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Membranes|October 27, 2022
Expression of Mutant Glycine Receptors in Xenopus Oocytes Using Canonical and Non-Canonical Amino Acids Reveals Distinct Roles of Conserved Proline ResiduesSarah C R Lummis, Dennis A DoughertyMolecular Pharmacology|June 9, 2019
Binding Interactions of NS6740, a Silent Agonist of the α7 Nicotinic Acetylcholine ReceptorCatriona E W Blunt, Dennis A DoughertyMolecular Pharmacology|June 27, 2014
Subtype-specific mechanisms for functional interaction between α6β4* nicotinic acetylcholine receptors and P2X receptorsWalrati Limapichat, Dennis A Dougherty, Henry A LesterThe Journal of Biological Chemistry|July 4, 2007
Establishing an ion pair interaction in the homomeric rho1 gamma-aminobutyric acid type A receptor that contributes to the gating pathwayJinti Wang, Henry A Lester, Dennis A DoughertyThe Journal of Biological Chemistry|January 14, 2010
Chemical scale studies of the Phe-Pro conserved motif in the cys loop of Cys loop receptorsWalrati Limapichat, Henry A Lester, Dennis A DoughertyCurrent Opinion in Neurobiology|July 10, 2003
Unnatural amino acid mutagenesis in mapping ion channel functionDarren L Beene, Dennis A Dougherty, Henry A LesterRNA (New York, N.Y.)|August 19, 2007
Improved amber and opal suppressor tRNAs for incorporation of unnatural amino acids in vivo. Part 2: evaluating suppression efficiencyErik A Rodriguez, Henry A Lester, Dennis A DoughertyACS Chemical Biology|February 3, 2012
Probing the effects of residues located outside the agonist binding site on drug-receptor selectivity in the nicotinic receptorNyssa L Puskar, Henry A Lester, Dennis A DoughertyNeuropharmacology|December 27, 2014
Allosteric activation of the 5-HT3AB receptor by mCPBGTimothy F Miles, Henry A Lester, Dennis A DoughertyACS Chemical Biology|August 10, 2012
Ondansetron and granisetron binding orientation in the 5-HT(3) receptor determined by unnatural amino acid mutagenesisNoah H Duffy, Henry A Lester, Dennis A DoughertyPageof 14