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Molecular Pharmacology|April 1, 1996
Suramin analogues as subtype-selective G protein inhibitorsM Freissmuth, S Boehm, W Beindl, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 21, 1998
Gsalpha-selective G protein antagonistsM Hohenegger, M Waldhoer, W Beindl, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|November 1, 1987
The role of a low beta 1-adrenoceptor selectivity of [3H]CGP-12177 for resolving subtype-selectivity of competitive ligandsC Nanoff, M Freissmuth, W Schütz
Cellular and Molecular Life Sciences : CMLS|April 3, 1999
G proteins as drug targetsC Höller, M Freissmuth, C Nanoff
The Journal of Biological Chemistry|December 23, 1994
Species difference in the G protein selectivity of the human and bovine A1-adenosine receptorR Jockers, M E Linder, M Hohenegger, et al.
Neuropharmacology|November 19, 1997
G protein coupling of the rat A1-adenosine receptor--partial purification of a protein which stabilizes the receptor-G protein associationC Nanoff, M Waldhoer, F Roka, et al.
European Journal of Pharmacology|June 12, 1987
Stimulation of adenylate cyclase activity via A2-adenosine receptors in isolated tubules of the rabbit renal cortexM Freissmuth, C Nanoff, E Tuisl, et al.
British Journal of Pharmacology|May 1, 1990
P2-, but not P1-purinoceptors mediate formation of 1, 4, 5-inositol trisphosphate and its metabolites via a pertussis toxin-insensitive pathway in the rat renal cortexC Nanoff, M Freissmuth, E Tuisl, et al.
Journal of Cardiovascular Pharmacology|February 1, 1989
A different desensitization pattern of cardiac beta-adrenoceptor subtypes by prolonged in vivo infusion of isoprenalineC Nanoff, M Freissmuth, E Tuisl, et al.
Trends in Pharmacological Sciences|June 15, 1999
G protein antagonistsM Freissmuth, M Waldhoer, E Bofill-Cardona, et al.
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