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H Mett

Showing results (21-30 of 53) with videos related to

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Bioorganic & Medicinal Chemistry Letters|February 17, 1999
2,6,9-trisubstituted purines: optimization towards highly potent and selective CDK1 inhibitorsP Imbach, H G Capraro, P Furet, et al.
European Journal of Biochemistry|July 1, 1992
Large-scale purification and characterisation of a recombinant epidermal growth-factor receptor protein-tyrosine kinase. Modulation of activity by multiple factorsE McGlynn, M Becker, H Mett, et al.
Journal of Medicinal Chemistry|June 7, 1996
4-(Phenylamino)pyrrolopyrimidines: potent and selective, ATP site directed inhibitors of the EGF-receptor protein tyrosine kinaseP M Traxler, P Furet, H Mett, et al.
Cancer Research|June 15, 1994
CGP 48664, a new S-adenosylmethionine decarboxylase inhibitor with broad spectrum antiproliferative and antitumor activityU Regenass, H Mett, J Stanek, et al.
The Journal of Biological Chemistry|February 3, 1995
Stable amplification of the S-adenosylmethionine decarboxylase gene in Chinese hamster ovary cellsD Kramer, H Mett, A Evans, et al.
Antimicrobial Agents and Chemotherapy|September 26, 1997
Alterations in ornithine decarboxylase characteristics account for tolerance of Trypanosoma brucei rhodesiense to D,L-alpha-difluoromethylornithineM Iten, H Mett, A Evans, et al.
The Journal of Antibiotics|May 1, 1997
Semicochliodinol A and B: inhibitors of HIV-1 protease and EGF-R protein tyrosine kinase related to asterriquinones produced by the fungus Chrysosporium merdariumA Fredenhagen, F Petersen, M Tintelnot-Blomley, et al.
Anticancer Research|September 1, 1996
Sequence specific antisense oligonucleotide analog interference with spermidine/spermine N1-acetyltransferase gene expressionM Fogel-Petrovic, S Vujcic, R Häner, et al.
Journal of Medicinal Chemistry|July 23, 1993
4-Amidinoindan-1-one 2'-amidinohydrazone: a new potent and selective inhibitor of S-Adenosylmethionine decarboxylaseJ Stanek, G Caravatti, J Frei, et al.
Cancer Research|September 10, 1998
Lysosomal sequestration of polyamine analogues in Chinese hamster ovary cells resistant to the S-adenosylmethionine decarboxylase inhibitor, CGP-48664D L Kramer, J D Black, H Mett, et al.
Pageof 6

Showing results (21-30 of 53) with videos related to

Sort By:
Pageof 6
Bioorganic & Medicinal Chemistry Letters|February 17, 1999
2,6,9-trisubstituted purines: optimization towards highly potent and selective CDK1 inhibitorsP Imbach, H G Capraro, P Furet, et al.
European Journal of Biochemistry|July 1, 1992
Large-scale purification and characterisation of a recombinant epidermal growth-factor receptor protein-tyrosine kinase. Modulation of activity by multiple factorsE McGlynn, M Becker, H Mett, et al.
Journal of Medicinal Chemistry|June 7, 1996
4-(Phenylamino)pyrrolopyrimidines: potent and selective, ATP site directed inhibitors of the EGF-receptor protein tyrosine kinaseP M Traxler, P Furet, H Mett, et al.
Cancer Research|June 15, 1994
CGP 48664, a new S-adenosylmethionine decarboxylase inhibitor with broad spectrum antiproliferative and antitumor activityU Regenass, H Mett, J Stanek, et al.
The Journal of Biological Chemistry|February 3, 1995
Stable amplification of the S-adenosylmethionine decarboxylase gene in Chinese hamster ovary cellsD Kramer, H Mett, A Evans, et al.
Antimicrobial Agents and Chemotherapy|September 26, 1997
Alterations in ornithine decarboxylase characteristics account for tolerance of Trypanosoma brucei rhodesiense to D,L-alpha-difluoromethylornithineM Iten, H Mett, A Evans, et al.
The Journal of Antibiotics|May 1, 1997
Semicochliodinol A and B: inhibitors of HIV-1 protease and EGF-R protein tyrosine kinase related to asterriquinones produced by the fungus Chrysosporium merdariumA Fredenhagen, F Petersen, M Tintelnot-Blomley, et al.
Anticancer Research|September 1, 1996
Sequence specific antisense oligonucleotide analog interference with spermidine/spermine N1-acetyltransferase gene expressionM Fogel-Petrovic, S Vujcic, R Häner, et al.
Journal of Medicinal Chemistry|July 23, 1993
4-Amidinoindan-1-one 2'-amidinohydrazone: a new potent and selective inhibitor of S-Adenosylmethionine decarboxylaseJ Stanek, G Caravatti, J Frei, et al.
Cancer Research|September 10, 1998
Lysosomal sequestration of polyamine analogues in Chinese hamster ovary cells resistant to the S-adenosylmethionine decarboxylase inhibitor, CGP-48664D L Kramer, J D Black, H Mett, et al.
Pageof 6