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1 uring development differ extensively between holometabolous and hemimetabolous insect species.
2 edicted that many other insect species, both holometabolous and hemimetabolous, express two Sema1a pr
3 es, such as the shift from hemimetabolous to holometabolous development, are therefore expected to ha
4 velopment in T. californicum to those of the holometabolous fly Drosophila melanogaster by reanalyzin
5   However, oskar has only been identified in holometabolous ("higher") insects that specify their ger
6           We review recent and older work on holometabolous insect development that sheds light on th
7 ar results were obtained in the more derived holometabolous insect Drosophila melanogaster, suggestin
8 utionary derived state restricted to several holometabolous insect lineages.
9 lusively by members of the four hyperdiverse holometabolous insect orders, has been more sparsely doc
10  show that endosymbiosis reorganization in a holometabolous insect relies on a synchronized host-symb
11  body reorganization during metamorphosis in holometabolous insect species outside of the Diptera.
12 or, was identified and investigated in three holometabolous insect species: Drosophila melanogaster,
13 -stranded RNA-mediated silencing, in a basal holometabolous insect, the beetle Tribolium castaneum.
14     A key regulatory gene in metamorphosing (holometabolous) insect life histories is the transcripti
15 lt transitions in both mammals (puberty) and holometabolous insects (metamorphosis).
16 phology of the CSD neurons originated in the holometabolous insects (those that undergo complete meta
17 mentation LXXLL motif was stably acquired in holometabolous insects after the appearance of striped e
18  may reflect evolutionary changes within the holometabolous insects and serves as a model to study in
19            We considered OXPHOS genes of six holometabolous insects and their orthologs from three Na
20  leading to segment formation: while several holometabolous insects are 'Drosophila-like', using PRG
21                      Corresponding events in holometabolous insects are simplified and lack formal na
22   This essential role of E93 is conserved in holometabolous insects as TcE93 RNAi in Tribolium castan
23         The timely onset of metamorphosis in holometabolous insects depends on their reaching the app
24                             The body form of holometabolous insects dramatically transforms from larv
25                        During metamorphosis, holometabolous insects eliminate obsolete larval tissues
26   Using a comparative approach, we find that holometabolous insects grow much faster than hemimetabol
27                                           In holometabolous insects growth ends at the onset of metam
28          Experiments in Drosophila and other holometabolous insects have demonstrated that either dam
29                  The key innovation of these holometabolous insects is a pupal stage between the larv
30                             Metamorphosis in holometabolous insects is an ecdysone-dependent process
31       The daily rhythm of adult emergence of holometabolous insects is one of the first circadian rhy
32                    The ventral nerve cord of holometabolous insects is reorganized during metamorphos
33                                              Holometabolous insects like Drosophila proceed through t
34                 The neuromuscular systems of holometabolous insects must be remodeled during metamorp
35 r subsequent transformation to appendages in holometabolous insects remains elusive at the developmen
36                          Adult structures in holometabolous insects such as Drosophila are generated
37  withstanding warming compared to beneficial holometabolous insects such as pollinators may exacerbat
38 have been studied functionally in only a few holometabolous insects that undergo metamorphosis.
39           Our data suggest that in ancestral holometabolous insects the female Dsx form is the defaul
40 tus of mosquitoes, flies, and possibly other holometabolous insects to be monitored.
41  (~345 Ma), and the major diversification of holometabolous insects to the Early Cretaceous.
42                                              Holometabolous insects undergo complete metamorphosis to
43  that the larval visual organs (stemmata) of holometabolous insects were derived from and are therefo
44 ature to adult life stages, particularly for holometabolous insects where there is radical restructur
45 nes occur only in Tribolium and not in other holometabolous insects with a sequenced genome.
46                                           In holometabolous insects, a species-specific size, known a
47  our understanding of the behaviors of early holometabolous insects, and enhances our knowledge of ma
48 mplicated in many developmental processes in holometabolous insects, but its mechanism of signaling r
49                                           In holometabolous insects, critical weight (CW) attainment
50                                Similarly, in holometabolous insects, immature juveniles transit to th
51 e situation exists in first instar larvae of holometabolous insects, in which absence of UbdA express
52  inherited germ plasm, in contrast with many holometabolous insects, including Drosophila.
53 he tobacco hornworm Manduca sexta, like many holometabolous insects, makes two versions of its thorac
54 s a wide variety of biological activities in holometabolous insects, ranging from vitellogenesis and
55                                           In holometabolous insects, segment identity may be specifie
56 ntrasts with the more evolutionarily derived holometabolous insects, such as the honey bee and the fr
57                                           In holometabolous insects, the adult appendages and interna
58 ult metamorphosis in both hemimetabolous and holometabolous insects, thus acting as the universal adu
59 has led to the successful diversification of holometabolous insects, yet the origin of the pupa remai
60 to its well-known essential germline role in holometabolous insects.
61 jor events, including the diversification of holometabolous insects.
62 use thus provides a reference for studies of holometabolous insects.
63 in Drosophila melanogaster, and possibly all holometabolous insects.
64 portant role in the evolution of the pupa in holometabolous insects.
65 iation was present in the common ancestor of holometabolous insects.
66 ifera, a member of the most basal lineage of holometabolous insects.
67 ocation originated in the common ancestor of holometabolous insects.
68 ents the ancestral form of CNS patterning in Holometabolous insects.
69 esis seen in the larva-to-pupa transition of holometabolous insects.
70 estigated during adult muscle development in holometabolous insects.
71 re sparsely known compared with more derived holometabolous insects.
72 ila well describe embryogenesis of advanced, holometabolous, insects generally.
73        Our work supports the notion that the holometabolous life history evolved to remove developmen
74 uent modification of JH action for hemi- and holometabolous lifestyles are discussed.
75 ment in hemimetabolous insects suggests that holometabolous metamorphosis combines patterning process
76 d several times in different lineages of the holometabolous, or fully metamorphosing, insects.
77 ionality of these constructs across multiple holometabolous orders suggests a high potential compatib
78 tion rates only occurred in the four richest holometabolous orders.
79 olve independently from each other even in a holometabolous species where the two life stages are sep
80                                           In holometabolous symbiotic insects, metamorphosis entails