関連する実験動画

Updated: Aug 14, 2026

Generating CRISPR/Cas9 Mediated Monoallelic Deletions to Study Enhancer Function in Mouse Embryonic Stem Cells
11:31

Generating CRISPR/Cas9 Mediated Monoallelic Deletions to Study Enhancer Function in Mouse Embryonic Stem Cells

Published on: April 2, 2016

ヒトのオルニチントランスカルバミラーゼロカスにおける遺伝子消去および制限断片長さのポリモルフィズム

R Rozen, J Fox, W A Fenton

    Nature
    |February 6, 1985
    PubMed
    まとめ

    X関連代謝障害であるオルニチントランスカルバミラーゼ (OTC) 欠乏症は,産前診断に課題をもたらします. 研究者らは,遺伝子の削除と一般的なDNAポリモルフィズムを特定し,多くの家族にとってキャリア状態の決定と産前診断の改善を可能にしました.

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