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1 (TLR4) and LPS and is a critical part of the LPS receptor.
2 nly two signalling pathways emanate from the LPS receptor.
3 R4 carbohydrates in LPS cross-linking to the LPS receptor.
4 logical activity, appears to be a functional LPS receptor.
5 a 55-kDa protein, has been identified as an LPS receptor.
6 ugh membrane CD14 (mCD14), a proinflammatory LPS receptor.
7 3 (polyinosinic-polycytidylic acid) or TLR4 (LPS) receptor.
8 ophages through the CD14 lipopolysaccharide (LPS) receptor.
9 fy components of the putatively shared Taxol/LPS receptor, a novel, photoactivatable Taxol analogue w
10 lthough CD14 has been identified as the main LPS receptor, accumulating evidence has suggested the po
12 receptor 4 (Tlr4) is the lipopolysaccharide (LPS) receptor and biochemical evidence that Tlr4 confers
13 eracts with ligand-binding protein and CD14 (LPS receptor) and activates expression of inflammatory g
15 the patient's monocytes expressed CD14, the LPS receptor, and bound LPS in a specific manner, but fa
16 uman neutrophils occurs via CD14, a proposed LPS receptor, and requires the presence of plasma contai
17 l. report that caspases 4/5/11 are cytosolic LPS receptors, becoming activated through oligomerizatio
19 a high affinity to monocytes but not to the LPS receptor CD14, and experiments performed at 4 degree
22 ing expression of either lipopolysaccharide (LPS) receptor CD14 or myeloid differentiation protein-88
24 by overexpression of the lipopolysaccharide (LPS) receptors CD14 and TLR4, which antagonize each othe
25 if LPS stimulation was mediated through the LPS receptor, CD14, surface receptors on HGF were assess
27 showed that monocytic TM interacted with the LPS receptors, CD14 and TLR4/myeloid differentiation fac
30 anscription factors, is the formation of the LPS receptor complex by LPS, LPS-binding protein (LBP),
31 TLR4.myeloid differentiation factor 2 (MD-2) LPS receptor complex is strongly activated by hexa-acyla
32 t that a signal transduction molecule in the LPS receptor complex may belong to the IL-1 receptor/tol
33 ding the function and biology of the corneal LPS receptor complex may lead to novel therapies for the
34 lls are capable of expressing the functional LPS receptor complex proteins, CD14 and Toll-like recept
36 ctions as the transmembrane component of the LPS receptor complex, an unduplicated pathway for the de
37 binding protein membrane CD14 to serve as an LPS receptor complex, and that LPS treatment enhances th
38 luable tools to characterize elements in the LPS receptor complex, as well as to activate or inhibit
39 ith decreased cell surface expression of the LPS receptor complex, Toll-like receptor 4 (TLR4)/MD-2.
45 uggests that the functional integrity of the LPS receptor depends both on the surface expression of a
47 e deletions essentially ablated soluble CD14 LPS receptor function, whereas only two of the deletions
53 (TLR4) is an important lipo-polysaccharide (LPS) receptor in gastric epithelial cell signaling trans
57 e receptor 4 (Tlr4), the lipopolysaccharide (LPS) receptor, is sufficient to induce nuclear factor ka
58 either lacking or expressing human CD14 (the LPS receptor), it was observed that expression of human
59 binding to the O-antigen lipopolysaccharide (LPS) receptor of Salmonella were examined at high temper
61 l half of the membrane CD14 was a functional LPS receptor on the cell membrane, we engineered a chime
62 een LPS responsiveness and the expression of LPS receptors or factors regulating LPS responsiveness o
63 colitis and in humans certain alleles of the LPS receptor protein TLR4 increase inflammatory bowel di
67 al epithelial cells expressed the functional LPS receptor-signaling protein TLR4, which was also augm
68 study, we investigated the importance of the LPS receptor TLR4 and MyD88, an adaptor molecule involve
69 of VEGF, NRP-1 directly interacted with the LPS receptor TLR4 and suppressed downstream signaling th
70 argeting of multiple elements, including the LPS receptor TLR4 and the key adaptor/signaling proteins
71 ry cytokines, along with upregulation of the LPS receptor TLR4 in lung tissue and increased activatio
72 velopment in mice requires activation of the LPS receptor TLR4 on the intestinal epithelium, through
75 t mice, we demonstrated that the presence of LPS receptor (TLR4) is not required on hematogenous immu
77 ve demonstrated that the lipopolysaccharide (LPS) receptor (TLR4) is expressed in TRPV1 containing tr
78 culture, we demonstrate that hRetn binds the LPS receptor Toll-like receptor 4 (TLR4) through its N t
80 at regulates signals transduced by the major LPS receptor Toll-like receptor 4 on the surface of mous
81 LPS without affecting the expression of the LPS receptor Toll-like receptor 4, demonstrating that RI
82 which acute lung inflammation depends on the LPS receptor (Toll-like receptor 4, TLR-4), the loss of
83 C3HHeJ, which has a mutation in the primary LPS receptor, Toll-like receptor 4 (TLR4), is extremely
85 Endotoxin-mediated down-regulation of the LPS receptor, Toll-like receptor 4, has been suggested a
91 is the signal transduction component of the LPS receptor, whereas MD-2 is the endotoxin-binding unit
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