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H Mett

Showing results (41-50 of 53) with videos related to

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Journal of Medicinal Chemistry|June 23, 1995
[(Alkylamino)methyl]acrylophenones: potent and selective inhibitors of the epidermal growth factor receptor protein tyrosine kinaseP Traxler, U Trinks, E Buchdunger, et al.
International Journal of Cancer|May 21, 1999
Author errataN Lydon, H Mett, M Mueller, et al.
Cancer Research|September 1, 1992
New S-adenosylmethionine decarboxylase inhibitors with potent antitumor activityU Regenass, G Caravatti, H Mett, et al.
Journal of Medicinal Chemistry|April 1, 1994
Dianilinophthalimides: potent and selective, ATP-competitive inhibitors of the EGF-receptor protein tyrosine kinaseU Trinks, E Buchdunger, P Furet, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 1, 1995
4,5-bis(4-fluoroanilino)phthalimide: A selective inhibitor of the epidermal growth factor receptor signal transduction pathway with potent in vivo antitumor activityE Buchdunger, H Mett, U Trinks, et al.
International Journal of Cancer|April 9, 1998
A potent protein-tyrosine kinase inhibitor which selectively blocks proliferation of epidermal growth factor receptor-expressing tumor cells in vitro and in vivoN B Lydon, H Mett, M Mueller, et al.
Journal of Medicinal Chemistry|November 14, 1997
Use of a pharmacophore model for the design of EGF-R tyrosine kinase inhibitors: 4-(phenylamino)pyrazolo[3,4-d]pyrimidinesP Traxler, G Bold, J Frei, et al.
The Biochemical Journal|November 1, 1992
Purification and biochemical characterization of non-myristoylated recombinant pp60c-src kinaseN B Lydon, B Gay, H Mett, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 15, 1994
4,5-Dianilinophthalimide: a protein-tyrosine kinase inhibitor with selectivity for the epidermal growth factor receptor signal transduction pathway and potent in vivo antitumor activityE Buchdunger, U Trinks, H Mett, et al.
European Journal of Biochemistry|November 15, 1995
Different susceptibility of protein kinases to staurosporine inhibition. Kinetic studies and molecular bases for the resistance of protein kinase CK2F Meggio, A Donella Deana, M Ruzzene, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Journal of Medicinal Chemistry|June 23, 1995
[(Alkylamino)methyl]acrylophenones: potent and selective inhibitors of the epidermal growth factor receptor protein tyrosine kinaseP Traxler, U Trinks, E Buchdunger, et al.
International Journal of Cancer|May 21, 1999
Author errataN Lydon, H Mett, M Mueller, et al.
Cancer Research|September 1, 1992
New S-adenosylmethionine decarboxylase inhibitors with potent antitumor activityU Regenass, G Caravatti, H Mett, et al.
Journal of Medicinal Chemistry|April 1, 1994
Dianilinophthalimides: potent and selective, ATP-competitive inhibitors of the EGF-receptor protein tyrosine kinaseU Trinks, E Buchdunger, P Furet, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 1, 1995
4,5-bis(4-fluoroanilino)phthalimide: A selective inhibitor of the epidermal growth factor receptor signal transduction pathway with potent in vivo antitumor activityE Buchdunger, H Mett, U Trinks, et al.
International Journal of Cancer|April 9, 1998
A potent protein-tyrosine kinase inhibitor which selectively blocks proliferation of epidermal growth factor receptor-expressing tumor cells in vitro and in vivoN B Lydon, H Mett, M Mueller, et al.
Journal of Medicinal Chemistry|November 14, 1997
Use of a pharmacophore model for the design of EGF-R tyrosine kinase inhibitors: 4-(phenylamino)pyrazolo[3,4-d]pyrimidinesP Traxler, G Bold, J Frei, et al.
The Biochemical Journal|November 1, 1992
Purification and biochemical characterization of non-myristoylated recombinant pp60c-src kinaseN B Lydon, B Gay, H Mett, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 15, 1994
4,5-Dianilinophthalimide: a protein-tyrosine kinase inhibitor with selectivity for the epidermal growth factor receptor signal transduction pathway and potent in vivo antitumor activityE Buchdunger, U Trinks, H Mett, et al.
European Journal of Biochemistry|November 15, 1995
Different susceptibility of protein kinases to staurosporine inhibition. Kinetic studies and molecular bases for the resistance of protein kinase CK2F Meggio, A Donella Deana, M Ruzzene, et al.
Pageof 6