Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P Clausen

Showing results (291-300 of 356) with videos related to

Pageof 36
Sort By:
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.
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.
Cytometry|April 1, 1995
Comparative sperm chromatin structure assay measurements on epiillumination and orthogonal axes flow cytometersD Evenson, L Jost, D Gandour, 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.
Scientific Reports|June 30, 2015
Cortical actin networks induce spatio-temporal confinement of phospholipids in the plasma membrane--a minimally invasive investigation by STED-FCSDébora M Andrade, Mathias P Clausen, Jan Keller, 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.
Journal of Medicinal Chemistry|December 17, 2021
Derivatives of (<i>R</i>)-3-(5-Furanyl)carboxamido-2-aminopropanoic Acid as Potent NMDA Receptor Glycine Site Agonists with GluN2 Subunit-Specific ActivityFabao Zhao, Unai Atxabal, Sofia Mariottini, et al.
Frontiers in Chemistry|December 5, 2022
Discovery of (<i>R</i>)-2-amino-3-triazolpropanoic acid derivatives as NMDA receptor glycine site agonists with GluN2 subunit-specific activityFabao Zhao, Georgios Mazis, Feng Yi, et al.
Nature Communications|March 28, 2026
Auxiliary subunits reshape structural asymmetry and functional plasticity in heterotetrameric GluA1/A2 AMPA receptor coreLaura Y Yen, Thomas P Newton, Maria V Yelshanskaya, et al.
Pageof 36

Showing results (291-300 of 356) with videos related to

Sort By:
Pageof 36
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.
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.
Cytometry|April 1, 1995
Comparative sperm chromatin structure assay measurements on epiillumination and orthogonal axes flow cytometersD Evenson, L Jost, D Gandour, 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.
Scientific Reports|June 30, 2015
Cortical actin networks induce spatio-temporal confinement of phospholipids in the plasma membrane--a minimally invasive investigation by STED-FCSDébora M Andrade, Mathias P Clausen, Jan Keller, 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.
Journal of Medicinal Chemistry|December 17, 2021
Derivatives of (<i>R</i>)-3-(5-Furanyl)carboxamido-2-aminopropanoic Acid as Potent NMDA Receptor Glycine Site Agonists with GluN2 Subunit-Specific ActivityFabao Zhao, Unai Atxabal, Sofia Mariottini, et al.
Frontiers in Chemistry|December 5, 2022
Discovery of (<i>R</i>)-2-amino-3-triazolpropanoic acid derivatives as NMDA receptor glycine site agonists with GluN2 subunit-specific activityFabao Zhao, Georgios Mazis, Feng Yi, et al.
Nature Communications|March 28, 2026
Auxiliary subunits reshape structural asymmetry and functional plasticity in heterotetrameric GluA1/A2 AMPA receptor coreLaura Y Yen, Thomas P Newton, Maria V Yelshanskaya, et al.
Pageof 36