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1 -specific CD8+ CTL have been suggested to be immunopathogenic.
2                For example, emerging, highly immunopathogenic adenovirus serotypes might induce incre
3           Lastly, an integrative analysis of immunopathogenic-associated SNPs suggests a role for dis
4    These data suggest a distinct genetic and immunopathogenic basis for AIH and PBC at the MIF locus.
5 n in AC22 mice, thereby providing us with an immunopathogenic basis for the fatal outcome of SARS-CoV
6 re profoundly inferior to Th1 cells in their immunopathogenic capacity.
7 g neutrophils and macrophages, suggesting an immunopathogenic component to neurovirulence.
8 he possibility that LIGHT may play a role in immunopathogenic conditions that are associated with loc
9 ignals transduced by HIV-1 envelope may have immunopathogenic consequences, including anergy, syncyti
10 ct the host, it centrally contributes to the immunopathogenic effects of HIV.
11                                          The immunopathogenic effects of myeloperoxidase and proteina
12 ur knowledge regarding immune-protective and immunopathogenic events in severe acute respiratory synd
13 APCs) known to be critically involved in the immunopathogenic events leading to type 1 diabetes, we h
14             Relatively little is known about immunopathogenic events occurring during the acute phase
15 ome serves as a prototype model to study the immunopathogenic features of a human organ-specific auto
16 25(+)Foxp3(+) regulatory T cells (Tregs) are immunopathogenic in cancers by impeding tumor-specific i
17 tion of normal mice with a foreign Ag can be immunopathogenic in certain transgenic recipients.
18 hepatocellular carcinoma, and virus-mediated immunopathogenic infections, affect billions of people w
19 Animal and clinical studies suggest that the immunopathogenic inflammatory condition of VVC is initia
20 ines of the Th17 lineage, and therefore, the immunopathogenic inflammatory response during VVC occurs
21 cting its vital function from the ravages of immunopathogenic injury.
22 ouse model of HSK is often used to delineate immunopathogenic mechanisms and bears many of the charac
23  an avenue to monitor MS and to characterize immunopathogenic mechanisms and therapeutic targets in t
24                                 Although the immunopathogenic mechanisms are currently unknown, virtu
25 plex array of multiphasic and multifactorial immunopathogenic mechanisms are involved in the establis
26 advances have increased understanding of the immunopathogenic mechanisms associated with the formatio
27                                              Immunopathogenic mechanisms have been implicated in schi
28 litis, tantalizing clues as to the potential immunopathogenic mechanisms in acute transverse myelitis
29 A, will be useful for the fine dissection of immunopathogenic mechanisms in EBA and for the developme
30               In this study, we examined the immunopathogenic mechanisms in this model, including ide
31                                          The immunopathogenic mechanisms leading to psoriasis remain
32 ensive cardiac inflammation, suggesting that immunopathogenic mechanisms may promote cardiomyopathy.
33                                          The immunopathogenic mechanisms mediating inflammation in mu
34                                          The immunopathogenic mechanisms of dry eye disease (DED), on
35                               Thus, defining immunopathogenic mechanisms of HSK in the mouse model wi
36                                          The immunopathogenic mechanisms of juvenile rheumatoid arthr
37      At this time, better delineation of the immunopathogenic mechanisms of this spectrum of diseases
38 ease that serves as a model for studying the immunopathogenic mechanisms of uveitis and organ-specifi
39 rting the role of p38 MAPK in regulating key immunopathogenic mechanisms underlying autoimmune inflam
40 the white matter to include a broad range of immunopathogenic mechanisms, axonal damage, and widespre
41 ), in which CD4(+) Th1 and/or Th17 cells are immunopathogenic, mimics various clinical features of no
42 n patients with TB reduces concentrations of immunopathogenic MMPs.
43 ults also show that beta-gal can serve as an immunopathogenic neural autoantigen, and that T cells ra
44  immune response could explain the increased immunopathogenic potential and associated increase in cl
45 in naive recipients and even exacerbated the immunopathogenic process in irradiated recipients.
46 rotein Hsp10 as a potential correlate to the immunopathogenic process in women with tubal factor infe
47              The role of Th17 lymphocytes in immunopathogenic processes has been well established, bu
48  molecular forms of antigen may initiate the immunopathogenic processes in the two forms of anti-GBM
49                        Th1 cells were highly immunopathogenic, producing disease in naive recipients
50 thepsin cleavage sites within mouse Tg, have immunopathogenic properties.
51 ated eyes, a complication possibly due to an immunopathogenic response to the RPE65 molecule.
52  be a previously unrecognized Notch-mediated immunopathogenic role for stromal cell niches in seconda
53 bserved in Clcn5 KO mice, suggesting a novel immunopathogenic role for the functional defects that re
54 with equine ocular components, suggesting an immunopathogenic role in leptospiral uveitis.
55 ndidate for the leishmaniases because of its immunopathogenic role in murine L. major infection.
56 oth Tfh and Th17 cells from entering the non-immunopathogenic site, the gut, and retained these T eff
57 e transfer of EAU to naive syngeneic mice by immunopathogenic T cells and suppressive effects of p28/
58 sely affecting the survival of SEA-reactive, immunopathogenic T lymphocytes.
59 mmune activation/suppression associated with immunopathogenic viruses such as hantaviruses; however,

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