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1 regulation of translation, fermentation, and amino acid biosynthesis.
2 (metB), proline (proC), or tryptophan (trpD) amino acid biosynthesis.
3 known functions, nearly all were involved in amino acid biosynthesis.
4  phosphorylation activates genes involved in amino acid biosynthesis.
5 rtant but not previously appreciated role in amino acid biosynthesis.
6 ic flow of intermediates from fatty acid and amino acid biosynthesis.
7 ases, both of which are involved in aromatic amino acid biosynthesis.
8 hosate and subsequent inhibition of aromatic amino acid biosynthesis.
9 quiring reactions such as photosynthesis and amino acid biosynthesis.
10 mediates (anaplerosis) is primarily used for amino acid biosynthesis.
11 ed-chain amino acid degradation and aromatic amino acid biosynthesis.
12 erts chorismate into prephenate for aromatic amino acid biosynthesis.
13 nsitions and sustaining growth by activating amino acid biosynthesis.
14 encoding enzymes involved in translation and amino acid biosynthesis.
15 o Salmonella exerts considerable pressure on amino acid biosynthesis.
16  activating amino acid promoters and de novo amino acid biosynthesis.
17 redients targeting two different branches of amino acid biosynthesis.
18 es and likely reflects different demands for amino acid biosynthesis.
19 se two enzymes have overlapping functions in amino acid biosynthesis.
20 volutionarily related to ligases involved in amino acid biosynthesis.
21  arginine and Gcn4p, the master regulator of amino acid biosynthesis.
22 uclear CIT2 gene in order to ensure adequate amino acid biosynthesis.
23 arvation, the kinase GCN2 in yeast activates amino acid biosynthesis.
24 mans cannot be associated only with costs of amino acid biosynthesis.
25 YjgF homolog have a defect in branched-chain amino acid biosynthesis.
26 yceride synthesis, lipid beta-oxidation, and amino acid biosynthesis.
27 and peroxisomal enzymes required for de novo amino acid biosynthesis.
28 cutive reactions in the aspartate pathway of amino acid biosynthesis.
29 cofactors in cells for use in nucleotide and amino acid biosynthesis.
30             The first enzyme of the aromatic amino acid biosynthesis, 3-deoxy-D-arabino-heptulosonate
31 or two stress-inducible enzymes unrelated to amino acid biosynthesis and accumulation of the indolic
32 tory P: rotein,' regulates genes involved in amino acid biosynthesis and catabolism and other cellula
33 e acts at the first branch-point of aromatic amino acid biosynthesis and catalyzes the conversion of
34 ffector protein that links OPDA signaling to amino acid biosynthesis and cellular redox homeostasis i
35 chondrial enzyme required for branched chain amino acid biosynthesis and for the stability of mitocho
36 myces cerevisiae required for branched-chain amino acid biosynthesis and for the stability of wild-ty
37 pression of genes involved in branched chain amino acid biosynthesis and in ammonia assimilation.
38 ses promoting colonization include essential amino acid biosynthesis and iron acquisition pathways, i
39 ation of genes encoding proteins involved in amino acid biosynthesis and iron metabolism, as well as
40 example, Ilv5 is required for branched chain amino acid biosynthesis and mtDNA stability.
41 termined and revealed physiological roles in amino acid biosynthesis and nutrient import.
42 a gene cohort responsible for stress-induced amino acid biosynthesis and observed markedly increased
43 servation of a common protein domain linking amino acid biosynthesis and protein synthesis implies an
44 pathways utilized for glucose catabolism and amino acid biosynthesis and revealed that the organism's
45 est a role for the Tsc1 and Tsc2 proteins in amino acid biosynthesis and sensing.
46  expected up-regulation of genes involved in amino acid biosynthesis and transport but also uncovered
47 xpression of many aminoacyl-tRNA synthetase, amino acid biosynthesis and transport genes in Bacillus
48 mal medium (n = 230) included those encoding amino acid biosynthesis and transport systems, outer mem
49 oup of genes that are essential for aromatic amino acid biosynthesis and transport.
50 eat part by the DksA-dependent regulation of amino acid biosynthesis and transport.
51  predominantly metabolic enzymes involved in amino acid biosynthesis and transport.
52 ters and activation of certain promoters for amino acid biosynthesis and transport.
53  of expression of aminoacyl-tRNA synthetase, amino acid biosynthesis and transporter gene expression
54 ng genes involved in cell cycle progression, amino acid biosynthesis, and carbohydrate transport and
55 eins required for oxidative stress response, amino acid biosynthesis, and fermentation together with
56 ysaccharide biosynthesis (wbkA), in aromatic amino acid biosynthesis, and in type IV secretion (virB1
57         Only then did water-soluble enzymes, amino acid biosynthesis, and intermediary metabolism evo
58 ciency led to changes in glucose metabolism, amino acid biosynthesis, and lipid biosynthesis that wer
59 rotein that also functions in branched chain amino acid biosynthesis, and one or more factors require
60 erential gene expression for myocyte growth, amino acid biosynthesis, and oxidative stress were relat
61 lish a role for CRP(Mt) in the regulation of amino acid biosynthesis, and show that reduced serine pr
62 s involved in translation, solute transport, amino acid biosynthesis, and tungsten and intermediary c
63 esponses, two to proteins involved in sulfur amino acid biosynthesis, and two having significant homo
64 olved in the Msn2/4 stress response pathway, amino-acid biosynthesis, and mitochondrial maintenance.
65 ster is that four genes involved in branched amino acid biosynthesis are located near its 5' end.
66 the established shikimic pathway of aromatic amino acid biosynthesis, are absent in most euryarchaeot
67 2O2 resistance included DNA repair, aromatic amino acid biosynthesis (aroBK), Fe-S cluster biosynthes
68 e the first committed step of branched-chain amino acid biosynthesis, but ilvG is unique for doing so
69 nts with the conserved metabolic pathways of amino acid biosynthesis can inform us about this history
70 he fourth enzyme in the aspartate pathway of amino acid biosynthesis, catalyzes the phosphorylation o
71 s cellular processes, including respiration, amino acid biosynthesis, cofactor biosynthesis, tRNA mod
72 ed downregulation of several photosynthesis, amino acid biosynthesis, energy metabolism genes; and an
73  variety of functional categories, including amino acid biosynthesis, energy metabolism, protein synt
74 roteins were predicted to be involved in the amino acid biosynthesis, energy metabolism, purines and
75  growth via inhibition of the branched-chain amino acid biosynthesis enzyme dihydroxyacid dehydratase
76  genes coding for shikimic acid and aromatic amino acid biosynthesis enzymes, leading to the producti
77            While Gcn2 promotes expression of amino acid biosynthesis enzymes, the mechanism and funct
78   Through transgenic expression of exogenous amino acid biosynthesis enzymes, vertebrate cells overco
79 on of genes involved in cysteine metabolism, amino acid biosynthesis, fermentation, energy metabolism
80 rough incorporating a network-based model of amino acid biosynthesis (from r = 0.07 to 0.80 for mRNA-
81  the fitness cost of synonymous mutations in amino acid biosynthesis genes and in the transcriptional
82 tabolism and a decrease in the expression of amino acid biosynthesis genes and transfer RNAs.
83                Approximately one-half of the amino acid biosynthesis genes downregulate during growth
84 ome production and increase transcription of amino acid biosynthesis genes during the stringent respo
85 abolic gene expression, but not induction of amino acid biosynthesis genes en masse.
86                                Expression of amino acid biosynthesis genes in bacteria is often repre
87 uired for the derepression of branched chain amino acid biosynthesis genes that seem to have a second
88  box family of aminoacyl-tRNA synthetase and amino acid biosynthesis genes, which are regulated by a
89 t only small increases in mRNA were seen for amino acid biosynthesis genes.
90 onments, we present evidence suggesting that amino acid biosynthesis has been broadly optimized to re
91     The mathematical model of branched chain amino acid biosynthesis in E. coli K12 presented here in
92 inase, an enzyme in the aspartate pathway of amino acid biosynthesis in Escherichia coli, catalyzes t
93 ne and valine binding control branched chain amino acid biosynthesis in Escherichia coli.
94 ell as decreased carbohydrate metabolism and amino acid biosynthesis in favor of nutrient transport a
95 phate (DKFP), a precursor sugar for aromatic amino acid biosynthesis in Methanocaldococcus jannaschii
96 f amino acids while diverting resources into amino acid biosynthesis in nutrient-poor environments.
97 s the first committed step of branched-chain amino acid biosynthesis in plants and bacteria.
98 amine into bacteriocytes, thereby regulating amino acid biosynthesis in the bacteriocyte.
99 compares favorably with 10 missing genes for amino acid biosynthesis in the complete Escherichia coli
100 should be physically separated from aromatic amino acid biosynthesis in the cytoplasm so as to avoid
101  complex control of the pathway for aromatic amino acid biosynthesis in the pathogen Mycobacterium tu
102  operation of the common pathway of aromatic amino acid biosynthesis in the reverse of its normal bio
103 onferring similar capabilities for essential amino acid biosynthesis, in both cases precisely complem
104 on factors or that mediate tRNA charging and amino acid biosynthesis increased or decreased, respecti
105  thailandensis, when exposed to the aromatic amino acid biosynthesis inhibitor glyphosate, induces (o
106  root and shoot levels of the branched-chain amino acid biosynthesis intermediate 2-oxobutanoate; Ser
107            Here we show that cognate bias in amino acid biosynthesis is present in the other domains
108 nresolved whether the supply of nitrogen for amino acid biosynthesis is supplemented by recycling of
109                            Genes involved in amino acid biosynthesis, lipid biosynthesis and oxygen t
110 analysis is applied to electron-transfer and amino acid biosynthesis networks yielding a more compreh
111 ulosis provide exquisite control of aromatic amino acid biosynthesis, not only controlling flux into
112    In addition to the toxin genes, genes for amino acid biosynthesis, nutrient transport, fermentatio
113 StlA], isocitrate lyase [Icl1], polyaromatic amino acid biosynthesis [PAA], NADH-dependent glutamate
114  overexpressed genes function in pathways of amino acid biosynthesis (particularly methionine) and su
115 ion, the aerobic/anaerobic diauxic shift and amino acid biosynthesis pathway repression.
116 ch is the first enzyme in the branched-chain amino acid biosynthesis pathway.
117 HAS), the first enzyme in the branched-chain amino acid biosynthesis pathway.
118  analyses while utilizing lifestyle specific amino acid biosynthesis pathways (where possible) to det
119 s revealed that strain 195 contains complete amino acid biosynthesis pathways, even though current ge
120 rophic mutations of one or more genes on the amino acid biosynthesis pathways.
121 tream of the Akt/mTOR pathway to promote the amino acid biosynthesis program, to reduce protein catab
122 reater abundance of genes for nucleotide and amino acid biosynthesis, repair of alkylated DNA and the
123              Unexpectedly, genes involved in amino acid biosynthesis represent only a quarter of the
124 tive stress tolerance and general control of amino acid biosynthesis, respectively.
125 rerouted to other metabolic pathways such as amino acid biosynthesis, results in the alleviation of a
126 ra's genome encodes most genes for essential amino acid biosynthesis, several genes in essential amin
127 sed our module to control flux into aromatic amino acid biosynthesis to increase titers of shikimate
128 numerous transcription units associated with amino acid biosynthesis, transport of macromolecules, an
129 lower rRNA promoter activity and much higher amino acid biosynthesis/transport promoter activity than
130 and from the inversely growth-rate-dependent amino acid biosynthesis/transport promoters PargI, PhisG
131  including regulation of gene expression and amino acid biosynthesis via transamidation pathways.
132                                              Amino acid biosynthesis was chosen to demonstrate the an
133                                   Enzymes of amino acid biosynthesis were higher in coculture than in
134            We found that 26 genes underlying amino acid biosynthesis were up-regulated in bacteriocyt
135 rexpressed pathways included sporulation and amino acid biosynthesis, whereas up-regulated pathways i

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