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1 g of critical neural circuits in response to alarm pheromone.
2 ral tests, the chemical structure of a mouse alarm pheromone.
3 lation of genes that mediate the response to alarm pheromone.
4 sive allomones, activity inhibitors, cryptic alarm pheromones, aggregative attractants, robbing agent
5 vidence that aphid perception of conspecific alarm pheromone aids in predator avoidance and thereby b
6 ulated biting of foragers or exposure to bee alarm pheromone also elicited signaling (88-fold and 14-
7 le, nest defenders were triggered by the bee alarm pheromone and live hornet presence to heat-ball th
8 foragers could eavesdrop upon heterospecific alarm pheromones, and would detect and avoid conspicuous
9 d avoidance of heterospecific alarm signals, alarm pheromones, at food sources in bees.
10 tarily warn the prey or by the production of alarm pheromones by the stressed prey alerting its consp
11 bee species can detect and use a specialized alarm pheromone component, benzyl acetate (BA), to avoid
12 hat OBP3 from M. viciae can bind to all four alarm pheromone components and the differential ligand b
13 xamine their molecular interactions with the alarm pheromone components.
14     We next examined responses to individual alarm pheromone compounds.
15  to release (E)-beta-farnesene (Ebetaf), the alarm pheromone for many pest aphids, using a synthetic
16                                              Alarm pheromones function in integrating defensive respo
17 e chemical structure of the identified mouse alarm pheromone has similar features as the sulfur-conta
18                       Continuous exposure to alarm pheromone in aphid colonies raised on transgenic A
19  (EBF) is the predominant constituent of the alarm pheromone in Myzus persicae (green peach aphid) an
20 n integrating defensive responses; honey bee alarm pheromone is an excellent example of a multicompon
21 f conservation with mammals, even though the alarm pheromone itself is bee-specific.
22 t Apis cerana foragers avoid the distinctive alarm pheromones of A. dorsata and A. mellifera, species
23                                          The alarm pheromones of many arthropods are also used as def
24 ided BA as strongly as they did to their own alarm pheromone on natural inflorescences.
25                     We analysed the volatile alarm pheromone produced by attacked workers of the most
26 ials or a closer imitation, in the plant, of alarm pheromone release.
27                                      For the alarm pheromone response gene set, we found a particular
28 onserved honey bee genes associated with the alarm pheromone response shows overrepresentation of pro
29 entially expressed gene sets associated with alarm pheromone response, the difference between old and
30 as the sensory organ through which mammalian alarm pheromones signal a threatening situation, the che
31 n predator attack, individual aphids emit an alarm pheromone to warn the colony of this danger.
32                             Both species use alarm pheromones to warn of dangers.
33 ato aphids showed that a reduced response to alarm pheromone was associated with both gene amplificat
34  obtained for EHB in response to exposure to alarm pheromone (which provokes aggression) and when com

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