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1 re negative in young leaves, and positive in mature leaves.
2 tion, but the transcript is less abundant in mature leaves.
3 eaves but increased transcription in healthy mature leaves.
4 nduced transcription of chloroplast genes in mature leaves.
5 treated, healthy potato organs or in wounded mature leaves.
6 n epidermal, mesophyll and vascular cells of mature leaves.
7 r from B supplied as a foliar application to mature leaves.
8  of the silique, pedicel and stem but not in mature leaves.
9 these processes were largely uncorrelated in mature leaves.
10 ver-expressed in developing primordia and in mature leaves.
11 equired to limit the spread of cell death in mature leaves.
12 ed with the mass-based carboxylation rate of mature leaves.
13 adjust the size and cell type composition of mature leaves.
14 oem cell wall ultrastructure in immature and mature leaves.
15 xhibit a significant cellulose deficiency in mature leaves.
16 hydrates metabolism were highly expressed in mature leaves.
17 he chlorophyll biosynthetic pathway, even in mature leaves.
18 n fruits, flowers and cotyledons, but not in mature leaves.
19 ves to an aliphatic wax-dominated profile in mature leaves.
20 inhibition effects, including the wilting of mature leaves.
21 ction were also significantly upregulated in mature leaves.
22 plete or nearly complete DNA loss already in mature leaves.
23  the upper leaf side was gained in young and mature leaves.
24 increased in the vein and mesophyll of young mature leaves.
25 , but relatively little initiation occurs in mature leaves.
26 t in immature leaves but are greater than in mature leaves.
27 umulated excess starch and soluble sugars in mature leaves.
28 he accumulation of neutral lipid droplets in mature leaves.
29 o high light and induced early senescence of mature leaves.
30 elopmental control and induces telomerase in mature leaves.
31 olated from the oil gland secretory cells of mature leaves.
32 ures on both adaxial and abaxial surfaces of mature leaves.
33 ndant transcript but was absent from healthy mature leaves.
34 the companion cells of the smallest veins of mature leaves.
35  immature leaves and was highly expressed in mature leaves.
36 expanding tissues, but substantially less in mature leaves.
37 ieved the repression of the PCNA promoter in mature leaves.
38  tips, shoots, and floral organs, but not to mature leaves.
39 or the full repression of PCNA expression in mature leaves.
40 important roles in the greater resistance of mature leaves against Xanthomonas citri compared with im
41                                           In mature leaves, all photosynthetic parameters were indist
42                         Induction of PHYB in mature leaves also rescues stomatal development in young
43 as a result of damage, increased >50-fold in mature leaves and decreased >1400-fold in immature leave
44 enerated a large data set of small RNAs from mature leaves and developing roots, shoots, and inflores
45 primarily expressed in chlorenchyma cells of mature leaves and internodes.
46                      This response occurs in mature leaves and may represent a strategy that is optim
47 0-fold above wild type, whereas the level in mature leaves and other tissues is no greater than wild
48 nly a subset of rops was highly expressed in mature leaves and pollen.
49 sink-source transition of immature leaves to mature leaves and provide knowledge regarding the differ
50 sink-source transition of immature leaves to mature leaves and provide knowledge regarding the differ
51 ted at 45.3% of the total soluble protein in mature leaves and remained stable even in old bleached l
52 ne, is shown to be specifically expressed in mature leaves and the developing pod walls of Brassica n
53 NMTase mRNA expression was high in young and mature leaves and was enhanced by light.
54 tants exhibited decreased phloem pressure in mature leaves, and altered phloem cell wall ultrastructu
55 , including seedlings, inflorescence rachis, mature leaves, and flowers.
56  accumulated high levels of carbohydrates in mature leaves, and had a higher shoot biomass, contrasti
57 l pattern of vascular bundles in cotyledons, mature leaves, and inflorescence stems.
58 highly expressed in the collection phloem of mature leaves, and its function in phloem loading is wel
59 , these morphological asymmetries persist in mature leaves, and we observe left-right asymmetries in
60 tyle of elongating siliques, the petioles of maturing leaves, and most of the root.
61 were up- or down-regulated in both young and mature leaves at both time points.
62  in gene expression varied between young and mature leaves at the same time point and between the sam
63                                          Its mature leaves bleached, and it showed an increased degre
64  in all tested tissues, was not expressed in mature leaves but was highly expressed in roots.
65 ese processes do not occur in the absence of maturing leaves but can be restored by application of C(
66 rol and sulfolipid levels were lower than in mature leaves, consistent with low photosynthetic rates
67 is machinery returned to wild-type levels in mature leaves, consistent with the developmental down-re
68                                              Mature leaves contained consistently higher residues of
69                             The epidermis of mature leaves contained the highest proportion of thiol
70 1b null mutant becomes depleted of CSP41a in mature leaves, correlating with a pale green phenotype a
71                                              Mature leaves detect these environmental signals and rel
72 he transcriptional control of acclimation in mature leaves distinct from other photoreceptor-regulate
73 nt on its catalytic activity was observed in mature leaves during mycotoxin-induced cell death.
74 n was not detected in floating leaf discs of mature leaves exposed to excess Mn.
75 t, which ensures the continual production of mature leaves following juvenile-adult transition, there
76 n nighttime leaf respiration rate (RN) among mature leaves from an Arabidopsis (Arabidopsis thaliana)
77                 Using this screening method, mature leaves from fully developed plants were analyzed,
78                                              Mature leaves grown under continuous illumination contai
79 y of organs to produce AsA from GAL-L showed mature leaves have a 3- to 10-fold higher biosynthetic c
80 nces in leaf patterning between juvenile and mature leaves in Arabidopsis.
81 Suc) found drastically decreased export from mature leaves in cpd28 and cpd47 mutants relative to wil
82 spectroscopy accurately predicts V(c,max) of mature leaves in Panamanian tropical forests (R(2) = 0.9
83                Ectopic expression of GAT1 in mature leaves increased plasmodesmal permeability and le
84               The photosynthetic capacity of mature leaves increases after several days' exposure to
85 n increased by more than 2-fold in young and mature leaves, indicating that phosphate stimulates prot
86                     The minor-vein phloem of mature leaves is developmentally and physiologically dis
87                      The transcript level in mature leaves is very low during the photoperiod, reache
88                    Our data suggest that, in mature leaves, isoprene emission rates are primarily det
89 ct DNA of any size in most chloroplasts from mature leaves, long before the onset of leaf senescence.
90                                   Stomata on mature leaves may act as stress signal-sensing and trans
91 synthesis, and immunity between immature and mature leaves may contribute to their different response
92 -off of cytochrome b6f complex biogenesis in mature leaves may represent part of the first dedicated
93 stemically, with the irradiance perceived by mature leaves modulating stomatal development in young l
94 onfers expression only in the minor veins of mature leaves, not in the transport phloem of larger lea
95 synthetic capacity with NSCs accumulation in mature leaves, observed most clearly with hexose, and ev
96 abolites, and key inorganic ions in recently mature leaves of 45 dicotyledonous species at midafterno
97 he nighttime O(2) consumption rate (R(N)) in mature leaves of Arabidopsis (Arabidopsis thaliana).
98                           Here, we show that mature leaves of Arabidopsis grown at higher photon irra
99                   Moreover, we show that the mature leaves of Arabidopsis thaliana supply young leave
100                    In contrast, B present in mature leaves of control tobacco lines could not be used
101 ssion in cultured cells and in young but not mature leaves of healthy transgenic plants.
102                    The same RNA was found in mature leaves of infected but not healthy plants.
103  distinct patterns of starch accumulation in mature leaves of PDLP5 and PDLP6 overexpressors.
104                      Foliar starch levels in mature leaves of plants transferred from LL to HL were n
105 l conductance (gs ) and transpiration (E) on mature leaves of R. stricta.
106                            Here we show that mature leaves of T-DNA insertion lines with diminished e
107 oter activity was detected in both young and mature leaves of TGMV-infected plants.
108 e examined the hydraulic architecture of the mature leaves of the model species Populus tremula x alb
109 o temperature (10 degrees C-40 degrees C) in mature leaves of tobacco (Nicotiana tabacum L. cv W38) w
110                                              Mature leaves of wild-type plants and arc mutants have a
111                                              Maturing leaves of myrosinase mutants had significantly
112 d whether responses differ between young and mature leaves or between morning and the end of the day.
113 ively dividing tissues of a plant and not in mature leaves or stems.
114 more IAA-Asp than in wild-type seedlings and mature leaves, respectively.
115 d photosynthetic functioning was observed in mature leaves, resulting in premature leaf aging.
116 n with earlier studies, we show that loss of mature leaves results in decreased sugar levels and incr
117           In addition, metabolic profiles of mature leaves revealed that several biosynthetic pathway
118         Analysis of the adaxial epidermis of mature leaves revealed that silenced lines had 70% to 90
119 d increases in the fatty acid content of the mature leaves, senescing leaves, and roots, respectively
120                                              Mature leaves showed the highest level of transgene expr
121          Transcriptome analyses of young and mature leaves, stems, stipules, and roots integrated wit
122                                           In mature leaves, submergence-induced auxin accumulation wa
123          At soil concentrations >4 mg/kg the mature leaves suffered from burnt edges and white spots
124 ilability or a defect in sucrose export from mature leaves, suggesting that isi1 mutant plants do not
125 significant impact on plant metabolism, with mature leaves tending to be more extensively affected th
126 bacco, superpromoter activity was greater in mature leaves than in young leaves, whereas in maize act
127 sing entire shoot tissues, most of which are mature leaves that do not elongate under submergence.
128  or clusters of leaves from the base of more mature leaves (the rosulate form).
129 te in young tissues and geminivirus-infected mature leaves, the GRIK-SnRK1 cascade may function in a
130 n young leaves of A. bisulcatus, but in more mature leaves, the Se-methylseleno-Cys concentration is
131 titutive in roots and inducible by copper in mature leaves; the reverse pattern was observed for MT2.
132  PetC was highly efficient in both young and mature leaves, these data indicate a lifetime of the cyt
133       The Calvin cycle was down-regulated in mature leaves to adjust to the reduced capacity of the l
134 slocation of the foliar-applied 10B from the mature leaves to the meristematic tissues verifies that
135         Sucrose is transported from sources (mature leaves) to sinks (importing tissues such as roots
136  to export sugars from regions of synthesis (mature leaves) to sugar sinks (roots, fruits).
137 ling pathways that control CHS expression in mature leaves using cryptochrome (cry) and phytochrome (
138    A differential response between young and mature leaves was also found in carbon metabolism, with
139 rformance of mannitol-accumulating calli and mature leaves was due to other stress-protective functio
140                 Foliar application of 10B to mature leaves was translocated to the meristematic tissu
141       Their transcript profiles in young and mature leaves were analyzed in response to phosphate sup
142   Lipid bodies, not observable in uninfected mature leaves, were found in and external to chloroplast
143 here AthDHS2 is highly expressed, but not in mature leaves, where AthDHS1 is predominantly expressed.
144  the formation of elliptical leaf laminae in mature leaves, whereas overexpression of GTE6 resulted i
145 te to the repression of the PCNA promoter in mature leaves, whereas the E2F1 site counters the repres
146 s, siliques, and roots than in dry seeds and mature leaves, whereas the polyphosphoinositide-dependen
147 endophyte-mediated protection was greater in mature leaves, which bear less intrinsic defense against
148 PFD, in 2% and 21% oxygen, in developing and mature leaves, which differed greatly in R in darkness.
149  mesophyll but not in the epidermis of young mature leaves, while this was reversed for zinc distribu
150 n immature leaves, but slightly expressed in mature leaves, while Vfa4 was active in immature leaves
151 eached rapidly and developed necroses, while mature leaves, whose photosynthetic apparatus was fully
152 and increased phospholipid concentrations in mature leaves, with concomitant changes in the expressio
153 s were notably different between growing and mature leaves, with greater anaplerotic, tricarboxylic a
154 nes by near-infrared spectroscopic screen of mature leaves yielded several dozen lines with heritable

 
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