Pharmacology
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Chris Hague, Ph.D.,
Assistant Professor

Lab Website
Publications
Course Website
  phcol402

Email: chague@uw.edu
Box 357280
HSC D431

Office: 206.221.4612
Lab: 206.543.8485
Fax: 206.685.3822
 

 

 

 

 

 

 

The research interests of the laboratory focus on the study of G-protein coupled receptors (GPCRs). GPCRs comprise ~1% of the entire genome and represent the target for >40% of all commerically available pharmaceutical drugs.

Our currents interests include the study of the adrenergic, sensory and orphan receptors. Using mass spectrometry and biochemical techniques, we are identifying novel protein binding partners for GPCRs. By combining expertise in pharmacology, cell biology and physiology, we determine the role of each binding partner in regulating GPCR function, trafficking, and drug binding. Our ultimate goal is to carefully characterize the mechanisms that regulate GPCR signaling complexes, in order to provide new information that may be used in the development of efficacious medicines to treat disease.



Recent Publications 

Reduced Iodine Load at CT Pulmonary Angiography with Dual-Energy Monochromatic Imaging: Comparison with Standard CT Pulmonary Angiography--A Prospective Randomized Trial. - ABSTRACT

Syntrophin isoforms play specific functional roles in the α1D-adrenergic receptor/DAPC signalosome. - ABSTRACT

The role of norepinephrine in differential response to stress in an animal model of posttraumatic stress disorder. - ABSTRACT

Alpha-dystrobrevin-1 recruits alpha-catulin to the alpha1D-adrenergic receptor/dystrophin-associated protein complex signalosome. - ABSTRACT

Differential regulation of GPR54 transcription by specificity protein-1 and partial estrogen response element in mouse pituitary cells. - ABSTRACT

View all recent publications