| scholarly article | Q13442814 |
| P2093 | author name string | Xueping Zhou | |
| Catherine Ledent | |||
| Stephen Tilley | |||
| S Jamal Mustafa | |||
| Bunyen Teng | |||
| P2860 | cites work | Endogenous adenosine increases coronary flow by activation of both A2A and A2B receptors in mice | Q44376976 |
| Blockade of the ATP-sensitive potassium channel modulates reactive hyperemia in the canine coronary circulation | Q44427462 | ||
| Hypoxic dilation of coronary arteries is mediated by ATP-sensitive potassium channels | Q46218245 | ||
| Comparison of buffer and red blood cell perfusion of guinea pig heart oxygenation | Q48970224 | ||
| Role of K(ATP)(+) channels and adenosine in the control of coronary blood flow during exercise. | Q52075780 | ||
| Adenosine is not responsible for local metabolic control of coronary blood flow in dogs during exercise. | Q52082669 | ||
| Role of adenosine in local metabolic coronary vasodilation. | Q52214971 | ||
| Adenosine A(2A) receptors mediate coronary microvascular dilation to adenosine: role of nitric oxide and ATP-sensitive potassium channels. | Q53923488 | ||
| Adenosine and coronary blood flow in conscious dogs during normal physiological stimuli. | Q54511363 | ||
| Hydrogen Peroxide | Q62000272 | ||
| Theophylline increases coronary vascular tone in humans: evidence for a role of endogenous adenosine in flow regulation | Q71053100 | ||
| Contribution of potassium channels to active hyperemia of the canine diaphragm | Q71628087 | ||
| Endogenous adenosine increases O2 utilisation efficiency in isoprenaline-stimulated canine myocardium | Q71635481 | ||
| High-energy phosphate concentrations in dog myocardium during stress | Q72346356 | ||
| Glibenclamide prevents coronary vasodilation induced by beta 1-adrenoceptor stimulation in dogs | Q72667213 | ||
| ATP sensitive potassium channels are involved in adenosine A2 receptor mediated coronary vasodilatation in the dog | Q72710663 | ||
| Role of K+ATP channels in coronary vasodilation during exercise | Q72885849 | ||
| Role of K+ATP channels in local metabolic coronary vasodilation | Q73278876 | ||
| Role of nitric oxide and adenosine in control of coronary blood flow in exercising dogs | Q73929767 | ||
| Impact of coronary risk factors on contribution of nitric oxide and adenosine to metabolic coronary vasodilation in humans | Q74530450 | ||
| Role of adenosine in the regulation of coronary blood flow in swine at rest and during treadmill exercise | Q77551534 | ||
| Cardiac nucleotides in hypoxia: possible role in regulation of coronary blood flow | Q79593218 | ||
| Adenosine receptors and the heart: role in regulation of coronary blood flow and cardiac electrophysiology | Q24598754 | ||
| Investigation of mechanisms that mediate reactive hyperaemia in guinea-pig hearts: role of K(ATP) channels, adenosine, nitric oxide and prostaglandins | Q28360156 | ||
| Hydrogen peroxide, an endogenous endothelium-derived hyperpolarizing factor, plays an important role in coronary autoregulation in vivo | Q31132587 | ||
| Role of K(ATP)(+) channels in regulation of systemic, pulmonary, and coronary vasomotor tone in exercising swine | Q31721911 | ||
| K(ATP)(+) channels, nitric oxide, and adenosine are not required for local metabolic coronary vasodilation | Q31833830 | ||
| Important role of endogenous hydrogen peroxide in pacing-induced metabolic coronary vasodilation in dogs in vivo | Q33299975 | ||
| Single channel and whole-cell K-currents evoked by levcromakalim in smooth muscle cells from the rabbit portal vein | Q34060925 | ||
| Endogenous adenosine mediates coronary vasodilation during exercise after K(ATP)+ channel blockade | Q34195568 | ||
| Control of myocardial oxygen consumption: relative influence of contractile state and tension development | Q34272361 | ||
| Mediators of coronary reactive hyperaemia in isolated mouse heart | Q35048663 | ||
| Contributions of A2A and A2B adenosine receptors in coronary flow responses in relation to the KATP channel using A2B and A2A/2B double-knockout mice | Q35601417 | ||
| Matching coronary blood flow to myocardial oxygen consumption. | Q35819031 | ||
| Ionic currents and inhibitory effects of glibenclamide in seminal vesicle smooth muscle cells | Q35872716 | ||
| Functional and RNA expression profile of adenosine receptor subtypes in mouse mesenteric arteries | Q36515316 | ||
| Interactions between A(2A) adenosine receptors, hydrogen peroxide, and KATP channels in coronary reactive hyperemia | Q36837892 | ||
| Up-regulation of A 2B adenosine receptor in A 2A adenosine receptor knockout mouse coronary artery | Q36979040 | ||
| CYP-epoxygenases contribute to A2A receptor-mediated aortic relaxation via sarcolemmal KATP channels. | Q37175460 | ||
| Regulation of coronary blood flow during exercise | Q37216075 | ||
| Role of K+ ATP channels and adenosine in the regulation of coronary blood flow during exercise with normal and restricted coronary blood flow | Q37352052 | ||
| A1 adenosine receptor negatively modulates coronary reactive hyperemia via counteracting A2A-mediated H2O2 production and KATP opening in isolated mouse hearts | Q37440228 | ||
| Role of potassium channels in coronary vasodilation | Q37733981 | ||
| Rosiglitazone inhibits vascular KATP channels and coronary vasodilation produced by isoprenaline. | Q39524834 | ||
| The role of adenosine in the regulation of coronary blood flow | Q40122505 | ||
| Blood pressure response to heart rate during exercise test and risk of future hypertension | Q40652987 | ||
| Adenosine is unimportant in controlling coronary blood flow in unstressed dog hearts | Q41363760 | ||
| Role of adenosine in coronary vasodilation during exercise | Q41434861 | ||
| Adenosine deaminase attenuates canine coronary vasodilation during systemic hypoxia | Q41494055 | ||
| Measurements of coronary plasma and pericardial infusate adenosine concentrations during exercise in conscious dog: relationship to myocardial oxygen consumption and coronary blood flow | Q41589193 | ||
| ATP-sensitive K+ channels, adenosine, and nitric oxide-mediated mechanisms account for coronary vasodilation during exercise | Q41714306 | ||
| Contribution of adenosine A(2A) and A(2B) receptors to ischemic coronary dilation: role of K(V) and K(ATP) channels | Q42005946 | ||
| ATP-sensitive potassium channel is essential to maintain basal coronary vascular tone in vivo | Q42460749 | ||
| Myocardial adenosine, flow, and metabolism during adenosine antagonism and adrenergic stimulation | Q42509879 | ||
| Role of adenosine in norepinephrine-induced coronary vasodilation | Q42547942 | ||
| Cardiac performance as a function of intracellular oxygen tension in buffer-perfused hearts | Q43799997 | ||
| Cardiac effects of adenosine in A(2A) receptor knockout hearts: uncovering A(2B) receptors | Q43852650 | ||
| P433 | issue | 7 | |
| P304 | page(s) | H1046-55 | |
| P577 | publication date | 2014-08-08 | |
| P1433 | published in | American Journal of Physiology Heart and Circulatory Physiology | Q3193662 |
| P1476 | title | Metabolic hyperemia requires ATP-sensitive K+ channels and H2O2 but not adenosine in isolated mouse hearts | |
| P478 | volume | 307 |
| Q35587846 | Involvement of NADPH oxidase in A2A adenosine receptor-mediated increase in coronary flow in isolated mouse hearts |
| Q39306627 | Kv1.3 channels facilitate the connection between metabolism and blood flow in the heart |
| Q39141080 | Potassium Channels in Regulation of Vascular Smooth Muscle Contraction and Growth |
| Q36832399 | Requisite Role of Kv1.5 Channels in Coronary Metabolic Dilation |
| Q36618711 | Role of Adenosine Receptor(s) in the Control of Vascular Tone in the Mouse Pudendal Artery |
| Q36093848 | Sex Difference in Coronary Endothelial Dysfunction in Apolipoprotein E Knockout Mouse: Role of NO and A2A Adenosine Receptor |
| Q39195631 | Smooth Muscle Ion Channels and Regulation of Vascular Tone in Resistance Arteries and Arterioles |
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