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1 s of red flour beetle populations (Tribolium castaneum).
2 hese genes in the red flour beetle Tribolium castaneum.
3 formation for the red flour beetle Tribolium castaneum.
4 heles gambiae and the flour beetle Tribolium castaneum.
5 21 genes during antenna metamorphosis in T. castaneum.
6 holometabolous insect, the beetle Tribolium castaneum.
7 erms of a model of antenna development in T. castaneum.
8 larval stages of the flour beetle, Tribolium castaneum.
9 h Bombyx mori and the flour beetle Tribolium castaneum.
10 gl orthologue of the flour beetle Tribolium castaneum.
11 in the coleopteran insect species Tribolium castaneum.
12 sciatus; and the red flour beetle, Tribolium castaneum.
13 nsects Drosophila melanogaster and Tribolium castaneum.
14 resistance in the red flour beetle Tribolium castaneum.
15 icularly stressful environment for Tribolium castaneum.
16 mbryonic patterning of the beetle, Tribolium castaneum.
17 ning leptophragmata development in Tribolium castaneum.
18 chitecture underlying dispersal in Tribolium castaneum.
19 B(2)Tubulin, Rad50-ATPase and enolase in T. castaneum.
20 using experimental populations of Tribolium castaneum.
21 the short germband model organism, Tribolium castaneum.
22 r cell intercalation in the beetle Tribolium castaneum.
23 ing GPCRs in the red flour beetle, Tribolium castaneum.
24 and (MAG) in the red flour beetle, Tribolium castaneum.
25 pest insect, the red flour beetle Tribolium castaneum.
26 the brain of the red flour beetle Tribolium castaneum.
27 arval head in the red flour beetle Tribolium castaneum.
28 ation of a regulator of Tcdsx splicing in T. castaneum.
29 ntified the dsx homolog (Tcdsx) in Tribolium castaneum.
30 xpression in the red flour beetle, Tribolium castaneum.
31 TcBuster from the red flour beetle Tribolium castaneum.
32 asciatus, and the red flour beetle Tribolium castaneum.
33 e observed in the QTC279 strain of Tribolium castaneum.
34 ceptor (Tcrk) in the model insect, Tribolium castaneum.
35 vehicle for dsRNA was assessed in Tribolium castaneum.
36 xpression in the red flour beetle, Tribolium castaneum.
37 pheles gambiae, Apis mellifera, or Tribolium castaneum.
38 es affected the growth and development of T. castaneum.
39 wing development in a coleopteran, Tribolium castaneum.
40 toy and ey in the red flour beetle Tribolium castaneum.
41 he larval stages of the red flour beetle, T. castaneum.
42 examined in the red flour beetle (Tribolium castaneum): 1) cardioacceleratory peptide 2b (CAPA); CAP
43 erase genes (TcAce1 and TcAce2) in Tribolium castaneum, a globally distributed major pest of stored g
44 silencing in the red flour beetle, Tribolium castaneum, a species that develops an appendage on the f
45 nsects Drosophila melanogaster and Tribolium castaneum achaete-scute homologues are initially express
47 ch has investigated how high densities of T. castaneum affect attraction to the aggregation pheromone
48 sequence from the red flour beetle Tribolium castaneum, along with those from other insect species, p
49 interactions with active site residues of T. castaneum alpha-amylase compared to C. chinensis alpha-a
50 genetics in insects, including in Tribolium castaneum, an important genetic model and agricultural p
51 euroblast lineages in D. melanogaster and T. castaneum and additional markers and information on line
52 ) were not inhibited by AhAI while Tribolium castaneum and Callosobruchus chinensis (Coleoptera) alph
58 ted communities of two Tribolium species (T. castaneum and T. confusum) to examine how intraspecific
61 mental system of the flour beetles Tribolium castaneum and Tribolium confusum, we show that interspec
62 traits using the red flour beetle (Tribolium castaneum) and the tapeworm parasite (Hymenolepis diminu
63 complex from the red flour beetle, Tribolium castaneum, and a cryo-EM structure of the complex at 3.5
65 iccation-tolerant red flour beetle Tribolium castaneum, and demonstrate its utility by identifying a
70 rthropod models such as the beetle Tribolium castaneum are shifting our knowledge of embryonic patter
72 hannel paralytic A (TcNav) gene in Tribolium castaneum as a viable means of controlling this insect p
74 study, using the red flour beetle, Tribolium castaneum, as a model insect species, we show that an en
75 sinases from the red flour beetle, Tribolium castaneum, as well as their developmental patterns of ex
76 ss family of the red flour beetle, Tribolium castaneum, based largely on sequences from bacterial art
77 this question in the flour beetle Tribolium castaneum by analyzing and comparing the development and
80 widespread in wild populations of Tribolium castaneum collected in Europe, North and South America,
83 er, the context of dispersal mattered, as T. castaneum dispersal was reduced in two-species communiti
87 ental validation in a model insect Tribolium castaneum evolving against two coinfecting bacterial pat
88 te populations of the model insect Tribolium castaneum exposed to over 10 years of experimental evolu
89 te populations of the flour beetle Tribolium castaneum for 6 to 7 years under conditions that differe
90 the hAT transposase TcBuster from Tribolium castaneum formed filamentous structures, or rodlets, in
96 isms, such as the red flour beetle Tribolium castaneum, have provided a wealth of insight into conser
97 of adults of the red flour beetle, Tribolium castaneum (Herbst) and the confused flour beetle, Tribol
99 and EMRE subunits from the beetle Tribolium castaneum in complex with a human MICU1-MICU2 heterodime
102 netic map of the red flour beetle (Tribolium castaneum) integrating molecular with morphological mark
105 We show that Medea(1) activity in Tribolium castaneum is associated with a composite Tc1 transposon
106 minal gene of the red flour beetle Tribolium castaneum is associated with an insertion of a novel ret
107 stoderm and germband of the beetle Tribolium castaneum is based on the same flexible mechanism: a gra
108 ific microRNAs in the early blastoderm of T. castaneum is consistent with previous findings in Drosop
112 e antenna of the red flour beetle, Tribolium castaneum, is composed of eleven articles, organized int
115 iochemical analyses and MS confirmed that T. castaneum JHR was a 1:1 heterodimer consisting of MET an
117 Application of JH analogs hydroprene to T. castaneum larvae and JH III to TcA cells suppressed HDAC
119 used RNA interference (RNAi) to show that T. castaneum larvae lacking functional Tcv or Tccn gene pro
121 ut in short-germ insects including Tribolium castaneum, loss of Wnt signaling affects development of
122 two species: No defects were observed in T. castaneum male genitalia, and while the male claspers of
124 ioxidative function and demonstrates that T. castaneum may use an alternative antioxidative system wh
126 short-germ insects like the beetle Tribolium castaneum) painted a different, very dynamic view of gen
129 etabolous insects as TcE93 RNAi in Tribolium castaneum prevented pupal-adult transition and produced
130 ertaken to assess the potential of Tribolium castaneum (Red flour beetle) acetylcholinesterase (Tc-AC
131 lele classes of Cephalothorax, the Tribolium castaneum (red flour beetle) ortholog of Sex combs reduc
132 lity in a laboratory population of Tribolium castaneum (red flour beetle), whereas using only the sta
134 in Diptera, as in the coleopteran Tribolium castaneum, repression of br by E93 is not sufficient to
135 the brain of the red flour beetle Tribolium castaneum respond to internal changes in osmolality by r
136 Knockdown of natalisin expression in T. castaneum resulted in significant reduction in the fecun
141 e three-dimensional structures of the two T. castaneum SKRs (TcSKR1 and TcSKR2) were generated from m
143 e show that an antioxidant enzyme, Tribolium castaneum superoxide dismutase 6 (TcSOD6), is secreted i
144 ies in Drosophila melanogaster and Tribolium castaneum support the hypothesis that oenocytes are of e
145 -product pest Tribolium species including T. castaneum, T. confusum, T. destructor, T. madens, T. fre
148 roteins from the red flour beetle, Tribolium castaneum (Tc), were examined by using gene-specific RNA
152 Here, we determined structures of Tribolium castaneum telomerase reverse transcriptase (TERT) throug
153 structure of 5-MeCITP bound to the Tribolium castaneum telomerase reverse transcriptase reveals an at
155 diminuta) in the red flour beetle (Tribolium castaneum) that serves as an intermediate host in its tr
157 sion patterns in the flour beetle (Tribolium castaneum), the honeybee (Apis mellifera) and the fruit
158 s, including the red flour beetle (Tribolium castaneum), the segment-polarity function of wg is conse
159 ribe cellularization in the beetle Tribolium castaneum, the embryos of which exhibit a thin blastoder
160 sue (serosa) epiboly in the insect Tribolium castaneum, the non-proliferative serosa becomes regional
162 rm tissue of the red flour beetle (Tribolium castaneum) tightly adheres in a temporally coordinated m
164 cently completed whole-genome sequence of T. castaneum to prepare custom microarrays and identified a
166 ent transgenic lines in the beetle Tribolium castaneum to show that the EE tissues dynamically form a
169 an invertebrate model, the beetle Tribolium castaneum Using controlled evolution experiments, we sel
170 ndibulate mouthparts of the beetle Tribolium castaneum, using RNA interference to deplete the express
171 two vitellogenins from the beetle Tribolium castaneum was 0.975, even though the two amino acid sequ
172 d here, egg cannibalism by two strains of T. castaneum was significantly enhanced in oat flour, and e
173 derived from the red flour beetle Tribolium castaneum, was shown to be highly active in previous stu
174 a model system, red flour beetles (Tribolium castaneum), we either allowed or constrained evolution o
178 n embryos and larvae of the beetle Tribolium castaneum, we provide the first molecular evidence for t
180 ap, we established a transgenic system in T. castaneum, which allows blocking an ongoing RNAi effect
181 hese processes in the flour beetle Tribolium castaneum, which develops ventral appendages during embr
182 assiana, and the red flour beetle, Tribolium castaneum, which has a well-documented external immune s
183 g and dpp in the red flour beetle, Tribolium castaneum, which retains more ancestral modes of limb an
184 pheles gambiae, Aedes aegypti, and Tribolium castaneum, while the PF repeats are reduced in size and
185 ive data from the red flour beetle Tribolium castaneum with its more insect-typical development.