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Open AccessNMR spectroscopy of HIV-1 gp120 outer domain
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Open AccessPartial germline reversions can increase VRC07 potency and breadth
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Open AccessStructure-guided modification and optimization of antibody VRC07
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Open AccessDeep sequencing with longitudinal sampling of a VRC01-like-antibody response in a chronically infected individual
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Open AccessHyperglycosylated resurfaced stabilized GP120 core as an immunogen elicits antibodies targeted at the CD4-binding site
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Open AccessCharacteristics of HIV-1 gp120 molecules that bind ancestor, intermediate and mature forms of VRC01-like antibodies
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Open AccessTransforming epitope-specific gp120 monomer-based probes into immunogens with N-linked glycan masking
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Open AccessDesign of an HIV Env antigen that binds with high affinity to antibodies against linear, conformational and broadly neutralizing epitopes within V1/V2
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Open AccessP14-10. Comparable immunogenicity of VRC DNA and rAd5 HIV-1 vaccines delivered by intramuscular, subcutaneous and intradermal routes in healthy adults (VRC 011)
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Open AccessP17-27. Development of recombinant adenovirus 28 vectors for HIV vaccines
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Open AccessP20-21 LB. Gene-to-gene differences in evolutionary rate between HIV-1 and natural SIV from sooty mangabeys: implications for vaccine tests in non-human primates
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Open AccessP13-01. Crystal structure and function of a monoclonal antibody against primate CD4 that blocks HIV/SIV infection
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Open AccessP13-07 LB. A human blocking antibody to CCR5 partially protects against lentiviral infection in non-human primates
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Open AccessP04-38. Crystal structure of gp120 in complex with the CD4-binding-site antibody b13 suggests precise targeting is needed for neutralization
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Open AccessP19-37. Replication-defective lymphocytic choriomeningitis virus vectors boost cellular and humoral immunity after DNA or adenovirus vector priming
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Open AccessRational Design of AIDS Vaccines
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Gene transfer into human umbilical cord blood-derived CD34+ cells by particle-mediated gene transfer
Delivery of genes into hematopoietic progenitor cells offers an attractive means for the introduction of corrective or protective genes into cells of both the myeloid and lymphoid lineage. Previously, investig...
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Combination gene transfer to potentiate tumor regression
Recent efforts to treat malignancy using gene transfer have met with varying degrees of success. In this paper, we report the results of studies using two recombinant adenoviral vectors to examine the efficacy...
