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American Journal of Hypertension|February 5, 2008
Ca2+ channel inactivation in small mesenteric arteries of WKY and SHRRobert H Cox, Irina M Lozinskaya
The Journal of Pharmacology and Experimental Therapeutics|May 1, 2010
Characterizing the role of Thr352 in the inhibition of the large conductance Ca2+-activated K+ channels by 1-[1-hexyl-6-(methyloxy)-1H-indazol-3-yl]-2-methyl-1-propanoneEarl Gordon, Simon F Semus, Irina M Lozinskaya, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 2, 2008
1-[1-Hexyl-6-(methyloxy)-1H-indazol-3-yl]-2-methyl-1-propanone, a potent and highly selective small molecule blocker of the large-conductance voltage-gated and calcium-dependent K+ channelHaoyu Zeng, Earl Gordon, Zuojun Lin, et al.
Channels (Austin, Tex.)|May 5, 2009
Functional TRPV4 channels and an absence of capsaicin-evoked currents in freshly-isolated, guinea-pig urothelial cellsXiaoping Xu, Earl Gordon, Zuojun Lin, et al.
The Journal of Pharmacology and Experimental Therapeutics|August 25, 2006
Mallotoxin is a novel human ether-a-go-go-related gene (hERG) potassium channel activatorHaoyu Zeng, Irina M Lozinskaya, Zuojun Lin, et al.
Molecular Pharmacology|November 29, 2007
2-[2-(3,4-dichloro-phenyl)-2,3-dihydro-1H-isoindol-5-ylamino]-nicotinic acid (PD-307243) causes instantaneous current through human ether-a-go-go-related gene potassium channelsEarl Gordon, Irina M Lozinskaya, Zuojun Lin, et al.
American Journal of Physiology. Heart and Circulatory Physiology|July 9, 2013
Human-induced pluripotent stem cell-derived cardiomyocytes exhibit temporal changes in phenotypeChristine Y Ivashchenko, Gordon C Pipes, Irina M Lozinskaya, et al.
Bioorganic & Medicinal Chemistry Letters|July 27, 2013
The discovery of potent blockers of the canonical transient receptor channels, TRPC3 and TRPC6, based on an anilino-thiazole pharmacophoreDavid G Washburn, Dennis A Holt, Jason Dodson, et al.
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