Ross Fellows

Insensitivity to pain induced by a potent selective closed-state Nav1.7 inhibitor

M.L. Flinspach, Q. Xu, Andrew D. Piekarz et al. · Scientific Reports · 2017 · 123 citations · Full text

Medicine, Medicinal Chemistry, Pharmacology +16

Analysis of the Structural and Molecular Basis of Voltage-sensitive Sodium Channel Inhibition by the Spider Toxin Huwentoxin-IV (μ-TRTX-Hh2a)

Natali A. Minassian, Alan C. Gibbs, Amy Y. Shih et al. · Journal of Biological Chemistry · 2013 · 70 citations · Full text

Natural Sciences, Neuroscience, Pharmacology +17

Targeting the Ion Channel Kv1.3 with Scorpion Venom Peptides Engineered for Potency, Selectivity, and Half-life

Wilson B. Edwards, Wai‐Ping Fung‐Leung, Chichi Huang et al. · Journal of Biological Chemistry · 2014 · 32 citations · Full text

Medicine, Medicinal Chemistry, Pharmacology +17

Comprehensive engineering of the tarantula venom peptide huwentoxin-IV to inhibit the human voltage-gated sodium channel hNa_v1.7

Robert A. Neff, M.L. Flinspach, Alan C. Gibbs et al. · Journal of Biological Chemistry · 2019 · 21 citations · Full text

Medicine, Medicinal Chemistry, Pharmacology +17

Evaluation of the role of three candidate human kinases in the conversion of the hepatitis C virus inhibitor 2′-C-methyl-cytidine to its 5′-monophosphate metabolite

Nina L. Golitsina, Francis T. Danehy, Ross Fellows et al. · Antiviral Research · 2009 · 15 citations

Life Sciences, Biochemistry, Molecular Virology +5