使用人源APOBEC3Bctd-Cas9融合蛋白对拟南芥中甲基化胞嘧啶进行精确编辑。 - Suppr | 超能文献

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Precise editing of methylated cytosine in Arabidopsis thaliana using a human APOBEC3Bctd-Cas9 fusion.使用人源APOBEC3Bctd-Cas9融合蛋白对拟南芥中甲基化胞嘧啶进行精确编辑。

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Generation of stable nulliplex autopolyploid lines of Arabidopsis thaliana using CRISPR/Cas9 genome editing.利用CRISPR/Cas9基因组编辑技术生成拟南芥稳定的零倍体同源多倍体系。

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MagnEdit-interacting factors that recruit DNA-editing enzymes to single base targets.MagnEdit 相互作用的因素将 DNA 编辑酶招募到单碱基靶标。

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Development and Application of Base Editors.碱基编辑器的开发与应用。

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pKAMA-ITACHI Vectors for Highly Efficient CRISPR/Cas9-Mediated Gene Knockout in Arabidopsis thaliana.用于拟南芥中高效CRISPR/Cas9介导的基因敲除的pKAMA-ITACHI载体

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CRISPR/Cas9-mediated base-editing system efficiently generates gain-of-function mutations in Arabidopsis.CRISPR/Cas9介导的碱基编辑系统在拟南芥中高效产生功能获得性突变。

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CRISPR-based targeting of DNA methylation in by a bacterial CG-specific DNA methyltransferase.基于 CRISPR 的靶向 DNA 甲基化技术通过一种细菌 CG 特异性 DNA 甲基转移酶实现。

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Targeting specificity of APOBEC-based cytosine base editor in human iPSCs determined by whole genome sequencing.基于 APOBEC 的胞嘧啶碱基编辑器在人诱导多能干细胞中的靶向特异性由全基因组测序确定。

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The gene for domains rearranged methyltransferase (DRM2) in Arabidopsis thaliana plants is methylated at both cytosine and adenine residues.拟南芥植物中结构域重排甲基转移酶（DRM2）的基因在胞嘧啶和腺嘌呤残基上均发生甲基化。

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Optimization of CRISPR/Cas9 genome editing to modify abiotic stress responses in plants.优化CRISPR/Cas9基因组编辑以改变植物的非生物胁迫反应。

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Targeted genome-modification tools and their advanced applications in crop breeding.靶向基因组修饰工具及其在作物育种中的应用进展。

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