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Showing results (91-100 of 129) with videos related to

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Biochemical Pharmacology|May 6, 2009
An inhibitor of Janus kinase 2 prevents polycythemia in miceAnjili Mathur, Jan-Rung Mo, Manfred Kraus, et al.
Bioorganic & Medicinal Chemistry Letters|June 8, 2001
Diaryl ether inhibitors of farnesyl-protein transferaseS C Mactough, S J Desolms, A W Shaw, et al.
Molecular Cancer Therapeutics|March 16, 2005
Identification of biomarkers for tumor endothelial cell proliferation through gene expression profilingJames S Hardwick, Yi Yang, Chunsheng Zhang, et al.
Bioorganic & Medicinal Chemistry Letters|June 21, 2006
3-Aryl-4-hydroxyquinolin-2(1H)-one derivatives as type I fatty acid synthase inhibitorsAlexey Rivkin, Yoona R Kim, Mark T Goulet, et al.
Journal of Medicinal Chemistry|November 7, 1998
Clavaric acid and steroidal analogues as Ras- and FPP-directed inhibitors of human farnesyl-protein transferaseR B Lingham, K C Silverman, H Jayasuriya, et al.
Journal of Medicinal Chemistry|August 28, 1999
Design and in vivo analysis of potent non-thiol inhibitors of farnesyl protein transferaseN J Anthony, R P Gomez, M D Schaber, et al.
Bioorganic & Medicinal Chemistry Letters|May 30, 2001
Aryloxy substituted N-arylpiperazinones as dual inhibitors of farnesyltransferase and geranylgeranyltransferase-IJ M Bergman, M T Abrams, J P Davide, et al.
Nature|April 17, 2020
Hydrothermal <sup>15</sup>N<sup>15</sup>N abundances constrain the origins of mantle nitrogenJ Labidi, P H Barry, D V Bekaert, et al.
Cancer Research|March 26, 2009
Inhibition of NOTCH signaling by gamma secretase inhibitor engages the RB pathway and elicits cell cycle exit in T-cell acute lymphoblastic leukemia cellsSudhir S Rao, Jennifer O'Neil, Cole D Liberator, et al.
Bioorganic & Medicinal Chemistry Letters|March 31, 2007
Kinesin spindle protein (KSP) inhibitors. Part V: discovery of 2-propylamino-2,4-diaryl-2,5-dihydropyrroles as potent, water-soluble KSP inhibitors, and modulation of their basicity by beta-fluorination to overcome cellular efflux by P-glycoproteinChristopher D Cox, Michael J Breslin, David B Whitman, et al.
Pageof 13

Showing results (91-100 of 129) with videos related to

Sort By:
Pageof 13
Biochemical Pharmacology|May 6, 2009
An inhibitor of Janus kinase 2 prevents polycythemia in miceAnjili Mathur, Jan-Rung Mo, Manfred Kraus, et al.
Bioorganic & Medicinal Chemistry Letters|June 8, 2001
Diaryl ether inhibitors of farnesyl-protein transferaseS C Mactough, S J Desolms, A W Shaw, et al.
Molecular Cancer Therapeutics|March 16, 2005
Identification of biomarkers for tumor endothelial cell proliferation through gene expression profilingJames S Hardwick, Yi Yang, Chunsheng Zhang, et al.
Bioorganic & Medicinal Chemistry Letters|June 21, 2006
3-Aryl-4-hydroxyquinolin-2(1H)-one derivatives as type I fatty acid synthase inhibitorsAlexey Rivkin, Yoona R Kim, Mark T Goulet, et al.
Journal of Medicinal Chemistry|November 7, 1998
Clavaric acid and steroidal analogues as Ras- and FPP-directed inhibitors of human farnesyl-protein transferaseR B Lingham, K C Silverman, H Jayasuriya, et al.
Journal of Medicinal Chemistry|August 28, 1999
Design and in vivo analysis of potent non-thiol inhibitors of farnesyl protein transferaseN J Anthony, R P Gomez, M D Schaber, et al.
Bioorganic & Medicinal Chemistry Letters|May 30, 2001
Aryloxy substituted N-arylpiperazinones as dual inhibitors of farnesyltransferase and geranylgeranyltransferase-IJ M Bergman, M T Abrams, J P Davide, et al.
Nature|April 17, 2020
Hydrothermal <sup>15</sup>N<sup>15</sup>N abundances constrain the origins of mantle nitrogenJ Labidi, P H Barry, D V Bekaert, et al.
Cancer Research|March 26, 2009
Inhibition of NOTCH signaling by gamma secretase inhibitor engages the RB pathway and elicits cell cycle exit in T-cell acute lymphoblastic leukemia cellsSudhir S Rao, Jennifer O'Neil, Cole D Liberator, et al.
Bioorganic & Medicinal Chemistry Letters|March 31, 2007
Kinesin spindle protein (KSP) inhibitors. Part V: discovery of 2-propylamino-2,4-diaryl-2,5-dihydropyrroles as potent, water-soluble KSP inhibitors, and modulation of their basicity by beta-fluorination to overcome cellular efflux by P-glycoproteinChristopher D Cox, Michael J Breslin, David B Whitman, et al.
Pageof 13