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1 ectaries) and Nicotiana attenuata (gynoecial nectaries).
2 th's proboscis as they search for a flower's nectary.
3 e the incision with bill-gaping to reach the nectary.
4 e role of MYB305 in the growth of the floral nectary.
5 on of the major nectarin genes in the floral nectary.
6 ional regulation of the NADPH oxidase in the nectary.
7  necessary for the subsequent development of nectaries.
8 olutionary origin and developmental basis of nectaries.
9 T), were induced during secretion in C. pepo nectaries.
10 e short stamens in the maturation of lateral nectaries.
11 is required for auxin-dependent responses in nectaries.
12 only weakly expressed in the earlier Stage 6 nectaries.
13  areas of lateral root emergence, and floral nectaries.
14 trong expression of At5g44630 in intrafloral nectaries.
15 gh levels of CAT expression in mature floral nectaries.
16 ned the convergent evolution of ant-guarding nectaries across ferns and flowering plants.
17 a nectary NADPH oxidase that was cloned from nectaries and identified as an rbohD-like NADPH oxidase.
18  the androecium, resulting in unusual floral nectaries and leading to a gradual sterilization of the
19 mulated to about 35% of total amino acids in nectaries and nectar during peak secretion; however, alt
20 te and nitrite, at least partially by NR, in nectaries and nectar.
21          Many plant species grow extrafloral nectaries and produce nectar to attract carnivore arthro
22 yledons, petals, sepals, filaments, stigmas, nectaries and siliques.
23 ucrose biosynthesis, are highly expressed in nectaries and that their expression is also essential fo
24                                    While the nectary and its nectar have been documented for two mill
25 opsis thaliana, Brassica rapa (extrastaminal nectaries) and Nicotiana attenuata (gynoecial nectaries)
26 es the continuous export of sucrose into the nectary apoplast.
27 rgans with continuous merocrine nectar flow, nectary appearance, nectar production, and flow.
28                                       Floral nectaries are an interesting example of a convergent tra
29                                              Nectaries are secretory organs that are widely present i
30  by nectar guides in the form of contrasting nectary area colouration.
31                            Nectar volume and nectary area displayed an evolutionary association with
32                                              Nectary area evolution involves parallel processes of ce
33 volutionary association of nectar volume and nectary area with pollination syndrome across 19 Penstem
34 ed trait correlations between nectar volume, nectary area, and the size of stamens on which nectaries
35 ion of STY homologs was also detected in the nectary-bearing petals of Delphinium and Epimedium.
36 ey-capturing traps of carnivorous plants and nectary-bearing petals of ranunculaceous species, are wi
37 ocumented for two millennia, many aspects of nectary biology are still unknown.
38      Four traits (purple fruits, extrafloral nectaries, bud scales and toothed leaves) were statistic
39 eporters displayed intense signal in lateral nectaries, but pin6 lateral nectaries showed little or n
40                    Production of extrafloral nectaries by Vachellia sp. that do not house ants is als
41                             We show that the nectary can form independently of any floral organ ident
42 p internal piece of nec4 cDNA from a stage 6 nectary cDNA library.
43 isolate a near full-length nec5 clone from a nectary-derived cDNA library.
44 ctary area, and the size of stamens on which nectaries develop.
45 w very little as to what genes contribute to nectary development and evolution, particularly in nonco
46 ocusing on the genetic mechanisms that drive nectary development and shape nectary diversity.
47 that NEC3 transcript is expressed throughout nectary development as well as in other floral organs.
48 factor was robustly expressed at Stage 12 of nectary development but was only weakly expressed in the
49 to CRABS CLAW, a gene involved in carpel and nectary development in Arabidopsis.
50 ral core eudicot species and is required for nectary development in both rosids and asterids, two maj
51 the relative importance of nectar volume and nectary development in defining Penstemon pollination sy
52 the only alternative loci for the control of nectary development in flowering plants, providing a cri
53 novel recruitment of STY homologs to control nectary development is likely to have occurred before th
54  it may have been co-opted as a regulator of nectary development within the eudicots, concomitant wit
55 tion and is strongly regulated during normal nectary development, we examined the accumulation of sta
56 s that have previously been shown to control nectary development.
57 nes revealed that they function in style and nectary development.
58                    Since in Arabidopsis, the nectary develops only at the base of stamens, its specif
59  to five persistent calyx lobes, a prominent nectary disk, persistent stamens, a semi-inferior ovary
60 sms that drive nectary development and shape nectary diversity.
61     Hypoxia-related processes are induced in nectaries during secretion, including lactic acid and et
62 , such as sugars, are synthesized within the nectary during secretion from both pre-stored and direct
63                   Passion flower extrafloral nectaries (EFNs) protrude from leaves and facilitate mut
64 es in which species have evolved extrafloral nectaries (EFNs), sugar-secreting organs that recruit ar
65                Here we report that PIN6 is a nectary-enriched gene whose expression level is positive
66                                          The nectary enzyme complex was distinct by migration on gels
67 vide a macroevolutionary framework of floral nectary evolution, focusing on the genetic mechanisms th
68 and removed nectar from their unique tubular nectary extensions.
69 pression is not sufficient to induce ectopic nectary formation.
70 We investigated the genetic basis of diverse nectary forms in eudicot angiosperm species using CRABS
71 on is conserved in morphologically different nectaries from several core eudicot species and is requi
72 N6 is required for proper auxin response and nectary function in Arabidopsis.
73 out the role(s) of nitrogen (N) compounds in nectary function.
74 thesis, it is most strongly expressed in the nectary gland after fertilization, indicating that inhib
75 ec5 expression is limited exclusively to the nectary gland during late stages of floral development.
76            While CRABS CLAW is essential for nectary gland formation, its ectopic expression is not s
77                                  Even though nectary glands arise from cells previously expressing th
78 of floral organ order in angiosperm flowers, nectary glands can be found in various floral and extraf
79                                       Floral nectaries have evolved many times independently, feature
80 i) has greatly reduced CWINV activity in the nectaries; (ii) produces a sucrose-rich nectar; but (iii
81  using CRABS CLAW (CRC), a gene required for nectaries in Arabidopsis.
82 nalyses in eudicots, we propose that diverse nectaries in core eudicots share conserved CRC gene regu
83                                        While nectaries in flowering plants evolved steadily through t
84 metabolism in Cucurbita pepo (squash) floral nectaries in order to understand how various N-containin
85 pecifically required for cell elongation and nectary maturation in the Aquilegia petal spur.
86 that MYB305 may also function in the tobacco nectary maturation program by controlling the expression
87 of terpenes, their production in stigmas and nectaries may serve to inhibit microbial infection at th
88 he expression of NOX1, a putative gene for a nectary NADPH oxidase that was cloned from nectaries and
89 2.26 kb fragment promoter, expressing GUS in nectaries, nodes, short style and in guard cells of the
90 nd that BrCWINV4A is highly expressed in the nectaries of Brassica rapa.
91                                          The nectaries of myb305 plants show juvenile character at la
92                                        Thus, nectaries of Ptr and Ptt seem to answer the same threat
93 se pyrophosphorylase (small subunit) gene in nectaries of the myb305 plants during the starch biosynt
94 e examined the accumulation of starch in the nectaries of the myb305 plants.
95 s concentrated expression in the presumptive nectary of the growing spur tip, and triple gene silenci
96            Reward secretions from the dorsal nectary organ (DNO) of Narathura japonica caterpillars f
97                       Here, we discover that nectaries originated in ferns and flowering plants concu
98 issues showed abundant expression: secreting nectaries, ovules early in development, and a set of sub
99 model in which sucrose is synthesized in the nectary parenchyma and subsequently secreted into the ex
100      Our results demonstrate that changes to nectary patterning are an important contributor to polli
101     Superoxide production was localized near nectary pores and inhibited by diphenylene iodonium but
102 Considering the phylogenetic distribution of nectary positions and CRC expression analyses in eudicot
103                        Owing to diversity in nectary positions and structures, they are thought to ha
104 served CRC gene regulation, and that derived nectary positions in eudicots have altered regulation of
105                                      In Ptt, nectaries represent constitutive organs with continuous
106 ew, we summarize the recent breakthroughs in nectary research and provide a macroevolutionary framewo
107                   The timing suggests oriole nectary-robbery may be a potent selection agent for an e
108 ignal in lateral nectaries, but pin6 lateral nectaries showed little or no signal for these reporters
109 NA-seq analyses of pin6-2 and myb57-2 mutant nectaries showed little overlap in terms of differential
110 we assessed cellular-level processes shaping nectary size.
111           This cDNA was then used to probe a nectary specific cDNA library and a full-length NEC3 cDN
112 lysis in transgenic plants revealed that the nectary-specific expression is the result of multiple pr
113                 Here we identify SWEET9 as a nectary-specific sugar transporter in three eudicot spec
114 alose 6-P play important regulatory roles in nectary starch degradation and nectar secretion.
115 r nectar secretion in Arabidopsis, including nectary starch degradation, Suc synthesis, and Suc expor
116 have accelerated our understanding of floral nectary structures and the genetic circuits behind their
117  accumulated lower levels of starch in their nectaries than did wild-type plants.
118 st, however, is the occurrence of staminodal nectaries that have structural characters intermediate b
119                 Angiosperms developed floral nectaries that reward pollinating insects.
120 ian" bodies, and sugar-secreting extrafloral nectaries-the "swollen thorn syndrome." We show that thi
121 nvolved in carbohydrate metabolism in squash nectaries throughout floral maturation and the associate
122     The induction of N metabolism in C. pepo nectaries thus plays an important role in the synthesis
123 e expression of Nectarin I was restricted to nectary tissues and to a much lower level in the ovary.
124                                       In the nectary tissues of tobacco flowers a quantitative increa
125                           It is expressed in nectary tissues only while nectar is being actively secr
126 t leads to hydrogen peroxide accumulation in nectary tissues, nectaries were stained with nitroblue t
127 promoter significantly reduced expression in nectary tissues.
128 oral nectar is a sugary solution produced by nectaries to attract and reward pollinators.
129 idopsis multiple factors act to restrict the nectary to the flower, and surprisingly, some of these f
130                                         Both nectary types strongly differ in morphology, nectar comp
131                                          Two nectary types that evolved with Populus trichocarpa (Ptr
132 ot species, no evidence of CRC expression in nectaries was found.
133                             In contrast, Ptr nectaries were found to be holocrine and inducible.
134 en peroxide accumulation in nectary tissues, nectaries were stained with nitroblue tetrazolium.
135 is produced by specialized structures termed nectaries, which can be found on different plant organs.
136 that the construct was expressed uniquely in nectaries with a small level of expression in ovary.
137 udicots, concomitant with the association of nectaries with reproductive organs in derived lineages.
138 ers extends to the epidermis of the staminal nectaries with strict boundaries at the second and fourt

 
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