Generation of conditional Acvrl1 knockout mice by CRISPR/Cas9-mediated gene targeting.
Molecular and Cellular Probes(2018)
摘要
•This study is to generate mutant mice containing the Alk1 gene flanked with LoxP sequences to allow the conditional deletion of Alk1 by the LoxP/Cre system.•CRISPR/Cas9 technique was used to edit Alk1.•CRISPR/Cas9 technique was able to efficiently modify Alk1 and create the target mice.
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关键词
CRISPR/Cas9,Acvrl1,Mouse,Arteriovenous malformation
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