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Titlebook: Subcellular Biochemistry; Volume 10 Donald B. Roodyn Book 1984 Plenum Press, New York 1984 Calcium.Chloroplast.DNA.Lipid.Nucleotide.RNA.bio

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Rafael Sentandreu,Enrique Herrero,José P. Martínez-García,Germán Larribairus. This chapter gives a general overview of how HIV-1 is neutralized by antibody, why the neutralizing antibody response fails to control infection and, finally, what is being done to develop an HIV-1 vaccine that has an effective antibody component.
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Héctor N. Seuánezypeptide composed of a C-terminal-truncated . peptide and the entire . peptide. The second stage involves the proteolytic processing of this fusion protein to generate mature structural and functional viral components (Debouck ., 1987; Lillehoj ., 1988). An HIV-specific protease cleaves the fusion p
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oduce some ten different recombinant baculoviruses expressing various gene products encoded by both HIV-1 and HIV-2. Here we describe four of these recombinant viruses that produce products encoded by the gag and . genes of HIV-1. We show that a feature of gag and . translation in HIV-1 infected cel
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Rafael Sentandreu,Enrique Herrero,José P. Martínez-García,Germán Larribacific antigens. Perhaps the most beneficial B cell response is one that is directed against the surface gp120 and transmembrane gp41 envelope glycoproteins of the virus; both glycoproteins are major targets for the antibody-mediated neutralization of HIV-1 infectivity. To ensure its survival, the vi
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B. B. Biswas,B. Ghosh,Arun Lahiri Majumdercific antigens. Perhaps the most beneficial B cell response is one that is directed against the surface gp120 and transmembrane gp41 envelope glycoproteins of the virus; both glycoproteins are major targets for the antibody-mediated neutralization of HIV-1 infectivity. To ensure its survival, the vi
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