sep;79:103484. doi: 10.1016/j.scr.2024.103484. Epub 2024 Jun 22.
5
Generation of heterozygous KCNA2 knockout induced pluripotent stem cell line.杂合型KCNA2基因敲除诱导多能干细胞系的产生。
Stem Cell Res. 2024 Dec;81:103596. doi: 10.1016/j.scr.2024.103596. Epub 2024 Oct 21.
6
Generation of a homozygous ABCA7 knockout cell line (AHMUCNi002-A) in human iPSCs using CRISPR/Cas9.使用CRISPR/Cas9在人诱导多能干细胞中生成纯合ABCA7基因敲除细胞系(AHMUCNi002-A)。
Stem Cell Res. 2025 Jun;85:103700. doi: 10.1016/j.scr.2025.103700. Epub 2025 Mar 25.
7
Generation of a homozygous ABCA7-knockout human iPSC line using the CRISPR/Cas9 system.使用CRISPR/Cas9系统生成纯合ABCA7基因敲除的人诱导多能干细胞系。
Stem Cell Res. 2023 Feb;66:103000. doi: 10.1016/j.scr.2022.103000. Epub 2022 Dec 7.
8
Generation of a TLR7 homozygous knockout human induced pluripotent stem cell line using CRISPR/Cas9.利用CRISPR/Cas9技术生成TLR7纯合敲除的人诱导多能干细胞系。
Stem Cell Res. 2019 Oct;40:101520. doi: 10.1016/j.scr.2019.101520. Epub 2019 Jul 31.
9
CRISPR/Cas9 Genome Editing of Human-Induced Pluripotent Stem Cells Followed by Granulocytic Differentiation.CRISPR/Cas9 基因组编辑的人类诱导多能干细胞,随后进行粒细胞分化。
Methods Mol Biol. 2020;2115:471-483. doi: 10.1007/978-1-0716-0290-4_27.
10
Generation of homozygous and heterozygous REEP1 knockout induced pluripotent stem cell lines by CRISPR/Cas9 gene editing.通过 CRISPR/Cas9 基因编辑技术生成纯合和杂合 REEP1 基因敲除诱导多能干细胞系。
Stem Cell Res. 2024 Jun;77:103378. doi: 10.1016/j.scr.2024.103378. Epub 2024 Mar 5.