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1 ng genetic variants of their major receptor, CC chemokine receptor 5.
5 ssion of coreceptors, cytokine regulation of CC chemokine receptor 5 (CCR5) and CD4 expression on mon
8 matory proteins 1alpha and 1beta to activate CC chemokine receptor 5 (CCR5) and the ability to inhibi
10 independent of the presence of a mutation in CC chemokine receptor 5 (CCR5) associated with resistanc
14 of a 32 bp deletion (Delta32) allele of the CC chemokine receptor 5 (CCR5) gene are reported to be m
16 n the present study, we explored the role of CC chemokine receptor 5 (CCR5) in a murine model of chro
25 us 24-bp deletion (Delta24) was found in the CC chemokine receptor 5 (CCR5) of 11 out of 15 red-cappe
26 eptor, CD4, and through a coreceptor, either CC chemokine receptor 5 (CCR5) or CXC chemokine receptor
27 f the viral envelope glycoprotein gp120 with CC chemokine receptor 5 (CCR5) or CXC chemokine receptor
28 glycoproteins, CD4 and a coreceptor, usually CC chemokine receptor 5 (CCR5) or CXC receptor 4 (CXCR4)
29 We demonstrate that signaling through the CC chemokine receptor 5 (CCR5) prevents uncontrolled pos
30 laria-infected women contain 3 times as much CC chemokine receptor 5 (CCR5) RNA as placentas of women
31 s of HIV-1 require the cell-surface receptor CC chemokine receptor 5 (CCR5) to infect specific leukoc
32 globulin (Ig) G4 monoclonal antibody against CC chemokine receptor 5 (CCR5) with robust in vitro acti
33 a32, a complete loss-of-function mutation in CC chemokine receptor 5 (CCR5), has been previously asso
34 of both CXC chemokine receptor 4 (CXCR4) and CC chemokine receptor 5 (CCR5), major coreceptors for T
39 8-coated beads are resistant to infection by CC chemokine receptor 5 (CCR5)-dependent HIV-1 isolates.
40 -SIGN1 is expressed on endothelial cells and CC chemokine receptor 5 (CCR5)-positive macrophage-like
44 iruses were found to play important roles in CC-chemokine receptor 5 (CCR5) coreceptor utilization, a
47 t on macrophagetropic viruses that enter via CC-chemokine receptor 5 (CCR5), despite binding to the s
50 detected for galactosyl ceramide but not for CC-chemokine receptor 5, CXC-chemokine receptor 4, or CD
51 normal CD45 splicing and the presence of the CC chemokine receptor 5 deletion 32 (CCR5del32) allele,
53 SIV hosts from AIDS and the discovery of low CC chemokine receptor 5 expression on CD4+ T cells as a
54 wed reduced CC chemokine receptor 1, but not CC chemokine receptor 5, expression by HaCaT cells at lo
55 chemokine receptor 4 (CXCR4), but not of the CC-chemokine receptor 5 in purified populations of prima
56 viral burden and further implicate roles for CC chemokine receptor 5, macrophages, and Vpr in the lif
57 ll expressed and secreted), a ligand for the CC chemokine receptor 5, potently inhibits HIV-1 replica
58 macaques with CXC chemokine receptor 4- and CC chemokine receptor 5-specific simian/human immunodefi
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