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1 ion and inhibition of the Krebs cycle enzyme alpha-ketoglutarate dehydrogenase.
2 CA cycle enzymes, pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase.
3 piration: the bc1 center and, more recently, alpha-ketoglutarate dehydrogenase.
4 A cycle enzymes isocitrate dehydrogenase and alpha-ketoglutarate dehydrogenase.
5 fects on intact mitochondria by inactivating alpha-ketoglutarate dehydrogenase.
6                          LSG184 is devoid of alpha-ketoglutarate dehydrogenase activity, indicating t
7 hough Nitrosomonas europaea lacks measurable alpha-ketoglutarate dehydrogenase activity, the recent c
8                       Despite the absence of alpha-ketoglutarate dehydrogenase activity, whole cells
9                        Here we show that the alpha-ketoglutarate dehydrogenase (alpha-KGDH) complex i
10 and, between phosphotransacetylase (PTA) and alpha-ketoglutarate dehydrogenase (alpha-KGDH) for their
11  and organization of the multienzyme complex alpha-ketoglutarate dehydrogenase (alpha-KGDH).
12 ansferase, and the E2 and E3 subunits of the alpha-ketoglutarate dehydrogenase (alphaKGDH) complex as
13 , we found an increase in phosphorylation of alpha-ketoglutarate dehydrogenase (alphaKGDH) in female
14 chondrial LipDH is part of the mitochondrial alpha-ketoglutarate dehydrogenase and branched chain alp
15  acid cofactor of pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase and other mitochondria
16 citrate dehydrogenase mutants, diminished in alpha-ketoglutarate dehydrogenase and succinyl-CoA ligas
17 ributions of regulation of the activities of alpha-ketoglutarate dehydrogenase and the aspartate-glut
18 ltiple proteins, including the E2 subunit of alpha-ketoglutarate dehydrogenase and the glutathione S-
19 complexes, including pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase, and branched-chain ke
20 ve E2 subunits of pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase, and Gcv3, the H prote
21 se components of the pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase, and glycine reductase
22 se components of the pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase, and glycine reductase
23  cardiac sarcoplasmic reticulum Ca2+-ATPase, alpha-ketoglutarate dehydrogenase, and the mitochondrial
24 lines in mitochondrial function and identify alpha-ketoglutarate dehydrogenase as a likely site of fr
25 id is a coenzyme for pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase, branched chain-ketoac
26 ltienzyme complexes: pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase, branched-chain alpha-
27                         Glutathionylation of alpha-ketoglutarate dehydrogenase can therefore be viewe
28 %), isocitrate dehydrogenase (-27%), and the alpha-ketoglutarate dehydrogenase complex (-57%).
29 hydrolipoamide dehydrogenase subunits of the alpha-ketoglutarate dehydrogenase complex (alphaKGDH), a
30 succinyltransferase, the E2 component of the alpha-ketoglutarate dehydrogenase complex (KDC).
31 m for 24 h, resulted in a pronounced loss of alpha-ketoglutarate dehydrogenase complex (KGDHC) activi
32                          The activity of the alpha-ketoglutarate dehydrogenase complex (KGDHC) declin
33                            The mitochondrial alpha-ketoglutarate dehydrogenase complex (KGDHC) is def
34     Brain metabolism and the activity of the alpha-ketoglutarate dehydrogenase complex (KGDHC), a mit
35                          The activity of the alpha-ketoglutarate dehydrogenase complex (KGDHC), an ar
36                              The activity of alpha-ketoglutarate dehydrogenase complex (KGDHC), an im
37  activity of a key mitochondrial enzyme, the alpha-ketoglutarate dehydrogenase complex (KGDHC), decli
38  a striking reduction in the activity of the alpha-ketoglutarate dehydrogenase complex (KGDHC).
39                                     Purified alpha-ketoglutarate dehydrogenase complex also is inacti
40  Lipoamide dehydrogenase, a component of the alpha-ketoglutarate dehydrogenase complex and two other
41 sferase to supply alpha-ketoglutarate to the alpha-ketoglutarate dehydrogenase complex and would, in
42 oxymethyl transferase, and components of the alpha-ketoglutarate dehydrogenase complex in conjunction
43                         Zn(2+) inhibition of alpha-ketoglutarate dehydrogenase complex required enzym
44                           Purified pig heart alpha-ketoglutarate dehydrogenase complex was strongly i
45 drogenase complex (OGHDC) (also known as the alpha-ketoglutarate dehydrogenase complex) is a rate-lim
46 d its target DLST-the E2 subcomponent of the alpha-ketoglutarate dehydrogenase complex, a rate-contro
47 ion of ThPP levels causes dysfunction of the alpha-ketoglutarate dehydrogenase complex, which explain
48 ced CoA to the reduction of NAD(+) using the alpha-ketoglutarate dehydrogenase complex.
49     This was attributed to inhibition of the alpha-ketoglutarate dehydrogenase complex.
50 notransferase, alanine aminotransferase, and alpha-ketoglutarate dehydrogenase complex.
51  respiration by reversible inhibition of the alpha-ketoglutarate dehydrogenase complex.
52 oteins, we demonstrate that the pyruvate and alpha-ketoglutarate dehydrogenase complexes directly cat
53 osttranslational lipoylation of pyruvate and alpha-ketoglutarate dehydrogenase complexes, resulting i
54  component of the pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase complexes.
55 ymes of central metabolism, the pyruvate and alpha-ketoglutarate dehydrogenase complexes.
56 d restored full activity to the pyruvate and alpha-ketoglutarate dehydrogenase complexes.
57 complex I during ischemia and complex IV and alpha-ketoglutarate dehydrogenase during reperfusion.
58 uld potentially compensate for inhibition of alpha-ketoglutarate dehydrogenase during symbiotic nitro
59                             Using a purified alpha-ketoglutarate dehydrogenase from pig hearts, the e
60 ken to identify the site and consequences of alpha-ketoglutarate dehydrogenase glutathionylation.
61 zobium japonicum sucA mutant that is missing alpha-ketoglutarate dehydrogenase is able to grow on mal
62                                              alpha-Ketoglutarate dehydrogenase is highly susceptible
63       It was determined that inactivation of alpha-ketoglutarate dehydrogenase is responsible, in lar
64 xylic acid cycle, but we recently found that alpha-ketoglutarate dehydrogenase (KDH) activity is lack
65 d lipoamide dehydrogenase (E3) components of alpha-ketoglutarate dehydrogenase (KDH).
66 ed chain amino acid dehydrogenase (BCDH) and alpha-ketoglutarate dehydrogenase (KDH).
67 e activities of specific Krebs cycle enzymes alpha-ketoglutarate dehydrogenase (KGDH) and succinate d
68 fects on the tricarboxylic acid cycle enzyme alpha-ketoglutarate dehydrogenase (KGDH) which provides
69 lexes, such as pyruvate dehydrogenase (PDH), alpha-ketoglutarate dehydrogenase (KGDH), and the glycin
70 plexes and Krebs cycle enzymes revealed that alpha-ketoglutarate dehydrogenase (KGDH), succinate dehy
71 ich inhibit pyruvate dehydrogenase (PDH) and alpha-ketoglutarate dehydrogenase (KGDH), we hypothesize
72 rts its effects on respiration by inhibiting alpha-ketoglutarate dehydrogenase (KGDH).
73                       Isolated mitochondrial alpha-ketoglutarate dehydrogenase (KGDHC) and pyruvate d
74 n of hypoxic/anaerobic genes was elevated in alpha-ketoglutarate dehydrogenase mutants, whereas expre
75 ial chaperones and assists in the folding of alpha-ketoglutarate dehydrogenase (OGDH), a rate-limitin
76 by using a coupled enzyme system with either alpha-ketoglutarate dehydrogenase or pyruvate dehydrogen
77 d) in association with peptides derived from alpha-ketoglutarate dehydrogenase (oxoglutarate dehydrog
78 utamine synthetase, glutamate dehydrogenase, alpha-ketoglutarate dehydrogenase, phosphate-activated g
79                         Glutathionylation of alpha-ketoglutarate dehydrogenase protected lipoic acid
80 l aspartate aminotransferase followed by the alpha-ketoglutarate dehydrogenase reaction.
81 zymes of the tricarboxylic acid (TCA) cycle, alpha-ketoglutarate dehydrogenase (sucAB) and succinyl c
82 lot analysis revealed that the E2 subunit of alpha-ketoglutarate dehydrogenase was reversibly glutath
83  The sucA gene, encoding the E1 component of alpha-ketoglutarate dehydrogenase, was cloned from Brady

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