机译:在牛中产生克隆的后代和CRISPR / CAS9基因组编辑牛的胚胎成纤维细胞
Ernst Fed Sci Ctr Anim Husb Podolsk Russia;
Moscow MV Lomonosov State Univ Inst Funct Genom Moscow Russia|Skolkovo Inst Sci & Technol Ctr Life Sci Skolkovo Russia|Moscow MV Lomonosov State Univ Fac Chem Moscow Russia;
Ernst Fed Sci Ctr Anim Husb Podolsk Russia;
Moscow MV Lomonosov State Univ Fac Chem Moscow Russia;
Ernst Fed Sci Ctr Anim Husb Podolsk Russia;
Res Ctr Biotechnol Moscow Russia;
Ernst Fed Sci Ctr Anim Husb Podolsk Russia;
Ernst Fed Sci Ctr Anim Husb Podolsk Russia;
Utah State Univ Dept Anim Dairy & Vet Sci Logan UT 84322 USA;
Ernst Fed Sci Ctr Anim Husb Podolsk Russia;
Univ Vet Med Dept Anim Breeding & Genet Vienna Austria;
Skolkovo Inst Sci & Technol Ctr Life Sci Skolkovo Russia|Moscow MV Lomonosov State Univ Fac Chem Moscow Russia|Moscow MV Lomonosov State Univ Belozersky Res Inst Physicochem Biol Moscow Russia|Shemyakin Ovchinnikov Inst Bioorgan Chem Moscow Russia;
Ernst Fed Sci Ctr Anim Husb Podolsk Russia;
Bos taurus; somatic cloning; gene editing; beta-lactoglobulin knock-out;
机译:使用CRISPR / CAS9 RiboNule蛋白接种对隐性营养不良表皮细胞释放方法的一步性IPSC重新编程和基因组编辑和基因组编辑
机译:CRISPR基因组编辑后从镰状细胞病患者血液中克隆的后代红细胞的细胞功能重建
机译:使用CRISPR / CAS9基因组编辑系统从小鼠颌下腺的功能产生功能性人体神经生长因子
机译:通过光学递送CRISPR / Cas9核糖核蛋白在马铃薯原生质体中进行靶向基因组编辑
机译:Chromothripsis作为CRISPR-CAS9基因组编辑的目标后果
机译:用于植物中基于CRISPR / Cas9的基因组编辑的高效连接无关克隆系统
机译:413使用Crispr / Cas9 RiboNule蛋白接种用于隐性营养不良结果的核细胞蛋白方法对原发性成纤维细胞的一步性IPSC重编程和基因组编辑