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1 f the Sh1 gene that encodes maize (Zea mays) sucrose synthase.
2 he fruit can be accomplished by invertase or sucrose synthase.
3 synthase, which promotes degradation of the sucrose synthase.
4 chimeric gene construction, in which a corn sucrose synthase-1 gene (Sh) promoter was used to direct
6 DP-glucose pyrophosphorylase 1a (TacAGPS1a), sucrose synthase 2 (TaSuS2), and other genes involved in
7 insight into the roles of this motif in rice sucrose synthase 3 (RSuS3), the two conserved glutamate
9 betaine aldehyde dehydrogenase) and sugars (sucrose synthase, acid invertase, trehalose-6-phosphate
10 development there is a transient increase in sucrose synthase activity and starch which is correlated
11 ol of a fruit-specific promoter we show that sucrose synthase activity can be reduced by up to 99% in
13 s and cleavage, as well as the regulation of sucrose synthase and its interactions with cellular targ
14 avage during expansion was sustained by both sucrose synthase and neutral invertase, associated with
15 ty in rs/rs roots whereas neutral invertase, sucrose synthase and sucrose phosphate synthase levels w
16 s increased accumulations of transcripts for sucrose synthase and vacuolar invertase were both observ
17 s the changing intracellular localization of sucrose synthase as a molecular switch between survival
20 , electron microscopic immunolocalization of sucrose synthase in cotton fibers, and phylogenetic rela
21 in vitro, and is required for expression of sucrose synthase in potato tubers and excised leaves.
22 result calls into question the importance of sucrose synthase in regulating sink strength in tomato f
28 ose synthase, possible regulation by Ca2+ of sucrose synthase localization, electron microscopic immu
29 eolus vulgaris roots, a Rhizobium-responsive sucrose synthase of soybean and a cell wall acid inverta
30 predominantly located in phloem tissues for sucrose synthase or the endodermis and phloem for solubl
31 included on phosphorylation of cotton fiber sucrose synthase, possible regulation by Ca2+ of sucrose
32 by a phloem-specific promoter (from the rice sucrose synthase RSs1 gene) and by a constitutive promot
39 e 170 (S170) of the maize (Zea mays L.) SUS1 sucrose synthase (SUS) protein as a possible, second pho
41 is tightly coexpressed with two isoforms of sucrose synthase (SUS5 and SUS6) known to be confined to
43 d cell-specific, yet functionally redundant, sucrose synthase (SuSy) genes, Sh1 and Sus1, which encod
44 eriments were conducted to determine whether sucrose synthase (SuSy) was phosphorylated in the elonga
45 lower expression of SbSUS4, a gene encoding sucrose synthase that generates UDP-glucose from sucrose
46 pose that UGT1 may transfer UDP-glucose from sucrose synthase to the callose synthase and thus help f
47 phofructokinase during cell division and for sucrose synthase, UDP-glucopyrophosphorylase, and phosph
48 ASE (VvPDC), ALCOHOL DEHYDROGENASE (VvADH2), SUCROSE SYNTHASE (VvSUSY), non-symbiotic HEMOGLOBIN (Vvn
50 s and fermentation genes and a gene encoding sucrose synthase were more strongly induced in the less
51 hey act as sugar brakes by phosphorylating a sucrose synthase, which promotes degradation of the sucr