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Molecular Pharmacology
|
June 24, 2010
Reversible, allosteric small-molecule inhibitors of regulator of G protein signaling proteins
Levi L Blazer, David L Roman, Alfred Chung, et al.
The Journal of Biological Chemistry
|
April 4, 2019
High-resolution structure of RGS17 suggests a role for Ca<sup>2+</sup> in promoting the GTPase-activating protein activity by RZ subfamily members
Monita Sieng, Michael P Hayes, Joseph B O'Brien, et al.
SLAS Discovery : Advancing Life Sciences R & D
|
January 20, 2018
Screen Targeting Lung and Prostate Cancer Oncogene Identifies Novel Inhibitors of RGS17 and Problematic Chemical Substructures
Christopher R Bodle, Josephine H Schamp, Joseph B O'Brien, et al.
Frontiers in Pharmacology
|
September 23, 2022
Protein-protein interaction-based high throughput screening for adenylyl cyclase 1 inhibitors: Design, implementation, and discovery of a novel chemotype
Tiffany S Dwyer, Joseph B O'Brien, Christopher P Ptak, et al.
Journal of Neurochemistry
|
December 17, 2009
Differential modulation of mu-opioid receptor signaling to adenylyl cyclase by regulators of G protein signaling proteins 4 or 8 and 7 in permeabilised C6 cells is Galpha subtype dependent
Jeffery N Talbot, David L Roman, Mary J Clark, et al.
BMC Pharmacology
|
May 26, 2009
A covalent peptide inhibitor of RGS4 identified in a focused one-bead, one compound library screen
Rebecca A Roof, David L Roman, Samuel T Clements, et al.
Chemical Biology & Drug Design
|
July 22, 2008
Novel peptide ligands of RGS4 from a focused one-bead, one-compound library
Rebecca A Roof, Katarzyna Sobczyk-Kojiro, Anjanette J Turbiak, et al.
Journal of Natural Products
|
June 17, 2017
Natural Products Discovered in a High-Throughput Screen Identified as Inhibitors of RGS17 and as Cytostatic and Cytotoxic Agents for Lung and Prostate Cancer Cell Lines
Christopher R Bodle, Duncan I Mackie, Michael P Hayes, et al.
Plos One
|
November 28, 2013
RABL6A, a novel RAB-like protein, controls centrosome amplification and chromosome instability in primary fibroblasts
Xuefeng Zhang, Jussara Hagen, Viviane P Muniz, et al.
British Journal of Pharmacology
|
September 16, 2021
THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: Introduction and Other Protein Targets
Stephen Ph Alexander, Eamonn Kelly, Alistair Mathie, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 42) with videos related to
Sort By:
Page
of 5
Molecular Pharmacology
|
June 24, 2010
Reversible, allosteric small-molecule inhibitors of regulator of G protein signaling proteins
Levi L Blazer, David L Roman, Alfred Chung, et al.
The Journal of Biological Chemistry
|
April 4, 2019
High-resolution structure of RGS17 suggests a role for Ca<sup>2+</sup> in promoting the GTPase-activating protein activity by RZ subfamily members
Monita Sieng, Michael P Hayes, Joseph B O'Brien, et al.
SLAS Discovery : Advancing Life Sciences R & D
|
January 20, 2018
Screen Targeting Lung and Prostate Cancer Oncogene Identifies Novel Inhibitors of RGS17 and Problematic Chemical Substructures
Christopher R Bodle, Josephine H Schamp, Joseph B O'Brien, et al.
Frontiers in Pharmacology
|
September 23, 2022
Protein-protein interaction-based high throughput screening for adenylyl cyclase 1 inhibitors: Design, implementation, and discovery of a novel chemotype
Tiffany S Dwyer, Joseph B O'Brien, Christopher P Ptak, et al.
Journal of Neurochemistry
|
December 17, 2009
Differential modulation of mu-opioid receptor signaling to adenylyl cyclase by regulators of G protein signaling proteins 4 or 8 and 7 in permeabilised C6 cells is Galpha subtype dependent
Jeffery N Talbot, David L Roman, Mary J Clark, et al.
BMC Pharmacology
|
May 26, 2009
A covalent peptide inhibitor of RGS4 identified in a focused one-bead, one compound library screen
Rebecca A Roof, David L Roman, Samuel T Clements, et al.
Chemical Biology & Drug Design
|
July 22, 2008
Novel peptide ligands of RGS4 from a focused one-bead, one-compound library
Rebecca A Roof, Katarzyna Sobczyk-Kojiro, Anjanette J Turbiak, et al.
Journal of Natural Products
|
June 17, 2017
Natural Products Discovered in a High-Throughput Screen Identified as Inhibitors of RGS17 and as Cytostatic and Cytotoxic Agents for Lung and Prostate Cancer Cell Lines
Christopher R Bodle, Duncan I Mackie, Michael P Hayes, et al.
Plos One
|
November 28, 2013
RABL6A, a novel RAB-like protein, controls centrosome amplification and chromosome instability in primary fibroblasts
Xuefeng Zhang, Jussara Hagen, Viviane P Muniz, et al.
British Journal of Pharmacology
|
September 16, 2021
THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: Introduction and Other Protein Targets
Stephen Ph Alexander, Eamonn Kelly, Alistair Mathie, et al.
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of 5