nad has been researched along with tetraphenylphosphonium in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (28.57) | 18.7374 |
1990's | 2 (28.57) | 18.2507 |
2000's | 3 (42.86) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Höfer, M; Sigler, K | 1 |
Kauppinen, RA; Nicholls, DG; Sihra, TS | 1 |
Burat, MK; Burat, T; Davis, EJ; Davis-Van Thienen, WI | 1 |
Baltscheffsky, H; Lundin, M; Pereira-da-Silva, L; Sherman, M | 1 |
Bodrova, ME; Dedukhova, VI; Mokhova, EN | 1 |
Deryabina, YI; Zvyagilskaya, RA | 1 |
Biel, S; Janausch, IG; Kröger, A; Schnorpfeil, M; Unden, G | 1 |
7 other study(ies) available for nad and tetraphenylphosphonium
Article | Year |
---|---|
Activation of the plasma membrane H(+)-ATPase of Saccharomyces cerevisiae by addition of hydrogen peroxide.
Topics: Buffers; Carbonyl Cyanide m-Chlorophenyl Hydrazone; Cell Membrane; Dicyclohexylcarbodiimide; Diethylstilbestrol; Enzyme Activation; Hydrogen Peroxide; Hydrogen-Ion Concentration; NAD; Onium Compounds; Organophosphorus Compounds; Oxidation-Reduction; Oxygen Consumption; Potassium; Proton-Translocating ATPases; Saccharomyces cerevisiae | 1991 |
Aminooxyacetic acid inhibits the malate-aspartate shuttle in isolated nerve terminals and prevents the mitochondria from utilizing glycolytic substrates.
Topics: Acetates; Aminooxyacetic Acid; Animals; Aspartic Acid; Glycolysis; Guinea Pigs; In Vitro Techniques; Malates; Membrane Potentials; Mitochondria; NAD; Onium Compounds; Organophosphorus Compounds; Oxygen Consumption; Synaptosomes | 1987 |
Control of cellular redox potential as measured in a steady-state, cell-free system.
Topics: 2,4-Dinitrophenol; Adenosine Diphosphate; Adenosine Triphosphate; Animals; Cell-Free System; Cytosol; Dinitrophenols; Homeostasis; Male; Mitochondria, Liver; NAD; Onium Compounds; Organophosphorus Compounds; Oxidation-Reduction; Proton-Translocating ATPases; Rats; Rats, Inbred Strains | 1984 |
Inorganic pyrophosphate gives a membrane potential in yeast mitochondria, as measured with the permeant cation tetraphenylphosphonium.
Topics: Adenosine Triphosphate; Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone; Diphosphates; Membrane Potentials; Mitochondria; NAD; Oligomycins; Onium Compounds; Organophosphorus Compounds; Pyrophosphatases; Saccharomyces cerevisiae | 1993 |
Generation of transmembrane electrical potential during NADH oxidation via the external pathway and the fatty acid uncoupling effect after transient opening of the Ca2+-dependent cyclosporin A-sensitive pore in liver mitochondria.
Topics: Animals; Calcium; Cyclosporine; Cytochrome c Group; Electron Transport; Electrophysiology; Enzyme Inhibitors; Fatty Acids; Hydrogen-Ion Concentration; Indicators and Reagents; Intracellular Membranes; Membrane Potentials; Mitochondria, Liver; NAD; Onium Compounds; Organophosphorus Compounds; Oxygen; Potassium Chloride; Rats; Time Factors | 2000 |
The Ca(2+)-transport system of yeast (Endomyces magnusii) mitochondria: independent pathways for Ca(2+) uptake and release.
Topics: Antifungal Agents; Biological Transport; Calcium; Cyclosporine; Dose-Response Relationship, Drug; Hydrogen-Ion Concentration; Indicators and Reagents; Ionophores; Kinetics; Lanthanum; Mitochondria; Models, Biological; NAD; Nigericin; Onium Compounds; Organophosphorus Compounds; Phosphates; Saccharomycetales; Sodium; Spectrophotometry; Spermine | 2000 |
Generation of a proton potential by succinate dehydrogenase of Bacillus subtilis functioning as a fumarate reductase.
Topics: Bacillus subtilis; Cations; Electron Transport; Electrons; Indicators and Reagents; Membrane Potentials; Models, Biological; Models, Chemical; Mutation; NAD; Onium Compounds; Organophosphorus Compounds; Protons; Quinone Reductases; Succinate Dehydrogenase; Vitamin K | 2001 |