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1 h higher lignin content at 25 DPA (Days Post Anthesis).
2 i2;1 mRNA begins to accumulate just prior to anthesis.
3 ript accumulation in pistils from flowers at anthesis.
4 ng plants by avoiding higher temperatures at anthesis.
5 ous photoperiodic stimulation for successful anthesis.
6 le in floral evocation, but a lesser role in anthesis.
7 h may help to identify these plants prior to anthesis.
8 ed pistils, where expression decreased after anthesis.
9  undergoes dynamic assembly processes during anthesis.
10 aries from eight developmental stages, up to anthesis.
11 at stress (38 C : 22 C) for up to 5 d at pre-anthesis.
12 nmasking of carotenoids from 31st days after anthesis.
13 ting heat stress effects on grain set during anthesis.
14 ss-lintless (fl) mutant at -3 and 0 day post-anthesis.
15 nol starts when flowers open and peaks after anthesis.
16  impacts better during grain filling than at anthesis.
17 flower buds and in the anther filaments upon anthesis.
18 ifferent QTLs were detected before and after anthesis.
19 he biological function of jasmonates in rice anthesis.
20 omoter is particularly active at 7 days post anthesis.
21 grees C : 22 degrees C) for up to 5 d at pre-anthesis.
22 r MD or N. attenuata, ir-EOBII flowers enter anthesis.
23 ransport to support high water demand during anthesis.
24 g from the stem xylem into the flower during anthesis.
25 ation between disease resistance and days to anthesis.
26 tapetum during meiosis and disappears before anthesis.
27 the formation of bicellular pollen grains at anthesis.
28 otyledons in embryos at around 13 days after anthesis.
29 obacterium were applied 5 d or more prior to anthesis.
30 ning Monsanto event 810) at the beginning of anthesis.
31  to form closed locules roughly 3 d prior to anthesis.
32 t accumulates in the stigma and style before anthesis.
33 ore anthesis, and in all floral organs after anthesis.
34 grees C night with additional heat stress at anthesis; 34 degrees C day/26 degrees C night; and 34 de
35  and parthenogenetic egg cells on the day of anthesis, a de novo transcriptome for the Cenchrus cilia
36  root TaNRT2.5 and TaNRT2.1 function in post-anthesis acquisition of soil nitrate.
37  meristem (IM) play a vital role in ensuring anthesis after floral commitment.
38 ta and pericarp at 20, 45, and 60 days after anthesis aiming at increasing our understanding of the m
39 genous, correlate inversely with the time of anthesis and directly with the number of flowers and the
40                        In the period between anthesis and fertilization, the protein content of ovary
41 ith two wheat cultivars under heat stress at anthesis and grain filling stages.
42 e variation during thermo-sensitive periods (anthesis and grain-filling; TSP) of wheat crop developme
43  model accurately simulated maize cultivar's anthesis and physiological maturity, with observed value
44 ent physiological responses, but its role in anthesis and pollinator attraction traits remains largel
45 N. attenuata, ir-EOBII flowers fail to enter anthesis and prematurely senesce.
46 re significant at a 5% false discovery rate: anthesis and silking dates in unrelated B73 and Oh43 lin
47 s in stems until approximately 7 days before anthesis and then down-regulated.
48 g', 'Mid Vegetative', 'Booting', 'Heading', 'Anthesis', and 'Milking', comprising 4496 images.
49 ion was observed in sepals and petals before anthesis, and in all floral organs after anthesis.
50  and declined during the next few days after anthesis, and it showed a strong, positive correlation w
51 l perception in the IM to promote successful anthesis, and that floral evocation and anthesis are two
52 ther filament, the opening of the stomium at anthesis, and the production of viable pollen.
53 ous groups being detected from 11 days after anthesis, and the proteins from about 14 days.
54  the premeiosis stage of development, or pre-anthesis anthers, however, the heat-mediated increase in
55 ontinuous photoperiodic stimulation promotes anthesis are not well understood.
56 sful anthesis, and that floral evocation and anthesis are two separate developmental events in chrysa
57 emission began to decline on the 2nd d after anthesis, BEAT activity continued to increase and remain
58 ts of both osjar1 alleles stayed open during anthesis because the lodicules, which control flower ope
59 nt levels only during the first 30 min after anthesis (before nectar is depleted in wild populations)
60 ate that a low dosage of CPPU applied in pre-anthesis can improve fruit weight/size without any negat
61 tis vinifera 'Chardonnay') 20 to 100 d after anthesis (DAA) and compared with observations of xylem a
62         In young developing seeds 25 d after anthesis (DAA) that did not exhibit OD, the lipid layer
63 tions were performed at 21 and 28 days after anthesis (DAA) under both water stress and control condi
64 l in leaf was manifested early at 12 d after anthesis (DAA), while global transcriptional and phenoty
65 on in the period between 6 and 42 days after anthesis (daa).
66 s were planted with four water regimes after anthesis: daily irrigation (control; S1), every 2days (S
67 sistently lower than those of simple traits (anthesis date and plant height) and prediction accuracy
68 ed with cessation of leaf and stem growth at anthesis, decreased expression of genes involved in stem
69                Delays in the phase of floral anthesis delay morning visits by pollinators, while disr
70                                          Pre-anthesis developing spikes were dipped into a solution o
71 sociated with very different profiles of pre-anthesis development which also depends on their interac
72 tly higher lutein contents from 20 days post anthesis (dpa) but lutein esters were not detected until
73  maximum concentration on the 30th days post-anthesis (dpa) for the young plant, while in the adult p
74  fibers harvested between 17 and 24 day post-anthesis (dpa) represent the greatest expressional dista
75 ccumulation occurred from 25 to 38 days post anthesis (DPA) under our growth conditions.
76  increased in abundance from 10 to 20 d post anthesis (DPA), GhTua1 and GhTua5 transcripts were abund
77 uated in the carpels from 10 to 30 days post-anthesis (DPA).
78 ssessed throughout ripening (30-50 days post-anthesis; dpa) in grafted and self-rooted plants.
79  NTS showed the highest contribution of post-anthesis dry matter translocation to grain yield (averag
80 uring male and female meiosis, and one after anthesis, during fertilization and early embryo developm
81 lopmental stages were identified, one before anthesis, during male and female meiosis, and one after
82 to generate iconic spiral phyllotaxy, during anthesis floret development occurs in discrete ring-like
83 la until floral initiation, then stems until anthesis, followed by panicles until grain maturity, and
84 Hsp101 transcript increased in the tassel at anthesis following a heat stress without an increase in
85 ribution of leaf N and light was analyzed at anthesis for 16 cultivars grown in the field in two cons
86 ected from planting until terminal height at anthesis for a panel of ~500 diverse maize inbred lines.
87 grees C night with additional heat stress at anthesis) for a suite of traits including five yield com
88                               Earlier floral anthesis has been suggested, in turn, to have a role in
89 GBS-SNP) markers to extreme response to post anthesis heat stress conditions.
90 ased removable chambers have shown that post-anthesis HNT stress can induce a significant reduction i
91         The system imposed a consistent post-anthesis HNT stress of + 3.8 degrees C until maturity an
92 ber-physical system to sense and impose post-anthesis HNT stress uniformly through physiological matu
93 hloroplast lines exhibited delayed growth at anthesis; however, at the time of harvest there was no s
94 anthesis (mature ovules) and two days before anthesis (immature ovules), as well as from a frk1 (fert
95             The reduction in An and gs after anthesis in both water conditions was mainly due a decli
96 al perception in the IM to ensure successful anthesis in chrysanthemum.
97 ssing the upper temperature threshold during anthesis in sweet corn.
98 verlap between susceptible monarchs and corn anthesis in the northern than the southern part of the s
99  timing of late-stage floret development, or anthesis, in domesticated sunflowers.
100 suggest that inflorescence water loss during anthesis is not limited by the xylem in our study specie
101         Yet in species that preform flowers, anthesis is one stage of a lengthy developmental process
102  indicate that, while expressed in nectar at anthesis, it is most strongly expressed in the nectary g
103 nd CYP76C3), are simultaneously expressed at anthesis, mainly in upper anther filaments and in petals
104 of ovules dissected from wild type plants at anthesis (mature ovules) and two days before anthesis (i
105                          However, anthers at anthesis, mature pollen, developing endosperm, and embry
106 nly a low level in the anthers and tassel at anthesis, mature pollen, roots, and leaves.
107                                      Days to anthesis, maturity, and plant height predictions had hig
108                    However, three days after anthesis, mRNA levels began a steep decline, whereas BEA
109 response pathways to tightly synchronize the anthesis of hundreds of florets each day, generating spa
110 opsis (Arabidopsis thaliana) seeds 13 d post anthesis of three transgenic lines, producing varying le
111  increased as the bud matured, and peaked at anthesis, paralleling changes in BEAT activity.
112 ), which occurred in a study with a rainless anthesis period.
113 other studies had rainfall events during the anthesis period.
114 eduction in node number, height, and days to anthesis (pollen shed).
115 quently increasing the R:FR near the time of anthesis promoted bud n-2 outgrowth and reduced topmost
116                    We show a requirement for ANTHESIS PROMOTING FACTOR 1 (APRF1), a homolog of yeast
117 ay spent above 30 [Formula: see text] during anthesis reduced crop yields by 0.5% and 2% in irrigated
118                               Heat stress at anthesis reduced observed grain numbers per unit area an
119 eatment of unripe melon fruits 20 days after anthesis showed that MEL2 and MEL7 mRNAs are only induce
120 rall, the study concluded that DS during the anthesis stage had the most significant negative impact
121 ght at tillering stage, and D(2): Drought at anthesis stage) and the application of Cu-nanoparticles
122 typic variation among wheat genotypes at the anthesis stage.
123  of photosynthates to grains during the post-anthesis stage.
124 n with terpene volatiles emission during the anthesis stage.
125 est level of expression was observed in post-anthesis styles.
126 iate upregulation of GA3ox1 and GA3ox4 after anthesis suggests that pollination and/or fertilization
127 e amplified from cDNA of fiber 14 days after anthesis, the A and D were found, indicating the presenc
128 to pollinator attraction (odour, colour) and anthesis time influenced diel pollination differences.
129 ops such as barley (Hordeum vulgare L.), pre-anthesis tip degeneration (PTD) starts with growth arres
130 es and five developmental stages from floral anthesis to enlarged fruits.
131 aita (Eugenia dysenterica) development, from anthesis to ripening.
132 In addition, time to flowering and time from anthesis to the onset of fruit ripening are increased by
133 the "break of sepals", about one week before anthesis, to study its effects on fruit weight/size and
134 d transcript profiling of TaSKP1-6B-4 during anthesis under ambient and terminal heat stress (THS) in
135 during 14 day intervals, from 10 weeks after anthesis until commercial maturity.
136 ast disintegration in fruits from 30 d after anthesis until ripening, suggesting that CmOr regulates
137                              Flowering date (anthesis) varied 91 days from late July to late November
138 ops like wheat (Triticum aestivum), the post-anthesis viability of unpollinated carpels has been over
139 ile the magnitude of effect of these QTLs on anthesis was similar, they are associated with very diff
140 ly growth temperature in the month preceding anthesis was the most influential environmental driver o
141      Biomass accumulation and N uptake after anthesis were significantly and positively correlated wi
142 ions of up to 200 ppm above-ambient CO(2) at anthesis, when nectar rewards are richest.
143 maximal levels of expression coinciding with anthesis, when stigmas are most receptive to pollen and
144 tunia flowers, scent production initiates at anthesis, when the flower is ready for pollination, and
145  development (approximately 26-30 days after anthesis), whereas homogalacturonan and pectic (1-->5)-a
146  in floral organs during the flowering time (anthesis), with the hypothesised primary functions being

 
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