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Thomas M Frimurer

Showing results (1-10 of 73) with videos related to

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Current Topics in Medicinal Chemistry|April 8, 2011
Drug design of GPCR ligands using physicogenetics and chemogenomics--principles and case studiesThomas M Frimurer, Thomas Högberg
Nature Chemical Biology|August 31, 2017
Structural biology: Full monty of family B GPCRsThue W Schwartz, Thomas M Frimurer
Bioorganic & Medicinal Chemistry Letters|September 8, 2012
Melanin concentrating hormone receptor 1 (MCHR1) antagonists-Still a viable approach for obesity treatment?Thomas Högberg, Thomas M Frimurer, Pradip K Sasmal
International Journal of Molecular Sciences|April 30, 2021
The Zinc-Sensing Receptor GPR39 in Physiology and as a Pharmacological TargetAnna Laitakari, Lingzhi Liu, Thomas M Frimurer, et al.
Current Opinion in Cell Biology|January 18, 2020
Structural basis for GPCR signaling by small polar versus large lipid metabolites-discovery of non-metabolite ligandsMichael Lückmann, Mette Trauelsen, Thomas M Frimurer, et al.
Cell Metabolism|February 8, 2018
The HETE Is on FFAR1 and Pancreatic Islet CellsMette Trauelsen, Michael Lückmann, Thomas M Frimurer, et al.
Molecular Informatics|August 6, 2016
In Silico Investigation of the Neurotensin Receptor 1 Binding Site: Overlapping Binding Modes for Small Molecule Antagonists and the Endogenous Peptide AgonistMichael Lückmann, Birgitte Holst, Thue W Schwartz, et al.
Plos One|July 12, 2013
Assessment and challenges of ligand docking into comparative models of G-protein coupled receptorsElizabeth Dong Nguyen, Christoffer Norn, Thomas M Frimurer, et al.
The Journal of Biological Chemistry|November 9, 2012
PheVI:09 (Phe6.44) as a sliding microswitch in seven-transmembrane (7TM) G protein-coupled receptor activationLouise Valentin-Hansen, Birgitte Holst, Thomas M Frimurer, et al.
Protein Science : a Publication of the Protein Society|September 22, 2022
Mechanistic basis of GPCR activation explored by ensemble refinement of crystallographic structuresJesper J Madsen, Libin Ye, Thomas M Frimurer, et al.
Pageof 8

Showing results (1-10 of 73) with videos related to

Sort By:
Pageof 8
Current Topics in Medicinal Chemistry|April 8, 2011
Drug design of GPCR ligands using physicogenetics and chemogenomics--principles and case studiesThomas M Frimurer, Thomas Högberg
Nature Chemical Biology|August 31, 2017
Structural biology: Full monty of family B GPCRsThue W Schwartz, Thomas M Frimurer
Bioorganic & Medicinal Chemistry Letters|September 8, 2012
Melanin concentrating hormone receptor 1 (MCHR1) antagonists-Still a viable approach for obesity treatment?Thomas Högberg, Thomas M Frimurer, Pradip K Sasmal
International Journal of Molecular Sciences|April 30, 2021
The Zinc-Sensing Receptor GPR39 in Physiology and as a Pharmacological TargetAnna Laitakari, Lingzhi Liu, Thomas M Frimurer, et al.
Current Opinion in Cell Biology|January 18, 2020
Structural basis for GPCR signaling by small polar versus large lipid metabolites-discovery of non-metabolite ligandsMichael Lückmann, Mette Trauelsen, Thomas M Frimurer, et al.
Cell Metabolism|February 8, 2018
The HETE Is on FFAR1 and Pancreatic Islet CellsMette Trauelsen, Michael Lückmann, Thomas M Frimurer, et al.
Molecular Informatics|August 6, 2016
In Silico Investigation of the Neurotensin Receptor 1 Binding Site: Overlapping Binding Modes for Small Molecule Antagonists and the Endogenous Peptide AgonistMichael Lückmann, Birgitte Holst, Thue W Schwartz, et al.
Plos One|July 12, 2013
Assessment and challenges of ligand docking into comparative models of G-protein coupled receptorsElizabeth Dong Nguyen, Christoffer Norn, Thomas M Frimurer, et al.
The Journal of Biological Chemistry|November 9, 2012
PheVI:09 (Phe6.44) as a sliding microswitch in seven-transmembrane (7TM) G protein-coupled receptor activationLouise Valentin-Hansen, Birgitte Holst, Thomas M Frimurer, et al.
Protein Science : a Publication of the Protein Society|September 22, 2022
Mechanistic basis of GPCR activation explored by ensemble refinement of crystallographic structuresJesper J Madsen, Libin Ye, Thomas M Frimurer, et al.
Pageof 8