| Year |
Citation |
Score |
| 2024 |
Dupont C, Blake B, Voss AA, Rich MM. BK channels promote action potential repolarization in skeletal muscle but contribute little to myotonia. Pflugers Archiv : European Journal of Physiology. PMID 39150500 DOI: 10.1007/s00424-024-03005-z |
0.316 |
|
| 2022 |
Wang X, Dupont C, Grant D, Voss AA, Rich MM. Plateau potentials contribute to myotonia in mouse models of myotonia congenita. Experimental Neurology. 361: 114303. PMID 36563835 DOI: 10.1016/j.expneurol.2022.114303 |
0.321 |
|
| 2021 |
Miranda DR, Voss AA, Bannister RA. Into the spotlight: RGK proteins in skeletal muscle. Cell Calcium. 98: 102439. PMID 34261001 DOI: 10.1016/j.ceca.2021.102439 |
0.311 |
|
| 2021 |
Myers JH, Denman K, DuPont C, Hawash AA, Novak KR, Koesters A, Grabner M, Dayal A, Voss AA, Rich MM. The mechanism underlying transient weakness in myotonia congenita. Elife. 10. PMID 33904400 DOI: 10.7554/eLife.65691 |
0.324 |
|
| 2020 |
Miranda DR, Reed E, Jama A, Bottomley M, Ren H, Rich MM, Voss AA. Mechanisms of altered skeletal muscle action potentials in the R6/2 mouse model of Huntington's disease. American Journal of Physiology. Cell Physiology. PMID 32432924 DOI: 10.1152/Ajpcell.00153.2020 |
0.363 |
|
| 2020 |
Dupont C, Novak K, Denman K, Myers JH, Sullivan JM, Walker PV, Brown NL, Ladle DR, Bogdanik L, Lutz CM, Voss A, Sumner CJ, Rich MM. TRPV4 antagonism prevents mechanically-induced myotonia. Annals of Neurology. PMID 32418267 DOI: 10.1002/Ana.25780 |
0.334 |
|
| 2020 |
Wang X, Burke SRA, Talmadge RJ, Voss AA, Rich MM. Depressed neuromuscular transmission causes weakness in mice lacking BK potassium channels. The Journal of General Physiology. 152. PMID 32243496 DOI: 10.1085/Jgp.201912526 |
0.385 |
|
| 2020 |
Burke SRA, Voss AA. In Vivo Force Experiments Suggest Calcium Handling Defects during Repetitive Activity in Huntingtion's Disease Skeletal Muscle Biophysical Journal. 118. DOI: 10.1016/J.Bpj.2019.11.2313 |
0.343 |
|
| 2019 |
Metzger S, Dupont C, Voss AA, Rich MM. The central role of subthreshold currents in myotonia. Annals of Neurology. PMID 31725924 DOI: 10.1002/Ana.25646 |
0.329 |
|
| 2019 |
Dupont C, Denman KS, Hawash AA, Voss AA, Rich MM. Treatment of myotonia congenita with retigabine in mice. Experimental Neurology. 315: 52-59. PMID 30738808 DOI: 10.1016/J.Expneurol.2019.02.002 |
0.391 |
|
| 2018 |
Burke SRA, Reed EJ, Romer SH, Voss AA. Levator Auris Longus Preparation for Examination of Mammalian Neuromuscular Transmission Under Voltage Clamp Conditions. Journal of Visualized Experiments : Jove. PMID 29782004 DOI: 10.3791/57482 |
0.309 |
|
| 2018 |
Romer SH, Bautista M, Hutcherson DE, Talmadge RJ, Voss AA. Architecture of Transverse Tubules and Triads in Huntington's Disease Skeletal Muscle Biophysical Journal. 114. DOI: 10.1016/J.Bpj.2017.11.2583 |
0.341 |
|
| 2017 |
Hawash AA, Voss AA, Rich MM. Inhibiting persistent inward sodium currents prevents myotonia. Annals of Neurology. PMID 28833464 DOI: 10.1002/Ana.25017 |
0.383 |
|
| 2017 |
Khedraki A, Reed EJ, Romer SH, Wang Q, Romine W, Rich MM, Talmadge RJ, Voss AA. Depressed Synaptic Transmission and Reduced Vesicle Release Sites in Huntington's Disease Neuromuscular Junctions. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 28724748 DOI: 10.1523/Jneurosci.0313-17.2017 |
0.37 |
|
| 2016 |
Miranda DR, Wong M, Romer SH, McKee C, Garza-Vasquez G, Medina AC, Bahn V, Steele AD, Talmadge RJ, Voss AA. Progressive Cl- channel defects reveal disrupted skeletal muscle maturation in R6/2 Huntington's mice. The Journal of General Physiology. PMID 27899419 DOI: 10.1085/Jgp.201611603 |
0.354 |
|
| 2016 |
Beqollari D, Romberg CF, Dobrowolny G, Martini M, Voss AA, MusarĂ² A, Bannister RA. 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 Muscle. 6: 24. PMID 27340545 DOI: 10.1186/S13395-016-0094-6 |
0.363 |
|
| 2009 |
Voss AA. Extracellular ATP inhibits chloride channels in mature mammalian skeletal muscle by activating P2Y1 receptors. The Journal of Physiology. 587: 5739-52. PMID 19805741 DOI: 10.1113/Jphysiol.2009.179275 |
0.383 |
|
| 2009 |
Voss A, Vergara J. ATP Regulates Mammalian Neuromuscular Transmission by Dramatically Decreasing the Resting Muscle Chloride Conductance via P2Y1 Biophysical Journal. 96: 165a. DOI: 10.1016/J.Bpj.2008.12.759 |
0.38 |
|
| 2008 |
Voss AA, Allen PD, Pessah IN, Perez CF. Allosterically coupled calcium and magnesium binding sites are unmasked by ryanodine receptor chimeras. Biochemical and Biophysical Research Communications. 366: 988-93. PMID 18096513 DOI: 10.1016/J.Bbrc.2007.12.058 |
0.5 |
|
| 2005 |
Gao J, Voss AA, Pessah IN, Lauer FT, Penning TM, Burchiel SW. Ryanodine receptor-mediated rapid increase in intracellular calcium induced by 7,8-benzo(a)pyrene quinone in human and murine leukocytes. Toxicological Sciences : An Official Journal of the Society of Toxicology. 87: 419-26. PMID 16049270 DOI: 10.1093/Toxsci/Kfi265 |
0.497 |
|
| 2004 |
Voss AA, Lango J, Ernst-Russell M, Morin D, Pessah IN. Identification of hyperreactive cysteines within ryanodine receptor type 1 by mass spectrometry. The Journal of Biological Chemistry. 279: 34514-20. PMID 15197184 DOI: 10.1074/Jbc.M404290200 |
0.462 |
|
| 2003 |
Perez CF, Voss A, Pessah IN, Allen PD. RyR1/RyR3 chimeras reveal that multiple domains of RyR1 are involved in skeletal-type E-C coupling. Biophysical Journal. 84: 2655-63. PMID 12668474 DOI: 10.1016/S0006-3495(03)75071-1 |
0.46 |
|
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