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1 iated by rat CD36 (rCD36), a closely related class B scavenger receptor.
2 uffices to generate high binding affinity to class B scavenger receptors.
4 Two macrophage surface receptors, CD36 (a class B scavenger receptor) and the macrophage scavenger
5 ylated, a property shared with CD36, another class B scavenger receptor, and other proteins that conc
7 s accompanied by augmented expression of the class B scavenger receptor CD36 (2.8+/-0.3-fold, P<0.001
11 ed cells to functionally link Parkin and the class B scavenger receptor CD36, suggesting a novel and
17 In the present study, we determined if the class B scavenger receptors, CD36 and SR-BI, are involve
19 e tested in mice the hypothesis that CD36, a class B scavenger receptor expressed on macrophages, has
20 tudied the effect of pitavastatin on CD36 (a class B scavenger receptor) expression by murine macroph
21 experimental evidence that CD36, a phagocyte class B scavenger receptor, functions as a novel SAA rec
23 Here, we investigated the role of CD36, a class B scavenger receptor, in a hypercholesterolemic mo
25 hat free fatty acid association with CD36, a class B scavenger receptor, induces the activation of en
28 , we demonstrated that activation of CD36, a class B scavenger receptor, mediates free radical produc
35 ipoprotein A-I mimetics are known to bind to class B scavenger receptors (SR-Bs), SR-BI, SR-BII, and
38 o results we conclude that both BBM-resident class B scavenger receptors, SR-BI and CD36, can facilit
41 ulated the protein levels of the class A and class B scavenger receptors, the membrane lipid transpor
42 ilities of SR-BI and CD36, both of which are class B scavenger receptors, to bind HDL and mediate cel
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