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Hansch

Showing results (101-110 of 383) with videos related to

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Optics Letters|October 31, 2009
High-precision intensity-selective observation of multiphoton ionization: a new method of photoelectron spectroscopyP Hansch, L D Van Woerkom
Chemico-Biological Interactions|August 1, 1997
A comparative QSAR analysis of acetylcholinesterase inhibitors currently studied for the treatment of Alzheimer's diseaseM Recanatini, A Cavalli, C Hansch
Science (New York, N.Y.)|October 16, 1981
Oculomotor reaction time in dementia reflects degree of cerebral dysfunctionF J Pirozzolo, E C Hansch
Chemico-Biological Interactions|January 1, 1985
Quantitative structure-activity relationships of cysteine hydrolases. Ficin hydrolysis of X-phenyl-N-methanesulfonyl glycinatesA Carotti, C Raguseo, C Hansch
Chemical Reviews|December 26, 2001
Comparative QSAR analysis of 5alpha-reductase inhibitorsA Kurup, R Garg, C Hansch
Bioorganic & Medicinal Chemistry|November 17, 2001
Possible allosteric effects in anticancer compoundsR Garg, A Kurup, C Hansch
Medicinal Research Reviews|January 3, 2001
Radical toxicity of phenols: a reference point for obtaining perspective in the formulation of QSARR Garg, S Kapur, C Hansch
Journal of Medicinal Chemistry|January 1, 1978
Structure-activity relationships in antitumor aniline mustardsA Panthananickal, C Hansch, A Leo
Biochemical Pharmacology|July 1, 1970
Fibrinolytic congeners of benzoic and salicylic acid. A mathematical analysis of correlation between structure and activityC Hansch, K N von Kaulla
Bioorganic & Medicinal Chemistry|March 16, 2001
Searching for allosteric effects via QSARsC Hansch, R Garg, A Kurup
Pageof 39

Showing results (101-110 of 383) with videos related to

Sort By:
Pageof 39
Optics Letters|October 31, 2009
High-precision intensity-selective observation of multiphoton ionization: a new method of photoelectron spectroscopyP Hansch, L D Van Woerkom
Chemico-Biological Interactions|August 1, 1997
A comparative QSAR analysis of acetylcholinesterase inhibitors currently studied for the treatment of Alzheimer's diseaseM Recanatini, A Cavalli, C Hansch
Science (New York, N.Y.)|October 16, 1981
Oculomotor reaction time in dementia reflects degree of cerebral dysfunctionF J Pirozzolo, E C Hansch
Chemico-Biological Interactions|January 1, 1985
Quantitative structure-activity relationships of cysteine hydrolases. Ficin hydrolysis of X-phenyl-N-methanesulfonyl glycinatesA Carotti, C Raguseo, C Hansch
Chemical Reviews|December 26, 2001
Comparative QSAR analysis of 5alpha-reductase inhibitorsA Kurup, R Garg, C Hansch
Bioorganic & Medicinal Chemistry|November 17, 2001
Possible allosteric effects in anticancer compoundsR Garg, A Kurup, C Hansch
Medicinal Research Reviews|January 3, 2001
Radical toxicity of phenols: a reference point for obtaining perspective in the formulation of QSARR Garg, S Kapur, C Hansch
Journal of Medicinal Chemistry|January 1, 1978
Structure-activity relationships in antitumor aniline mustardsA Panthananickal, C Hansch, A Leo
Biochemical Pharmacology|July 1, 1970
Fibrinolytic congeners of benzoic and salicylic acid. A mathematical analysis of correlation between structure and activityC Hansch, K N von Kaulla
Bioorganic & Medicinal Chemistry|March 16, 2001
Searching for allosteric effects via QSARsC Hansch, R Garg, A Kurup
Pageof 39