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Journal of Medicinal Chemistry
|
February 28, 2016
Discovery of GluN2A-Selective NMDA Receptor Positive Allosteric Modulators (PAMs): Tuning Deactivation Kinetics via Structure-Based Design
Matthew Volgraf, Benjamin D Sellers, Yu Jiang, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 22, 2013
Discovery of 2-methylpyridine-based biaryl amides as γ-secretase modulators for the treatment of Alzheimer's disease
Jian Jeffrey Chen, Wenyuan Qian, Kaustav Biswas, et al.
Nature Chemical Biology
|
May 24, 2016
An inhibitor of KDM5 demethylases reduces survival of drug-tolerant cancer cells
Maia Vinogradova, Victor S Gehling, Amy Gustafson, et al.
Ebiomedicine
|
July 6, 2025
Effectorless Fc-fusion improves FLT3L drug-like properties for cancer immunotherapy combinations
Jérémie Decalf, Evangeline Toy, Dongping He, et al.
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of 6
Search research articles
Search
Showing results (51-60 of 54) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 54 results.
Journal of Medicinal Chemistry
|
February 28, 2016
Discovery of GluN2A-Selective NMDA Receptor Positive Allosteric Modulators (PAMs): Tuning Deactivation Kinetics via Structure-Based Design
Matthew Volgraf, Benjamin D Sellers, Yu Jiang, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 22, 2013
Discovery of 2-methylpyridine-based biaryl amides as γ-secretase modulators for the treatment of Alzheimer's disease
Jian Jeffrey Chen, Wenyuan Qian, Kaustav Biswas, et al.
Nature Chemical Biology
|
May 24, 2016
An inhibitor of KDM5 demethylases reduces survival of drug-tolerant cancer cells
Maia Vinogradova, Victor S Gehling, Amy Gustafson, et al.
Ebiomedicine
|
July 6, 2025
Effectorless Fc-fusion improves FLT3L drug-like properties for cancer immunotherapy combinations
Jérémie Decalf, Evangeline Toy, Dongping He, et al.
Page
of 6