The N-terminal domain of APJ, a CNS-based coreceptor for HIV-1, is essential for its receptor function and coreceptor activity (Q28191538)

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Xiaoling Zhang

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Xuejun Fan

3

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Elias Argyris

4

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Jianhua Fang

5

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Edward Acheampong

6

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Garrett C DuBois

CXC Chemokines Bind to Unique Sets of Selectivity Determinants That Can Function Independently and Are Broadly Distributed on Multiple Domains of Human Interleukin-8 Receptor B

7

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language of work or name

English

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publication date

5 December 2003

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published in

Virology

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volume

317

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issue

1

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page(s)

84-94

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cites work

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A new possible mechanism of human immunodeficiency virus type 1 infection of neural cells

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Identification of residues of CXCR4 critical for human immunodeficiency virus coreceptor and chemokine receptor activities

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Apelin, the natural ligand of the orphan seven-transmembrane receptor APJ, inhibits human immunodeficiency virus type 1 entry.

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Cloning, pharmacological characterization and brain distribution of the rat apelin receptor

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Identification of a major co-receptor for primary isolates of HIV-1

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Amino acid sequence and embryonic expression of msr/apj, the mouse homolog of Xenopus X-msr and human APJ

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Antigen recognition by helper T cells elicits a sequence of distinct changes of their shape and intracellular calcium

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A dual-tropic primary HIV-1 isolate that uses fusin and the beta-chemokine receptors CKR-5, CKR-3, and CKR-2b as fusion cofactors

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HIV-1 entry into CD4+ cells is mediated by the chemokine receptor CC-CKR-5

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Structural and functional study of the apelin-13 peptide, an endogenous ligand of the HIV-1 coreceptor, APJ.

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The role of post-translational modifications of the CXCR4 amino terminus in stromal-derived factor 1 alpha association and HIV-1 entry

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Tyrosine sulfation of the amino terminus of CCR5 facilitates HIV-1 entry

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Sulfated tyrosines contribute to the formation of the C5a docking site of the human C5a anaphylatoxin receptor.

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HIV-1 Entry Cofactor: Functional cDNA Cloning of a Seven-Transmembrane, G Protein-Coupled Receptor

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Apelin, the natural ligand of the orphan receptor APJ, is abundantly secreted in the colostrum

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Dissociation of the signalling and antiviral properties of SDF-1-derived small peptides

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The interleukin-8-receptor family: from chemokines to malaria

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Molecular and functional characteristics of APJ. Tissue distribution of mRNA and interaction with the endogenous ligand apelin

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Characterization of apelin, the ligand for the APJ receptor

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The Promiscuous Chemokine Binding Profile of the Duffy Antigen/Receptor for Chemokines Is Primarily Localized to Sequences in the Amino-terminal Domain

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Low stringency hybridization study of the dopamine D4 receptor revealed D4-like mRNA distribution of the orphan seven-transmembrane receptor, APJ, in human brain

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A human gene that shows identity with the gene encoding the angiotensin receptor is located on chromosome 11

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Monocyte chemotactic protein-1 receptor CCR2B is a glycoprotein that has tyrosine sulfation in a conserved extracellular N-terminal region

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Expression and coreceptor function of APJ for primate immunodeficiency viruses

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Physiological role of a novel neuropeptide, apelin, and its receptor in the rat brain.

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Distribution of apelin-synthesizing neurons in the adult rat brain.

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Apelin, the novel endogenous ligand of the orphan receptor APJ, regulates cardiac contractility

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The effects of centrally administered apelin-13 on food intake, water intake and pituitary hormone release in rats

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Isolation and characterization of a novel endogenous peptide ligand for the human APJ receptor

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The novel peptide apelin lowers blood pressure via a nitric oxide-dependent mechanism

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Cell-cell fusion and internalization of the CNS-based, HIV-1 co-receptor, APJ

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Apelin peptides block the entry of human immunodeficiency virus (HIV).

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An orphan seven-transmembrane domain receptor expressed widely in the brain functions as a coreceptor for human immunodeficiency virus type 1 and simian immunodeficiency virus

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A tyrosine-rich region in the N terminus of CCR5 is important for human immunodeficiency virus type 1 entry and mediates an association between gp120 and CCR5

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Fusogenic mechanisms of enveloped-virus glycoproteins analyzed by a novel recombinant vaccinia virus-based assay quantitating cell fusion-dependent reporter gene activation.

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Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

14675627

1 reference

Consolidated OpenCitations Corpus – April 2017