Earl Gordon

发表

RNA Interference Reveals That EndogenousXenopus MinK-related Peptides Govern Mammalian K+ Channel Function in Oocyte Expression Studies*

G. Abbott, A. Anantharam, A. Lewis, 2003, The Journal of Biological Chemistry.

Acetic acid opens large-conductance Ca2+-activated K+ channels in guinea pig detrusor smooth muscle cells.

R. Willette, D. Brooks, I. Lozinskaya, 2007, European journal of pharmacology.

N-((1S)-1-{[4-((2S)-2-{[(2,4-Dichlorophenyl)sulfonyl]amino}-3-hydroxypropanoyl)-1-piperazinyl]carbonyl}-3-methylbutyl)-1-benzothiophene-2-carboxamide (GSK1016790A), a Novel and Potent Transient Receptor Potential Vanilloid 4 Channel Agonist Induces Urinary Bladder Contraction and Hyperactivity: Part

D. Demarini, D. Brooks, N. Laping, 2008, Journal of Pharmacology and Experimental Therapeutics.

Functional TRPV4 channels and an absence of capsaicin-evoked currents in freshly-isolated, guinea-pig urothelial cells

K. Thorneloe, I. Lozinskaya, Xiaoping Xu, 2009, Channels.

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+ Channel

R. Willette, Haoyu Zeng, I. Lozinskaya, 2008, Journal of Pharmacology and Experimental Therapeutics.

JPET #139733 1 1-[1-hexyl-6-(methyloxy)-1H-indazol-3-yl]-2-methyl-1-propanone (HMIMP), a Potent and Highly Selective Small Molecule Blocker of the Large-Conductance Voltage-gated and Calcium-dependent K Channel

R. Willette, Haoyu Zeng, I. Lozinskaya, 2008 .

RNAi in Xenopus Laevis Oocytes

G. Abbott, Earl Gordon, 2004 .

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 Channels

S. Semus, R. Willette, F. Blaney, 2008, Molecular Pharmacology.

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-propanone

S. Semus, I. Lozinskaya, Xiaoping Xu, 2010, Journal of Pharmacology and Experimental Therapeutics.

CHARACTERIZING THE ROLE OF T352 IN THE INHIBITION OF THE LARGE CONDUCTANCE Ca 2+ -ACTIVATED K + (BK) CHANNELS BY 1-[1-HEXYL-6-(METHYLOXY)-1

S. Semus, I. Lozinskaya, Xiaoping Xu, 2010 .

Correction: MPX-004 and MPX-007: New Pharmacological Tools to Study the Physiology of NMDA Receptors Containing the GluN2A Subunit

M. Fagiolini, R. Volkmann, F. Menniti, 2016, PloS one.

MPX-004 and MPX-007: New Pharmacological Tools to Study the Physiology of NMDA Receptors Containing the GluN2A Subunit

M. Fagiolini, R. Volkmann, F. Menniti, 2016, PloS one.

1,4-Diazabicyclo[2.2.2]octane Derivatives: A Novel Class of Voltage-Gated Potassium Channel Blockers

G. Abbott, Earl Gordon, R. Engel, 2006, Molecular Pharmacology.

A KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalance.

H. Ostrer, W. Chung, C. Basson, 2008, Cardiovascular research.

An Orally Active TRPV4 Channel Blocker Prevents and Resolves Pulmonary Edema Induced by Heart Failure

H. Alsaid, W. Bao, R. Willette, 2012, Science Translational Medicine.

Endogenous KCNE subunits govern Kv2.1 K+ channel activation kinetics in Xenopus oocyte studies.

G. Abbott, T. K. Roepke, Earl Gordon, 2006, Biophysical journal.

PTC-174, a positive allosteric modulator of NMDA receptors containing GluN2C or GluN2D subunits

R. Volkmann, F. Menniti, K. Hansen, 2020, Neuropharmacology.