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Sub-Cellular Biochemistry
|
March 9, 2017
The Structure and Function of the PRMT5:MEP50 Complex
Stephen Antonysamy
Bioorganic & Medicinal Chemistry Letters
|
November 21, 2008
Fragment-based discovery of JAK-2 inhibitors
Stephen Antonysamy, Gavin Hirst, Frances Park, et al.
Mabs
|
July 4, 2024
Engineering a tumor-selective prodrug T-cell engager bispecific antibody for safer immunotherapy
Amelia C McCue, Stephen J Demarest, Karen J Froning, et al.
Plos One
|
September 11, 2020
Rapid and robust antibody Fab fragment crystallization utilizing edge-to-edge beta-sheet packing
Ricky Lieu, Stephen Antonysamy, Zhanna Druzina, et al.
Plos One
|
December 25, 2013
Structural context of disease-associated mutations and putative mechanism of autoinhibition revealed by X-ray crystallographic analysis of the EZH2-SET domain
Stephen Antonysamy, Bradley Condon, Zhanna Druzina, et al.
Journal of Medicinal Chemistry
|
May 12, 2015
Crystal Structures of mPGES-1 Inhibitor Complexes Form a Basis for the Rational Design of Potent Analgesic and Anti-Inflammatory Therapeutics
John Gately Luz, Stephen Antonysamy, Steven L Kuklish, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 17, 2012
Crystal structure of the human PRMT5:MEP50 complex
Stephen Antonysamy, Zahid Bonday, Robert M Campbell, et al.
Plos One
|
January 13, 2018
Utilization of peptide phage display to investigate hotspots on IL-17A and what it means for drug discovery
Joey P Ting, Frances Tung, Stephen Antonysamy, et al.
ACS Medicinal Chemistry Letters
|
July 24, 2018
LLY-283, a Potent and Selective Inhibitor of Arginine Methyltransferase 5, PRMT5, with Antitumor Activity
Zahid Q Bonday, Guillermo S Cortez, Michael J Grogan, et al.
Biochimica Et Biophysica Acta. General Subjects
|
November 27, 2020
Structure-based, multi-targeted drug discovery approach to eicosanoid inhibition: Dual inhibitors of mPGES-1 and 5-lipoxygenase activating protein (FLAP)
Joseph D Ho, Matthew R Lee, Charles T Rauch, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 2
Sub-Cellular Biochemistry
|
March 9, 2017
The Structure and Function of the PRMT5:MEP50 Complex
Stephen Antonysamy
Bioorganic & Medicinal Chemistry Letters
|
November 21, 2008
Fragment-based discovery of JAK-2 inhibitors
Stephen Antonysamy, Gavin Hirst, Frances Park, et al.
Mabs
|
July 4, 2024
Engineering a tumor-selective prodrug T-cell engager bispecific antibody for safer immunotherapy
Amelia C McCue, Stephen J Demarest, Karen J Froning, et al.
Plos One
|
September 11, 2020
Rapid and robust antibody Fab fragment crystallization utilizing edge-to-edge beta-sheet packing
Ricky Lieu, Stephen Antonysamy, Zhanna Druzina, et al.
Plos One
|
December 25, 2013
Structural context of disease-associated mutations and putative mechanism of autoinhibition revealed by X-ray crystallographic analysis of the EZH2-SET domain
Stephen Antonysamy, Bradley Condon, Zhanna Druzina, et al.
Journal of Medicinal Chemistry
|
May 12, 2015
Crystal Structures of mPGES-1 Inhibitor Complexes Form a Basis for the Rational Design of Potent Analgesic and Anti-Inflammatory Therapeutics
John Gately Luz, Stephen Antonysamy, Steven L Kuklish, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 17, 2012
Crystal structure of the human PRMT5:MEP50 complex
Stephen Antonysamy, Zahid Bonday, Robert M Campbell, et al.
Plos One
|
January 13, 2018
Utilization of peptide phage display to investigate hotspots on IL-17A and what it means for drug discovery
Joey P Ting, Frances Tung, Stephen Antonysamy, et al.
ACS Medicinal Chemistry Letters
|
July 24, 2018
LLY-283, a Potent and Selective Inhibitor of Arginine Methyltransferase 5, PRMT5, with Antitumor Activity
Zahid Q Bonday, Guillermo S Cortez, Michael J Grogan, et al.
Biochimica Et Biophysica Acta. General Subjects
|
November 27, 2020
Structure-based, multi-targeted drug discovery approach to eicosanoid inhibition: Dual inhibitors of mPGES-1 and 5-lipoxygenase activating protein (FLAP)
Joseph D Ho, Matthew R Lee, Charles T Rauch, et al.
Page
of 2