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1 of the Arabidopsis mutant rgr1 (reduced root gravitropism).
2 d plants with respect to the gravity vector (gravitropism).
3 bidopsis show reduced shoot phototropism and gravitropism.
4 Y) is required for normal root and hypocotyl gravitropism.
5 been proposed to be a major player in plant gravitropism.
6 ttle is understood about the early events of gravitropism.
7 enting amyloplasts function as statoliths in gravitropism.
8 enes previously implicated to be involved in gravitropism.
9 nes have not been previously associated with gravitropism.
10 t observed in aux1 mutants is a loss of root gravitropism.
11 nt is primary and Ca2+ movement secondary in gravitropism.
12 increased basipetal auxin transport impedes gravitropism.
13 n the early signaling pathways of maize stem gravitropism.
14 or examining the participation of calcium in gravitropism.
15 a model system for the response component of gravitropism.
16 and that DEZ cells play an important role in gravitropism.
17 eption and signal transduction components of gravitropism.
18 ssociated with light-induced changes in root gravitropism.
19 s these changes are also important in normal gravitropism.
20 lls curved away from the HGMF, comparable to gravitropism.
21 oot tropic responses must be antagonistic to gravitropism.
22 tid sedimentation, and have severely reduced gravitropism.
23 ells of story 2 contributed the most to root gravitropism.
24 diagravitropism or of an alteration in root gravitropism.
25 ng root formation, vascular development, and gravitropism.
26 a unique role for the N-terminus of GTRC in gravitropism.
27 ponent, whose loss-of-function enhances root gravitropism.
28 utated, reverses the direction of protonemal gravitropism.
29 , act as statoliths to facilitate downstream gravitropism.
30 f conserved wavelength in response linked to gravitropism.
31 d phototropism and light-regulated hypocotyl gravitropism.
32 's gravity field by a dynamic process called gravitropism.
33 iana root development, response to auxin and gravitropism.
34 anges in cell growth that contribute to root gravitropism.
35 , and mechanosensing in the control of plant gravitropism.
36 activating auxin biosynthesis in response to gravitropism.
37 natural variation in monocot and dicot root gravitropism.
38 ition of root growth and early phase of root gravitropism.
39 ate in the early gravity signaling for shoot gravitropism.
40 subcellular processes for phenomena such as gravitropism.
41 nditions previously found to be important to gravitropism.
42 enerated insight into functions of GLR3.3 in gravitropism.
43 a positive regulatory loop required for root gravitropism.
44 timulus response parameters such as onset of gravitropism.
45 t are required for normal root and hypocotyl gravitropism.
46 h-related tropisms, such as phototropism and gravitropism.
47 rowth but contributes surprisingly little to gravitropism.
48 is a modulator of root cap morphogenesis and gravitropism.
49 e in Arabidopsis (Arabidopsis thaliana) root gravitropism.
50 erscoring the link between endomembranes and gravitropism.
51 blished between endomembrane trafficking and gravitropism.
52 gp1-100 mutants also displayed enhanced root gravitropism.
53 in regulating polar auxin transport and root gravitropism.
54 f these were confirmed to inhibit or enhance gravitropism.
55 eton has been implicated in regulating plant gravitropism.
56 lyzed the hypergravity response in the shoot gravitropism 2 (sgr2) mutant, which exhibits neither a s
60 d that straightening is not a consequence of gravitropism, although gravity has some effect on the ph
63 l inhibitors of protein phosphatases on root gravitropism and basipetal auxin transport, as well as t
65 st that reduced PID kinase function inhibits gravitropism and basipetal indole-3-acetic acid transpor
70 t the mdr mutants display faster and greater gravitropism and enhanced phototropism instead of the im
71 s, and that RCN1 and EIN2 modulate hypocotyl gravitropism and ethylene responses through independent
73 ve strengths of negative phototropism and of gravitropism and how much phototropism affects gravitrop
74 is governed by nutrient gradients, positive gravitropism and hydrotropism, negative phototropism and
75 us chemicals and genetic backgrounds on both gravitropism and hydrotropism, to provide an up-to-date
80 ht-induced response is weak relative to both gravitropism and negative phototropism, we used a novel
81 in tuning root tropic responses by promoting gravitropism and negatively regulating hydrotropism.
86 y, each render TIR1 ineffective in mediating gravitropism and sustained auxin-induced root growth inh
87 ism-regulating factors function to attenuate gravitropism and the interplay between these various fac
88 escribed and demonstrated in the analysis of gravitropism and thigmomorphogenesis in corn seedlings (
89 s NPH4 is required for both phototropism and gravitropism and thus may function directly in the diffe
91 re presented, along with descriptions of how gravitropisms and reaction woods contribute to the survi
92 onses, including seed germination, hypocotyl gravitropism, and chlorophyll biosynthesis, by physicall
93 ion, increased adventitious rooting, no root gravitropism, and ectopic expression from the SAUR-AC1 p
95 opsis thaliana) has altered auxin transport, gravitropism, and ethylene response, providing an opport
96 ction of cotyledon opening, randomization of gravitropism, and gene regulation, were investigated in
97 ased chlorophyll accumulation, modulation of gravitropism, and induction of side branches in darkness
98 LAZY proteins are known as key regulators of gravitropism, and lazy mutants show striking gravitropic
99 ella cells of the root cap are important for gravitropism, and starchless mutants such as pgm1 displa
100 stimulate adventitious rooting, mediate root gravitropism, and stimulate transcription from the SAUR-
101 Basipetal indole-3-acetic acid transport and gravitropism are reduced in pid-9 seedlings, while acrop
102 -mediated root basipetal auxin transport and gravitropism, as well as auxin response in the root cent
104 functions in gravity signaling during shoot gravitropism, being a functional ortholog of rice LAZY1.
106 leton is proposed to play important roles in gravitropism, but the underlying mechanisms are obscure.
107 R2 is required for the PIN2 asymmetry during gravitropism by acting as a negative regulator of the ce
108 n of gravity but likely acts to downregulate gravitropism by continuously resetting the gravitropic-s
109 versial, is that auxins play a major role in gravitropism by controlling the rate of cell extension.
111 rter suggest that AUX1 is necessary for root gravitropism by facilitating basipetal auxin transport t
112 essments of the participation of ethylene in gravitropism by hypocotyls of tomato (Lycopersicon escul
114 Therefore, actin could function in root gravitropism by providing a mechanism to regulate the pr
116 ments suggest that the induction of positive gravitropism by red light involves a rise in cytoplasmic
117 y varying components of a conserved process (gravitropism) by making it feasible to conduct the same
118 Lycopersicon esculentum Mill.) indicate that gravitropism can occur without substantial change in eth
119 sitely oriented and LAZY-independent form of gravitropism causes the inflorescence stems of a lazy qu
120 AGRAVITROPIC 1 (AGR1) gene involved in root gravitropism confer increased root-growth sensitivity to
129 idopsis aux1 mutants, including altered root gravitropism, fewer lateral roots, shorter root hairs, a
130 s of knockout mutants demonstrated a role in gravitropism for four of the seven: CCT2 functions in ph
133 that individuals with extreme differences in gravitropism had more sterile crosses than individuals w
134 eption, response, and behavior), research on gravitropism has been dominated by different theories at
136 ildflower, Senecio lautus We find that shoot gravitropism has evolved multiple times in association w
140 p swing rate as a function of condition cast gravitropism in a multidimensional response space that p
143 auxin and (b) compare these patterns during gravitropism in control roots and roots pretreated with
148 cesses such as touch and hearing in animals, gravitropism in plants, and bacterial osmoregulation.
150 ondary site/mechanism of gravity sensing for gravitropism in roots, and the possibility that the earl
152 o the horizontal displayed distinct negative gravitropism in solutions of iodixanol with densities of
153 is study is comparable to earlier studies of gravitropism in starch-deficient mutants of higher plant
154 nstream of phytochromes to control hypocotyl gravitropism in the light and act early in phototropin s
159 rowth, lateral root formation, and timing of gravitropism, indicating that SHY2/IAA3 regulates multip
161 ontrols both shoot and root architecture.(1) Gravitropism is a dynamic process whereby gravistimulati
166 onal growth and morphogenesis in plants, and gravitropism is the process by which plants perceive and
169 of a rod-like organ and compared it with the gravitropism kinematics of different organs from 11 angi
170 iments with Brassica rapa verified that that gravitropism-like induction of curvature is possible in
171 and characterized a key RSA regulatory gene, GRAVITROPISM LOSS 1 (OsGLS1), in rice (Oryza sativa L.).
172 If so, pairs of orthologous genes affecting gravitropism may be present within the maize and Arabido
175 the ein2 mutation abrogates the accelerated gravitropism observed in rcn1 hypocotyls, indicating tha
176 uss the molecular mechanisms that govern the gravitropism of angiosperm roots, where a physical separ
178 se chemicals for compounds that affected the gravitropism of Arabidopsis seedlings positively or nega
180 The role of reactive oxygen species (ROS) in gravitropism of maize and Arabidopsis (Arabidopsis thali
182 lated-seedling growth by inhibiting negative gravitropism of the hypocotyls via modulating auxin home
185 default mechanism of downward growth, termed gravitropism, often functions to counteract hydrotropism
187 We have characterized auxin transport and gravitropism phenotypes of rcn1 hypocotyls and have expl
189 al growth responses, including phototropism, gravitropism, phytochrome-dependent hypocotyl curvature,
190 ochrome primarily responsible for inhibiting gravitropism, proving the utility of the mutant library.
196 tro, leads to a reduction in root growth and gravitropism, similar to the effects of synthetic auxin
197 lthough previous reports of Arabidopsis root gravitropism suggest latent periods of approximately 30
199 e, we show that adaptive divergence in shoot gravitropism, the ability of a plant's shoot to bend upw
204 t Ca2+ does not redistribute actively during gravitropism: the asymmetry arises because of its releas
205 s, we assessed the roles of AGB1 and XLG3 in gravitropism, thigmotropism and hormonal responses.
207 fied at three loci using this cold effect on gravitropism to screen for gravity persistence signal (g
208 tyl to the presence of obstacles, overriding gravitropism, to enable efficient circumnavigation throu
209 B), a potent actin-disrupting drug, on root gravitropism using various parameters that included deta
210 ted ethylene levels negatively regulate root gravitropism, using EIN2- and ETR1-dependent pathways, a
211 motor that determines the direction of plant gravitropism via mediating the asymmetric distribution o
216 wall pH mediates the initial stages of root gravitropism, we combined a novel cell wall pH sensor (a
217 To delineate the role of InsP3 in plant gravitropism, we generated Arabidopsis (Arabidopsis thal
218 ved genetic elements affecting seedling root gravitropism, we measured the process in a set of Zea ma
219 periods of illumination found to exaggerate gravitropism were 45 min of continuous illumination and
221 ed roots, and its developmental consequence (gravitropism), were inhibited by micromolar concentratio
222 abidopsis display altered root and hypocotyl gravitropism, whereas their inflorescence stems are full
224 t growth towards gravity in a process termed gravitropism, which is necessary for roots to grow into
226 to have altered auxin transport, growth, and gravitropism, while rcn1 hypocotyl elongation exhibited
227 PIN proteins, the lip5 roots showed abnormal gravitropism with an enhanced response within the first
228 rabidopsis thaliana alter root and hypocotyl gravitropism without affecting phototropism, root growth
229 s of PID activity alters auxin transport and gravitropism without causing an obvious change in cellul