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从携带 FXN 基因第一内含子中 GAA 三核苷酸重复扩增的三位弗里德赖希共济失调(FRDA)患者中生成无转基因 iPSC 系。

Generation of transgene-free iPSC lines from three patients with Friedreich's ataxia (FRDA) carrying GAA triplet expansions in the first intron of FXN gene.

机构信息

School of Medicine, Koc University, Istanbul, Turkey.

Diagnostic Center for Genetic Diseases, Koc University Hospital, Koc University, Istanbul, Turkey.

出版信息

Stem Cell Res. 2021 Jul;54:102438. doi: 10.1016/j.scr.2021.102438. Epub 2021 Jun 27.

Abstract

Friedreich's ataxia (FRDA) is a rare neurodegenerative disorder which is caused by triplet repeat expansion (GAA) in the first intron of FXN gene. In this present study, we generated induced pluripotent stem cells (iPSC) lines from fibroblasts of three unrelated FRDA patients using integration-free episomal vectors. All iPSC lines express the pluripotency markers such as OCT4 and SSEA4, display normal karyotypes and can differentiate into all three germ layers via in vivo teratoma formation assay.

摘要

弗里德里希共济失调(FRDA)是一种罕见的神经退行性疾病,由 FXN 基因第一内含子中的三核苷酸重复扩展(GAA)引起。在本研究中,我们使用无整合的附加体载体从三位无关联 FRDA 患者的成纤维细胞中生成诱导多能干细胞(iPSC)系。所有 iPSC 系均表达多能性标志物,如 OCT4 和 SSEA4,显示正常核型,并可通过体内畸胎瘤形成试验分化为三个胚层。

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