ライフサイエンスコーパス: Tribolium castaneum

1 el habitat using experimental populations of Tribolium castaneum.

2 at alter embryonic patterning of the beetle, Tribolium castaneum.

3 opment of the short germband model organism, Tribolium castaneum.

4 equired for cell intercalation in the beetle Tribolium castaneum.

5 een targeting GPCRs in the red flour beetle, Tribolium castaneum.

6 cessory gland (MAG) in the red flour beetle, Tribolium castaneum.

7 model and pest insect, the red flour beetle Tribolium castaneum.

8 uropils in the brain of the red flour beetle Tribolium castaneum.

9 s of the larval head in the red flour beetle Tribolium castaneum.

10 We identified the dsx homolog (Tcdsx) in Tribolium castaneum.

11 Vg) gene expression in the red flour beetle, Tribolium castaneum.

12 gypti and TcBuster from the red flour beetle Tribolium castaneum.

13 copeltus fasciatus, and the red flour beetle Tribolium castaneum.

14 resistance observed in the QTC279 strain of Tribolium castaneum.

15 ursicon receptor (Tcrk) in the model insect, Tribolium castaneum.

16 egulated expression in the red flour beetle, Tribolium castaneum.

17 not in Anopheles gambiae, Apis mellifera, or Tribolium castaneum.

18 analyzed wing development in a coleopteran, Tribolium castaneum.

19 nction of toy and ey in the red flour beetle Tribolium castaneum.

20 ction of these genes in the red flour beetle Tribolium castaneum.

21 genomic information for the red flour beetle Tribolium castaneum.

22 quito Anopheles gambiae and the flour beetle Tribolium castaneum.

23 in a basal holometabolous insect, the beetle Tribolium castaneum.

24 - to late-larval stages of the flour beetle, Tribolium castaneum.

25 he silkmoth Bombyx mori and the flour beetle Tribolium castaneum.

26 sis of the gl orthologue of the flour beetle Tribolium castaneum.

27 c/sc genes in the coleopteran insect species Tribolium castaneum.

28 opeltus fasciatus; and the red flour beetle, Tribolium castaneum.

29 ic model insects Drosophila melanogaster and Tribolium castaneum.

30 secticide resistance in the red flour beetle Tribolium castaneum.

31 is a particularly stressful environment for Tribolium castaneum.

32 ptors were examined in the red flour beetle (Tribolium castaneum): 1) cardioacceleratory peptide 2b (

33 lcholinesterase genes (TcAce1 and TcAce2) in Tribolium castaneum, a globally distributed major pest o

34 ated gene silencing in the red flour beetle, Tribolium castaneum, a species that develops an appendag

35 In the insects Drosophila melanogaster and Tribolium castaneum achaete-scute homologues are initial

36 rotein extracts of elytra (wing covers) from Tribolium castaneum adults.

37 le genome sequence from the red flour beetle Tribolium castaneum, along with those from other insect

38 epidoptera) were not inhibited by AhAI while Tribolium castaneum and Callosobruchus chinensis (Coleop

39 demonstrated high similarity with the ELO of Tribolium castaneum and Drosophila melanogaster.

40 However, in the beetle Tribolium castaneum and most other arthropods, a number

41 ities) between two species of flour beetles, Tribolium castaneum and T. freemani.

42 d fitness traits using the red flour beetle (Tribolium castaneum) and the tapeworm parasite (Hymenole

43 ous insect species: Drosophila melanogaster, Tribolium castaneum, and Bombyx mori.

44 s on new arthropod models such as the beetle Tribolium castaneum are shifting our knowledge of embryo

45 otic selector genes of the red flour beetle, Tribolium castaneum, are located in a single cluster.

46 dium ion channel paralytic A (TcNav) gene in Tribolium castaneum as a viable means of controlling thi

47 In this study, using the red flour beetle, Tribolium castaneum, as a model insect species, we show

48 s and tyrosinases from the red flour beetle, Tribolium castaneum, as well as their developmental patt

49 a backcross family of the red flour beetle, Tribolium castaneum, based largely on sequences from bac

50 we address this question in the flour beetle Tribolium castaneum by analyzing and comparing the devel

51 present the high-resolution structure of the Tribolium castaneum catalytic subunit of telomerase, TER

52 ound to be widespread in wild populations of Tribolium castaneum collected in Europe, North and South

53 In the flour beetle, Tribolium castaneum, ectopic wingless also induced engra

54 ng replicate populations of the flour beetle Tribolium castaneum for 6 to 7 years under conditions th

55 found that the hAT transposase TcBuster from Tribolium castaneum formed filamentous structures, or ro

56 Drosophila melanogaster, Apis mellifera and Tribolium castaneum have 23, 21 and 24, respectively.

57 The Tribolium castaneum homeotic gene maxillopedia (mxp) is

58 een replicated invasions of the flour beetle Tribolium castaneum in laboratory microcosms.

59 Using the flour beetle (Tribolium castaneum) in a microcosm experiment, we disen

60 A genetic map of the red flour beetle (Tribolium castaneum) integrating molecular with morpholo

61 Tribolium castaneum is a member of the most species-rich

62 We show that Medea(1) activity in Tribolium castaneum is associated with a composite Tc1 t

63 eotic Abdominal gene of the red flour beetle Tribolium castaneum is associated with an insertion of a

64 th the blastoderm and germband of the beetle Tribolium castaneum is based on the same flexible mechan

65 The red flour beetle Tribolium castaneum is widely used as a model insect spe

66 The red flour beetle (Tribolium castaneum) is an important model organism for

67 The red flour beetle, Tribolium castaneum, is an emerging model organism separ

68 lt capitate antenna of the red flour beetle, Tribolium castaneum, is composed of eleven articles, org

69 how that TcBuster, from the red flour beetle Tribolium castaneum, is highly active in human cells.

70 In beetles, such as Tribolium castaneum, it is the forewings that are modifi

71 terning, but in short-germ insects including Tribolium castaneum, loss of Wnt signaling affects devel

72 Tribolium castaneum paired (Tc-prd) and sloppy-paired (T

73 We report the structure of Tribolium castaneum PINK1 (TcPINK1), revealing several u

74 d in holometabolous insects as TcE93 RNAi in Tribolium castaneum prevented pupal-adult transition and

75 mutant allele classes of Cephalothorax, the Tribolium castaneum (red flour beetle) ortholog of Sex c

76 of variability in a laboratory population of Tribolium castaneum (red flour beetle), whereas using on

77 , while other insects, like the flour beetle Tribolium castaneum, retain an ancestral robo2/3 gene.

78 In the red flour beetle, Tribolium castaneum, RNA interference studies indicate t

79 netic studies in Drosophila melanogaster and Tribolium castaneum support the hypothesis that oenocyte

80 as putative Cry3Ba toxin-binding proteins in Tribolium castaneum (Tc) larvae.

81 d ADC and DDC genes in the red flour beetle, Tribolium castaneum (Tc), and investigated their functio

82 ase-like proteins from the red flour beetle, Tribolium castaneum (Tc), were examined by using gene-sp

83 fied homolog of dsx in the red flour beetle, Tribolium castaneum (Tcdsx).

84 menolepis diminuta) in the red flour beetle (Tribolium castaneum) that serves as an intermediate host

85 ically test the function of the elytra using Tribolium castaneum (the red flour beetle) as a model.

86 ene expression patterns in the flour beetle (Tribolium castaneum), the honeybee (Apis mellifera) and

87 erm insects, including the red flour beetle (Tribolium castaneum), the segment-polarity function of w

88 ut to describe cellularization in the beetle Tribolium castaneum, the embryos of which exhibit a thin

89 In the red flour beetle, Tribolium castaneum, the only currently available system

90 w fluorescent transgenic lines in the beetle Tribolium castaneum to show that the EE tissues dynamica

91 Here we use flour beetles (Tribolium castaneum) to show experimentally that mean ex

92 ning of mandibulate mouthparts of the beetle Tribolium castaneum, using RNA interference to deplete t

93 o acids in two vitellogenins from the beetle Tribolium castaneum was 0.975, even though the two amino

94 son system derived from the red flour beetle Tribolium castaneum, was shown to be highly active in pr

95 Using a model system, red flour beetles (Tribolium castaneum), we either allowed or constrained e

96 In the red flour beetle, Tribolium castaneum, we have isolated loss-of-function m

97 Using the red flour beetle, Tribolium castaneum, we identify major fitness benefits

98 ng genes in embryos and larvae of the beetle Tribolium castaneum, we provide the first molecular evid

99 As RNAi works well in Tribolium castaneum, we utilized this insect and RNAi to

100 compared these processes in the flour beetle Tribolium castaneum, which develops ventral appendages d

101 eauveria bassiana, and the red flour beetle, Tribolium castaneum, which has a well-documented externa

102 tions of wg and dpp in the red flour beetle, Tribolium castaneum, which retains more ancestral modes

103 ded in Anopheles gambiae, Aedes aegypti, and Tribolium castaneum, while the PF repeats are reduced in