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1 mmitted step of plastoquinone and tocopherol biosyntheses.
2  features, biological activity, and proposed biosyntheses.
3 eners" are not derived from enantiodivergent biosyntheses.
4 antipodes arising from separate enantiomeric biosyntheses.
5 y disruption of peptidoglycan and fatty acid biosyntheses.
6 y share parallels with the natural products' biosyntheses.
7 und in bacterial and other fungal polyketide biosyntheses.
8 yl THF to formate and THF for purine and Gly biosyntheses.
9  in coordinating phospholipid and fatty acid biosyntheses.
10 rsors in leucine, isoleucine, and coenzyme B biosyntheses.
11 s between aromatic polyketide and fatty acid biosyntheses.
12 lvement in both heme and iron-sulfur cluster biosyntheses.
13 al role of WsMYC2 in the regulation of their biosyntheses.
14 r lipid, cofactor, amino acid, or nucleotide biosyntheses.
15 een recruited for sulfolactate or sulfolipid biosyntheses.
16 at are required for riboflavin and pteridine biosyntheses.
17 principal genes of amino acid and nucleotide biosyntheses.
18 their electronic structures, mechanisms, and biosyntheses.
19  unclear, despite extensive studies of their biosyntheses.
20 sis, but also for heme a and lipoyl cofactor biosyntheses.
21  in context to withanolides and stigmasterol biosyntheses.
22 gulatory steps in cholesterol and fatty acid biosyntheses, 3-hydroxy-3-methylglutaryl-coenzyme A (HMG
23                                 During their biosyntheses, a peptide aminoacyl-transfer ribonucleic a
24                                        These biosyntheses all involve polycyclization via cationic in
25 y of proteins involved in FeMo-co and FeV-co biosyntheses, allows us to define a new family of iron a
26 nsduction, chromatin repair, metabolism, and biosyntheses, among others.
27 gins with a brief discussion of the proposed biosyntheses and biosynthetic connections among the poly
28 depend on NADPH production to feed essential biosyntheses and for oxidative stress defense.
29 oxylipin, glucosinolate, and brassinosteroid biosyntheses and have shown that both P450 and non-P450
30 lipid and glycosylphosphatidylinositol (GPI) biosyntheses and may harbor sterol trafficking defects.
31 functions including ATP production, cofactor biosyntheses, apoptosis, lipid synthesis, and steroid me
32 ed xanthone, ergochrome, and bianthraquinone biosyntheses are discussed.
33     Yet, the mechanisms of most endoperoxide biosyntheses are not well understood.
34                                        Their biosyntheses are typically initiated by hydroxylation of
35  and amino acid, sugar, nucleotide and lipid biosyntheses can be reconstituted in high yield under mi
36 ed to deoxyribose triphosphate, and in vitro biosyntheses could be successfully performed with severa
37 carotenoid, brassinosteroid, and gibberellin biosyntheses have been added from the literature.
38 sulfur-containing sugars in nature and their biosyntheses have not been studied.
39 lutathione, F420, folate, and murein peptide biosyntheses illustrate convergent evolution of nonribos
40 t optimization in recapitulating complex PNP biosyntheses in microbial hosts and illustrates the util
41 e mammals cannot form 24-alkylsterols, their biosyntheses in P. carinii are attractive targets for th
42 s even higher due to inhibition of estrogens biosyntheses in peripheral tissue by the aromatase (CYP1
43  in maintaining both oxidative and reductive biosyntheses in response to changing nutrient availabili
44 of both peptidoglycan and wall teichoic acid biosyntheses in S. aureus.
45 role vis-a-vis withanolides and stigmasterol biosyntheses in Withania somnifera.
46 auxin can reciprocally regulate each other's biosyntheses, influence each other's response pathways,
47 o be involved in cofactor and small molecule biosyntheses, intermediary metabolism, transport, nitrog
48               The key chemical step in these biosyntheses is amide bond formation between aminoacyl b
49 d in the study of other complex Fe-S cluster biosyntheses is discussed.
50                           The structures and biosyntheses of "odd" siderophores can reveal the evolut
51               Recently, we reported that the biosyntheses of 3-thiaglutamate and ammosamide, single a
52                    However, the heterologous biosyntheses of bisBIAs have thus far been largely unexp
53                     The de novo heterologous biosyntheses of bisBIAs presented here provide the found
54           Therefore, the relatively distinct biosyntheses of cysteine and methionine in E. coli and S
55 ence of LpxC inhibitors, suggesting that the biosyntheses of fatty acids and lipid A are tightly regu
56                                Together, the biosyntheses of histidine, purines, and thiamine pyropho
57 hereas Apd6 LmbY and partially GriH from the biosyntheses of lincomycin and griselimycin, respectivel
58 ces methylmalonyl-CoA, the substrate for the biosyntheses of multimethyl-branched fatty acids such as
59 tative dyotropic rearrangement (DR), and the biosyntheses of other Callophycus secondary metabolites,
60  finding, which we consider relevant for the biosyntheses of other class III lantibiotics, underlines
61 o-installing di-iron amine oxygenases in the biosyntheses of other natural products.
62  our recent reports describing the bacterial biosyntheses of PBDEs, we predicted the presence of addi
63 efense signalling, transcription regulation, biosyntheses of secondary metabolites, and other biologi
64       In addition, new results indicate that biosyntheses of signal recognition particle RNA and telo
65 in share marked structural similarities, the biosyntheses of their bicyclic nuclei are wholly dissimi
66 enating enzymes postulated to be involved in biosyntheses of these unusual monomers.
67 ere also suggested to play key roles for the biosyntheses of various natural products.
68                                These complex biosyntheses, once only in the realm of the biopharmaceu
69  nature, yet the mechanisms underlying their biosyntheses remain largely unknown.
70 andidate genes suppressed glycogen and lipid biosyntheses resulting in inhibition of long-term carbon
71 inia carotovora, genes common to phosphonate biosyntheses were found in neighboring positions of thos
72 ymes, the ones involved in protein and lipid biosyntheses were observed to be particularly active.
73 ted in O antigen and capsular polysaccharide biosyntheses with those facilitating teichoic acid and N