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1 l for studying apically localized endogenous asialoglycoprotein receptor.
2 uent of N-acetylgalactosamine in the hepatic asialoglycoprotein receptor.
3 up nearly exclusively by hepatocytes via the asialoglycoprotein receptor.
4 ding site similar to the binding site in the asialoglycoprotein receptor.
5 lin 1 structures had no asialoorosomucoid or asialoglycoprotein receptor.
6 sfer into HuH-7 human hepatoma cells via the asialoglycoprotein receptor.
7 se, making it a good functional mimic of the asialoglycoprotein receptor.
8 the gene coding for the major subunit of the asialoglycoprotein receptor.
9 i.v., and targeted to the hepatocyte via the asialoglycoprotein receptor.
10 or inhibition of in vitro translation of the asialoglycoprotein receptor.
11  efficiency in targeting hepatocytes via the asialoglycoprotein receptor.
12 al N-acetylgalactosamine binding site of the asialoglycoprotein receptor.
13 ical to the major subunit (RHL-1) of the rat asialoglycoprotein receptor.
14 ticular, there is a striking loss of State 2 asialoglycoprotein receptors.
15 nal HLCs using the hepatocyte surface marker asialoglycoprotein receptor 1 (ASGR1).
16                                              Asialoglycoprotein receptor-1 (ASGR1) mediates capture a
17 n 4 of ASGR1, which encodes a subunit of the asialoglycoprotein receptor, a lectin that plays a role
18                        The mammalian hepatic asialoglycoprotein receptor, a member of the C-type anim
19                                         This asialoglycoprotein receptor activity remains a key facto
20  4 degrees C with metal did not lose surface asialoglycoprotein receptor activity.
21 ral colorectal cancer cell lines express the asialoglycoprotein receptor, although no significant lev
22 of the CRD is very similar to the CRD of the asialoglycoprotein receptor and other galactose-specific
23  cells produce a functional apically located asialoglycoprotein receptor and provide a model for rece
24                                          The asialoglycoprotein receptors and many other C-type (Ca2+
25 docytosed transferrin, transferrin receptor, asialoglycoprotein receptor, and low amounts of the cati
26              These studies showed that human asialoglycoprotein receptor (ASGP-R) and the terminal la
27                                    Using the asialoglycoprotein receptor (ASGP-R) as a model, we have
28 ative functional imaging techniques that use asialoglycoprotein receptor (ASGP-R) binding is based on
29                 Polyclonal antibodies to the asialoglycoprotein receptor (ASGP-R) demonstrated the pr
30                                              Asialoglycoprotein receptor (ASGP-R) has been actively i
31                        Within the liver, the asialoglycoprotein receptor (ASGP-R) has been shown to b
32 acids in their sequences, orthologues of the asialoglycoprotein receptor (ASGP-R) in different mammal
33                                  The hepatic asialoglycoprotein receptor (ASGP-R) internalizes desial
34                 The functional human hepatic asialoglycoprotein receptor (ASGP-R) is a hetero-oligome
35                                          The asialoglycoprotein receptor (ASGP-R) is an abundant, car
36                                  The hepatic asialoglycoprotein receptor (ASGP-R) is an endocytic rec
37                        The mammalian hepatic asialoglycoprotein receptor (ASGP-R) is an endocytic rec
38                                  The hepatic asialoglycoprotein receptor (ASGP-R) is posttranslationa
39  efficient uptake of the nucleic acid by the asialoglycoprotein receptor (ASGP-R) on hepatocytes.
40 ae lipooligosaccharide (LOS) can bind to the asialoglycoprotein receptor (ASGP-R) on human sperm.
41 ly in situ, the endocytic trafficking of the asialoglycoprotein receptor (ASGP-R) was impaired in eth
42 nd was partially prevented by ligands of the asialoglycoprotein receptor (ASGP-R), thyroglobulin, asi
43 s of the experimentally intractable trimeric asialoglycoprotein receptor (ASGP-R), which consists of
44 s have not, to date, been identified for the asialoglycoprotein receptor (ASGP-R), which is abundantl
45 endocytic receptor on hepatocytes called the asialoglycoprotein receptor (ASGP-R), which is known to
46  may be preferentially localized through the asialoglycoprotein receptor (ASGP-R).
47                      Functional rat or human asialoglycoprotein receptors (ASGP-Rs) are hetero-oligom
48                                          The asialoglycoprotein-receptor (ASGP-R) located on liver pa
49 of FcF241A via impaired interaction with the asialoglycoprotein receptor ASGPR.
50 S mutant of alpha1-AT and H2a subunit of the asialoglycoprotein receptor (ASGPR H2a) were expressed i
51          In addition, protein content of the asialoglycoprotein receptor (ASGPR) and three traffickin
52                                          The asialoglycoprotein receptor (ASGPR) is a high-capacity g
53                                The mammalian asialoglycoprotein receptor (ASGPR) is located on the si
54 erfering RNA (siRNA) mediates binding to the asialoglycoprotein receptor (ASGPR) on the surface of he
55 age-galactose-type lectin (MGL) receptor and asialoglycoprotein receptor (ASGPR) was also significant
56                                    Likewise, asialoglycoprotein receptor (ASGPR) was up-regulated in
57 raders of extracellular proteins through the asialoglycoprotein receptor (ASGPR)), which mediate the
58    Here, we developed LYTACs that engage the asialoglycoprotein receptor (ASGPR), a liver-specific ly
59 -affinity ligand for the hepatocyte-specific asialoglycoprotein receptor (ASGPR), enhances the potenc
60 in-like growth factor 2 receptor (IGF2R) and asialoglycoprotein receptor (ASGPR), sortilin and transf
61 ific antibody to the thyroid apical membrane asialoglycoprotein receptor (ASGPR), which is related to
62                                              Asialoglycoprotein receptor (ASGPR)-mediated endocytosis
63 amine (GalNAc), the ligand recognized by the asialoglycoprotein receptor (ASGPR).
64 e novel binding polymers for a case study of asialoglycoprotein receptor (ASGPR).
65 dged ketal was developed as a ligand for the asialoglycoprotein receptor (ASGPR).
66 actosamine = GalNAc) for hepatocyte-specific asialoglycoprotein receptors (ASGPR) to enhance uptake t
67 bohydrate-specific, endocytic receptors, the asialoglycoprotein receptor (ASGR) and the mannose recep
68                            Expression of the asialoglycoprotein receptor (ASGR) by the human hepatoce
69                                The exclusive asialoglycoprotein receptor (ASGR) expression on hepatoc
70 ligonucleotides (ASO) to hepatocytes via the asialoglycoprotein receptor (ASGR) has improved the pote
71                     The human hepatic lectin asialoglycoprotein receptor (ASGR) is selectively expres
72 ell-surface receptors for asialoorosomucoid (asialoglycoprotein receptor (ASGR)), transferrin, and ma
73 dylethanolamine (Lac-DOPE), a ligand for the asialoglycoprotein receptor (ASGR), and an antibiotic pe
74         Liver-mediated uptake is through the asialoglycoprotein receptor (ASGR), since clearance can
75 ylgalactosamine (GalNAc)-conjugated ASOs for Asialoglycoprotein Receptor (ASGR)-mediated uptake into
76  into cultured hepatic cells (HepG2) via the asialoglycoprotein receptor (ASGR).
77        The mannose receptor (ManR, Mrc1) and asialoglycoprotein receptor (ASGR, Asgr1 and Asgr2) are
78         The hepatic carbohydrate-recognizing asialoglycoprotein receptor (ASGR1) mediates the endocyt
79 rate-recognition domain (CRD) of the hepatic asialoglycoprotein receptor at endosomal pH requires a s
80  terminal galactosylation leading to reduced asialoglycoprotein-receptor binding and to improved phar
81            We recently reported that the rat asialoglycoprotein receptor binds oligosaccharides termi
82                            Expression of the asialoglycoprotein receptor by the human hepatocellular
83 simultaneous detection of asialoorosomucoid, asialoglycoprotein receptor, caveolin 1, and microtubule
84                        Pretreatment of Huh7, asialoglycoprotein receptor (+) cells, with antisense co
85                                              Asialoglycoprotein receptor colocalized with asialooroso
86 inetic analysis that estimates the subject's asialoglycoprotein receptor concentration [R]o.
87 In this study, we report that ligation of DC-asialoglycoprotein receptor (DC-ASGPR), a C-type lectin
88                                           DC-asialoglycoprotein receptor (DC-ASGPR), a lectinlike rec
89 s confirmed 40 days after transplantation by asialoglycoprotein receptor-directed nuclear scanning.
90 cells can be enriched and recovered based on asialoglycoprotein-receptor expression and potentially c
91 tocytes were isolated by sorting for surface asialoglycoprotein-receptor expression.
92 hat an IgA receptor, distinct from the pIgR, asialoglycoprotein receptor, galactosyltransferase, and
93                                    The human asialoglycoprotein receptor H2a subunit contains a charg
94 d ERAD substrate, the uncleaved precursor of asialoglycoprotein receptor H2a, its nonglycosylated mut
95  cells with deletion constructs encoding the asialoglycoprotein receptor H2b subunit localized the cG
96  COS-7 cells with deletion constructs of the asialoglycoprotein receptor H2b subunit localized the cG
97                   We found expression of the asialoglycoprotein receptor in FLC to be maintained at s
98 tudies on the functional role of the hepatic asialoglycoprotein receptor in mammals.
99 f binding to the mannose receptor and/or the asialoglycoprotein receptor in the liver.
100  keratinocytes; cell surface levels of human asialoglycoprotein receptor increase following gonococca
101 0 nm; asialofetuin, a natural ligand for the asialoglycoprotein receptor, inhibited this process by u
102 ity; zinc-treated cells accumulated inactive asialoglycoprotein receptors intracellularly, whereas co
103                                  The hepatic asialoglycoprotein receptor is responsible for rapid cle
104 ells lost approximately 50% of their surface asialoglycoprotein receptor ligand binding activity; zin
105 ation of small interfering RNA (siRNA) to an asialoglycoprotein receptor ligand derived from N-acetyl
106 he introduction of an optimized GalNAc-based asialoglycoprotein receptor ligand to the nanoparticle s
107 erases mask galactose linkages implicated as asialoglycoprotein receptor ligands, only ST3Gal-IV defi
108                                          The asialoglycoprotein receptor localizes to the basolateral
109                DNA delivered to the liver by asialoglycoprotein receptor-mediated endocytosis is degr
110         In a cell-free system, initiation of asialoglycoprotein receptor mRNA translation was depende
111 acting factor associating with the 5'-UTR of asialoglycoprotein receptor mRNAs, thereby inhibiting tr
112                                              Asialoglycoprotein receptors on hepatocytes lose endocyt
113 ns, and N-acetylgalactosamine, which targets asialoglycoprotein receptors on hepatocytes, were synthe
114 the endocytic and ligand binding activity of asialoglycoprotein receptors on isolated rat hepatocytes
115                                              Asialoglycoprotein receptors on the surfaces of both hep
116 gA binding to HT-29/19A cells was due to the asialoglycoprotein receptor or beta-1, 4-galactosyltrans
117                                          The asialoglycoprotein receptor or other lectin-like recepto
118  TM2 by the transmembrane domain of CD4, the asialoglycoprotein receptor, or the transferrin receptor
119             We show that the two subunits of asialoglycoprotein receptor [rat hepatic lectin 1 (RHL1)
120 did not detect the minor subunits of the rat asialoglycoprotein receptor (RHL-2/3) in p45 preparation
121 beta nerve growth factor (NGF) and a soluble asialoglycoprotein receptor (sASGPR) assay from human se
122 he red cell anion exchange protein (Band 3), asialoglycoprotein receptor subunits, sucrase-isomaltase
123                  We have previously used the asialoglycoprotein receptor system to elucidate the path
124                         SRCL shares with the asialoglycoprotein receptor the ability to mediate endoc
125        Here, we address this problem for the asialoglycoprotein receptor using ensemble FRET imaging,
126  corresponding to residue 256 of the hepatic asialoglycoprotein receptor was found to cause a 14-fold
127                                  The hepatic asialoglycoprotein receptor was the first of the mammali
128 t of the transmembrane domain of CD74 or the asialoglycoprotein receptor with Astn2 TM2 leads to the
129 sting a decrease in the number of functional asialoglycoprotein receptors with concomitant increase i

 
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