Martin D. Brand focuses on Biochemistry, Mitochondrion, Superoxide, Reactive oxygen species and UCP3. Within one scientific family, Martin D. Brand focuses on topics pertaining to Biophysics under Biochemistry, and may sometimes address concerns connected to ATP–ADP translocase. His study in Mitochondrion is interdisciplinary in nature, drawing from both Oxidative stress and Oxidative phosphorylation.
The study incorporates disciplines such as Lipid peroxidation, Electron Transport Complex I and Dehydrogenase in addition to Superoxide. His Reactive oxygen species research is multidisciplinary, incorporating elements of Superoxide dismutase, Radical, Hydroxyl radical, Hydrogen peroxide and Reverse electron flow. His UCP3 study integrates concerns from other disciplines, such as Phospholipid and Mitochondrial ROS.
Biochemistry, Mitochondrion, Biophysics, Oxidative phosphorylation and Superoxide are his primary areas of study. Reactive oxygen species, Uncoupling protein, Cellular respiration, UCP3 and Electron transport chain are the primary areas of interest in his Biochemistry study. Martin D. Brand combines subjects such as Endocrinology, Internal medicine and Membrane potential with his study of Mitochondrion.
His work deals with themes such as Proton pump, Membrane, Adenosine triphosphate and Respiration rate, which intersect with Biophysics. His Oxidative phosphorylation study incorporates themes from Metabolic control analysis and Phosphorylation. His research integrates issues of Superoxide dismutase, Coenzyme Q – cytochrome c reductase, Electron Transport Complex I, Hydrogen peroxide and Reverse electron flow in his study of Superoxide.
Martin D. Brand mainly investigates Mitochondrion, Biochemistry, Superoxide, Reactive oxygen species and Cell biology. His biological study spans a wide range of topics, including Biophysics, Membrane potential, UCP3 and Oxidative phosphorylation. His Membrane potential research is multidisciplinary, incorporating perspectives in Depolarization and Respiration.
His studies deal with areas such as Electron transport chain, Coenzyme Q – cytochrome c reductase, Reverse electron flow, Flavin group and Hydrogen peroxide as well as Superoxide. His research in Reactive oxygen species intersects with topics in Oxidative stress, Superoxide dismutase and NAD+ kinase. His work carried out in the field of Cell biology brings together such families of science as Apoptosis and Adenosine triphosphate.
His scientific interests lie mostly in Biochemistry, Mitochondrion, Superoxide, Reactive oxygen species and Coenzyme Q – cytochrome c reductase. His Biochemistry research is multidisciplinary, relying on both Biophysics and Respiration. His Mitochondrion research is multidisciplinary, incorporating elements of UCP3, Uncoupling protein and Oxidative phosphorylation.
His work deals with themes such as Endocrinology, Internal medicine, Carbohydrate metabolism, Bioenergetics and Phosphorylation, which intersect with Oxidative phosphorylation. The various areas that Martin D. Brand examines in his Superoxide study include Electron transport chain, Antimycin A, Hydrogen peroxide, Reverse electron flow and Dehydrogenase. The concepts of his Coenzyme Q – cytochrome c reductase study are interwoven with issues in Electron Transport Complex II, Succinate dehydrogenase, Palmitoylcarnitine, Electron Transport Complex I and Flavin group.
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Assessing mitochondrial dysfunction in cells
Martin D. Brand;David G. Nicholls.
Biochemical Journal (2011)
Topology of Superoxide Production from Different Sites in the Mitochondrial Electron Transport Chain
Julie St-Pierre;Julie A. Buckingham;Stephen J. Roebuck;Martin D. Brand.
Journal of Biological Chemistry (2002)
Superoxide activates mitochondrial uncoupling proteins
Karim S. Echtay;Damien Roussel;Julie St-Pierre;Mika B. Jekabsons.
Nature (2002)
Mitochondrial superoxide: production, biological effects, and activation of uncoupling proteins.
Martin D Brand;Charles Affourtit;Telma C Esteves;Katherine Green.
Free Radical Biology and Medicine (2004)
The sites and topology of mitochondrial superoxide production
Martin D. Brand.
Experimental Gerontology (2010)
Mitofusin-2 Determines Mitochondrial Network Architecture and Mitochondrial Metabolism A NOVEL REGULATORY MECHANISM ALTERED IN OBESITY
Daniel Bach;Sara Pich;Francesc X. Soriano;Nathalie Vega.
Journal of Biological Chemistry (2003)
Uncoupling to survive? The role of mitochondrial inefficiency in ageing.
M.D Brand.
Experimental Gerontology (2000)
Physiological functions of the mitochondrial uncoupling proteins UCP2 and UCP3
Martin D. Brand;Telma C. Esteves.
Cell Metabolism (2005)
Mice overexpressing human uncoupling protein-3 in skeletal muscle are hyperphagic and lean
John C. Clapham;Jonathan R. S. Arch;Helen Chapman;Andrea Haynes.
Nature (2000)
A hierarchy of ATP-consuming processes in mammalian cells.
F Buttgereit;M D Brand.
Biochemical Journal (1995)
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