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1 KOs for carnitine palmitoyltransferase 2 and pyruvate carboxylase.
2 hydrogenase 1, malic enzyme 1, and cytosolic pyruvate carboxylase.
3  gluconeogenesis by allosteric activation of pyruvate carboxylase.
4 lso contain a biotinylated protein, probably pyruvate carboxylase.
5 yl-CoA and propionyl-CoA carboxylases and of pyruvate carboxylase.
6 on of glutamine into lipids does not involve pyruvate carboxylase.
7              Furthermore, enzyme activity of pyruvate carboxylase, a key regulator of pyruvate cyclin
8 APDHS mediates this shift through changes in pyruvate carboxylase activity and aspartate synthesis, b
9 -body lipolysis, hepatic acetyl CoA content, pyruvate carboxylase activity and hepatic glucose produc
10 spartate indicated high rates of anaplerotic pyruvate carboxylase activity and incomplete equilibrati
11 ese two carboxylases in the islet and of low pyruvate carboxylase activity in the islet in NIDDM.
12 arbamoylphosphate synthetase 1 (urea cycle), pyruvate carboxylase (anaplerosis, gluconeogenesis), pro
13 ficial miRNAs for simultaneous repression of pyruvate carboxylase and glutaminase by selecting all se
14  fibroblasts, and this flux depended on both pyruvate carboxylase and malic enzyme 1 activity.
15 f mRNAs encoding two malate-forming enzymes, pyruvate carboxylase and malic enzyme, are observed in t
16 termediates and bicarbonate is diagnostic of pyruvate carboxylase and PEPCK flux in the liver.
17 esses two oxaloacetate-synthesizing enzymes, pyruvate carboxylase and phosphoenolpyruvate carboxylase
18 rmed that flux rates through PDH, as well as pyruvate carboxylase and pyruvate cycling activities, ar
19 glucose oxidation partially occurred through pyruvate carboxylase and rendered NNT knockdown cells mo
20 ts differentiation-dependent expression like pyruvate carboxylase and the cytosolic isozymes CA II an
21 ndrial glycerol phosphate dehydrogenase, and pyruvate carboxylase), and ion channels/pumps (Kir6.2, V
22  non-neuronal SNAP25-like protein homolog 1, pyruvate carboxylase, and BCKDC kinase.
23 , phosphoenolpyruvate carboxykinase (PEPCK), pyruvate carboxylase, and glucose-6-phosphatase, and the
24 ic acetyl-CoA content, a potent activator of pyruvate carboxylase, and increased glycerol conversion
25 CCA-1/propionyl-CoA carboxylase alpha, PYC-1/pyruvate carboxylase, and MCCC-1/methylcrotonyl-CoA carb
26 rial carboxylases propionyl-CoA carboxylase, pyruvate carboxylase, and methylcrotonoyl-CoA carboxylas
27 C]pyruvate into the hepatic TCA cycle is via pyruvate carboxylase, and that cataplerotic flux through
28 tion-based model selection method identified pyruvate carboxylase as a key model component.
29 te entering the Krebs cycle is converted via pyruvate carboxylase as an anaplerotic route at a rate m
30 lipogenesis involves an inhibitory effect on pyruvate carboxylase as opposed to acetyl CoA carboxylas
31                               Interestingly, pyruvate carboxylase ASO also reduced adiposity, plasma
32                                              Pyruvate carboxylase ASO did not alter de novo fatty aci
33                                              Pyruvate carboxylase ASO had similar effects in Zucker D
34                                              Pyruvate carboxylase ASO reduced plasma glucose concentr
35     Here we report the complete structure of pyruvate carboxylase at 2.0 angstroms resolution, which
36                                Chicken liver pyruvate carboxylase catalyzes a nonclassical ping-pong
37 o urea cycle defects, organic acidurias, and pyruvate carboxylase deficiency as a treatable condition
38  and pyruvate conversion to oxaloacetate via pyruvate carboxylase (DET0119-0120).
39        In addition, C. elegans homologues of pyruvate carboxylase, DNA gyrase, beta-adrenergic recept
40 arbon entry into the TCA cycle via increased pyruvate carboxylase expression.
41 tochondrial citrate synthase flux (V CS) and pyruvate carboxylase flux (V PC) in vivo.
42 ted mitochondrial TCA cycle flux and induced pyruvate carboxylase flux and gluconeogenesis in lean ra
43 rates of hepatic mitochondrial oxidation and pyruvate carboxylase flux in healthy volunteers followin
44 gnal generated by anaplerosis from increased pyruvate carboxylase flux is essential for glucose-stimu
45 xidation decreased, whereas rates of hepatic pyruvate carboxylase flux remained unchanged.
46                                      Hepatic pyruvate carboxylase flux was impaired with ChREBP delet
47  tricarboxylic acid (TCA) cycle activity and pyruvate carboxylase flux were normal in newly diabetic
48 ic lipolysis, hepatic acetyl-CoA content and pyruvate carboxylase flux, while also increasing mitocho
49 dipose tissue (WAT) leading to reductions in pyruvate carboxylase flux.
50  hepatic acetyl-CoA allosteric activation of pyruvate carboxylase flux.
51 ative pyruvate dehydrogenase and anaplerotic pyruvate carboxylase fluxes.
52                     In addition, SNPs in the pyruvate carboxylase gene showed evidence of association
53 arboxyl transferase domain of Rhizobium etli pyruvate carboxylase have been determined for the forwar
54 ondrial enzyme that provides bicarbonate for pyruvate carboxylase in liver and kidney.
55                      We assessed the role of pyruvate carboxylase in regulating glucose and lipid met
56      We conclude that the decreased mGPD and pyruvate carboxylase in the pancreatic islet of the GK r
57  also exhibited increased sensitivity to the pyruvate carboxylase inhibitor phenylacetate.
58                Tissue-specific inhibition of pyruvate carboxylase is a potential therapeutic approach
59           In particular, we demonstrate that pyruvate carboxylase is essential to re-supply the deple
60 ty fits the suggestion that in M. smegmatis, pyruvate carboxylase is not anaplerotic but rather gluco
61 gh C. reinhardtii has a single gene encoding pyruvate carboxylase, it has six genes encoding putative
62  in Listeria monocytogenes by inhibiting its pyruvate carboxylase (LmPC), a biotin-dependent enzyme w
63 tors, including the central metabolic enzyme pyruvate carboxylase (LmPC).
64                             This decrease in pyruvate carboxylase-mediated [14C] carbon fixation was
65 CanB is crucial in bicarbonate provision for pyruvate carboxylase-mediated oxaloacetate synthesis.
66 demonstrate a potentially important role for pyruvate carboxylase-mediated pyruvate cycling pathways
67        Moreover, the result is a function of pyruvate-carboxylase, mitochondrial pyruvate transporter
68 tate production in the gut, modulating liver pyruvate carboxylase, MPC1/2, and FBP1, establishing a g
69  flux through three anaplerotic pathways: 1) pyruvate carboxylase of pyruvate derived from glycolytic
70 pyruvate derived from glycolytic sources; 2) pyruvate carboxylase of pyruvate derived from nonglycoly
71 phate dehydrogenase (mGPD) (EC 1.1.99.5) and pyruvate carboxylase (PC) (EC 6.4.1.1) have been reporte
72 ited apparent correlation with gluconeogenic pyruvate carboxylase (PC) activity in hepatocytes.
73 ial pyruvate carrier 1/2 (MPC1/2) levels and pyruvate carboxylase (PC) activity, in comparison to nor
74 and glutamine, which require the activity of pyruvate carboxylase (PC) and glutaminase 1 (GLS1), resp
75        The reason was increased flux through pyruvate carboxylase (PC) and the malate-pyruvate and ci
76  correlation of insulin secretion rates with pyruvate carboxylase (PC) flux suggest that a pyruvate-m
77                                              Pyruvate carboxylase (PC) has important roles in metabol
78  observed in the structure of the tetrameric pyruvate carboxylase (PC) holoenzyme.
79                                              Pyruvate carboxylase (PC) is a tetrameric enzyme that co
80 ive mRNA level of the key anaplerotic enzyme pyruvate carboxylase (PC) were 80-90% lower in human pan
81                                              Pyruvate carboxylase (PC), a multifunctional biotin-depe
82 pensatory anaplerotic mechanism catalyzed by pyruvate carboxylase (PC), allowing the cells to use glu
83                                 5S and human pyruvate carboxylase (PC), an enzyme crucial to gluconeo
84 s the expression of the mitochondrial enzyme pyruvate carboxylase (PC), resulting in diminished produ
85 nsulin secretion, we lowered the activity of pyruvate carboxylase (PC), the major enzyme of anapleros
86 thermore, we discovered that A3-6 bound with pyruvate carboxylase (PC), then inhibited PC activity, r
87  secretion (GSIS) is tightly correlated with pyruvate carboxylase (PC)-catalyzed anaplerotic flux int
88 cetate in the carboxyl transferase domain of pyruvate carboxylase (PC).
89 e generated mice with a liver-specific KO of pyruvate carboxylase (Pcx(L-/-)) to understand the role
90 -dependent carboxylation to oxaloacetate via pyruvate carboxylase (Pcx).
91 plets was suggested by the identification of pyruvate carboxylase, prohibitin, and a subunit of ATP s
92 y metabolism: carbamoylphosphate synthetase, pyruvate carboxylase, propionyl-CoA carboxylase and 3-me
93 biopsy specimens and found that only hepatic pyruvate carboxylase protein levels related strongly wit
94         The assayable activity and amount of pyruvate carboxylase protein were decreased approximatel
95 egmatis for biotin auxotrophs and identified pyruvate carboxylase (Pyc) as required for biotin biosyn
96  thermoautotrophicum strain DeltaH possessed pyruvate carboxylase (PYC), and this biotin prototroph r
97 4)beta(4)-type acetyl coenzyme A-independent pyruvate carboxylase (PYC), composed of 64.2-kDa biotiny
98 ted under low CO2 , including both PEPCs and pyruvate carboxylase (PYC), whereas ME abundance did not
99  mutations in the acetyl-CoA binding site of pyruvate carboxylase (PycA) rescued cefuroxime resistanc
100                                       A high pyruvate carboxylase rate (V(PC), approximately 0.14-0.1
101  found that the otherwise integrative enzyme pyruvate carboxylase (TgPyC) is dispensable not only in
102 sulinotropic polypeptide (GIP) receptor, and pyruvate carboxylase) that are important regulators of b
103                        With the exception of pyruvate carboxylase, the activities of other enzymes we
104                              The activity of pyruvate carboxylase, the predominant enzyme for anapler
105 ing a conversion of lactate to pyruvate, via pyruvate carboxylase to oxaloacetate, and via PCK2 to ph
106 d the biotin carrying polypeptide from yeast pyruvate carboxylase to the carboxyl terminus of Cin8p.
107 ate-malate shuttle is suggested by unchanged pyruvate carboxylase Vmax and a fourfold higher release
108                              The activity of pyruvate carboxylase was low in muscle, and no PEP carbo
109  propionyl-CoA carboxylase and mitochondrial pyruvate carboxylase, was inhibited.
110              The activities of both mGPD and pyruvate carboxylase were also normalized by insulin tre
111                                              Pyruvate carboxylase, which catalyzes the first step of
112                      Inactivation studies of pyruvate carboxylase, which has an analogous mode of act
113 nzyme of the glycerol phosphate shuttle, and pyruvate carboxylase, which is the key component of the
114          Pyruvate carboxylation catalyzed by pyruvate carboxylase will supply oxaloacetate to mitocho

 
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