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1 t mediate some of the cell responses to this plant hormone.
2 ABA biosynthesis and also responses to this plant hormone.
3 oculation with V. dahliae and application of plant hormone.
4 nt-kaurene as a precursor to the gibberellin plant hormones.
5 by altering chemical defenses via changes in plant hormones.
6 ene, the olefin precursor to the gibberellin plant hormones.
7 results suggest this is driven by changes in plant hormones.
8 ts, which includes the important gibberellin plant hormones.
9 sm, carbon fixation, and the biosynthesis of plant hormones.
10 related collection of small molecules called plant hormones.
11 es, utilisation of nitrogen and synthesis of plant hormones.
12 ransport, perception and signalling of major plant hormones.
13 to tryptophan and the storage forms of auxin plant hormones.
14 mplex network of interactions among multiple plant hormones.
15 ronmental signals transduced by a variety of plant hormones.
28 hat ios1-1 plants were hypersensitive to the plant hormone abscisic acid (ABA), displaying enhanced A
31 nducible transcription factor regulating the plant hormone abscisic acid (ABA)-independent drought re
34 xidases required for the biosynthesis of the plant hormones abscisic acid (ABA) and indole-acetic aci
36 es in redox signaling, retrograde signaling, plant hormone action, programmed cell death, and defense
37 ly act as critical prereceptor modulators of plant hormone action; however, the molecular basis for t
38 ic acid, and these differential responses of plant hormones affect specific secondary chemical pathwa
39 using these simple principles to study other plant hormone and small molecule responses in temporally
44 ve shed light on how BRs interact with other plant hormones and environmental cues to shape the growt
45 olling the biosynthesis and modifications of plant hormones and how these enzymes contribute to the n
46 sts convened in Keystone, Colorado, for the "Plant Hormones and Signaling" symposium, which was organ
48 into branches is regulated systemically via plant hormones and the demand of growing shoot tips for
49 and enlarged SAM, including those related to plant hormones and those involved in cell wall developme
51 t into the interaction between these two key plant hormones, and suggest that endogenous ethylene dir
56 A relatively recently discovered class of plant hormones are the strigolactones; strigolactones in
61 lled by a positive feedback loop between the plant hormone auxin and its efflux carrier PIN-FORMED1 (
62 s mediated by an asymmetric signaling of the plant hormone auxin between the upper and lower side of
65 fferentiation and concentration peaks of the plant hormone auxin direct organ initiation and mediate
67 ane proteins, which facilitate efflux of the plant hormone auxin from cells, is important for plants
69 d, recently, the morphogenic activity of the plant hormone auxin has been found to mediate patterning
73 This study also demonstrated the role of plant hormone auxin in determining the Au induced root s
86 employment of OEIPs for the delivery of the plant hormone auxin to induce differential concentration
89 m, with cell-type-specific production of the plant hormone auxin, and identifies a downstream compone
106 ifferences in the concentrations of selected plant hormones (auxins, cytokinins, abscisic acid and ja
107 a lack of technology that precisely delivers plant hormones, based on cyclic alkanes or aromatic stru
110 ts protein-coding genes that are involved in plant hormone biosynthesis and signaling pathways, inclu
114 imary and specialized metabolites, including plant hormones, cofactors, defense compounds, and attrac
115 imary and specialized metabolites, including plant hormones, cofactors, defense compounds, and attrac
119 We find that localized perception of the plant hormone cytokinin establishes a spatial domain in
126 s have recognized that varying ratios of the plant hormones cytokinin and auxin induce plant cells to
127 s on the roles they play in signaling by the plant hormones cytokinin and ethylene, in phytochrome-me
129 t brassinosteroids (BRs), a class of natural plant hormones, decreased residues of common organophosp
130 des modulate biological pathways involved in plant hormone, defense, cell signaling, cytoskeleton and
131 caused changes in the homeostasis of several plant hormones especially auxin and the ethylene precurs
132 ied major roles in pathogen response for the plant hormone ethylene and the secondary metabolite 4-me
135 hanges in response to elevated levels of the plant hormone ethylene in roots from light-grown Arabido
140 to identify mechanisms by which the gaseous plant hormone ethylene reduces lateral root formation an
142 mming of epidermal cell fate by the volatile plant hormone ethylene requires two signals: mechanosens
143 ogen-fixation in legumes is regulated by the plant hormone ethylene, but it has remained unclear whet
144 ipening of tomato fruits is triggered by the plant hormone ethylene, but its effect is restricted by
156 a proof of concept, we demonstrate that the plant hormone gibberellic acid induces a spatial gradien
158 echanistic link between the growth-promoting plant hormone gibberellin and cortical microtubule organ
159 Both efficient carbon metabolism and the plant hormone gibberellin are required to guarantee opti
160 cinerea and salt stress but repressed by the plant hormone gibberellin, indicating a complex regulati
162 cid), ranging in complexity from methanol to plant hormones (gibberellins, containing eight stereocen
163 During the last 15 years the number of known plant hormones has grown from five to at least ten.
168 trategy is effector-mediated manipulation of plant hormone homeostasis, which leads to the suppressio
169 ls of any of the UBA2 transcripts, and other plant hormones implicated in wound responses, ethylene a
171 method provides quantification of most major plant hormones in a single run from 50 mg of fresh plant
172 regulator of development and is unique among plant hormones in that its function requires polarized t
174 nd developmental signals, often mediated via plant hormones, including auxin, strigolactone and cytok
175 isms of karrikins, strigolactones, and other plant hormones, including auxins, jasmonates, and gibber
176 are bacterial Nod Factors (NFs) and several plant hormones, including cytokinins (CKs) and gibberell
177 wever, the spatial distribution of the other plant hormones, including gibberellic acid (GA), is larg
182 ally, CaMYB31 expression was affected by the plant hormones indoleacetic acid, jasmonic acid, salicyl
186 were recently rediscovered as a new class of plant hormones involved in the control of shoot branchin
189 thesis and perception mutants show that this plant hormone is not only required for male fertility bu
197 rticular, recent studies have identified the plant hormone jasmonate (JA) receptor as one of the comm
200 co-chaperone SGT1b impairs responses to the plant hormones jasmonate, auxin and gibberellic acid, bu
201 , we report a previously unknown role of the plant hormone jasmonic acid (JA) in determining rice (Or
202 mutants, exhibit reduced sensitivity to the plant hormone jasmonic acid (JA) in JA-dependent root in
204 produces coronatine, a toxin that mimics the plant hormone jasmonic acid isoleucine and promotes open
206 al of which have been shown to adenylate the plant hormones jasmonic acid, indole acetic acid and sal
209 sis, profound and multifarious modulation of plant hormone levels, and of chromatin structure, transc
210 structurally resembling tryptophan and auxin plant hormones; <1% remained as parent compound.
212 ults suggest that the homeostasis of various plant hormones might be altered in 35S::XERICO plants, p
214 This revealed changes in the responses to plant hormones, most notably auxin, strigolactone, gibbe
215 utants in brassinosteroids (BRs), a class of plant hormones necessary for normal plant growth and the
217 s production and insect control by releasing plant hormones or sugar esters from their conjugates sto
218 ablishing this pattern, as well as roles for plant hormones, particularly auxin, in the earliest step
220 nterferes with normal functioning of several plant hormone pathways and alters transcriptional regula
221 proteins were implicated in light reaction, plant hormone pathways and cell-wall-related metabolism,
222 ve model showing the role and interaction of plant hormone pathways in defense of this monocot crop a
223 wn that pathogens exert extensive effects on plant hormone pathways not only to defeat immunity, but
234 lant hormones quantitatively is important as plant hormones regulate plant growth, development and re
242 Abscisic acid (ABA) is one of the central plant hormones, responsible for controlling both maturat
246 been shown to function as a receptor of the plant hormone salicylic acid and to mediate proteosomal
250 ranscription factor is induced by pathogens, plant hormones, salinity and oxidative stress, suggestin
253 l evidence for KEG as an important factor in plant hormone signaling and a positive regulator of JAZ1
254 nscriptional activation of genes involved in plant hormone signaling and synthesis, removal of reacti
256 eeding of citrate to mutants with defects in plant hormone signaling pathways did not completely abol
257 remodeling factors, notably expansins, while plant hormone signaling pathways maintain remarkable hom
258 remodeling factors, notably expansins, while plant hormone signaling pathways maintain remarkable hom
260 urthermore, many of the proteins involved in plant hormone signalling pathways have been identified,
263 in the Orobanchaceae germinate after sensing plant hormones, strigolactones, exuded from host roots.
265 stem for studying the interplay of light and plant hormones, such as brassinosteroids (BRs), in the r
266 unctional drug aspirin, but also serves as a plant hormone that affects diverse processes during grow
277 of indole-3-acetic acid (IAA), a ubiquitous plant hormone that signals bacterial stress-tolerance an
280 Gibberellins are a class of tetracyclic plant hormones that are well known to promote plant grow
284 Brassinosteroids (BRs) are growth-promoting plant hormones that play a role in abiotic stress respon
293 Strigolactones (SLs) are carotenoid-derived plant hormones that regulate shoot branching, secondary
297 The prominent pathways in this network are plant hormone transduction, starch and sucrose metabolis
299 ns are found in smoke and strigolactones are plant hormones, yet both molecules are likely recognized
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