Chloroquine or Hydroxychloroquine for COVID‐19: Is Cardiotoxicity a Concern?

por Kamp, Timothy J., Hamdan, Mohamed H., January, Craig T.
Publicado 2020

Atrial Fibrillation and Long QT Syndrome Presenting in a 12-Year-Old Girl

por Knoche, Jonathan W., Orland, Kate M., January, Craig T., Maginot, Kathleen R.
Publicado 2012

Molecular pathogenesis of long QT syndrome type 2

por Smith, Jennifer L., Anderson, Corey L., Burgess, Don E., Elayi, Claude S., January, Craig T., Delisle, Brian P.
Publicado 2016

Large-scale Mutational Analysis of Kv11.1 Reveals Molecular Insights into Type 2 Long QT Syndrome

por Anderson, Corey L., Kuzmicki, Catherine E., Childs, Ryan R., Hintz, Caleb J., Delisle, Brian P., January, Craig T.
Publicado 2014

A rapid solubility assay of protein domain misfolding for pathogenicity assessment of rare DNA sequence variants

por Anderson, Corey L., Routes, Tim C., Eckhardt, Lee L., Delisle, Brian P., January, Craig T., Kamp, Timothy J.
Publicado 2020

Visualizing Mutation-Specific Differences in the Trafficking-Deficient Phenotype of Kv11.1 Proteins Linked to Long QT Syndrome Type 2

por Hall, Allison R., Anderson, Corey L., Smith, Jennifer L., Mirshahi, Tooraj, Elayi, Claude S., January, Craig T., Delisle, Brian P.
Publicado 2018

How Functional Genomics Can Keep Pace With VUS Identification

por Anderson, Corey L., Munawar, Saba, Reilly, Louise, Kamp, Timothy J., January, Craig T., Delisle, Brian P., Eckhardt, Lee L.
Publicado 2022

Flecainide treats a novel KCNJ2 mutation associated with Andersen-Tawil syndrome

por Van Ert, Hanora A., McCune, Elise C., Orland, Kate M., Maginot, Kathleen R., Von Bergen, Nicholas H., January, Craig T., Eckhardt, Lee L.
Publicado 2016

Mouse ERG K(+) Channel Clones Reveal Differences in Protein Trafficking and Function

por Lin, Eric C., Moungey, Brooke M., Lim, Evi, Concannon, Sarah P., Anderson, Corey L., Kyle, John W., Makielski, Jonathan C., Balijepalli, Sadguna Y., January, Craig T.
Publicado 2014

Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 KCNH2 (hERG) Mutations and Identifying New Patients

por Ono, Makoto, Burgess, Don E., Schroder, Elizabeth A., Elayi, Claude S., Anderson, Corey L., January, Craig T., Sun, Bin, Immadisetty, Kalyan, Kekenes-Huskey, Peter M., Delisle, Brian P.
Publicado 2020

Mutation-Specific Differences in Kv7.1 (KCNQ1) and Kv11.1 (KCNH2) Channel Dysfunction and Long QT Syndrome Phenotypes

por Kekenes-Huskey, Peter M., Burgess, Don E., Sun, Bin, Bartos, Daniel C., Rozmus, Ezekiel R., Anderson, Corey L., January, Craig T., Eckhardt, Lee L., Delisle, Brian P.
Publicado 2022

Calcium Transients Closely Reflect Prolonged Action Potentials in iPSC Models of Inherited Cardiac Arrhythmia

por Spencer, C. Ian, Baba, Shiro, Nakamura, Kenta, Hua, Ethan A., Sears, Marie A.F., Fu, Chi-cheng, Zhang, Jianhua, Balijepalli, Sadguna, Tomoda, Kiichiro, Hayashi, Yohei, Lizarraga, Paweena, Wojciak, Julianne, Scheinman, Melvin M., Aalto-Setälä, Katriina, Makielski, Jonathan C., January, Craig T., Healy, Kevin E., Kamp, Timothy J., Yamanaka, Shinya, Conklin, Bruce R.
Publicado 2014