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Assessment of mitochondrial energy coupling in vivo by 13C/31P NMR

Assessment of mitochondrial energy coupling in vivo by 13C/31P NMR

http://www.wikidata.org/entity/Q28344306

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Regulation of skeletal muscle mitochondrial activity by thyroid hormones: focus on the "old" triiodothyronine and the "emerging" 3,5-diiodothyronine Effect of triiodothyronine on mitochondrial energy coupling in human skeletal muscle Mitochondrial GTP regulates glucose-stimulated insulin secretion Changes in uncoupling protein-2 and -3 expression in aging rat skeletal muscle, liver, and heart.Muscle mitochondrial ATP synthesis and glucose transport/phosphorylation in type 2 diabetes.Studying Enzymes by In Vivo C Magnetic Resonance Spectroscopy Integration of microRNA changes in vivo identifies novel molecular features of muscle insulin resistance in type 2 diabetes.Burn injury causes mitochondrial dysfunction in skeletal muscle.Energy metabolism, fuel selection and body weight regulation.Exchange kinetics by inversion transfer: integrated analysis of the phosphorus metabolite kinetic exchanges in resting human skeletal muscle at 7 T Impaired mitochondrial substrate oxidation in muscle of insulin-resistant offspring of type 2 diabetic patients.Control of energy metabolism by iodothyronines.Increased uncoupling protein 3 content does not affect mitochondrial function in human skeletal muscle in vivo.A small volatile bacterial molecule triggers mitochondrial dysfunction in murine skeletal muscle.Standard magnetic resonance-based measurements of the Pi→ATP rate do not index the rate of oxidative phosphorylation in cardiac and skeletal muscles.Thyroid hormone and uncoupling proteins.Human uncoupling protein-3 and obesity: an update.What do magnetic resonance-based measurements of Pi→ATP flux tell us about skeletal muscle metabolism?³¹P-magnetization transfer magnetic resonance spectroscopy measurements of in vivo metabolism.Amplification of the effects of magnetization exchange by (31) P band inversion for measuring adenosine triphosphate synthesis rates in human skeletal muscle Methods for assessing mitochondrial function in diabetes.ESCI Award 2006. Mitochondrial function and endocrine diseases.Mitochondria-targeted antioxidant promotes recovery of skeletal muscle mitochondrial function after burn trauma assessed by in vivo 31P nuclear magnetic resonance and electron paramagnetic resonance spectroscopy Paradoxical effects of increased expression of PGC-1alpha on muscle mitochondrial function and insulin-stimulated muscle glucose metabolism.Nuclear magnetic resonance in conjunction with functional genomics suggests mitochondrial dysfunction in a murine model of cancer cachexia Multimodal neuroimaging provides a highly consistent picture of energy metabolism, validating 31P MRS for measuring brain ATP synthesis.Hypophosphatemia promotes lower rates of muscle ATP synthesis.The role of mitochondria in insulin resistance and type 2 diabetes mellitus.Mitochondrial dysfunction as a central event for mechanisms underlying insulin resistance: the roles of long chain fatty acids.Metabolic syndrome and the environmental pollutants from mitochondrial perspectives.Assessing the Mitochondrial Membrane Potential in Cells and In Vivo using Targeted Click Chemistry and Mass Spectrometry.A Flux Balance of Glucose Metabolism Clarifies the Requirements of the Warburg Effect.AMPK/Mitochondria in Metabolic Diseases.Resistance to thyroid hormone is associated with raised energy expenditure, muscle mitochondrial uncoupling, and hyperphagia.Tracer-based assessments of hepatic anaplerotic and TCA cycle flux: practicality, stoichiometry, and hidden assumptions.A simple approach to evaluate the kinetic rate constant for ATP synthesis in resting human skeletal muscle at 7 T.A practical multinuclear transceiver volume coil for in vivo MRI/MRS at 7 T.Uncoupling protein downregulation in doxorubicin-induced heart failure improves mitochondrial coupling but increases reactive oxygen species generation.Skeletal muscle mitochondrial free-fatty-acid content and membrane potential sensitivity in different thyroid states: involvement of uncoupling protein-3 and adenine nucleotide translocase.Hypercaloric cafeteria-like diet induced UCP3 gene expression in skeletal muscle is impaired by hypothyroidism.

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P2860

Assessment of mitochondrial energy coupling in vivo by 13C/31P NMR

http://www.wikidata.org/entity/Q28344306

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2000 nî lūn-bûn

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2000 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2000 թվականի հունիսին հրատարակված գիտական հոդված

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2000年の論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年论文

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name

Assessment of mitochondrial energy coupling in vivo by 13C/31P NMR

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Assessment of mitochondrial energy coupling in vivo by 13C/31P NMR

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Assessment of mitochondrial energy coupling in vivo by 13C/31P NMR

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Assessment of mitochondrial energy coupling in vivo by 13C/31P NMR

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Assessment of mitochondrial energy coupling in vivo by 13C/31P NMR

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Assessment of mitochondrial energy coupling in vivo by 13C/31P NMR

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Assessment of mitochondrial energy coupling in vivo by 13C/31P NMR

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Assessment of mitochondrial energy coupling in vivo by 13C/31P NMR

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Assessment of mitochondrial energy coupling in vivo by 13C/31P NMR

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Proceedings of the National Academy of Sciences of the United States of America

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Assessment of mitochondrial energy coupling in vivo by 13C/31P NMR

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P2093

B M Jucker

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B Underhill

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G I Shulman

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J Ren

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K S Cadman

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S Dufour

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S F Previs

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X Cao

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P2860

Uncoupling protein-3: a new member of the mitochondrial carrier family with tissue-specific expression

UCP3: an uncoupling protein homologue expressed preferentially and abundantly in skeletal muscle and brown adipose tissue

Uncoupling protein-3 is a mediator of thermogenesis regulated by thyroid hormone, beta3-adrenergic agonists, and leptin

Kinetic analysis of dynamic 13C NMR spectra: metabolic flux, regulation, and compartmentation in hearts.

31P nuclear magnetic resonance measurements of ATPase kinetics in aerobic Escherichia coli cells

Brown adipose tissue thermogenesis and obesity.

NMR studies of enzymatic rates in vitro and in vivo by magnetization transfer.

The flux from glucose to glutamate in the rat brain in vivo as determined by 1H-observed, 13C-edited NMR spectroscopy.

NMR determination of the TCA cycle rate and alpha-ketoglutarate/glutamate exchange rate in rat brain.

In vivo 13C NMR measurements of hepatocellular tricarboxylic acid cycle flux.

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6880-4

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scholarly article

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4752215

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10.1073/PNAS.120131997

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12

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97

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2000-06-06T00:00:00Z

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12493997

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10823916

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18769

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