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S L Graham

Showing results (71-80 of 96) with videos related to

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Bioorganic & Medicinal Chemistry|September 1, 1994
Synthesis and biological activity of ras farnesyl protein transferase inhibitors. Tetrapeptide analogs with amino methyl and carbon linkagesJ S Wai, D L Bamberger, T E Fisher, et al.
Journal of Medicinal Chemistry|November 1, 1989
Topically active carbonic anhydrase inhibitors. 1. O-acyl derivatives of 6-hydroxybenzothiazole-2-sulfonamideO W Woltersdorf, H Schwam, J B Bicking, et al.
Journal of Medicinal Chemistry|March 18, 1994
Pseudopeptide inhibitors of Ras farnesyl-protein transferaseS L Graham, S J deSolms, E A Giuliani, et al.
Nature Medicine|August 1, 1995
Inhibition of farnesyltransferase induces regression of mammary and salivary carcinomas in ras transgenic miceN E Kohl, C A Omer, M W Conner, 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.
Journal of Medicinal Chemistry|December 1, 1989
Topically active carbonic anhydrase inhibitors. 2. Benzo[b]thiophenesulfonamide derivatives with ocular hypotensive activityS L Graham, K L Shepard, P S Anderson, et al.
Science (New York, N.Y.)|June 25, 1993
Selective inhibition of ras-dependent transformation by a farnesyltransferase inhibitorN E Kohl, S D Mosser, S J deSolms, et al.
Journal of Medicinal Chemistry|September 1, 1991
Design and synthesis of HIV protease inhibitors. Variations of the carboxy terminus of the HIV protease inhibitor L-682,679S J deSolms, E A Giuliani, J P Guare, et al.
Biochemical Society Transactions|August 1, 1996
Farnesyltransferase inhibitors: a new class of cancer chemotherapeuticsK S Koblan, N E Kohl, C A Omer, et al.
Pageof 10

Showing results (71-80 of 96) with videos related to

Sort By:
Pageof 10
Bioorganic & Medicinal Chemistry|September 1, 1994
Synthesis and biological activity of ras farnesyl protein transferase inhibitors. Tetrapeptide analogs with amino methyl and carbon linkagesJ S Wai, D L Bamberger, T E Fisher, et al.
Journal of Medicinal Chemistry|November 1, 1989
Topically active carbonic anhydrase inhibitors. 1. O-acyl derivatives of 6-hydroxybenzothiazole-2-sulfonamideO W Woltersdorf, H Schwam, J B Bicking, et al.
Journal of Medicinal Chemistry|March 18, 1994
Pseudopeptide inhibitors of Ras farnesyl-protein transferaseS L Graham, S J deSolms, E A Giuliani, et al.
Nature Medicine|August 1, 1995
Inhibition of farnesyltransferase induces regression of mammary and salivary carcinomas in ras transgenic miceN E Kohl, C A Omer, M W Conner, 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.
Journal of Medicinal Chemistry|December 1, 1989
Topically active carbonic anhydrase inhibitors. 2. Benzo[b]thiophenesulfonamide derivatives with ocular hypotensive activityS L Graham, K L Shepard, P S Anderson, et al.
Science (New York, N.Y.)|June 25, 1993
Selective inhibition of ras-dependent transformation by a farnesyltransferase inhibitorN E Kohl, S D Mosser, S J deSolms, et al.
Journal of Medicinal Chemistry|September 1, 1991
Design and synthesis of HIV protease inhibitors. Variations of the carboxy terminus of the HIV protease inhibitor L-682,679S J deSolms, E A Giuliani, J P Guare, et al.
Biochemical Society Transactions|August 1, 1996
Farnesyltransferase inhibitors: a new class of cancer chemotherapeuticsK S Koblan, N E Kohl, C A Omer, et al.
Pageof 10