A polyvalent DNA prime with matched polyvalent proteinGLASE boost regimen elicited the most robust and broad lgG and V1V2 binding antibody and antibody and CV4 T cell responses among 13 HIV vaccine trials
dc.article.end-page | 20 | en |
dc.article.start-page | 1 | en |
dc.citation.doi | 10.1080/22221751.2025.2485317 | en |
dc.contributor.author | Z Moodie | en |
dc.contributor.author | Shuying Sue Li | en |
dc.contributor.author | Elena E Giorgi | en |
dc.contributor.author | LaTonya D Williams | en |
dc.contributor.author | Fatima Laher | en |
dc.contributor.author | Glenda Gray | en |
dc.contributor.author | E et al | en |
dc.date.accessioned | 2025-07-31T08:49:46Z | |
dc.faculty | FACULTY OF HEALTH SCIENCES | en |
dc.identifier.citation | WOS | en |
dc.identifier.uri | https://hdl.handle.net/10539/45720 | |
dc.journal.title | A polyvalent DNA prime with matched polyvalent proteinGLASE boost regimen elicited the most robust and broad lgG and V1V2 binding antibody and antibody and CV4 T cell responses among 13 HIV vaccine trials | en |
dc.journal.volume | 14 | en |
dc.title | A polyvalent DNA prime with matched polyvalent proteinGLASE boost regimen elicited the most robust and broad lgG and V1V2 binding antibody and antibody and CV4 T cell responses among 13 HIV vaccine trials | en |
dc.type | Journal Article | en |
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