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1 ns identified in an individual with inactive dihydrolipoamide dehydrogenase.
2 es in a yeast strain deficient in endogenous dihydrolipoamide dehydrogenase.
3 sposon insertion into the A. phagocytophilum dihydrolipoamide dehydrogenase 1 gene (lpda1 [APH_0065])
4 ons to phenazines through the common subunit dihydrolipoamide dehydrogenase, a flavoprotein encoded b
5 ion while a P453L change resulted in reduced dihydrolipoamide dehydrogenase abundance in the mitochon
6 ls lacking endogenous DLD even when residual dihydrolipoamide dehydrogenase activity was as low as 21
7 these mutations decreased to various degrees dihydrolipoamide dehydrogenase activity, whereas dimer i
8 roteins in subcellular organelles, including dihydrolipoamide dehydrogenase and catalase, and show th
9 ervation through evolution, it is unknown if dihydrolipoamide dehydrogenases are functionally equival
10                                          The dihydrolipoamide dehydrogenase-binding protein (E3BP) an
11                                          The dihydrolipoamide dehydrogenase-binding protein (E3BP), a
12                  Protein X, recently renamed dihydrolipoamide dehydrogenase-binding protein (E3BP), i
13 protein (BP), and the BP associated with its dihydrolipoamide dehydrogenase (BP.E3).
14                                 In vivo, the dihydrolipoamide dehydrogenase component (E3) is associa
15 ds, is essentially devoid of the constituent dihydrolipoamide dehydrogenase component (E3).
16                                    The mouse dihydrolipoamide dehydrogenase (Dld) gene has been clone
17                                              Dihydrolipoamide dehydrogenase (DLD) is a multifunctiona
18                    The mitochondrial enzyme, dihydrolipoamide dehydrogenase (DLD), is essential for e
19 hages while the PDH E3 enzyme, also known as dihydrolipoamide dehydrogenase (DLD), is irreversibly in
20 al and genomic analyses, we further identify dihydrolipoamide dehydrogenase (DLD), the E3 subunit of
21 acid sequence of TGP2 has high similarity to dihydrolipoamide dehydrogenase (DLDH) from a variety of
22  describes the enzymatic characterization of dihydrolipoamide dehydrogenase (DLDH) from Streptococcus
23 the present study, we have characterized the dihydrolipoamide dehydrogenase (DLDH) of Strepto-coccus
24 coccus pneumoniae strains lacking the enzyme dihydrolipoamide dehydrogenase (DLDH) show markedly redu
25 cing, but also identifies Hsp60 polymers and dihydrolipoamide dehydrogenase (DLDH).
26 ehydrogenase (E(1)) and about 6 molecules of dihydrolipoamide dehydrogenase (E(3)) with its binding p
27 ding sites for two other component proteins, dihydrolipoamide dehydrogenase (E3) and pyruvate dehydro
28  and smaller pyruvate dehydrogenase (E1) and dihydrolipoamide dehydrogenase (E3) complexes.
29                                              Dihydrolipoamide dehydrogenase (E3) is a flavoprotein co
30 dihydrolipoamide acetyltransferase (E2), and dihydrolipoamide dehydrogenase (E3) subunits of the pyru
31 ng protein (E3BP), is required for anchoring dihydrolipoamide dehydrogenase (E3) to the dihydrolipoam
32 -keto acid decarboxylase/dehydrogenase (E1), dihydrolipoamide dehydrogenase (E3), BCKD kinase, and BC
33 1p), dihydrolipoyl transacetylase (E2p), and dihydrolipoamide dehydrogenase (E3), to carry out the ox
34 ranched-chain amino acids was diagnosed with dihydrolipoamide dehydrogenase (E3; dihydrolipoamide: NA
35  E426 is conserved throughout non-halophilic dihydrolipoamide dehydrogenases, E423 is only present in
36                            The gene encoding dihydrolipoamide dehydrogenase from Mycobacterium tuberc
37             A homology-modelled structure of dihydrolipoamide dehydrogenase from the halophilic archa
38 our site-directed mutations of the Haloferax dihydrolipoamide dehydrogenase have been made (E423D, E4
39                                        Human dihydrolipoamide dehydrogenase (hE3) is an enzymatic com
40                                        Human dihydrolipoamide dehydrogenase (hLADH, hE3) deficiency (
41                               Regions within dihydrolipoamide dehydrogenase involved in association w
42                                              Dihydrolipoamide dehydrogenase is a common component of
43                                              Dihydrolipoamide dehydrogenase is a flavoenzyme that rev
44 arasites possess two distinct genes encoding dihydrolipoamide dehydrogenases (LipDH), which are indis
45                                              Dihydrolipoamide dehydrogenase (Lpd) and dihydrolipoamid
46        In this study, we identify the 57-kDa dihydrolipoamide dehydrogenase (Lpd) as a surface-expose
47 d, the mutation was in the lpd gene encoding dihydrolipoamide dehydrogenase (LPD), a component of PDH
48 ntified a virulence-associated gene encoding dihydrolipoamide dehydrogenase (lpd).
49                                         This dihydrolipoamide dehydrogenase null mutant will not grow
50               The Dld gene product, known as dihydrolipoamide dehydrogenase or the E3 component, cata
51            Enzymatic assays for catalase and dihydrolipoamide dehydrogenase show that sample preparat
52 tified the lipoamide succinyltransferase and dihydrolipoamide dehydrogenase subunits of the alpha-ket
53  OGDH, dihydrolipoyl succinyltransferase and dihydrolipoamide dehydrogenase to form a hybrid 2-oxoglu
54  enzymes that include glutathione reductase, dihydrolipoamide dehydrogenase, trypanothione reductase,
55                                        Human dihydrolipoamide dehydrogenases with selected amino acid