Andrew Voss Lab https://validator.w3.org/feed/docs/rss2.html Action potential properties affect excitation-contraction coupling in skeletal muscle Ohio Physiological Society Meeting – 2021 Undergraduate Keisha Barnes receives summer fellowship award Skeletal Muscle Denervation In Huntington’s Disease? Maybe Not. News Wright State Research Contracting Acetylcholine receptor subunit expression in Huntington’s disease mouse muscle Katie Trittschuh Our Team Conferences And Talks Privacy Policy Future Member Journal Articles Contact Us Helping Birds of Prey: Eggcellent Results With 3D Printing RyR1/RyR3 chimeras reveal that multiple domains of RyR1 are involved in skeletal-type E-C coupling Identification of Hyperreactive Cysteines within Ryanodine Receptor Type 1 by Mass Spectrometry Ryanodine receptor-mediated rapid increase in intracellular calcium induced by 7,8-benzo(a)pyrene quinone in human and murine leukocytes Dr. Voss Neuromuscular Physiology Lab – Welcome to our new Website! Steve Burke Imino sugars are potent agonists of the human glucose sensor SGLT3 Elton Nguyen Allosterically coupled calcium and magnesium binding sites are unmasked by ryanodine receptor chimeras Glucose transport by human renal Na+/d-glucose cotransporters SGLT1 and SGLT2 Increase the Production of Poly-3-Hydroxybutyrate in Genetically Engineered Escherichia coli Extracellular ATP inhibits chloride channels in mature mammalian skeletal muscle by activating P2Y1 receptors Daniel Miranda Dr. Andrew Voss Progressive Cl− channel defects reveal disrupted skeletal muscle maturation in R6/2 Huntington’s mice A Forward-Design Approach to Increase the Production of Poly-3-Hydroxybutyrate in Genetically Depressed Synaptic Transmission and Reduced Vesicle Release Sites in Huntington’s Disease Neuromuscular Junctions Levator Auris Longus Preparation for Examination of Mammalian Neuromuscular Transmission Under Voltage Clamp Conditions Treatment of myotonia congenita with retigabine in mice Central Role of Subthreshold Currents in Myotonia Depressed neuromuscular transmission causes weakness in mice lacking BK potassium channels TRPV4 Antagonism Prevents Mechanically Induced Myotonia Mechanisms of altered skeletal muscle action potentials in the R6/2 mouse model of Huntington’s disease Loss of membrane integrity drives myofiber death in lipin1deficient skeletal muscle A mouse model of Huntington’s disease shows altered ultrastructure of transverse tubules in skeletal muscle fibers Increase the Production of Poly-3-Hydroxybutyrate in Genetically Engineered Escherichia coli A Forward-Design Approach to Increase the Production of Poly-3-Hydroxybutyrate in Genetically Increase the Production of Poly-3-Hydroxybutyrate in Genetically Engineered Escherichia coli Increase the Production of Poly-3-Hydroxybutyrate in Genetically Engineered Escherichia coli Huntington disease skeletal muscle is hyperexcitable owing to chloride and potassium channel dysfunction A Forward-Design Approach to Increase the Production of Poly-3-Hydroxybutyrate in Genetically Increase the Production of Poly-3-Hydroxybutyrate in Genetically Engineered Escherichia coli Progressive impairment of CaV1.1 function in the skeletal muscle of mice expressing a mutant type 1 Cu/Zn superoxide dismutase (G93A) linked to amyotrophic lateral sclerosis A Forward-Design Approach to Increase the Production of Poly-3-Hydroxybutyrate in Genetically Haematopoietic stem cell transplantation for autoimmune diseases Dr. Voss Neuromuscular Physiology Lab