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Cells|September 28, 2021
P-Rex1 Controls Sphingosine 1-Phosphate Receptor Signalling, Morphology, and Cell-Cycle Progression in Neuronal CellsElizabeth Hampson, Elpida Tsonou, Martin J Baker, et al.
Nature Structural & Molecular Biology|August 20, 2013
Defining the structural relationship between kainate-receptor deactivation and desensitizationG Brent Dawe, Maria Musgaard, Elizabeth D Andrews, et al.
ACS Chemical Neuroscience|August 3, 2023
Side Groups Convert the α7 Nicotinic Receptor Agonist Ether Quinuclidine into a Type I Positive Allosteric ModulatorFranco Viscarra, Juan Facundo Chrestia, Yaima Sanchez, et al.
The Journal of Biological Chemistry|June 18, 2014
Non-equivalent ligand selectivity of agonist sites in (α4β2)2α4 nicotinic acetylcholine receptors: a key determinant of agonist efficacySimone Mazzaferro, Federica Gasparri, Karina New, et al.
FEBS Letters|November 25, 2003
Ion channel gating: insights via molecular simulationsOliver Beckstein, Philip C Biggin, Peter Bond, et al.
The Journal of Biological Chemistry|September 7, 2015
Tripartite ATP-independent Periplasmic (TRAP) Transporters Use an Arginine-mediated Selectivity Filter for High Affinity Substrate BindingMarcus Fischer, Adam P Hopkins, Emmanuele Severi, et al.
Nature Structural & Molecular Biology|October 3, 2017
Crystal structures of a GABAA-receptor chimera reveal new endogenous neurosteroid-binding sitesDuncan Laverty, Philip Thomas, Martin Field, et al.
Journal of Chemical Information and Modeling|December 8, 2015
The Fragment Molecular Orbital Method Reveals New Insight into the Chemical Nature of GPCR-Ligand InteractionsAlexander Heifetz, Ewa I Chudyk, Laura Gleave, et al.
Nature Communications|August 18, 2022
Structural basis for cannabinoid-induced potentiation of alpha1-glycine receptors in lipid nanodiscsArvind Kumar, Kayla Kindig, Shanlin Rao, et al.
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