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1 ing domain of a large multienzyme complex, 2-oxoglutarate dehydrogenase.
2 ion by inhibiting the mitochondrial enzyme 2-oxoglutarate dehydrogenase.
3        The tricarboxylic acid cycle enzyme 2-oxoglutarate dehydrogenase (2-OGDH) converts 2-oxoglutar
4 tae, activation of mitochondrial AMPK, and 2-oxoglutarate dehydrogenase, a rate-liming enzyme in tric
5 mplete in many other anaerobes (absence of 2-oxoglutarate dehydrogenase activity), isotopic labeling
6 ccinyltransferase (Dlst), a subunit of the 2-oxoglutarate dehydrogenase (alpha-KGDH) complex.
7 ficient PDAC cells through the inhibition of oxoglutarate dehydrogenase-an enzyme of the tricarboxyli
8 cid as a cofactor (pyruvate dehydrogenase, 2-oxoglutarate dehydrogenase and glycine decarboxylase).
9 to succinate and thus functionally replace 2-oxoglutarate dehydrogenase and succinyl-CoA synthetase.
10 boxylic acid (TCA) cycle because they lack 2-oxoglutarate dehydrogenase and thus cannot convert 2-oxo
11                               Pyruvate and 2-oxoglutarate dehydrogenases are substituted by 'ancient'
12 ganisms in which three enzymes compose the 2-oxoglutarate dehydrogenase complex (ODH), actinobacteria
13    Pyruvate dehydrogenase complex (PDHC) and oxoglutarate dehydrogenase complex (OGDC), which belong
14 id dehydrogenase complex (BCOADC), and the 2-oxoglutarate dehydrogenase complex (OGDC).
15 ensitive and -sensitive E1 subunits of the 2-oxoglutarate dehydrogenase complex (OGDHC) regulate tiss
16 nate selectively reduced the expression of 2-oxoglutarate dehydrogenase complex (OGDHc), the enzyme f
17                                        The 2-oxoglutarate dehydrogenase complex (OGHDC) (also known a
18 ependent E1o component (EC 1.2.4.2) of the 2-oxoglutarate dehydrogenase complex catalyses a rate-limi
19 hydrogenase complex E (BCOADC-E2), and the 2-oxoglutarate dehydrogenase complex E (OGDC-E2).
20 2) in 6 of 19 patients (31.6%), and to the 2-oxoglutarate dehydrogenase complex E2 (OGDC-E2) in 1 of
21 (BCOADC-E2) in 4 of 49 (8%), to PDC-E2 and 2-oxoglutarate dehydrogenase complex E2 (OGDC-E2) in 9 of
22 of the gene encoding the E1 subunit of the 2-oxoglutarate dehydrogenase complex in the antisense orie
23                              A traditional 2-oxoglutarate dehydrogenase complex is missing in the cya
24 regenerated by Complex I is reduced by the 2-oxoglutarate dehydrogenase Complex yielding succinyl-CoA
25 e enzymes, pyruvate dehydrogenase complex, 2-oxoglutarate dehydrogenase complex, NAD-malic enzyme, an
26 ered with pyruvate dehydrogenase complex and oxoglutarate dehydrogenase complex-RNS can cause inactiv
27 -oxo-acid dehydrogenase, and E2 subunit of 2-oxoglutarate dehydrogenase complex.
28  2-oxoglutarate decarboxylase (E1o) of the 2-oxoglutarate dehydrogenase complex.
29 ents of pyruvate dehydrogenase complex and 2-oxoglutarate dehydrogenase complex.
30  includes pyruvate dehydrogenase complex and oxoglutarate dehydrogenase complex.
31     We report that the intact pyruvate and 2-oxoglutarate dehydrogenase complexes specifically copuri
32 yl CoA ligase, aconitase, and pyruvate and 2-oxoglutarate dehydrogenase complexes.
33                 (a) Functionally competent 2-oxoglutarate dehydrogenase (E1o-h) and dihydrolipoyl suc
34 ow nuclear localization of aconitase 2 and 2-oxoglutarate dehydrogenase in mouse embryonic stem cells
35 h engineered variants of the E2 subunit of 2-oxoglutarate dehydrogenase indicate that binding sites f
36 n this organism, even though a traditional 2-oxoglutarate dehydrogenase is lacking.
37  to enzymes of the tricarboxylic acid cycle (oxoglutarate dehydrogenase, isocitrate dehydrogenase) an
38                                        The 2-oxoglutarate dehydrogenase-like (OGDHL) protein is a rat
39  OPN knockout or AAV9-mediated delivery of 2-oxoglutarate dehydrogenase-like (Ogdhl) to the heart.
40 re reported unique properties of the human 2-oxoglutarate dehydrogenase multienzyme complex (OGDHc),
41 nit binding domain from Escherichia coli's 2-oxoglutarate dehydrogenase multienzyme complex (termed B
42 succinyltransferase (E2o) component of the 2-oxoglutarate dehydrogenase multienzyme complex is compos
43 ccinyltransferase polypeptide chain of the 2-oxoglutarate dehydrogenase multienzyme complex of Escher
44  interactions with other components of the 2-oxoglutarate dehydrogenase multienzyme complex.
45  (E2p, E2o) components of the pyruvate and 2-oxoglutarate dehydrogenase multienzyme complexes are spe
46 see text]-fatty acid oxidation pathway and 2-oxoglutarate dehydrogenase of the citric acid cycle, res
47              We further examined the role of oxoglutarate dehydrogenase (OGDH) and its transcription
48 arker glutarylcarnitine and demonstrate that oxoglutarate dehydrogenase (OGDH) is responsible for thi
49 ogenase E1 component subunit beta (PDHB) and oxoglutarate dehydrogenase (OGDH) required dual phosphor
50 ived from alpha-ketoglutarate dehydrogenase (oxoglutarate dehydrogenase (OGDH)), a ubiquitous intrace
51 in RBR E3 ubiquitin protein ligase (parkin), oxoglutarate dehydrogenase (OGDH), and leucine rich repe
52                               However, the 2-oxoglutarate dehydrogenase (OGDH), branched-chain 2-oxoa
53                              Inhibition of 2-oxoglutarate dehydrogenase (OGDH), the E1 subunit of the
54 mouse models and organoids, we reveal that 2-oxoglutarate dehydrogenase (OGDH), the enzymatic subunit
55 edundancy with the ubiquitous OGDH-encoded 2-oxoglutarate dehydrogenase (OGDH).
56 ire the expression of the TCA cycle enzyme 2-oxoglutarate dehydrogenase (OGDH).
57 pha-ketoglutarate dehydrogenase (kdh), and 2-oxoglutarate dehydrogenase (sucA), were responsive to ac
58 s and thus upregulates ATP citrate lyase and oxoglutarate dehydrogenase, two key enzymes that determi
59 ine diphosphate-dependent Escherichia coli 2-oxoglutarate dehydrogenase, which is a key component of