A P IJzerman - JoVE Visualize

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Proteins|October 31, 2000

Receptors coupling to G proteins: is there a signal behind the sequence?F Horn, E M van der Wenden, L Oliveira, et al.

European Journal of Pharmacology|March 15, 1994

Full and partial agonistic behaviour and thermodynamic binding parameters of adenosine A1 receptor ligandsP A Borea, K Varani, A Dalpiaz, et al.

British Journal of Pharmacology|December 1, 1994

Pharmacological analysis of ecto-ATPase inhibition: evidence for combined enzyme inhibition and receptor antagonism in P2X-purinoceptor ligandsB E Crack, M W Beukers, K C McKechnie, et al.

Journal of Medicinal Chemistry|March 1, 1991

1H-imidazo[4,5-c]quinolin-4-amines: novel non-xanthine adenosine antagonistsP J van Galen, P Nissen, I van Wijngaarden, et al.

European Journal of Pharmacology|April 25, 1991

Mapping the xanthine C8-region of the adenosine A1 receptor with computer graphicsE M Van der Wenden, P J Van Galen, A P IJzerman, et al.

Pharmaceutical Research|August 18, 1999

Thermodynamic in vitro studies as a method to investigate the pharmacodynamic behavior of adenosine A1 receptor ligandsA Dalpiaz, A Scatturin, B Pavan, et al.

Molecular Pharmacology|November 28, 2000

Why are A(2B) receptors low-affinity adenosine receptors? Mutation of Asn273 to Tyr increases affinity of human A(2B) receptor for 2-(1-Hexynyl)adenosineM W Beukers, H den Dulk, E W van Tilburg, et al.

British Journal of Pharmacology|October 1, 1995

Deoxyribose analogues of N6-cyclopentyladenosine (CPA): partial agonists at the adenosine A1 receptor in vivoR A Mathôt, E M Van der Wenden, W Soudijn, et al.

Molecular Pharmacology|April 1, 1996

Suramin analogues as subtype-selective G protein inhibitorsM Freissmuth, S Boehm, W Beindl, et al.

Bioorganic & Medicinal Chemistry Letters|September 22, 2000

2-Nitro analogues of adenosine and 1-deazaadenosine: synthesis and binding studies at the adenosine A1, A2A and A3 receptor subtypesM J Wanner, J K Von Frijtag Drabbe Künzel, A P Ijzerman, et al.

Pageof 14

Showing results (61-70 of 136) with videos related to

Sort By:

Pageof 14

Proteins|October 31, 2000

Receptors coupling to G proteins: is there a signal behind the sequence?F Horn, E M van der Wenden, L Oliveira, et al.

European Journal of Pharmacology|March 15, 1994

Full and partial agonistic behaviour and thermodynamic binding parameters of adenosine A1 receptor ligandsP A Borea, K Varani, A Dalpiaz, et al.

British Journal of Pharmacology|December 1, 1994

Pharmacological analysis of ecto-ATPase inhibition: evidence for combined enzyme inhibition and receptor antagonism in P2X-purinoceptor ligandsB E Crack, M W Beukers, K C McKechnie, et al.

Journal of Medicinal Chemistry|March 1, 1991

1H-imidazo[4,5-c]quinolin-4-amines: novel non-xanthine adenosine antagonistsP J van Galen, P Nissen, I van Wijngaarden, et al.

European Journal of Pharmacology|April 25, 1991

Mapping the xanthine C8-region of the adenosine A1 receptor with computer graphicsE M Van der Wenden, P J Van Galen, A P IJzerman, et al.

Pharmaceutical Research|August 18, 1999

Thermodynamic in vitro studies as a method to investigate the pharmacodynamic behavior of adenosine A1 receptor ligandsA Dalpiaz, A Scatturin, B Pavan, et al.

Molecular Pharmacology|November 28, 2000

Why are A(2B) receptors low-affinity adenosine receptors? Mutation of Asn273 to Tyr increases affinity of human A(2B) receptor for 2-(1-Hexynyl)adenosineM W Beukers, H den Dulk, E W van Tilburg, et al.

British Journal of Pharmacology|October 1, 1995

Deoxyribose analogues of N6-cyclopentyladenosine (CPA): partial agonists at the adenosine A1 receptor in vivoR A Mathôt, E M Van der Wenden, W Soudijn, et al.

Molecular Pharmacology|April 1, 1996

Suramin analogues as subtype-selective G protein inhibitorsM Freissmuth, S Boehm, W Beindl, et al.

Bioorganic & Medicinal Chemistry Letters|September 22, 2000

2-Nitro analogues of adenosine and 1-deazaadenosine: synthesis and binding studies at the adenosine A1, A2A and A3 receptor subtypesM J Wanner, J K Von Frijtag Drabbe Künzel, A P Ijzerman, et al.

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