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S Pickering

Showing results (201-210 of 225) with videos related to

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Neuron|March 9, 2000
Neuropilin-2 is required in vivo for selective axon guidance responses to secreted semaphorinsR J Giger, J F Cloutier, A Sahay, et al.
The FEBS Journal|December 25, 2023
Small-molecule positive allosteric modulation of homomeric kainate receptors GluK1-3: development of screening assays and insight into GluK3 structureYasmin Bay, Raminta Venskutonytė, Stine M Frantsen, et al.
Annals of Neurology|August 12, 1999
Frequency of tau mutations in three series of non-Alzheimer's degenerative dementiaH Houlden, M Baker, J Adamson, et al.
Journal of Medicinal Chemistry|April 4, 2019
Use of the 4-Hydroxytriazole Moiety as a Bioisosteric Tool in the Development of Ionotropic Glutamate Receptor LigandsStefano Sainas, Piero Temperini, Jill C Farnsworth, et al.
Journal of Medicinal Chemistry|April 26, 2007
A tetrazolyl-substituted subtype-selective AMPA receptor agonistStine B Vogensen, Karla Frydenvang, Jeremy R Greenwood, et al.
Journal of Medicinal Chemistry|May 31, 2011
Selective kainate receptor (GluK1) ligands structurally based upon 1H-cyclopentapyrimidin-2,4(1H,3H)-dione: synthesis, molecular modeling, and pharmacological and biostructural characterizationRaminta Venskutonyte, Stefania Butini, Salvatore Sanna Coccone, et al.
Annals of Neurology|December 16, 2000
Pick's disease is associated with mutations in the tau geneS Pickering-Brown, M Baker, S H Yen, et al.
Journal of Medicinal Chemistry|December 14, 2001
Characterization of the 1H-cyclopentapyrimidine-2,4(1H,3H)-dione derivative (S)-CPW399 as a novel, potent, and subtype-selective AMPA receptor full agonist with partial desensitization propertiesG Campiani, E Morelli, V Nacci, et al.
European Journal of Medicinal Chemistry|December 15, 2023
Exploring thienothiadiazine dioxides as isosteric analogues of benzo- and pyridothiadiazine dioxides in the search of new AMPA and kainate receptor positive allosteric modulatorsPierre Francotte, Yasmin Bay, Eric Goffin, et al.
Journal of Medicinal Chemistry|December 23, 2016
Design and Synthesis of a Series of l-trans-4-Substituted Prolines as Selective Antagonists for the Ionotropic Glutamate Receptors Including Functional and X-ray Crystallographic Studies of New Subtype Selective Kainic Acid Receptor Subtype 1 (GluK1) Antagonist (2S,4R)-4-(2-Carboxyphenoxy)pyrrolidine-2-carboxylic AcidNiels Krogsgaard-Larsen, Claudia G Delgar, Karina Koch, et al.
Pageof 23

Showing results (201-210 of 225) with videos related to

Sort By:
Pageof 23
Neuron|March 9, 2000
Neuropilin-2 is required in vivo for selective axon guidance responses to secreted semaphorinsR J Giger, J F Cloutier, A Sahay, et al.
The FEBS Journal|December 25, 2023
Small-molecule positive allosteric modulation of homomeric kainate receptors GluK1-3: development of screening assays and insight into GluK3 structureYasmin Bay, Raminta Venskutonytė, Stine M Frantsen, et al.
Annals of Neurology|August 12, 1999
Frequency of tau mutations in three series of non-Alzheimer's degenerative dementiaH Houlden, M Baker, J Adamson, et al.
Journal of Medicinal Chemistry|April 4, 2019
Use of the 4-Hydroxytriazole Moiety as a Bioisosteric Tool in the Development of Ionotropic Glutamate Receptor LigandsStefano Sainas, Piero Temperini, Jill C Farnsworth, et al.
Journal of Medicinal Chemistry|April 26, 2007
A tetrazolyl-substituted subtype-selective AMPA receptor agonistStine B Vogensen, Karla Frydenvang, Jeremy R Greenwood, et al.
Journal of Medicinal Chemistry|May 31, 2011
Selective kainate receptor (GluK1) ligands structurally based upon 1H-cyclopentapyrimidin-2,4(1H,3H)-dione: synthesis, molecular modeling, and pharmacological and biostructural characterizationRaminta Venskutonyte, Stefania Butini, Salvatore Sanna Coccone, et al.
Annals of Neurology|December 16, 2000
Pick's disease is associated with mutations in the tau geneS Pickering-Brown, M Baker, S H Yen, et al.
Journal of Medicinal Chemistry|December 14, 2001
Characterization of the 1H-cyclopentapyrimidine-2,4(1H,3H)-dione derivative (S)-CPW399 as a novel, potent, and subtype-selective AMPA receptor full agonist with partial desensitization propertiesG Campiani, E Morelli, V Nacci, et al.
European Journal of Medicinal Chemistry|December 15, 2023
Exploring thienothiadiazine dioxides as isosteric analogues of benzo- and pyridothiadiazine dioxides in the search of new AMPA and kainate receptor positive allosteric modulatorsPierre Francotte, Yasmin Bay, Eric Goffin, et al.
Journal of Medicinal Chemistry|December 23, 2016
Design and Synthesis of a Series of l-trans-4-Substituted Prolines as Selective Antagonists for the Ionotropic Glutamate Receptors Including Functional and X-ray Crystallographic Studies of New Subtype Selective Kainic Acid Receptor Subtype 1 (GluK1) Antagonist (2S,4R)-4-(2-Carboxyphenoxy)pyrrolidine-2-carboxylic AcidNiels Krogsgaard-Larsen, Claudia G Delgar, Karina Koch, et al.
Pageof 23