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1 andom location (so-called KO-plus-transgenic humanization).
2 rine lungs and spleens indicating successful humanization.
3 2.5-A resolution and used as a template for humanization.
4 rent and random location; KO-plus-transgenic humanization.
5 facilitate further antibody optimization and humanization.
6 f immunodeficient mouse strains suitable for humanization.
7 ts were allowed to heal on naive mice before humanization.
8 e changes necessary to regain activity after humanization.
9 and also suggest a possible means of enzyme "humanization."
14 the Ebola virus now provides a framework for humanization and development of a postexposure immunothe
15 the immunogenicity of rodent antibodies via humanization and generation of antibodies in transgenic
16 gn strategy could be applied during antibody humanization and library design for in vitro display met
18 Here, we present data on the identification, humanization, and in vitro pharmacology of an antidote f
19 ovides a detailed description of our genetic humanization approach, and the companion paper reports t
21 rparts at the same genetic location (in situ humanization), but such efforts involved laborious proce
22 oach (i) provides a rapid route for antibody humanization constraining the content of original mouse
25 notransplantation with human immune systems (humanization) has been problematic because C57BL/6 SIRPa
30 of its high affinity and its high degree of humanization, JC-7U IgG1 is an excellent drug candidate
36 Here we demonstrate marked effects of this humanization of Foxp2 on learning and striatal neuroplas
38 it immune repertoires for the generation and humanization of monoclonal antibodies that bind with str
42 designed combinatorial V gene libraries, the humanization of mouse monoclonal antibody LM609 directed
47 ural information and computational tools the humanization of rodent antibodies for clinical use often
53 themes emerged: 1) a feeling of support, 2) humanization of the medical system, 3) an opportunity fo
54 r findings have significant implications for humanization of the mouse IgG1 currently in clinical tri
56 ell-binding antibodies, these data show that humanization offers a significant reduction in immunogen
58 tibody-derived antibody sequence used during humanization, only the CDR3 region from a murine antibod
59 hus overcoming the major drawback of current humanization procedures, the requirement to construct an
60 ut these systems involve a long and variable humanization process, are expensive, and require the use
62 cells and stromal cells occurs 2 weeks after humanization, so investigators should expect to observe
65 highly successful in the clinic, all current humanization techniques have potential limitations, such
67 for very large, in situ, and precise genetic humanization using large compound bacterial artificial c
70 immunodeficiency virus, type 1 disease, its humanization was desired to minimize the potential for i
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