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Transgenic Stra8-EYFP pigs: a model for developing male germ cell technologies.转基因 Stra8-EYFP 猪:开发雄性生殖细胞技术的模型。
Transgenic Res. 2012 Apr;21(2):383-92. doi: 10.1007/s11248-011-9542-6. Epub 2011 Aug 9.
2
Genetically modified pigs for medicine and agriculture.用于医学和农业的基因编辑猪。
Biotechnol Genet Eng Rev. 2008;25:245-65. doi: 10.7313/upo9781904761679.011.
3
The ΔF508 mutation causes CFTR misprocessing and cystic fibrosis-like disease in pigs.ΔF508 突变导致 CFTR 加工错误和猪的囊性纤维化样疾病。
Sci Transl Med. 2011 Mar 16;3(74):74ra24. doi: 10.1126/scitranslmed.3001868.
4
Disruption of the Survival Motor Neuron (SMN) gene in pigs using ssDNA.利用单链 DNA 破坏猪的生存运动神经元 (SMN) 基因。
Transgenic Res. 2011 Dec;20(6):1293-304. doi: 10.1007/s11248-011-9496-8. Epub 2011 Feb 25.
5
Gene targeting with zinc finger nucleases to produce cloned eGFP knockout pigs.利用锌指核酸酶进行基因靶向以生产克隆的增强绿色荧光蛋白(eGFP)基因敲除猪。
Mol Reprod Dev. 2011 Jan;78(1):2. doi: 10.1002/mrd.21271.
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Vascular endothelium-specific overexpression of human catalase in cloned pigs.克隆猪血管内皮细胞特异性过表达人过氧化氢酶。
Transgenic Res. 2011 Oct;20(5):989-1001. doi: 10.1007/s11248-010-9473-7. Epub 2010 Dec 18.
7
Prediabetes as a therapeutic target.糖尿病前期作为治疗靶点。
Clin Chem. 2011 Feb;57(2):215-20. doi: 10.1373/clinchem.2010.149096. Epub 2010 Nov 9.
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Murine models of acute and chronic lung infection with cystic fibrosis pathogens.鼠类急性和慢性肺部感染囊性纤维化病原体模型。
Int J Med Microbiol. 2010 Dec;300(8):584-93. doi: 10.1016/j.ijmm.2010.08.012. Epub 2010 Oct 14.
9
Activation method does not alter abnormal placental gene expression and development in cloned pigs.激活方法不会改变克隆猪中异常胎盘基因的表达和发育。
Mol Reprod Dev. 2010 Dec;77(12):1016-30. doi: 10.1002/mrd.21235. Epub 2010 Oct 5.
10
Generation of antibody- and B cell-deficient pigs by targeted disruption of the J-region gene segment of the heavy chain locus.通过靶向敲除重链基因座 J 区基因片段生成抗体和 B 细胞缺陷型猪。
Transgenic Res. 2011 Jun;20(3):625-41. doi: 10.1007/s11248-010-9444-z. Epub 2010 Sep 26.

用于医学和农业的猪的基因修饰。

Genetic modifications of pigs for medicine and agriculture.

机构信息

National Swine Resource and Research Center, University of Missouri, Columbia, Missouri 65211, USA.

出版信息

Mol Reprod Dev. 2011 Oct-Nov;78(10-11):879-91. doi: 10.1002/mrd.21333. Epub 2011 Jun 10.

DOI:10.1002/mrd.21333
PMID:21671302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3522184/
Abstract

Genetically modified swine hold great promise in the fields of agriculture and medicine. Currently, these swine are being used to optimize production of quality meat, to improve our understanding of the biology of disease resistance, and to reduced waste. In the field of biomedicine, swine are anatomically and physiologically analogous to humans. Alterations of key swine genes in disease pathways provide model animals to improve our understanding of the causes and potential treatments of many human genetic disorders. The completed sequencing of the swine genome will significantly enhance the specificity of genetic modifications, and allow for more accurate representations of human disease based on syntenic genes between the two species. Improvements in both methods of gene alteration and efficiency of model animal production are key to enabling routine use of these swine models in medicine and agriculture.

摘要

转基因猪在农业和医学领域具有巨大的应用潜力。目前,这些猪被用于优化优质肉类的生产,以增进我们对疾病抗性生物学的理解,并减少浪费。在生物医学领域,猪在解剖学和生理学上与人类相似。改变疾病途径中的关键猪基因可提供模型动物,以增进我们对许多人类遗传疾病的病因和潜在治疗方法的理解。猪基因组的完成测序将极大地提高遗传修饰的特异性,并允许基于两个物种之间的同线性基因,更准确地模拟人类疾病。基因修饰方法的改进和模型动物生产效率的提高是使这些猪模型在医学和农业中得到常规应用的关键。