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1 orms are induced as a primary response to 20-hydroxyecdysone.
2 omosomes initiated by the molting hormone 20-hydroxyecdysone.
3 o become pupally committed in response to 20-hydroxyecdysone.
4 ion of cholesterol to the molting hormone 20-hydroxyecdysone.
5 that includes the insect steroid hormone 20-hydroxyecdysone.
6 mutant larvae the insect steroid hormone 20-hydroxyecdysone.
7 R, IR, and mass spectra not only for pure 20-hydroxyecdysone (100-400 microg on column) but also the
9 ections and find that the steroid hormone 20-hydroxyecdysone (20-HE) can regulate the quality of the
10 influential roles of the steroid hormone 20-hydroxyecdysone (20-HE) during development, we tested th
14 droxyecdysone-3-O-beta-D-glycopyranoside, 20-hydroxyecdysone, 20-hydroxyecdysone-3-O-beta-D-xylose an
15 d wing disk growth in vitro requires both 20-hydroxyecdysone (20E) and either brain extract or bombyx
16 ryos have very low titers of ecdysone and 20-hydroxyecdysone (20E) and fail to express IMP-E1 and L1,
17 utonomous response to the steroid hormone 20-hydroxyecdysone (20E) and involves mitochondrial demise
18 show that the Drosophila steroid hormone 20-hydroxyecdysone (20E) and its nuclear receptor directly
19 nduction of BR-C mRNA in the epidermis by 20-hydroxyecdysone (20E) and its suppression by JH were sho
20 sstalk between two major insect hormones, 20-hydroxyecdysone (20E) and juvenile hormone (JH) to elici
21 aximal levels within 12h by low levels of 20-hydroxyecdysone (20E) and repressed by physiologically r
22 ture, AaFTZ-F1 expression is inhibited by 20-hydroxyecdysone (20E) and superactivated by its withdraw
23 and developmental hormones, the steroidal 20-hydroxyecdysone (20E) and the sesquiterpenoid juvenile h
24 squito Anopheles gambiae, the ecdysteroid 20-hydroxyecdysone (20E) appears to have evolved to both co
25 or genes activated by the steroid hormone 20-hydroxyecdysone (20E) are dually controlled by the ecdys
26 n occurs as levels of the steroid hormone 20-hydroxyecdysone (20E) are rising during the pupal stage.
27 of the tobacco hornworm Manduca sexta by 20-hydroxyecdysone (20E) during larval and pupal molts, wit
31 competence factor for the steroid hormone 20-hydroxyecdysone (20E) in Drosophila melanogaster metamor
32 day 2 fifth larval epidermis in vitro by 20-hydroxyecdysone (20E) in the absence of JH with dose-res
33 ormone receptor family that is induced by 20-hydroxyecdysone (20E) in the epidermis of the tobacco ho
34 a key requirement for the steroid hormone 20-hydroxyecdysone (20E) in the maintenance of numerous pat
35 hen day 2 fourth epidermis was exposed to 20-hydroxyecdysone (20E) in vitro, MHR4 mRNA appeared betwe
38 that the male-transferred steroid hormone 20-hydroxyecdysone (20E) is a key regulator of monandry and
39 insect metamorphosis, the steroid hormone 20-hydroxyecdysone (20E) is responsible for coordinating th
41 nowledge, because exposure to the steroid 20-hydroxyecdysone (20E) leads to a robust regulated secret
42 n successive phases of rising and falling 20-hydroxyecdysone (20E) levels, leading to a cascade of nu
45 vealed that pulses of the steroid hormone 20-hydroxyecdysone (20E) regulate ganglionic fusion, but li
46 In Drosophila, the primary steroid twenty-hydroxyecdysone (20E) regulates ovarian germline stem ce
47 that the ecdysone receptor (EcR)-mediated 20-hydroxyecdysone (20E) signaling regulates miRNA expressi
49 sexta in a pattern-specific manner as the 20-hydroxyecdysone (20E) titer rises for the larval molt.
50 t includes the principal molting hormone, 20-hydroxyecdysone (20E), and ecdysone (E), which is the pr
52 activated in larval organs cultured with 20-hydroxyecdysone (20E), consistent with EcR/USP acting as
53 Upon blood feeding, a steroid hormone, 20-hydroxyecdysone (20E), initiates a reproductive program
55 converts ecdysone (E) to the more active 20-hydroxyecdysone (20E), specifically in mature follicle c
57 nly thought to be a hormone precursor and 20-hydroxyecdysone (20E), the physiologically active steroi
59 n direct response to the prepupal rise in 20-hydroxyecdysone (20E), whereas APR(4)s survive through t
60 d by the male-synthetized steroid hormone 20-hydroxyecdysone (20E), which is packaged together with o
61 ssion of DHR3 and betaFTZ-F1 is part of a 20-hydroxyecdysone (20E)-triggered transcriptional cascade
73 , juvenile hormone (JH) and ecdysteroids (20-hydroxyecdysone, 20E, is the most active form) govern fe
75 that the most prevalent phytoecdysteroid, 20-hydroxyecdysone (20HE), was secreted (leached) from inta
76 d and used to identify four ecdysteroids: 20-hydroxyecdysone-3-O-beta-D-glycopyranoside, 20-hydroxyec
77 ta-D-glycopyranoside, 20-hydroxyecdysone, 20-hydroxyecdysone-3-O-beta-D-xylose and a hydroxyecdystero
80 imal concentration of the steroid hormone 20-hydroxyecdysone and with hemolymph taken from growing la
81 posure to the hormone and lower levels of 20-hydroxyecdysone, and by being sensitive to either 20-hyd
82 We examine the role of juvenile hormone, 20-hydroxyecdysone, and insulin/insulin-like growth factor-
83 en used for the analysis of a standard of 20-hydroxyecdysone- and ecdysteroid-containing plant extrac
85 y induced in larval epidermis in vitro by 20-hydroxyecdysone, but EcR-B1 mRNA accumulated more rapidl
89 ion in Drosophila Schneider S2 cells in a 20-hydroxyecdysone-dependent manner, via its interaction wi
93 Drosophila, pulses of the steroid hormone 20-hydroxyecdysone (ecdysone) control the timing of the tra
94 amorphosis, pulses of the steroid hormone 20-hydroxyecdysone (ecdysone) direct the destruction of obs
96 ich is coordinated by the steroid hormone 20-hydroxyecdysone (ecdysone) through the ecdysone receptor
97 Drosophila melanogaster, fluctuations in 20-hydroxyecdysone (ecdysone) titer coordinate gene express
100 in the production of the steroid hormone 20-hydroxyecdysone from the prothoracic gland, the primary
101 studies have suggested that production of 20-hydroxyecdysone in Drosophila and other arthropods invol
103 of premoult concentrations (10(-6) M) of 20-hydroxyecdysone in the epidermal and muscle tissue of th
104 ntral nervous system, the steroid hormone 20-hydroxyecdysone induces a wide spectrum of cellular resp
108 atory mechanism upon a hormonal stimulus (20-hydroxyecdysone) is to influence pause-release rather th
109 exogenous and endogenous compounds, like 20-hydroxyecdysone (natural ligand of the ecdysone receptor
113 g the mutants the steroid molting hormone 20-hydroxyecdysone, or the precursors of ecdysone biosynthe
114 ments stimulating direct development (the 20-hydroxyecdysone pathway: Ecr, Shd, Broad; the Wnt pathwa
115 lly identified in these extracts included 20-hydroxyecdysone, polypodine B, and integristerone A.
118 oad-Complex (BR-C) is a key member of the 20-hydroxyecdysone regulatory hierarchy that coordinates ch
119 d in vitro by the insect molting hormone, 20-hydroxyecdysone, suggesting that this, or some related s
121 depends on ecdysone signaling, as feeding 20-hydroxyecdysone to PTTH mutants reverses the effect.
122 Bombyxin evidently acts together with 20-hydroxyecdysone to stimulate cell division and growth of
123 Importantly, AaGATAr can override the 20-hydroxyecdysone transactivation of YPP genes, and its tr
126 e have shown that the fly steroid hormone 20-hydroxyecdysone triggers both the elongation itself and
127 d and orchestrated by the steroid hormone 20-hydroxyecdysone, which initiates a cascade of coordinate