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1 uent of N-acetylgalactosamine in the hepatic asialoglycoprotein receptor.
2 ding site similar to the binding site in the asialoglycoprotein receptor.
3 lin 1 structures had no asialoorosomucoid or asialoglycoprotein receptor.
4 sfer into HuH-7 human hepatoma cells via the asialoglycoprotein receptor.
5 se, making it a good functional mimic of the asialoglycoprotein receptor.
6 the gene coding for the major subunit of the asialoglycoprotein receptor.
7 i.v., and targeted to the hepatocyte via the asialoglycoprotein receptor.
8 or inhibition of in vitro translation of the asialoglycoprotein receptor.
9 efficiency in targeting hepatocytes via the asialoglycoprotein receptor.
10 al N-acetylgalactosamine binding site of the asialoglycoprotein receptor.
11 ical to the major subunit (RHL-1) of the rat asialoglycoprotein receptor.
12 l for studying apically localized endogenous asialoglycoprotein receptor.
13 ticular, there is a striking loss of State 2 asialoglycoprotein receptors.
16 n 4 of ASGR1, which encodes a subunit of the asialoglycoprotein receptor, a lectin that plays a role
20 ral colorectal cancer cell lines express the asialoglycoprotein receptor, although no significant lev
21 of the CRD is very similar to the CRD of the asialoglycoprotein receptor and other galactose-specific
22 cells produce a functional apically located asialoglycoprotein receptor and provide a model for rece
24 docytosed transferrin, transferrin receptor, asialoglycoprotein receptor, and low amounts of the cati
27 ative functional imaging techniques that use asialoglycoprotein receptor (ASGP-R) binding is based on
31 acids in their sequences, orthologues of the asialoglycoprotein receptor (ASGP-R) in different mammal
38 ae lipooligosaccharide (LOS) can bind to the asialoglycoprotein receptor (ASGP-R) on human sperm.
39 ly in situ, the endocytic trafficking of the asialoglycoprotein receptor (ASGP-R) was impaired in eth
40 nd was partially prevented by ligands of the asialoglycoprotein receptor (ASGP-R), thyroglobulin, asi
41 s of the experimentally intractable trimeric asialoglycoprotein receptor (ASGP-R), which consists of
42 s have not, to date, been identified for the asialoglycoprotein receptor (ASGP-R), which is abundantl
43 endocytic receptor on hepatocytes called the asialoglycoprotein receptor (ASGP-R), which is known to
47 S mutant of alpha1-AT and H2a subunit of the asialoglycoprotein receptor (ASGPR H2a) were expressed i
52 -affinity ligand for the hepatocyte-specific asialoglycoprotein receptor (ASGPR), enhances the potenc
53 ific antibody to the thyroid apical membrane asialoglycoprotein receptor (ASGPR), which is related to
56 actosamine = GalNAc) for hepatocyte-specific asialoglycoprotein receptors (ASGPR) to enhance uptake t
57 bohydrate-specific, endocytic receptors, the asialoglycoprotein receptor (ASGR) and the mannose recep
59 ligonucleotides (ASO) to hepatocytes via the asialoglycoprotein receptor (ASGR) has improved the pote
60 ell-surface receptors for asialoorosomucoid (asialoglycoprotein receptor (ASGR)), transferrin, and ma
61 dylethanolamine (Lac-DOPE), a ligand for the asialoglycoprotein receptor (ASGR), and an antibiotic pe
63 ylgalactosamine (GalNAc)-conjugated ASOs for Asialoglycoprotein Receptor (ASGR)-mediated uptake into
66 rate-recognition domain (CRD) of the hepatic asialoglycoprotein receptor at endosomal pH requires a s
67 terminal galactosylation leading to reduced asialoglycoprotein-receptor binding and to improved phar
70 simultaneous detection of asialoorosomucoid, asialoglycoprotein receptor, caveolin 1, and microtubule
75 s confirmed 40 days after transplantation by asialoglycoprotein receptor-directed nuclear scanning.
76 cells can be enriched and recovered based on asialoglycoprotein-receptor expression and potentially c
78 hat an IgA receptor, distinct from the pIgR, asialoglycoprotein receptor, galactosyltransferase, and
80 d ERAD substrate, the uncleaved precursor of asialoglycoprotein receptor H2a, its nonglycosylated mut
81 cells with deletion constructs encoding the asialoglycoprotein receptor H2b subunit localized the cG
82 COS-7 cells with deletion constructs of the asialoglycoprotein receptor H2b subunit localized the cG
85 keratinocytes; cell surface levels of human asialoglycoprotein receptor increase following gonococca
86 0 nm; asialofetuin, a natural ligand for the asialoglycoprotein receptor, inhibited this process by u
87 ity; zinc-treated cells accumulated inactive asialoglycoprotein receptors intracellularly, whereas co
89 ells lost approximately 50% of their surface asialoglycoprotein receptor ligand binding activity; zin
90 ation of small interfering RNA (siRNA) to an asialoglycoprotein receptor ligand derived from N-acetyl
91 erases mask galactose linkages implicated as asialoglycoprotein receptor ligands, only ST3Gal-IV defi
95 acting factor associating with the 5'-UTR of asialoglycoprotein receptor mRNAs, thereby inhibiting tr
97 ns, and N-acetylgalactosamine, which targets asialoglycoprotein receptors on hepatocytes, were synthe
98 the endocytic and ligand binding activity of asialoglycoprotein receptors on isolated rat hepatocytes
100 gA binding to HT-29/19A cells was due to the asialoglycoprotein receptor or beta-1, 4-galactosyltrans
102 TM2 by the transmembrane domain of CD4, the asialoglycoprotein receptor, or the transferrin receptor
104 did not detect the minor subunits of the rat asialoglycoprotein receptor (RHL-2/3) in p45 preparation
105 he red cell anion exchange protein (Band 3), asialoglycoprotein receptor subunits, sucrase-isomaltase
109 corresponding to residue 256 of the hepatic asialoglycoprotein receptor was found to cause a 14-fold
111 t of the transmembrane domain of CD74 or the asialoglycoprotein receptor with Astn2 TM2 leads to the
112 sting a decrease in the number of functional asialoglycoprotein receptors with concomitant increase i
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