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1 tion with synapses via a mechanism involving apolipoprotein E receptors.
3 elin and VLDLR was similar but expression of apolipoprotein E receptor 2 (ApoER2) (the reelin recepto
5 s by binding to two transmembrane receptors, apolipoprotein E receptor 2 (Apoer2) and very-low-densit
6 identification of bound proteins identified apolipoprotein E receptor 2 (ApoER2) as a candidate test
7 density lipoprotein receptor (VLDLR) and the apolipoprotein E receptor 2 (ApoER2) exhibit identical n
8 low density lipoprotein receptor (VLDLR) and apolipoprotein E receptor 2 (apoER2) results in either p
9 carrying apolipoprotein E (ApoE) to receptor apolipoprotein E receptor 2 (ApoER2) triggers the endocy
10 . apoE3, and also greater risk with the LRP8/apolipoprotein E receptor 2 (ApoER2) variant ApoER2-R952
12 Selenoprotein P (Sepp1) and its receptor, apolipoprotein E receptor 2 (apoER2), account for brain
13 low density lipoprotein receptor (VLDLR) and apolipoprotein E receptor 2 (ApoER2), but the exact mech
14 human monocytic-like U937 cells to evaluate apolipoprotein E receptor 2 (ApoER2)-dependent signaling
18 ow density lipoprotein receptor (VLDLR), the apolipoprotein E receptor 2 (ApoER2; refs 9-11 ), alpha3
19 low density lipoprotein receptor family, the apolipoprotein E receptor 2 and the very low density lip
20 ls, triggers a signal in granulosa cells via apolipoprotein E receptor 2 and the very low density lip
21 lipids and with the intracellular domains of apolipoprotein E receptor 2 and very low density lipopro
22 ery low density lipoprotein receptor and the apolipoprotein E receptor 2 on the surface of neurons.
23 r very-low-density lipoprotein receptors and apolipoprotein E receptor 2 receptors but by a distinct
24 itiated by reelin and its receptors, apoER2 (apolipoprotein E receptor 2) and VLDLR (very-low-density
26 s, very low-density lipoprotein receptor and apolipoprotein E receptor 2, the cytoplasmic adaptor pro
27 he very low density lipoprotein receptor and apolipoprotein E receptor 2, thereby inducing tyrosine p
28 s, very-low-density lipoprotein receptor and apolipoprotein E receptor 2, to stimulate phosphorylatio
29 c evidence that this cascade is dependent on apolipoprotein E receptor 2, very low density lipoprotei
31 ic alterations of Sepp1, the Sepp1 receptors apolipoprotein E receptor-2 (apoER2) and megalin, and Gp
36 es take up plasma Sepp1 for its selenium via apolipoprotein E receptor-2 (apoER2)-mediated endocytosi
38 on to their expression of the Sepp1 receptor apolipoprotein E receptor-2, creating a tissue selenium
40 nctionalized with a peptide derived from the apolipoprotein-E receptor-binding domain for blood-brain
41 lin-dependent kinase 2 (CDK2) in carotids of apolipoprotein-E receptor null (ApoE(-/-)) mice and in C
42 e repeat in the 5' untranslated region of an apolipoprotein E receptor, the very-low-density lipoprot
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