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1 dust contamination and possible dispersal of fungal spores.
2 hogenic implications of infections caused by fungal spores.
3 (Hck), p72(Syk), and p77(Btk) in response to fungal spores.
4 e infected flies by dusting the cuticle with fungal spores.
5 ecific areas on the nematode's surface where fungal spores adhere preferentially.
6 drophobins have been suggested to facilitate fungal spore adhesion and to direct the action of the en
7  insights into the host factors that mediate fungal spore adhesion.
8                               Pollen, algal, fungal spore and micro-charcoal data from sediments demo
9 dusts, biological species (pollen, bacteria, fungal spores and plankton), carbonaceous combustion pro
10 permicron particles such as bacterial cells, fungal spores and pollen grains.
11       Airborne biological particles, such as fungal spores and pollen, are ubiquitous in the Earth's
12 and other molds leading to aerosolization of fungal spores and potential exposure for patients.
13 e (ESEM), we observed rupturing of Amazonian fungal spores and subsequent release of submicrometer si
14 ing mite and insect cuticles, pollen grains, fungal spores, and insect eggs.
15              Finally, to negate discharge of fungal spores, and/or archaeal and/or bacterial cells, c
16 s striking implications for the evolution of fungal-spore- and plant-pollen-profilins as allergens.
17                    Furthermore, rupturing of fungal spores at high humidity may explain the bursting
18  geographic structure in pine-associated ECM fungal spore banks across the North American continent.
19             Similar to plant seed banks, ECM fungal spore banks are, in general, depauperate, and rep
20 owth, the structure of ectomycorrhizal (ECM) fungal spore banks remains poorly understood.
21 th light) sharply reduced the infectivity of fungal spores but did not affect host susceptibility to
22                 The minimal concentration of fungal spores by air sampling for acquisition of fungal
23                   Long-distance dispersal of fungal spores by the wind can spread plant diseases acro
24                                              Fungal spores (conidia) are rapidly ingested by ECs deri
25 al for host survival following inhalation of fungal spores (conidia).
26                                  The average fungal spore counts per cubic metre of air in the bedroo
27 sists in the plant until head emergence when fungal spores develop and are released from sori formed
28 nes to contribute to better understanding of fungal spore dispersal, plant disease epidemiology, and
29 unique Raman spectral signatures from intact fungal spores dispersed on commercially available alumin
30 nogaster flies with a standardized amount of fungal spores from clinical Zygomycetes isolates to stud
31             Strategies to efficiently remove fungal spores from hospital surfaces and, ideally, patie
32 uclear migration, and death of the conidium (fungal spore) from which the infection originated.
33                                       During fungal spore germination, a resting spore returns to a c
34 rmination medium reduced M. sexta growth and fungal spore germination, respectively.
35 ans to accurately enumerate and localize the fungal spores in the pulmonary tissues.
36          Early epithelial internalization of fungal spores in vivo cannot explain the bronchial/bronc
37                 While immunization with live fungal spores induced antibody responses, we found a mar
38                  LDD of small particles like fungal spores is often a result of turbulent wind disper
39 Neurospora, meiotic drive can be observed in fungal spore killing.
40 dox based on wind-gust aerodynamic models of fungal-spore liberation.
41 stead revealed that the sum of bacterial and fungal spores mass represented only a minor OMCOARSE fra
42 ls consisting of: i) soil samples containing fungal spores of B. bassiana and B. brongniartii in know
43 rom palaeoecological records of coprophilous fungal spores of the formerly more extensive geographica
44                Despite the serious impact of fungal spores on human health, little is known about the
45 acing billions of stochastic trajectories of fungal spores over dynamically changing host and environ
46 sion models controlling for weekend days and fungal spores, personal O3 was associated with asthma se
47 nd daily counts of ambient concentrations of fungal spores, pollen, and air pollutants.
48 es between metabolically active and inactive fungal spores remains an important question.
49                Live but not heat-inactivated fungal spores resulted in recruitment of gamma interfero
50                 Exposures to several outdoor fungal spore taxa, including some not reported in previo
51 l responses are restricted to challenge with fungal spores that have the potential to germinate and c
52  dynamics of experimental murine exposure to fungal spores, thereby highlighting the potential of mat
53 , some insects can detect and actively avoid fungal spores to reduce infection risk.
54 ves to create robust protein coats that help fungal spores to resist wetting and thus facilitate thei
55 risk to global wheat production, because the fungal spores transmitting the disease can be wind-dispe
56                         Control root tips or fungal spores treated with nuclease alone exhibited norm
57                                              Fungal spores were significantly associated with symptom

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