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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.
6                        Recombinant major cat dander allergen Fel d 1 was fused to a translocation seq
7 s cockroach, fungal, and mite growth and (2) dander allergens are known to be present in schools and
8        Sera from 59 patients IgE positive to dander and 55 patients IgE negative to dander but with s
9 -old man hypersensitive to grass pollen, cat dander and Alternaria tenuis with a history of urticaria
10 e naive animals and mice sensitized with cat dander and challenged with OVA-peptide or PBS.
11 n induction of allergic sensitization to cat dander and common pollens relevant to human allergic dis
12  combination of allergy to dust mites or cat dander and high levels of the allergen.
13 ls was significantly decreased with both cat dander and P3-1, after final ocular challenge (P < 0.001
14                                 For both cat dander and P3-1, Muc5AC and Muc4 mRNA was found to be de
15 y one to two allergens, with very few animal danders and without an association with asthma.
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
19               Among patients IgE negative to dander, but with symptoms to dog, 20% were IgE positive
20 dog were analysed for IgE against saliva and dander by ELISA.
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
24 ing proteins was found in saliva compared to dander extract and varied among dog breeds.
25                                     However, dander extract in routine diagnostics is not an optimal
26     Basophil stimulation with dog saliva and dander extract was measured by flow cytometry among thre
27       IgE-binding proteins in dog saliva and dander extract were analysed by immunoblot and mass spec
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
30 l epitopes for the principal allergen of cat dander, Fel d 1.
31  and ragweed pollen, midge larvae, and horse dander; food allergens from peanut, cow's milk, and toma
32                      IgE specific for animal dander had the highest prevalence and strongest relation
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
37 e were sensitized intraperitoneally with cat dander or the peptide P3-1 from the protein Fel d1.
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
40                      Sensitization to animal dander, pollen, or Aspergillus fumigatus was associated
41                   The majority of the 59 dog dander-positive sera (n = 44) were IgE positive to dog s
42           Multiple sensitizations and animal dander sensitization are more common among Finnish asthm
43                             Here, twenty cat dander-sensitized patients were randomized to receive th
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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