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Zi-Xuan Wang

Researcher at University of Louisville

Publications -  13
Citations -  755

Zi-Xuan Wang is an academic researcher from University of Louisville. The author has contributed to research in topics: Chemokine receptor & Chemokine. The author has an hindex of 9, co-authored 13 publications receiving 736 citations.

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Journal ArticleDOI

The Duffy antigen/receptor for chemokines (DARC) is expressed in endothelial cells of Duffy negative individuals who lack the erythrocyte receptor.

TL;DR: It is reported here that DARC is indeed expressed in endothelial cells lining postcapillary venules and splenic sinusoids in individuals who lack the erythrocyte receptor, and the DARC may play a critical role in mediating the effects of proinflammatory chemokines on the interactions between leukocyte and endothelial Cells.
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The Duffy antigen receptor for chemokines: structural analysis and expression in the brain

TL;DR: Immunohistochemical examination of human archival sections of the brain with monoclonal antibodies specific for DARC localize expression of DARC to cell bodies and processes of Purkinjie cells in the cerebellum and suggests that chemokines may play an important role in the modulation of neuronal activity by glial cells.
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Evolution of the Human Immunodeficiency Virus Type 1 Envelope during Infection Reveals Molecular Corollaries of Specificity for Coreceptor Utilization and AIDS Pathogenesis

TL;DR: These experiments demonstrate that progression from the R5 to X4 phenotype may occur through a multi- or dual-tropic intermediate and that multiple domains contribute to this process.
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Identification of ENV determinants in V3 that influence the molecular anatomy of CCR5 utilization.

TL;DR: It is demonstrated that sequences in the third hypervariable region determine the specificity of coreceptor utilization for fusion, and that a conserved motif in the crown directly influences the molecular anatomy of the interaction between gp120 and CCR5.
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Molecular anatomy of CCR5 engagement by physiologic and viral chemokines and HIV-1 envelope glycoproteins: differences in primary structural requirements for RANTES, MIP-1 alpha, and vMIP-II Binding.

TL;DR: It is suggested that the molecular anatomy of CCR5 binding plays a critical role in antagonism of coreceptor activity and monoclonal antibodies to N-ter epitopes did not block chemokine binding, but those mapped to ECL2 were effective inhibitors.