Daniel C. Bartos, Ph.D.
Affiliations: | 2013 | Physiology | University of Kentucky, Lexington, KY |
Area:
Physiology Biology, General BiophysicsGoogle:
"Daniel Bartos"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Brian P. Delisle | grad student | 2013 | University of Kentucky | |
| (Mechanistic basis for atrial and ventricular arrhythmias caused by KCNQ1 mutations.) | ||||
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Publications
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| Kekenes-Huskey PM, Burgess DE, Sun B, et al. (2022) Mutation-Specific Differences in Kv7.1 () and Kv11.1 () Channel Dysfunction and Long QT Syndrome Phenotypes. International Journal of Molecular Sciences. 23 |
| Liao Z, Ginsburg KS, Bartos DC, et al. (2017) High Diastolic Sodium Influx in Heart Failure has Drug-Sensitivities Like Late Sodium Current, but Produces Inward Current at Diastolic Potentials Biophysical Journal. 112: 333a |
| Grandi E, Sanguinetti MC, Bartos DC, et al. (2016) Potassium channels in the heart: structure, function and regulation. The Journal of Physiology |
| Ackerman JP, Bartos DC, Kapplinger JD, et al. (2016) The Promise and Peril of Precision Medicine: Phenotyping Still Matters Most. Mayo Clinic Proceedings |
| Bartos DC, Grandi E, Ripplinger CM. (2015) Ion Channels in the Heart. Comprehensive Physiology. 5: 1423-64 |
| Schroder EA, Burgess DE, Zhang X, et al. (2015) The cardiomyocyte molecular clock regulates the circadian expression of Kcnh2 and contributes to ventricular repolarization. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 12: 1306-14 |
| Bartos DC, Giudicessi JR, Tester DJ, et al. (2014) A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 459-68 |
| Smith JL, Reloj AR, Nataraj PS, et al. (2013) Pharmacological correction of long QT-linked mutations in KCNH2 (hERG) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulum. American Journal of Physiology. Cell Physiology. 305: C919-30 |
| Crotti L, Tester DJ, White WM, et al. (2013) Long QT syndrome-associated mutations in intrauterine fetal death. Jama. 309: 1473-82 |
| McBride CM, Smith AM, Smith JL, et al. (2013) Mechanistic basis for type 2 long QT syndrome caused by KCNH2 mutations that disrupt conserved arginine residues in the voltage sensor. The Journal of Membrane Biology. 246: 355-64 |