Vaccination with Gag, Vif, and Nef gene fragments affords partial control of viral replication after mucosal challenge with SIVmac239.

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Published in J Virol on April 16, 2014

Authors

Mauricio A Martins1, Nancy A Wilson2, Shari M Piaskowski3, Kim L Weisgrau3, Jessica R Furlott3, Myrna C Bonaldo4, Marlon G Veloso de Santana1, Richard A Rudersdorf3, Eva G Rakasz3, Karen D Keating5, Maria J Chiuchiolo6, Michael Piatak7, David B Allison5, Christopher L Parks6, Ricardo Galler8, Jeffrey D Lifson7, David I Watkins9

Author Affiliations

1: Department of Pathology, University of Miami Miller School of Medicine, Miami, Florida, USA.
2: Department of Medicine, University of Wisconsin-Madison, Madison, Wisconsin, USA.
3: Wisconsin National Primate Research Center, University of Wisconsin-Madison, Madison, Wisconsin, USA.
4: Laboratório de Biologia Molecular de Flavivírus, Instituto Oswaldo Cruz, Rio de Janeiro, Brazil.
5: Section on Statistical Genetics, Department of Biostatistics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
6: International AIDS Vaccine Initiative, AIDS Vaccine Design and Development Laboratory, Brooklyn Army Terminal, Brooklyn, New York, USA.
7: AIDS and Cancer Virus Program, Leidos Biomedical Research, Inc., Frederick National Laboratory, Frederick, Maryland, USA.
8: Instituto de Tecnologia em Imunobiológicos, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
9: Department of Pathology, University of Miami Miller School of Medicine, Miami, Florida, USA dwatkins@med.miami.edu.

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