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ACS Chemical Biology
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September 21, 2017
Mapping Protein Targets of Bioactive Small Molecules Using Lipid-Based Chemical Proteomics
Kenneth M Lum, Yoshiaki Sato, Brittney A Beyer, et al.
Journal of the American Chemical Society
|
April 5, 2023
A Cell Type Selective YM155 Prodrug Targets Receptor-Interacting Protein Kinase 2 to Induce Brain Cancer Cell Death
Thomas J West, Junfeng Bi, Francisco Martínez-Peña, et al.
Nature Communications
|
April 11, 2025
Distinct oligomeric assemblies of STING induced by non-nucleotide agonists
Anant Gharpure, Ariana Sulpizio, Johannes R Loeffler, et al.
The Journal of Biological Chemistry
|
August 12, 2011
Structural and kinetic analysis of substrate binding to the sialyltransferase Cst-II from Campylobacter jejuni
Ho Jun Lee, Luke L Lairson, Jamie R Rich, et al.
The Journal of Biological Chemistry
|
April 13, 2004
Intermediate trapping on a mutant retaining alpha-galactosyltransferase identifies an unexpected aspartate residue
Luke L Lairson, Cecilia P C Chiu, Hoa D Ly, et al.
Nature Chemistry
|
February 12, 2020
Electronic complementarity permits hindered butenolide heterodimerization and discovery of novel cGAS/STING pathway antagonists
Benjamin J Huffman, Shuming Chen, J Luca Schwarz, et al.
Biochemistry
|
June 22, 2005
Mutational, structural, and kinetic evidence for a dissociative mechanism in the GDP-mannose mannosyl hydrolase reaction
Zuyong Xia, Hugo F Azurmendi, Luke L Lairson, et al.
ACS Combinatorial Science
|
June 18, 2016
High-Throughput Screening Uncovers Novel Botulinum Neurotoxin Inhibitor Chemotypes
Kristin M Bompiani, Dejan Caglič, Michelle C Krutein, et al.
Biochemistry
|
October 15, 2009
NMR spectroscopic characterization of the sialyltransferase CstII from Campylobacter jejuni: histidine 188 is the general base
Patrick H W Chan, Luke L Lairson, Ho Jun Lee, et al.
European Journal of Medicinal Chemistry
|
August 24, 2022
Synthesis and biological evaluation of novel FiVe1 derivatives as potent and selective agents for the treatment of mesenchymal cancers
Francisco Martínez-Peña, Aaron D Pearson, Eileen L Tang, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 60) with videos related to
Sort By:
Page
of 6
ACS Chemical Biology
|
September 21, 2017
Mapping Protein Targets of Bioactive Small Molecules Using Lipid-Based Chemical Proteomics
Kenneth M Lum, Yoshiaki Sato, Brittney A Beyer, et al.
Journal of the American Chemical Society
|
April 5, 2023
A Cell Type Selective YM155 Prodrug Targets Receptor-Interacting Protein Kinase 2 to Induce Brain Cancer Cell Death
Thomas J West, Junfeng Bi, Francisco Martínez-Peña, et al.
Nature Communications
|
April 11, 2025
Distinct oligomeric assemblies of STING induced by non-nucleotide agonists
Anant Gharpure, Ariana Sulpizio, Johannes R Loeffler, et al.
The Journal of Biological Chemistry
|
August 12, 2011
Structural and kinetic analysis of substrate binding to the sialyltransferase Cst-II from Campylobacter jejuni
Ho Jun Lee, Luke L Lairson, Jamie R Rich, et al.
The Journal of Biological Chemistry
|
April 13, 2004
Intermediate trapping on a mutant retaining alpha-galactosyltransferase identifies an unexpected aspartate residue
Luke L Lairson, Cecilia P C Chiu, Hoa D Ly, et al.
Nature Chemistry
|
February 12, 2020
Electronic complementarity permits hindered butenolide heterodimerization and discovery of novel cGAS/STING pathway antagonists
Benjamin J Huffman, Shuming Chen, J Luca Schwarz, et al.
Biochemistry
|
June 22, 2005
Mutational, structural, and kinetic evidence for a dissociative mechanism in the GDP-mannose mannosyl hydrolase reaction
Zuyong Xia, Hugo F Azurmendi, Luke L Lairson, et al.
ACS Combinatorial Science
|
June 18, 2016
High-Throughput Screening Uncovers Novel Botulinum Neurotoxin Inhibitor Chemotypes
Kristin M Bompiani, Dejan Caglič, Michelle C Krutein, et al.
Biochemistry
|
October 15, 2009
NMR spectroscopic characterization of the sialyltransferase CstII from Campylobacter jejuni: histidine 188 is the general base
Patrick H W Chan, Luke L Lairson, Ho Jun Lee, et al.
European Journal of Medicinal Chemistry
|
August 24, 2022
Synthesis and biological evaluation of novel FiVe1 derivatives as potent and selective agents for the treatment of mesenchymal cancers
Francisco Martínez-Peña, Aaron D Pearson, Eileen L Tang, et al.
Page
of 6