Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Craig T January

Showing results (11-20 of 58) with videos related to

Pageof 6
Sort By:
Journal of Cardiovascular Pharmacology|March 13, 2010
Rescue of mutated cardiac ion channels in inherited arrhythmia syndromesSadguna Y Balijepalli, Corey L Anderson, Eric C Lin, et al.
Cardiovascular Research|May 29, 2002
Rate-dependent QT shortening mechanism for the LQT3 deltaKPQ mutantToshihisa Nagatomo, Craig T January, Bin Ye, et al.
American Journal of Physiology. Heart and Circulatory Physiology|July 14, 2009
Reduction of repolarization reserve unmasks the proarrhythmic role of endogenous late Na(+) current in the heartLin Wu, Sridharan Rajamani, Hong Li, et al.
American Journal of Physiology. Heart and Circulatory Physiology|April 10, 2016
IK1-enhanced human-induced pluripotent stem cell-derived cardiomyocytes: an improved cardiomyocyte model to investigate inherited arrhythmia syndromesRavi Vaidyanathan, Yogananda S Markandeya, Timothy J Kamp, et al.
The Journal of Biological Chemistry|July 3, 2003
Thapsigargin selectively rescues the trafficking defective LQT2 channels G601S and F805CBrian P Delisle, Corey L Anderson, Ravi C Balijepalli, et al.
American Journal of Physiology. Cell Physiology|April 15, 2011
Trafficking-deficient hERG K⁺ channels linked to long QT syndrome are regulated by a microtubule-dependent quality control compartment in the ERJennifer L Smith, Christie M McBride, Parvathi S Nataraj, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 2, 2020
A rapid solubility assay of protein domain misfolding for pathogenicity assessment of rare DNA sequence variantsCorey L Anderson, Tim C Routes, Lee L Eckhardt, et al.
Journal of Arrhythmia|October 21, 2016
Molecular pathogenesis of long QT syndrome type 2Jennifer L Smith, Corey L Anderson, Don E Burgess, et al.
Current Cardiology Reports|August 10, 2002
Genetic basis for the origin of cardiac arrhythmias: implications for therapyMackenzi Mbai, Sridharan Rajamani, Brian P Delisle, et al.
Nature Communications|November 25, 2014
Large-scale mutational analysis of Kv11.1 reveals molecular insights into type 2 long QT syndromeCorey L Anderson, Catherine E Kuzmicki, Ryan R Childs, et al.
Pageof 6

Showing results (11-20 of 58) with videos related to

Sort By:
Pageof 6
Journal of Cardiovascular Pharmacology|March 13, 2010
Rescue of mutated cardiac ion channels in inherited arrhythmia syndromesSadguna Y Balijepalli, Corey L Anderson, Eric C Lin, et al.
Cardiovascular Research|May 29, 2002
Rate-dependent QT shortening mechanism for the LQT3 deltaKPQ mutantToshihisa Nagatomo, Craig T January, Bin Ye, et al.
American Journal of Physiology. Heart and Circulatory Physiology|July 14, 2009
Reduction of repolarization reserve unmasks the proarrhythmic role of endogenous late Na(+) current in the heartLin Wu, Sridharan Rajamani, Hong Li, et al.
American Journal of Physiology. Heart and Circulatory Physiology|April 10, 2016
IK1-enhanced human-induced pluripotent stem cell-derived cardiomyocytes: an improved cardiomyocyte model to investigate inherited arrhythmia syndromesRavi Vaidyanathan, Yogananda S Markandeya, Timothy J Kamp, et al.
The Journal of Biological Chemistry|July 3, 2003
Thapsigargin selectively rescues the trafficking defective LQT2 channels G601S and F805CBrian P Delisle, Corey L Anderson, Ravi C Balijepalli, et al.
American Journal of Physiology. Cell Physiology|April 15, 2011
Trafficking-deficient hERG K⁺ channels linked to long QT syndrome are regulated by a microtubule-dependent quality control compartment in the ERJennifer L Smith, Christie M McBride, Parvathi S Nataraj, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 2, 2020
A rapid solubility assay of protein domain misfolding for pathogenicity assessment of rare DNA sequence variantsCorey L Anderson, Tim C Routes, Lee L Eckhardt, et al.
Journal of Arrhythmia|October 21, 2016
Molecular pathogenesis of long QT syndrome type 2Jennifer L Smith, Corey L Anderson, Don E Burgess, et al.
Current Cardiology Reports|August 10, 2002
Genetic basis for the origin of cardiac arrhythmias: implications for therapyMackenzi Mbai, Sridharan Rajamani, Brian P Delisle, et al.
Nature Communications|November 25, 2014
Large-scale mutational analysis of Kv11.1 reveals molecular insights into type 2 long QT syndromeCorey L Anderson, Catherine E Kuzmicki, Ryan R Childs, et al.
Pageof 6