Hyperglycosylated resurfaced stabilized GP120 core as an immunogen elicits antibodies targeted at the CD4-binding site

K Dai; JC Boyington; W Shi; SD Schmidt; I Georgiev; D Lingwood; PD Kwong; JR Mascola; Z Yang; GJ Nabel

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Hyperglycosylated resurfaced stabilized GP120 core as an immunogen elicits antibodies targeted at the CD4-binding site

机译：高糖基化表面稳定的GP120核心作为免疫原引发针对CD4结合位点的抗体

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《Retrovirology》 |2012年第s2期|共页
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K Dai; JC Boyington; W Shi; SD Schmidt; I Georgiev; D Lingwood; PD Kwong; JR Mascola; Z Yang; GJ Nabel;
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中图分类细胞生物化学;
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1. Hyperglycosylated resurfaced stabilized GP120 core as an immunogen elicits antibodies targeted at the CD4-binding site [J] . K Dai, JC Boyington, W Shi, Retrovirology . 2012,第S2期

机译：高糖基化表面稳定的GP120核心作为免疫原引发针对CD4结合位点的抗体
2. Hyperglycosylated gp120 mutants elicit improved CD4-binding site directed antibodies in a heterologous prime:boost regimen [J] . FK Ahmed, BE Clark, R Pantophlet Retrovirology . 2012,第S2期

机译：高糖基化的GP120突变体引发改进的CD4结合位点，在异源性素数：升压方案
3. An engineered mutant of HIV-1 gp120 formulated with adjuvant Quil A promotes elicitation of antibody responses overlapping the CD4-binding site. [J] . Ahmed F. K., Clark B. E., Burton D. R., Vaccine . 2012,第5期

机译：用佐剂Quil A配制的HIV-1 gp120的工程突变体可促进引起与CD4结合位点重叠的抗体反应。
4. Chapter 6 Strategies for Designing Peptide Immunogens To Elicit a-Helical Conformation-Specific Antibodies Reactive with Native Proteins [C] . Zhe Yan, Wendy J. Hartsock, Zhaohui Qian, American Chemical Society. . 2012

机译：第6章设计肽免疫原的策略，以引发与天然蛋白质反应的α-螺旋构象特异性抗体
5. Designing immunogens to elicit broadly reactive neutralizing antibodies to the HIV envelope. [D] . Derby, Nina Rafterman. 2007

机译：设计免疫原以引发针对HIV包膜的广泛反应性中和抗体。
6. Hyperglycosylated resurfaced stabilized GP120 core as an immunogen elicits antibodies targeted at the CD4-binding site [O] . K Dai, JC Boyington, W Shi, 2012

机译：高糖基化的表面稳定化GP120核心作为免疫原引发针对CD4结合位点的抗体
7. Hyperglycosylated resurfaced stabilized GP120 core as an immunogen elicits antibodies targeted at the CD4-binding site [O] . K Dai, JC Boyington, W Shi, 2012

机译：高糖基化的表面稳定化GP120核心作为免疫原引发针对CD4结合位点的抗体

Hyperglycosylated resurfaced stabilized GP120 core as an immunogen elicits antibodies targeted at the CD4-binding site

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