Craig T. January
Affiliations: | Biophysics | University of Wisconsin, Madison, Madison, WI |
Area:
General Biophysics, Biochemistry, Physiology BiologyGoogle:
"Craig January"Mean distance: (not calculated yet)
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Publications
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| Anderson CL, Munawar S, Reilly L, et al. (2022) How Functional Genomics Can Keep Pace With VUS Identification. Frontiers in Cardiovascular Medicine. 9: 900431 |
| 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 |
| Ono M, Burgess DE, Schroder EA, et al. (2020) Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 () Mutations and Identifying New Patients. Biomolecules. 10 |
| Ng K, Titus EW, Lieve KV, et al. (2020) An International Multi-Center Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of - Catecholaminergic Polymorphic Ventricular Tachycardia. Circulation |
| Anderson CL, Routes TC, Eckhardt LL, et al. (2020) A rapid solubility assay of protein domain misfolding for pathogenicity assessment of rare DNA sequence variants. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Qile M, Ji Y, Golden TD, et al. (2020) LUF7244 plus dofetilide rescues aberrant Kv11.1 trafficking and produces functional IKv11.1. Molecular Pharmacology |
| Mellor GJ, Panwar P, Lee AK, et al. (2019) Type 8 long QT syndrome: pathogenic variants in CACNA1C-encoded Cav1.2 cluster in STAC protein binding site. Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups On Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology |
| Hall AR, Anderson CL, Smith JL, et al. (2018) Visualizing Mutation-Specific Differences in the Trafficking-Deficient Phenotype of Kv11.1 Proteins Linked to Long QT Syndrome Type 2. Frontiers in Physiology. 9: 584 |
| Smith JL, Tester DJ, Hall AR, et al. (2018) Functional Invalidation of Putative Sudden Infant Death Syndrome-Associated Variants in the -Encoded Kv11.1 Channel. Circulation. Arrhythmia and Electrophysiology. 11: e005859 |
| Delisle BP, January CT. (2018) Advancing precision medicine for the treatment of long-QT syndrome type 2: shedding light on lumacaftor. European Heart Journal. 39: 1456-1458 |