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1 inflammation induced by the fungal allergen Alternaria alternata.
2 asally on days 0, 3 and 6 with a filtrate of Alternaria alternata.
3 ys were exposed to a common fungal allergen, Alternaria alternata.
4 for pathogenicity in the necrotrophic fungus Alternaria alternata.
5 /musty odour and increased concentrations of Alternaria alternata allergen, Aspergillus fumigatus ant
6 associated mold sensitivity, particularly to Alternaria alternata and Cladosporium herbarum, with the
9 gic airway inflammation (house dust mice and Alternaria alternata) and OVA-induced models of active a
10 cts from seven environmental airborne fungi (Alternaria alternata, Aspergillus versicolor, Bipolaris
11 d, and specific IgE levels were measured for Alternaria alternata, cat, cockroach, dog, Dermatophagoi
12 whole extract fungal (Aspergillus fumigatus, Alternaria alternata, Cryptococcus neoformans and Candid
13 ies identifying proteins from fungal species Alternaria alternata due to significant interspecies pro
14 s farinae, dog, cat, timothy grass, ragweed, Alternaria alternata, egg, peanut, milk, and German cock
15 ure to extract from the respiratory pathogen Alternaria alternata elicits profound epithelial cell (E
16 rmal and asthmatic subjects to extracts from Alternaria alternata evoked a rapid and sustained releas
17 (-/-) mice were challenged intranasally with Alternaria alternata extract for 4 consecutive days to i
21 and secretion in the phytopathogenic fungus Alternaria alternata in the presence of host-plant extra
22 nically relevant ubiquitous fungal allergen, Alternaria alternata, increases bronchoalveolar lavage l
23 ommon environmental aeroallergen, the fungus Alternaria alternata, induces rapid release of IL-33 int
26 Fusarium moniliforme toxins (fumonisins) and Alternaria alternata lycopersici (AAL) toxins are member
27 (NAPT) with Dermatophagoides pteronyssinus, Alternaria alternata, Olea europaea and grass pollen wer
28 n tests with Dermatophagoides pteronyssinus, Alternaria alternata, Olea europea, and a mix of grass p
29 mice were subjected to acute challenge with Alternaria alternata or house dust mite, and secretion o
33 ulated pomegranate fruits with six different Alternaria alternata species complex isolates, known to
34 ecretion of mannitol in the tobacco pathogen Alternaria alternata suggested that, like their animal c
35 ponses after exposure to the fungal allergen Alternaria alternata Thus, CysLT1R promotes LTC4- and Al
36 nst Phytophthora parasitica var. nicotianae, Alternaria alternata var. nicotianae and Rhizoctonia sol
38 in the presence or absence of VCs emitted by Alternaria alternata We found that volatile emissions fr
39 iveness to cold dry air and sensitisation to Alternaria alternata were determined before age 6 years.
40 vigorously to a common environmental fungus, Alternaria alternata, which is implicated in the develop
41 skin infection with phaeohyphomycosis due to Alternaria alternata, which we treated with topical anti
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