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1 ting to carbon assimilation, which differ by plant type.
2 pe discrimination and values among different plant types.
3 el differences in acclimation capacity among plant types.
4            Rd acclimation was similar across plant types.
5 tter than previous MST models for a range of plant types.
6 e of this study was to determine whether the plant type 1 peroxisomal targeting signal (PTS1) utilize
7 ucoseen reductase (E3), is an NADH dependent plant type [2Fe-2S] containing flavoenzyme.
8  The enzyme exhibits a strong preference for plant type [2Fe-2S] ferredoxins; however, flavodoxin can
9 wo electrons from NADH were allocated to the plant-type [2Fe-2S] cluster and to FMN in the form of a
10 s of the flavin mononucleotide (FMN) and the plant-type [2Fe-2S] cluster of CntB and also of the Ries
11 rotein with one Rieske [2Fe-2S] cluster, one plant-type [2Fe-2S] cluster, and one flavin mononucleoti
12 vided by essential interactions with reduced plant-type [2Fe-2S] ferredoxin (Fd).
13        A reductase, which contains FMN and a plant-type [2Fe-2S] ferredoxin domain, transfers electro
14 tional composition increased and key-species plant types and functional composition-productivity rela
15 obustness of its temperature response across plant types and growth conditions.
16 act that E(max) was roughly conserved across plant types and scales with the product of xylem saturat
17 y composition surpassed the variation due to plant type, and microbial communities under each crop di
18  energy into biomass is 4.6-6%, depending on plant type, and the best year-long efficiencies realized
19 adients of precipitation, edaphic qualities, plant types, and/or land use change.
20 eu is critical for the catalytic function of plant-type APS reductases by promoting the interdomain i
21  elucidated the first N-terminal nucleophile plant-type asparaginase structure in the covalent interm
22 e maturation of hedgehog signaling proteins, plant-type asparaginases, and pyruvoyl enzymes.
23                      Similar to nonmammalian plant-type asparaginases, hASRGL1 is shown to be an Ntn
24 tivity consistent with enzymes designated as plant-type asparaginases, which had thus far been found
25  a subunit fold similar to that observed in "plant"-type beta class carbonic anhydrases.
26            Here we report on the first known plant-type (beta-class) carbonic anhydrase in the archae
27 t carbon exchange is common across different plant types, but that acclimation to warmer temperatures
28 nd shrubs and competitive interactions among plant types, confirmed by structural equation analysis.
29  evolution from bacterial-type SRP to higher plant-type cpSRP system.
30                 The stereoselectivity of the plant-type desaturation pathway expressed in E. coli is
31 e also important determinants in controlling plant-type distributions.
32 known 'bacterial-type' PEPC, along with the 'plant-type' exclusively used in other CAM and C4 plants
33  study provides experimental evidence that a plant-type FA beta-oxidation involving H2 O2 -producing
34 Chlamydomonas reinhardtii genome encodes six plant type [Fe2S2] ferredoxins, products of PETF, FDX2-F
35 by the [Fe-Fe]-hydrogenase HYDA1, which uses plant type ferredoxin PETF/FDX1 (PETF) as an electron do
36 (+) reductase (ptFNR) and its redox partner, plant-type ferredoxin (ptFd).
37 t contains flavin mononucleotide (FMN) and a plant-type ferredoxin [2Fe-2S] center.
38  is the first structural information for the plant-type ferredoxin domain in a complex state, was als
39 s heterodimeric; SDH2N and SDH2C contain the plant-type ferredoxin domain in the N-terminal half and
40 ast, the ferredoxin redox system consists of plant-type ferredoxin-NADP(+) reductase (ptFNR) and its
41  center is not distinguishable from those in plant-type ferredoxins.
42  < 0.001) and was relatively conserved among plant types (for a given plant size), while increasing a
43  recently discovered in Arabidopsis thaliana plant-type histidinol phosphate phosphatase (HPP) shares
44                    Together with a few other plant type I OMTs, we demonstrated that our Gibbs' reage
45 vities in vitro and in vivo, and some of the plant type II MCPs exhibit Ca(2+) dependence for their e
46            CPA and U-73122 are inhibitors of plant type IIA calcium pumps and phospholipase C, respec
47 oward tailoring the biosynthetic activity of plant type III PKS.
48 emble the most recent common ancestor of the plant type III PKSs.
49                                          The plant type III polyketide synthases (PKSs), which produc
50 shown its improved yield potential over tall plant type in cereals which further leads to 'Green revo
51 arf alleles have continued to develop better plant types in all cereals.
52  but significant impacts from soil depth and plant type (invasive vs. native).
53 erence between the susceptible and resistant plant types is determined at an earlier stage in saponin
54                                            A plant-type lycopene beta-cyclase gene crtL was identifie
55       Two varieties, japonica (tropical; new plant type [NPT]) and indica (IR72) were compared.
56  to explore the effects of fertilization and plant type on spatiotemporal variations of N- and P-hydr
57 ted with either high-phosphate iron mineral (plant-type) or low-phosphate iron mineral (animal-type)
58 As and identifying their cellular targets in plant-type organisms.
59 ises from a tight interaction between 107-kD plant-type PEPC and 118-kD bacterial-type (BTPC) subunit
60 r and that they both originate from the same plant-type PEPC gene.
61 complex stress-related (LHCSR)-dependent and plant-type S subunit of Photosystem II (PSBS)-dependent
62                                         Both plant types showed toxicity tolerance, but metal accumul
63 modern carbon isotope compositions in all C3 plant types shows a monotonic increase in delta(13)C wit
64 ic acid, regardless of fullerene presence or plant type, significantly decreased the p,p'-DDE uptake.
65 chemical-induced CAC, oral administration of plant-type sphingolipids called sphingadienes increased
66 ding can be used more efficiently to develop plant types that can combine all or most of the benefici
67                            Dwarf/ semi dwarf plant type varieties has shown its improved yield potent
68                                   Unlike the plant-type VDE that is located in the thylakoid lumen, t
69                               Two transgenic plant types were used; in the first, functional antibody
70 ntent) and plant agronomy (harvest index and plant type) were investigated.
71 nificantly structured according to sites and plant type (wild vs cultivated).
72 ies of cereals, most of them had undesirable plant types with defects including extreme dwarfism and
73 different photosynthetic processes varied by plant type, with C3 species tending to preferentially ac
74 es to productivity in a variety of different plant types, with an emphasis on fruit and cereal crops.