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Birgit S Hansen

Showing results (1-10 of 9) with videos related to

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Journal of Clinical Pharmacology|October 30, 2013
Investigation of safety, tolerability, pharmacokinetics, and pharmacodynamics of single and multiple doses of a long-acting α-MSH analog in healthy overweight and obese subjectsJane E Royalty, Gitte Konradsen, Ole Eskerod, et al.
Bioorganic & Medicinal Chemistry Letters|December 31, 2003
Parallel solid-phase synthesis of disubstituted (5-biphenyltetrazolyl) hydantoins and thiohydantoins targeting the growth hormone secretagogue receptorRune Severinsen, Jesper F Lau, Kent Bondensgaard, et al.
Journal of Medicinal Chemistry|February 6, 2004
Recognition of privileged structures by G-protein coupled receptorsKent Bondensgaard, Michael Ankersen, Henning Thøgersen, et al.
The Biochemical Journal|July 5, 2007
Mitochondrial uncouplers with an extraordinary dynamic rangePhing-How Lou, Birgit S Hansen, Preben H Olsen, et al.
European Journal of Endocrinology|June 29, 2002
Nateglinide, but not repaglinide, stimulates growth hormone release in rat pituitary cells by inhibition of K channels and stimulation of cyclic AMP-dependent exocytosisJesper Gromada, Krister Bokvist, Marianne Høy, et al.
Bioorganic & Medicinal Chemistry Letters|December 12, 2001
Synthesis and biological evaluation of novel thio-substituted chromanes as high-affinity partial agonists for the estrogen receptorLise B Christiansen, Martin Wenckens, Paul S Bury, et al.
Bioorganic & Medicinal Chemistry|December 12, 2001
Synthesis and pharmacological evaluation of novel cis-3,4-diaryl-hydroxychromanes as high affinity partial agonists for the estrogen receptorPaul S Bury, Lise B Christiansen, Poul Jacobsen, et al.
Journal of Medicinal Chemistry|February 17, 2012
Identification and in vivo and in vitro characterization of long acting and melanocortin 4 receptor (MC4-R) selective α-melanocyte-stimulating hormone (α-MSH) analoguesKilian Conde-Frieboes, Henning Thøgersen, Jesper F Lau, et al.
Journal of Medicinal Chemistry|May 28, 2004
Arylcyanoguanidines as activators of Kir6.2/SUR1K ATP channels and inhibitors of insulin releaseTina M Tagmose, Søren C Schou, John P Mogensen, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Journal of Clinical Pharmacology|October 30, 2013
Investigation of safety, tolerability, pharmacokinetics, and pharmacodynamics of single and multiple doses of a long-acting α-MSH analog in healthy overweight and obese subjectsJane E Royalty, Gitte Konradsen, Ole Eskerod, et al.
Bioorganic & Medicinal Chemistry Letters|December 31, 2003
Parallel solid-phase synthesis of disubstituted (5-biphenyltetrazolyl) hydantoins and thiohydantoins targeting the growth hormone secretagogue receptorRune Severinsen, Jesper F Lau, Kent Bondensgaard, et al.
Journal of Medicinal Chemistry|February 6, 2004
Recognition of privileged structures by G-protein coupled receptorsKent Bondensgaard, Michael Ankersen, Henning Thøgersen, et al.
The Biochemical Journal|July 5, 2007
Mitochondrial uncouplers with an extraordinary dynamic rangePhing-How Lou, Birgit S Hansen, Preben H Olsen, et al.
European Journal of Endocrinology|June 29, 2002
Nateglinide, but not repaglinide, stimulates growth hormone release in rat pituitary cells by inhibition of K channels and stimulation of cyclic AMP-dependent exocytosisJesper Gromada, Krister Bokvist, Marianne Høy, et al.
Bioorganic & Medicinal Chemistry Letters|December 12, 2001
Synthesis and biological evaluation of novel thio-substituted chromanes as high-affinity partial agonists for the estrogen receptorLise B Christiansen, Martin Wenckens, Paul S Bury, et al.
Bioorganic & Medicinal Chemistry|December 12, 2001
Synthesis and pharmacological evaluation of novel cis-3,4-diaryl-hydroxychromanes as high affinity partial agonists for the estrogen receptorPaul S Bury, Lise B Christiansen, Poul Jacobsen, et al.
Journal of Medicinal Chemistry|February 17, 2012
Identification and in vivo and in vitro characterization of long acting and melanocortin 4 receptor (MC4-R) selective α-melanocyte-stimulating hormone (α-MSH) analoguesKilian Conde-Frieboes, Henning Thøgersen, Jesper F Lau, et al.
Journal of Medicinal Chemistry|May 28, 2004
Arylcyanoguanidines as activators of Kir6.2/SUR1K ATP channels and inhibitors of insulin releaseTina M Tagmose, Søren C Schou, John P Mogensen, et al.
Pageof 1