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1 lding domain of a large multienzyme complex, 2-oxoglutarate dehydrogenase.
2 ction by inhibiting the mitochondrial enzyme 2-oxoglutarate dehydrogenase.
4 istae, activation of mitochondrial AMPK, and 2-oxoglutarate dehydrogenase, a rate-liming enzyme in tr
5 complete in many other anaerobes (absence of 2-oxoglutarate dehydrogenase activity), isotopic labelin
7 acid as a cofactor (pyruvate dehydrogenase, 2-oxoglutarate dehydrogenase and glycine decarboxylase).
8 e to succinate and thus functionally replace 2-oxoglutarate dehydrogenase and succinyl-CoA synthetase
9 arboxylic acid (TCA) cycle because they lack 2-oxoglutarate dehydrogenase and thus cannot convert 2-o
11 organisms in which three enzymes compose the 2-oxoglutarate dehydrogenase complex (ODH), actinobacter
13 nsensitive and -sensitive E1 subunits of the 2-oxoglutarate dehydrogenase complex (OGDHC) regulate ti
14 cinate selectively reduced the expression of 2-oxoglutarate dehydrogenase complex (OGDHc), the enzyme
16 -dependent E1o component (EC 1.2.4.2) of the 2-oxoglutarate dehydrogenase complex catalyses a rate-li
18 -E2) in 6 of 19 patients (31.6%), and to the 2-oxoglutarate dehydrogenase complex E2 (OGDC-E2) in 1 o
19 2 (BCOADC-E2) in 4 of 49 (8%), to PDC-E2 and 2-oxoglutarate dehydrogenase complex E2 (OGDC-E2) in 9 o
20 t of the gene encoding the E1 subunit of the 2-oxoglutarate dehydrogenase complex in the antisense or
22 ) regenerated by Complex I is reduced by the 2-oxoglutarate dehydrogenase Complex yielding succinyl-C
23 cle enzymes, pyruvate dehydrogenase complex, 2-oxoglutarate dehydrogenase complex, NAD-malic enzyme,
30 show nuclear localization of aconitase 2 and 2-oxoglutarate dehydrogenase in mouse embryonic stem cel
31 ith engineered variants of the E2 subunit of 2-oxoglutarate dehydrogenase indicate that binding sites
34 al OPN knockout or AAV9-mediated delivery of 2-oxoglutarate dehydrogenase-like (Ogdhl) to the heart.
35 are reported unique properties of the human 2-oxoglutarate dehydrogenase multienzyme complex (OGDHc)
36 bunit binding domain from Escherichia coli's 2-oxoglutarate dehydrogenase multienzyme complex (termed
37 e succinyltransferase (E2o) component of the 2-oxoglutarate dehydrogenase multienzyme complex is comp
38 succinyltransferase polypeptide chain of the 2-oxoglutarate dehydrogenase multienzyme complex of Esch
40 se (E2p, E2o) components of the pyruvate and 2-oxoglutarate dehydrogenase multienzyme complexes are s
41 : see text]-fatty acid oxidation pathway and 2-oxoglutarate dehydrogenase of the citric acid cycle, r
44 d mouse models and organoids, we reveal that 2-oxoglutarate dehydrogenase (OGDH), the enzymatic subun
47 alpha-ketoglutarate dehydrogenase (kdh), and 2-oxoglutarate dehydrogenase (sucA), were responsive to
48 amine diphosphate-dependent Escherichia coli 2-oxoglutarate dehydrogenase, which is a key component o