コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ocytoses galactose-terminated glycoproteins (asialoglycoproteins).
2 mumol/L, and was competable by an excess of asialoglycoprotein.
3 (CL) were labeled with asialofetuin (AF), an asialoglycoprotein.
4 asialo-orosomucoid rather than generally to asialoglycoproteins.
6 ction of Texas red asialoorosomucoid contain asialoglycoprotein and its receptor and move and undergo
7 In contrast, antibodies to the receptors for asialoglycoproteins and mannose-6-phosphate or to the ly
10 rafficking mutant (Trf1) of HuH-7 alters the asialoglycoprotein (ASGPR) and transferrin receptor subc
11 and to chemically modified siRNA has enabled asialoglycoprotein (ASGPR)-mediated targeted delivery of
13 ligands, only ST3Gal-IV deficiency promotes asialoglycoprotein clearance mechanisms with a reduction
16 leotides anti-III and anti-IV in the form of asialoglycoprotein-polylysine complexes were administere
17 e-1 (pSVK3-hBUGT1) genes were complexed with asialoglycoprotein-polylysine conjugates, and 1 mg of th
21 ative functional imaging techniques that use asialoglycoprotein receptor (ASGP-R) binding is based on
25 acids in their sequences, orthologues of the asialoglycoprotein receptor (ASGP-R) in different mammal
33 ae lipooligosaccharide (LOS) can bind to the asialoglycoprotein receptor (ASGP-R) on human sperm.
34 ly in situ, the endocytic trafficking of the asialoglycoprotein receptor (ASGP-R) was impaired in eth
35 nd was partially prevented by ligands of the asialoglycoprotein receptor (ASGP-R), thyroglobulin, asi
36 s of the experimentally intractable trimeric asialoglycoprotein receptor (ASGP-R), which consists of
37 s have not, to date, been identified for the asialoglycoprotein receptor (ASGP-R), which is abundantl
38 endocytic receptor on hepatocytes called the asialoglycoprotein receptor (ASGP-R), which is known to
40 S mutant of alpha1-AT and H2a subunit of the asialoglycoprotein receptor (ASGPR H2a) were expressed i
44 erfering RNA (siRNA) mediates binding to the asialoglycoprotein receptor (ASGPR) on the surface of he
45 age-galactose-type lectin (MGL) receptor and asialoglycoprotein receptor (ASGPR) was also significant
47 raders of extracellular proteins through the asialoglycoprotein receptor (ASGPR)), which mediate the
48 Here, we developed LYTACs that engage the asialoglycoprotein receptor (ASGPR), a liver-specific ly
49 -affinity ligand for the hepatocyte-specific asialoglycoprotein receptor (ASGPR), enhances the potenc
50 in-like growth factor 2 receptor (IGF2R) and asialoglycoprotein receptor (ASGPR), sortilin and transf
51 ific antibody to the thyroid apical membrane asialoglycoprotein receptor (ASGPR), which is related to
56 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
61 ell-surface receptors for asialoorosomucoid (asialoglycoprotein receptor (ASGR)), transferrin, and ma
62 dylethanolamine (Lac-DOPE), a ligand for the asialoglycoprotein receptor (ASGR), and an antibiotic pe
64 ylgalactosamine (GalNAc)-conjugated ASOs for Asialoglycoprotein Receptor (ASGR)-mediated uptake into
68 In this study, we report that ligation of DC-asialoglycoprotein receptor (DC-ASGPR), a C-type lectin
70 did not detect the minor subunits of the rat asialoglycoprotein receptor (RHL-2/3) in p45 preparation
71 beta nerve growth factor (NGF) and a soluble asialoglycoprotein receptor (sASGPR) assay from human se
76 of the CRD is very similar to the CRD of the asialoglycoprotein receptor and other galactose-specific
77 cells produce a functional apically located asialoglycoprotein receptor and provide a model for rece
79 rate-recognition domain (CRD) of the hepatic asialoglycoprotein receptor at endosomal pH requires a s
85 d ERAD substrate, the uncleaved precursor of asialoglycoprotein receptor H2a, its nonglycosylated mut
86 COS-7 cells with deletion constructs of the asialoglycoprotein receptor H2b subunit localized the cG
87 cells with deletion constructs encoding the asialoglycoprotein receptor H2b subunit localized the cG
91 keratinocytes; cell surface levels of human asialoglycoprotein receptor increase following gonococca
93 ells lost approximately 50% of their surface asialoglycoprotein receptor ligand binding activity; zin
94 ation of small interfering RNA (siRNA) to an asialoglycoprotein receptor ligand derived from N-acetyl
95 he introduction of an optimized GalNAc-based asialoglycoprotein receptor ligand to the nanoparticle s
96 erases mask galactose linkages implicated as asialoglycoprotein receptor ligands, only ST3Gal-IV defi
99 acting factor associating with the 5'-UTR of asialoglycoprotein receptor mRNAs, thereby inhibiting tr
100 gA binding to HT-29/19A cells was due to the asialoglycoprotein receptor or beta-1, 4-galactosyltrans
102 he red cell anion exchange protein (Band 3), asialoglycoprotein receptor subunits, sucrase-isomaltase
106 corresponding to residue 256 of the hepatic asialoglycoprotein receptor was found to cause a 14-fold
108 t of the transmembrane domain of CD74 or the asialoglycoprotein receptor with Astn2 TM2 leads to the
109 n 4 of ASGR1, which encodes a subunit of the asialoglycoprotein receptor, a lectin that plays a role
111 ral colorectal cancer cell lines express the asialoglycoprotein receptor, although no significant lev
112 docytosed transferrin, transferrin receptor, asialoglycoprotein receptor, and low amounts of the cati
113 simultaneous detection of asialoorosomucoid, asialoglycoprotein receptor, caveolin 1, and microtubule
114 hat an IgA receptor, distinct from the pIgR, asialoglycoprotein receptor, galactosyltransferase, and
115 0 nm; asialofetuin, a natural ligand for the asialoglycoprotein receptor, inhibited this process by u
116 TM2 by the transmembrane domain of CD4, the asialoglycoprotein receptor, or the transferrin receptor
118 s confirmed 40 days after transplantation by asialoglycoprotein receptor-directed nuclear scanning.
134 terminal galactosylation leading to reduced asialoglycoprotein-receptor binding and to improved phar
135 cells can be enriched and recovered based on asialoglycoprotein-receptor expression and potentially c
138 actosamine = GalNAc) for hepatocyte-specific asialoglycoprotein receptors (ASGPR) to enhance uptake t
140 ity; zinc-treated cells accumulated inactive asialoglycoprotein receptors intracellularly, whereas co
142 ns, and N-acetylgalactosamine, which targets asialoglycoprotein receptors on hepatocytes, were synthe
143 the endocytic and ligand binding activity of asialoglycoprotein receptors on isolated rat hepatocytes
145 sting a decrease in the number of functional asialoglycoprotein receptors with concomitant increase i
148 e have previously shown decreased binding of asialoglycoproteins to this receptor after as early as 1