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1 rts its role in the systemic distribution of photoassimilate.
2 ntirely, inhibited exudation of radiolabeled photoassimilate.
3  controlled primarily by the availability of photoassimilates.
4 ght requirement and the hyperaccumulation of photoassimilates.
5  crucial roles played by uridine salvage for photoassimilate allocation and partitioning.
6                     Mannitol is an important photoassimilate, as well as providing plants with resist
7     Therefore, avoiding stresses which limit photoassimilates availability particularly during early
8 effect of light intensity on the quantity of photoassimilates available to the fruits without a clear
9 otosynthesis is dependent on partitioning of photoassimilate between starch and sucrose, and varies i
10 leaves, Tre6P influences the partitioning of photoassimilates between Suc, organic acids, and amino a
11 cesses such as growth and tissue patterning, photoassimilate distribution and defense against pathoge
12 ow that the only vital function of AtSUC2 in photoassimilate distribution is phloem loading.
13 sential functions as they provide routes for photoassimilate distribution, the exchange of developmen
14        Phloem loading is the initial step in photoassimilate export and the one that creates the driv
15 ild type, vte1 and vte2 had reduced rates of photoassimilate export as early as 6 h into low-temperat
16 nt of transfer cell walls and maintenance of photoassimilate export capacity during low-temperature (
17                       The rapid reduction in photoassimilate export in vte2 coincides with callose de
18 ng impacts on LT-induced sugar accumulation, photoassimilate export reduction and vascular-specific c
19 d facilitate greater yields through enhanced photoassimilate export to sink tissues.
20 rrelated with their extent of suppression of photoassimilate export.
21  predictable pattern, each bundle conducting photoassimilate from a specific region of the blade.
22 istance is likely not caused by diversion of photoassimilates from growth to defense but rather by a
23                                 Transport of photoassimilates from leaf tissues (source regions) to t
24                 However, as the transport of photoassimilates from leaves (sources) to flowers (sinks
25 potential of regulating the translocation of photoassimilates from source to sink tissues represents
26 ocities and volume flow to supply sinks with photoassimilates greatly depend on the geometry of the m
27             Leaves are the primary source of photoassimilate in crop plants, and understanding the ge
28 r veins for transport rather than loading of photoassimilates in source tissue does not preclude viru
29                                Conversion of photoassimilate into mannitol and glycerol for carbon se
30 hat BnaC02.TPS8 enhanced the partitioning of photoassimilate into starch and sucrose, as opposed to g
31 hesis, but exhibit increased partitioning of photoassimilate into sucrose and have delayed photosynth
32                                    Uptake of photoassimilates into the leaf phloem is the key step in
33 ty of Fru-2,6-P2 to modulate partitioning of photoassimilate is an important determinant of growth an
34 ally devoid of P-protein structures and lost photoassimilates more rapidly after injury than control
35 expressed can be predicted by a knowledge of photoassimilate movement patterns in vivo.
36                                              Photoassimilates play crucial roles during plant-pathoge
37 (35S::AVP1 cassette) enhanced shoot biomass, photoassimilate production and transport, rhizosphere ac
38                                              Photoassimilates regulate circadian timing 1750 III.
39 ccharides is an adaptive strategy to improve photoassimilate retention, and consequently translocatio
40                                              Photoassimilates such as sugars are transported through
41 te uptake is potentiated by increased carbon photoassimilate (sucrose) levels.
42 number of loading strategies for the primary photoassimilates, sucrose and sugar alcohols.
43  associated with a concentration gradient of photoassimilates (the non-mobile solutes) that exists in
44 gen-poor soils at the cost of diverting some photoassimilate to their microsymbionts.
45 eferential allocation by the fungus of plant photoassimilate to weather grains of limestone and silic
46 mature seeds indicated reduced conversion of photoassimilates to oil.
47 nd tissues, which are critical for water and photoassimilate transport at long distances, point to ma
48 ective in transfer cell wall development and photoassimilate transport at low temperature (LT).
49                               Sucrose is the photoassimilate transported from the leaves to the fruit