Stephan Bour

Summary

Affiliation: National Institutes of Health
Country: USA

Publications

  1. ncbi Naturally occurring amino acid substitutions in the HIV-2 ROD envelope glycoprotein regulate its ability to augment viral particle release
    Stephan Bour
    Viral Biochemistry Section, Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892 0460, USA
    Virology 309:85-98. 2003
  2. ncbi The HIV-1 Vpu protein: a multifunctional enhancer of viral particle release
    Stephan Bour
    Bioinformatics Core Facility, Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 4, Center Drive, Room 337, Bethesda, MD 20892 0460, USA
    Microbes Infect 5:1029-39. 2003
  3. ncbi DAVID Knowledgebase: a gene-centered database integrating heterogeneous gene annotation resources to facilitate high-throughput gene functional analysis
    Brad T Sherman
    Laboratory of Immunopathogenesis and Bioinformatics, Clinical Services Program, SAIC Frederick, Inc, National Cancer Institute at Frederick, Frederick, MD 21702, USA
    BMC Bioinformatics 8:426. 2007
  4. ncbi dCAS: a desktop application for cDNA sequence annotation
    Yongjian Guo
    Bioinformatics and Computational Biosciences Branch, Office of Cyber Infrastructure and Computational Biology and Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA
    Bioinformatics 25:1195-6. 2009
  5. ncbi Codon optimization of the HIV-1 vpu and vif genes stabilizes their mRNA and allows for highly efficient Rev-independent expression
    Kim Lien Nguyen
    Viral Biochemistry Section, Laboratory of Molecular Microbiology, National Institutes of Allergy Diseases, Bethesda, MD 20892, USA
    Virology 319:163-75. 2004
  6. ncbi Expression, purification, and activities of full-length and truncated versions of the integral membrane protein Vpu from HIV-1
    Che Ma
    Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, California 92093, USA
    Protein Sci 11:546-57. 2002
  7. ncbi Mutual functional destruction of HIV-1 Vpu and host TASK-1 channel
    Kate Hsu
    Institute of Molecular Cardiobiology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Mol Cell 14:259-67. 2004
  8. ncbi Specific interaction of CXCR4 with CD4 and CD8alpha: functional analysis of the CD4/CXCR4 interaction in the context of HIV-1 envelope glycoprotein-mediated membrane fusion
    Stephane Basmaciogullari
    Department of Cancer Immunology and AIDS, Dana Farber Cancer Institute, Boston, MA 02115, USA
    Virology 353:52-67. 2006

Collaborators

Detail Information

Publications8

  1. ncbi Naturally occurring amino acid substitutions in the HIV-2 ROD envelope glycoprotein regulate its ability to augment viral particle release
    Stephan Bour
    Viral Biochemistry Section, Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892 0460, USA
    Virology 309:85-98. 2003
    ....
  2. ncbi The HIV-1 Vpu protein: a multifunctional enhancer of viral particle release
    Stephan Bour
    Bioinformatics Core Facility, Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 4, Center Drive, Room 337, Bethesda, MD 20892 0460, USA
    Microbes Infect 5:1029-39. 2003
    ..This review focuses on presenting our current knowledge of the HIV-1-specific Vpu protein and its essential role in regulating viral particle release, viral load and expression of the CD4 receptor...
  3. ncbi DAVID Knowledgebase: a gene-centered database integrating heterogeneous gene annotation resources to facilitate high-throughput gene functional analysis
    Brad T Sherman
    Laboratory of Immunopathogenesis and Bioinformatics, Clinical Services Program, SAIC Frederick, Inc, National Cancer Institute at Frederick, Frederick, MD 21702, USA
    BMC Bioinformatics 8:426. 2007
    ..Thus, a highly centralized and ready-to-use gene-annotation knowledgebase is in demand for high throughput gene functional analysis...
  4. ncbi dCAS: a desktop application for cDNA sequence annotation
    Yongjian Guo
    Bioinformatics and Computational Biosciences Branch, Office of Cyber Infrastructure and Computational Biology and Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA
    Bioinformatics 25:1195-6. 2009
    ..AVAILABILITY: The dCAS package is distributed freely. A cross-platform installer and associated sequence databases can be downloaded at: http://exon.niaid.nih.gov/applications.html...
  5. ncbi Codon optimization of the HIV-1 vpu and vif genes stabilizes their mRNA and allows for highly efficient Rev-independent expression
    Kim Lien Nguyen
    Viral Biochemistry Section, Laboratory of Molecular Microbiology, National Institutes of Allergy Diseases, Bethesda, MD 20892, USA
    Virology 319:163-75. 2004
    ....
  6. ncbi Expression, purification, and activities of full-length and truncated versions of the integral membrane protein Vpu from HIV-1
    Che Ma
    Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, California 92093, USA
    Protein Sci 11:546-57. 2002
    ..The C-terminal alpha-helices modulate or promote the oligomerization of Vpu in the membrane and stabilize the conductive state of the channel, in addition to their involvement in CD4 degradation...
  7. ncbi Mutual functional destruction of HIV-1 Vpu and host TASK-1 channel
    Kate Hsu
    Institute of Molecular Cardiobiology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Mol Cell 14:259-67. 2004
    ..This virus-host interaction may influence HIV-1/AIDS progression, as well as electrical signaling in infected host tissues...
  8. ncbi Specific interaction of CXCR4 with CD4 and CD8alpha: functional analysis of the CD4/CXCR4 interaction in the context of HIV-1 envelope glycoprotein-mediated membrane fusion
    Stephane Basmaciogullari
    Department of Cancer Immunology and AIDS, Dana Farber Cancer Institute, Boston, MA 02115, USA
    Virology 353:52-67. 2006
    ..The CD4/CXCR4 and CD8alpha/CXCR4 interactions may thus be involved in cellular signaling pathways shared by the CD4 and CD8alpha molecules...