コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ATHIONINE gamma-SYNTHASE (AtCGS), Met's main regulatory enzyme.
2 the molecular architecture of this important regulatory enzyme.
3 of structure-function relationships of this regulatory enzyme.
4 ct binding of a kinesin-related protein to a regulatory enzyme.
5 nit interactions, resulting in an allosteric regulatory enzyme.
6 biopterin (BH4) is a cofactor of a number of regulatory enzymes.
7 operties and effector sensitivities of these regulatory enzymes.
8 y functional human E2 that mediated enhanced regulatory enzyme activities but, lacking E3BP, supporte
9 '-AMP, is a potent activator of an important regulatory enzyme, AMP-activated protein kinase (AMPK).
10 that HDAC3 represses the synthesis of a key regulatory enzyme and reveal a novel mechanism by which
12 ssociated with hyperlipidemia, altered lipid regulatory enzymes and receptors, and increased risk of
13 his issue, we examined the expression of S1P regulatory enzymes and S1P receptors during cardiac deve
14 sed to describe the allosteric properties of regulatory enzymes and subsequently extended to receptor
16 e self-association and activity of important regulatory enzymes, and examined conformational properti
18 e macromolecular complex suggests that these regulatory enzymes are coordinately positioned to regula
21 ,4-trisphosphate 5/6-kinase (ITPK1) is a key regulatory enzyme at the branch point for the synthesis
22 moserine dehydrogenase (HSD) function as key regulatory enzymes at branch points in the aspartate ami
23 encodes a member of the Pak family of actin-regulatory enzymes, but whose in vivo function is unknow
24 ulations of MASS models explicitly show that regulatory enzymes can control dynamic states of network
25 dvances in our understanding of how PTMs and regulatory enzymes control the signaling activity of RLR
26 suggest the EGAP NAT complex is an essential regulatory enzyme controlling the function of a subset o
27 we demonstrate that prostaglandin E2 and its regulatory enzyme, COX-2, are also targets of Tpl2-trans
28 nthesis by increasing phosphorylation of the regulatory enzyme CTP:phosphocholine cytidylyltransferas
29 ectively inhibiting the activity of the rate-regulatory enzyme, CTP:phosphocholine cytdylyltransferas
31 is frequently considered vested in classical regulatory enzymes, each strongly displaced from equilib
32 Protein kinases constitute a large family of regulatory enzymes, each with a distinct specificity to
33 hat S. mutans ADP-Glc PPase is an allosteric regulatory enzyme exhibiting sensitivity to modulation b
34 ine cytidylyltransferase (Pcyt2) is the main regulatory enzyme for de novo biosynthesis of phosphatid
35 he expression of ent-kaurene synthase, a key regulatory enzyme for gibberellin synthesis, the followi
36 ee-fold increase in the activity of the rate-regulatory enzyme for PC synthesis, cytidylyltransferase
37 '-phosphate hydrolase has been proposed as a regulatory enzyme for vitamin B-6, but we found B-6 vita
39 r structural principles operate in bacterial regulatory enzymes, gene repressors (and the related nuc
40 il now the identity or the function of these regulatory enzymes has not been defined in any crop plan
43 ndritic cells (DCs) competent to express the regulatory enzyme IDO in mice are a small but distinctiv
44 inactivate GS kinase-3beta (GSK-3beta), the regulatory enzyme immediately upstream of GS, by serine
45 de strong evidence that NCED is indeed a key regulatory enzyme in ABA biosynthesis in leaves, and dem
46 Although it has never been reported as a regulatory enzyme in any system studied to date, kinetic
47 ene determining the activity of an important regulatory enzyme in catecholamine inactivation is assoc
48 of phosphoglucomutase 1 (PGM), an important regulatory enzyme in cellular glucose utilization and en
50 ivates acetyl-CoA carboxylase (ACC), the key regulatory enzyme in fatty acid biosynthesis, in the arc
51 er fructose-1,6-bisphosphatase (FBPase) is a regulatory enzyme in gluconeogenesis that is elevated by
57 cceptor) oxidoreductase, EC 1.7.99.5), a key regulatory enzyme in one-carbon metabolism, results in a
58 idermal ornithine decarboxylase (ODC), a key regulatory enzyme in polyamine biosynthesis, may suppres
59 cose (Glc) pyrophosphorylase (AGPase), a key regulatory enzyme in starch biosynthesis, is highly regu
67 latter group as purF, which encodes the key regulatory enzyme in the de novo purine synthetic pathwa
68 ic acid (ACC) synthase which is an important regulatory enzyme in the ethylene biosynthetic pathway.
71 a polypeptide revealed its identity as a key regulatory enzyme in the glycolytic pathway, namely phos
72 endent isocitrate dehydrogenase (IDH), a key regulatory enzyme in the Krebs cycle, is a multi-tetrame
73 ansferase (AANAT) is the penultimate and key regulatory enzyme in the melatonin biosynthetic pathway.
74 e to acetyl-CoA in mitochondria and is a key regulatory enzyme in the metabolism of glucose to acetyl
75 rnesyl pyrophosphate synthase (hFPPS), a key regulatory enzyme in the mevalonate pathway, catalyzes t
76 tors of IkappaB kinase-beta (IKKbeta), a key regulatory enzyme in the nuclear factor-kappaB (NF-kappa
78 e to acetyl-CoA in mitochondria and is a key regulatory enzyme in the oxidation of glucose to acetyl-
81 lutaryl coenzyme A (HMG-CoA) synthase, a key regulatory enzyme in the pathway for endogenous choleste
82 lutaryl-coenzyme A (HMG-CoA) synthase, a key regulatory enzyme in the pathway for endogenous choleste
83 din-endoperoxide synthase 2 (PTGS2) is a key regulatory enzyme in the synthesis of the antifibrotic a
84 (PDE) of retinal photoreceptors is a central regulatory enzyme in the visual transduction pathway of
85 bifunctional substrate preference of the key regulatory enzyme in tocopherol (vitamin E) biosynthesis
88 stinct compartmentalization of PP2A and PP2A regulatory enzymes in plasma membrane microdomains and i
90 use the total amount of one of the principle regulatory enzymes in the extract (ACP, the enzyme compl
91 minant negative and dominant active forms of regulatory enzymes in the Ras/MAPK and PKB pathways and
92 apeutic potential of inhibiting two critical regulatory enzymes in this pathway-kynurenine-3-monooxyg
93 nfection stimulated expression of the immune regulatory enzyme indoleamine 2,3 dioxygenase (IDO) in l
94 is uniquely competent to express the T-cell regulatory enzyme indoleamine 2,3-dioxygenase (IDO) in m
95 brain, AKAP79/150 incorporates PKA and other regulatory enzymes into signal transduction networks tha
98 alterations in protein expression levels of regulatory enzymes involved in glucose and choline metab
99 erations in the protein expression levels of regulatory enzymes involved in lipid metabolism, includi
101 e previously shown declining activity of the regulatory enzyme lactosylceramide N-acetylglucosaminylt
102 affinity of receptors or in the activity of regulatory enzymes may alter the susceptibility of certa
103 -glucose pyrophosphorylase (AGPase) is a key regulatory enzyme of bacterial glycogen and plant starch
104 clopropane-1-carboxylic acid synthase, a key regulatory enzyme of ethylene biosynthesis) and LeIAA (A
105 encoding acetyl-CoA carboxylase-alpha, a key regulatory enzyme of fatty acid synthesis, is transcribe
113 ose-5-phosphate synthase (DXS), an important regulatory enzyme of the mevalonate-independent pathway
114 onine decarboxylase (AdoMetDC) is a critical regulatory enzyme of the polyamine biosynthetic pathway
116 In the yeast Saccharomyces cerevisiae, key regulatory enzymes of gluconeogenesis such as fructose-1
118 nd neutral sphingomyelinase (NSMase) are key regulatory enzymes of sphingolipid metabolism, promoting
119 oA reductase and acetyl-CoA carboxylase (key regulatory enzymes of sterol synthesis and fatty acid sy
121 expression of the myofibrils and the calcium-regulatory enzyme SERCA2, and reduced the magnitude and
122 y showed that androgen induces the first and regulatory enzyme spermidine/spermine N1-acetyltransfera
123 es, which phosphorylate and thereby activate regulatory enzymes such as phospholipase C-gamma 1 and p
124 are reflected in the fractional states of a regulatory enzyme, such as the fraction of the total enz
125 rofiling to identify candidate substrates of regulatory enzymes, such as kinases and ubiquitin ligase
126 nsferase (plsB) of Escherichia coli is a key regulatory enzyme that catalyzes the first committed ste
128 on in catechol-O-methyltransferase (COMT), a regulatory enzyme that controls dopamine availability.
132 merous functional aspects of a key metabolic regulatory enzyme that is important for high-titer viral
134 cible 6-phosphofructo-2-kinase, a glycolysis-regulatory enzyme that protects against diet-induced int
135 tosolic phospholipase A(2) (cPLA(2)alpha), a regulatory enzyme that releases arachidonic acid (AA) fo
136 ndoleamine 2,3-dioxygenase 1 (IDO1) is a key regulatory enzyme that supports Treg function and periph
139 ansferase subunit is a member of a family of regulatory enzymes that are known to control a range of
141 is a complex process involving a variety of regulatory enzymes that control the intracellular respon
142 ons along with the transcription factors and regulatory enzymes that have been previously identified
144 increased by 40%) and the involvement of key regulatory enzymes, using isolated working rat hearts ex
145 hanism of tissue-specific expression of this regulatory enzyme, we characterized the major (type 2) C
146 1%; beta-HAD, 32%) and glycolytic (PFK, 18%) regulatory enzymes were also increased in mVEGF-/- mice.
147 redoxin reductases (TRs) are important redox regulatory enzymes, which control the redox state of thi
149 mic, effector-modified interactions of these regulatory enzymes with the flexibly held outer domains
150 choline cytidylyltransferase (CCT), the rate-regulatory enzyme within the CDP-choline pathway, by 40%
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。