Expression of Nef from unintegrated HIV-1 DNA downregulates cell surface CXCR4 and CCR5 on T-lymphocytes
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1742-4690
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Expression of Nef from unintegrated HIV-1 DNA downregulates cell surface CXCR4 and CCR5 on T-lymphocytes ; volume:7 ; number:1 ; day:13 ; month:5 ; year:2010 ; pages:1-10 ; date:12.2010
Retrovirology ; 7, Heft 1 (13.5.2010), 1-10, 12.2010
- Creator
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Sloan, Richard D.
- Contributor
- DOI
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10.1186/1742-4690-7-44
- URN
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urn:nbn:de:1111-2016080712277
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:59 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Sloan, Richard D.
- Donahue, Daniel A.
- Kuhl, Björn D.
- Bar-Magen, Tamara
- Wainberg, Mark A.
- SpringerLink (Online service)
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CCR5 and CXCR4 antagonist and agonist binding sites
Spermine and spermidine bind CXCR4 and inhibit CXCR4- but not CCR5-tropic HIV-1 infection
Structural basis of dimerization of chemokine receptors CCR5 and CXCR4
Recombinant soluble CCR5 AND CXCR4 chemokine receptors as anti-HIV drug targets
Establishment of a novel CCR5 and CXCR4 expressing CD4+ cell line which is highly sensitive to HIV and suitable for high-throughput evaluation of CCR5 and CXCR4 antagonists
Effekte chemisch induzierter β-Arrestin-1-Translokation an die Chemokinrezeptoren CXCR4 und CCR5
Identification of an unique CXCR4 epitope whose ligation inhibits infection by both CXCR4 and CCR5 tropic human immunodeficiency type-I viruses
Chemokine receptors CXCR4 and CCR5: Cell surface expression, signaling and modulation by β-arrestin 2
Macrocyclic polyamines inhibit HIV infection by interacting with the cellular HIV co-receptors CXCR4 and CCR5
Enhanced CXCR4 expression of human CD8Low T lymphocytes is driven by S1P4
Organisationsdiagramm NEF; Fotoalbum NEF, S.5.; 1946
Bedeutung der N-Glykosylierung der Chemokinrezeptoren CXCR4 und CCR5 für die Infektion mit dem humanen Immundefizienzvirus Typ-1
CCR5 and CXCR4 antagonist and agonist binding sites
Spermine and spermidine bind CXCR4 and inhibit CXCR4- but not CCR5-tropic HIV-1 infection
Structural basis of dimerization of chemokine receptors CCR5 and CXCR4
Recombinant soluble CCR5 AND CXCR4 chemokine receptors as anti-HIV drug targets
Establishment of a novel CCR5 and CXCR4 expressing CD4+ cell line which is highly sensitive to HIV and suitable for high-throughput evaluation of CCR5 and CXCR4 antagonists
Effekte chemisch induzierter β-Arrestin-1-Translokation an die Chemokinrezeptoren CXCR4 und CCR5
Identification of an unique CXCR4 epitope whose ligation inhibits infection by both CXCR4 and CCR5 tropic human immunodeficiency type-I viruses
Chemokine receptors CXCR4 and CCR5: Cell surface expression, signaling and modulation by β-arrestin 2
Macrocyclic polyamines inhibit HIV infection by interacting with the cellular HIV co-receptors CXCR4 and CCR5
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Organisationsdiagramm NEF; Fotoalbum NEF, S.5.; 1946