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Journal of Medicinal Chemistry|February 1, 1990
Topically active carbonic anhydrase inhibitors. 3. Benzofuran- and indole-2-sulfonamidesS L Graham, J M Hoffman, P Gautheron, et al.
Journal of Medicinal Chemistry|September 29, 1995
Pseudodipeptide inhibitors of protein farnesyltransferaseS J deSolms, A A Deana, E A Giuliani, et al.
Journal of Medicinal Chemistry|October 1, 1991
Topically active carbonic anhydrase inhibitors. 4. [(Hydroxyalkyl)sulfonyl]benzene and [(hydroxyalkyl)sulfonyl]thiophenesulfonamidesK L Shepard, S L Graham, R J Hudcosky, et al.
Deutsche Medizinische Wochenschrift (1946)|September 21, 2007
[Treatment of the acute coronary syndrome in Germany: experiences in a German cluster of the GRACE registry]U Tebbe, P Bramlage, P von Löwis of Menar, et al.
Pharmacogenomics|April 27, 2010
Role of genetic variation in the cannabinoid type 1 receptor gene (CNR1) in the pathophysiology of human obesityDorit Schleinitz, Solveig Carmienke, Yvonne Böttcher, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 10, 1998
Long-term beta adrenoceptor-mediated alteration in contractility and expression of phospholamban and sarcoplasmic reticulum Ca(++)-ATPase in mammalian ventricleB Linck, P Bokník, H A Baba, et al.
Journal of Medicinal Chemistry|July 3, 1998
N-Arylalkyl pseudopeptide inhibitors of farnesyltransferaseS J deSolms, E A Giuliani, S L Graham, et al.
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