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Department Of Pharmacology Asahika Wa Medical College | 論文
- Protective Effect of Amiloride Against Reperfusion Damage as Evidenced by Inhibition of Accumulation of Free Fatty Acids in Working Rat Hearts
- ACCUMULATION OF MYOCARDIAL FREE FATTY ACIDS DURING ISCHEMIA AND REPERFUSION AND ITS RELATION TO ANTI-ISCHEMIC ACTION OF DRUGS
- -18-RELEASE OF ADENOSINE AND LACTATE FROM THE HEART DURING ATRIAL PACING IN PATIENTS WITH ISCHEMIC HEART DISEASE
- Cardioprotecvtive Effect of K-7259,a Novel Dlazep Derivative,against Ischemia-Reperfusion Damage in Isolated,Working Rat Hearts
- A Study on Dilazep: II. Dilazep Attenuates Lysophosphatidylcholine-Induced Mechanical and Metabolic Derangements in the Isolated, Working Rat Heart
- A Study on Dilazep: I. Mechanism of Anti-ischemic Action of Dilazep Is Not Coronary Vasodilation but Decreased Cardiac Mechanical Function in the Isolated, Working Rat Heart
- Protective effect of propranolol and lidocaine on accumulation of non-esterified fatty acid induced by paraquat in the lung, kidney, liver and heart in rats
- Protective Effect of Quinaprilat, an Active Metabolite of Quinapril, on Ca^-Overload Induced by Lysophosphatidylcholine in Isolated Rat Cardiomyocytes
- Protective Effects of Ranolazine, a Novel Anti-ischemic Drug, on the Hydrogen Peroxide-Induced Derangements in Isolated, Per fused Rat Heart: Comparison With Dichloroacetate
- Beneficial Effects of Dilazep on the Palmitoyl : L : carnitine : Induced Derangements in Isolated, Per fused Rat Heart: Comparison with Tetrodotoxin
- EFFECT OF CARTEOLOL, A NEW BETA-ADRENERGIC BLOCKING AGENT, ON MYOCARDIAL METABOLIC RESPONSE TO CORONARY ARTERY LIGATION IN DOGS
- Crossover Plot Study of Glycolytic Intermediates in the Ischemic Canine Heart
- MAIN CAUSES OF MYOCARDIAL ISCHEMIC DAMAGE
- TISSUE DISTRIBUTION OF ARSENIC AFTER SUBCUTANEOUS IMPLANTATION OF ARSENIC TRIOXIDE PELLET IN RATS
- A New Approach to the Development of Anti-ischemic Drugs. Substances that Counteract the Deleterious Effect of Lysophosphatidylcholine on the Heart.:Substances that Counteract the Deleterious Effect of Lysophosphatidylcholine on the Heart
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