ライフサイエンスコーパス: castaneum

1 using experimental populations of Tribolium castaneum.

2 h Bombyx mori and the flour beetle Tribolium castaneum.

3 gl orthologue of the flour beetle Tribolium castaneum.

4 in the coleopteran insect species Tribolium castaneum.

5 sciatus; and the red flour beetle, Tribolium castaneum.

6 nsects Drosophila melanogaster and Tribolium castaneum.

7 resistance in the red flour beetle Tribolium castaneum.

8 icularly stressful environment for Tribolium castaneum.

9 mbryonic patterning of the beetle, Tribolium castaneum.

10 the short germband model organism, Tribolium castaneum.

11 r cell intercalation in the beetle Tribolium castaneum.

12 ing GPCRs in the red flour beetle, Tribolium castaneum.

13 and (MAG) in the red flour beetle, Tribolium castaneum.

14 pest insect, the red flour beetle Tribolium castaneum.

15 the brain of the red flour beetle Tribolium castaneum.

16 arval head in the red flour beetle Tribolium castaneum.

17 ation of a regulator of Tcdsx splicing in T. castaneum.

18 ntified the dsx homolog (Tcdsx) in Tribolium castaneum.

19 xpression in the red flour beetle, Tribolium castaneum.

20 TcBuster from the red flour beetle Tribolium castaneum.

21 asciatus, and the red flour beetle Tribolium castaneum.

22 e observed in the QTC279 strain of Tribolium castaneum.

23 ceptor (Tcrk) in the model insect, Tribolium castaneum.

24 xpression in the red flour beetle, Tribolium castaneum.

25 pheles gambiae, Apis mellifera, or Tribolium castaneum.

26 es affected the growth and development of T. castaneum.

27 wing development in a coleopteran, Tribolium castaneum.

28 toy and ey in the red flour beetle Tribolium castaneum.

29 he larval stages of the red flour beetle, T. castaneum.

30 hese genes in the red flour beetle Tribolium castaneum.

31 formation for the red flour beetle Tribolium castaneum.

32 heles gambiae and the flour beetle Tribolium castaneum.

33 21 genes during antenna metamorphosis in T. castaneum.

34 holometabolous insect, the beetle Tribolium castaneum.

35 erms of a model of antenna development in T. castaneum.

36 larval stages of the flour beetle, Tribolium castaneum.

37 examined in the red flour beetle (Tribolium castaneum): 1) cardioacceleratory peptide 2b (CAPA); CAP

38 erase genes (TcAce1 and TcAce2) in Tribolium castaneum, a globally distributed major pest of stored g

39 silencing in the red flour beetle, Tribolium castaneum, a species that develops an appendage on the f

40 nsects Drosophila melanogaster and Tribolium castaneum achaete-scute homologues are initially express

41 racts of elytra (wing covers) from Tribolium castaneum adults.

42 sequence from the red flour beetle Tribolium castaneum, along with those from other insect species, p

43 interactions with active site residues of T. castaneum alpha-amylase compared to C. chinensis alpha-a

44 euroblast lineages in D. melanogaster and T. castaneum and additional markers and information on line

45 ) were not inhibited by AhAI while Tribolium castaneum and Callosobruchus chinensis (Coleoptera) alph

46 ed high similarity with the ELO of Tribolium castaneum and Drosophila melanogaster.

47 We searched the genome sequence of T. castaneum and identified 53 bHLH genes.

48 However, in the beetle Tribolium castaneum and most other arthropods, a number of anterio

49 ween two species of flour beetles, Tribolium castaneum and T. freemani.

50 traits using the red flour beetle (Tribolium castaneum) and the tapeworm parasite (Hymenolepis diminu

51 species: Drosophila melanogaster, Tribolium castaneum, and Bombyx mori.

52 Most strains of T. castaneum appear to harbor approximately 25-35 copies of

53 When sires from T. castaneum are mated to conspecific and heterospecific fe

54 rthropod models such as the beetle Tribolium castaneum are shifting our knowledge of embryonic patter

55 tor genes of the red flour beetle, Tribolium castaneum, are located in a single cluster.

56 hannel paralytic A (TcNav) gene in Tribolium castaneum as a viable means of controlling this insect p

57 egating among four natural populations of T. castaneum as well as within these populations.

58 study, using the red flour beetle, Tribolium castaneum, as a model insect species, we show that an en

59 sinases from the red flour beetle, Tribolium castaneum, as well as their developmental patterns of ex

60 ss family of the red flour beetle, Tribolium castaneum, based largely on sequences from bacterial art

61 this question in the flour beetle Tribolium castaneum by analyzing and comparing the development and

62 e high-resolution structure of the Tribolium castaneum catalytic subunit of telomerase, TERT.

63 widespread in wild populations of Tribolium castaneum collected in Europe, North and South America,

64 In the flour beetle, Tribolium castaneum, ectopic wingless also induced engrailed expre

65 small RNA and mRNA complements throughout T. castaneum embryogenesis.

66 In contrast, similar analysis of T. castaneum even-skipped (Tc-eve), runt (Tc-run), or odd-s

67 te populations of the flour beetle Tribolium castaneum for 6 to 7 years under conditions that differe

68 the hAT transposase TcBuster from Tribolium castaneum formed filamentous structures, or rodlets, in

69 Systemic RNA interference in T. castaneum functions differently from that in Caenorhabdi

70 a melanogaster, Apis mellifera and Tribolium castaneum have 23, 21 and 24, respectively.

71 Females of T. castaneum have a terminal ovipositor ending in short sty

72 The Tribolium castaneum homeotic gene maxillopedia (mxp) is the orthol

73 ated invasions of the flour beetle Tribolium castaneum in laboratory microcosms.

74 Using the flour beetle (Tribolium castaneum) in a microcosm experiment, we disentangled th

75 netic map of the red flour beetle (Tribolium castaneum) integrating molecular with morphological mark

76 Tribolium castaneum is a member of the most species-rich eukaryoti

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

78 minal gene of the red flour beetle Tribolium castaneum is associated with an insertion of a novel ret

79 stoderm and germband of the beetle Tribolium castaneum is based on the same flexible mechanism: a gra

80 ific microRNAs in the early blastoderm of T. castaneum is consistent with previous findings in Drosop

81 The red flour beetle Tribolium castaneum is widely used as a model insect species.

82 The red flour beetle (Tribolium castaneum) is an important model organism for genetics,

83 The red flour beetle, Tribolium castaneum, is an emerging model organism separated from

84 e antenna of the red flour beetle, Tribolium castaneum, is composed of eleven articles, organized int

85 cBuster, from the red flour beetle Tribolium castaneum, is highly active in human cells.

86 In beetles, such as Tribolium castaneum, it is the forewings that are modified (to for

87 is protected from chitinase action by the T. castaneum Knickkopf (TcKnk) protein.

88 used RNA interference (RNAi) to show that T. castaneum larvae lacking functional Tcv or Tccn gene pro

89 ut in short-germ insects including Tribolium castaneum, loss of Wnt signaling affects development of

90 two species: No defects were observed in T. castaneum male genitalia, and while the male claspers of

91 ng of large gonocoxopodites and claspers; T. castaneum males have relatively simple genitalia.

92 ioxidative function and demonstrates that T. castaneum may use an alternative antioxidative system wh

93 Only the styli of the T. castaneum ovipositor were affected by RNAi depletion of

94 Tribolium castaneum paired (Tc-prd) and sloppy-paired (Tc-slp) gen

95 We report the structure of Tribolium castaneum PINK1 (TcPINK1), revealing several unique exte

96 etabolous insects as TcE93 RNAi in Tribolium castaneum prevented pupal-adult transition and produced

97 lele classes of Cephalothorax, the Tribolium castaneum (red flour beetle) ortholog of Sex combs reduc

98 lity in a laboratory population of Tribolium castaneum (red flour beetle), whereas using only the sta

99 Knockdown of natalisin expression in T. castaneum resulted in significant reduction in the fecun

100 her insects, like the flour beetle Tribolium castaneum, retain an ancestral robo2/3 gene.

101 In the red flour beetle, Tribolium castaneum, RNA interference studies indicate that 5MP fa

102 e three-dimensional structures of the two T. castaneum SKRs (TcSKR1 and TcSKR2) were generated from m

103 T. castaneum SOD2 (TcSOD2) is composed of 215 amino acids,

104 ies in Drosophila melanogaster and Tribolium castaneum support the hypothesis that oenocytes are of e

105 -product pest Tribolium species including T. castaneum, T. confusum, T. destructor, T. madens, T. fre

106 e Cry3Ba toxin-binding proteins in Tribolium castaneum (Tc) larvae.

107 DDC genes in the red flour beetle, Tribolium castaneum (Tc), and investigated their functions.

108 roteins from the red flour beetle, Tribolium castaneum (Tc), were examined by using gene-specific RNA

109 og of dsx in the red flour beetle, Tribolium castaneum (Tcdsx).

110 diminuta) in the red flour beetle (Tribolium castaneum) that serves as an intermediate host in its tr

111 t the function of the elytra using Tribolium castaneum (the red flour beetle) as a model.

112 sion patterns in the flour beetle (Tribolium castaneum), the honeybee (Apis mellifera) and the fruit

113 s, including the red flour beetle (Tribolium castaneum), the segment-polarity function of wg is conse

114 ribe cellularization in the beetle Tribolium castaneum, the embryos of which exhibit a thin blastoder

115 In the red flour beetle, Tribolium castaneum, the only currently available system for germl

116 Comparing metamorphic patterning in T. castaneum to embryonic and post-embryonic development in

117 cently completed whole-genome sequence of T. castaneum to prepare custom microarrays and identified a

118 ent transgenic lines in the beetle Tribolium castaneum to show that the EE tissues dynamically form a

119 Here we use flour beetles (Tribolium castaneum) to show experimentally that mean expansion sp

120 cific and one female-specific isoforms of T. castaneum transformer (Tctra) were identified.

121 ndibulate mouthparts of the beetle Tribolium castaneum, using RNA interference to deplete the express

122 two vitellogenins from the beetle Tribolium castaneum was 0.975, even though the two amino acid sequ

123 d here, egg cannibalism by two strains of T. castaneum was significantly enhanced in oat flour, and e

124 derived from the red flour beetle Tribolium castaneum, was shown to be highly active in previous stu

125 a model system, red flour beetles (Tribolium castaneum), we either allowed or constrained evolution o

126 In the red flour beetle, Tribolium castaneum, we have isolated loss-of-function mutations o

127 Using the red flour beetle, Tribolium castaneum, we identify major fitness benefits of polyand

128 To evaluate TcSOD2 function in T. castaneum, we performed RNAi and also assessed the pheno

129 n embryos and larvae of the beetle Tribolium castaneum, we provide the first molecular evidence for t

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

131 hese processes in the flour beetle Tribolium castaneum, which develops ventral appendages during embr

132 assiana, and the red flour beetle, Tribolium castaneum, which has a well-documented external immune s

133 g and dpp in the red flour beetle, Tribolium castaneum, which retains more ancestral modes of limb an

134 pheles gambiae, Aedes aegypti, and Tribolium castaneum, while the PF repeats are reduced in size and