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1 owth and enhanced production of side shoots (tiller).
2 mes participate in systemic invasion of each tiller.
3 uptake and a higher proportion of productive tillers.
4 from the cob upon maturity, as well as fewer tillers.
5 RCS had greater benefit in plants with fewer tillers.
6 -type buds continue growing and develop into tillers.
7 by panicles until grain maturity, and apical tillers.
8 t diverts sucrose (Suc) away from developing tillers.
9  older leaves, younger leaves, and secondary tillers.
10 lates less Striga germination, and is highly tillered.
11 rhizomatous growth and with QTLs influencing tillering.
12 cription of OsTCP19, a negative modulator of tillering.
13 ly associated with increased germination and tillering.
14 tussock root necromass and density-dependent tillering.
15  SPL4 seriously suppressed bud formation and tillering.
16 ea and developing thicker roots and moderate tillering.
17 results in reduced chlorophyll and increased tillering.
18             We have identified a gene (Wheat Tiller-1, WT-1) that regulates numbers of these two very
19 020 and 2020-2021, respectively) and damaged tillers (3.4%) in CA-based practices.
20  Plants grown at phi values of 0.55 and 0.33 tillered 43 and 56%, less compared with plants grown at
21 cifically, DSR exhibited a greater number of tillers (635-650) and panicles (510-529) m(- 2), along w
22                                      Reduced tillering allowed testing the transgenic plants under hi
23                              Here, we mapped tiller and biomass QTLs with ~ 250 recombinant inbred li
24                          This suppression of tiller and lateral branch growth is an important trait s
25          Expression of the genes involved in tiller and leaf angle control was also affected in the m
26 ene via stable RNAi showed reduction in both tiller and spikelet number.
27                                              Tiller and spikelet numbers are important agronomic trai
28 : FA ratio, reduced plant stature, increased tillering and an approx. threefold increase in sugar rel
29 to a quantitative trait locus that regulates tillering and lateral branching in maize and shows evide
30 b1), a major domestication locus controlling tillering and lateral branching.
31                                              Tillering and plant biomass are key determinants of rice
32 seminal axile roots) and stem-borne tissues (tillers and coleoptile and leaf node axile roots) plus b
33 matic activity, showing reduced formation of tillers and internodes and extensive adventitious root/s
34        Furthermore, triple mutants have more tillers and leaves-phenotypes seen in Corngrass1 mutants
35          The transgenic plants produced more tillers and more seed than wild-type plants.
36 ield, mutants exhibited increased numbers of tillers and panicles.
37  host plant as assessed by immunoblotting of tillers and quantitative PCR.
38  similar to the wild type but produced fewer tillers and seeds.
39 f spikelet nodes per spike and produces more tillers and spikes, thereby enhancing grain yield in tra
40 rative genomics reveal that basal branching (tillering) and axillary branching are partially controll
41 hat stalk width, number of lateral branches (tillers), and branching of the inflorescence decline wit
42 evels of PPF resulted in more dry mass, more tillering, and a more advanced Haun stage.
43 ypes including very narrow leaves, increased tillering, and failure of the main shoot.
44 rait loci--qSLB1.1--for the exudation of SL, tillering, and induction of Striga germination was detec
45 pmental processes, including shoot-branching/tillering, and mediate rhizospheric interactions.
46 with respect to flowering, as well as short, tillering, and segregating for yellow kernel color.
47 ce similarity searches identified rice TAC1 (tiller angle control 1) as a putative ortholog, and we t
48                      Restoration of a normal tiller angle in fuct-1 by complementation demonstrated t
49                                              Tiller angle is an important determinant of plant archit
50 ncluding LAZY1, a key gene controlling plant tiller angle) were under selection during the mimicry pr
51 his weed in rice paddies has evolved a small tiller angle, allowing it to phenocopy cultivated rice a
52 d-type cv Kitaake, fuct-1 displayed a larger tiller angle, shorter internode and panicle lengths, and
53 duced gravitropic response and the increased tiller angle.
54 ead to less compact growth by increasing the tiller angle.
55 es indicated that the effects of OsbZIP49 on tiller angles are mediated through changes in shoot grav
56 enables nitrogen-induced stimulation of rice tillering: APETALA2-domain transcription factor NGR5 (NI
57                                              Tillers are vegetative branches that develop from axilla
58                                              Tillering at the vegetative stage is associated with wee
59  of tillering, leading to a larger number of tillers bearing fertile spikes, and increases in seed nu
60                    However, its asynchronous tillering behavior and fast growth rate helps recovering
61                                              Tillers, branches initiated at the base of grass plants,
62                                              Tillering (branching) is a major yield component and, th
63                             Active growth of tiller bud (TB) requires high amount of mineral nutrient
64 mulates root meristem cell proliferation and tiller bud formation and promotes photosynthetic efficie
65 ts showed that silencing of WT-1 reduced the tiller bud initiation.
66 illering in tin is due to early cessation of tiller bud outgrowth during the transition of the shoot
67 wn region showed that differentiation of the tiller buds and apical meristem into spikelets occurs du
68                                The growth of tiller buds in the first leaf axil of wild-type (100M, P
69  branching and the possibility of optimizing tillering by manipulating the timing of internode elonga
70 ant, which produces an exaggerated number of tillers compared to wild-type plants, is caused by a gai
71                               Shoot size and tillers correlated positively with roots with irrigation
72 t, dry matter accumulation, leaf area index, tiller count, SPAD (Soil Plant Analysis Development) val
73 ty and necromass bulk density and less so by tiller demography.
74  barley Uniculme4 (Cul4) locus cause reduced tillering, deregulation of the number of axillary buds i
75 s known about the molecular genetic bases of tiller development in important Triticeae crops such as
76 ile trying to understand the early events of tiller development in wheat, cross section analysis of t
77 s showed that the average mass of the rotary tiller device was 49.44 kg, while the required soil lift
78  and the soil throwing process of the rotary tiller device was simulated using the discrete element m
79 ich causes enhanced main shoot dominance and tiller dwarfism by an unknown mechanism.
80                                         This tillering effect was transferable between grass species,
81           Semi-dwarf rice varieties with low tiller formation but high seed production per panicle an
82                       Meanwhile, it promotes tiller formation by repressing the transcription of OsTC
83  as a key coordinator of nitrogen uptake and tiller formation in rice.
84 water-dependent water uptake and xylem flow; tiller formation; evapotranspiration; simultaneous simul
85 s studies have largely focused on basal bud (tiller) formation but scarcely touched on aerial buds, w
86 creased NGR5 activity consequently uncouples tillering from nitrogen regulation, boosting rice yield
87     Furthermore, the ba2 mutation suppresses tiller growth in the teosinte branched1 mutant, indicati
88 transcription factor NGR5 (NITROGEN-MEDIATED TILLER GROWTH RESPONSE 5) facilitates nitrogen-dependent
89                             Wheat emergence, tillering, growth, and biomass increased in wild type co
90 lopment, lateral root structure and density, tiller height and number, panicle and grain morphologies
91 cy, improved grain homogeneity and increased tillering in a vrs4 background, while with vrs5, decreas
92               Chlorophyll deficit suppressed tillering in multiple maize mutants, including teosinte
93 ting that SLs are not the sole regulators of tillering in response to N availability.
94  enables plants to modify shoot branching or tillering in response to varying light intensities and r
95                                  The reduced tillering in tin is due to early cessation of tiller bud
96 ogen promotes the formation of nonproductive tillers in rice, which decreases nitrogen use efficiency
97  caused by RGSV, such as dwarfing and excess tillering, in transgenic rice plants.
98 eaf Zn uptake (r = 0.60, P < 0.01) at active tillering, indicating dependence on remobilization for g
99 e characterize a reduced tillering (tin, for tiller inhibition) mutant of wheat (Triticum aestivum).
100                      Genetic manipulation of tillering is a major objective in breeding for improved
101                                              Tillering is inhibited in sorghum genotypes that lack ph
102                                     However, tillering is regulated by complex interactions of endoge
103 sed yield was controlled by a higher rate of tillering, leading to a larger number of tillers bearing
104  covering seven growth phases 'Crown Root', 'Tillering', 'Mid Vegetative', 'Booting', 'Heading', 'Ant
105  that tin represents a novel type of reduced tillering mutant associated with precocious internode el
106 erization of naturally occurring and induced tillering mutants in the major crops.
107 nstructed high-quality cell atlases for rice tiller nodes, rhizomes of wild rice and maize crown root
108 antitative trait loci (QTLs) associated with tiller number (qTN), root biomass (qRB), and shoot bioma
109  associated with major effects on leaf size, tiller number and ABA accumulation in wheat.
110  vrs4 background, while with vrs5, decreased tiller number and increased grain weight.
111 ion, showing role of the gene in controlling tiller number and spikelet number per spike.
112  surpassed a threshold height of 1.1 m, both tiller number and survival of S. scoparium plants were d
113                     An application to a rice tiller number data set is given.
114 i regulating ABA accumulation, leaf size and tiller number in the two crops is discussed.
115                                              Tiller number is one of the most important agronomic tra
116 2)(%), GCV, PCV, GA and GA% mean observed in tiller number per plant (23.81, 17.65, 5.71, 28, 30.86%)
117 ed from wheat resulted in uniculm and reduce tiller number phenotype.
118 nd the knowledge required to achieve optimal tiller number through genetic and agronomic means is sti
119 ught-induced ABA accumulation, leaf size and tiller number were compared between rice and wheat.
120 reased leaf greenness, reduction of leaf and tiller number, and affects yield parameters.
121 ants display shortened internodes, increased tiller number, and upright growth.
122 ed a reduction in spikelet number per spike, tiller number, and yield in the outdoor experiments.
123 e indica OsNR2 to confer increased effective tiller number, grain yield and NUE on japonica rice, eff
124    Plant growth parameters including height, tiller number, leaf area and biomass were generally high
125 inued to respond to N limitation by reducing tiller number, suggesting that SLs are not the sole regu
126 d growth, reduced grain yield, and increased tiller number.
127 ion is particularly related to a decrease in tiller numbers and by sterile spikelets in some cultivar
128  RNAi events, variation in both spikelet and tiller numbers correlated with the level of reduction in
129                                              Tiller numbers of S. scoparium plants were unaffected by
130 R109944 exhibited early flowering, increased tiller numbers, and increased susceptibility to R. solan
131  GID1-NGR5 interaction and explain increased tillering of green revolution varieties.
132 with distinct chromosome constitutions among tillers of the same plant and also between root and shoo
133 me rhizomes are similar to those that become tillers--one QTL appears to influence the number of such
134 olecular responses of the plant at advanced (tillering or reproductive) stage of growth.
135 e whether individual buds differentiate into tillers or rhizomes.
136                            However, leaf and tiller orientation and inclination characteristics were
137  the exception of the number of panicles and tillers per hill, low genetic advance was also found for
138  number of grains per panicle, and number of tillers per plant of hybrid rice (derived from recombina
139 orrelations were found between the number of tillers per plant, plant height, spike length, number of
140 ith more than three leaves at the end of the tillering period.
141              Despite exhibiting an increased tillering phenotype, Tad17 mutants continued to respond
142 ght, panicle and panicle base length, but no tillering phenotype.
143 lag hypothesis by measuring both short-term (tiller population growth rates) and long-term (17-year s
144 ions and a mass balance model coupled with a tiller population model.
145                                              Tillering produced up to 7000 heads per square meter at
146 ophyte infection increased plant biomass and tiller production by 10-15% in both treatments.
147 rogen uptake and the formation of productive tillers remains a long-standing challenge, yet how these
148 imal tussock size was primarily regulated by tiller root productivity and necromass bulk density and
149         Uniform growth of the main shoot and tillers significantly influences rice plant architecture
150                            Genotype leaf and tiller size, leaf lamina thickness, leaf mass per area (
151 ructure and working parameters of the rotary tiller soil throwing device, soil lifting device, track-
152 e plants overexpressing OsbZIP49 displayed a tiller-spreading phenotype with reduced plant height and
153 terregion and codingregion of Bt rice during tillering stage (cv. HH1 expressing fused Cry1Ab/Cry1Ac)
154  of iron plaque on rice roots at the maximum tillering stage and the mature stage were also determine
155 o' cross using data collected at the maximum tillering stage from two years of greenhouse study, and
156 tin architecture/epigenetic modifications at tillering stage of growth under phosphorus deficiency st
157 e methane emissions occur in June during the tillering stage of rice, decreasing toward ripening, ind
158 o decipher the strategies adopted by rice at tillering stage under P deficiency stress, a pair of con
159 (qRB), and shoot biomass (qSB) at the active tillering stage which occurs approximately 6 weeks after
160 , and qRB5-1 were significant at the maximum tillering stage while qTN3-2 was detected only at the ha
161  wheat crop (D(0): Control, D(1): Drought at tillering stage, and D(2): Drought at anthesis stage) an
162 n the lateral meristems generated vegetative tillers subtended by leaves instead of spikelets.
163 ping population was replicated using a split-tiller technique to control and better estimate the envi
164               Here we characterize a reduced tillering (tin, for tiller inhibition) mutant of wheat (
165 aacetic acid)-extractable soil Zn from early tillering to flowering.
166 eaths, and between the mainstem and axillary tillers) to model the dynamics of canopy development.
167 so inhibit shoot branching, Azucena is a low-tillering variety.
168 d by warming, but the number of reproductive tillers was increasingly suppressed by intensified droug
169 es dark green, semidwarf plants with reduced tillering, whereas RNA interference knockdown results in
170  area and leaf rank for the mainstem and its tillers, which was robust across a range of sowing dates
171 eat cultivars, early-maturing Scout and high-tillering Yitpi, under non-limiting water and nutrients

 
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