ライフサイエンスコーパス: primary metabolism

1 of histone deacetylases on genes involved in primary metabolism.

2 origins of natural product biosynthesis from primary metabolism.

3 f the essential amino acid leucine, and thus primary metabolism.

4 ncH, -I, and -J and the enzyme homologues of primary metabolism.

5 rotective mechanisms and a downregulation of primary metabolism.

6 ation is the first reported in streptomycete primary metabolism.

7 l CoA:ACP transacylase (MAT), recruited from primary metabolism.

8 or pravastatin depend on cytochrome P450 for primary metabolism.

9 rage proteins synthesized by the pathways of primary metabolism.

10 ion and focused on the genetic variation for primary metabolism.

11 e less affected by environment than mQTLs of primary metabolism.

12 elated to herbivore-induced changes in plant primary metabolism.

13 antly influence the induced changes in plant primary metabolism.

14 ysis suggesting that Xpp1 is an activator of primary metabolism.

15 ecting target gene expression and ultimately primary metabolism.

16 binds promoters of genes encoding enzymes of primary metabolism.

17 t herbivory causes numerous changes in plant primary metabolism.

18 products of monosaccharide autoxidation and primary metabolism.

19 id cycle and is central to the regulation of primary metabolism.

20 ss cost, as resources are diverted away from primary metabolism.

21 ynthetic pathway, beginning from products of primary metabolism.

22 en balancing and highlight the robustness of primary metabolism.

23 f secondary metabolites, to the reactions of primary metabolism.

24 eatedly by duplication of a gene involved in primary metabolism.

25 g-opening of a purine heterocycle for use in primary metabolism.

26 lated to energy production, respiration, and primary metabolism.

27 and participates in the regulation of plant primary metabolism.

28 y one or more treatment; 28 were involved in primary metabolism.

29 metabolism, and fewer diterpenes of general (primary) metabolism.

30 ed into 19 categories with highest scores in primary metabolism (17%) and transcription (12%).

31 n numerous physiological processes including primary metabolism, although knowledge about the functio

32 tis elegans uses simple building blocks from primary metabolism and a strategy of modular assembly to

33 A), an essential cofactor utilized in ~4% of primary metabolism and central to fatty acid, polyketide

34 and underscores an important linkage between primary metabolism and epigenetic gene regulation.

35 es such as sterols and carotenes are part of primary metabolism and found essentially in all plants.

36 nk the production of a tRNA-modified base to primary metabolism and further clarify the biosynthetic

37 at AsCYP51H10 enzyme has been recruited from primary metabolism and has acquired a different function

38 upstream of the cAMP-PKA pathway, influences primary metabolism and hyphal growth, while represses se

39 s and they play numerous functional roles in primary metabolism and in ecological interactions.

40 ming recognized as major regulators of plant primary metabolism and of other cellular processes.

41 e has been validated as an essential gene to primary metabolism and presents a target for the identif

42 ger gene set that includes genes involved in primary metabolism and production of other specialized c

43 nover compares with filament growth rate and primary metabolism and provided new insights into the bi

44 mpartmentalized into regions responsible for primary metabolism and reproduction (core genome), and p

45 rk during drought stress, linking changes in primary metabolism and the initiation of stress response

46 -regulation of a series of genes involved in primary metabolism and the phenylpropanoid pathway, and

47 infer the level of global reconfiguration of primary metabolism and the subsequent changes in downstr

48 discuss examples of enzyme recruitment from primary metabolism and the variety of paths taken by dup

49 er understanding of the relationship between primary metabolism and virus infection.

50 oxylation step in both leucine biosynthesis (primary metabolism) and methionine chain elongation of g

51 at SN1 silencing affects cell division, leaf primary metabolism, and cell wall composition in potato

52 er cellular functions such as transcription, primary metabolism, and stress resistance.

53 relationships of leaf gas-exchange with leaf primary metabolism are still limited.

54 mix of chemistry that has been adopted from primary metabolism as well as those with no chemical pre

55 esize basic metabolites needed for survival (primary metabolism), but different taxa produce distinct

56 synthesis, the pentose phosphate pathway and primary metabolism, but lower levels of defense-related

57 ived from terpene synthase genes involved in primary metabolism by duplication and divergence in stru

58 d for two model systems, liver and adipocyte primary metabolism, by applying an algorithm for top-dow

59 Primary metabolism can be measured by the universally co

60 pectrometry-based profiling of lipidomic and primary metabolism changes in the liver and plasma revea

61 gnals derived from combinatorial assembly of primary metabolism-derived building blocks, play a centr

62 trong down-regulation of genes implicated in primary metabolism, detoxication apparatus and signal tr

63 but also increases the supply of carbon from primary metabolism, energy and reducing power, which may

64 permit rapid reconstruction and modeling of primary metabolism for all plant genomes in the database

65 co-opting the sulphur-delivery machinery of primary metabolism for the biosynthesis of sulphur-conta

66 Isotopic labeling studies of primary metabolism frequently utilize GC/MS to quantify

67 some results were similar, the expression of primary metabolism genes and heat shock proteins was hig

68 Although primary metabolism genes have been retained, the E. webe

69 athway leads to widespread downregulation of primary metabolism genes, an upregulation in virulence f

70 In contrast to most primary metabolism genes, the genes involved in secondar

71 A (CoA) synthase, the homologous enzyme from primary metabolism, HMGS has several differences at the

72 Compartmentation of primary metabolism in developing embryos poses a signifi

73 dition, we studied the genetic regulation of primary metabolism in dry and imbibed Arabidopsis (Arabi

74 further highlights how genes associated with primary metabolism in nonpathogenic Streptomyces species

75 the genetic factors underlying variation in primary metabolism in potato (Solanum tuberosum), we hav

76 that host plants receive from altering their primary metabolism in response to insect herbivory.

77 resolution proteomics is used to investigate primary metabolism in techniques such as stable isotope

78 play essential roles in enzymes involved in primary metabolism including energy transduction and deo

79 l molecules from modified building blocks of primary metabolism, including an unusual xylopyranose-ba

80 l of plant development, stress response, and primary metabolism, including nutrient homeostasis.

81 suggested, the extent to which autophagy and primary metabolism interact to support plant respiration

82 sive picture of (13)C distribution along the primary metabolism is elaborated.

83 Our results revealed that primary metabolism is reconfigured in many ways during T

84 t to other rice studies, the heritability of primary metabolism is similar to Arabidopsis.

85 ependent TRB1 target genes, many involved in primary metabolism, is decreased in the absence of TRB1

86 corbate, and inositol metabolism, as well as primary metabolisms like amino acid synthesis and glycol

87 ulated whereas for several genes involved in primary metabolism lower expression was detected.

88 uinate (secondary metabolism) and shikimate (primary metabolism) metabolic activities are encoded by

89 In plant primary metabolism, metabolic fine-tuning involves feed-

90 grape leaf development to alter patterns of primary metabolism, nutrient mobilization, and defense i

91 study were compared with previous results on primary metabolism obtained from the same material and t

92 ctances, alongside the 53 data profiles from primary metabolism of 14 species grown in different expe

93 RV) in order to investigate the influence of primary metabolism on virus infection.

94 ith known functions mostly encode enzymes of primary metabolism or other key biochemical components,

95 ontology analysis for 538 genes involved in primary metabolism, oxidation reduction and response to

96 st hints for coregulation patterns involving primary metabolism plus leaf water and carbon balances t

97 ent with species relationships inferred from primary-metabolism (PM) gene genealogies, and FUM cluste

98 me-dependent protein synthesis and essential primary metabolism processes, such as targeted protein d

99 In addition to the importance of their primary metabolism, some cyanobacteria are prolific prod

100 r evolutionarily constrained counterparts in primary metabolism, specialized metabolic enzymes may be

101 Mutants demonstrate changes in primary metabolism, such as modulation of fatty acid com

102 ne (Cys) is a master control switch of plant primary metabolism that coordinates the flux of sulfur w

103 siological trait by measuring the changes in primary metabolism that occur during the transition in o

104 wledge has existed for sulfur trafficking in primary metabolism, the secondary metabolism involving s

105 ication between organelles and regulation of primary metabolism through redox-mediated signaling are

106 four enzymes are proposed to siphon CoA from primary metabolism to create the side chains for the pre

107 remains one of the least understood areas of primary metabolism to date.

108 r, little is known about the contribution of primary metabolism to the evolution of specialized metab

109 diverts the central flux of carbon from the primary metabolism to the synthesis of myriad phenolics.

110 ; it diverts the central flux of carbon from primary metabolism to the synthesis of myriad phenolics.

111 A substantial proportion of primary metabolism transcripts were decreased in border

112 plant, leaf, and cellular level showed that primary metabolism was reduced by growth in limiting N,

113 omata suggests a significant manipulation of primary metabolism, we also characterized the gall trans

114 onserved and evolutionarily ancient genes of primary metabolism were activated at intermediate time p

115 d activities of the main enzymes involved in primary metabolism were compared.

116 Major pathways in primary metabolism were identified, indicating significa

117 quires JA-Ile signaling-dependent changes in primary metabolism, which are not compromised in the COI

118 d expressed sequence tags several enzymes of primary metabolism whose expression during spore germina

119 this pathway is an important link connecting primary metabolism with development.

120 biosynthesis is an important link connecting primary metabolism with development.