Generation of Dip2a homozygous knockout murine ES cell line IBMSe001-A-1 via CRISPR/Cas9 technology

DIP2A mutation is associated with abnormal brain development and diseases including dyslexia, autism and Alzheimer's disease. However, the role and the involved mechanisms remain unknown. To study the biological function of DIP2A during mESCs neural differentiation in early neural development,...

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מידע ביבליוגרפי
Main Authors: Mingze Yao, Qian Yang, Mengqiao Lian, Pengfei Su, Xiaogang Cui, Tinglin Ren, Xiedong Wang, Changxin Wu, Yaowu Zheng
פורמט: Artigo
שפה:Inglês
יצא לאור: Elsevier 2020-05-01
סדרה:Stem Cell Research
גישה מקוונת:http://www.sciencedirect.com/science/article/pii/S1873506120300829
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