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Journal of Medicinal Chemistry
|
March 4, 2014
Differences in conformational dynamics between Plasmodium falciparum and human Hsp90 orthologues enable the structure-based discovery of pathogen-selective inhibitors
Tai Wang, William H Bisson, Pascal Mäser, et al.
Journal of Medicinal Chemistry
|
August 5, 2005
Ligand selectivity for the acetylcholine binding site of the rat alpha4beta2 and alpha3beta4 nicotinic subtypes investigated by molecular docking
William H Bisson, Leonardo Scapozza, Gerrit Westera, et al.
Carcinogenesis
|
June 17, 2009
Alpha-keto acid metabolites of organoselenium compounds inhibit histone deacetylase activity in human colon cancer cells
Hui Nian, William H Bisson, Wan-Mohaiza Dashwood, et al.
Comparative Biochemistry and Physiology. Toxicology & Pharmacology : CBP
|
May 29, 2012
Alternate glucocorticoid receptor ligand binding structures influence outcomes in an in vivo tissue regeneration model
Sumitra Sengupta, William H Bisson, Lijoy K Mathew, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology
|
October 18, 2017
TCDD, FICZ, and Other High Affinity AhR Ligands Dose-Dependently Determine the Fate of CD4+ T Cell Differentiation
Allison K Ehrlich, Jamie M Pennington, William H Bisson, et al.
Environmental Health Perspectives
|
August 13, 2016
Low-Dose Mixture Hypothesis of Carcinogenesis Workshop: Scientific Underpinnings and Research Recommendations
Mark F Miller, William H Goodson, Masoud H Manjili, et al.
European Journal of Medicinal Chemistry
|
March 21, 2006
Synthesis and binding studies of epibatidine analogues as ligands for the nicotinic acetylcholine receptors
Linjing Mu, Konstantin Drandarov, William H Bisson, et al.
Chemical Biology & Drug Design
|
November 18, 2008
Binding properties of the C-terminal domain of VIAF
William H Bisson, Ziming Zhang, Kate Welsh, et al.
Aquatic Toxicology (Amsterdam, Netherlands)
|
May 29, 2014
Mono-substituted isopropylated triaryl phosphate, a major component of Firemaster 550, is an AHR agonist that exhibits AHR-independent cardiotoxicity in zebrafish
Cory V Gerlach, Siba R Das, David C Volz, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology
|
December 18, 2010
Estrogen-like activity of perfluoroalkyl acids in vivo and interaction with human and rainbow trout estrogen receptors in vitro
Abby D Benninghoff, William H Bisson, Daniel C Koch, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 63) with videos related to
Sort By:
Page
of 7
Journal of Medicinal Chemistry
|
March 4, 2014
Differences in conformational dynamics between Plasmodium falciparum and human Hsp90 orthologues enable the structure-based discovery of pathogen-selective inhibitors
Tai Wang, William H Bisson, Pascal Mäser, et al.
Journal of Medicinal Chemistry
|
August 5, 2005
Ligand selectivity for the acetylcholine binding site of the rat alpha4beta2 and alpha3beta4 nicotinic subtypes investigated by molecular docking
William H Bisson, Leonardo Scapozza, Gerrit Westera, et al.
Carcinogenesis
|
June 17, 2009
Alpha-keto acid metabolites of organoselenium compounds inhibit histone deacetylase activity in human colon cancer cells
Hui Nian, William H Bisson, Wan-Mohaiza Dashwood, et al.
Comparative Biochemistry and Physiology. Toxicology & Pharmacology : CBP
|
May 29, 2012
Alternate glucocorticoid receptor ligand binding structures influence outcomes in an in vivo tissue regeneration model
Sumitra Sengupta, William H Bisson, Lijoy K Mathew, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology
|
October 18, 2017
TCDD, FICZ, and Other High Affinity AhR Ligands Dose-Dependently Determine the Fate of CD4+ T Cell Differentiation
Allison K Ehrlich, Jamie M Pennington, William H Bisson, et al.
Environmental Health Perspectives
|
August 13, 2016
Low-Dose Mixture Hypothesis of Carcinogenesis Workshop: Scientific Underpinnings and Research Recommendations
Mark F Miller, William H Goodson, Masoud H Manjili, et al.
European Journal of Medicinal Chemistry
|
March 21, 2006
Synthesis and binding studies of epibatidine analogues as ligands for the nicotinic acetylcholine receptors
Linjing Mu, Konstantin Drandarov, William H Bisson, et al.
Chemical Biology & Drug Design
|
November 18, 2008
Binding properties of the C-terminal domain of VIAF
William H Bisson, Ziming Zhang, Kate Welsh, et al.
Aquatic Toxicology (Amsterdam, Netherlands)
|
May 29, 2014
Mono-substituted isopropylated triaryl phosphate, a major component of Firemaster 550, is an AHR agonist that exhibits AHR-independent cardiotoxicity in zebrafish
Cory V Gerlach, Siba R Das, David C Volz, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology
|
December 18, 2010
Estrogen-like activity of perfluoroalkyl acids in vivo and interaction with human and rainbow trout estrogen receptors in vitro
Abby D Benninghoff, William H Bisson, Daniel C Koch, et al.
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of 7