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1 of the Arabidopsis mutant rgr1 (reduced root gravitropism).
2  been proposed to be a major player in plant gravitropism.
3 ttle is understood about the early events of gravitropism.
4 enting amyloplasts function as statoliths in gravitropism.
5 enes previously implicated to be involved in gravitropism.
6 nes have not been previously associated with gravitropism.
7 t observed in aux1 mutants is a loss of root gravitropism.
8 nt is primary and Ca2+ movement secondary in gravitropism.
9  increased basipetal auxin transport impedes gravitropism.
10 n the early signaling pathways of maize stem gravitropism.
11 or examining the participation of calcium in gravitropism.
12 a model system for the response component of gravitropism.
13 and that DEZ cells play an important role in gravitropism.
14 eption and signal transduction components of gravitropism.
15 ssociated with light-induced changes in root gravitropism.
16 s these changes are also important in normal gravitropism.
17 lls curved away from the HGMF, comparable to gravitropism.
18 tid sedimentation, and have severely reduced gravitropism.
19 ells of story 2 contributed the most to root gravitropism.
20  diagravitropism or of an alteration in root gravitropism.
21 ng root formation, vascular development, and gravitropism.
22 ate in the early gravity signaling for shoot gravitropism.
23  subcellular processes for phenomena such as gravitropism.
24 nditions previously found to be important to gravitropism.
25 enerated insight into functions of GLR3.3 in gravitropism.
26 a positive regulatory loop required for root gravitropism.
27 timulus response parameters such as onset of gravitropism.
28 t are required for normal root and hypocotyl gravitropism.
29 h-related tropisms, such as phototropism and gravitropism.
30 rowth but contributes surprisingly little to gravitropism.
31 is a modulator of root cap morphogenesis and gravitropism.
32 e in Arabidopsis (Arabidopsis thaliana) root gravitropism.
33 erscoring the link between endomembranes and gravitropism.
34 blished between endomembrane trafficking and gravitropism.
35 gp1-100 mutants also displayed enhanced root gravitropism.
36 in regulating polar auxin transport and root gravitropism.
37 f these were confirmed to inhibit or enhance gravitropism.
38 oot tropic responses must be antagonistic to gravitropism.
39 eton has been implicated in regulating plant gravitropism.
40 bidopsis show reduced shoot phototropism and gravitropism.
41 Y) is required for normal root and hypocotyl gravitropism.
42 lyzed the hypergravity response in the shoot gravitropism 2 (sgr2) mutant, which exhibits neither a s
43                                              Gravitropism allows plant organs to direct their growth
44                                              Gravitropism allows plant organs to guide their growth i
45 d that straightening is not a consequence of gravitropism, although gravity has some effect on the ph
46                 apm1 alleles show defects in gravitropism and auxin transport.
47 l inhibitors of protein phosphatases on root gravitropism and basipetal auxin transport, as well as t
48 es an auxin efflux component regulating root gravitropism and basipetal auxin transport.
49 st that reduced PID kinase function inhibits gravitropism and basipetal indole-3-acetic acid transpor
50 -L-methionine pathway in the control of root gravitropism and cap morphogenesis.
51  of the moss Ceratodon purpureus show upward gravitropism and contain amyloplasts that sediment.
52 t the mdr mutants display faster and greater gravitropism and enhanced phototropism instead of the im
53 s, and that RCN1 and EIN2 modulate hypocotyl gravitropism and ethylene responses through independent
54  for dissecting endomembrane trafficking and gravitropism and for cognate target identification.
55 ve strengths of negative phototropism and of gravitropism and how much phototropism affects gravitrop
56  is governed by nutrient gradients, positive gravitropism and hydrotropism, negative phototropism and
57 tional regulation during the early stages of gravitropism and mechanical stimulation.
58 ht-induced response is weak relative to both gravitropism and negative phototropism, we used a novel
59 in tuning root tropic responses by promoting gravitropism and negatively regulating hydrotropism.
60 d ARL2, behave similarly to the wild type in gravitropism and other related assays.
61                      The interaction between gravitropism and phototropism results in an alignment of
62                   Land plants rely mainly on gravitropism and phototropism to control their posture a
63 escribed and demonstrated in the analysis of gravitropism and thigmomorphogenesis in corn seedlings (
64 s NPH4 is required for both phototropism and gravitropism and thus may function directly in the diffe
65                       The chemicals affected gravitropism and vacuole morphology in concert in a tiss
66 re presented, along with descriptions of how gravitropisms and reaction woods contribute to the survi
67 ion, increased adventitious rooting, no root gravitropism, and ectopic expression from the SAUR-AC1 p
68 nhibitors of basipetal root auxin transport, gravitropism, and elongation growth.
69 opsis thaliana) has altered auxin transport, gravitropism, and ethylene response, providing an opport
70 ction of cotyledon opening, randomization of gravitropism, and gene regulation, were investigated in
71 ased chlorophyll accumulation, modulation of gravitropism, and induction of side branches in darkness
72 ella cells of the root cap are important for gravitropism, and starchless mutants such as pgm1 displa
73 stimulate adventitious rooting, mediate root gravitropism, and stimulate transcription from the SAUR-
74 Basipetal indole-3-acetic acid transport and gravitropism are reduced in pid-9 seedlings, while acrop
75 -mediated root basipetal auxin transport and gravitropism, as well as auxin response in the root cent
76 abnormal amyloplast distribution and reduced gravitropism at 1 g.
77  functions in gravity signaling during shoot gravitropism, being a functional ortholog of rice LAZY1.
78                 Blue light also affects root gravitropism but the sensitivity of roots to blue is 50
79 n of gravity but likely acts to downregulate gravitropism by continuously resetting the gravitropic-s
80 versial, is that auxins play a major role in gravitropism by controlling the rate of cell extension.
81  concentration-dependent modulation of shoot gravitropism by ethylene.
82 rter suggest that AUX1 is necessary for root gravitropism by facilitating basipetal auxin transport t
83 essments of the participation of ethylene in gravitropism by hypocotyls of tomato (Lycopersicon escul
84                        The onset of positive gravitropism by lateral roots is positively correlated w
85      Therefore, actin could function in root gravitropism by providing a mechanism to regulate the pr
86 e consistent with a reciprocal regulation of gravitropism by RCN1 and PID.
87 ments suggest that the induction of positive gravitropism by red light involves a rise in cytoplasmic
88 Lycopersicon esculentum Mill.) indicate that gravitropism can occur without substantial change in eth
89  AGRAVITROPIC 1 (AGR1) gene involved in root gravitropism confer increased root-growth sensitivity to
90                                          The gravitropism defective 2 (grv2) mutants of Arabidopsis s
91                                          The gravitropism defective 2 (grv2) mutants of Arabidopsis t
92                   The root morphogenesis and gravitropism defects of adk1-1 are accompanied by altere
93 rabidopsis thaliana) gene ETHYLENE-DEPENDENT GRAVITROPISM DEFICIENT AND YELLOW-GREEN1.
94                       Here we show that root gravitropism depends on the novel protein, NEGATIVE GRAV
95                       This resulted in rapid gravitropism even though the elongation rate of the root
96 nting for phototropism in the design of root gravitropism experiments in Arabidopsis.
97 idopsis aux1 mutants, including altered root gravitropism, fewer lateral roots, shorter root hairs, a
98                                Although root gravitropism has been studied extensively, no conclusive
99 rhizoids are impaired in the early stages of gravitropism (i.e. gravity perception).
100                                     However, gravitropism improved dramatically when NS458 seedlings
101 p swing rate as a function of condition cast gravitropism in a multidimensional response space that p
102 at basipetally transported IAA controls root gravitropism in Arabidopsis.
103 impaired lateral root formation and abnormal gravitropism in both hypocotyl and root.
104  auxin and (b) compare these patterns during gravitropism in control roots and roots pretreated with
105                                              Gravitropism in dark-grown hypocotyls of the wild type w
106 with Latrunculin B (Lat B) strongly promoted gravitropism in maize roots.
107 l analysis of plasticity in general and root gravitropism in particular.
108 cesses such as touch and hearing in animals, gravitropism in plants, and bacterial osmoregulation.
109       The red light requirement for positive gravitropism in roots of corn (Zea mays cv "Merit") prov
110 ondary site/mechanism of gravity sensing for gravitropism in roots, and the possibility that the earl
111 fect both inflorescence development and root gravitropism in S. viridis.
112 o the horizontal displayed distinct negative gravitropism in solutions of iodixanol with densities of
113 is study is comparable to earlier studies of gravitropism in starch-deficient mutants of higher plant
114                       We propose a model for gravitropism in the woody stem in which the peripheral l
115 e kinetics of the light requirement for root gravitropism in this cultivar.
116                                Plasticity of gravitropism in wild-type Arabidopsis (Arabidopsis thali
117                                         Root gravitropism in wild-type Arabidopsis and in two starchl
118 rowth, lateral root formation, and timing of gravitropism, indicating that SHY2/IAA3 regulates multip
119                        Maize (Zea mays) stem gravitropism involves differential elongation of cells w
120  ATP gradient in auxin export and plant root gravitropism is discussed.
121                                 The study of gravitropism is hindered by the fact that as a root resp
122  phosphoinositide signaling pathway in plant gravitropism is not well understood.
123                                    In roots, gravitropism is the predominant tropistic response, but
124                                        Shoot gravitropism is triggered when statocysts sense the loca
125            Conversely, hydrotropism, but not gravitropism, is inhibited by preventing differential ce
126 of a rod-like organ and compared it with the gravitropism kinematics of different organs from 11 angi
127                                Time-resolved gravitropism measurements of atlazy1 hypocotyls and prim
128 be due at least in part to a reversal in the gravitropism mechanism.
129  the ein2 mutation abrogates the accelerated gravitropism observed in rcn1 hypocotyls, indicating tha
130 uss the molecular mechanisms that govern the gravitropism of angiosperm roots, where a physical separ
131 imilar to those found inside cells can block gravitropism of Arabidopsis roots.
132 se chemicals for compounds that affected the gravitropism of Arabidopsis seedlings positively or nega
133                 Here, we report that in root gravitropism of Arabidopsis thaliana, auxin regulates ro
134 The role of reactive oxygen species (ROS) in gravitropism of maize and Arabidopsis (Arabidopsis thali
135             Red light-induced changes in the gravitropism of roots of Zea mays variety Merit is a ver
136 lated-seedling growth by inhibiting negative gravitropism of the hypocotyls via modulating auxin home
137 ental traits, such as epidermal twisting and gravitropism of the root.
138 rong contractile force resulting in negative gravitropism of the stem.
139 en media denser than the cell should prevent gravitropism or reverse its direction.
140    We have characterized auxin transport and gravitropism phenotypes of rcn1 hypocotyls and have expl
141 onses of the roots to the environment (e.g., gravitropism, phototropism, and thigmotropism).
142 al growth responses, including phototropism, gravitropism, phytochrome-dependent hypocotyl curvature,
143                             Phototropism and gravitropism represent adaptive growth responses induced
144 , loss of NGR reverses the direction of root gravitropism, resulting in roots growing upward.
145 g1-2 double mutant roots display kinetics of gravitropism similar to those of single mutants.
146 tro, leads to a reduction in root growth and gravitropism, similar to the effects of synthetic auxin
147 lthough previous reports of Arabidopsis root gravitropism suggest latent periods of approximately 30
148              The tt4(2YY6) roots had delayed gravitropism that was chemically complemented with a fla
149                                              Gravitropism, the bending of plants in response to gravi
150         In addition, unlike its role in root gravitropism, the elongation zone performs a dual functi
151                                              Gravitropism, the slow reorientation of plant growth in
152 t Ca2+ does not redistribute actively during gravitropism: the asymmetry arises because of its releas
153 s, we assessed the roles of AGB1 and XLG3 in gravitropism, thigmotropism and hormonal responses.
154                                     For root gravitropism to occur, AUX1 and PIN2 must transport auxi
155 fied at three loci using this cold effect on gravitropism to screen for gravity persistence signal (g
156 tyl to the presence of obstacles, overriding gravitropism, to enable efficient circumnavigation throu
157  B), a potent actin-disrupting drug, on root gravitropism using various parameters that included deta
158 ted ethylene levels negatively regulate root gravitropism, using EIN2- and ETR1-dependent pathways, a
159 grew as straight as the wild type, but their gravitropism was enhanced.
160 However, upon 90 degrees reorientation, mdr1 gravitropism was inseparable from the wild type.
161                                         Root gravitropism was selected as the process to study with h
162                                              Gravitropism was stronger than phototropism in some but
163  wall pH mediates the initial stages of root gravitropism, we combined a novel cell wall pH sensor (a
164      To delineate the role of InsP3 in plant gravitropism, we generated Arabidopsis (Arabidopsis thal
165  periods of illumination found to exaggerate gravitropism were 45 min of continuous illumination and
166 icroM NPA, hypocotyl and root elongation and gravitropism were strongly inhibited.
167 ed roots, and its developmental consequence (gravitropism), were inhibited by micromolar concentratio
168 abidopsis display altered root and hypocotyl gravitropism, whereas their inflorescence stems are full
169               Both molecules do disrupt root gravitropism, which is a developmental process requiring
170 t growth towards gravity in a process termed gravitropism, which is necessary for roots to grow into
171 on inhibitor diphenylene iodonium attenuated gravitropism while enhancing hydrotropism.
172 to have altered auxin transport, growth, and gravitropism, while rcn1 hypocotyl elongation exhibited
173 PIN proteins, the lip5 roots showed abnormal gravitropism with an enhanced response within the first
174 rabidopsis thaliana alter root and hypocotyl gravitropism without affecting phototropism, root growth
175 s of PID activity alters auxin transport and gravitropism without causing an obvious change in cellul

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