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Updated: Apr 24, 2026

Highly Efficient Gene Disruption of Murine and Human Hematopoietic Progenitor Cells by CRISPR/Cas9
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Published on: April 10, 2018

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类似病毒的颗粒使得向基因工程和在人类初级髓状细胞中进行聚合CRISPR查成为可能

Hyuncheol Jung, Pascal Devant, Carter Ching

    bioRxiv : the preprint server for biology
    |December 19, 2025
    PubMed
    概括

    一个新的病毒样粒子 (VLP) 工具包有效地设计了用于免疫治疗的初级人类髓状细胞. 这项技术使基因编辑和功能查成为可能,揭示了巨细胞炎症反应的关键调节者.

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    CRISPR01:59

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    Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...
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