In Memoriam: Harry A. Fozzard, MD, 1931–2014

Por Kamp, Timothy J., January, Craig T.
Publicado no Circ Res (2015)

Differences in action potential and early afterdepolarization properties in LQT2 and LQT3 models of long QT syndrome

Por Studenik, Christian R, Zhou, Zhengfeng, January, Craig T
Publicado em 2001

Protein trafficking abnormalities: a new mechanism in drug-induced long QT syndrome

Por Eckhardt, Lee L, Rajamani, Sridharan, January, Craig T
Publicado em 2005

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

Por Kamp, Timothy J., Hamdan, Mohamed H., January, Craig T.
Publicado no J Am Heart Assoc (2020)

Effect of microculture on cell metabolism and biochemistry: Do cells get stressed in microchannels?

Por Su, Xiaojing, Theberge, Ashleigh B., January, Craig T., Beebe, David J.
Publicado em 2013

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 em 2012

Rescue of Mutated Cardiac Ion Channels in Inherited Arrhythmia Syndromes

Por Balijepalli, Sadguna Y., Anderson, Corey L., Lin, Eric C., January, Craig T.
Publicado no J Cardiovasc Pharmacol (2010)

I(K1)-enhanced human-induced pluripotent stem cell-derived cardiomyocytes: an improved cardiomyocyte model to investigate inherited arrhythmia syndromes

Por Vaidyanathan, Ravi, Markandeya, Yogananda S., Kamp, Timothy J., Makielski, Jonathan C., January, Craig T., Eckhardt, Lee L.
Publicado no Am J Physiol Heart Circ Physiol (2016)

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 no J Arrhythm (2016)

Microfluidic Cell Culture and Its Application in High Throughput Drug Screening: Cardiotoxicity Assay for hERG Channels

Por Su, Xiaojing, Young, Edmond W.K., Underkofler, Heather A. S., Kamp, Timothy J., January, Craig T., Beebe, David J.
Publicado em 2010

Trafficking-deficient hERG K(+) channels linked to long QT syndrome are regulated by a microtubule-dependent quality control compartment in the ER

Por Smith, Jennifer L., McBride, Christie M., Nataraj, Parvathi S., Bartos, Daniel C., January, Craig T., Delisle, Brian P.
Publicado em 2011

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 no Nat Commun (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 no Genet Med (2020)

Blockade of HERG cardiac K(+) current by antifungal drug miconazole

Por Kikuchi, Kan, Nagatomo, Toshihisa, Abe, Haruhiko, Kawakami, Kazunobu, Duff, Henry J, Makielski, Jonathan C, January, Craig T, Nakashima, Yasuhide
Publicado em 2004

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 no Front Physiol (2018)

Comparison of HERG channel blocking effects of various β-blockers – implication for clinical strategy

Por Kawakami, Kazunobu, Nagatomo, Toshihisa, Abe, Haruhiko, Kikuchi, Kan, Takemasa, Hiroko, Anson, Blake D, Delisle, Brian P, January, Craig T, Nakashima, Yasuhide
Publicado em 2005

Small GTPase Rab11b regulates degradation of surface membrane L-type Ca(v)1.2 channels

Por Best, Jabe M., Foell, Jason D., Buss, Courtney R., Delisle, Brian P., Balijepalli, Ravi C., January, Craig T., Kamp, Timothy J.
Publicado em 2011

Novel Chemical Suppressors of Long QT Syndrome Identified by an in vivo Functional Screen

Por Peal, David S., Mills, Robert W., Lynch, Stacey N., Mosley, Janet M., Lim, Evi, Elllinor, Patrick T., January, Craig T., Peterson, Randall T., Milan, David J.
Publicado em 2010

The common African American polymorphism SCN5A-S1103Y interacts with mutation SCN5A-R680H to increase late Na current

Por Cheng, Jianding, Tester, David J., Tan, Bi-Hua, Valdivia, Carmen R., Kroboth, Stacie, Ye, Bin, January, Craig T., Ackerman, Michael J., Makielski, Jonathan C.
Publicado em 2011

KCNJ2 Mutation Causes an Adrenergic-Dependent Rectification Abnormality with Calcium Sensitivity and Ventricular Arrhythmia

Por Kalscheur, Matthew M., Vaidyanathan, Ravi, Orland, Kate M., Abozeid, Sara, Fabry, Nicholas, Maginot, Kathleen R., January, Craig T., Makielski, Jonathan C., Eckhardt, Lee L.
Publicado no Heart Rhythm (2014)