ライフサイエンスコーパス: mature leaf

1 CN7/ZCN8 messenger RNA in florigen-producing mature leaf.

2 development affects stomatal density on the mature leaf.

3 ncrease vein and plasmodesmatal density in a mature leaf.

4 ieved the repression of the PCNA promoter in mature leaves.

5 tips, shoots, and floral organs, but not to mature leaves.

6 or the full repression of PCNA expression in mature leaves.

7 re negative in young leaves, and positive in mature leaves.

8 tion, but the transcript is less abundant in mature leaves.

9 eaves but increased transcription in healthy mature leaves.

10 nduced transcription of chloroplast genes in mature leaves.

11 treated, healthy potato organs or in wounded mature leaves.

12 n epidermal, mesophyll and vascular cells of mature leaves.

13 r from B supplied as a foliar application to mature leaves.

14 these processes were largely uncorrelated in mature leaves.

15 of the silique, pedicel and stem but not in mature leaves.

16 ed with the mass-based carboxylation rate of mature leaves.

17 ver-expressed in developing primordia and in mature leaves.

18 equired to limit the spread of cell death in mature leaves.

19 adjust the size and cell type composition of mature leaves.

20 oem cell wall ultrastructure in immature and mature leaves.

21 hydrates metabolism were highly expressed in mature leaves.

22 xhibit a significant cellulose deficiency in mature leaves.

23 he chlorophyll biosynthetic pathway, even in mature leaves.

24 n fruits, flowers and cotyledons, but not in mature leaves.

25 ves to an aliphatic wax-dominated profile in mature leaves.

26 inhibition effects, including the wilting of mature leaves.

27 ction were also significantly upregulated in mature leaves.

28 plete or nearly complete DNA loss already in mature leaves.

29 the upper leaf side was gained in young and mature leaves.

30 increased in the vein and mesophyll of young mature leaves.

31 , but relatively little initiation occurs in mature leaves.

32 t in immature leaves but are greater than in mature leaves.

33 he accumulation of neutral lipid droplets in mature leaves.

34 umulated excess starch and soluble sugars in mature leaves.

35 o high light and induced early senescence of mature leaves.

36 elopmental control and induces telomerase in mature leaves.

37 olated from the oil gland secretory cells of mature leaves.

38 ures on both adaxial and abaxial surfaces of mature leaves.

39 ndant transcript but was absent from healthy mature leaves.

40 the companion cells of the smallest veins of mature leaves.

41 immature leaves and was highly expressed in mature leaves.

42 expanding tissues, but substantially less in mature leaves.

43 important roles in the greater resistance of mature leaves against Xanthomonas citri compared with im

44 In mature leaves, all photosynthetic parameters were indist

45 Induction of PHYB in mature leaves also rescues stomatal development in young

46 bidopsis microarrays with labeled cDNAs from mature leaf and shoot apices from several different spec

47 as a result of damage, increased >50-fold in mature leaves and decreased >1400-fold in immature leave

48 enerated a large data set of small RNAs from mature leaves and developing roots, shoots, and inflores

49 primarily expressed in chlorenchyma cells of mature leaves and internodes.

50 This response occurs in mature leaves and may represent a strategy that is optim

51 0-fold above wild type, whereas the level in mature leaves and other tissues is no greater than wild

52 nly a subset of rops was highly expressed in mature leaves and pollen.

53 sink-source transition of immature leaves to mature leaves and provide knowledge regarding the differ

54 sink-source transition of immature leaves to mature leaves and provide knowledge regarding the differ

55 ted at 45.3% of the total soluble protein in mature leaves and remained stable even in old bleached l

56 ne, is shown to be specifically expressed in mature leaves and the developing pod walls of Brassica n

57 NMTase mRNA expression was high in young and mature leaves and was enhanced by light.

58 per-binding proteins purified from seedling, mature leaf, and mature root tissues.

59 tants exhibited decreased phloem pressure in mature leaves, and altered phloem cell wall ultrastructu

60 , including seedlings, inflorescence rachis, mature leaves, and flowers.

61 accumulated high levels of carbohydrates in mature leaves, and had a higher shoot biomass, contrasti

62 l pattern of vascular bundles in cotyledons, mature leaves, and inflorescence stems.

63 highly expressed in the collection phloem of mature leaves, and its function in phloem loading is wel

64 , these morphological asymmetries persist in mature leaves, and we observe left-right asymmetries in

65 tyle of elongating siliques, the petioles of maturing leaves, and most of the root.

66 Mature leaf area (LA) is a showcase of diversity - varyi

67 were up- or down-regulated in both young and mature leaves at both time points.

68 in gene expression varied between young and mature leaves at the same time point and between the sam

69 d transcriptomic data from seedling leaf and mature leaf blade tissues of maize hybrids and their inb

70 hese developing zones to one another and the mature leaf blade.

71 in all green tissues, with highest levels in maturing leaf blades.

72 Its mature leaves bleached, and it showed an increased degre

73 in all tested tissues, was not expressed in mature leaves but was highly expressed in roots.

74 ese processes do not occur in the absence of maturing leaves but can be restored by application of C(

75 y roles in glucosinolate allocation within a mature leaf by effectively importing apoplastically loca

76 plants reduces the number of chloroplasts in mature leaf cells from 100 to one, indicating that both

77 are specifically targeted for proteolysis in mature leaf cells.

78 rol and sulfolipid levels were lower than in mature leaves, consistent with low photosynthetic rates

79 is machinery returned to wild-type levels in mature leaves, consistent with the developmental down-re

80 Mature leaves contained consistently higher residues of

81 The epidermis of mature leaves contained the highest proportion of thiol

82 We found that the matured leaf contains a longitudinal gene expression gra

83 1b null mutant becomes depleted of CSP41a in mature leaves, correlating with a pale green phenotype a

84 Mature leaves detect these environmental signals and rel

85 he transcriptional control of acclimation in mature leaves distinct from other photoreceptor-regulate

86 nt on its catalytic activity was observed in mature leaves during mycotoxin-induced cell death.

87 n was not detected in floating leaf discs of mature leaves exposed to excess Mn.

88 t, which ensures the continual production of mature leaves following juvenile-adult transition, there

89 )) content comparable to coffee beans, while mature leaf from plant pruning presented not only high c

90 n nighttime leaf respiration rate (RN) among mature leaves from an Arabidopsis (Arabidopsis thaliana)

91 Using this screening method, mature leaves from fully developed plants were analyzed,

92 Mature leaves grown under continuous illumination contai

93 y of organs to produce AsA from GAL-L showed mature leaves have a 3- to 10-fold higher biosynthetic c

94 nces in leaf patterning between juvenile and mature leaves in Arabidopsis.

95 Suc) found drastically decreased export from mature leaves in cpd28 and cpd47 mutants relative to wil

96 spectroscopy accurately predicts V(c,max) of mature leaves in Panamanian tropical forests (R(2) = 0.9

97 Ectopic expression of GAT1 in mature leaves increased plasmodesmal permeability and le

98 The photosynthetic capacity of mature leaves increases after several days' exposure to

99 n increased by more than 2-fold in young and mature leaves, indicating that phosphate stimulates prot

100 The minor-vein phloem of mature leaves is developmentally and physiologically dis

101 The transcript level in mature leaves is very low during the photoperiod, reache

102 Our data suggest that, in mature leaves, isoprene emission rates are primarily det

103 ct DNA of any size in most chloroplasts from mature leaves, long before the onset of leaf senescence.

104 Stomata on mature leaves may act as stress signal-sensing and trans

105 synthesis, and immunity between immature and mature leaves may contribute to their different response

106 -off of cytochrome b6f complex biogenesis in mature leaves may represent part of the first dedicated

107 stemically, with the irradiance perceived by mature leaves modulating stomatal development in young l

108 onfers expression only in the minor veins of mature leaves, not in the transport phloem of larger lea

109 synthetic capacity with NSCs accumulation in mature leaves, observed most clearly with hexose, and ev

110 abolites, and key inorganic ions in recently mature leaves of 45 dicotyledonous species at midafterno

111 he nighttime O(2) consumption rate (R(N)) in mature leaves of Arabidopsis (Arabidopsis thaliana).

112 Here, we show that mature leaves of Arabidopsis grown at higher photon irra

113 Moreover, we show that the mature leaves of Arabidopsis thaliana supply young leave

114 In contrast, B present in mature leaves of control tobacco lines could not be used

115 ssion in cultured cells and in young but not mature leaves of healthy transgenic plants.

116 The same RNA was found in mature leaves of infected but not healthy plants.

117 distinct patterns of starch accumulation in mature leaves of PDLP5 and PDLP6 overexpressors.

118 Foliar starch levels in mature leaves of plants transferred from LL to HL were n

119 l conductance (gs ) and transpiration (E) on mature leaves of R. stricta.

120 Here we show that mature leaves of T-DNA insertion lines with diminished e

121 oter activity was detected in both young and mature leaves of TGMV-infected plants.

122 e examined the hydraulic architecture of the mature leaves of the model species Populus tremula x alb

123 o temperature (10 degrees C-40 degrees C) in mature leaves of tobacco (Nicotiana tabacum L. cv W38) w

124 Mature leaves of wild-type plants and arc mutants have a

125 Maturing leaves of myrosinase mutants had significantly

126 d whether responses differ between young and mature leaves or between morning and the end of the day.

127 ively dividing tissues of a plant and not in mature leaves or stems.

128 ision and differentiation to yield the fully mature leaf organ.

129 of cellular differentiation of relevance for mature leaf photosynthetic performance.

130 more IAA-Asp than in wild-type seedlings and mature leaves, respectively.

131 d photosynthetic functioning was observed in mature leaves, resulting in premature leaf aging.

132 n with earlier studies, we show that loss of mature leaves results in decreased sugar levels and incr

133 In addition, metabolic profiles of mature leaves revealed that several biosynthetic pathway

134 Analysis of the adaxial epidermis of mature leaves revealed that silenced lines had 70% to 90

135 ivities are the major source of variation in mature leaf RN under favorable controlled conditions.

136 iced cyclin was detected in apical meristem, mature leaf, root tip and mature root.

137 d increases in the fatty acid content of the mature leaves, senescing leaves, and roots, respectively

138 patterning, and the establishment of complex mature leaf shapes.

139 Mature leaves showed the highest level of transgene expr

140 mass) failed to keep pace with increases in mature leaf size.

141 Transcriptome analyses of young and mature leaves, stems, stipules, and roots integrated wit

142 In mature leaves, submergence-induced auxin accumulation wa

143 At soil concentrations >4 mg/kg the mature leaves suffered from burnt edges and white spots

144 ilability or a defect in sucrose export from mature leaves, suggesting that isi1 mutant plants do not

145 significant impact on plant metabolism, with mature leaves tending to be more extensively affected th

146 bacco, superpromoter activity was greater in mature leaves than in young leaves, whereas in maize act

147 sing entire shoot tissues, most of which are mature leaves that do not elongate under submergence.

148 or clusters of leaves from the base of more mature leaves (the rosulate form).

149 te in young tissues and geminivirus-infected mature leaves, the GRIK-SnRK1 cascade may function in a

150 n young leaves of A. bisulcatus, but in more mature leaves, the Se-methylseleno-Cys concentration is

151 titutive in roots and inducible by copper in mature leaves; the reverse pattern was observed for MT2.

152 PetC was highly efficient in both young and mature leaves, these data indicate a lifetime of the cyt

153 days contained predominantly selenate in the mature leaf tissue at a concentration of 0.3-0.6 mM, whe

154 TWAS using mature leaf tissue identified known true-positive flower

155 omal regions via RNA-seq of maize (Zea mays) mature leaf tissue to reveal new aspects of genomic imba

156 ature root and nodules but the reaction with mature leaf tissue was low compared to other tissues.

157 ere found to be significantly upregulated in mature leaf tissue, suggesting that oil production incre

158 RNA expression using RNA-seq data from maize mature leaf tissue.

159 is a common target of MYB31 and MYB42 in the mature leaf tissues of maize, sorghum and rice, as evide

160 lated from the root elongation zone and from mature leaf tissues.

161 The Calvin cycle was down-regulated in mature leaves to adjust to the reduced capacity of the l

162 slocation of the foliar-applied 10B from the mature leaves to the meristematic tissues verifies that

163 Sucrose is transported from sources (mature leaves) to sinks (importing tissues such as roots

164 to export sugars from regions of synthesis (mature leaves) to sugar sinks (roots, fruits).

165 ling pathways that control CHS expression in mature leaves using cryptochrome (cry) and phytochrome (

166 A differential response between young and mature leaves was also found in carbon metabolism, with

167 rformance of mannitol-accumulating calli and mature leaves was due to other stress-protective functio

168 Foliar application of 10B to mature leaves was translocated to the meristematic tissu

169 Their transcript profiles in young and mature leaves were analyzed in response to phosphate sup

170 Lipid bodies, not observable in uninfected mature leaves, were found in and external to chloroplast

171 here AthDHS2 is highly expressed, but not in mature leaves, where AthDHS1 is predominantly expressed.

172 the formation of elliptical leaf laminae in mature leaves, whereas overexpression of GTE6 resulted i

173 te to the repression of the PCNA promoter in mature leaves, whereas the E2F1 site counters the repres

174 s, siliques, and roots than in dry seeds and mature leaves, whereas the polyphosphoinositide-dependen

175 endophyte-mediated protection was greater in mature leaves, which bear less intrinsic defense against

176 PFD, in 2% and 21% oxygen, in developing and mature leaves, which differed greatly in R in darkness.

177 mesophyll but not in the epidermis of young mature leaves, while this was reversed for zinc distribu

178 n immature leaves, but slightly expressed in mature leaves, while Vfa4 was active in immature leaves

179 eached rapidly and developed necroses, while mature leaves, whose photosynthetic apparatus was fully

180 and increased phospholipid concentrations in mature leaves, with concomitant changes in the expressio

181 s were notably different between growing and mature leaves, with greater anaplerotic, tricarboxylic a

182 nes by near-infrared spectroscopic screen of mature leaves yielded several dozen lines with heritable