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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
8 ficantly up-regulated after stimulated by 20-hydroxyecdysone (20-E) in vivo.
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
11  by the prepupal peak of the ecdysteroid, 20-hydroxyecdysone (20-HE).
12 ating titer of the insect molting hormone 20-hydroxyecdysone (20-HE).
13 Kc167) that differentiates in response to 20-hydroxyecdysone (20-HE).
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 aximal levels within 12h by low levels of 20-hydroxyecdysone (20E) and repressed by physiologically r
21 ture, AaFTZ-F1 expression is inhibited by 20-hydroxyecdysone (20E) and superactivated by its withdraw
22 and developmental hormones, the steroidal 20-hydroxyecdysone (20E) and the sesquiterpenoid juvenile h
23 or genes activated by the steroid hormone 20-hydroxyecdysone (20E) are dually controlled by the ecdys
24 n occurs as levels of the steroid hormone 20-hydroxyecdysone (20E) are rising during the pupal stage.
25  of the tobacco hornworm Manduca sexta by 20-hydroxyecdysone (20E) during larval and pupal molts, wit
26                               Remarkably, 20-hydroxyecdysone (20E) has opposite effects on USP isofor
27                  Blood feeding triggers a 20-hydroxyecdysone (20E) hormonal cascade, which activates
28 competence factor for the steroid hormone 20-hydroxyecdysone (20E) in Drosophila melanogaster metamor
29  day 2 fifth larval epidermis in vitro by 20-hydroxyecdysone (20E) in the absence of JH with dose-res
30 ormone receptor family that is induced by 20-hydroxyecdysone (20E) in the epidermis of the tobacco ho
31 a key requirement for the steroid hormone 20-hydroxyecdysone (20E) in the maintenance of numerous pat
32 hen day 2 fourth epidermis was exposed to 20-hydroxyecdysone (20E) in vitro, MHR4 mRNA appeared betwe
33 d the Manduca GV1 cell line is induced by 20-hydroxyecdysone (20E) in vitro.
34                       The steroid hormone 20-hydroxyecdysone (20E) initiates metamorphosis in insects
35 that the male-transferred steroid hormone 20-hydroxyecdysone (20E) is a key regulator of monandry and
36 insect metamorphosis, the steroid hormone 20-hydroxyecdysone (20E) is responsible for coordinating th
37                               The steroid 20-hydroxyecdysone (20E) is the primary regulatory hormone
38 nowledge, because exposure to the steroid 20-hydroxyecdysone (20E) leads to a robust regulated secret
39 n successive phases of rising and falling 20-hydroxyecdysone (20E) levels, leading to a cascade of nu
40      Tonic exposure to moderate levels of 20-hydroxyecdysone (20E) or its precursor, ecdysone, are re
41 vealed that pulses of the steroid hormone 20-hydroxyecdysone (20E) regulate ganglionic fusion, but li
42    In Drosophila, the primary steroid twenty-hydroxyecdysone (20E) regulates ovarian germline stem ce
43 blished that fat-body remodeling requires 20-hydroxyecdysone (20E) signaling.
44 sexta in a pattern-specific manner as the 20-hydroxyecdysone (20E) titer rises for the larval molt.
45 t includes the principal molting hormone, 20-hydroxyecdysone (20E), and ecdysone (E), which is the pr
46                          The mechanism of 20-hydroxyecdysone (20E), but not of JH action, is well und
47  activated in larval organs cultured with 20-hydroxyecdysone (20E), consistent with EcR/USP acting as
48  converts ecdysone (E) to the more active 20-hydroxyecdysone (20E), specifically in mature follicle c
49                        Here, we show that 20-hydroxyecdysone (20E), the active metabolite of ecdysone
50 nly thought to be a hormone precursor and 20-hydroxyecdysone (20E), the physiologically active steroi
51 n direct response to the prepupal rise in 20-hydroxyecdysone (20E), whereas APR(4)s survive through t
52 ssion of DHR3 and betaFTZ-F1 is part of a 20-hydroxyecdysone (20E)-triggered transcriptional cascade
53 evelopment and metamorphosis regulated by 20-hydroxyecdysone (20E).
54 ests its regulation by a steroid hormone, 20-hydroxyecdysone (20E).
55 tamorphosis through its active metabolite 20-hydroxyecdysone (20E).
56 osis is controlled by the steroid hormone 20-hydroxyecdysone (20E).
57  under the control of the steroid hormone 20-hydroxyecdysone (20E).
58 , and the JH I induction is suppressed by 20-hydroxyecdysone (20E).
59 nesis is regulated by the steroid hormone 20 hydroxyecdysone (20E).
60 ly candidate for sexual selection is male 20-hydroxyecdysone (20E).
61  cell autonomously by the steroid hormone 20-hydroxyecdysone (20E).
62 a blood-meal-initiated, elevated titer of 20-hydroxyecdysone (20E).
63 sis and is essential for molting hormone (20-hydroxyecdysone; 20E) biosynthesis.
64 that the most prevalent phytoecdysteroid, 20-hydroxyecdysone (20HE), was secreted (leached) from inta
65 d and used to identify four ecdysteroids: 20-hydroxyecdysone-3-O-beta-D-glycopyranoside, 20-hydroxyec
66 ta-D-glycopyranoside, 20-hydroxyecdysone, 20-hydroxyecdysone-3-O-beta-D-xylose and a hydroxyecdystero
67                 After ingestion of blood, 20-hydroxyecdysone activates yolk protein precursor (YPP) g
68                          We conclude that 20-hydroxyecdysone acts through the Broad-Complex to contro
69 imal concentration of the steroid hormone 20-hydroxyecdysone and with hemolymph taken from growing la
70 posure to the hormone and lower levels of 20-hydroxyecdysone, and by being sensitive to either 20-hyd
71  We examine the role of juvenile hormone, 20-hydroxyecdysone, and insulin/insulin-like growth factor-
72 en used for the analysis of a standard of 20-hydroxyecdysone- and ecdysteroid-containing plant extrac
73  residues were identified as critical for 20-hydroxyecdysone binding.
74 y induced in larval epidermis in vitro by 20-hydroxyecdysone, but EcR-B1 mRNA accumulated more rapidl
75                       The holoreceptor of 20-hydroxyecdysone consists of two nuclear receptors (NRs)
76                       The steroid hormone 20-hydroxyecdysone coordinates the stages of Drosophila dev
77 ion in Drosophila Schneider S2 cells in a 20-hydroxyecdysone-dependent manner, via its interaction wi
78                       The steroid hormone 20-hydroxyecdysone (ecdysone) activates a relatively small
79 development is regulated by two hormones, 20-hydroxyecdysone (ecdysone) and juvenile hormone.
80      Following an increase in the steroid 20-hydroxyecdysone (ecdysone) at the end of larval developm
81 Drosophila, pulses of the steroid hormone 20-hydroxyecdysone (ecdysone) control the timing of the tra
82 amorphosis, pulses of the steroid hormone 20-hydroxyecdysone (ecdysone) direct the destruction of obs
83                       The steroid hormone 20-hydroxyecdysone (ecdysone) is the key regulator of poste
84 ich is coordinated by the steroid hormone 20-hydroxyecdysone (ecdysone) through the ecdysone receptor
85  Drosophila melanogaster, fluctuations in 20-hydroxyecdysone (ecdysone) titer coordinate gene express
86 hological response to the steroid hormone 20-hydroxyecdysone (ecdysone).
87                The insect steroid hormone 20-hydroxyecdysone enhanced BrdU incorporation into the nuc
88  in the production of the steroid hormone 20-hydroxyecdysone from the prothoracic gland, the primary
89 studies have suggested that production of 20-hydroxyecdysone in Drosophila and other arthropods invol
90  elevated response to the steroid hormone 20-hydroxyecdysone in mosquitoes in a state of arrest.
91  of premoult concentrations (10(-6) M) of 20-hydroxyecdysone in the epidermal and muscle tissue of th
92 ntral nervous system, the steroid hormone 20-hydroxyecdysone induces a wide spectrum of cellular resp
93                       The steroid hormone 20-hydroxyecdysone is a key regulatory factor, controlling
94        The steroid insect molting hormone 20-hydroxyecdysone is believed to control critical aspects
95 most abundant phytoecdysteroids including 20-hydroxyecdysone is yet to be clarified.
96  exogenous and endogenous compounds, like 20-hydroxyecdysone (natural ligand of the ecdysone receptor
97                 Precocious application of 20-hydroxyecdysone on the first day of pupal life accelerat
98 reasing the levels of the steroid hormone 20-hydroxyecdysone or by decapitation.
99 cdysone, and by being sensitive to either 20-hydroxyecdysone or its precursor, ecdysone.
100 g the mutants the steroid molting hormone 20-hydroxyecdysone, or the precursors of ecdysone biosynthe
101 ments stimulating direct development (the 20-hydroxyecdysone pathway: Ecr, Shd, Broad; the Wnt pathwa
102 lly identified in these extracts included 20-hydroxyecdysone, polypodine B, and integristerone A.
103                       The steroid hormone 20-hydroxyecdysone (referred to here as ecdysone) directs D
104                      The Broad-Complex, a 20-hydroxyecdysone-regulated gene, is essential for the dev
105 oad-Complex (BR-C) is a key member of the 20-hydroxyecdysone regulatory hierarchy that coordinates ch
106 d in vitro by the insect molting hormone, 20-hydroxyecdysone, suggesting that this, or some related s
107     Bombyxin evidently acts together with 20-hydroxyecdysone to stimulate cell division and growth of
108     Importantly, AaGATAr can override the 20-hydroxyecdysone transactivation of YPP genes, and its tr
109 tured fat body became less abundant after 20-hydroxyecdysone treatment.
110                     Later, high levels of 20-hydroxyecdysone trigger a wave of apoptosis within the a
111 e have shown that the fly steroid hormone 20-hydroxyecdysone triggers both the elongation itself and
112 d and orchestrated by the steroid hormone 20-hydroxyecdysone, which initiates a cascade of coordinate
113                The insect steroid hormone 20-hydroxyecdysone works through a ligand-activated nuclear

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