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1 leukotriene (cysLT) levels were measured in nasal lavage fluid.
3 ction through analysis of cytokine levels in nasal lavage fluid and stimulated peripheral blood monon
4 tion of macrophage inflammatory protein 2 in nasal lavage fluid and subsequent recruitment of neutrop
5 antibodies was measured in tissue extracts, nasal lavage fluid, and sera by using multiplex bead arr
7 the mouse, human CD49d(+) PMNs isolated from nasal lavage fluid during a viral respiratory tract infe
8 +) PMN frequency was significantly higher in nasal lavage fluid during acute respiratory symptoms in
9 e assessed, the inflammatory cell content in nasal lavage fluids estimated, and the activation patter
15 We sought to compare MP types and levels in nasal lavage fluids (NLFs) from controls and patients wi
16 and measured the total leukocyte content of nasal lavage fluid obtained from 10 min to 4 h after the
17 cell differential counts were evaluated from nasal lavage fluid obtained from wild-type and IL-17A-de
18 ergen significantly increased NGF protein in nasal lavage fluids of subjects with allergic rhinitis,
19 nts with acute bronchiolitis was elevated in nasal lavage fluid on both Days 1-2 (p = 0.014) and Days
20 We found that IL-6 and IFN-alpha levels in nasal lavage fluids peaked early (day 2) and correlated
21 IL-8, IFN-alpha, TGF-beta, and TNF-alpha in nasal lavage fluid, plasma, and serum obtained serially
22 ning cytokine and chemokine levels in serial nasal lavage fluid samples from 15 volunteers experiment
23 higher level of NTHI 2019 per milliliter of nasal lavage fluid than chinchillas colonized with predo
25 The percentage of leukocytes observed in nasal lavage fluid was significantly increased 12, 24, 4
26 ores, and concentrations of IL-6 and IL-8 in nasal lavage fluids were compared between treatment grou
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