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Development of Humanized Mice in the Age of Genome Editing

机译:基因组编辑时代人源小鼠的发展

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ABSTRACT Mice are the most commonly used model organisms to study human disease. Many genetic human diseases can be recapitulated by modifying the mouse genome allowing the testing of existing and novel therapeutics, including combinatorial therapeutics, without putting humans at risk. Specifically, the development of “humanized” mice, that is, severely immunodeficient mice engrafted with functional human hematopoietic and immune cells and tissues, has revolutionized our ability to study and model human diseases in preclinical in vivo systems. Until recently it has been challenging to develop strains of humanized mice with targeted mutations or that transgenically express human genes with site‐specific mutations, and can permit optimal growth of functional human cells and tissues. However, recent advances in targeted nuclease‐based genetic engineering have enabled precise modification and development of humanized mouse models at an unprecedented pace. These modifications permit optimal growth of functional human cells and tissues and can be used to replicate human genetically determined diseases. J. Cell. Biochem. 118: 3043–3048, 2017. ? 2017 Wiley Periodicals, Inc.
机译:摘要小鼠是研究人类疾病最常用的模型生物。通过修饰小鼠基因组可以重新携带许多遗传人类疾病,允许测试存在的现有和新的治疗剂,包括组合治疗剂,而不会使人类处于风险。具体而言,“人源化”小鼠的发展,即携带功能性人造血和免疫细胞和组织的严重免疫缺陷小鼠,已经彻底改变了我们在体内体内研究和模拟人类疾病的能力。直到最近,它一直挑战,具有靶向突变的人源化小鼠的菌株或转基因特异性突变的原始表达人类基因,并且可以允许官能性人细胞和组织的最佳生长。然而,近期基于核酸酶的基因工程的最新进展使得以前所未有的速度使人性化小鼠模型的精确改性和发展能够。这些修饰允许功能性人细胞和组织的最佳生长,并且可用于复制人类遗传确定的疾病。 J.Cell。生物学习。 118:3043-3048,2017 2017年Wiley期刊,Inc。

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