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1 n alpha-glycol-3-phosphate dehydrogenase and l-lactate dehydrogenase.
2 graphic analysis of allosterically inhibited L-lactate dehydrogenase.
3 rogenase (GAPDH), L-lactate dehydrogenase B, L-lactate dehydrogenase A chain, L-lactate dehydrogenase
4 that these CD dimers inhibit the activity of L-lactate dehydrogenase and citrate synthase at least in
5           Initial screening showed that only L-lactate dehydrogenase and citrate synthase were inhibi
6 uce D(-)-lactate by deleting the native ldh (L-lactate dehydrogenase) and alsS (acetolactate synthase
7 rogenase B, L-lactate dehydrogenase A chain, L-lactate dehydrogenase, and ATP synthase subunit beta,
8 ctase, holo-[acyl-carrier-protein] synthase, l-lactate dehydrogenase, and uncharacterized protein.
9 es, LdhD (D-lactate dehydrogenase) and LldD (L-lactate dehydrogenase) are correctly annotated.
10 tion, employing cystathionine beta-lyase and L-lactate dehydrogenase as coupling enzymes, are describ
11 tion, employing cystathionine beta-lyase and L-lactate dehydrogenase as coupling enzymes, is describe
12 raldehyde-3-phosphate dehydrogenase (GAPDH), L-lactate dehydrogenase B, L-lactate dehydrogenase A cha
13 3-phosphate-dehydrogenase, alpha enolase and L-lactate dehydrogenase B-chain) and in oxidative stress
14 pha E-beta D) of Bacillus stearothermophilus L-lactate dehydrogenase (bsLDH).
15 s generated by the reduction of pyruvate via l-lactate dehydrogenase, but this enzyme does not effici
16 permease and candidate genes for both d- and l-lactate dehydrogenase enzymes.
17                                      Catfish L-lactate dehydrogenase, glyceraldehyde-3-phosphate dehy
18 overexpression of a Lactobacillus helveticus L-lactate dehydrogenase in M. buryatense resulted in an
19 g of lldA, a Neisseria meningitidis gene for L-lactate dehydrogenase (L-LDH).
20 cus mutans NG8 which produces a thermolabile L-(+)-lactate dehydrogenase (LDH) activity.
21 duced amino acid sequences of cDNAs encoding L-lactate dehydrogenase (LDH) isozymes A (muscle) and B
22 ldehyde-3-phosphate dehydrogenase (GAPDH) to L-lactate Dehydrogenase (LDH) using enzymes from differe
23 ed on reduced graphene oxide (RGO-AuNPs) and l-lactate dehydrogenase (LDH) was developed for the sens
24                         The up-regulation of L-lactate dehydrogenase (LDH), an intracellular enzyme p
25 d elongation factor thermo-unstable (EF-Tu), l-lactate dehydrogenase (LDH), protein D (PD), and pepti
26 bumin, 3.4 g/dL; beta2-microglobulin, 5.7 mg/L; lactate dehydrogenase (LDH), 397 IU/L; and normal liv
27 sative stress by expressing an NO.-inducible L-lactate dehydrogenase (ldh1, SACOL0222) divergently tr
28 ty in sequence and catalytic properties, the l-lactate dehydrogenases (LDHs) in lactic acid bacteria
29 mylase level, 1435 U/L (normal level, <140 U/L); lactate dehydrogenase level, 253 U/L (normal level,
30 ranscriptional regulation of the respiratory l-lactate dehydrogenase LldD in vitro and in mouse model
31 ACB), that is distinct from the flavoprotein L-lactate dehydrogenase (LldD).
32  alternative, iron-sulfur cluster-containing L-lactate dehydrogenase (LutACB), that is distinct from
33 ing GWAS and metabolomic data identified two L-lactate dehydrogenases, one polyamine oxidase, and one
34 l dehydrogenase, D-glucose dehydrogenase and L-lactate dehydrogenase respectively.
35 ate kinase, phosphate acetyltransferase, and L-lactate dehydrogenase) resulted in a strain able to pr
36 alpha-glycerol-3-phosphate dehydrogenase and l-lactate dehydrogenase was reported.