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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.
7 hough Nitrosomonas europaea lacks measurable alpha-ketoglutarate dehydrogenase activity, the recent c
10 and, between phosphotransacetylase (PTA) and alpha-ketoglutarate dehydrogenase (alpha-KGDH) for their
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-
29 hydrolipoamide dehydrogenase subunits of the alpha-ketoglutarate dehydrogenase complex (alphaKGDH), a
31 m for 24 h, resulted in a pronounced loss of alpha-ketoglutarate dehydrogenase complex (KGDHC) activi
34 Brain metabolism and the activity of the alpha-ketoglutarate dehydrogenase complex (KGDHC), a mit
37 activity of a key mitochondrial enzyme, the alpha-ketoglutarate dehydrogenase complex (KGDHC), decli
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
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
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
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
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
64 xylic acid cycle, but we recently found that alpha-ketoglutarate dehydrogenase (KDH) activity is lack
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
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
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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