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Organic Letters
|
April 21, 2006
New air-stable catalysts for general and efficient suzuki-miyaura cross-coupling reactions of heteroaryl chlorides
Anil S Guram, Anthony O King, John G Allen, et al.
Chemmedchem
|
October 10, 2017
Minor Structural Variations of Small Molecules Tune Regulatory Activities toward Pathological Factors in Alzheimer's Disease
Michael W Beck, Jeffrey S Derrick, Jong-Min Suh, et al.
Biorxiv : the Preprint Server for Biology
|
October 10, 2024
Caspase-Activated DNase localizes to cancer causing translocation breakpoints during cell differentiation
Dalal Alsowaida, Brian D Larsen, Sarah Hachmer, et al.
Journal of Virology
|
August 8, 2014
A chimeric virus-mouse model system for evaluating the function and inhibition of papain-like proteases of emerging coronaviruses
Xufang Deng, Sudhakar Agnihothram, Anna M Mielech, et al.
Heart Rhythm
|
July 19, 2015
Gap junction modifier rotigaptide decreases the susceptibility to ventricular arrhythmia by enhancing conduction velocity and suppressing discordant alternans during therapeutic hypothermia in isolated rabbit hearts
Yu-Cheng Hsieh, Jiunn-Cherng Lin, Chen-Ying Hung, et al.
Journal of Medicinal Chemistry
|
March 22, 2017
Structure-Based Design of Highly Selective and Potent G Protein-Coupled Receptor Kinase 2 Inhibitors Based on Paroxetine
Helen V Waldschmidt, Kristoff T Homan, Marilyn C Cato, et al.
Journal of Virology
|
July 18, 2014
Novel indole-2-carboxamide compounds are potent broad-spectrum antivirals active against western equine encephalitis virus in vivo
Phillip C Delekta, Craig J Dobry, Janice A Sindac, et al.
Journal of Medicinal Chemistry
|
June 13, 2019
Correction to "Structure-Based Design of Highly Selective and Potent G Protein-Coupled Receptor Kinase 2 Inhibitors Based on Paroxetine"
Helen V Waldschmidt, Kristoff T Homan, Marilyn C Cato, et al.
Biochemical Pharmacology
|
July 1, 2008
Development of XPA067.06, a potent high affinity human anti-gastrin monoclonal antibody
Ssucheng J Hsu, Amita Patel, Paul D Larsen, et al.
Bioorganic & Medicinal Chemistry
|
June 15, 2007
Discovery of pyrrole-based hepatoselective ligands as potent inhibitors of HMG-CoA reductase
Larry D Bratton, Bruce Auerbach, Chulho Choi, et al.
Page
of 67
Search research articles
Search
Showing results (591-600 of 666) with videos related to
Sort By:
Page
of 67
Organic Letters
|
April 21, 2006
New air-stable catalysts for general and efficient suzuki-miyaura cross-coupling reactions of heteroaryl chlorides
Anil S Guram, Anthony O King, John G Allen, et al.
Chemmedchem
|
October 10, 2017
Minor Structural Variations of Small Molecules Tune Regulatory Activities toward Pathological Factors in Alzheimer's Disease
Michael W Beck, Jeffrey S Derrick, Jong-Min Suh, et al.
Biorxiv : the Preprint Server for Biology
|
October 10, 2024
Caspase-Activated DNase localizes to cancer causing translocation breakpoints during cell differentiation
Dalal Alsowaida, Brian D Larsen, Sarah Hachmer, et al.
Journal of Virology
|
August 8, 2014
A chimeric virus-mouse model system for evaluating the function and inhibition of papain-like proteases of emerging coronaviruses
Xufang Deng, Sudhakar Agnihothram, Anna M Mielech, et al.
Heart Rhythm
|
July 19, 2015
Gap junction modifier rotigaptide decreases the susceptibility to ventricular arrhythmia by enhancing conduction velocity and suppressing discordant alternans during therapeutic hypothermia in isolated rabbit hearts
Yu-Cheng Hsieh, Jiunn-Cherng Lin, Chen-Ying Hung, et al.
Journal of Medicinal Chemistry
|
March 22, 2017
Structure-Based Design of Highly Selective and Potent G Protein-Coupled Receptor Kinase 2 Inhibitors Based on Paroxetine
Helen V Waldschmidt, Kristoff T Homan, Marilyn C Cato, et al.
Journal of Virology
|
July 18, 2014
Novel indole-2-carboxamide compounds are potent broad-spectrum antivirals active against western equine encephalitis virus in vivo
Phillip C Delekta, Craig J Dobry, Janice A Sindac, et al.
Journal of Medicinal Chemistry
|
June 13, 2019
Correction to "Structure-Based Design of Highly Selective and Potent G Protein-Coupled Receptor Kinase 2 Inhibitors Based on Paroxetine"
Helen V Waldschmidt, Kristoff T Homan, Marilyn C Cato, et al.
Biochemical Pharmacology
|
July 1, 2008
Development of XPA067.06, a potent high affinity human anti-gastrin monoclonal antibody
Ssucheng J Hsu, Amita Patel, Paul D Larsen, et al.
Bioorganic & Medicinal Chemistry
|
June 15, 2007
Discovery of pyrrole-based hepatoselective ligands as potent inhibitors of HMG-CoA reductase
Larry D Bratton, Bruce Auerbach, Chulho Choi, et al.
Page
of 67