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Acronym | Full Name | Score | Rating | Judge me | Search |
ATP | adenosine triphosphate | 838 | 1 | good bad | |
ATP | adenosine 5'-triphosphate | 188 | 3 | good bad | |
ATP | ATP-sensitive K(+) channels (K | 20 | 3 | good bad | |
ATP | Adult Treatment Panel | 12 | -1 | good bad | |
ATP | antitachycardia pacing | 11 | 5 | good bad | |
ATP | ATP-sensitive K(+) channel (K | 10 | 3 | good bad | |
ATP | ATP-sensitive K(+) (mitoK | 7 | 4 | good bad | |
ATP | adenosinetriphosphate | 6 | 3 | good bad | |
ATP | Annual Transmission Potential | 5 | 8 | good bad | |
ATP | adenosine triphosphatase | 4 | 5 | good bad | |
ATP | adenosine 5' triphosphate | 4 | 4 | good bad | |
ATP | activation of ATP-sensitive K(+) (K | 4 | 2 | good bad | |
ATP | mitochondrial K | 4 | 2 | good bad | |
ATP | substrate | 4 | 1 | good bad | |
ATP | K(+) | 4 | 0 | good bad | |
ATP | at the K | 3 | 2 | good bad | |
ATP | ATP-sensitive K(+) channel (mitoK | 3 | 0 | good bad | |
ATP | autoimmune thrombocytopenia | 3 | 0 | good bad | |
ATP | Angstrom Technology Partnership | 3 | -1 | good bad | |
ATP | absence of adenosine 5'-triphosphate | 3 | -2 | good bad | |
ATP | adenosine and adenosine 5'-triphosphate | 3 | -2 | good bad | |
ATP | adenosine 5-triphosphate | 2 | 6 | good bad | |
ATP | activation of mitochondrial K | 2 | 5 | good bad | |
ATP | adenosine 5'triphosphate | 2 | 5 | good bad | |
ATP | activation of mitochondrial ATP-sensitive K(+) (mitoK | 2 | 5 | good bad | |
ATP | aspirative transthoracic puncture | 2 | 4 | good bad | |
ATP | sarcK | 2 | 4 | good bad | |
ATP | adenosine triphosphate (ATP)-sensitive K+ (K | 2 | 4 | good bad | |
ATP | applied adenosine 5'-triphosphate | 2 | 2 | good bad | |
ATP | Arabidopsis TILLING Project | 2 | 2 | good bad | |
ATP | aggregation and adenosine 5'-triphosphate | 2 | 2 | good bad | |
ATP | antagonist of responses to adenosine 5'-triphosphate | 2 | 2 | good bad | |
ATP | ATP-dependent K(+) (mitoK | 2 | 1 | good bad | |
ATP | ability to regenerate adenosine triphosphate | 2 | 1 | good bad | |
ATP | activation of the K(+) | 2 | 1 | good bad | |
ATP | Acetylcholine (ACh) and adenosine 5'-triphosphate | 2 | 0 | good bad | |
ATP | activation of K | 2 | 0 | good bad | |
ATP | adenosine triphosphate content | 2 | 0 | good bad | |
ATP | Activation of the K | 2 | 0 | good bad | |
ATP | Adenosine-5-triphosphate | 2 | -1 | good bad | |
ATP | application of adenosine 5'-triphosphate | 2 | -1 | good bad | |
ATP | adenosine-tri-phosphate | 2 | -1 | good bad | |
ATP | triphosphate | 2 | -2 | good bad | |
ATP | short T1 | 1 | 20 | good bad | |
ATP | assay of adenosine 5'-triphosphate | 1 | 9 | good bad | |
ATP | above findings indicate that K | 1 | 8 | good bad | |
ATP | activity of inward rectifier K | 1 | 8 | good bad | |
ATP | apparent KM | 1 | 8 | good bad | |
ATP | tested as putative K | 1 | 7 | good bad | |
ATP | autoimmune (or idiopathic) thrombocytopenic purpura | 1 | 7 | good bad | |
ATP | atrial ATP-sensitive K(+) (K | 1 | 7 | good bad | |
ATP | analyzed for adenosine 5'-triphosphate | 1 | 7 | good bad | |
ATP | attempt to maintain adequate adenosine triphosphate | 1 | 7 | good bad | |
ATP | altered expression of a K | 1 | 6 | good bad | |
ATP | ATP-sensitive K(+) channel (K(+) | 1 | 6 | good bad | |
ATP | at 575 nm | 1 | 6 | good bad | |
ATP | activates K | 1 | 6 | good bad | |
ATP | altered by inhibitors of K+ | 1 | 5 | good bad | |
ATP | ATP-sensitive potassium (K | 1 | 5 | good bad | |
ATP | any enzimatic system for energy production | 1 | 5 | good bad | |
ATP | adenosine S-triphosphate | 1 | 5 | good bad | |
ATP | after due consideration of substrate | 1 | 5 | good bad | |
ATP | adenosin triphosphate | 1 | 5 | good bad | |
ATP | Phosphomonoester/beta-adenosine triphosphate | 1 | 5 | good bad | |
ATP | expresses ATP-sensitive K(+) (K | 1 | 5 | good bad | |
ATP | shows a Km | 1 | 5 | good bad | |
ATP | cardioselective K | 1 | 4 | good bad | |
ATP | on Km | 1 | 4 | good bad | |
ATP | assay measures intracellular adenosintriphosphate | 1 | 4 | good bad | |
ATP | adenosonine triphosphate | 1 | 4 | good bad | |
ATP | analogue of S1-adenosine 5'-triphosphate | 1 | 4 | good bad | |
ATP | activation of 70 pS K | 1 | 4 | good bad | |
ATP | active calcium transport and adenosine 5'-triphosphate | 1 | 4 | good bad | |
ATP | approximately equal to adenosine 5'-triphosphate | 1 | 4 | good bad | |
ATP | adenosine tetraphosphate (5'AdoP4) from adenosine triphosphate | 1 | 4 | good bad | |
ATP | ability to produce adenosine triphosphate | 1 | 4 | good bad | |
ATP | co-factor | 1 | 4 | good bad | |
ATP | taurine-sensitive K(+) channel (K | 1 | 4 | good bad | |
ATP | attenuates postischemic dysfunction through K | 1 | 4 | good bad | |
ATP | antitachycardia | 1 | 4 | good bad | |
ATP | affect the ability of adenosine 5'-triphosphate | 1 | 3 | good bad | |
ATP | role for K | 1 | 3 | good bad | |
ATP | activation of IK | 1 | 3 | good bad | |
ATP | ADP-beta-S and adenosine 5'-triphosphate | 1 | 3 | good bad | |
ATP | activation and adenosine on K | 1 | 3 | good bad | |
ATP | allowed to accumulate adenosine 5'-triphosphate | 1 | 3 | good bad | |
ATP | Although the ATP-sensitive K(+) (K | 1 | 3 | good bad | |
ATP | A2A adenosine receptor(s) by K+ | 1 | 3 | good bad | |
ATP | acting on the Cl(-)-adenosine triphosphate | 1 | 3 | good bad | |
ATP | shift in Km | 1 | 3 | good bad | |
ATP | administration of the K | 1 | 3 | good bad | |
ATP | used for energy | 1 | 3 | good bad | |
ATP | PEPCK | 1 | 3 | good bad | |
ATP | activity induced by exogenous adenosine 5'-triphosphate | 1 | 3 | good bad | |
ATP | cofactor | 1 | 3 | good bad | |
ATP | Fe3+ | 1 | 3 | good bad | |
ATP | atrial tachyarrhythmias actively by antitachycardia pacing | 1 | 3 | good bad | |
ATP | important role in neurotransmitter | 1 | 3 | good bad | |
ATP | Adenosintriphosphats | 1 | 3 | good bad | |
ATP | adenosine triphosphate (ATP)-sensitive potassium (K+ | 1 | 3 | good bad | |
ATP | assay based on adenosine 5(')-triphosphate | 1 | 2 | good bad | |
ATP | adenosine triphosphate-sensitive (ATP-sensitive) K+ channels (K | 1 | 2 | good bad | |
ATP | actions at K | 1 | 2 | good bad | |
ATP | action on the K(+) | 1 | 2 | good bad | |
ATP | adenosine triphosphate-sensitive K(+) (K | 1 | 2 | good bad | |
ATP | diminished markedly by energy | 1 | 2 | good bad | |
ATP | adenosine triphosphate (ATP)-sensitive K(+) (sarcK | 1 | 2 | good bad | |
ATP | ability to release adenosine 5'-triphosphate | 1 | 2 | good bad | |
ATP | calcium metabolism | 1 | 2 | good bad | |
ATP | blockade of K | 1 | 2 | good bad | |
ATP | application of 1 mM-adenosine-5'-triphosphate | 1 | 2 | good bad | |
ATP | structure-activity relationships (QSARs) studies on K | 1 | 2 | good bad | |
ATP | highly selective K | 1 | 2 | good bad | |
ATP | cellular energy content | 1 | 2 | good bad | |
ATP | at low adenosine 5'-triphosphate | 1 | 2 | good bad | |
ATP | activators of the ATP-sensitive K(+) (K | 1 | 2 | good bad | |
ATP | activator of ATP-sensitive K(+) channels (K | 1 | 2 | good bad | |
ATP | activation of K(Ca) and ROMK-type K | 1 | 2 | good bad | |
ATP | involvement of K | 1 | 2 | good bad | |
ATP | adentriphos | 1 | 2 | good bad | |
ATP | kcat/Km | 1 | 2 | good bad | |
ATP | ATP-dependent K(+) (K | 1 | 2 | good bad | |
ATP | adenosine-5'-diphosphate (ADP) and adenosine-5'-triphosphate | 1 | 2 | good bad | |
ATP | applications of adenosine 5'-triphosphate | 1 | 1 | good bad | |
ATP | ATP-sensitive K(+) channels (K(+) | 1 | 1 | good bad | |
ATP | myocardial adenosine 5'-triphosphate | 1 | 1 | good bad | |
ATP | associated with ligand binding in K | 1 | 1 | good bad | |
ATP | novelK | 1 | 1 | good bad | |
ATP | ATP4- and M | 1 | 1 | good bad | |
ATP | autogenic training phrases | 1 | 1 | good bad | |
ATP | ATP with an apparent Km | 1 | 1 | good bad | |
ATP | ATP-inhibited K(+) channels (K | 1 | 1 | good bad | |
ATP | ATP dependent potassium current IK | 1 | 1 | good bad | |
ATP | ATP-dependent and Ca(2+)-activated K(+) channels (K | 1 | 1 | good bad | |
ATP | atrial triggered pacemakers | 1 | 1 | good bad | |
ATP | ATP-dependent potassium (K | 1 | 1 | good bad | |
ATP | against ischaemia by opening mitochondrial K | 1 | 1 | good bad | |
ATP | activator of adenosine 5'-triphosphate | 1 | 1 | good bad | |
ATP | All three detergents blocked K | 1 | 1 | good bad | |
ATP | agonists adenosine 5'-triphosphate | 1 | 1 | good bad | |
ATP | adenosine triphosphatase (ATP)-sensitive K(+) (K | 1 | 1 | good bad | |
ATP | agents was unaffected by the K | 1 | 1 | good bad | |
ATP | acetylcholine and adenosine 5'-triphosphate | 1 | 1 | good bad | |
ATP | adenosin 5' triphosphate | 1 | 1 | good bad | |
ATP | activates an IK | 1 | 1 | good bad | |
ATP | adenosine triphosphate (ATP)-sensitive potassium channel (K | 1 | 1 | good bad | |
ATP | Adenosine Triphosphate level | 1 | 1 | good bad | |
ATP | actions of various ATP-sensitive K(+) (K | 1 | 1 | good bad | |
ATP | immediately measure adenosine 5(')-triphosphate | 1 | 1 | good bad | |
ATP | Although these modulatory effects on K | 1 | 1 | good bad | |
ATP | adenosine 5'-monophosphate (AMP) and adenosine 5'-triphosphate | 1 | 1 | good bad | |
ATP | antagonist adenosine 5'-triphosphate | 1 | 1 | good bad | |
ATP | Alterations in energy | 1 | 1 | good bad | |
ATP | Alzheimer-type pathology | 1 | 1 | good bad | |
ATP | adenosine phosphate | 1 | 0 | good bad | |
ATP | actions of the K | 1 | 0 | good bad | |
ATP | endogenous cofactor | 1 | 0 | good bad | |
ATP | adenosine trisphosphate | 1 | 0 | good bad | |
ATP | adenosine 5'-monophosphate (AMP) or adenosine 5'-triphosphate | 1 | 0 | good bad | |
ATP | adenosine 5'-phosphates such as adenosine 5'-triphosphate | 1 | 0 | good bad | |
ATP | attenuates the fall in adenosine 5'-triphosphate | 1 | 0 | good bad | |
ATP | availability of high-energy cofactors | 1 | 0 | good bad | |
ATP | (CP)----adenosine 5'-triphosphate | 1 | 0 | good bad | |
ATP | acid conditions implies that the Km | 1 | 0 | good bad | |
ATP | augment secretagogue | 1 | 0 | good bad | |
ATP | adult frogs express the K | 1 | 0 | good bad | |
ATP | actions of adenosine 5'-triphosphate | 1 | 0 | good bad | |
ATP | accumulation of macroergic phosphates | 1 | 0 | good bad | |
ATP | accelerates adenosinetriphosphate | 1 | 0 | good bad | |
ATP | an energy generating source | 1 | 0 | good bad | |
ATP | associated with inhibition of whole-cell K | 1 | 0 | good bad | |
ATP | assayed by adenosine 5'-triphosphate | 1 | 0 | good bad | |
ATP | accelerate the adenosine 5'-triphosphate | 1 | 0 | good bad | |
ATP | analogue of adenosine 5'-triphosphate | 1 | 0 | good bad | |
ATP | antagonist of K | 1 | 0 | good bad | |
ATP | transient psychotic disorders | 1 | 0 | good bad | |
ATP | ATP-dependent K(+)-current (K | 1 | 0 | good bad | |
ATP | Application of the K | 1 | 0 | good bad | |
ATP | activate K+ | 1 | 0 | good bad | |
ATP | actin-activated adenosine 5'-triphosphate | 1 | 0 | good bad | |
ATP | affinity for K | 1 | 0 | good bad | |
ATP | after injection of striadyne | 1 | 0 | good bad | |
ATP | ATP-regulated K(+) channels (IK | 1 | 0 | good bad | |
ATP | lower Km | 1 | -1 | good bad | |
ATP | ATP-sensitive K+ channels (K | 1 | -1 | good bad | |
ATP | adenine or adenosine 5'-triphosphate | 1 | -1 | good bad | |
ATP | abolished by K | 1 | -1 | good bad | |
ATP | activated by actin with low K | 1 | -1 | good bad | |
ATP | nucleotide | 1 | -1 | good bad | |
ATP | activators of ATP sensitive K(+) (K | 1 | -1 | good bad | |
ATP | potential adenosine 5'-triphosphate | 1 | -1 | good bad | |
ATP | increase in adenosine 5'-triphosphate | 1 | -1 | good bad | |
ATP | enzyme-ATP complex or of the enzyme | 1 | -1 | good bad | |
ATP | ATP-sensitive potassium (K(+) | 1 | -1 | good bad | |
ATP | adenylate cyclase for its substrate | 1 | -1 | good bad | |
ATP | administration of a K+ | 1 | -1 | good bad | |
ATP | application of 10(-4) M-adenosine-5'-triphosphate | 1 | -1 | good bad | |
ATP | affinity complexes of myosin-adenosine triphosphate | 1 | -1 | good bad | |
ATP | against-the-power | 1 | -1 | good bad | |
ATP | agonist and antagonist of mitochondria K | 1 | -1 | good bad | |
ATP | an ATP-sensitive K(+) (K | 1 | -1 | good bad | |
ATP | apparent Km values were 48 | 1 | -1 | good bad | |
ATP | adenosine triphosphate (ATP)-sensitive K(+)i (K | 1 | -1 | good bad | |
ATP | adenosine triphosphate (ATP) sensitive K+ (K | 1 | -1 | good bad | |
ATP | activating mitochondrial K | 1 | -1 | good bad | |
ATP | Adenosine tri-phosphate | 1 | -1 | good bad | |
ATP | adenosine ribonucleoside triphosphate | 1 | -1 | good bad | |
ATP | adenosine 5'-triphosphate (ATP)-dependent K+-channels (K | 1 | -1 | good bad | |
ATP | adenosine 5'-triphosphate (ATP) sensitive potassium (K | 1 | -1 | good bad | |
ATP | absolute requirement for adenosine 5'-triphosphate | 1 | -2 | good bad | |
ATP | about the K | 1 | -2 | good bad | |
ATP | corresponding Ymax | 1 | -2 | good bad | |
ATP | apparent retardation of loss by metabolic | 1 | -2 | good bad | |
ATP | 5'-triphosphate | 1 | -2 | good bad | |
ATP | triphosphates | 1 | -2 | good bad | |
ATP | addition of exogenous adenosine 5'-triphosphate | 1 | -2 | good bad | |
ATP | ATP sensitive K(+) channel (K | 1 | -2 | good bad | |
ATP | acyl-CoA would not inhibit adenosine 5'-triphosphate | 1 | -2 | good bad | |
ATP | affinity for myocardial K | 1 | -2 | good bad | |
ATP | Purpose- ATP-sensitive K(+) (K | 1 | -2 | good bad | |
ATP | affecting K | 1 | -2 | good bad | |
ATP | activation by adenine nucleotides | 1 | -2 | good bad | |
ATP | adenosine triphosphoric acid | 1 | -2 | good bad | |
ATP | affect vascular K | 1 | -2 | good bad |
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Text2Knowledge ... Yong Huang
2002
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