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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
43 flowering stages to test the following: how seed dormancy affects germination responses to the envir
46 RMINATION1 (DOG1) gene is a key regulator of seed dormancy and a major quantitative trait locus in Ar
49 l repressors HSI2/VAL1 and HSL1/VAL2 silence seed dormancy and enable the subsequent germination and
51 liana segregating early and late alleles for seed dormancy and flowering time in a field experiment.
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.
60 after-ripening and incubation conditions on seed dormancy and germination of Stipa bungeana, a peren
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
70 ensities) and key species traits (seed mass, seed dormancy and life form) for 2350 species of angiosp
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
75 reasing temperature variability can increase seed dormancy and reduce germination rates, especially i
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
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
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.
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
104 Consistent with a role for clock genes in seed dormancy control, CCA1 expression is transcriptiona
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
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
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
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
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
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
141 determining the sex of ferns to controlling seed dormancy in the earliest seed plants before being c
156 it, breeding of crop cultivars with suitable seed dormancy is hindered by limited useful regulatory g
161 entral cell that primes the depth of primary seed dormancy later established during seed maturation.
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
170 reen for genetic suppressors of the enhanced seed dormancy phenotype of max2 in Arabidopsis (Arabidop
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
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
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
185 th and development, including embryogenesis, seed dormancy, root and shoot growth, transpiration, and
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
191 opulations must consider year of collection, seed dormancy states and germination test conditions whe
194 mechanism to explain ecotypic differences in seed dormancy that are controlled by the DOG1 locus.
197 gressively silenced DOG1 expression to break seed dormancy through ABI5-BINDING PROTEIN 2 (AFP2) as t
202 rabidopsis caused two remarkable phenotypes: seed dormancy was abolished and time to flowering was re
208 ression; Overexpressing WRKY36 broke primary seed dormancy, whereas wrky36 mutants showed strong prim