Bhuiyan Mohiuddin | Department Of Pharmacology Faculty Of Pharmaceutical Sciences Niigata University Of Pharmacy And App

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概要

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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
Constitutively Active Mutant N111G of Angiotensin II Type 1 (AT_1) Receptor Induces Homologous Internalization Through Mediation of AT_1-Receptor Antagonist
Assessment of Binding Affinity to 5-Hydroxytryptamine 2A (5-HT_) Receptor and Inverse Agonist Activity of Naftidrofuryl : Comparison With Those of Sarpogrelate
Mutation of Important Amino Acid Residue of Asp104Lys in Human β_1-Adrenergic Receptor Triggers Functional and Constitutive Inactivation(Pharmacology)
Identification of a Key Amino Acid of the Human 5-HT_ Serotonin Receptor Important for Sarpogrelate Binding
Selectivity of Sarpogrelate to the Recombinant Human 5-HT_ Receptors as Assessed by Molecular Pharmacology and Molecular Modeling
Inverse Agonist Activity of Sarpogrelate, a Selective 5-HT_-Receptor Antagonist, at the Constitutively Active Human 5-HT_ Receptor
Internalization of Constitutively Active N111G Mutant of AT1 Receptor Induced by Angiotensin II–Receptor Antagonists Candesartan, Losartan, and Telmisartan: Comparison With Valsartan
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
Asp125 and Thr130 in Transmembrane Domain 3 Are Major Sites of α_-Adrenergic Receptor Antagonist Binding(Pharmacology)
Identification of a Key Amino Acid of the Human 5-HT2B Serotonin Receptor Important for Sarpogrelate Binding
Engineered Mutation of Some Important Amino Acids in Angiotensin II Type 1 (AT_1) Receptor Increases the Binding Affinity of AT_1-Receptor Antagonists
Internalization of Constitutively Active N111G Mutant of AT_1 Receptor Induced by Angiotensin II-Receptor Antagonists Candesartan, Losartan, and Telmisartan : Comparison With Valsartan
Effect of Site-directed Mutagenesis in Some Important Amino Acids of AT_1 Receptor on the Binding Affinity of the Agonist and Antagonists
Selectivity of Valsartan to the Human Angiotensin II Type One Receptors as Assessed by Binding Affinity, Functional Activity and Molecular Modeling
Pharmacological and Molecular Studies for the Regulation of β_1-Adrenergic Receptors that Reveals Activation and Inactivation
Mechanism of Inverse Agonist Action of Sarpogrelate at the Constitutively Active Mutant of Human 5-HT2A Receptor Revealed by Molecular Modeling

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