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J M Cassady

Showing results (41-50 of 73) with videos related to

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Journal of Medicinal Chemistry|August 1, 1978
Potential antitumor agents. Synthesis, reactivity, and cytoxicity of alpha-methylene carbonyl compoundsJ M Cassady, S R Byrn, I K Stamos, et al.
Journal of Natural Products|March 1, 1992
Isolation of potential cancer chemopreventive agents from Eriodictyon californicumY L Liu, D K Ho, J M Cassady, et al.
Biochemistry|November 20, 1990
Metabolic activation of 2-substituted derivatives of myristic acid to form potent inhibitors of myristoyl CoA:protein N-myristoyltransferaseL A Paige, G Q Zheng, S A DeFrees, et al.
Journal of Natural Products|March 1, 1987
New xanthones from Psorospermum febrifugumA M Habib, K S Reddy, T G McCloud, et al.
Journal of Medicinal Chemistry|November 1, 1977
Ergot alkaloids. Synthesis of 6-alkyl-8-ergolenes and 6-methyl-8-aminoergolines as potential prolactin inhibitorsA M Crider, J M Robinson, H G Floss, et al.
Life Sciences|January 1, 1988
Pyrimidine nucleosides enhance the efficacy of inhibitors of pyrimidine biosynthesis in cultured hepatocellular carcinoma cellsL B Jacobsen, J E Putnam, D P Sawick, et al.
Journal of Medicinal Chemistry|August 1, 1989
S-(2-oxopentadecyl)-CoA, a nonhydrolyzable analogue of myristoyl-CoA, is a potent inhibitor of myristoyl-CoA:protein N-myristoyltransferaseL A Paige, G Q Zheng, S A DeFrees, et al.
The Journal of Biological Chemistry|April 25, 1993
Reversible palmitoylation of the protein-tyrosine kinase p56lckL A Paige, M J Nadler, M L Harrison, et al.
Journal of Medicinal Chemistry|March 1, 1974
Ergot alkaloids. Ergolines and related compounds as inhibitors of prolactin releaseJ M Cassady, G S Li, E B Spitzner, et al.
Biochemistry|September 7, 1993
Treatment of T cells with 2-hydroxymyristic acid inhibits the myristoylation and alters the stability of p56lckM J Nadler, M L Harrison, C L Ashendel, et al.
Pageof 8

Showing results (41-50 of 73) with videos related to

Sort By:
Pageof 8
Journal of Medicinal Chemistry|August 1, 1978
Potential antitumor agents. Synthesis, reactivity, and cytoxicity of alpha-methylene carbonyl compoundsJ M Cassady, S R Byrn, I K Stamos, et al.
Journal of Natural Products|March 1, 1992
Isolation of potential cancer chemopreventive agents from Eriodictyon californicumY L Liu, D K Ho, J M Cassady, et al.
Biochemistry|November 20, 1990
Metabolic activation of 2-substituted derivatives of myristic acid to form potent inhibitors of myristoyl CoA:protein N-myristoyltransferaseL A Paige, G Q Zheng, S A DeFrees, et al.
Journal of Natural Products|March 1, 1987
New xanthones from Psorospermum febrifugumA M Habib, K S Reddy, T G McCloud, et al.
Journal of Medicinal Chemistry|November 1, 1977
Ergot alkaloids. Synthesis of 6-alkyl-8-ergolenes and 6-methyl-8-aminoergolines as potential prolactin inhibitorsA M Crider, J M Robinson, H G Floss, et al.
Life Sciences|January 1, 1988
Pyrimidine nucleosides enhance the efficacy of inhibitors of pyrimidine biosynthesis in cultured hepatocellular carcinoma cellsL B Jacobsen, J E Putnam, D P Sawick, et al.
Journal of Medicinal Chemistry|August 1, 1989
S-(2-oxopentadecyl)-CoA, a nonhydrolyzable analogue of myristoyl-CoA, is a potent inhibitor of myristoyl-CoA:protein N-myristoyltransferaseL A Paige, G Q Zheng, S A DeFrees, et al.
The Journal of Biological Chemistry|April 25, 1993
Reversible palmitoylation of the protein-tyrosine kinase p56lckL A Paige, M J Nadler, M L Harrison, et al.
Journal of Medicinal Chemistry|March 1, 1974
Ergot alkaloids. Ergolines and related compounds as inhibitors of prolactin releaseJ M Cassady, G S Li, E B Spitzner, et al.
Biochemistry|September 7, 1993
Treatment of T cells with 2-hydroxymyristic acid inhibits the myristoylation and alters the stability of p56lckM J Nadler, M L Harrison, C L Ashendel, et al.
Pageof 8