戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ERMINATION1 (DOG1) is a primary regulator of seed dormancy.
2 ative correlation between seed longevity and seed dormancy.
3 ays induced earlier flowering, regardless of seed dormancy.
4 nondormant mutants tt3 and tt4 reestablished seed dormancy.
5  fertility, delayed flowering, and increased seed dormancy.
6 dividual's offspring, such as differences in seed dormancy.
7  in early developing seeds to induce primary seed dormancy.
8 tal stress responses, embryo development and seed dormancy.
9 r was found to be the primary determinant of seed dormancy.
10 he GA-insensitive sly1 mutants show variable seed dormancy.
11 t be a result of selective breeding to alter seed dormancy.
12 y roles in the initiation and maintenance of seed dormancy.
13 iosynthesis, showing increased guttation and seed dormancy.
14 elongation, earlier flowering, and decreased seed dormancy.
15 whereas wrky36 mutants showed strong primary seed dormancy.
16 or, which underlies the natural variation of seed dormancy.
17 acid and gibberellins, central regulators of seed dormancy.
18 cid sequence with DOG1, a major regulator of seed dormancy.
19 hibition of DOG1 expression to break primary seed dormancy.
20  epigenetically, thereby fine-tuning primary seed dormancy.
21 no significant effect on the distribution of seed dormancy.
22 rease grain size but have minimal effects on seed dormancy.
23 ate is just one of several global drivers of seed dormancy.
24  regulatory pathways to increase Arabidopsis seed dormancy.
25 n of ALN expression and further promotion of seed dormancy.
26 ) could potentially be overcome by improving seed dormancy.
27 ests an important role of DNA methylation in seed dormancy.
28 ication traits, including flowering time and seed dormancy.
29 tion can be prevented by a property known as seed dormancy.
30  its components, and quantified selection on seed dormancy.
31 e as well as developmental processes such as seed dormancy.
32 ature variation affects Arabidopsis thaliana seed dormancy.
33 olved in abscisic acid signaling and control seed dormancy.
34 sgenic analyses indicated that APUM9 reduces seed dormancy.
35    Abscisic acid is an essential hormone for seed dormancy.
36 t was isolated based on its strongly reduced seed dormancy.
37 (MFT) that we show here promotes Arabidopsis seed dormancy.
38 le both reduces seed longevity and increases seed dormancy.
39 CnAIP2 impaired seed development and reduced seed dormancy; (2) CnAIP2 promoted root development, par
40 als, we report a quantitative genetic locus, Seed Dormancy 6 (SD6), from aus-type rice, encoding a ba
41 estigate the genetic architecture underlying seed dormancy, a critical adaptive trait in plants.
42        Most alpine plants show physiological seed dormancy, a strong need for cold stratification, wa
43  flowering stages to test the following: how seed dormancy affects germination responses to the envir
44                          Seed lots with high seed dormancy after-ripened slowly, with stronger allele
45                      These data suggest that seed dormancy, an adaptive trait that arose evolutionari
46 RMINATION1 (DOG1) gene is a key regulator of seed dormancy and a major quantitative trait locus in Ar
47                                   Changes in seed dormancy and ABA-induced Pro accumulation consisten
48       In Arabidopsis (Arabidopsis thaliana), seed dormancy and embryogenesis are initiated by the tra
49 l repressors HSI2/VAL1 and HSL1/VAL2 silence seed dormancy and enable the subsequent germination and
50                            Major alleles for seed dormancy and flowering time are well studied, and c
51 liana segregating early and late alleles for seed dormancy and flowering time in a field experiment.
52                               To examine how seed dormancy and flowering time shape annual plant life
53  thaliana, APA is involved in the control of seed dormancy and flowering.
54                   Thus, studies on comparing seed dormancy and germination among populations must con
55                   Therefore, genes affecting seed dormancy and germination are among those under stro
56             It has long been recognized that seed dormancy and germination are regulated by the plant
57 scisic acid (ABA) is a hormone that controls seed dormancy and germination as well as the overall pla
58 n shown to be important in the regulation of seed dormancy and germination by environmental cues.
59                                              Seed dormancy and germination of S. bungeana differed wi
60  after-ripening and incubation conditions on seed dormancy and germination of Stipa bungeana, a peren
61 ull understanding of mechanisms that control seed dormancy and germination remains elusive.
62 le for FTase in ABA signaling that modulates seed dormancy and germination.
63 identify new components in the regulation of seed dormancy and germination.
64 een 2 complex and highly interlinked stages: seed dormancy and germination.
65 Ontology clustering revealed novel actors of seed dormancy and germination.
66  and nondormant seeds and revealed actors in seed dormancy and germination.
67 during seed set is an important modulator of seed dormancy and impacts the performance of crop seeds
68 Although cold plasma has been found to break seed dormancy and improve germination rate, only a few s
69 ) antagonistically control the shift between seed dormancy and its alleviation.
70 ensities) and key species traits (seed mass, seed dormancy and life form) for 2350 species of angiosp
71 rivers, and evolutionary transitions between seed dormancy and nondormancy.
72 -type levels of sHSPs are not sufficient for seed dormancy and not necessary for desiccation toleranc
73    Abscisic acid (ABA) is a key regulator of seed dormancy and plant responses to environmental chall
74                                    GA breaks seed dormancy and promotes germination.
75 reasing temperature variability can increase seed dormancy and reduce germination rates, especially i
76                     In contrast, plants have seed dormancy and seed longevity described as two traits
77             QTL were identified for depth of seed dormancy and seedling emergence timing (SET).
78 at mutations in one MIR156 subfamily enhance seed dormancy and suppress PHS with negligible effects o
79 A) plays a central role in the regulation of seed dormancy and that transcriptional regulation of gen
80           We show that ice1 or zou increases seed dormancy and the double mutant has an additive phen
81 heses on the evolution of different kinds of seed dormancy and their association with lineage diversi
82 l environment can influence the intensity of seed dormancy and thus seasonal germination timing and p
83 s of the Arabidopsis seed that contribute to seed dormancy and to learn more about how dormancy and g
84 se activity cause increased ABA sensitivity, seed dormancy, and stomatal closure, consistent with the
85  one case of memory in the form of increased seed dormancy, and that persisted one generation removed
86  history and transgenerational plasticity in seed dormancy are adaptations of I. violascens to its de
87 based on extant plants that tiny embryos and seed dormancy are basic for angiosperms as a whole.
88         The molecular mechanisms controlling seed dormancy are not well understood.
89 ral hormones, such as abscisic acid-mediated seed dormancy, auxin-dependent lateral shoot initiation,
90 ansitions, and differences in adaptations of seed dormancy between life-forms are poorly understood.
91              Six months of dry storage broke seed dormancy, broadened the temperature range for germi
92                        ABA not only promotes seed dormancy but also triggers growth arrest in postger
93 tor that determines the intensity of primary seed dormancy, but its underlying regulatory mechanism i
94  trans Therefore, the negative regulation of seed dormancy by asDOG1 in cis results in allele-specifi
95 E2) function antagonistically in controlling seed dormancy by directly regulating the ABA catabolism
96 EL3) maintains maternal control over progeny seed dormancy by establishing an epigenetic state in the
97  content of seeds, the regulation of lettuce seed dormancy by red and far red light was determined at
98    Mechanistically, mir156 mutations enhance seed dormancy by suppressing the gibberellin (GA) pathwa
99                                              Seed dormancy, by controlling the timing of germination,
100                                            * Seed dormancy can affect life history through its effect
101                                 The depth of seed dormancy can be influenced by a number of different
102 l defects to leaf somatic embryos, including seed dormancy characteristics.
103       Combining the most updated data set on seed dormancy classes for > 10 000 species with > 4 mill
104    Consistent with a role for clock genes in seed dormancy control, CCA1 expression is transcriptiona
105                                              Seed dormancy controls the start of a plant's life cycle
106 e plant hormone abscisic acid (ABA) mediates seed dormancy, controls seedling development and trigger
107    A negative correlation was observed, deep seed dormancy correlating with low seed longevity and vi
108                  Of the pleiotropic effects, seed dormancy could contribute most to the weed adaptati
109                                          RIL seed dormancy could explain variation in seedling establ
110                                              Seed dormancy cycling plays a crucial role in the lifecy
111  that further suberin-deficient mutants have seed dormancy defects.
112                                              Seed dormancy determines germination timing and contribu
113 l-length transcripts related to ABA-mediated seed dormancy discovered a conserved isoform of PIF6-B a
114 lation plays critical roles in regulation of seed dormancy during seed germination and early seedling
115 higher plants; it plays an important role in seed dormancy, embryo development, and adaptation to env
116 undant but essential roles in the release of seed dormancy epistatic to DOG1.
117  are considered to be the ancestral state in seed dormancy evolution.
118 ent plants are viable yet show phenotypes in seed dormancy, flowering time, lateral root, and stomata
119 resented that separates the action of ABA in seed dormancy from AR and dry storage regulated gene exp
120 r results add to the current knowledge about seed dormancy from macro-adaptive perspectives and the p
121 -mediated mechanism limiting the duration of seed dormancy functions across the Brassicaceae.
122 Gs), the proteins from which are crucial for seed dormancy, germination, and reserve accumulation, ar
123 ABA) is an important phytohormone regulating seed dormancy, germination, seedling growth, and plant t
124                                              Seed dormancy governs the timing of germination, one of
125                                              Seed dormancy has been associated with red grain color i
126 ants, the association of seed longevity with seed dormancy has not been studied in detail.
127 lude that seed coat suberin is essential for seed dormancy imposition by low temperature and that the
128 elay of Germination 1) is a key regulator of seed dormancy in Arabidopsis (Arabidopsis thaliana) and
129  genetic regulators and its association with seed dormancy in Arabidopsis (Arabidopsis thaliana).
130 mRNA is a key player in the establishment of seed dormancy in Arabidopsis and characterizes a set of
131 G1 is the major quantitative trait locus for seed dormancy in Arabidopsis and has been shown to contr
132 ignaling pathway that mediates ABA-regulated seed dormancy in Arabidopsis.
133 ses.The DOG1 protein is a major regulator of seed dormancy in Arabidopsis.
134 perature and light are well known to control seed dormancy in many plant species.
135                                  ABA induces seed dormancy in maturing embryos and inhibits germinati
136  networks in the regulation of variation for seed dormancy in natural populations and make it critica
137 n RNA 3' processing complex display weakened seed dormancy in parallel with defects in DOG1 proximal
138 L3 is retained in mature seeds, and controls seed dormancy in part through repression of programmed c
139  that the mother plant modulates its progeny seed dormancy in response to seasonal temperature change
140 portant grain yield regulator, also controls seed dormancy in rice.
141  determining the sex of ferns to controlling seed dormancy in the earliest seed plants before being c
142                                * In summary, seed dormancy influences flowering time and hence life h
143                                              Seed dormancy is a block to the completion of germinatio
144                                              Seed dormancy is a common phase of the plant life cycle,
145                                              Seed dormancy is a complex life history trait that deter
146                                              Seed dormancy is a key adaptive trait under polygenic co
147                                              Seed dormancy is a trait of considerable adaptive signif
148                                              Seed dormancy is a widespread and key adaptive trait tha
149                                              Seed dormancy is an adaptive trait defining where and wh
150                                              Seed dormancy is an adaptive trait preventing premature
151                                              Seed dormancy is an important developmental process that
152                                              Seed dormancy is an important life history state that in
153                       In many plant species, seed dormancy is broken by cold stratification, a pre-ch
154                                              Seed dormancy is defined as a temporary failure of a via
155                                              Seed dormancy is expected to provide ecological advantag
156 it, breeding of crop cultivars with suitable seed dormancy is hindered by limited useful regulatory g
157                               In Arabidopsis seed dormancy is imposed by the embryo-surrounding tissu
158                                              Seed dormancy is one of the most crucial process transit
159                                              Seed dormancy is prevalent in seasonally cold and dry cl
160       When the favorable season is fleeting, seed dormancy is the only adaptive strategy.
161 entral cell that primes the depth of primary seed dormancy later established during seed maturation.
162 mutants, but there is a striking increase in seed dormancy levels.
163                     GAAS loci colocated with seed dormancy loci, Delay Of Germination (DOG), earlier
164                                              Seed dormancy maximizes plant recruitment in habitats wi
165                                 Reduction of seed dormancy mechanisms, allowing for rapid germination
166 rates a jasmonic acid-dependent reduction in seed dormancy, mediated by alteration of gibberellin and
167  We compiled global distribution records for seed dormancy of 12 743 species and their phylogeny to e
168  turn explains the opposite effect of SPT on seed dormancy of the two ecotypes analyzed here.
169 C7, a cluster of quantitative trait loci for seed dormancy/pericarp color in weedy red rice.
170 reen for genetic suppressors of the enhanced seed dormancy phenotype of max2 in Arabidopsis (Arabidop
171 overexpression can relieve the strong sly1-2 seed dormancy phenotype.
172  of nondormancy and the different classes of seed dormancy: physiological dormancy, morphophysiologic
173 The phytohormone abscisic acid (ABA) acts in seed dormancy, plant development, drought tolerance, and
174  was located in the same region as the major seed dormancy QTL and the dormancy gene DELAY OF GERMINA
175                             qSD12 is a major seed dormancy quantitative trait locus (QTL) identified
176 states in a way that related to the depth of seed dormancy, rather than the type of environmental exp
177 ing RNA that regulates expression of the key seed dormancy regulator, DELAY OF GERMINATION1, is a typ
178  seasonal germination depends on patterns of seed dormancy release or induction by cold and interacts
179  freshly harvested seeds acts as a timer for seed dormancy release, which functions largely independe
180 nd HSL1 in regulation of DOG1 expression and seed dormancy remain elusive.
181 ence phenotypes, but whether it also affects seed dormancy remains unexplored.
182 FGs) in Arabidopsis thaliana are involved in seed dormancy, reserve accumulation, and desiccation tol
183 e development, floral organ development, and seed dormancy), resistance to abiotic and biotic stresse
184                       It appears that sly1-2 seed dormancy results from abscisic acid (ABA) signaling
185 th and development, including embryogenesis, seed dormancy, root and shoot growth, transpiration, and
186                                              Seed dormancy (SD) and longevity (SL) may share developm
187 d development, including embryo development, seed dormancy, seedling development, lateral root initia
188    Preharvest sprouting (PHS) due to lack of seed dormancy seriously threatens crop production worldw
189            We show here that homologs of the seed dormancy-specific gene delay of germination1 (DOG1)
190 cides with a temperature-sensitive switch in seed dormancy state.
191 opulations must consider year of collection, seed dormancy states and germination test conditions whe
192                                       Strong seed dormancy suppressed mid-summer germination in both
193                 Weedy rice has much stronger seed dormancy than cultivated rice.
194 mechanism to explain ecotypic differences in seed dormancy that are controlled by the DOG1 locus.
195                                              Seed dormancy-the absence of seed germination under favo
196                                  The kind of seed dormancy, therefore, can influence both population
197 gressively silenced DOG1 expression to break seed dormancy through ABI5-BINDING PROTEIN 2 (AFP2) as t
198                         In turn, FT controls seed dormancy through inhibition of proanthocyanidin syn
199 n seeds, leaf somatic embryogenesis bypasses seed dormancy to form viable plantlets.
200 regulating the developmental transition from seed dormancy to germination.
201 terns and environmental correlates of global seed dormancy variation.
202 rabidopsis caused two remarkable phenotypes: seed dormancy was abolished and time to flowering was re
203                                              Seed dormancy was analysed by measurement of maximum ger
204                                The increased seed dormancy was reversed by addition of the carotenoid
205                                              Seed dormancy was the dominating state during the evolut
206                                After >5 y of seed dormancy, we triggered germination from the seedban
207               Loss of PIF6 increases primary seed dormancy, whereas overexpression of the beta form,
208 ression; Overexpressing WRKY36 broke primary seed dormancy, whereas wrky36 mutants showed strong prim
209                 This timing is controlled by seed dormancy, which prevents germination under favourab
210                               Association of seed dormancy with shattering, awn, and black hull and r

 
Page Top