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Humanized Mouse Models of Clinical Disease.临床疾病的人源化小鼠模型
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ANIMAL RESEARCH. Chimpanzee sanctuaries open door to more research.动物研究。黑猩猩保护区为更多研究敞开大门。
Science. 2016 Jul 29;353(6298):433-4. doi: 10.1126/science.353.6298.433.
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Simple, Efficient CRISPR-Cas9-Mediated Gene Editing in Mice: Strategies and Methods.小鼠中简单、高效的CRISPR-Cas9介导的基因编辑:策略与方法
Methods Mol Biol. 2016;1438:19-53. doi: 10.1007/978-1-4939-3661-8_2.
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Site-specific recombinases: molecular machines for the Genetic Revolution.位点特异性重组酶:基因革命的分子机器。
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Generation of improved humanized mouse models for human infectious diseases.生成改良的人类感染疾病的人源化小鼠模型。
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Humanized NOD-SCID IL2rg–/– mice as a preclinical model for cancer research and its potential use for individualized cancer therapies.人源化 NOD-SCID IL2rg–/– 小鼠作为癌症研究的临床前模型及其在个体化癌症治疗中的潜在应用。
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Nonhuman primate models in the genomic era: a paradigm shift.基因组时代的非人灵长类动物模型:范式转变。
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Human immune system development and survival of non-obese diabetic (NOD)-scid IL2rγ(null) (NSG) mice engrafted with human thymus and autologous haematopoietic stem cells.人免疫系统的发育和非肥胖型糖尿病(NOD)-scid IL2rγ(null)(NSG)小鼠植入人胸腺和自体造血干细胞的存活。
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ZFN, TALEN, and CRISPR/Cas-based methods for genome engineering.基于 ZFN、TALEN 和 CRISPR/Cas 的基因组编辑方法。
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基因组编辑时代人源化小鼠的发展

Development of Humanized Mice in the Age of Genome Editing.

作者信息

Hosur Vishnu, Low Benjamin E, Avery Cindy, Shultz Leonard D, Wiles Michael V

机构信息

The Jackson Laboratory, Bar Harbor 04609, Maine.

出版信息

J Cell Biochem. 2017 Oct;118(10):3043-3048. doi: 10.1002/jcb.26002. Epub 2017 May 15.

DOI:10.1002/jcb.26002
PMID:28332231
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5550330/
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.

摘要

小鼠是研究人类疾病最常用的模式生物。通过修饰小鼠基因组可以重现许多人类遗传疾病,从而能够在不危及人类的情况下测试现有的和新型的治疗方法,包括联合治疗。具体而言,“人源化”小鼠的开发,即植入功能性人类造血和免疫细胞及组织的严重免疫缺陷小鼠,彻底改变了我们在临床前体内系统中研究和模拟人类疾病的能力。直到最近,开发具有靶向突变或转基因表达具有位点特异性突变的人类基因、并能使功能性人类细胞和组织实现最佳生长的人源化小鼠品系一直具有挑战性。然而,基于靶向核酸酶的基因工程的最新进展使得以前所未有的速度精确修饰和开发人源化小鼠模型成为可能。这些修饰能使功能性人类细胞和组织实现最佳生长,并可用于复制人类基因决定的疾病。《细胞生物化学杂志》118: 3043 - 3048, 2017年。© 2017威利期刊公司。