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Nature Chemical Biology
|
July 22, 2008
Turning down tau phosphorylation
Peter M Fischer
Trends in Pharmacological Sciences
|
April 22, 2008
Cyclin-dependent kinase 9: a key transcriptional regulator and potential drug target in oncology, virology and cardiology
Shudong Wang, Peter M Fischer
Current Pharmaceutical Design
|
May 17, 2005
Strategies for the design of potent and selective kinase inhibitors
Campbell McInnes, Peter M Fischer
Nature Reviews. Drug Discovery
|
June 2, 2007
Untangling tau hyperphosphorylation in drug design for neurodegenerative diseases
Michael P Mazanetz, Peter M Fischer
Expert Opinion on Investigational Drugs
|
June 5, 2003
CDK inhibitors in clinical development for the treatment of cancer
Peter M Fischer, Athos Gianella-Borradori
Expert Opinion on Investigational Drugs
|
May 11, 2005
Recent progress in the discovery and development of cyclin-dependent kinase inhibitors
Peter M Fischer, Athos Gianella-Borradori
Journal of Peptide Science : an Official Publication of the European Peptide Society
|
October 10, 2002
Liquid-phase peptide synthesis on polyethylene glycol (PEG) supports using strategies based on the 9-fluorenylmethoxycarbonyl amino protecting group: application of PEGylated peptides in biochemical assays
Peter M Fischer, Daniella I Zheleva
Nature
|
February 27, 2004
Turning the key on p53
David P Lane, Peter M Fischer
Trends in Pharmacological Sciences
|
June 29, 2004
Small-molecule inhibitors of the p53 suppressor HDM2: have protein-protein interactions come of age as drug targets?
Peter M Fischer, David P Lane
Drug Discovery Today
|
January 3, 2007
Pharmacological targeting of lysine acetyltransferases in human disease: a progress report
David M Heery, Peter M Fischer
Page
of 12
Search research articles
Search
Showing results (11-20 of 118) with videos related to
Sort By:
Page
of 12
Nature Chemical Biology
|
July 22, 2008
Turning down tau phosphorylation
Peter M Fischer
Trends in Pharmacological Sciences
|
April 22, 2008
Cyclin-dependent kinase 9: a key transcriptional regulator and potential drug target in oncology, virology and cardiology
Shudong Wang, Peter M Fischer
Current Pharmaceutical Design
|
May 17, 2005
Strategies for the design of potent and selective kinase inhibitors
Campbell McInnes, Peter M Fischer
Nature Reviews. Drug Discovery
|
June 2, 2007
Untangling tau hyperphosphorylation in drug design for neurodegenerative diseases
Michael P Mazanetz, Peter M Fischer
Expert Opinion on Investigational Drugs
|
June 5, 2003
CDK inhibitors in clinical development for the treatment of cancer
Peter M Fischer, Athos Gianella-Borradori
Expert Opinion on Investigational Drugs
|
May 11, 2005
Recent progress in the discovery and development of cyclin-dependent kinase inhibitors
Peter M Fischer, Athos Gianella-Borradori
Journal of Peptide Science : an Official Publication of the European Peptide Society
|
October 10, 2002
Liquid-phase peptide synthesis on polyethylene glycol (PEG) supports using strategies based on the 9-fluorenylmethoxycarbonyl amino protecting group: application of PEGylated peptides in biochemical assays
Peter M Fischer, Daniella I Zheleva
Nature
|
February 27, 2004
Turning the key on p53
David P Lane, Peter M Fischer
Trends in Pharmacological Sciences
|
June 29, 2004
Small-molecule inhibitors of the p53 suppressor HDM2: have protein-protein interactions come of age as drug targets?
Peter M Fischer, David P Lane
Drug Discovery Today
|
January 3, 2007
Pharmacological targeting of lysine acetyltransferases in human disease: a progress report
David M Heery, Peter M Fischer
Page
of 12