Site-Directed Mutagenesis of the Gerbil and Human Angiotensin II AT1Receptors Identifies Amino Acid Residues Attributable to the Binding Affinity for the Nonpeptidic Antagonist Losartan-Reference-Cited by-同舟云学术

Site-Directed Mutagenesis of the Gerbil and Human Angiotensin II AT1Receptors Identifies Amino Acid Residues Attributable to the Binding Affinity for the Nonpeptidic Antagonist Losartan

Published:2002-06-01 Issue:6 Volume:61 Page:1404-1415
ISSN:0026-895X
Container-title:Molecular Pharmacology
language:en
Short-container-title:Mol Pharmacol

Author:

Hoe Kwang-Lae,Saavedra Juan M.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference36 articles.

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4. The Ligand Binding Signatures of the Rat AT1A, AT1B and the Human AT1 Receptors Are Essentially Identical

5. International Union of Pharmacology. XXIII. The Angiotensin II Receptors.;De Gasparo;Pharmacol Rev,2000

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