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1 ER2 (apolipoprotein E receptor 2) and VLDLR (very-low-density lipoprotein receptor).
2 (d), approximately 30 nM) but not to soluble very low density lipoprotein receptor.
3 e gene expression for lipoprotein lipase and very-low-density lipoprotein receptor.
4 rs, apolipoprotein E receptor 2 (Apoer2) and very-low-density lipoprotein receptor.
5 s cortical layering by signaling through the very low density lipoprotein receptor and apolipoprotein
6 orylated form in mice lacking Reelin or both very low density lipoprotein receptor and apolipoprotein
7 ons for two LDL receptor family members, the very low density lipoprotein receptor and the apoE recep
8 eted extracellular protein that binds to the very low density lipoprotein receptor and the apolipopro
9 gnaling pathway that requires its receptors, very low-density lipoprotein receptor and apolipoprotein
10 by binding to the two lipoprotein receptors, very-low-density lipoprotein receptor and apolipoprotein
11  Reelin that is not mediated by Disabled1 or very-low-density lipoprotein receptors and apolipoprotei
12 y, including the receptors ApoER2 and VLDLR (very low density lipoprotein receptor) and the adapter p
13 is dependent on apolipoprotein E receptor 2, very low density lipoprotein receptor, and Dab1.
14 ily, the apolipoprotein E receptor 2 and the very low density lipoprotein receptor, and regulates neu
15 eceptors for Reelin, including integrins and very-low-density lipoprotein receptor/apolipoprotein E2
16 ransfer experiments, we demonstrate that the very low density lipoprotein receptor can also bind and
17 r domains of apolipoprotein E receptor 2 and very low density lipoprotein receptor, Dab1 is preferent
18 l blood vessels invading photoreceptors: the very low-density lipoprotein receptor-deficient (Vldlr(-
19                                              Very low density lipoprotein receptor gene knock-out (Vl
20 the likelihood that this polymorphism in the very-low-density lipoprotein receptor gene is strongly a
21  We determined the allele frequencies of the very-low-density lipoprotein receptor in 3 white populat
22  region of an apolipoprotein E receptor, the very-low-density lipoprotein receptor, is genetically as
23 ation and vascular leakage in the eyecups of very low-density lipoprotein receptor knockout mice, a m
24                                              Very low-density lipoprotein receptor mutant mice (Vldlr
25 ells via apolipoprotein E receptor 2 and the very low density lipoprotein receptor, resulting in the
26 ptor proteins, apolipoprotein receptor 2 and very low density lipoprotein receptor, results in a Reln
27 an interaction with the RELN receptor VLDLR (very low-density lipoprotein receptor); this was confirm
28 ails of the lipoprotein receptors ApoER2 and very low density lipoprotein receptor through an amino-t
29 runcated TFPI molecule, is recognized by the very low density lipoprotein receptor (VLDL receptor) in
30  the LDL receptor-related protein (LRP), the very low density lipoprotein receptor (VLDL), and apoE r
31                                          The very low density lipoprotein receptor (VLDL-R) binds and
32 rototype of this family, which also contains very-low-density lipoprotein receptors (VLDL-R), apolipo
33                                Activation of very low density lipoprotein receptor (VLDLR) and apolip
34 Reelin signals via the lipoprotein receptors very low density lipoprotein receptor (VLDLR) and apolip
35 ther proteins, cell surface receptors termed very low density lipoprotein receptor (VLDLR) and apolip
36  to apolipoprotein E receptor 2 (ApoER2) and very low density lipoprotein receptor (VLDLR) and is int
37      We discovered that miR-200c targets the very low density lipoprotein receptor (Vldlr) and its li
38                            For instance, the very low density lipoprotein receptor (VLDLR) and the ap
39 lves two neuronal cell surface proteins, the very low density lipoprotein receptor (VLDLR) and the ap
40             ApoE Receptor 2 (ApoER2) and the very low density lipoprotein receptor (VLDLR) are type I
41                                          The very low density lipoprotein receptor (VLDLr) binds dive
42 ransfer to study the in vivo function of the very low density lipoprotein receptor (VLDLR) in low den
43                                          The very low density lipoprotein receptor (VLDLR) is a membe
44               Previously, we have shown that very low density lipoprotein receptor (VLDLR) is virtual
45  include the LDLR-related protein (LRP), the very low density lipoprotein receptor (VLDLR), the apoli
46 migrating cortical neurons by binding to the very low density lipoprotein receptor (VLDLR), the apoli
47 induced choroidal neovascularization and the very low density lipoprotein receptor (Vldlr)-knockout m
48 red the cooperative function of uPAR and the very low density lipoprotein receptor (VLDLr).
49 le seven-module cluster, vertebrate VgRs and very low density lipoprotein receptors (VLDLR) which hav
50 tly to lipoprotein receptors, preferably the very low-density lipoprotein receptor (VLDLR) and apolip
51 nt in Reelin, Disabled 1 (Dab1), or both the very low-density lipoprotein receptor (VLDLR) and the ap
52                                          The very low-density lipoprotein receptor (VLDLR) knockout (
53 le pathways including through the receptors, Very low-density lipoprotein receptor (Vldlr), Apolipopr
54   Mice deficient in another Reelin receptor, very low-density lipoprotein receptor (VLDLR), had norma
55 ng embryonic neurons requires binding to the very-low-density lipoprotein receptor (VLDLR) and the ap
56 revealed a point mutation, c.2239C>T, in the very-low-density lipoprotein receptor (Vldlr) gene.
57                                              Very-low-density lipoprotein receptor (VLDLR) in knockou
58                                              Very-low-density lipoprotein receptor (VLDLR) is a multi
59                                          The very-low-density lipoprotein receptor (VLDLR) negatively
60                                              Very-low-density lipoprotein receptor (Vldlr), which is
61  retinopathy and another angiogenic model of very-low-density lipoprotein receptor (Vldlr)-deficient
62  the brain involves the binding of Reelin to very-low-density lipoprotein receptors (VLDLR) and apoli
63 scular entothelial growth factor [VEGF], and very low density lipoprotein receptor [VLDLR]) were test
64 uncation disrupts an interaction with VLDLR (very low-density lipoprotein receptor), while the APOER2

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