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1 e (MAs(III)), which is a potent inhibitor of glycerol-3-phosphate dehydrogenase.
2 acetone phosphate transport system and an sn-glycerol-3-phosphate dehydrogenase.
3 e and suppression of GLUT2, glucokinase, and glycerol-3-phosphate dehydrogenase.
4 ncluding pyruvate dehydrogenase kinase 4 and glycerol 3-phosphate dehydrogenase 1, was acutely induce
5                                     In yeast glycerol-3-phosphate dehydrogenase 1 is essential for sy
6 , both the malate/oxaloacetate shuttle and a glycerol-3-phosphate dehydrogenase 1(Gpd1p)-dependent sh
7  co-imported with the PTS2-containing enzyme Glycerol-3-phosphate dehydrogenase 1, Gpd1.
8 ion (A280V) in a conserved amino acid of the glycerol-3-phosphate dehydrogenase 1-like (GPD1-L) gene.
9 lic cohorts and detected the upregulation of glycerol-3-phosphate dehydrogenase 1-like (GPD1L) among
10                 Here, we identify the enzyme glycerol-3-phosphate dehydrogenase 1-like (GPD1L) as a n
11  production of the mature miRNA, derepresses glycerol-3-phosphate dehydrogenase 1-like enzyme (GPD1L)
12            Recently, a novel mutation in the glycerol-3-phosphate dehydrogenase 1-like gene (GPD1-L)
13 azepam also blocked the mutant A280V GPD1-L (glycerol-3-phosphate dehydrogenase 1-like) effect on red
14 luted and identified by mass spectrometry as glycerol-3-phosphate dehydrogenase 2 (Gpd2).
15 nthase activity (P<0.001), a 48% increase in glycerol-3-phosphate dehydrogenase activity (P<0.01) and
16 ve effects by inducing maximal mitochondrial glycerol-3-phosphate dehydrogenase activity in rat liver
17 d by 12 +/- 0.4 % in TG SOL and single fibre glycerol-3-phosphate dehydrogenase activity was decrease
18 nergy metabolism (triosephosphate isomerase, glycerol-3-phosphate-dehydrogenase, alpha enolase and L-
19                                  They encode glycerol-3-phosphate dehydrogenase, an ABC transporter,
20 viously characterized glpD gene, encoding sn-glycerol-3-phosphate dehydrogenase, an open reading fram
21 s that apicoplast-targeted Plasmodium yoelii glycerol 3-phosphate dehydrogenase and glycerol 3-phosph
22 ons of Escherichia coli encode the anaerobic glycerol 3-phosphate dehydrogenase and glycerol 3-phosph
23 pathic protein, which interacts with aerobic glycerol-3-phosphate dehydrogenase and increases dehydro
24 dulated formation of a complex between alpha-glycerol-3-phosphate dehydrogenase and l-lactate dehydro
25 sure and a glycerol synthesis gene, gpd1(+) (glycerol-3-phosphate dehydrogenase), and is independent
26 rogenase, glucose 6-phosphate dehydrogenase, glycerol 3-phosphate dehydrogenase, and glucose oxidase.
27 rug tolerance loci, glpABC, the anaerobic sn-glycerol-3-phosphate dehydrogenase, and plsB, an sn-glyc
28  and the glycerol-3-phosphate shuttle (Gut2, glycerol-3-phosphate dehydrogenase) are novel longevity
29                       The activation of pure glycerol-3-phosphate dehydrogenase by either L-ascorbic
30                       MicroRNA-210 targeting glycerol-3-phosphate dehydrogenase controls mitochondria
31 oglucomutase, triosephosphate isomerase, and glycerol 3-phosphate dehydrogenase define a cluster of s
32 ol kinase encoded by glpK and suggest that a glycerol-3-phosphate dehydrogenase encoded by the upstre
33                                              Glycerol-3-phosphate dehydrogenase from pig brain mitoch
34  uncoupling protein (Ucp1) and mitochondrial glycerol-3-phosphate dehydrogenase (Gdm) result in mice
35 xpress the gene for the conserved aerobic sn-glycerol-3-phosphate dehydrogenase GlpD.
36                                           Sn-glycerol-3-phosphate dehydrogenase (GlpD) is an essentia
37 a glycerol-3-phosphate transporter (GlpT), a glycerol-3-phosphate dehydrogenase (GlpD), and a thiored
38 stabilize the integral membrane flavoenzyme, glycerol-3-phosphate dehydrogenase (GlpD), and the solub
39 three-step reaction utilizing three enzymes: glycerol 3-phosphate dehydrogenase, glycerol 3-phosphate
40 osphoserine phosphatase (PSP) motif fused to glycerol-3-phosphate dehydrogenase (GPD) domains.
41              The high flux through cytosolic glycerol-3-phosphate dehydrogenase (GPD) is required to
42 r glycerol levels because of a defect in the glycerol-3-phosphate dehydrogenase (GPD1) gene: deletion
43 nes encoding stress-related proteins such as glycerol-3-phosphate dehydrogenase (gpd1+) and trehalose
44  Saccharomyces cerevisiae has two homologous glycerol-3-phosphate dehydrogenases, Gpd1 and Gpd2, that
45          The glycerol-producing PTS2 protein glycerol-3-phosphate dehydrogenase Gpd1p shows a tripart
46 rial lipopolysaccharide (LPS), mitochondrial glycerol 3-phosphate dehydrogenase (GPD2) regulates gluc
47 hain cation of R269 lies at the surface of l-glycerol 3-phosphate dehydrogenase (GPDH) and forms an i
48 ion and activity (P<0.02), a 61% increase in glycerol-3-phosphate dehydrogenase (GPDH) activity (P<0.
49              Here we evaluate the effects of glycerol-3-phosphate dehydrogenase (Gpdh) and cytosolic
50  An extensive investigation of two proteins, glycerol-3-phosphate dehydrogenase (GPDH) and superoxide
51                                 We find that glycerol-3-phosphate dehydrogenase (GPDH) is localized a
52                  In fruit flies, the encoded glycerol-3-phosphate dehydrogenase (GPDH) protein evolve
53 nd hence their glycolytic enzymes, including glycerol-3-phosphate dehydrogenase (GPDH), are considere
54 n extensive investigation of three proteins, glycerol-3-phosphate dehydrogenase (GPDH), superoxide di
55 ehyde-3-phosphate dehydrogenase (GAPDH), and glycerol-3-phosphate dehydrogenase (GPDH).
56        We have investigated the evolution of glycerol-3-phosphate dehydrogenase (Gpdh).
57 ate decarboxylase (ScOMPDC), and human liver glycerol 3-phosphate dehydrogenase (hlGPDH) for catalysi
58                        The R269A mutation of glycerol-3-phosphate dehydrogenase (hlGPDH) results in a
59 robic conditions, increasing the activity of glycerol-3-phosphate dehydrogenase induces complex dynam
60                                   Aerobic sn-glycerol 3-phosphate dehydrogenase is a cytoplasmic memb
61 echanistically, we showed that mitochondrial glycerol-3-phosphate dehydrogenase is a novel target of
62 ng the activity of its ancillary subunit-the glycerol-3-phosphate dehydrogenase-like protein.
63            For the heavily entangled protein glycerol-3-phosphate dehydrogenase, limited-proteolysis
64  sn-glycerol 3-phosphate by mitochondrial sn-glycerol 3-phosphate dehydrogenase (mGPDH) is a major pa
65           Pancreatic beta-cell mitochondrial glycerol-3-phosphate dehydrogenase (mGPDH) plays a major
66 letion within the glpD gene encoding aerobic glycerol-3-phosphate dehydrogenase might account for the
67              The mitochondrial FAD-dependent glycerol-3-phosphate dehydrogenase (mtGPD) plays an impo
68 mology, the closest structural neighbors are glycerol-3-phosphate dehydrogenase, N-(1-d-carboxylethyl
69  truncated substrate glycolaldehyde (GLY) by glycerol 3-phosphate dehydrogenase (NAD (+), GPDH) satur
70  triosephosphate isomerase (EC 5.3.1.1), and glycerol-3-phosphate dehydrogenase (NAD+)(EC 1.1.1.8).
71                                 Knockdown of glycerol-3-phosphate dehydrogenase negated microRNA-210
72 ally linked to the gpdC gene of the putative glycerol-3-phosphate dehydrogenase operon (gpdABC), base
73 is shifted towards the pentose phosphate and glycerol-3-phosphate dehydrogenase pathways.
74 plasmic reticulum Ca2+-ATPase, mitochondrial glycerol 3-phosphate dehydrogenase, PGC1alpha, CoxII, an
75 d gain-of-function experiments revealed that glycerol-3-phosphate dehydrogenase played a key role in
76 e glycerol facilitator, glycerol kinase, and glycerol-3-phosphate dehydrogenase, respectively, all of
77 -3-phosphate acyltransferase or GLY1-encoded glycerol-3-phosphate dehydrogenase restored 18:1 levels
78 n upstream gene, gpdA, encoding a homolog of glycerol-3-phosphate dehydrogenase subunit A, were upreg
79        Gpd1p is a cytosolic NAD(+)-dependent glycerol 3-phosphate dehydrogenase that also localizes t
80 equire GPD1, which encodes an NADH-dependent glycerol-3-phosphate dehydrogenase that is important for
81 s a physiological activator of mitochondrial glycerol-3-phosphate dehydrogenase, that the enzyme is p
82          Homogeneous pig brain mitochondrial glycerol-3-phosphate dehydrogenase was activated by eith
83 rom NADL to glycolaldehyde (GA) catalyzed by glycerol-3-phosphate dehydrogenase were determined over
84     GPD1-L has >80% amino acid homology with glycerol-3-phosphate dehydrogenase, which is involved in