Get started
Author

Walter A. Volberg

Observed names: W .A. VOLBERG, W A Volberg, W Volberg, W. A. VOLBERG, W. A. Volberg, Walt Volberg, Walter A Volberg, Walter Volberg
OpenAlex ID: A5042398673
Blockade of Human Cardiac Potassium Channel Human Ether-a-go-go-Related Gene (HERG) by Macrolide Antibiotics
2002 · Walter A. Volberg, Bryan J. Koci, et al. · Journal of Pharmacology and Experimental Therapeutics · 153
Novel Potent Human Ether-à-Go-Go-Related Gene (hERG) Potassium Channel Enhancers and Their in Vitro Antiarrhythmic Activity
2005 · Jun Zhou, Corinne E Augelli-Szafran, et al. · Molecular Pharmacology · 137
Chemical synthesis and characterization of ShK toxin: a potent potassium channel inhibitor from a sea anemone
1995 · M. W. PENNINGTON, M. E. BYRNES, et al. · International journal of peptide & protein research · 103
Identification of a specific radioligand for the cardiac rapidly activating delayed rectifier K+ channel.
1993 · C C Chadwick, A M Ezrin, et al. · Circulation Research · 54
Synthesis and Structure-Activity Relationships of 6-Heterocyclic-Substituted Purines as Inactivation Modifiers of Cardiac Sodium Channels
1995 · Kimberly G. Estep, Kurt A. Josef, et al. · Journal of Medicinal Chemistry · 47
An impedance-based approach using human iPSC-derived cardiomyocytes significantly improves in vitro prediction of in vivo cardiotox liabilities
2017 · Bryan Koci, Gregory Luerman, et al. · Toxicology and Applied Pharmacology · 37
(3R,4S)-3-[4-(4-Fluorophenyl)-4-hydroxypiperidin-1-yl]chroman-4,7-diol: A Conformationally Restricted Analogue of the NR2B Subtype-Selective NMDA Antagonist (1S,2S)-1-(4-Hydroxyphenyl)-2- (4-hydroxy-4-phenylpiperidino)-1-propanol
1998 · Todd W. Butler, James F. Blake, et al. · Journal of Medicinal Chemistry · 33
Novel Inhibitors of Potassium Ion Channels on Human T Lymphocytes
1995 · William F. Michne, Joseph W. Guiles, et al. · Journal of Medicinal Chemistry · 33
Voltage Dependence of Cardiac Delayed Rectifier Block by Methanesulfonamide Class III Antiarrhythmic Agents
1994 · Douglas S. Krafte, Walter A. Volberg · Journal of Cardiovascular Pharmacology · 33
WIN 17317-3: novel nonpeptide antagonist of voltage-activated K+ channels in human T lymphocytes.
1995 · R J Hill, A M Grant, et al. · Molecular Pharmacology · 31
Characterization of endogenous sodium channel gene expressed in Chinese hamster ovary cells
1993 · P. H. Lalik, D. S. Krafte, et al. · American Journal of Physiology-Cell Physiology · 30
Structure–activity relationships of triazolopyridine oxazole p38 inhibitors: Identification of candidates for clinical development
2006 · Kim F. McClure, Michael A. Letavic, et al. · Bioorganic & Medicinal Chemistry Letters · 29
Expression of cardiac Na channels with appropriate physiological and pharmacological properties in Xenopus oocytes.
1991 · D S Krafte, W A Volberg, et al. · Proceedings of the National Academy of Sciences · 27
Electrical alternans and hemodynamics in the anesthetized guinea pig can discriminate the cardiac safety of antidepressants
2006 · Anthony A. Fossa, William Gorczyca, et al. · Journal of Pharmacological and Toxicological Methods · 26
Inhibition of calmodulin and protein kinase C by amiodarone and other class III antiarrhythmic agents
1989 · Paul J. Silver, Mary J. Connell, et al. · Cardiovascular Drugs and Therapy · 18
4,5-Dihydro-3-(methanesulfonamidophenyl)-1-phenyl-1H-2,4-benzodiazepines: A Novel Class III Antiarrhythmic Agents
1995 · Robert E. Johnson, Paul J. Silver, et al. · Journal of Medicinal Chemistry · 16
Properties of endogenous voltage-dependent sodium currents in Xenopus laevis oocytes
1992 · Douglas S. Krafte, Walter A. Volberg · Journal of Neuroscience Methods · 14
Stable expression and functional characterization of a human cardiac Na+ channel gene in mammalian cells
1995 · Douglas S. Krafte, Walter A. Volberg, et al. · Journal of Molecular and Cellular Cardiology · 9
Evidence for multiple antiarrhythmic binding sites on the cardiac rapidly activating delayed rectifier K+ channel
1995 · Christopher C. Chadwick, Douglas S. Krafte, et al. · Drug Development Research · 3
ChemInform Abstract: Synthesis and Structure‐Activity Relationships of 6‐Heterocyclic‐ Substituted Purines as Inactivation Modifiers of Cardiac Sodium Channels.
1995 · K. G. ESTEP, K. A. JOSEF, et al. · ChemInform · 1
Impedance-Based Assessment of Preclinical Cardiac Structural Toxicity Using Human iPSC-Derived Cardiomyocytes and its Correlation to In Vivo (dog) Exposures
2017 · Bryan Koci, Greg Luerman, et al. · Journal of Pharmacological and Toxicological Methods
Works count: 21
Citation count: 834
H-index: 16
I10-index: 17
Year
Topic
Type