Publications by authors named "Andrew A Voss"

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Discovery and Treatment of Action Potential-Independent Myotonia in Hyperkalemic Periodic Paralysis.
Chris Dupont, Adam Deardorff, Murad Nawaz, Andrew A Voss, Mark M Rich

Ann Clin Transl Neurol· October 2025

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BK channels promote action potential repolarization in skeletal muscle but contribute little to myotonia.
Chris Dupont, Brianna Blake, Andrew A Voss, Mark M Rich

Pflugers Arch· November 2024

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Exploring lipin1 as a promising therapeutic target for the treatment of Duchenne muscular dystrophy.
Abdulrahman Jama, Abdullah A Alshudukhi, Steve Burke, Lixin Dong, John Karanja Kamau, Andrew Alvin Voss

J Transl Med· July 2024

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Voltage sensor current, SR Ca release, and Ca channel current during trains of action potential-like depolarizations of skeletal muscle fibers.
Hugo Bibollet, Elton L Nguyen, Daniel R Miranda, Christopher W Ward, Andrew A Voss

Physiol Rep· May 2023

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Plateau potentials contribute to myotonia in mouse models of myotonia congenita.
Xueyong Wang, Chris Dupont, Delaney Grant, Andrew A Voss, Mark M Rich

Exp Neurol· March 2023

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Lipin1 plays complementary roles in myofibre stability and regeneration in dystrophic muscles.
Abdulrahman Jama, Abdullah A Alshudukhi, Steve Burke, Lixin Dong, John Karanja Kamau, Andrew Alvin Voss

J Physiol· March 2023

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The role of action potential changes in depolarization-induced failure of excitation contraction coupling in mouse skeletal muscle.
Xueyong Wang, Murad Nawaz, Chris DuPont, Jessica H Myers, Steve Ra Burke, Andrew A Voss

Elife· January 2022

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Acetylcholine receptor subunit expression in Huntington's disease mouse muscle.
Briana Simpson, Mark M Rich, Andrew A Voss, Robert J Talmadge

Biochem Biophys Rep· December 2021

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Into the spotlight: RGK proteins in skeletal muscle.
Daniel R Miranda, Andrew A Voss, Roger A Bannister

Cell Calcium· September 2021

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A mouse model of Huntington's disease shows altered ultrastructure of transverse tubules in skeletal muscle fibers.
Shannon H Romer, Sabrina Metzger, Kristiana Peraza, Matthew C Wright, D Scott Jobe, Andrew A Voss

J Gen Physiol· April 2021

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The mechanism underlying transient weakness in myotonia congenita.
Jessica H Myers, Kirsten Denman, Chris DuPont, Ahmed A Hawash, Kevin R Novak, Andrew A Voss

Elife· April 2021

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Loss of membrane integrity drives myofiber death in lipin1-deficient skeletal muscle.
Sandhya Ramani Sattiraju, Abdulrahman Jama, Abdullah A Alshudukhi, Nicholas Edward Townsend, Daniel Reynold Miranda, Andrew A Voss

Physiol Rep· October 2020

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TRPV4 Antagonism Prevents Mechanically Induced Myotonia.
Chris Dupont, Kevin Novak, Kirsten Denman, Jessica H Myers, Jeremy M Sullivan, Andrew A Voss

Ann Neurol· August 2020

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Mechanisms of altered skeletal muscle action potentials in the R6/2 mouse model of Huntington's disease.
Daniel R Miranda, Eric Reed, Abdulrahman Jama, Michael Bottomley, Hongmei Ren, Andrew A Voss

Am J Physiol Cell Physiol· July 2020

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Depressed neuromuscular transmission causes weakness in mice lacking BK potassium channels.
Xueyong Wang, Steven R A Burke, Robert J Talmadge, Andrew A Voss, Mark M Rich

J Gen Physiol· May 2020

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Central Role of Subthreshold Currents in Myotonia.
Sabrina Metzger, Chris Dupont, Andrew A Voss, Mark M Rich

Ann Neurol· February 2020

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Treatment of myotonia congenita with retigabine in mice.
Chris Dupont, Kirsten S Denman, Ahmed A Hawash, Andrew A Voss, Mark M Rich

Exp Neurol· May 2019

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Levator Auris Longus Preparation for Examination of Mammalian Neuromuscular Transmission Under Voltage Clamp Conditions.
Steven R A Burke, Eric J Reed, Shannon H Romer, Andrew A Voss

J Vis Exp· May 2018

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Inhibiting persistent inward sodium currents prevents myotonia.
Ahmed A Hawash, Andrew A Voss, Mark M Rich

Ann Neurol· September 2017

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Depressed Synaptic Transmission and Reduced Vesicle Release Sites in Huntington's Disease Neuromuscular Junctions.
Ahmad Khedraki, Eric J Reed, Shannon H Romer, Qingbo Wang, William Romine, Andrew A Voss

J Neurosci· August 2017

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Progressive Cl- channel defects reveal disrupted skeletal muscle maturation in R6/2 Huntington's mice.
Daniel R Miranda, Monica Wong, Shannon H Romer, Cynthia McKee, Gabriela Garza-Vasquez, Andrew A Voss

J Gen Physiol· January 2017

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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.
Donald Beqollari, Christin F Romberg, Gabriella Dobrowolny, Martina Martini, Andrew A Voss

Skelet Muscle· October 2016

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Huntington disease skeletal muscle is hyperexcitable owing to chloride and potassium channel dysfunction.
Christopher W Waters, Grigor Varuzhanyan, Robert J Talmadge, Andrew A Voss

Proc Natl Acad Sci U S A· May 2013

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Glucose transport by human renal Na+/D-glucose cotransporters SGLT1 and SGLT2.
Charles S Hummel, Chuan Lu, Donald D F Loo, Bruce A Hirayama, Andrew A Voss

Am J Physiol Cell Physiol· January 2011

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Extracellular ATP inhibits chloride channels in mature mammalian skeletal muscle by activating P2Y1 receptors.
Andrew A Voss

J Physiol· December 2009

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