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Depressed neuromuscular transmission causes weakness in mice lacking BK potassium channels Journal of General PhysiologyDepressed neuromuscular transmission causes weakness in mice lacking BK potassium channels

Levator Auris Longus Preparation for Examination of Mammalian Neuromuscular Transmission Under Voltage Clamp Conditions Journal of Visualized ExperimentsLevator Auris Longus Preparation for Examination of Mammalian Neuromuscular Transmission Under Voltage Clamp Conditions

Depressed Synaptic Transmission and Reduced Vesicle Release Sites in Huntington’s Disease Neuromuscular Junctions The Journal of NeuroscienceDepressed Synaptic Transmission and Reduced Vesicle Release Sites in Huntington's Disease Neuromuscular Junctions

Extracellular ATP inhibits chloride channels in mature mammalian skeletal muscle by activating P2Y1 receptors The Journal of PhysiologyExtracellular ATP inhibits chloride channels in mature mammalian skeletal muscle by activating P2Y1 receptors

TRPV4 Antagonism Prevents Mechanically Induced Myotonia Annals of NeurologyTRPV4 Antagonism Prevents Mechanically Induced Myotonia

Central Role of Subthreshold Currents in Myotonia Annals of NeurologyCentral Role of Subthreshold Currents in Myotonia

Treatment of myotonia congenita with retigabine in mice Experimental NeurologyTreatment of myotonia congenita with retigabine in mice

Loss of membrane integrity drives myofiber death in lipin1deficient skeletal muscle Physiological Reports

Loss of membrane integrity drives myofiber death in lipin1deficient skeletal muscle Physiological Reports

TRPV4 Antagonism Prevents Mechanically Induced Myotonia Annals of NeurologyTRPV4 Antagonism Prevents Mechanically Induced Myotonia

Acetylcholine receptor subunit expression in Huntington’s disease mouse muscle Biochemistry and Biophysics Reports

A mouse model of Huntington’s disease shows altered ultrastructure of transverse tubules in skeletal muscle fibers Journal of General Physiology

Mechanisms of altered skeletal muscle action potentials in the R6/2 mouse model of Huntington’s disease American Journal of Physiology - Cell PhysiologyMechanisms of altered skeletal muscle action potentials in the R6/2 mouse model of Huntington’s disease

Depressed neuromuscular transmission causes weakness in mice lacking BK potassium channels Journal of General PhysiologyDepressed neuromuscular transmission causes weakness in mice lacking BK potassium channels

Depressed Synaptic Transmission and Reduced Vesicle Release Sites in Huntington’s Disease Neuromuscular Junctions The Journal of NeuroscienceDepressed Synaptic Transmission and Reduced Vesicle Release Sites in Huntington's Disease Neuromuscular Junctions

Progressive Cl− channel defects reveal disrupted skeletal muscle maturation in R6/2 Huntington’s mice Journal of General PhysiologyProgressive Cl− channel defects reveal disrupted skeletal muscle maturation in R6/2 Huntington’s mice

Huntington disease skeletal muscle is hyperexcitable owing to chloride and potassium channel dysfunction National Academy of SciencesHuntington disease skeletal muscle is hyperexcitable owing to chloride and potassium channel dysfunction

Glucose transport by human renal Na+/d-glucose cotransporters SGLT1 and SGLT2 American Journal of Physiology - Cell Physiology

Imino sugars are potent agonists of the human glucose sensor SGLT3 Molecular Pharmacology

A mouse model of Huntington’s disease shows altered ultrastructure of transverse tubules in skeletal muscle fibers Journal of General Physiology

Mechanisms of altered skeletal muscle action potentials in the R6/2 mouse model of Huntington’s disease American Journal of Physiology - Cell PhysiologyMechanisms of altered skeletal muscle action potentials in the R6/2 mouse model of Huntington’s disease

TRPV4 Antagonism Prevents Mechanically Induced Myotonia Annals of NeurologyTRPV4 Antagonism Prevents Mechanically Induced Myotonia

Central Role of Subthreshold Currents in Myotonia Annals of NeurologyCentral Role of Subthreshold Currents in Myotonia

Treatment of myotonia congenita with retigabine in mice Experimental NeurologyTreatment of myotonia congenita with retigabine in mice

Progressive Cl− channel defects reveal disrupted skeletal muscle maturation in R6/2 Huntington’s mice Journal of General PhysiologyProgressive Cl− channel defects reveal disrupted skeletal muscle maturation in R6/2 Huntington’s mice

Huntington disease skeletal muscle is hyperexcitable owing to chloride and potassium channel dysfunction National Academy of SciencesHuntington disease skeletal muscle is hyperexcitable owing to chloride and potassium channel dysfunction

Glucose transport by human renal Na+/d-glucose cotransporters SGLT1 and SGLT2 American Journal of Physiology - Cell Physiology

Extracellular ATP inhibits chloride channels in mature mammalian skeletal muscle by activating P2Y1 receptors The Journal of PhysiologyExtracellular ATP inhibits chloride channels in mature mammalian skeletal muscle by activating P2Y1 receptors

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 Skeletal MuscleProgressive 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

Allosterically coupled calcium and magnesium binding sites are unmasked by ryanodine receptor chimeras Biochemical and Biophysical Research Communications Allosterically coupled calcium and magnesium binding sites are unmasked by ryanodine receptor chimeras

Ryanodine receptor-mediated rapid increase in intracellular calcium induced by 7,8-benzo(a)pyrene quinone in human and murine leukocytes Toxicological SciencesRyanodine receptor-mediated rapid increase in intracellular calcium induced by 7,8-benzo(a)pyrene quinone in human and murine leukocytes

Identification of Hyperreactive Cysteines within Ryanodine Receptor Type 1 by Mass Spectrometry The Journal of Biological Chemistry Vol. 279, No. 33Identification of Hyperreactive Cysteines within Ryanodine Receptor Type 1 by Mass Spectrometry

RyR1/RyR3 chimeras reveal that multiple domains of RyR1 are involved in skeletal-type E-C coupling Biophysical Journal Volume 84 Issue 4RyR1/RyR3 Chimeras Reveal that Multiple Domains of RyR1 Are Involved in Skeletal-Type E-C Coupling

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 Skeletal MuscleProgressive 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