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1 ASGPR is composed of two highly homologous subunits, ter
2 dified siRNA has enabled asialoglycoprotein (ASGPR)-mediated targeted delivery of therapeutically act
3 rf1) of HuH-7 alters the asialoglycoprotein (ASGPR) and transferrin receptor subcellular distribution
5 uman primates with antigens fused to anti-DC-ASGPR monoclonal antibody generates antigen-specific CD4
7 that targeting antigens to human DCs via DC-ASGPR, but not lectin-like oxidized-LDL receptor, Dectin
9 on experiments suggest that other endogenous ASGPR ligands, the nature of which remain to be determin
10 new ligands were obtained with affinity for ASGPR as good as or better than that of the parent N-ace
12 njugated ASOs showed high affinity for mouse ASGPR, which results in enhanced ASO delivery to hepatoc
15 ference in the kinetics of ER degradation of ASGPR H2a in susceptible as compared with protected host
17 dase gene (LacZ) resulted in transduction of ASGPR-positive cells (rat hepatocytes or Hepa1 cell line
19 the function of these compounds showed rapid ASGPR-dependent cellular uptake in vitro and high levels
20 subunit of the asialoglycoprotein receptor (ASGPR H2a) were expressed in skin fibroblast cell lines
21 content of the asialoglycoprotein receptor (ASGPR) and three trafficking proteins, Rab3D, Rab7and Ra
23 The mammalian asialoglycoprotein receptor (ASGPR) is located on the sinusoidal membrane of hepatocy
25 tocyte-specific asialoglycoprotein receptor (ASGPR), enhances the potency of second-generation gapmer
26 apical membrane asialoglycoprotein receptor (ASGPR), which is related to the ASGPR of liver cells.
29 ocyte-specific asialoglycoprotein receptors (ASGPR) to enhance uptake to hepatocytes and to increase
31 dependent sorting proteins from cytosol, the ASGPR cytoplasmic domain was expressed as a GST fusion p
32 provide a hitherto unsuspected role for the ASGPR in transcriptional signaling, aside from its role
34 provide evidence that phosphorylation of the ASGPR cytoplasmic domain is required for the binding of
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