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Journal of Medicinal Chemistry
|
September 6, 2008
Multiple and single binding modes of fragment-like kinase inhibitors revealed by molecular modeling, residue type-selective protonation, and nuclear overhauser effects
Keith L Constantine, Luciano Mueller, William J Metzler, et al.
Molecular Pharmacology
|
June 25, 2017
A Functional Na<sub>V</sub>1.7-Na<sub>V</sub>Ab Chimera with a Reconstituted High-Affinity ProTx-II Binding Site
Ramkumar Rajamani, Sophie Wu, Iyoncy Rodrigo, et al.
Journal of Biomolecular Screening
|
September 25, 2013
Development of novel, 384-well high-throughput assay panels for human drug transporters: drug interaction and safety assessment in support of discovery research
Huaping Tang, Ding Ren Shen, Yong-Hae Han, et al.
Acta Crystallographica. Section F, Structural Biology Communications
|
October 14, 2024
Improving the diffraction quality of heat-shock protein 47 crystals
Kevin Kish, Stephen Cobell, Nicolas Szapiel, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
June 12, 2014
Pharmacologic profile of the Adnectin BMS-962476, a small protein biologic alternative to PCSK9 antibodies for low-density lipoprotein lowering
Tracy Mitchell, Ginger Chao, Doree Sitkoff, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
December 12, 2018
Characterization of Mauritian Cynomolgus Macaque FcγR Alleles Using Long-Read Sequencing
Amelia K Haj, Jaren M Arbanas, Aaron P Yamniuk, et al.
Bioconjugate Chemistry
|
April 22, 2016
Biotechnology Based Process for Production of a Disulfide-Bridged Peptide
Animesh Goswami, Steven L Goldberg, Ronald L Hanson, et al.
Journal of Medicinal Chemistry
|
September 3, 2011
Small molecule receptor protein tyrosine phosphatase γ (RPTPγ) ligands that inhibit phosphatase activity via perturbation of the tryptophan-proline-aspartate (WPD) loop
Steven Sheriff, Brett R Beno, Weixu Zhai, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 5, 2020
Structure-based amelioration of PXR transactivation in a novel series of macrocyclic allosteric inhibitors of HIV-1 integrase
Prasanna Sivaprakasam, Zhongyu Wang, Nicholas A Meanwell, et al.
Journal of Molecular Biology
|
January 13, 2015
Developing Adnectins that target SRC co-activator binding to PXR: a structural approach toward understanding promiscuity of PXR
Javed A Khan, Daniel M Camac, Simon Low, et al.
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Search research articles
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Showing results (21-30 of 34) with videos related to
Sort By:
Page
of 4
Journal of Medicinal Chemistry
|
September 6, 2008
Multiple and single binding modes of fragment-like kinase inhibitors revealed by molecular modeling, residue type-selective protonation, and nuclear overhauser effects
Keith L Constantine, Luciano Mueller, William J Metzler, et al.
Molecular Pharmacology
|
June 25, 2017
A Functional Na<sub>V</sub>1.7-Na<sub>V</sub>Ab Chimera with a Reconstituted High-Affinity ProTx-II Binding Site
Ramkumar Rajamani, Sophie Wu, Iyoncy Rodrigo, et al.
Journal of Biomolecular Screening
|
September 25, 2013
Development of novel, 384-well high-throughput assay panels for human drug transporters: drug interaction and safety assessment in support of discovery research
Huaping Tang, Ding Ren Shen, Yong-Hae Han, et al.
Acta Crystallographica. Section F, Structural Biology Communications
|
October 14, 2024
Improving the diffraction quality of heat-shock protein 47 crystals
Kevin Kish, Stephen Cobell, Nicolas Szapiel, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
June 12, 2014
Pharmacologic profile of the Adnectin BMS-962476, a small protein biologic alternative to PCSK9 antibodies for low-density lipoprotein lowering
Tracy Mitchell, Ginger Chao, Doree Sitkoff, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
December 12, 2018
Characterization of Mauritian Cynomolgus Macaque FcγR Alleles Using Long-Read Sequencing
Amelia K Haj, Jaren M Arbanas, Aaron P Yamniuk, et al.
Bioconjugate Chemistry
|
April 22, 2016
Biotechnology Based Process for Production of a Disulfide-Bridged Peptide
Animesh Goswami, Steven L Goldberg, Ronald L Hanson, et al.
Journal of Medicinal Chemistry
|
September 3, 2011
Small molecule receptor protein tyrosine phosphatase γ (RPTPγ) ligands that inhibit phosphatase activity via perturbation of the tryptophan-proline-aspartate (WPD) loop
Steven Sheriff, Brett R Beno, Weixu Zhai, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 5, 2020
Structure-based amelioration of PXR transactivation in a novel series of macrocyclic allosteric inhibitors of HIV-1 integrase
Prasanna Sivaprakasam, Zhongyu Wang, Nicholas A Meanwell, et al.
Journal of Molecular Biology
|
January 13, 2015
Developing Adnectins that target SRC co-activator binding to PXR: a structural approach toward understanding promiscuity of PXR
Javed A Khan, Daniel M Camac, Simon Low, et al.
Page
of 4