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1 on of house dust mite or the fungal allergen Alternaria alternata.
2 inflammation induced by the fungal allergen Alternaria alternata.
3 asally on days 0, 3 and 6 with a filtrate of Alternaria alternata.
4 ys were exposed to a common fungal allergen, Alternaria alternata.
5 for pathogenicity in the necrotrophic fungus Alternaria alternata.
6 on the major allergen Alt a 1 of the fungus Alternaria alternata.
7 goides pteronyssinus) or the fungal allergen Alternaria alternata.
8 d were highest for Candida albicans (18.6%), Alternaria alternata (16.6%), Stemphylium herbarum (14.9
9 AC with Dermatophagoides pteronyssinus (DP), Alternaria alternata (AA), grass (GP) and olive (OP) pol
10 /musty odour and increased concentrations of Alternaria alternata allergen, Aspergillus fumigatus ant
11 nut extract (PNE), an environmental allergen Alternaria alternata (Alt) and a detergent induce food a
12 ut extract (PNE), the environmental allergen Alternaria alternata (Alt), and detergent (4% SDS); oral
14 trinum, Aspergillus flavus, Fusarium solani, Alternaria alternata, Alternaria citri, Pseudomonas syri
15 associated mold sensitivity, particularly to Alternaria alternata and Cladosporium herbarum, with the
18 ungal LOV-domain blue-light receptor LreA of Alternaria alternata and show that it predominantly cont
20 gic airway inflammation (house dust mice and Alternaria alternata) and OVA-induced models of active a
22 ppb) and with FS (defined as IgE specific to Alternaria alternata, Aspergillus fumigatus or Cladospor
23 ally challenged with PBS or mixed allergen ( Alternaria alternata, Aspergillus fumigatus, house dust
24 cts from seven environmental airborne fungi (Alternaria alternata, Aspergillus versicolor, Bipolaris
25 ls of Streptococcus pneumoniae infection and Alternaria alternata asthma, we show that sensory neuron
26 d, and specific IgE levels were measured for Alternaria alternata, cat, cockroach, dog, Dermatophagoi
28 whole extract fungal (Aspergillus fumigatus, Alternaria alternata, Cryptococcus neoformans and Candid
30 ies identifying proteins from fungal species Alternaria alternata due to significant interspecies pro
31 s farinae, dog, cat, timothy grass, ragweed, Alternaria alternata, egg, peanut, milk, and German cock
32 ure to extract from the respiratory pathogen Alternaria alternata elicits profound epithelial cell (E
33 rmal and asthmatic subjects to extracts from Alternaria alternata evoked a rapid and sustained releas
34 ild-type (WT) and IP knockout (KO) mice with Alternaria alternata extract (Alt) to induce ILC2 activa
35 bese) mice were challenged intranasally with Alternaria alternata extract (Alt-Ext) or PBS for 4 cons
36 (DKO) mice were challenged intranasally with Alternaria alternata extract (Alt-Ext) or vehicle to eva
38 T cells from lungs of mice sensitized with Alternaria alternata extract displayed genetic signature
39 (-/-) mice were challenged intranasally with Alternaria alternata extract for 4 consecutive days to i
40 ive mice were intranasally exposed to fungus Alternaria alternata extract or house dust mite for up t
41 ta-catenin-deficient mice were exposed to an Alternaria alternata extract sensitization and challenge
42 ated lung inflammation following exposure to Alternaria alternata extract, marked by increased IL-5 a
48 sed in the mouse models of IL-33, IL-25, and Alternaria alternata ILC2-dependent airway inflammation.
49 and secretion in the phytopathogenic fungus Alternaria alternata in the presence of host-plant extra
50 nically relevant ubiquitous fungal allergen, Alternaria alternata, increases bronchoalveolar lavage l
52 ommon environmental aeroallergen, the fungus Alternaria alternata, induces rapid release of IL-33 int
58 ichia coli or the fungi Botrytis cinerea and Alternaria alternata, likely due to limited ZnO release
59 Fusarium moniliforme toxins (fumonisins) and Alternaria alternata lycopersici (AAL) toxins are member
60 ic utility of MIS416 was investigated in the Alternaria alternata model of allergic asthma and in hum
62 y, we studied the effect of IL-33trap in the Alternaria alternata mouse model of allergic airway infl
63 (NAPT) with Dermatophagoides pteronyssinus, Alternaria alternata, Olea europaea and grass pollen wer
64 n tests with Dermatophagoides pteronyssinus, Alternaria alternata, Olea europea, and a mix of grass p
65 mice were subjected to acute challenge with Alternaria alternata or house dust mite, and secretion o
70 derived from the common saprophytic fungus, Alternaria alternata release ATP, which in turn stimulat
71 ulated pomegranate fruits with six different Alternaria alternata species complex isolates, known to
72 ecretion of mannitol in the tobacco pathogen Alternaria alternata suggested that, like their animal c
73 ere repeatedly exposed to house dust mite or Alternaria alternata three times a week for up to 5 week
74 ponses after exposure to the fungal allergen Alternaria alternata Thus, CysLT1R promotes LTC4- and Al
75 oallergens, such as house dust mite (HDM) or Alternaria alternata, to induce experimental asthma.
76 nst Phytophthora parasitica var. nicotianae, Alternaria alternata var. nicotianae and Rhizoctonia sol
78 in the presence or absence of VCs emitted by Alternaria alternata We found that volatile emissions fr
79 iveness to cold dry air and sensitisation to Alternaria alternata were determined before age 6 years.
80 hibition in growth of Rhizoctonia solani and Alternaria alternata were observed in response to ZNsw.
81 vigorously to a common environmental fungus, Alternaria alternata, which is implicated in the develop
82 skin infection with phaeohyphomycosis due to Alternaria alternata, which we treated with topical anti