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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
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(-
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
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
32 rototype of this family, which also contains very-low-density lipoprotein receptors (VLDL-R), apolipo
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
39 lves two neuronal cell surface proteins, the very low density lipoprotein receptor (VLDLR) and the ap
42 ransfer to study the in vivo function of the very low density lipoprotein receptor (VLDLR) in low den
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
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
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
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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