Dong Liu

Discovery and biological evaluation of potent, selective, orally bioavailable, pyrazine-based blockers of the Na(v)1.8 sodium channel with efficacy in a model of neuropathic pain.

Matthew S. Johnson, C. Shieh, James B. Thomas, 2010, Bioorganic & medicinal chemistry.

A-803467, a potent and selective Nav1.8 sodium channel blocker, attenuates neuropathic and inflammatory pain in the rat

Matthew S. Johnson, J. Sullivan, C. Shieh, 2007, Proceedings of the National Academy of Sciences.

Discovery and biological evaluation of 5-aryl-2-furfuramides, potent and selective blockers of the Nav1.8 sodium channel with efficacy in models of neuropathic and inflammatory pain.

Matthew S. Johnson, C. Shieh, James B. Thomas, 2008, Journal of medicinal chemistry.

(−)-(9S)-9-(3-Bromo-4-fluorophenyl)-2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-Dioxide (A-278637): A Novel ATP-Sensitive Potassium Channel Opener Efficacious in Suppressing Urinary Bladder Contractions. I. In Vitro Characterization

J. Sullivan, R. Chess-Williams, M. Williams, 2002, Journal of Pharmacology and Experimental Therapeutics.

The Association of Low Molecular Weight Heparin Use and In-hospital Mortality Among Patients Hospitalized with COVID-19

E. Peterson, Ying Xiao, Daowen Wang, 2021, Cardiovascular Drugs and Therapy.

Tenidap, a novel anti-inflammatory agent, is an opener of the inwardly rectifying K+ channel hKir2.3.

M. Coghlan, Dong Liu, Yi Liu, 2002, European journal of pharmacology.

Decrease of inward rectification as a mechanism for arachidonic acid-induced potentiation of hKir2.3

Dong Liu, Yi Liu, D. Krafte, 2002, European Biophysics Journal.

Voltage-dependent inhibition of brain Na(+) channels by American ginseng.

C. Yuan, J. W. Kyle, A. Attele, 2001, European journal of pharmacology.