長友孝文 | Department Of Pharmacology Faculty Of Pharmaceutical Sciences Niigata University Of Pharmacy And App

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著作論文

Cardiomyopathic Hamster Hearts : Long-Term Effects of Drugs on Catecholamine Contents and Binding Characteristics of α_1- and β_1-Adrenergic Receptors
Alterations of Binding Characteristics of α_1-, β_1-Adrenoceptors and Ca^ Binding Sites in the Myocardium of Spontaneously Hypertensive Rats (SHR) by Chronically Administered Bunazosin, Atenolol, Ketanserin and Verapamil
Binding Characteristics of [^3H] Dihydroalprenolol to β-Adrenergic Receptors of Rat Brain : Comparison with Those of Rat Heart Treated with Neuraminidase
Effects of Ketanserin and 3-[2-[4-(o-Methoxyphenyl)-1-piperazinyl]ethyl]-2,4(1H, 3H)-quinazolinedione Monohydrochloride (SGB-1534), Anti-hypertensive Agents, on ^3H-Serotonin and ^3H^Ketanserin Bindings to Serotonergic (5HT_1 and 5HT_2) Receptors in Dog B
Effect of 3-[2-[4-(o-Methoxyphenyl)-1-piperazinyl]ethyl]-2,4(1H, 3H)-quinazolinedione Monohydrochloride (SGB-1534), an Anthihypertensive Agent, on ^3H-Prazosin and ^3H-p-Aminoclonidine Binding to α_1-and α_2-Adrenoceptors in Dog Brain and Arta
Effects of Choline and Inositol on ^3H-Dihydroalprenolol and ^I-Iodocyanopindolol Bindings to β-Adrenegic Receptors of the Guinea Pig Cerebral Cortical Membranes
Characterization of ^3H-Dihydroalprenolol Binding to β-Adrenergic Receptors of Rat Brain : Two Binding Sites of Racemic Propranolol in Displacement Experiments(Pharmacological)
Biphasic Binding of ^I-Iodocyanopindolol to β-Adrenergic Receptors in Rat Cerebral Cortical Membranes. I. Assessment by the Use of Agonists(Pharmacological)
Adrenergic and Serotonergic Receptor-Blocking Potencies of Terazosin, a New Antihypertensive Agent, as Assessed by Radioligand Binding Assay(Pharmacological)
The Affinity of Bopindolol and Its Two Metabolites for a β_2-Adrenoceptor in the Bovine Mesenteric Artery
Comparison of Displacemental Potencies of Terazosin Enantiomers for α_1-Adrenoceptor Subtypes
Bopindolol Is a Slowly Dissociating β_1-Adrenoceptor Antagonist When Compared to Other β-Blockers

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