检索结果 - Gloriam, David E

The G protein-coupled receptor subset of the rat genome 由 Gloriam, David E, Fredriksson, Robert, Schiöth, Helgi B

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SMARTCyp: A 2D Method for Prediction of Cytochrome P450-Mediated Drug Metabolism 由 Rydberg, Patrik, Gloriam, David E., Zaretzki, Jed, Breneman, Curt, Olsen, Lars

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Integrating structural and mutagenesis data to elucidate GPCR ligand binding 由 Munk, Christian, Harpsøe, Kasper, Hauser, Alexander, Isberg, Vignir, Gloriam, David E.

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Novel approaches leading towards peptide GPCR de‐orphanisation 由 Hauser, Alexander S., Gloriam, David E., Bräuner‐Osborne, Hans, Foster, Simon R.

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Pharmacology and function of the orphan GPR139 G protein‐coupled receptor 由 Vedel, Line, Nøhr, Anne Cathrine, Gloriam, David E., Bräuner‐Osborne, Hans

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The G protein-coupled receptor subset of the dog genome is more similar to that in humans than rodents 由 Haitina, Tatjana, Fredriksson, Robert, Foord, Steven M, Schiöth, Helgi B, Gloriam, David E

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Structure-Activity Relationships of Constrained Phenylethylamine Ligands for the Serotonin 5-HT(2) Receptors 由 Isberg, Vignir, Paine, James, Leth-Petersen, Sebastian, Kristensen, Jesper L., Gloriam, David E.

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Correction: Structure-Activity Relationships of Constrained Phenylethylamine Ligands for the Serotonin 5-HT(2) Receptors 由 Isberg, Vignir, Paine, James, Leth-Petersen, Sebastian, Kristensen, Jesper L., Gloriam, David E.

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Structural insight to mutation effects uncover a common allosteric site in class C GPCRs 由 Harpsøe, Kasper, Boesgaard, Michael W, Munk, Christian, Bräuner-Osborne, Hans, Gloriam, David E

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Selectivity determinants of GPCR-G protein binding 由 Flock, Tilman, Hauser, Alexander S., Lund, Nadia, Gloriam, David E., Balaji, Santhanam, Babu, M. Madan

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Trends in GPCR drug discovery: new agents, targets and indications 由 Hauser, Alexander S., Attwood, Misty M., Rask-Andersen, Mathias, Schiöth, Helgi B., Gloriam, David E.

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Common coupling map advances GPCR-G protein selectivity 由 Hauser, Alexander S, Avet, Charlotte, Normand, Claire, Mancini, Arturo, Inoue, Asuka, Bouvier, Michel, Gloriam, David E

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The G Protein–Coupled Receptor Subset of the Chicken Genome 由 Lagerström, Malin C, Hellström, Anders R, Gloriam, David E, Larsson, Thomas P, Schiöth, Helgi B, Fredriksson, Robert

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Pharmacogenomics of GPCR Drug Targets 由 Hauser, Alexander S., Chavali, Sreenivas, Masuho, Ikuo, Jahn, Leonie J., Martemyanov, Kirill A., Gloriam, David E., Babu, M. Madan

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Ligand-directed bias of G protein signaling at the dopamine D(2) receptor 由 Moo, Ee Von, Harpsøe, Kasper, Hauser, Alexander S, Masuho, Ikuo, Bräuner-Osborne, Hans, Gloriam, David E., Martemyanov, Kirill A.

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A novel red fluorescence dopamine biosensor selectively detects dopamine in the presence of norepinephrine in vitro 由 Nakamoto, Chihiro, Goto, Yuhei, Tomizawa, Yoko, Fukata, Yuko, Fukata, Masaki, Harpsøe, Kasper, Gloriam, David E., Aoki, Kazuhiro, Takeuchi, Tomonori

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Selective Negative Allosteric Modulation Of Metabotropic Glutamate Receptors – A Structural Perspective of Ligands and Mutants 由 Harpsøe, Kasper, Isberg, Vignir, Tehan, Benjamin G., Weiss, Dahlia, Arsova, Angela, Marshall, Fiona H., Bräuner-Osborne, Hans, Gloriam, David E.

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Identification of Histamine H(3) Receptor Ligands Using a New Crystal Structure Fragment-based Method 由 Frandsen, Ida Osborn, Boesgaard, Michael W., Fidom, Kimberley, Hauser, Alexander S., Isberg, Vignir, Bräuner-Osborne, Hans, Wellendorph, Petrine, Gloriam, David E.

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GPCRdb in 2018: adding GPCR structure models and ligands 由 Pándy-Szekeres, Gáspár, Munk, Christian, Tsonkov, Tsonko M, Mordalski, Stefan, Harpsøe, Kasper, Hauser, Alexander S, Bojarski, Andrzej J, Gloriam, David E

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Structure of the class D GPCR Ste2 dimer coupled to two G proteins 由 Velazhahan, Vaithish, Ma, Ning, Pándy-Szekeres, Gáspár, Kooistra, Albert J., Lee, Yang, Gloriam, David E., Vaidehi, Nagarajan, Tate, Christopher G.

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