Ishiguro Masaji | Laboratory Of Chemical Biology Faculty Of Applied Life Sciences Niigata University Of Pharmacy And A

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著作論文

Engineered Mutation of Some Important Amino Acids in Angiotensin II Type 1 (AT1) Receptor Increases the Binding Affinity of AT1-Receptor Antagonists
Mutation of Important Amino Acid Residue of Asp104Lys in Human β_1-Adrenergic Receptor Triggers Functional and Constitutive Inactivation(Pharmacology)
Inverse Agonist Activity of Sarpogrelate, a Selective 5-HT_-Receptor Antagonist, at the Constitutively Active Human 5-HT_ Receptor
Molecular modeling of the interaction of sarpogrelate and human 5-HT_, 5-HT_ and 5-HT_ receptor subtypes
Mutational Analysis of the α_-Adrenergic Receptor Binding Pocket of Antagonists by Radioligand Binding Assay(Pharmacology)
Amino Acids of the Human α_-Adrenergic Receptor Involved in Antagonist Binding
Beta-Blockers Show Inverse Agonism to a Novel Constitutively Active Mutant of β_1-Adrenoceptor
Pharmacological and Molecular Characterization of Novel SWR-Compounds for β-Adrenergic Receptors as assessed by Molecular Modeling, Site-Directed Mutagenesis, Binding Affinity and Functional Activity
β-Adrenoceptors: Three-Dimensional Structures and Binding Sites for Ligands
Engineered Mutation of Some Important Amino Acids in Angiotensin II Type 1 (AT_1) Receptor Increases the Binding Affinity of AT_1-Receptor Antagonists
Mechanism of Inverse Agonist Action of Sarpogrelate at the Constitutively Active Mutant of Human 5-HT2A Receptor Revealed by Molecular Modeling
Identification of a C26-sterol in urine and serum of patient with congenital adrenal hyperplasia.

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