戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

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 ntained within the cytoplasmic domain of the neonatal Fc receptor.
2 t on binding to human FcgammaRI, C1q, or the neonatal Fc receptor.
3 /H435Q) with minimal affinity for the murine neonatal Fc receptor.
4 vent capsid spike interaction with the human neonatal Fc receptor.
5 gagement with its cognate cellular recycling neonatal Fc receptor.
6 cations of an increase in IgG binding to the neonatal Fc receptor.
7 ion complexes, which are transcytosed by the neonatal Fc receptor across syncytiotrophoblasts, infect
8 red to increase affinity at acidic pH to the neonatal Fc receptor, and to reduce effector functions.
9 a gravis (gMG) treated with efgartigimod, an neonatal Fc receptor antagonist, under the Early Access
10    m01s bound to a recombinant soluble human neonatal Fc receptor at pH 6.0 more strongly than CH2.
11 nt deposition, opsonophagocytic killing, and neonatal Fc receptor binding while tested against capsul
12                         Rozanolixizumab is a neonatal Fc receptor blocker that might provide a novel
13 erefore, we aimed to evaluate nipocalimab, a neonatal Fc receptor blocker that reduces circulating Ig
14                         Nipocalimab, an anti-neonatal Fc receptor blocker, inhibits transplacental Ig
15                               Nipocalimab, a neonatal Fc receptor blocker, was associated with dose-d
16 lly, improvements directed at binding to the neonatal Fc receptor can endow therapeutic antibodies wi
17 rint has some overlap with that seen for the neonatal Fc receptor complexed with enterovirus E6 but i
18 alent in endothelial cells, macrophages, and neonatal Fc receptor-expressing cells in the placental t
19 natriuretic peptide receptor A IgG4 with the neonatal Fc receptor, Fcgamma receptors, and complement-
20                                          The neonatal Fc receptor FcRn plays a critical role in the t
21                                          The neonatal Fc receptor FcRn provides IgG molecules with th
22 ctions have recently been identified for the neonatal Fc receptor FcRn.
23  fusion cytokine with reduced binding to the neonatal Fc receptor FcRn.
24  knockout and activation screens to identify neonatal Fc receptor (FcRn) and dipeptidyl-peptidase IV
25 iometry of immunoglobulin G (IgG) binding to neonatal Fc receptor (FcRn) and Fcgamma receptor (Fcgamm
26 th diverse types of receptors, including the neonatal Fc receptor (FcRn) and Fcgamma receptors (Fcgam
27 ibody fragments lack the ability to bind the neonatal Fc receptor (FcRn) and have reduced half-lives.
28 blood by transcytosis across the BBB via the neonatal Fc receptor (FcRn) and the low-density lipoprot
29                        Here, we identify the neonatal Fc receptor (FcRn) as a pan-echovirus receptor.
30                            We identified the neonatal Fc receptor (FcRn) as an important pro-viral ho
31 (Fv) of IgG antibodies on the binding to the neonatal Fc receptor (FcRn) as well as on FcRn-dependent
32 A) and IgG, through its Fc part, bind to the neonatal Fc receptor (FcRn) at low pH in the endosome af
33 erved Fc methionine residues and the loss of neonatal Fc receptor (FcRn) binding and complement-depen
34    Functional studies by antigen binding and neonatal Fc receptor (FcRn) binding correlated very well
35 igimod), an engineered IgG1 Fc with enhanced neonatal Fc receptor (FcRn) binding, which reduced total
36                                          The neonatal Fc receptor (FcRn) binds maternal immunoglobuli
37 ort the three-dimensional structure of human neonatal Fc receptor (FcRn) bound concurrently to its tw
38                       The widely distributed neonatal Fc receptor (FcRn) contributes to maintaining s
39                                          The neonatal Fc receptor (FcRn) controls IgG transport from
40                                          The neonatal Fc receptor (FcRn) directs the transfer of mate
41  albumin (HSA(QMP)) engineered for favorable neonatal Fc receptor (FcRn) engagement.
42 me MHC class I-related molecules such as the neonatal Fc receptor (FcRn) execute their function witho
43 ansferred across the placenta by binding the neonatal Fc receptor (FcRn) expressed within the endosom
44                                          The neonatal Fc receptor (FcRn) facilitates the transfer of
45                                          The neonatal Fc receptor (FcRn) for IgG, an MHC class I-rela
46                                              Neonatal Fc receptor (FcRn) has a key role in the homeos
47                                          The neonatal Fc receptor (FcRn) has been known to modulate I
48                     The endothelial cellular neonatal Fc receptor (FcRn) has been suggested to play a
49 (monoFc) maintained the binding affinity for neonatal Fc receptor (FcRn) in a pH-dependent manner.
50 ellular traffic of IgG mediated by the human neonatal Fc receptor (FcRn) in fibroblast cell lines wit
51 tudy the involvement of immune complexes and neonatal Fc receptor (FcRn) in the emergence of ADAs in
52                            Given the role of neonatal Fc receptor (FcRn) in transferring IgG across p
53                In light of the fact that the neonatal Fc receptor (FcRn) is a key regulator of albumi
54                                          The neonatal Fc receptor (FcRn) is a major histocompatibilit
55                                          The neonatal Fc receptor (FcRn) is a major regulator of IgG
56                    Improved affinity for the neonatal Fc receptor (FcRn) is known to extend antibody
57 nd in vivo analyses, the MHC class I-related neonatal Fc receptor (FcRn) is known to play a central r
58                                              Neonatal Fc receptor (FcRn) is the homeostatic receptor
59                 Here, we find that the human neonatal Fc receptor (FcRn) is the vehicle that transpor
60                    We also identify that the neonatal Fc receptor (FcRn) is upregulated in the cornea
61 ects proteins for lysosomal degradation, the neonatal Fc receptor (FcRn) located at the brush border
62                       Increasing affinity to neonatal Fc receptor (FcRn) may extend the pharmacokinet
63                                          The neonatal Fc receptor (FcRn) mediates the transport of Ig
64         We found that PVIgGs associated with neonatal Fc receptor (FcRn) on the cell membrane, and th
65                                    Silencing neonatal Fc Receptor (FcRn) or CAMK4 prevented the podoc
66 (PPI-Fc) is delivered to fetuses through the neonatal Fc receptor (FcRn) pathway, which physiological
67                                          The neonatal Fc receptor (FcRn) performs two distinct but re
68      The interaction of the IgG1 Fc with the neonatal Fc receptor (FcRn) plays a critical role in mai
69                                          The neonatal Fc receptor (FcRn) plays a critical role in reg
70                                          The neonatal Fc receptor (FcRn) plays an important role in r
71 -dependent affinity of IgG molecules for the neonatal Fc receptor (FcRn) receptor primarily arises fr
72 ct Fc region is controlled by the protective neonatal Fc receptor (FcRn) receptor.
73 ed endothelial cell (EC) injury, loss of the neonatal Fc receptor (FcRn) responsible for IgG recyclin
74  Serum half-life of IgG is controlled by the neonatal Fc receptor (FcRn) that interacts with the IgG
75                                          The neonatal Fc receptor (FcRn) that mediates IgG and albumi
76 t in blood, syncytiotrophoblasts express the neonatal Fc receptor (FcRn) that transports IgG for pass
77                                          The neonatal Fc receptor (FcRn) transfers IgG across epithel
78                                          The neonatal Fc receptor (FcRn) transports IgG across barrie
79                                          The neonatal Fc receptor (FcRn) transports IgG across epithe
80                                          The neonatal Fc receptor (FcRn) transports immunoglobulin G
81                                          The neonatal Fc receptor (FcRn) transports immunoglobulin G
82                                          The neonatal Fc receptor (FcRn) transports maternal IgG acro
83                                          The neonatal Fc receptor (FcRn) transports maternal immunogl
84 gG1 IC and formed a ternary complex with the neonatal Fc receptor (FcRn) under acidic conditions.
85 bodies via pharmacological inhibition of the neonatal Fc receptor (FcRn) using high-dose IgG therapy.
86            In contrast, in mice in which the neonatal Fc receptor (FcRn) was deleted, the half-life o
87 c fragment of immunoglobulin G (IgG) and the neonatal Fc receptor (FcRn) was determined at low resolu
88                                 Recently the neonatal Fc receptor (FcRn) was identified as a receptor
89                                          The neonatal Fc receptor (FcRn) was initially discovered as
90 eered to enhance interactions with the human neonatal Fc receptor (FcRn) without loss of the oligomer
91 ologic inhibition or genetic deletion of the neonatal Fc receptor (FcRn) would attenuate mechanical h
92 ng site on Fcgamma overlaps with that of the neonatal Fc receptor (FcRn), an interaction that is crit
93 regulated the constitutive expression of the neonatal Fc receptor (FcRn), an MHC class I-related mole
94 crossed the placenta, dependent on the fetal neonatal Fc receptor (FcRN), and sensitized fetal MCs fo
95 by the cells, the binding affinity of mAb to neonatal Fc receptor (FcRn), and the intracellular degra
96 pH-dependent interaction between IgG and the neonatal Fc receptor (FcRn), as FcRn is the main homeost
97  expression of the relevant receptor, namely neonatal Fc receptor (FcRn), by Calu-3 cell layers simul
98 roperties, via modified interaction with the neonatal Fc receptor (FcRn), has been achieved.
99 logue of the primary echovirus receptor, the neonatal Fc receptor (FcRn), is not sufficient for infec
100            The MHC class I-related receptor, neonatal Fc receptor (FcRn), plays a central role in reg
101 s, facilitated by interaction with the human neonatal Fc receptor (FcRn), that promotes it as a highl
102                 Here we demonstrate that the neonatal Fc receptor (FcRn), which is highly expressed a
103                     Here, involvement of the neonatal Fc receptor (FcRn), which mediates IgG recyclin
104 gG is transported across the placenta by the neonatal Fc receptor (FcRn), which recognizes the Fc dom
105                      Genetic deletion of the neonatal Fc receptor (FcRn), which rescues albumin and I
106 gGs is ensured by their interaction with the neonatal Fc receptor (FcRn), which salvages IgG from int
107 tibodies at these sites is influenced by the neonatal Fc receptor (FcRn), whose role in protecting ag
108  conjugate (rHA-CpG) designed to exploit the neonatal Fc receptor (FcRn)-driven albumin cellular sort
109 ediated effector functions and benefits from neonatal Fc receptor (FcRn)-mediated recycling.
110 offspring by instructing T reg formation via neonatal Fc receptor (FcRn)-mediated transfer and uptake
111 ties that are conferred by interactions with neonatal Fc receptor (FcRn).
112 in part, regulated by their interaction with neonatal Fc receptor (FcRn).
113 , neutrophils also express the intracellular neonatal Fc receptor (FcRn).
114 F9DHS, HY6-F9YTE) to increase binding to the neonatal Fc receptor (FcRn).
115 due to its pH-dependent interaction with the neonatal Fc receptor (FcRn).
116 ch is attributed to its interaction with the neonatal Fc receptor (FcRn).
117 alf-life requires interaction of Fc with the neonatal Fc receptor (FcRn).
118 ting fusion proteins interact with the human neonatal Fc receptor (FcRn).
119 gG by saturation of the MHC-like Fc receptor neonatal Fc receptor (FcRn).
120 rum half-life of IgG Abs is regulated by the neonatal Fc receptor (FcRn).
121 heir ability to interact with the protective neonatal Fc receptor (FcRn, Brambell receptor) present o
122  on half-life, pharmacokinetics defining the neonatal Fc receptors (FcRn) and most important safety o
123  airway epithelium through interactions with neonatal Fc receptors (FcRn).
124 udy was to determine the contribution of the neonatal Fc-receptor (FcRn) in rat brain efflux employin
125                                              Neonatal Fc-receptor (FcRn), the major histocompatibilit
126                                          The neonatal Fc receptor, FcRn mediates an endocytic salvage
127 r histocompatibility complex class I-related neonatal Fc receptor, FcRn, assembles as a heterodimer c
128                        The expression of the neonatal Fc receptor, FcRn, in APCs and its localization
129                 We demonstrate here that the neonatal Fc receptor, FcRn, is expressed in female genit
130                                          The neonatal Fc receptor, FcRn, is responsible for the long
131                                          The neonatal Fc receptor, FcRn, regulates the half-life of I
132                                          The neonatal Fc receptor, FcRn, transports immunoglobulin G
133  of these proteins, suggesting a lack of the neonatal Fc receptor, FcRn.
134                                          The neonatal Fc receptor for IgG (FcRn) functions to transpo
135               Immunoglobulin G (IgG) and the neonatal Fc receptor for IgG (FcRn) have an important fu
136                                          The neonatal Fc receptor for IgG (FcRn) is a distant member
137                                          The neonatal Fc receptor for IgG (FcRn) plays a major role i
138 ocyte-derived CD8(-)CD11b(+) DCs require the neonatal Fc receptor for IgG (FcRn) to conduct cross-pre
139                                          The neonatal Fc receptor for IgG (FcRn) transfers maternal I
140 Darby canine kidney cells expressing the rat neonatal Fc receptor for IgG (FcRn), it significantly re
141                                          The neonatal Fc receptor for immunoglobulin (Ig)G (FcRn) pro
142 ment crystallizable (Fc) domain to the human neonatal Fc receptor (hFcRn).
143 engagement with the human cellular recycling neonatal Fc receptor (hFcRn).
144 ntal transport, are facilitated by the human neonatal Fc receptor (hFcRn).
145                The human MHC class I-related neonatal Fc receptor, hFcRn, mediates bidirectional tran
146         This study reveals the importance of neonatal Fc receptor in the biology of pemphigus and the
147  findings support the mechanism of action of neonatal Fc receptor inhibition in generalised myastheni
148 imab are clinically approved for PV, but the neonatal Fc receptor inhibitor efgartigimod and Bruton's
149                              We assessed the neonatal Fc receptor inhibitor rozanolixizumab for CIDP
150 830 is a humanized IgG4 antibody that blocks neonatal Fc receptor interactions with IgG.
151 ected wild-type, but not Fcgamma-receptor or neonatal Fc-receptor knock-out mice.
152 I but also the related CD1a, CD1b, CD1c, and neonatal Fc receptor molecules were absent from the surf
153                               In a humanized neonatal Fc receptor mouse model, Bangladeshi sera led t
154  IgG, supporting data that saturation of the neonatal Fc-receptor occurs at ~ 16 mg IgG/ml.
155 y CD1), transport of immunoglobulins (by the neonatal Fc receptor), regulation of iron metabolism (by
156                                       Absent neonatal Fc receptor surface expression led to low serum
157                              By engaging the neonatal Fc receptor the Fc domain extends the in vivo l
158 mediates transcytosis through binding to the neonatal Fc receptor, the peptidomimetic introduces cros
159                                Pups used the neonatal Fc receptor to transfer IgG from milk into seru
160 we show that this effect is dependent on the neonatal Fc receptor, which rescues the dissociated anti
161 lass novel human IgG1 Fc fragment, binds the neonatal Fc receptor with high affinity and thus reduces

 
Page Top