Genetically engineered humanized mouse models for preclinical antibody studies.

Genetically engineered humanized mouse models for preclinical antibody studies.
复制标题

DOI:
10.1007/s40259-013-0071-0
复制
发表时间:
2014-04
期刊:
BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy
影响因子:
--
通讯作者:
Roopenian DC
Roopenian DC
中科院分区:
其他
文献类型:
--
作者:
Proetzel G;Wiles MV;Roopenian DC

文献摘要

参考文献

相似文献

基因工程的使用极大地提高了我们在临床前研究中创建动物模型的能力。随着基因编辑技术的最新进展,现在可以根据需要非常快速地创建高度可调的小鼠模型。在这里,我们概述了基因工程方法,以及人源化新生儿Fc受体(FcRn)模型的发展及其在单克隆抗体体内研究中的应用。
The use of genetic engineering has vastly improved our capabilities to create animal models relevant in preclinical research. With the recent advances in gene-editing technologies, it is now possible to very rapidly create highly tunable mouse models as needs arise. Here, we provide an overview of genetic engineering methods, as well as the development of humanized neonatal Fc receptor (FcRn) models and their use for monoclonal antibody in vivo studies.
DOI: 10.1006/bbrc.1997.7124
发表时间: 1997-08-28
影响因子: 3.1
作者:
Feil, R;Wagner, J;Chambon, P
通讯作者: Chambon, P
DOI: 10.1074/jbc.m110.164848
发表时间: 2011-02-18
影响因子: 4.8
作者:
Andersen, Jan Terje;Pehrson, Rikard;Ekblad, Caroline
通讯作者: Ekblad, Caroline
DOI: 10.1172/jci200418838
发表时间: 2004-05-01
影响因子: 15.9
作者:
Akilesh, S;Petkova, S;Roopenian, D
通讯作者: Roopenian, D
DOI: 10.1182/blood-2011-08-367813
发表时间: 2012-03-29
期刊: BLOOD
影响因子: 20.3
作者:
Dumont, Jennifer A.;Liu, Tongyao;Jiang, Haiyan
通讯作者: Jiang, Haiyan
DOI: 10.1038/ng794
发表时间: 2002-01-01
期刊: NATURE GENETICS
影响因子: 30.8
作者:
Anderson, MG;Smith, RS;John, SWM
通讯作者: John, SWM