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1 as a major effect on feeding behavior in the pea aphid.
2 luded potential apparent competition with AR pea aphids.
3 herefore been retained following transfer to pea aphids.
4 tic basis of a male wing polymorphism in the pea aphid Acyrthosiphon pisum (Hemiptera: Aphididae).
5 d to the symbiosomal membrane separating the pea aphid Acyrthosiphon pisum from its intracellular sym
6 not negatively affect the performance of the pea aphid Acyrthosiphon pisum Harris, a sap-feeding inse
7                     Genetic diversity in the pea aphid Acyrthosiphon pisum was investigated by a rest
8  bean aphid Aphis fabae and non-ant-attended Pea aphid Acyrthosiphon pisum were monitored over two ye
9 widespread defensive mutualism involving the pea aphid Acyrthosiphon pisum, and its heritable symbion
10  in two highly specialized host races of the pea aphid (Acyrthosiphon pisum pisum; Hemiptera : Aphidi
11 f a mutually obligate symbiosis, between the pea aphid (Acyrthosiphon pisum) and its maternally trans
12 lf-matings between two parental genotypes of pea aphid (Acyrthosiphon pisum) differing in virulence o
13 re, we investigated the genetic cause of the pea aphid (Acyrthosiphon pisum) male wing dimorphism, wh
14  protein is important in the survival of the pea aphid (Acyrthosiphon pisum) on fava bean, a host pla
15                                   We use the pea aphid (Acyrthosiphon pisum) to address this problem.
16 ants are also compromised in immunity to the pea aphid (Acyrthosiphon pisum), for which Arabidopsis i
17 e three most common facultative symbionts of pea aphid (Acyrthosiphon pisum), the bacterium Regiella
18 nsa, increase the fitness of their host, the pea aphid (Acyrthosiphon pisum), under natural condition
19 l for the study of incipient speciation, the pea aphid (Acyrthosiphon pisum).
20 esistance has been previously documented for pea aphids (Acyrthosiphon pisum) attacked by the parasit
21                               Experiments on pea aphids (Acyrthosiphon pisum) have demonstrated that
22  of settling and survival on dodder vines by pea aphids (Acyrthosiphon pisum) were reduced significan
23 oth ecological and evolutionary responses of pea aphids (Acyrthosiphon pisum), a common agricultural
24                                           In pea aphids (Acyrthosiphon pisum), several inherited endo
25                                           In pea aphids (Acyrthosiphon pisum), strain-level variation
26 hanced binding and toxicity against both the pea aphid, Acyrthosiphon pisum, and the green peach aphi
27                                          The pea aphid, Acyrthosiphon pisum, maintains extreme variat
28 s (PEMV) coat protein (CP) in the gut of the pea aphid, Acyrthosiphon pisum, using a far-Western blot
29  Armet, namely as an effector protein in the pea aphid, Acyrthosiphon pisum.
30 ivery of fused proteins into the hemocoel of pea aphids, Acyrthosiphon pisum, without virion assembly
31 an) in red and green colour morphs of clonal pea aphids, Acyrthosiphon pisum.
32 ions of secondary symbionts carried by 1,104 pea aphids, Acyrthosiphon pisum.
33                                           CR pea aphids always had fitness losses when on broad bean
34 nomes were consistently abundant in infected pea aphids, and related phages were found in all tested
35  on seedlings from unmowed plants, while cow pea aphid (Aphis craccivora), a generalist, established
36                                              Pea aphids are typically unwinged but produce winged off
37                               Inoculation of pea aphid Armet protein into tobacco leaves induced a tr
38                                              Pea aphid Armet's physical and chemical properties and i
39 ) were found to differ in ability to protect pea aphids attacked by the parasitoid Aphidius ervi.
40 ound that both alleles were present prior to pea aphid biotype lineage diversification, we estimated
41 atiles that attract parasitic wasps, and the pea aphid can carry facultative endosymbiotic bacteria t
42               We confirm that three types of pea aphid clones coexist in natural populations, those p
43  predation in complex agricultural mosaic on pea aphid clover and alfalfa races.
44                     Host-associated races of pea aphid discriminate between plant species in race-spe
45                                              Pea aphids display a red-green color polymorphism, which
46 tative symbioses in Acyrthosiphon pisum (the pea aphid) for vulnerability of the aphid host to a hyme
47                                  We compared pea aphid gene expression between bacteriocytes and othe
48 pped reads from the re-sequencing data of 33 pea aphid genomes from individuals specialized on differ
49 lycosylated receptor aminopeptidase N in the pea aphid gut and is transcytosed across the gut epithel
50                         Insertion of a 12-aa pea aphid gut-binding peptide by adding to or replacing
51                                              Pea aphids have an obligate nutritional symbiosis with t
52 he presence or absence of fava bean foliage; pea aphids have very low sterol content.
53 as dramatic effects on the heat tolerance of pea aphid hosts (Acyrthosiphon pisum).
54 vestigated a host-parasitoid system in which pea aphid hosts rapidly evolve resistance to Aphidius er
55 ng seven strains of Buchnera aphidicola from pea aphid hosts.
56 atiotemporal expression of a selected set of pea aphid IAPs and showed that they are differentially e
57 rial symbionts, which occur in a majority of pea aphids in field populations.
58 distributed across the tribe Coccinellini-on pea aphids in the presence or absence of fava bean folia
59                                              Pea aphids infected with the bacterial endosymbiont, Fuk
60                      The wing polyphenism of pea aphids is a compelling laboratory model with which t
61 lysis reveals that male wing polymorphism in pea aphids is determined by a single locus, two alleles
62  potential source of physiological stress in pea aphids is infection by other microorganisms, includi
63 Our results suggest that feeding behavior in pea aphids is neither simple nor highly polygenic.
64    We placed experimental populations of two pea aphid lines, each with and without symbionts, in fiv
65 olyphenism is transgenerational, in that the pea aphid mother experiences the environmental signals,
66 rotein C002 is crucial in the feeding of the pea aphid on fava bean.
67 ss on clover race (CR) and alfalfa race (AR) pea aphids on broad bean, red clover and alfalfa alone.
68                           Plants fed upon by pea aphids release volatiles that attract parasitic wasp
69 a bellii (a tick-associated bacterium) and a pea-aphid Rickettsia.
70 lassic example of phenotypic plasticity: the pea aphid's ability to produce winged offspring in respo
71                                       In the pea aphid, some of the seven known species of facultativ
72 ed proteins have extensive homology with the pea aphid SymL and Escherichia coli GroEL chaperonin.
73                                           In pea aphids, the bacterial symbiont Buchnera is confined
74                                              Pea aphids thus obtain protection from natural enemies t
75 lant virus pea enation mosaic virus into the pea aphid vector.
76 By amplifying DNA from hemolymph of infected pea aphids, we obtained a set of genomic sequences of H.
77 he genetic basis of wing polymorphism in the pea aphid, which can produce either winged or wingless m
78 rol profile of four beetle species reared on pea aphids-with or without foliage-and compared their st