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1 petes with Abeta for cellular uptake through apoE receptors.
2 ing them to cellular catabolism via neuronal APOE receptors.
3 complexes despite proper expression of other APOE receptors.
4  these lipoproteins from blood by binding to ApoE receptors.
5 by an isoform-specific process that requires apoE receptors.
6  activation and decreased JNK activation via apoE receptors.
7  apoE3:Abeta complex formation and uptake by apoE receptors.
8                                              ApoE Receptor 2 (ApoER2) and the very low density lipopr
9 density lipoprotein receptor (VLDLR) and the apoE receptor 2 (ApoER2) as well as a cytosolic adaptor
10 y was to determine the effect of X11alpha on ApoE receptor 2 (ApoEr2) trafficking and the functional
11  low density lipoprotein (VLDL) receptor and apoE receptor 2 (apoER2), are also receptors for Reelin,
12 elin and apolipoprotein E (apoE), ligands of apoE receptor 2 (ApoER2), are involved in retinal develo
13 cts with amyloid precursor protein (APP) and apoE receptor 2 (apoEr2), increases their levels on the
14 ntially spliced isoform of an ApoE receptor, ApoE receptor 2 (Apoer2), is essential for protection ag
15 osely related LDLR family members, VLDLR and ApoE receptor 2 (ApoER2), proteins implicated in both ne
16 bly mutant for the VLDL receptor (VLDLR) and ApoE receptor 2 (ApoER2), show disorders of cerebral cor
17 t F-spondin interacts with an apoE receptor (apoE receptor 2 [ApoEr2]) through the thrombospondin dom
18  to negatively charged cellular surfaces and ApoE receptor 2.
19 low density lipoprotein receptor (VLDL), and apoE receptor-2 in mouse aortic smooth muscle cells.
20 ery low density lipoprotein receptor and the apoE receptor-2, in the transmission of extracellular si
21 ells isolated from LDLR-null, VLDL-null, and apoE receptor-2-null mice were responsive to apoE inhibi
22                        The apolipoprotein E (apoE) receptor-2 (apoER2), another member of the LDL rec
23          We demonstrate that ApoE binding to ApoE receptors activates dual leucine-zipper kinase (DLK
24      Of note, postnatal administration of an APOE receptor agonist (APOE-RA) mitigates motor learning
25   Over the past few years, apolipoprotein E (ApoE) receptors, also known as LDL receptor-related prot
26                                        ApoE, ApoE receptors and APP cooperate in the pathogenesis of
27  (VLDLR) is a multi ligand apolipoprotein E (apoE) receptor and is involved in brain development thro
28 rotein that interacts with apolipoprotein E (ApoE) receptors and controls neuronal positioning during
29 emonstrated that F-spondin interacts with an apoE receptor (apoE receptor 2 [ApoEr2]) through the thr
30  that a differentially spliced isoform of an ApoE receptor, ApoE receptor 2 (Apoer2), is essential fo
31       Our previous data demonstrate that the apoE receptor ApoEr2 co-precipitated with APP and sugges
32 ission by signaling through the postsynaptic ApoE receptors Apoer2 and Vldlr and thereby potently enh
33 ation experiments an interaction between the apoE receptor, ApoEr2, and NMDAR1 through their extracel
34 ase cleavage of APP and an apolipoprotein E (apoE) receptor, ApoER2.
35                                              ApoE receptors are essential for the development of the
36                                     Neuronal ApoE receptors are linked to learning and memory, but th
37 ted for by the interaction with the proposed ApoE receptor binding region; therefore, we speculate th
38 s on ApoE have illuminated the physiology of ApoE, receptor binding, and interaction with amyloid-B (
39 s on ApoE have illuminated the physiology of ApoE, receptor binding, and interaction with amyloid-bet
40          Using single chain multimers of the apoE receptor-binding domain (N-apoE), we also show that
41 E2, ApoE3, and ApoE4, which exhibit distinct ApoE receptor-binding properties and differentially affe
42 ited by a synthetic peptide derived from the apoE receptor-binding region.
43 xists as to whether a single lipid-activated apoE receptor-binding site within a particle is capable
44                      Thus, the impairment of apoE receptor-dependent neuromodulation may contribute t
45 lly-lipidated apoE from premature binding to apoE receptors during receptor biogenesis.
46 acts with APP as well as with members of the apoE receptor family.
47 ed mRNA and protein for an apolipoprotein E (ApoE) receptor family member, SorLA (LR11) has been foun
48                       The expanding roles of ApoE receptors for cellular signal transduction at the s
49                                              ApoE receptors have been indirectly implicated in memory
50 n receptor-related protein 1 (LRP1), a major apoE receptor in the brain that is abundantly expressed
51 nsity lipoprotein receptor (LDLR) is a major apoE receptor in the brain that strongly regulates amylo
52                        Since LDLR is a major apoE receptor in the brain, we hypothesized that rs688 m
53 oE and apoJ levels and the potential role of apoE receptors in astrocyte activation have not been add
54 en be cleared from the interstitial space by apoE receptors in the brain or become part of an extrace
55 mer's disease , a direct or indirect role of ApoE receptors in the disease process is likely.
56 ing in mice to investigate possible roles of ApoE receptors in the regulation of neuronal survival.
57 eceptor-associated protein (RAP), suggesting apoE receptor involvement, ATP-stimulated migration was
58                     Genetic knockdown of the APOE receptor lipoprotein receptor-related protein 1 (LR
59 w that APOE4-mediated surface trafficking of APOE receptor low-density lipoprotein receptor-related p
60                                          The apoE receptors low-density lipoprotein receptor (LDLR) a
61                    The identification of the apoE receptor, low-density lipoprotein receptor-related
62                            Intriguingly, the ApoE receptor LRP4 and APP are also required for normal
63                             Interaction with apoE receptors may not mediate the toxic actions of apoE
64 he present work examines the hypothesis that apoE receptors mediate uptake of apoE/Abeta complex into
65  propose a model in which Abeta, Reelin, and ApoE receptors modulate neurotransmission and thus synap
66                            Blocking LRP1, an apoE receptor on the neuronal membrane, also blocked the
67 receptor-associated protein, an inhibitor of apoE receptors, particularly the LDL-receptor-related pr
68 e, such as the heparan-sulphate proteoglycan-APOE receptor pathway, the TREM-2-driven signalling path
69 gle nucleotide polymorphisms (SNPs) in brain apoE receptors represent excellent candidates for associ
70 summary, these studies identify a functional apoE receptor SNP that is associated with AD in a sex-de
71 model for studying the relationships between ApoE receptors, tau hyperphosphorylation, and Alzheimer'
72                                  The primary apoE receptor that regulates levels of apoE in the brain
73                        Two apolipoprotein E (apoE) receptors, the very low density lipoprotein (VLDL)
74                      These data suggest that apoE receptors translate the presence of extracellular A
75 receptor-associated protein, an inhibitor of apoE receptors with a differential affinity for the low
76 tery, but the numerous critical functions of ApoE receptors within and outside the nervous system tha