Structural Basis for Ligand Recognition and Functional Selectivity at Angiotensin Receptor
about
Angiotensin Receptors: Structure, Function, Signaling and Clinical ApplicationsDifferential Contribution of Transmembrane Domains IV, V, VI, and VII to Human Angiotensin II Type 1 Receptor Homomer Formation.Supporting precision medicine by data mining across multi-disciplines: an integrative approach for generating comprehensive linkages between single nucleotide variants (SNVs) and drug-binding sites.Molecular docking, 3D-QSAR and structural optimization on imidazo-pyridine derivatives dually targeting AT1 and PPARg.Angiotensin II type 1/adenosine A 2A receptor oligomers: a novel target for tardive dyskinesia.Insights into Basal Signaling Regulation, Oligomerization, and Structural Organization of the Human G-Protein Coupled Receptor 83.Structural basis for selectivity and diversity in angiotensin II receptorsDrug Binding Poses Relate Structure with Efficacy in the μ Opioid Receptor.Hitchhiking on the heptahelical highway: structure and function of 7TM receptor complexes.Biased agonism and allosteric modulation of G protein-coupled receptor 183 - a 7TM receptor also known as Epstein-Barr virus-induced gene 2.Unravelling the Lesser Known Facets of Angiotensin II Type 1 Receptor.Impact of Non-Human Leukocyte Antigen-Specific Antibodies in Kidney and Heart Transplantation.Current topics in angiotensin II type 1 receptor research: Focus on inverse agonism, receptor dimerization and biased agonism.Dissecting binding of a β-barrel membrane protein by phage display.Biased signalling: from simple switches to allosteric microprocessors.Challenges and Opportunities in Drug Discovery of Biased Ligands.A Structural Framework for GPCR Chemogenomics: What's In a Residue Number?Characterization of Ligand Binding to GPCRs Through Computational Methods.Divergent Spatiotemporal Interaction of Angiotensin Receptor Blocking Drugs with Angiotensin Type 1 Receptor.Computational design of Phe-Tyr dipeptide and preparation, characterization, cytotoxicity studies of Phe-Tyr dipeptide loaded PLGA nanoparticles for the treatment of hypertension.Molecular requirements involving the human platelet protease-activated receptor-4 mechanism of activation by peptide analogues of its tethered-ligand.In silico studies targeting G-protein coupled receptors for drug research against Parkinson's disease.Exploring G Protein-Coupled Receptors (GPCRs) Ligand Space via Cheminformatics Approaches: Impact on Rational Drug Design.Apelinergic System Structure and Function.G protein-coupled receptors: the evolution of structural insight.
P2860
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P2860
Structural Basis for Ligand Recognition and Functional Selectivity at Angiotensin Receptor
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2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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name
Structural Basis for Ligand Re ...... tivity at Angiotensin Receptor
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Structural Basis for Ligand Re ...... tivity at Angiotensin Receptor
@en
type
label
Structural Basis for Ligand Re ...... tivity at Angiotensin Receptor
@ast
Structural Basis for Ligand Re ...... tivity at Angiotensin Receptor
@en
prefLabel
Structural Basis for Ligand Re ...... tivity at Angiotensin Receptor
@ast
Structural Basis for Ligand Re ...... tivity at Angiotensin Receptor
@en
P2093
P2860
P356
P1476
Structural Basis for Ligand Re ...... tivity at Angiotensin Receptor
@en
P2093
Gye Won Han
Hamiyet Unal
Nilkanth Patel
Raymond C Stevens
Russell Desnoyer
Sadashiva S Karnik
Vadim Cherezov
P2860
P304
29127-29139
P356
10.1074/JBC.M115.689000
P407
P577
2015-09-29T00:00:00Z