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Rasmus P Clausen

Showing results (31-40 of 83) with videos related to

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ACS Chemical Biology|July 12, 2014
Substrate- and cofactor-independent inhibition of histone demethylase KDM4CUlrike Leurs, Brian Lohse, Kasper D Rand, et al.
Journal of Medicinal Chemistry|December 5, 2008
Novel high-affinity and selective biaromatic 4-substituted gamma-hydroxybutyric acid (GHB) analogues as GHB ligands: design, synthesis, and binding studiesSigne Høg, Petrine Wellendorph, Birgitte Nielsen, et al.
Brain Research|January 13, 2015
Differential role of AMPA receptors in mouse tests of antidepressant and anxiolytic actionJesper T Andreasen, Ciaran M Fitzpatrick, Maria Larsen, et al.
Neurochemical Research|April 6, 2020
Pharmacological Characterization of a Betaine/GABA Transporter 1 (BGT1) Inhibitor Displaying an Unusual Biphasic Inhibition Profile and Anti-seizure EffectsMaria E K Lie, Stefanie Kickinger, Jonas Skovgaard-Petersen, et al.
Journal of Medicinal Chemistry|April 29, 2005
Convergent synthesis and pharmacology of substituted tetrazolyl-2-amino-3-(3-hydroxy-5-methyl-4-isoxazolyl)propionic acid analoguesStine B Vogensen, Rasmus P Clausen, Jeremy R Greenwood, et al.
International Journal of Biological Macromolecules|July 13, 2016
A parallel panning scheme used for selection of a GluA4-specific Fab targeting the ligand-binding domainRasmus P Clausen, Andreas Ø Mohr, Erik Riise, et al.
Journal of Medicinal Chemistry|September 24, 2013
New synthesis and tritium labeling of a selective ligand for studying high-affinity γ-hydroxybutyrate (GHB) binding sitesStine B Vogensen, Aleš Marek, Tina Bay, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 15, 2005
Novel cyclic gamma-hydroxybutyrate (GHB) analogs with high affinity and stereoselectivity of binding to GHB sites in rat brainPetrine Wellendorph, Signe Høg, Jeremy R Greenwood, et al.
Biological Chemistry|November 25, 2022
<i>In vitro</i> ADME characterization of a very potent 3-acylamino-2-aminopropionic acid-derived GluN2C-NMDA receptor agonist and its ester prodrugsElena Bechthold, Lucie Grey, Emil Diamant, et al.
Biochemical Pharmacology|June 25, 2013
Discovery of a subtype selective inhibitor of the human betaine/GABA transporter 1 (BGT-1) with a non-competitive pharmacological profileBolette Kragholm, Trine Kvist, Karsten K Madsen, et al.
Pageof 9

Showing results (31-40 of 83) with videos related to

Sort By:
Pageof 9
ACS Chemical Biology|July 12, 2014
Substrate- and cofactor-independent inhibition of histone demethylase KDM4CUlrike Leurs, Brian Lohse, Kasper D Rand, et al.
Journal of Medicinal Chemistry|December 5, 2008
Novel high-affinity and selective biaromatic 4-substituted gamma-hydroxybutyric acid (GHB) analogues as GHB ligands: design, synthesis, and binding studiesSigne Høg, Petrine Wellendorph, Birgitte Nielsen, et al.
Brain Research|January 13, 2015
Differential role of AMPA receptors in mouse tests of antidepressant and anxiolytic actionJesper T Andreasen, Ciaran M Fitzpatrick, Maria Larsen, et al.
Neurochemical Research|April 6, 2020
Pharmacological Characterization of a Betaine/GABA Transporter 1 (BGT1) Inhibitor Displaying an Unusual Biphasic Inhibition Profile and Anti-seizure EffectsMaria E K Lie, Stefanie Kickinger, Jonas Skovgaard-Petersen, et al.
Journal of Medicinal Chemistry|April 29, 2005
Convergent synthesis and pharmacology of substituted tetrazolyl-2-amino-3-(3-hydroxy-5-methyl-4-isoxazolyl)propionic acid analoguesStine B Vogensen, Rasmus P Clausen, Jeremy R Greenwood, et al.
International Journal of Biological Macromolecules|July 13, 2016
A parallel panning scheme used for selection of a GluA4-specific Fab targeting the ligand-binding domainRasmus P Clausen, Andreas Ø Mohr, Erik Riise, et al.
Journal of Medicinal Chemistry|September 24, 2013
New synthesis and tritium labeling of a selective ligand for studying high-affinity γ-hydroxybutyrate (GHB) binding sitesStine B Vogensen, Aleš Marek, Tina Bay, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 15, 2005
Novel cyclic gamma-hydroxybutyrate (GHB) analogs with high affinity and stereoselectivity of binding to GHB sites in rat brainPetrine Wellendorph, Signe Høg, Jeremy R Greenwood, et al.
Biological Chemistry|November 25, 2022
<i>In vitro</i> ADME characterization of a very potent 3-acylamino-2-aminopropionic acid-derived GluN2C-NMDA receptor agonist and its ester prodrugsElena Bechthold, Lucie Grey, Emil Diamant, et al.
Biochemical Pharmacology|June 25, 2013
Discovery of a subtype selective inhibitor of the human betaine/GABA transporter 1 (BGT-1) with a non-competitive pharmacological profileBolette Kragholm, Trine Kvist, Karsten K Madsen, et al.
Pageof 9