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1 els are not needed for bud release following decapitation.
2     Planarians famously can regenerate after decapitation.
3 gulated in axillary meristems upon main stem decapitation.
4 d (3) circulating catecholamine levels after decapitation.
5 prolonged culture on cytokinins or following decapitation.
6 d collected either by cardiac puncture or by decapitation.
7 ced every 2 h from 09.00 to 21.00 h by rapid decapitation.
8 the steroid hormone 20-hydroxyecdysone or by decapitation.
9  c-fos mRNA expression occurred at 1 h after decapitation.
10 , or removal of tissues from other organs by decapitation.
11 rgic nervous system can regenerate following decapitation.
12 xcises cilia tips in a process we call cilia decapitation.
13                           By contrast, after decapitation AEs were dramatically elevated (anandamide,
14  brains obtained from rats immediately after decapitation and 30 min later were used to determine the
15 r paradormancy release (growth induction) by decapitation and in response to seasonal signals.
16  and CK changes were largely associated with decapitation and/or root removal and auxin response, whe
17 oss in these cells is accompanied by ciliary decapitation, and kinase activity does not change the ti
18 idents were subsequently sacrificed by rapid decapitation, and their brains were removed and processe
19  findings demonstrate that the initiation of decapitation- and cytokinin-induced axillary bud outgrow
20 docking to the nucleus, leading to spermatid decapitation as a result of a failure to form a stable h
21 , and diminished responses to auxin in shoot decapitation assays.
22 ponds to 6-benzylaminopurine application and decapitation by increasing axillary bud length, implicat
23 ed throughout the Arabidopsis hypocotyl, yet decapitation experiments have localized the site of ligh
24                                 Grafting and decapitation experiments indicate that the rn phenotype
25                                              Decapitation experiments suggested that if teneral reser
26 increase eye progenitor production following decapitation, facilitating regeneration.
27  onset of status epilepticus (SE) by CO2 and decapitation for the assay of COx activity and by head-f
28  of stem cell proliferation occurs following decapitation, forming a blastema at the oral pole within
29 s and bud outgrowth after shoot tip removal (decapitation) in the pea (Pisum sativum).
30 hich auxin and CK are dominant regulators of decapitation-induced branching, whereas SLs are more imp
31               Finally, we propose that cilia decapitation induces mitogenic signaling and constitutes
32                        Our data confirm that decapitation induces the expression of at least one ISOP
33 basal conditions and in brain after one-hour decapitation ischemia, using liquid chromatography with
34 aviors that are exhibited spontaneously upon decapitation, namely, grooming, grasping, righting, and
35                                              Decapitation of o-carborane clusters made these extended
36 leolytic processing, and occasionally robust decapitation of the 5' guanine (G) of mirtron-5p species
37 decapitation reduced the inductive effect of decapitation on bud evagination.
38 Removing the main shoot PATS auxin source by decapitation or chemically inhibiting the PATS strongly
39 had no effect on initial bud outgrowth after decapitation or cytokinin (benzyladenine; BA) treatment.
40 y does not change the timing or frequency of decapitation or the rate of cilia loss but increases the
41            New findings indicate that, after decapitation, planarians build an organizing center from
42 ies of growth-induced (2 h, 2, and 4 d after decapitation) plants were used to identify differentiall
43 ow that an acute loss of IFT-B through cilia decapitation precedes resorption.
44        Removal of the PF at the same time as decapitation reduced the inductive effect of decapitatio
45          Here, we show that leafy shoot apex decapitation releases apical dominance through massive a
46 d more normal head-body proportions prior to decapitation resulted in animals which were capable of r
47                                 TAB-meristem decapitation resulted in the development of increasing n
48  accumulation of reaper transcripts, whereas decapitation results in the accumulation of lower levels
49       Circulating catecholamine levels after decapitation stress generally dropped with increasing ag
50    After testing, all animals were killed by decapitation, their brains were removed for c-fos in sit
51                                        After decapitation, trunk blood was collected and plasma was i
52 lices received dizocilpine immediately after decapitation, TUNEL-positive staining no longer occurred