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1 a targets VEGF-A, glucose transporter-1, and lactate dehydrogenase A.
2 tions in NOX2 activity and the production of lactate dehydrogenase A.
3 g the expression of hexokinase II (HKII) and lactate dehydrogenase A.
4 (HIF-1) in the transcriptional activation of lactate dehydrogenase A, aldolase-A, phosphoglycerate ki
5 lpha including those involved in glycolysis (lactate dehydrogenase A and enolase 2), oxidant stress (
6 rast, genes barely expressed in sham islets (lactate dehydrogenase A and hexokinase I) were markedly
7 Myc oncogenic transcription factor regulates lactate dehydrogenase A and induces lactate overproducti
8 to the hypoxia response element site in the lactate dehydrogenase A and PKM2 loci and mediates the r
12 YND8 directly regulates the transcription of lactate dehydrogenase A by promoting the recruitment of
16 genase (GAPDH), L-lactate dehydrogenase B, L-lactate dehydrogenase A chain, L-lactate dehydrogenase,
18 se transporter 2 expression, glucose uptake, lactate dehydrogenase A expression, and NAD + level.
20 ow that removal of Glucose transporter 1 and Lactate dehydrogenase A gene activity from developing re
23 , including those for the glycolytic enzymes lactate dehydrogenase A, hexokinase II, and 6-phosphofru
24 s normally suppressed in beta-cells, such as lactate dehydrogenase-A, hexokinase I, glucose-6-phospha
25 ate dehydrogenase A (LDHA) or stiripentol, a lactate dehydrogenase A inhibitor used clinically for an
26 CHK-336 is a liver-targeted, small-molecule lactate dehydrogenase A inhibitor with potential to trea
27 triction were treated with oxamate (an LDHA [lactate dehydrogenase A] inhibitor) or sodium lactate to
28 xpression of glycolysis-regulating molecules lactate dehydrogenase A (LDH-A) and heat shock factor 1
30 s used to correlate metabolite labeling with lactate dehydrogenase A (LDH-A) expression and some immu
32 regulation of heat shock factor 1 (HSF1) and lactate dehydrogenase A (LDH-A) in ErbB2-positive cancer
33 r basis of the cAMP-induced stabilization of lactate dehydrogenase A (LDH-A) mRNA and identified four
34 ces, the multiprotein complex binding to the lactate dehydrogenase A (LDH-A) promoter was characteriz
36 ation of c-Myc target genes, such as rcl and lactate dehydrogenase A (LDH-A), is critical for underst
38 ed the contributions of macrophage-expressed lactate dehydrogenase-A (LDH-A) to tumor formation in a
39 es barely expressed in sham islets including lactate dehydrogenase-A (LDH-A), lactate (monocarboxylat
41 ntially metabolized to lactate by the enzyme lactate dehydrogenase-A (LDH-A), suggesting a possible v
42 of the genes encoding hexokinase 1 (HK1) and lactate dehydrogenase A (LDHA) - both of which regulate
43 ssive tumors to enhanced glycolytic flux and lactate dehydrogenase A (LDHA) activity (Warburg effect)
44 t-converts glucose to lactate via the enzyme lactate dehydrogenase A (LDHA) and is a metabolic featur
45 present article delineates the detection of lactate dehydrogenase A (LDHA) by exploiting the AIE pro
47 ing hematopoietic stem cells (HSCs), whereas lactate dehydrogenase A (LDHA) deletion significantly in
50 pproaches, we show that lactate reduction by lactate dehydrogenase A (LDHA) inactivation heightens ty
53 reduction using either genetic depletion of lactate dehydrogenase A (LDHA) or stiripentol, a lactate
54 olytic as manifested by strong expression of lactate dehydrogenase A (LDHA) that converts pyruvate to
55 ate Kinase 1 (PGK1), Hexokinase 2 (HK2), and Lactate Dehydrogenase A (LDHA) were each significantly h
56 Treg cells, and inhibiting PI3K, Rictor, or lactate dehydrogenase A (Ldha), a key Myc target enzyme
57 t that phosphorylation-induced activation of lactate dehydrogenase A (LDHA), an enzyme that catalyses
58 monophosphate synthetase (UMPS), as well as lactate dehydrogenase A (LDHA), establishing a mechanism
59 n cells also generate G3P upon inhibition of lactate dehydrogenase A (LDHA), our findings hint at a c
60 housekeeping genes - such as those encoding lactate dehydrogenase A (LDHA), solute transporter MCT1,
61 ression of the pyruvate transporter MCT1 and lactate dehydrogenase A (LDHA), the enzyme catalyzing la
64 take up glucose and generate lactate through lactate dehydrogenase A (LDHA), which is encoded by a ta
65 st cancer cells by binding to and activating lactate dehydrogenase A (LDHA), which promoted histones
66 ing lymphocytes have been shown to undertake lactate dehydrogenase A (LDHA)-dependent aerobic glycoly
67 ling and functional studies demonstrate that lactate dehydrogenase A (LDHA)-directed extracellular si
72 rpin RNA against GBP-5) release twofold less lactate dehydrogenase (a marker of membrane permeability
73 enase, a marker of lipolytic metabolism; and lactate dehydrogenase, a marker of glycolytic metabolism
75 ycolytic enzymes, with notable expression of lactate dehydrogenase A occurring in the airway epitheli
78 re, we show that pharmacologic inhibition of lactate dehydrogenase-A suppressed the conversion of hyp
80 c downregulation decreased the expression of lactate dehydrogenase A, the enzyme catalyzing the conve
81 es key beta cell "disallowed" genes, such as lactate dehydrogenase A We propose that C2CD4A is a tran
82 is enzymes pyruvate dehydrogenase kinase and lactate dehydrogenase A within cortical and hippocampal