Pages that link to "Q51941651"
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The following pages link to Christopher A. Reynolds (Q51941651):
Displaying 36 items.
- A Hydrogen-Bonded Polar Network in the Core of the Glucagon-Like Peptide-1 Receptor Is a Fulcrum for Biased Agonism: Lessons from Class B Crystal Structures (Q27345100) (← links)
- The Extracellular Surface of the GLP-1 Receptor Is a Molecular Trigger for Biased Agonism (Q28276469) (← links)
- Receptor Activity-modifying Protein-directed G Protein Signaling Specificity for the Calcitonin Gene-related Peptide Family of Receptors (Q28278110) (← links)
- Key interactions by conserved polar amino acids located at the transmembrane helical boundaries in Class B GPCRs modulate activation, effector specificity and biased signalling in the glucagon-like peptide-1 receptor (Q28278129) (← links)
- Assessing the effect of dynamics on the closed-loop protein-folding hypothesis (Q30355826) (← links)
- Closed loop folding units from structural alignments: experimental foldons revisited. (Q30393591) (← links)
- A prototype bioreductive DNA groove binding ligand (Q33262211) (← links)
- Genetically encoded photocross-linkers determine the biological binding site of exendin-4 peptide in the N-terminal domain of the intact human glucagon-like peptide-1 receptor (GLP-1R) (Q33615669) (← links)
- Dimerization and domain swapping in G-protein-coupled receptors: a computational study (Q34047431) (← links)
- Towards new transition metal-based hypoxic selective agents for therapy and imaging (Q34264345) (← links)
- Understanding the molecular functions of the second extracellular loop (ECL2) of the calcitonin gene-related peptide (CGRP) receptor using a comprehensive mutagenesis approach (Q34557426) (← links)
- Bioinformatics and molecular modelling approaches to GPCR oligomerization. (Q37656672) (← links)
- Criteria for confirming sequence periodicity identified by Fourier transform analysis: application to GCR2, a candidate plant GPCR? (Q46845571) (← links)
- Extracellular loops 2 and 3 of the calcitonin receptor selectively modify agonist binding and efficacy. (Q49898093) (← links)
- Computed redox potentials and the design of bioreductive agents (Q51657113) (← links)
- Connectivity and binding-site recognition: applications relevant to drug design. (Q51661480) (← links)
- Classical polarization in hybrid QM/MM methods (Q51941603) (← links)
- Studies on the mechanism of hypoxic selectivity in copper bis(thiosemicarbazone) radiopharmaceuticals. (Q52044357) (← links)
- Modeling GPCR active state conformations: The β2‐adrenergic receptor (Q53437310) (← links)
- Toward a consistent treatment of polarization in model QM/MM calculations. (Q53524928) (← links)
- Assessing the role of polarization in docking. (Q53524934) (← links)
- Quantitative measurement of protease ligand conformation. (Q53551924) (← links)
- Conservation of closed loops. (Q53572265) (← links)
- A multilayered approach to approximating solute polarization. (Q53643501) (← links)
- Dimerization of G-protein-coupled receptors. (Q53676491) (← links)
- Accurate numerical determination of Kohn-Sham potentials from electronic densities: I. Two-electron systems (Q58228107) (← links)
- Potential energy surfaces from Kohn-Sham potentials (Q58228116) (← links)
- Rational drug design: binding free energy differences of carbonic anhydrase inhibitors (Q59614548) (← links)
- Correlated mutations and subtype specificity in the adrenergic receptor (Q64997987) (← links)
- Hypoxia-targeting copper bis(selenosemicarbazone) complexes: comparison with their sulfur analogues (Q73800334) (← links)
- Simulations on dimeric peptides: evidence for domain swapping in G-protein-coupled receptors? (Q73920684) (← links)
- Correlated mutations amongst the external residues of G-protein coupled receptors (Q73921179) (← links)
- A New Approach to Docking in the β2-Adrenergic Receptor That Exploits the Domain Structure of G-Protein-Coupled Receptors (Q73938121) (← links)
- Structure and dynamics of the active Gs-coupled human secretin receptor (Q98564759) (← links)
- Addressing free fatty acid receptor 1 (FFAR1) activation using supervised molecular dynamics (Q98772845) (← links)
- Partial agonism improves the anti-hyperglycaemic efficacy of an oxyntomodulin-derived GLP-1R/GCGR co-agonist (Q112583678) (← links)