コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 replicates of red flour beetle populations (Tribolium castaneum).
2 opeltus fasciatus; and the red flour beetle, Tribolium castaneum.
3 ic model insects Drosophila melanogaster and Tribolium castaneum.
4 secticide resistance in the red flour beetle Tribolium castaneum.
5 is a particularly stressful environment for Tribolium castaneum.
6 at alter embryonic patterning of the beetle, Tribolium castaneum.
7 s underpinning leptophragmata development in Tribolium castaneum.
8 gogenic architecture underlying dispersal in Tribolium castaneum.
9 el habitat using experimental populations of Tribolium castaneum.
10 opment of the short germband model organism, Tribolium castaneum.
11 equired for cell intercalation in the beetle Tribolium castaneum.
12 een targeting GPCRs in the red flour beetle, Tribolium castaneum.
13 cessory gland (MAG) in the red flour beetle, Tribolium castaneum.
14 model and pest insect, the red flour beetle Tribolium castaneum.
15 uropils in the brain of the red flour beetle Tribolium castaneum.
16 s of the larval head in the red flour beetle Tribolium castaneum.
17 a delivery vehicle for dsRNA was assessed in Tribolium castaneum.
18 We identified the dsx homolog (Tcdsx) in Tribolium castaneum.
19 Vg) gene expression in the red flour beetle, Tribolium castaneum.
20 gypti and TcBuster from the red flour beetle Tribolium castaneum.
21 copeltus fasciatus, and the red flour beetle Tribolium castaneum.
22 resistance observed in the QTC279 strain of Tribolium castaneum.
23 ursicon receptor (Tcrk) in the model insect, Tribolium castaneum.
24 egulated expression in the red flour beetle, Tribolium castaneum.
25 not in Anopheles gambiae, Apis mellifera, or Tribolium castaneum.
26 analyzed wing development in a coleopteran, Tribolium castaneum.
27 nction of toy and ey in the red flour beetle Tribolium castaneum.
28 ction of these genes in the red flour beetle Tribolium castaneum.
29 genomic information for the red flour beetle Tribolium castaneum.
30 quito Anopheles gambiae and the flour beetle Tribolium castaneum.
31 in a basal holometabolous insect, the beetle Tribolium castaneum.
32 - to late-larval stages of the flour beetle, Tribolium castaneum.
33 he silkmoth Bombyx mori and the flour beetle Tribolium castaneum.
34 sis of the gl orthologue of the flour beetle Tribolium castaneum.
35 c/sc genes in the coleopteran insect species Tribolium castaneum.
36 ptors were examined in the red flour beetle (Tribolium castaneum): 1) cardioacceleratory peptide 2b (
37 lcholinesterase genes (TcAce1 and TcAce2) in Tribolium castaneum, a globally distributed major pest o
38 ated gene silencing in the red flour beetle, Tribolium castaneum, a species that develops an appendag
39 In the insects Drosophila melanogaster and Tribolium castaneum achaete-scute homologues are initial
41 le genome sequence from the red flour beetle Tribolium castaneum, along with those from other insect
42 we conduct genetics in insects, including in Tribolium castaneum, an important genetic model and agri
43 epidoptera) were not inhibited by AhAI while Tribolium castaneum and Callosobruchus chinensis (Coleop
48 ies experimental system of the flour beetles Tribolium castaneum and Tribolium confusum, we show that
49 d fitness traits using the red flour beetle (Tribolium castaneum) and the tapeworm parasite (Hymenole
50 MCU-EMRE complex from the red flour beetle, Tribolium castaneum, and a cryo-EM structure of the comp
52 onally desiccation-tolerant red flour beetle Tribolium castaneum, and demonstrate its utility by iden
53 lable datasets from Drosophila melanogaster, Tribolium castaneum, Arabidopsis thaliana and C. elegans
54 s on new arthropod models such as the beetle Tribolium castaneum are shifting our knowledge of embryo
55 otic selector genes of the red flour beetle, Tribolium castaneum, are located in a single cluster.
56 dium ion channel paralytic A (TcNav) gene in Tribolium castaneum as a viable means of controlling thi
57 In this study, using the red flour beetle, Tribolium castaneum, as a model insect species, we show
58 s and tyrosinases from the red flour beetle, Tribolium castaneum, as well as their developmental patt
59 a backcross family of the red flour beetle, Tribolium castaneum, based largely on sequences from bac
60 we address this question in the flour beetle Tribolium castaneum by analyzing and comparing the devel
61 present the high-resolution structure of the Tribolium castaneum catalytic subunit of telomerase, TER
62 ound to be widespread in wild populations of Tribolium castaneum collected in Europe, North and South
65 nd experimental validation in a model insect Tribolium castaneum evolving against two coinfecting bac
66 ng replicate populations of the model insect Tribolium castaneum exposed to over 10 years of experime
67 ng replicate populations of the flour beetle Tribolium castaneum for 6 to 7 years under conditions th
68 found that the hAT transposase TcBuster from Tribolium castaneum formed filamentous structures, or ro
71 Drosophila melanogaster, Apis mellifera and Tribolium castaneum have 23, 21 and 24, respectively.
72 odel organisms, such as the red flour beetle Tribolium castaneum, have provided a wealth of insight i
73 mortality of adults of the red flour beetle, Tribolium castaneum (Herbst) and the confused flour beet
75 rising MCU and EMRE subunits from the beetle Tribolium castaneum in complex with a human MICU1-MICU2
82 eotic Abdominal gene of the red flour beetle Tribolium castaneum is associated with an insertion of a
83 th the blastoderm and germband of the beetle Tribolium castaneum is based on the same flexible mechan
87 lt capitate antenna of the red flour beetle, Tribolium castaneum, is composed of eleven articles, org
88 how that TcBuster, from the red flour beetle Tribolium castaneum, is highly active in human cells.
90 terning, but in short-germ insects including Tribolium castaneum, loss of Wnt signaling affects devel
91 rates and short-germ insects like the beetle Tribolium castaneum) painted a different, very dynamic v
94 d in holometabolous insects as TcE93 RNAi in Tribolium castaneum prevented pupal-adult transition and
95 dy was undertaken to assess the potential of Tribolium castaneum (Red flour beetle) acetylcholinester
96 mutant allele classes of Cephalothorax, the Tribolium castaneum (red flour beetle) ortholog of Sex c
97 of variability in a laboratory population of Tribolium castaneum (red flour beetle), whereas using on
99 e acquired in Diptera, as in the coleopteran Tribolium castaneum, repression of br by E93 is not suff
100 neurons in the brain of the red flour beetle Tribolium castaneum respond to internal changes in osmol
101 , while other insects, like the flour beetle Tribolium castaneum, retain an ancestral robo2/3 gene.
104 Here, we show that an antioxidant enzyme, Tribolium castaneum superoxide dismutase 6 (TcSOD6), is
105 netic studies in Drosophila melanogaster and Tribolium castaneum support the hypothesis that oenocyte
107 d ADC and DDC genes in the red flour beetle, Tribolium castaneum (Tc), and investigated their functio
108 ase-like proteins from the red flour beetle, Tribolium castaneum (Tc), were examined by using gene-sp
113 e crystal structure of 5-MeCITP bound to the Tribolium castaneum telomerase reverse transcriptase rev
114 menolepis diminuta) in the red flour beetle (Tribolium castaneum) that serves as an intermediate host
115 ically test the function of the elytra using Tribolium castaneum (the red flour beetle) as a model.
116 ene expression patterns in the flour beetle (Tribolium castaneum), the honeybee (Apis mellifera) and
117 erm insects, including the red flour beetle (Tribolium castaneum), the segment-polarity function of w
118 ut to describe cellularization in the beetle Tribolium castaneum, the embryos of which exhibit a thin
119 ryonic tissue (serosa) epiboly in the insect Tribolium castaneum, the non-proliferative serosa become
121 e blastoderm tissue of the red flour beetle (Tribolium castaneum) tightly adheres in a temporally coo
122 al Ca(2+)-conducting complex, MCU-EMRE, from Tribolium castaneum to probe ion selectivity mechanisms.
123 w fluorescent transgenic lines in the beetle Tribolium castaneum to show that the EE tissues dynamica
125 ificity in an invertebrate model, the beetle Tribolium castaneum Using controlled evolution experimen
126 ning of mandibulate mouthparts of the beetle Tribolium castaneum, using RNA interference to deplete t
127 o acids in two vitellogenins from the beetle Tribolium castaneum was 0.975, even though the two amino
128 son system derived from the red flour beetle Tribolium castaneum, was shown to be highly active in pr
129 Using a model system, red flour beetles (Tribolium castaneum), we either allowed or constrained e
132 ng genes in embryos and larvae of the beetle Tribolium castaneum, we provide the first molecular evid
134 compared these processes in the flour beetle Tribolium castaneum, which develops ventral appendages d
135 eauveria bassiana, and the red flour beetle, Tribolium castaneum, which has a well-documented externa
136 tions of wg and dpp in the red flour beetle, Tribolium castaneum, which retains more ancestral modes
137 ded in Anopheles gambiae, Aedes aegypti, and Tribolium castaneum, while the PF repeats are reduced in
138 by extensive data from the red flour beetle Tribolium castaneum with its more insect-typical develop