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1 ed (grass pollen) or remained unchanged (cat dander).
2 d with the titer of IgE antibodies to animal dander.
3 e cutaneous late-phase reaction to whole cat dander.
4 late-phase cutaneous reactions to whole cat dander.
5 05-2.88], P = 0.03), sensitization to animal dander (1.93 [1.21-3.09], P = 0.006) or pollen (1.16 [1.
7 s cockroach, fungal, and mite growth and (2) dander allergens are known to be present in schools and
9 -old man hypersensitive to grass pollen, cat dander and Alternaria tenuis with a history of urticaria
11 n induction of allergic sensitization to cat dander and common pollens relevant to human allergic dis
13 ls was significantly decreased with both cat dander and P3-1, after final ocular challenge (P < 0.001
16 on Survey identified several pollens and cat dander as among the most common allergens that induce al
17 the size of their late reaction to whole cat dander between baseline and both follow-ups, but the dif
18 ve to dander and 55 patients IgE negative to dander but with symptoms to dog were analysed for IgE ag
21 e (Der p1), peanut allergen (Ara h1) and dog dander (Can f1) and immuno-kinetic assay was performed t
22 e intratracheally sensitized with OVA or cat dander extract (CDE) alone or together with SEA and then
23 RWPE, other pollen allergic extracts, or cat dander extract (CDE), and activation of nuclear factor k
26 Basophil stimulation with dog saliva and dander extract was measured by flow cytometry among thre
28 ), dust mites (Der p 1 and Der f 1), and cat dander (Fel d 1) in household dust using monoclonal-anti
29 ionalized with four different allergens, cat dander (Fel d1), dust mite (Der p1), peanut allergen (Ar
31 and ragweed pollen, midge larvae, and horse dander; food allergens from peanut, cow's milk, and toma
33 A/J mice sensitized and challenged with cat dander in the eye were treated with topical IL-1Ra or ve
34 the role of MD2 in inducing pollen- and cat dander-induced innate and allergic airway inflammation.
35 coreceptor, but its role in pollen- and cat dander-induced innate and allergic inflammation has not
36 thma related to any IgE antibodies to animal dander or high-titer IgE antibodies (>/=17.5 IU/mL) were
38 receptor given inhaled house dust mite, cat dander, or Alternaria, and the effect of inhibiting alle
39 Among subjects challenged with ragweed, cat dander, or house dust mite, there were no differences in
44 nses (P = .026 vs placebo) and increased cat dander-specific IgG(4) levels by 5.66-fold (P = .003).
45 5) for wheat flour, rye flour, soy, cow hair/dander, storage mites (Tyrophagus putrescentiae, Lepidog
46 ly reaction to Fel D 1, but not to whole cat dander was significantly reduced in those on peptides co
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