ライフサイエンスコーパス: juvenile hormone

1 n with insect hormones, such as ecdysone and juvenile hormone.

2 oid hormone ecdysone and the sesquiterpenoid juvenile hormone.

3 r inhibited by diet, ovarian development, or juvenile hormone.

4 hormones, 20-hydroxyecdysone (ecdysone) and juvenile hormone.

5 related roles of insulin-IGF-1 signaling and juvenile hormone.

6 als but the latter because of suppression by juvenile hormone.

7 ith the formation of sesquiterpenes, such as juvenile hormones.

8 We examine the role of juvenile hormone, 20-hydroxyecdysone, and insulin/insuli

9 m methyltransferase, Drosophila melanogaster Juvenile Hormone Acid O-Methyltransferase (DmJHAMT).

10 Juvenile hormone affected the expression of Vg and insul

11 developmental arrest with an application of juvenile hormone, an endocrine trigger known to terminat

12 Juvenile hormone, an important regulator of development

13 Juvenile hormone analog (JHA) insecticides are relativel

14 In S2 cells, Ecd and the juvenile hormone analog methoprene exert opposite effect

15 reatment of the long-lived InR dwarfs with a juvenile hormone analog restores life expectancy toward

16 Application of hydroprene, a juvenile hormone analog, during the penultimate instar c

17 their fundamental behaviors to disseminate a juvenile hormone analogue (JHA) between resting and ovip

18 rmone titers and their regulation implicates juvenile hormone and ecdysone in the control of wing-mor

19 lated JHAMT and up-regulated CYP307A1 in the juvenile hormone and ecdysteroid pathways, respectively,

20 This includes genes related to juvenile hormone and insulin, two hormones shown previou

21 Adult ants use saliva to transfer juvenile hormone and other chemical signals to their lar

22 ns, which are inducible by the morphogenetic juvenile hormone and which constitute a significant prop

23 Our work suggests not only a new role for juvenile hormone and/or serotonin in Drosophila ovarian

24 hat the interplay between insulin signaling, juvenile hormone, and vitellogenin regulates maternal ef

25 47b neurons requires a reproductive hormone, juvenile hormone, as well as its binding protein Methopr

26 ty to two ligand binding proteins, including juvenile hormone binding protein.

27 JH-binding protein, given the name mosquito juvenile hormone-binding protein (mJHBP), which circulat

28 he inhibitory effect of synthetic Ae-AS-C on juvenile hormone biosynthesis by the isolated corpora al

29 t characterized as a peptide that stimulated juvenile hormone biosynthesis in adult lepidopteran corp

30 e various functions, including inhibition of juvenile hormone biosynthesis in cockroaches and cricket

31 Farnesol is an intermediate in juvenile hormone biosynthesis, but is also produced by r

32 gene involved in an insect-specific step of juvenile hormone biosynthesis.

33 arch circadian clockwork; all members of the juvenile hormone biosynthetic pathway whose regulation s

34 We conclude that juvenile hormone deficiency, which results from InR sign

35 mRNA levels of Kruppel homolog 1 (Kr-h1), a juvenile hormone-dependent transcription factor that rep

36 roportion of total termite protein, suppress juvenile-hormone-dependent worker differentiation to the

37 Manduca sexta juvenile hormone diol kinase (JHDK) catalyzes the conver

38 The gene sequence of Manduca sexta juvenile hormone diol kinase (JHDK) codes for an enzyme

39 , the insulin/IGF signaling pathway, and the juvenile hormone/ecdysteroid pathway.

40 Juvenile hormone epoxide hydrolase (JHEH) has attracted

41 One pathway of this degradation is through juvenile hormone esterase (JHE), which cleaves the JH es

42 Juvenile hormone esterase (JHE; EC 3.1.1.1), which is in

43 Juvenile hormone esterase degrades juvenile hormone, whi

44 up by pericardial cells and native M. sexta juvenile hormone esterase in fat body tissue, where the

45 Circulating juvenile hormone esterase is removed from insect blood b

46 Binding assays showed that P29 bound juvenile hormone esterase more strongly than it did a mu

47 experiments, P29 bound injected recombinant juvenile hormone esterase taken up by pericardial cells

48 terase) and in an insect enzyme preparation (juvenile hormone esterase).

49 rize proteins involved in the degradation of juvenile hormone esterase, a pericardial cell cDNA phage

50 e et al., and down-regulated genes including juvenile hormone esterase-like protein et al.

51 cells to facilitate lysosomal degradation of juvenile hormone esterase.

52 structed and screened for proteins that bind juvenile hormone esterase.

53 tions in follicle formation were enhanced by juvenile hormone exposure and phenocopied by serotonin f

54 The presence of juvenile hormone had no effect on accumulation of either

55 ristoneura fumiferana is directly induced by juvenile hormone I (JH I), and the JH I induction is sup

56 ressed by physiologically relevant levels of juvenile hormone I (JH I).

57 Dramatically increased titer of the juvenile hormone III (JH III) is essential for the acqui

58 Juvenile hormone III (JH) plays a key role in regulating

59 The isoprenoids farnesol and juvenile hormone III (JH), metabolites of the cholestero

60 regulated in part by the positive effect of juvenile hormone III (JHIII) on gene expression for HMG-

61 -day-old males resulted in identification of juvenile hormone III bisepoxide and juvenile hormone III

62 ation of juvenile hormone III bisepoxide and juvenile hormone III in a ratio of 2.5:1.

63 the sesquiterpenoid methyl epoxyfarnesoate (juvenile hormone III) to Sf9 cells induces transcription

64 farnesoid X-activated receptor (farnesol or juvenile hormone III), or liver X receptor (22R-hydroxyc

65 ferator-activated receptor-alpha ligand, and juvenile hormone III, a farnesoid X-activated receptor a

66 The FXR activators, all-trans farnesol and juvenile hormone III, also accelerated epidermal barrier

67 1-epoxy-3,7,11-trimethyl-2,6-dodecadienoate [juvenile hormone III, JH III] with a turnover of 3-5 nmo

68 GPPS expression levels are regulated by juvenile hormone III, similar to other mevalonate pathwa

69 te (MF), the unepoxidised analogue of insect juvenile hormone-III (JH-III).

70 Without juvenile hormone, imaginal discs form and grow despite s

71 of amphibians that is equivalent to that of juvenile hormone in insect metamorphosis.

72 of farnesoic acid, an immediate precursor of juvenile hormone, indicating that the Ae-AS-C target is

73 e Carrier) transporter family member JhI-21 (Juvenile hormone Inducible-21), which is expressed in Dr

74 lly, the results support the hypothesis that juvenile hormone is a pivotal hormone coordinating the d

75 transcription factor that plays key roles in juvenile hormone (JH) action] mRNA in the penultimate ny

76 r result in resistance to both methoprene, a juvenile hormone (JH) agonist insecticide, and JH.

77 In experiment 1, drones treated with the juvenile hormone (JH) analog methoprene started flying a

78 is exposed to ecdysteroids in the absence of juvenile hormone (JH) and becomes committed to pupal dif

79 Metamorphosis in insects is regulated by juvenile hormone (JH) and ecdysteroids.

80 Our recent studies identified juvenile hormone (JH) and nutrition as the two key signa

81 on the disappearance of the antimetamorphic juvenile hormone (JH) and the transcription factors Krup

82 Ecdysone and juvenile hormone (JH) are important regulators of insect

83 mporally directed manipulations, we identify juvenile hormone (JH) as an anticipatory endocrine signa

84 Juvenile hormone (JH) biosynthesis in the corpus allatum

85 Juvenile hormone (JH) coordinates timing of female repro

86 ol kinase (JHDK) catalyzes the conversion of juvenile hormone (JH) diol to JH diol phosphate.

87 lay of mRNA technique we discovered that the juvenile hormone (JH) esterase gene (Cfjhe) from Chorist

88 Juvenile hormone (JH) governs a great diversity of proce

89 Juvenile hormone (JH) has been implicated in many develo

90 Application of a high dose of juvenile hormone (JH) III or its mimics (JHM) to Drosoph

91 component, ipsdienol, de novo in response to juvenile hormone (JH) III.

92 se of its critical role in the regulation of juvenile hormone (JH) in insects.

93 To elucidate the role of juvenile hormone (JH) in metamorphosis of Drosophila mel

94 The role of juvenile hormone (JH) in regulating the timing and natur

95 is review explores the roles of ecdysone and juvenile hormone (JH) in the evolution of complete metam

96 Juvenile hormone (JH) is a key insect developmental horm

97 Juvenile hormone (JH) is a key regulator of insect devel

98 The synthesis of juvenile hormone (JH) is an attractive target for contro

99 Juvenile hormone (JH) is an important regulator of both

100 Juvenile hormone (JH) is an insect hormone containing an

101 Juvenile hormone (JH) is critical for multiple aspects o

102 the endocrine glands that produce the insect juvenile hormone (JH) is most closely related to P450 pr

103 l for courtship memory through regulation of juvenile hormone (JH) levels in adult males.

104 tion of a supernumerary nymphal stage with a juvenile hormone (JH) mimic prevented the disappearance

105 Juvenile hormone (JH) plays crucial roles in many aspect

106 Juvenile hormone (JH) prevents these changes in earlier

107 ons as an obligatory allatotropin to promote juvenile hormone (JH) production and reproduction.

108 Juvenile hormone (JH) receptor, Methoprene-tolerant (Met

109 Juvenile hormone (JH) regulates a wide variety of biolog

110 Juvenile hormone (JH) regulates insect development by a

111 om fourth instar larvae with high endogenous juvenile hormone (JH) showed a 10-fold higher sensitivit

112 Despite longstanding efforts, the juvenile hormone (JH) signaling pathway remains unknown.

113 s rising, and this increase was prevented by juvenile hormone (JH) that prevented adult development.

114 Once critical weight is reached, juvenile hormone (JH) titers decline, resulting in the r

115 an controls and receiving aggression reduces juvenile hormone (JH) titers.

116 lopmental transition that is induced by high juvenile hormone (JH) titers.

117 Treatment with the insect hormone juvenile hormone (JH), a key regulator of metamorphosis,

118 The molecular action of juvenile hormone (JH), a regulator of vital importance t

119 ycles, which are in turn driven by cycles of juvenile hormone (JH), can be eliminated by application

120 in, vitellogenin (Vg), and endocrine factor, juvenile hormone (JH), functions as a pacemaker driving

121 lated but were largely related to effects of juvenile hormone (JH), suggesting that the increase in J

122 ster is attributable to the endocrine signal juvenile hormone (JH), which promotes the development of

123 portant status quo role in the regulation of juvenile hormone (JH)-dependent caste differentiation.

124 ed in mediating vitellogenin (Vg) uptake and juvenile hormone (JH)-regulated remodeling of follicular

125 The promoters of three juvenile hormone (JH)-sensitive, and one JH-insensitive

126 ponses of the Lepidoptera and the Diptera to juvenile hormone (JH).

127 is is under the dual control of ecdysone and juvenile hormone (JH).

128 ydroxyecdysone (20E) and the sesquiterpenoid juvenile hormone (JH).

129 cally transmitted throughout the organism by juvenile hormone (JH).

130 ark conditions, starvation, temperature, and juvenile hormone (JH).

131 Juvenile hormones (JH) are a class of regulatory sesquit

132 or identification and quantitation of insect juvenile hormones (JH) has been developed using capillar

133 is of high specific activity insect [10-(3)H]juvenile hormones (JH) I, II, and III which affords both

134 Juvenile hormones (JH) regulate a wide variety of develo

135 Juvenile hormones (JH), a sesquiterpenoid group of ligan

136 affinity analogs of the natural lepidopteran juvenile hormones, JH I and II [epoxy[3H]bishomofarnesyl

137 We conclude that juvenile hormone mediated a positive feedback system tha

138 mating was induced by topical application of juvenile hormone, methoprene, or fenoxycarb.

139 Early treatments with juvenile hormone mimic (JHm) appear to repress extension

140 vents could be prevented by application of a juvenile hormone mimic (JHM).

141 The juvenile hormone mimic, pyriproxyfen is a suppressor of

142 Topical application of a juvenile-hormone mimic to the flight-capable morph cause

143 domatuic acid, juvabione, and related insect juvenile hormone mimics.

144 Although the hemolymph titer of juvenile hormone normally decreases to low levels early

145 olactin (PRL) is widely considered to be the juvenile hormone of anuran tadpoles and to counteract th

146 ormal schedule, and the inhibitory action of juvenile hormone on this checkpoint.

147 f insects studied, they act as inhibitors of juvenile hormone production in only some groups.

148 onse that ultimately leads to a cessation of juvenile hormone production.

149 The insect juvenile hormone receptor is a basic helix-loop-helix (b

150 the role of GPCRs in insect reproduction and juvenile hormone-regulated Vg uptake, we performed a com

151 Juvenile hormone regulation of Vg synthesis has been kno

152 We show that a mutation in the juvenile hormone-regulatory pathway in Manduca sexta ena

153 A juvenile hormone response element (JHRE) has been identi

154 at 4 element and is designated as a putative juvenile hormone response element (JHRE).

155 Insulin and juvenile hormone signaling direct entry of the mosquito

156 storage proteins are implicated in silencing juvenile hormone signaling, which is a prerequisite for

157 ests that this decision is regulated through juvenile hormone signaling.

158 homolog 1 (Kr-h1), one of the key players in juvenile hormone signaling.

159 For example, we conclude that juvenile hormone signalling evolved with the emergence o

160 h inhibitory effects on visceral muscles and juvenile hormone synthesis.

161 one function in insects is the inhibition of juvenile hormone synthesis.

162 racts from mated males contained 3-fold more juvenile hormone than did extracts from virgins.

163 l cells of the ring gland, which produce the juvenile hormone that controls progression through devel

164 udy identifies a direct neural substrate for juvenile hormone that permits coordination of courtship

165 tar, eye disc development begins even if the juvenile hormone titer is artificially maintained at hig

166 ion on allatectomized (CAX) larvae that lack juvenile hormone to impose the critical weight checkpoin

167 ynthesis and degradation of ecdysteroids and juvenile hormones to the metabolism of foreign chemicals

168 Starvation and juvenile hormone treatments allowed the separation of in

169 Juvenile hormone esterase degrades juvenile hormone, which acts in conjunction with ecdyste

170 insect corpora allata, produce precursors of juvenile hormone with putatively similar functions.