Interactions of ATP, oestradiol, genistein and the anti-oestrogens, faslodex (ICI 182780) and tamoxifen, with the human erythrocyte glucose transporter, GLUT1.
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Real-Time Tracking of BODIPY-C12 Long-Chain Fatty Acid in Human Term Placenta Reveals Unique Lipid Dynamics in Cytotrophoblast CellsThe disaccharide moiety of bleomycin facilitates uptake by cancer cellsTime-lapse 3-D measurements of a glucose biosensor in multicellular spheroids by light sheet fluorescence microscopy in commercial 96-well plates.Isoflavones, their Glycosides and Glycoconjugates. Synthesis and Biological Activity.Predicting the three-dimensional structure of the human facilitative glucose transporter glut1 by a novel evolutionary homology strategy: insights on the molecular mechanism of substrate migration, and binding sites for glucose and inhibitory molecuDocking studies show that D-glucose and quercetin slide through the transporter GLUT1.Homology modeling of GLUT4, an insulin regulated facilitated glucose transporter and docking studies with ATP and its inhibitors.Interactions of androgens, green tea catechins and the antiandrogen flutamide with the external glucose-binding site of the human erythrocyte glucose transporter GLUT1.Caffeine inhibits glucose transport by binding at the GLUT1 nucleotide-binding site.Structural features facilitating tumor cell targeting and internalization by bleomycin and its disaccharide.Human red blood cells: rheological aspects, uptake, and release of cytotoxic drugs.AMP-activated protein kinase and the regulation of glucose transport.Preclinical evaluation of the anti-tumor effects of the natural isoflavone genistein in two xenograft mouse models monitored by [18F]FDG, [18F]FLT, and [64Cu]NODAGA-cetuximab small animal PET.GLUT1 as a therapeutic target in hepatocellular carcinoma.Dietary Isoflavones as Modulators of Drug Metabolizing Enzymes and Transporters: Effect on Prescription Medicines.Piracetam and TRH analogues antagonise inhibition by barbiturates, diazepam, melatonin and galanin of human erythrocyte D-glucose transport.Myricetin, quercetin and catechin-gallate inhibit glucose uptake in isolated rat adipocytes.Endofacial competitive inhibition of the glucose transporter 1 activity by gossypol.Resolution of the direct interaction with and inhibition of the human GLUT1 hexose transporter by resveratrol from its effect on glucose accumulation.2-Methoxyoestradiol inhibits glucose transport in rodent skeletal muscle.Genistein inhibits glucose and sulphate transport in isolated rat liver lysosomes.Kinetic Basis of Cis- and Trans-Allostery in GLUT1-Mediated Sugar Transport.Evaluating the Efficacy of GLUT Inhibitors Using a Seahorse Extracellular Flux Analyzer.
P2860
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P2860
Interactions of ATP, oestradiol, genistein and the anti-oestrogens, faslodex (ICI 182780) and tamoxifen, with the human erythrocyte glucose transporter, GLUT1.
description
2002 nî lūn-bûn
@nan
2002年の論文
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2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Interactions of ATP, oestradio ...... te glucose transporter, GLUT1.
@en
Interactions of ATP, oestradio ...... te glucose transporter, GLUT1.
@nl
type
label
Interactions of ATP, oestradio ...... te glucose transporter, GLUT1.
@en
Interactions of ATP, oestradio ...... te glucose transporter, GLUT1.
@nl
prefLabel
Interactions of ATP, oestradio ...... te glucose transporter, GLUT1.
@en
Interactions of ATP, oestradio ...... te glucose transporter, GLUT1.
@nl
P2860
P356
P1433
P1476
Interactions of ATP, oestradio ...... yte glucose transporter, GLUT1
@en
P2093
Iram Afzal
Philip Cunningham
P2860
P304
P356
10.1042/BJ20011624
P407
P577
2002-08-01T00:00:00Z