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1 growth factor receptor and G-protein-coupled CXC chemokine receptor 4.
2 ceptor 5 (CCR5), whereas 84%-99% coexpressed CXC chemokine receptor 4.
3 nterleukin-10-induced apoptosis, all through CXC chemokine receptor-4.
5 a promising protein therapeutic and implies CXC chemokine receptor 4 as a drug target after polytrau
8 demonstrates cell surface expression of both CXC chemokine receptor 4 (CXCR4) and CC chemokine recept
11 ll-derived factor-1 (SDF-1) and its receptor CXC chemokine receptor 4 (CXCR4) are important regulator
14 romal cell-derived factor 1 and its receptor CXC chemokine receptor 4 (CXCR4) critically mediate the
17 terferes with the expression and function of CXC chemokine receptor 4 (CXCR4) in CD4+ T lymphocytes.
18 have investigated the expression of surface CXC chemokine receptor 4 (CXCR4) in enriched populations
19 east cancer, GnRH in ovarian carcinomas, and CXC chemokine receptor 4 (CXCR4) in multiple malignancie
24 38+ cells in the blood, higher leukemic cell CXC chemokine receptor 4 (CXCR4) levels, and increased r
25 al use of CC chemokine receptor 5 (CCR5) and CXC chemokine receptor 4 (CXCR4) may be intimately invol
28 crophage-tropic coreceptor for HIV-1 whereas CXC chemokine receptor 4 (CXCR4) serves the counterpart
29 The stromal cell-derived factor-1 (SDF-1)/CXC chemokine receptor 4 (CXCR4) signaling axis appears
30 lls expressed elevated levels of CD95, CD25, CXC chemokine receptor 4 (CXCR4), and CC chemokine recep
35 gous to the V3 loop of HIV-1, which binds to CXC chemokine receptor 4 (CXCR4), we hypothesized that B
36 ations covering all 352 residues of the GPCR CXC chemokine receptor 4 (CXCR4), we identified 41 amino
37 , indicating that PTEN was not requisite for CXC chemokine receptor 4 (CXCR4)-mediated chemotaxis of
45 we reported that human RMS cells express the CXC chemokine receptor-4 (CXCR4) and postulated a role f
46 howed that inducible knockdown of endogenous CXC chemokine receptor-4 (CXCR4) gene expression in brea
47 romal cell-derived factor-1 and its receptor CXC chemokine receptor-4 (CXCR4) have received considera
48 tic parental cells (686LN-Ps), we found that CXC chemokine receptor-4 (CXCR4) mRNA levels were signif
50 Most importantly, BDNF reduced the levels of CXC chemokine receptor-4 (CXCR4), a receptor that mediat
51 d, these cells expressed substantial surface CXC chemokine receptor-4 (CXCR4), and CXCL12 stimulation
57 iae lacking FimCDE fail to interact with the CXC-chemokine receptor 4 (CXCR4), and bacteria expressin
58 , up-regulates the surface expression of the CXC-chemokine receptor 4 (CXCR4), but not of the CC-chem
59 -derived factor (SDF)-1alpha (the ligand for CXC chemokine receptor 4 [CXCR4]) did not affect T(GFP)
61 ells with 12G5, an antibody specific for the CXC chemokine receptor-4, eliminates this response indic
62 ral differentiation, we observed that CXCR4 (CXC chemokine receptor-4) expressing central nervous sys
66 le describes the transient expression of the CXC chemokine receptor-4 in Xenopus laevis melanophores
71 vels and corresponding surface expression of CXC chemokine receptor 4 on clonal PCs, suggesting that
73 s, such as protease-activated receptor 1 and CXC chemokine receptor 4, RGS4 disrupted Rac1-dependent
74 bone marrow; in particular, the role of the CXC chemokine receptor 4/stromal-derived factor 1 axis,
76 The HIV envelope glycoprotein interacts with CXC chemokine receptor 4 to activate the lysosomal degra
78 upregulated in tissues infected ex vivo with CXC chemokine receptor 4-tropic but not CCR5-tropic HIV-
79 stem cell mobilizer or its receptor, CXCR4 (CXC chemokine receptor 4), would attenuate and reverse h
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