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1 l species Chironomus riparius (Chironomidae, Diptera).
2 anchiopods, copepods and isopods, and insect diptera).
3 er is concerned with the flight mechanism of diptera.
4 t body- and female-specific gene activity in Diptera.
5 on limit ecological overlap among the higher Diptera.
6 uccession of blood barriers form in immature Diptera.
7 to trypsin genes of selected Lepidoptera and Diptera.
8 n are discussed as they occur throughout the Diptera.
9 y reflects the ancestral karyotype of higher Diptera.
10 biologically the best-known group of higher Diptera.
11 or the evolution of embryonic development in Diptera.
12 ebiidae as the sister group to all remaining Diptera.
13 that have been reported from three genera of Diptera.
14 f the network have evolved within the higher Diptera.
15 clear that bcd is a unique feature of higher Diptera.
16 e flies; it may be a general property of the Diptera.
17 ecologically important families in the order Diptera.
18 holometabolous insect species outside of the Diptera.
19 ced three episodes of rapid radiation--lower Diptera (220 Ma), lower Brachycera (180 Ma), and Schizop
21 rast the patterns found within the parasitic Diptera against those found in the better studied parasi
23 nebrio, Coleoptera) and the mosquito (Aedes, Diptera), all 50 neurons showed increases in cGMP immuno
24 creased in the lineage leading to the higher Diptera, allowing the development of stereotyped bristle
29 ins is abundantly expressed in blood-feeding Diptera and is distantly related to the odorant-binding
30 tudies suggest an evolutionary split between Diptera and Lepidoptera in how the ecdysone biosynthetic
31 this direct repression is conserved between Diptera and Lepidoptera, but is absent in the Crustacea
35 tabase covering the Coleoptera, Lepidoptera, Diptera and Lepidoptera/Diptera specificity classes.
37 pecies belonging to 22 different families of Diptera and uncover tremendous hidden diversity in sex c
38 he Triassic specimens are a nematoceran fly (Diptera) and two disparate species of mites, Triasacarus
39 aluable information in studying phylogeny of Diptera, and developing genetic markers for species iden
40 ed taxa such as many families of Coleoptera, Diptera, and Hymenoptera and on poorly sampled parts of
41 iruses from hosts of the orders Lepidoptera, Diptera, and Hymenoptera, was reconstructed based on seq
42 play sequence conservation relative to other Diptera, and low similarity to SFPs from other studied s
43 n as the dorsal ridge is not specific to the Diptera but is homologous to structures found in other i
44 ropoda, Arachnida, Hexapoda, Coleoptera, and Diptera) but do not support monophyly for Deuterostomia,
46 me of the Hessian fly (Mayetiola destructor; Diptera: Cecidomyiidae), a plant parasitic gall midge an
49 rs of the Chironomus cucini larvae (Insecta, Diptera, Chironomidae) living in the harbor area were re
50 s of organisms such as bloodworms (larvae of Diptera, Chironomidae), has substantial impacts on sedim
53 ere found in other Lepidoptera, Trichoptera, Diptera, Coleoptera, and Neuroptera but not in the Hymen
54 (AP) patterning within at least a subset of Diptera, conservation of this process has not yet been d
56 opheles gambiae, and Culex quinquefasciatus (Diptera: Culicidae), representing 2 subfamilies (Culicin
57 biodiversity and ecological roles of higher Diptera, cyclorraphous flies are often numerous and spec
59 in protocerebral neuropils of two species of Diptera, Drosophila melanogaster and Phaenicia sericata;
60 sophila (SWD), Drosophila suzukii Matsumura (Diptera: Drosophilidae), with seven "reported" hosts (bl
64 ex-chromosomes have formed repeatedly across Diptera from ordinary autosomes, and X-chromosomes mostl
65 resentative insect species from Hemiptera to Diptera, from published and novel genome sequence data,
67 gglesworthia glossinidia) of the tsetse fly (Diptera: Glossinidae) are known to supplement dietary de
71 discuss medically significant tsetse flies (Diptera: Glossinidae), a group comprised of over 30 spec
72 ture of SFPs in the viviparous tsetse flies (Diptera: Glossinidae), vectors of Human and Animal Afric
73 of tsetse fly, Glossina morsitans morsitans (Diptera: Glossinidae), was differentially screened, and
77 ation in diversification within some orders (Diptera, Hemiptera) or shows no significant relationship
78 es disperse phoretically on parasitic flies (Diptera: Hippoboscidae), but body lice seldom engage in
79 or brood site in many insect groups such as Diptera, Hymenoptera and Coleoptera, and frugivorous ver
83 properties of the main photoreceptors of the Diptera indicates that the transition of the brown eye c
89 Orthoptera, Isoptera, Hemiptera, Coleoptera, Diptera, Lepidoptera, and Hymenoptera), GABA-like immuno
90 representing diverse insect orders including Diptera, Lepidoptera, Coleoptera, and Hymenoptera as wel
92 tion of wingless transcripts is conserved in Diptera, localisation of even-skipped and hairy pair-rul
94 roduced parasitic nest fly Philornis downsi (Diptera: Muscidae) has been implicated in the decline of
95 homicrodon belongs to the Phoridae (Insecta: Diptera), not the Syrphidae where it was first placed, a
96 ete mitochondrial genome (mtgenome) data for Diptera, one of the largest metazoan orders, in public d
97 ities and differences between two species of Diptera, one of which has neurons large enough for intra
102 Comparative studies of gene regulation among Diptera reveal that divergent sequences can underlie con
104 e elementary motion are conserved across the Diptera, selective pressure has resulted in modification
106 on pipeline to identify Y-linked genes in 22 Diptera species, revealing patterns of Y-chromosome gene
107 content evolution of Y-chromosomes across 22 Diptera species, using a subtraction pipeline that infer
109 multiple structure alignment found that the Diptera-specific Cry4Ba is structurally more closely sim
112 t body morphology is presented by the higher diptera, such as Drosophila, in which males develop fewe
113 yoni (Froggatt) and B. neohumeralis (Hardy) (Diptera: Tephritidae) are sympatric species which hybrid
114 ntial radiation in the Rhagoletis pomonella (Diptera: Tephritidae) complex, a model for sympatric spe
115 ion in the melon fly, Bactrocera cucurbitae (Diptera: Tephritidae) is described here using a newly ge
116 that the apple maggot, Rhagoletis pomonella (Diptera: Tephritidae) is undergoing sympatric speciation
118 orn-infesting races of Rhagoletis pomonella (Diptera: Tephritidae) to approximately 6% per generation
119 nd apple host races of Rhagoletis pomonella (Diptera: Tephritidae), a model for contemporary speciati
120 ested the olive fruit fly, Bactrocera oleae (Diptera: Tephritidae), as a model system to evaluate the
121 Olive fruit fly, Bactrocera oleae (Rossi) (Diptera: Tephritidae), is the major pest of commercial o
123 a unique and overlooked foregut organ in the Diptera that affects many physiological and behavioral f
125 and endoparasitic species of myiasis-causing Diptera, the evolutionary affinities of which remain to
126 and endoparasitic species of myiasis-causing Diptera, the evolutionary affinities of which remain to
127 gh it has a similar number of genes as other Diptera, the midge genome has very low repeat density an
129 red within the radiation of the insect order Diptera, thereby illustrating the magnitude of the contr
132 ibution of sensory bristles on the thorax of Diptera (true flies) provides a useful model for the stu
133 n family found in blood-feeding nematocerous Diptera will function as biogenic amine-binding proteins
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