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1 ed (grass pollen) or remained unchanged (cat dander).
2 osis in airways of naive mice exposed to cat dander.
3 d with the titer of IgE antibodies to animal dander.
4 e cutaneous late-phase reaction to whole cat dander.
5  late-phase cutaneous reactions to whole cat dander.
6 tigens such as dust mite, pollen, and animal dander.
7 s d 6, beef, pork, milk, dog dander, and cat dander.
8 05-2.88], P = 0.03), sensitization to animal dander (1.93 [1.21-3.09], P = 0.006) or pollen (1.16 [1.
9                        Recombinant major cat dander allergen Fel d 1 was fused to a translocation seq
10 s cockroach, fungal, and mite growth and (2) dander allergens are known to be present in schools and
11        Sera from 59 patients IgE positive to dander and 55 patients IgE negative to dander but with s
12 -old man hypersensitive to grass pollen, cat dander and Alternaria tenuis with a history of urticaria
13 e naive animals and mice sensitized with cat dander and challenged with OVA-peptide or PBS.
14 n induction of allergic sensitization to cat dander and common pollens relevant to human allergic dis
15  dog allergy by repeatedly administering dog dander and epithelium extracts via the intranasal route.
16  combination of allergy to dust mites or cat dander and high levels of the allergen.
17 ls was significantly decreased with both cat dander and P3-1, after final ocular challenge (P < 0.001
18                                 For both cat dander and P3-1, Muc5AC and Muc4 mRNA was found to be de
19 y one to two allergens, with very few animal danders and without an association with asthma.
20 d 2, Sus s 1, Bos d 6, beef, pork, milk, dog dander, and cat dander.
21                                          Cat dander- and Fel d 1-specific IgG(4) concentrations were
22 on Survey identified several pollens and cat dander as among the most common allergens that induce al
23 the size of their late reaction to whole cat dander between baseline and both follow-ups, but the dif
24 ve to dander and 55 patients IgE negative to dander but with symptoms to dog were analysed for IgE ag
25               Among patients IgE negative to dander, but with symptoms to dog, 20% were IgE positive
26 dog were analysed for IgE against saliva and dander by ELISA.
27 e (Der p1), peanut allergen (Ara h1) and dog dander (Can f1) and immuno-kinetic assay was performed t
28 ed high specific IgE (>=50UA/ml) against cat dander, dog dander, pork, Sus s 1, Fel d 2, Can f 1, Can
29 sted allergens (dust mite, cedar pollen, dog dander, egg white, milk, and candida) were measured by t
30 e intratracheally sensitized with OVA or cat dander extract (CDE) alone or together with SEA and then
31 RWPE, other pollen allergic extracts, or cat dander extract (CDE), and activation of nuclear factor k
32                  Basophil sensitivity to cat dander extract and Fel d 1 was lower in WC versus WoC su
33 ing proteins was found in saliva compared to dander extract and varied among dog breeds.
34 ced experimental asthma using repetitive cat dander extract exposure.
35                                     However, dander extract in routine diagnostics is not an optimal
36 e, crossreactivity between pork meat and dog dander extract was also noted.
37     Basophil stimulation with dog saliva and dander extract was measured by flow cytometry among thre
38       IgE-binding proteins in dog saliva and dander extract were analysed by immunoblot and mass spec
39 pots on 67-kDa proteins in pork meat and cat dander extract.
40 had the same molecular weight (67kDa) as cat dander extracts, and also cross-reactivity between these
41 tivity was confirmed for beef, milk, and cat dander extracts.
42 ), dust mites (Der p 1 and Der f 1), and cat dander (Fel d 1) in household dust using monoclonal-anti
43 ionalized with four different allergens, cat dander (Fel d1), dust mite (Der p1), peanut allergen (Ar
44 l epitopes for the principal allergen of cat dander, Fel d 1.
45                            Total IgE and cat dander-, Fel d 1- and Fel d 7-specific IgE concentration
46                 The dominant allergen in cat dander, Felis domesticus allergen 1 (Fel d 1), is a pers
47  and ragweed pollen, midge larvae, and horse dander; food allergens from peanut, cow's milk, and toma
48           The prevalence of sensitization to dander from various animals appears to be increasing wor
49                      IgE specific for animal dander had the highest prevalence and strongest relation
50                     The anti-Fel d 1 IgE/cat dander IgE ratio in pretreatment serum correlated with T
51  A/J mice sensitized and challenged with cat dander in the eye were treated with topical IL-1Ra or ve
52 -kappaB-inducible BRD4 activity mediates cat dander-induced inflammation and remodeling.
53  We sought to elucidate the mechanism of cat dander-induced inflammation-remodeling.
54  the role of MD2 in inducing pollen- and cat dander-induced innate and allergic airway inflammation.
55  coreceptor, but its role in pollen- and cat dander-induced innate and allergic inflammation has not
56                                          Cat dander induces innate inflammation through NF-kappaB sig
57                                          Cat dander induces NF-kappaB/RelA to complex with and activa
58                                          Cat dander is an aeroallergen associated with asthma risk.
59 thma related to any IgE antibodies to animal dander or high-titer IgE antibodies (>/=17.5 IU/mL) were
60 e were sensitized intraperitoneally with cat dander or the peptide P3-1 from the protein Fel d1.
61  receptor given inhaled house dust mite, cat dander, or Alternaria, and the effect of inhibiting alle
62  Among subjects challenged with ragweed, cat dander, or house dust mite, there were no differences in
63                      Sensitization to animal dander, pollen, or Aspergillus fumigatus was associated
64 ific IgE (>=50UA/ml) against cat dander, dog dander, pork, Sus s 1, Fel d 2, Can f 1, Can f 2, and Ca
65                   The majority of the 59 dog dander-positive sera (n = 44) were IgE positive to dog s
66           Multiple sensitizations and animal dander sensitization are more common among Finnish asthm
67                             Here, twenty cat dander-sensitized patients were randomized to receive th
68 nses (P = .026 vs placebo) and increased cat dander-specific IgG(4) levels by 5.66-fold (P = .003).
69 5) for wheat flour, rye flour, soy, cow hair/dander, storage mites (Tyrophagus putrescentiae, Lepidog
70 ly reaction to Fel D 1, but not to whole cat dander was significantly reduced in those on peptides co
71          Specific IgE levels for cat and dog dander were measured.