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1                                              Arthus responses in NZB/NZW mice pretreated with R788 or
2      This local reaction, which is likely an Arthus hypersensitivity reaction caused by high levels o
3 with the classical histologic features of an Arthus reaction.
4 ed with viable T. pallidum; and 2) classical Arthus reactions when challenged intradermally with eith
5 ter formation of cutaneous immune complexes (Arthus reaction).
6 and neutrophil infiltration in the cutaneous Arthus reaction in mice.
7                     By imaging the cutaneous Arthus reaction through a skin window, we observed in re
8  injury in mice, as modeled by the cutaneous Arthus reaction, requires receptors for the Fc portion o
9 n immune complex-mediated FcgammaR-dependent Arthus reaction.
10 mune complexes, which can trigger a type III Arthus reaction.
11 ssary for neutrophil influx in skin and lung Arthus reactions and agonist-induced neutrophilia in the
12 d glomerulonephritis and the reverse passive Arthus (RPA) reaction and FcR-bearing macrophages, and m
13                   We induced reverse passive Arthus (RPA) reactions in the skin of rodents and found
14  hemorrhage and edema in the reverse passive Arthus in the lung and skin.
15 ulation (DIC) in mice; (2) a reverse passive Arthus model in guinea pigs; and (3) vasoregulatory effe
16                    Using the reverse passive Arthus reaction and experimental models of immune hemoly
17 we re-examined the cutaneous reverse passive Arthus reaction and observed that IC-activated neutrophi
18 erleukin 6 in the peritoneal reverse passive Arthus reaction compared to their wild-type littermates.
19                          The reverse passive Arthus reaction could be induced in HoxB8 chimeras but n
20 e C5aR and its ligand in the reverse passive Arthus reaction in the lung and a synergistic role toget
21                       In the reverse passive Arthus reaction in the skin the C5aR was also required f
22          Furthermore, in the reverse passive Arthus reaction, soluble immune complexes induce equival
23 disease, as well as from the reverse passive Arthus reaction, with functional overlap between the thr
24 uired for development of the reverse passive Arthus reaction.
25 e DIC model and a guinea pig reverse passive Arthus reaction.
26 lammation, we established a mouse peritoneal Arthus reaction model.
27  exaggerated responses to reverse peritoneal Arthus reaction characterized by increased infiltration
28 riggered responses in the reverse peritoneal Arthus reaction in mice.
29 g in vitro and in vivo, with blockade of rat Arthus reaction, kidney protection in mouse Ab-induced n
30        R788 pretreatment resulted in reduced Arthus responses in NZB/NZW mice, similar to results obt
31 d extravasation of neutrophils in a reversed Arthus reaction.
32 n of complement in vivo, inhibiting both the Arthus reaction and Forssman shock in guinea pigs.
33 ted processes are of major importance in the Arthus reaction in rats and guinea pigs, and suggest tha
34                                    Using the Arthus reaction in rabbits as an in vivo model of immune
35                    To determine whether this Arthus-like response occurred via a B cell superantigeni