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1 longated collagen-like binding domain of the macrophage scavenger receptor.
2 binding domain of OxLDL with respect to some macrophage scavenger receptors.
3 utations and common sequence variants of the macrophage scavenger receptor 1 (MSR1) gene have recentl
6 oprotein J (APOJ), lipoprotein lipase (LPL), macrophage scavenger receptor 1 (MSR1), and tumor necros
10 hree [steroid 5-alpha-reductase 2 (Srd5A-2), macrophage scavenger receptor-1 (MSR-1), and tumor necro
11 r-1alpha, vascular cell adhesion molecule-1, macrophage scavenger receptor-1, and cyclophilin A compa
13 ould regulate the expression and function of macrophage scavenger receptor A (SR-A) in macrophages.
16 M-CSFR overexpression increased the mRNA for macrophage scavenger receptor A, and fucoidan blocking o
18 binding adaptor Iba-1, lysosome marker CD68, macrophage scavenger receptor A, Fcgamma receptors I (CD
19 amyloid-beta42 load correlated directly with macrophage scavenger receptor A-positive clusters and in
20 ger receptor A, CD64, CD32 and the number of macrophage scavenger receptor A-positive plaque-related
21 CD36 (a class B scavenger receptor) and the macrophage scavenger receptor (a class A scavenger recep
22 of low-density lipoprotein into a ligand for macrophage scavenger receptor A1 recognition, cholestero
23 l proliferation, increased expression of the macrophage scavenger receptor and apolipoprotein E, and
24 found for the group-A SRCR domain of type-1 macrophage scavenger receptor and MARCO, the macrophage
28 have examined human brain for expression of macrophage scavenger receptor as part of ongoing studies
31 as endogenous high-affinity ligands for the macrophage scavenger receptor CD36 (oxPC(CD36)) was rece
34 endogenous oxidized phospholipid ligand for macrophage scavenger receptor CD36, where the truncated
36 Together, these results demonstrate that macrophage scavenger receptor class A contributes signif
37 homogeneity and find that it belongs to the macrophage scavenger receptor cysteine rich (SRCR) famil
39 se results indicate that TNF-alpha regulates macrophage scavenger receptor expression in PMA-differen
40 tment divergently regulated CD36 and class A macrophage-scavenger receptor expression and failed to i
42 ma (IFN-gamma) inhibits transcription of the macrophage scavenger receptor gene by antagonizing the R
43 The effect of CsA on the mRNA expression of macrophage scavenger receptor genes including CD36, CD68
46 to lipoproteins increases expression of the macrophage scavenger receptor implies that lipoproteins
47 uch oxidized phospholipids are recognized by macrophage scavenger receptors, implying that these inna
48 goal of this study is to examine the role of macrophage scavenger receptors in immune cell recruitmen
49 avenger receptor A, and fucoidan blocking of macrophage scavenger receptors inhibited uptake of A bet
50 om recent studies suggested that some of the macrophage scavenger receptors involved in the uptake of
52 ptake of oxidized low-density lipoprotein by macrophage scavenger receptors is largely responsible fo
53 oxidized low-density lipoprotein (OxLDL) by macrophage scavenger receptors is thought to be a key pr
54 nsity lipoprotein receptor (LDLR) repeats, a macrophage scavenger receptor-like domain, and a trypsin
55 low density lipoprotein receptor repeats, a macrophage scavenger receptor-like domain, and a trypsin
56 or betaine promoted upregulation of multiple macrophage scavenger receptors linked to atherosclerosis
67 oncentrations demonstrated the modulation of macrophage scavenger receptors (MSRs) involved in athero
68 reased the luciferase activity driven by the macrophage scavenger receptor promoter in the transfecte
69 egulatory pathway in fibrogenesis in which a macrophage scavenger receptor protects against organ fib
70 LDL binding was paralleled by a reduction of macrophage scavenger receptor protein as detected by the
74 fected cultured cells overexpressing RAGE or macrophage scavenger receptor (SR), type A, displayed bi
77 ry defense against inhaled oxidants in mice: macrophage scavenger receptors (SRs) bind proinflammator
78 f this study was to test the expression of 3 macrophage scavenger receptors (SRs) that are responsibl
80 d the mechanism by which TNF-alpha inhibited macrophage scavenger receptor surface expression and bin
81 ing places cosmid CI8-2644 telomeric to MSR (macrophage scavenger receptor), the reverse of a previou
82 a charged surface in a manor similar to the macrophage scavenger receptor to "capture" LPS ligands a
84 ing showed that NKX3.1 is proximal to MSR32 (macrophage scavenger receptor type II) and LPL (human li
86 ted forms of the human type I and II class A macrophage scavenger receptors were studied using bioche
87 d expression cloning approach, we identified macrophage scavenger receptor with collagenous structure
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