ライフサイエンスコーパス: plant height

1 and a premature stop codon, leading to short plant height.

2 s in mean specific leaf area, shoot mass and plant height.

3 s tremula x P. alba achieved up to a 200% in plant height.

4 elopment, and also affect flowering time and plant height.

5 ficant effect on leaf number, leaf area, and plant height.

6 ID1B could play a major role in reducing the plant height.

7 e and latitude, including dispersal mode and plant height.

8 lting in accumulation of STF1/2, and reduced plant height.

9 onships between vessel diameter, climate and plant height.

10 cy for traits with high heritability such as plant height.

11 ability to change hydraulic properties with plant height.

12 resulted in a significant increase in mutant plant height.

13 coupled meristem and inflorescence size from plant height.

14 ly associated with number of records, as was plant height.

15 y the vey1 (Mo17) allele resulted in reduced plant height.

16 ORICAULA of Antirrhinum, was associated with plant height.

17 tative variation of maize flowering time and plant height.

18 ely, without delaying maturity or increasing plant height.

19 days to 50% flowering (68.3-126.3 days), and plant height (128.9-298.3 cm) were among traits that exh

20 at SMH-2 chalked up utmost values in growth (plant height 189.4 cm) and periodic leaf area index and

21 enhanced various growth parameters, such as plant height (3.22%, 6.58%), shoot fresh weight (17.4%,

22 ve and reproductive parameters, particularly plant height (32-58%), flower and siliques dimensions, a

23 Drought stress significantly reduced plant height (34.24%), 1000-grain weight (49.05%), and p

24 tress in shoot biomass (60.20%), followed by plant height (42.40%), root biomass (31.50%), while as l

25 erved in key morphological traits, including plant height (98.3-143.3 cm), days to 50% flowering (50.

26 We measured functional traits, including plant height, absolute and specific leaf area, leaf dry

27 between vessel diameter, climate and maximum plant height across angiosperm species with different pi

28 arger changes in vessel diameter and maximum plant height across climates for species with vestures a

29 daptive syndrome including excessive ear and plant heights along with later flowering; this was reduc

30 reased photosynthesis, and up to 35% greater plant height and 88% biomass in poplar accessions under

31 except bentazon, which caused a 28% drop in plant height and a 29% decrease in total biomass compare

32 Stem internode growth impacts plant height and biomass accumulation and is regulated b

33 Plant height and canopy width under the AVS were not sig

34 For the experimental study, lettuce growth (plant height and canopy width) and yields (fresh and dry

35 Reduced plant height and culm robustness are quantitative charac

36 f dispersal structures, dispersal investment plant height and dispersal distance.

37 ay explain the positive relationship between plant height and dispersal distance.

38 lking dates in unrelated B73 and Oh43 lines; plant height and ear height in unrelated Oh43 and PH207

39 ent-independent for grain yield, ear height, plant height and ear leaf area and largely environment d

40 ade avoidance responses, including increased plant height and enhanced apical dominance.

41 letted phenotype with pleiotropic effects on plant height and fertility.

42 Parallelly, molecular links between plant height and flowering time have been explored.

43 the number of fruits per plant, followed by plant height and fruit weight, suggesting substantial ge

44 + M-CTT-33 and E-AGG + M-CGT-22 markers with plant height and glucomannan content.

45 gle nucleotide polymorphisms associated with plant height and growth rate at different parts of the g

46 GRAIN NUMBER, PLANT HEIGHT AND HEADING DATE 7 (SbGhd7) is one of the s

47 ion factor (Ghd8) that control grain number, plant height and heading date in rice.

48 i plants of TaABCB1 gene resulted in reduced plant height and increased seed width.

49 ed a tiller-spreading phenotype with reduced plant height and internode lengths.

50 e genetic and molecular mechanisms governing plant height and its correlation with yield and yield co

51 steroids (BRs) play a key role in regulating plant height and leaf angle in plants.

52 ow vessel diameter related to wood porosity, plant height and leaf length.

53 Reduced growth rate as measured by plant height and leaf number was consistent with the DHA

54 stem branching, rosette branching, and final plant height and observed several strong positive and ne

55 and direct measurements were used to monitor plant height and photosynthetic activity.

56 ic root length) and the plant size gradient (plant height and rooting depth).

57 erexpression of AtDJ-1C and AtDJ-1E improved plant height and rosette formation under physiological c

58 tern is driven mainly by specific leaf area, plant height and seed mass, followed by genome size.

59 Thiamethoxam-treated seedlings had greater plant height and shoot fresh mass compared to clothianid

60 fzt plants have dramatically reduced plant height and shorter, narrower leaves with leaf pola

61 eight, suggesting close associations between plant height and spike-related traits.

62 e evaluated for their accuracy in estimating plant height and stem diameter.

63 eral novel putative genomic associations for plant height and tannin content, which were not identifi

64 a GWAS found loci associated with changes in plant height and the amount of damaged tissue under stre

65 dopsis thaliana included a reduction in both plant height and tracheary element length and an increas

66 an those of simple traits (anthesis date and plant height) and prediction accuracy under stress condi

67 orrelated significantly with lignin content, plant height, and dry matter yield, suggesting that meta

68 ecophysiological traits and flowering time, plant height, and ecological guild were examined.

69 ress reduced shoot fresh weight, dry weight, plant height, and flag leaf length by 77%, 73%, 25%, and

70 In -mtlD plants, fresh weight, dry weight, plant height, and flag leaf length were reduced by 70%,

71 s based on multi-environment FHB resistance, plant height, and maturity phenotypic data was conducted

72 uated except days to flowering and maturity, plant height, and number of unfilled grains.

73 lant strategy variation (specific leaf area, plant height, and seed mass) in tree assemblages spannin

74 nd tenacity, rachis fragility, spike length, plant height, and spike emergence time.

75 to squamosa mutants regarding heading time, plant height, and spikelets per spike, but it exhibited

76 ative water content, leaf area, root length, plant height, and total fresh, and dry weights.

77 ing photoperiod responses in flowering time, plant height, and total leaf number.

78 e it is a known regulator of flowering time, plant height, and trichome development.

79 f predictions for grain yield, heading date, plant height, and yield components in soft red winter wh

80 er, specific root length, rooting depth, and plant height are drivers in Doma.

81 dry matter content, specific root length and plant height are the drivers in Akwanga.

82 ibution, Leaf area, Specific root length and plant height are the drivers in Lafia.

83 With plant height as a covariate, vegetative biomass of ASP a

84 ent and vigor, delayed flowering and reduced plant height at maturity.

85 le variance explained for biomass (7.6%) and plant height (average of 3.1% across all stages).

86 ts affecting seed coat roughness and colour, plant height, axil ring pigmentation, leaflet number and

87 sistance in the phloem scales inversely with plant height because of a shift in sieve element structu

88 ental modulation of overall plant growth and plant height better for understanding genotypic modulati

89 s evolved multiple times in association with plant height between adjacent populations inhabiting con

90 ee distinct BjuGy type subunits, to regulate plant height (BjuGByA2 and BjuGByC), seed weight (BjuGBG

91 n the means for leaf number, flowering time, plant height, branching and growth rate; across-treatmen

92 positively correlated to stalk diameter and plant height, but negatively correlated to moisture cont

93 Plant height can be an indicator of plant health across

94 and correlation between vessel diameter and plant height can obscure the mechanisms linking vessel d

95 GWAS maps several classical loci for plant height, candidate genes for inflorescence architec

96 Maize growth was evaluated by measuring plant height, chlorophyll concentration, and biomass acc

97 ed genome-wide association studies (GWAS) on plant height components and inflorescence architecture.

98 gth OsbZIP48 in rice transgenics reduced the plant height considerably.

99 c plasticity via the reanalysis of published plant height data involving 3502 recombinant inbred line

100 To assess variation throughout development, plant height data was collected from planting until term

101 were obtained in a sorghum (Sorghum bicolor) plant height dataset, demonstrating that trait measureme

102 SoyNAM project and the following phenotypes: plant height, days to maturity, grain yield, and seed pr

103 many secondary inflorescence stems, reduced plant height, decreased stem diameter, and increased sec

104 Plant height, dispersal syndrome and dispersal investmen

105 wed improved growth characteristics, such as plant height, dry matter accumulation, leaf area index,

106 We found that plant height, dry weight and net photosynthetic rate dec

107 d to Dw3 do not associate significantly with plant height due to allele sharing between Dw3 and dw3 i

108 onhyperploid plants by measuring leaf width, plant height, ear height, internode length, stalk circum

109 In field experiment, plant height, ear length, ear weight/plot, grain yield/p

110 Plant height, economic yield, photosynthetic rate, and r

111 Individually, alleles conferring taller plant height exhibited complete dominance over alleles c

112 al reconstruction; (2) Automatic Hedge-based Plant Height Extraction (Auto-PHe) based on dense stereo

113 e following: (1) User-interactive Individual Plant Height Extraction (UsIn-PHe) based on dense stereo

114 ion and enhanced our toolbox for fine-tuning plant height for crop improvement.

115 individual plants should lead to changes in plant height, for example, shedding terminal branches an

116 riod, five of the seven species decreased in plant height, four of these decreased in leaf size, and

117 Data were collected on plant height, fresh biomass and leaf area.

118 agronomic traits, i.e., yield, heading date, plant height, grain length, and grain width.

119 r Frechet distance stability was observed in plant height growth curves than for canopy cover.

120 When plant height growth curves were compared to growth curve

121 MST) posits that the scaling exponents among plant height H, diameter D, and biomass M will covary ac

122 tic, molecular, and anatomical regulation of plant height have been discussed.

123 Overexpression of MdTCP11 in apple decreases plant height, highlighting its important role in the dev

124 ucted a vGWAS using both the BFT and DGLM on plant height in a maize diversity panel.

125 tion was found to be associated with reduced plant height in a natural recessive allele.

126 However, the genetic basis of plant height in adaptation to these regions remains uncl

127 um bicolor) genetic population evaluated for plant height in seven natural field conditions, we inves

128 armers used the semi-dwarf allele to improve plant height in sorghum long before efforts to introduce

129 Vessel diameter increased across ontogeny as plant height increased.

130 Manipulating plant height is an essential component of crop improveme

131 Typically plant height is measured at a single timepoint when plan

132 sults and those of previous studies indicate plant height is still the best proxy for estimating spec

133 Agriculturally advantageous reduction in plant height is usually achieved by blocking the action

134 es with dispersal structures on their seeds, plant height is very weakly related to dispersal investm

135 The size-dependent variations of plant height L and mass M with respect to basal stem dia

136 Using plant trait data (plant height, leaf area and flower length) for 895 nativ

137 Leaf photosynthetic rate, transpiration, plant height, leaf area index (LAI), biomass, and yield

138 The plant height, leaf greenness, shoot biomass, and yield w

139 r plasticity index values for traits such as plant height, leaf mass ratio, and root : shoot ratio.

140 ion (PDO) in the year of collection affected plant height, leaf size, and flower number, and asked wh

141 oots, (2) covariation among economic traits, plant height, leaf size, and seed mass, and (3) relation

142 diversification of three functional traits (plant height, leaf size, and seed size) were estimated f

143 t site of AP2L2 were associated with reduced plant height, more compact spikes, promotion of lemma-li

144 ormant and stress responsive QTL regions for plant height, new leaf and dry biomass weight.

145 unexpectedly wide range of traits including plant height, node number, leaf length, and flowering ti

146 r features from UAV images: vegetative area, plant height, Normalized Green-Red Difference Index, and

147 Yield and growth attributes: stem diameter, plant height, number of branches per plant, number of po

148 The plant height, number of branches, total dry weight, SPAD

149 served between populations of both weeds for plant height, number of leaves and biomass, however, the

150 ed seedling leaf protein levels to the adult plant height of 15 hybrids.

151 The overall plant height of overexpression lines was reduced due to

152 meristem cell proliferation, root diameter, plant height or ploidy.

153 0.0001), root mass fraction (p = 0.003) and plant height (p < 0.0001).

154 Moreover, Os1400 mutants showed shorter plant height, panicle and panicle base length, but no ti

155 ociated with two important agronomic traits, plant height (PH) and heading date (HD).

156 Plant height (PH) is an essential trait in maize (Zea ma

157 verage of Absolute Scores index, considering plant height (PH), number of days to maturity (NDM), and

158 (CGR), root volume (RV), root density (RD), plant height, pod plant(-1), pod length, seeds pod(-1),

159 Days to anthesis, maturity, and plant height predictions had high heritability and gave

160 even traits (days to maturity, lodging, oil, plant height, protein, seed size, and seed yield) for 39

161 separate quantitative trait locus (QTL) for plant height (qHT7.1) was identified near the genomic re

162 rtholog, SbBr1, co-segregates with the major plant height QTL qHT7.1 and is alternatively spliced.

163 GWAS linked a sorghum plant height QTL with the Br1 homolog by resequencing a

164 on chromosome 5A: 5A1 was co-located with a plant height QTL, and 5A2 with a major maturity QTL.

165 Here, we positionally cloned a plant height quantitative trait locus (QTL) qHT7.1 as a

166 of 100 years, there was a negative trend in plant height (r2= 0.4361, P < 0.001) for the intensely c

167 positively correlated with hybrid/midparent plant height ratios for the chloroplast ribosomal protei

168 in two maize inbred lines showed significant plant height reduction.

169 genome-wide association study, we identify a plant height regulating gene on chromosome 13 (PH13) enc

170 This enriched our understanding of plant height regulation and enhanced our toolbox for fin

171 encode genes controlling flowering time and plant height, respectively, which are critical for desig

172 ); plant body length L (i.e., cell length or plant height) scales, on average, as the 1/4-power of M

173 depth and root biomass significantly impact plant height, shoot biomass and number of leaves further

174 t architecture 1 (par1), which shows reduced plant height, shorter and narrower leaves, and larger le

175 grassy tillers1 In contrast to these traits, plant height showed a nonlinear response to chlorophyll

176 m channel tetramerization domain protein for plant height, Sobic.010G186600, a nucleoporin-related ge

177 n burden correlated negatively with biomass, plant height, specific leaf area (SLA), and tissue starc

178 ined plant biomass, species-specific traits (plant height, specific leaf area (SLA), root aerenchyma,

179 aspects of wheat growth and yield, including plant height, spike length, 1000 grain weight, stomatal

180 alyzed essential agronomic traits, including plant height, spike length, grain number, and thousand-k

181 und between the number of tillers per plant, plant height, spike length, number of grains per spike,

182 mowing community, and significantly positive plant height - SRA relationship was found in the enclosu

183 Significant variations in plant height, stem diameter, and budbreak were observed

184 exhibited growth promotry effect in terms of plant height, stem diameter, root length, root number an

185 cation of GA3 to bioenergy sorghum increased plant height, stem internode length, cell length and the

186 Plant height, stem length, number of flowers, bulb fresh

187 these SNPs closely localized to the SNPs for plant height, suggesting close associations between plan

188 The percent variance explained in plant height throughout the season was significantly exp

189 e source for manipulating flowering time and plant height to develop the full range of sorghum types:

190 a significant reduction in the root length, plant height, total fresh and dry weights, as well as ch

191 al agronomically important traits, including plant height, transitions to flowering and axillary bran

192 Evaluating plant height using unoccupied aerial vehicles allows for

193 trait loci was assessed through analysis of plant height variation.

194 V tended to be greater for whole-plant (e.g. plant height) vs. organ-level traits and for leaf chemic

195 an optimization of end wall resistance with plant height was discovered, but found to be independent

196 Plant height was generally reduced through breeding in w

197 Plant height was highly heritable (91.9%), followed by t

198 eCO(2) exhibited two trends across species: plant height was taller in 44% of species and flower num

199 Variation in spike compactness and plant height were associated with the level of transgene

200 ions between Delta(13)C, flowering time, and plant height were not significant.

201 Similar trends with plant height were observed.

202 d Auto-PHe were accurate methods to estimate plant height, while Auto-PHe had the additional advantag

203 mapping, a genome-wide association study of plant height with a sorghum diversity panel pinpointed g

204 ion may explain why the Rht-1 alleles reduce plant height without affecting dormancy.