Brian P. Delisle

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Anees P, Saminathan A, Rozmus ER, et al. (2023) Detecting organelle-specific activity of potassium channels with a DNA nanodevice. Nature Biotechnology
Fang X, Immadisetty K, Ramon GS, et al. (2023) Prediction of Kv11.1 potassium channel PAS-domain variants trafficking via machine learning. Journal of Molecular and Cellular Cardiology
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
Schroder EA, Wayland JL, Samuels KM, et al. (2021) Cardiomyocyte Deletion of Exacerbates QT- and RR-Interval Prolongation in Mice. Frontiers in Physiology. 12: 681011
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
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
van der Heyden MAG, Delisle BP, Abriel H. (2018) Editorial: Ion Channel Trafficking and Cardiac Arrhythmias. Frontiers in Physiology. 9: 1254
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