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Corey L Anderson

Showing results (21-30 of 28) with videos related to

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International Journal of Molecular Sciences|July 9, 2022
Mutation-Specific Differences in Kv7.1 (<i>KCNQ1</i>) and Kv11.1 (<i>KCNH2</i>) Channel Dysfunction and Long QT Syndrome PhenotypesPeter M Kekenes-Huskey, Don E Burgess, Bin Sun, et al.
Biomolecules|August 8, 2020
Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 <i>KCNH2</i> (<i>hERG</i>) Mutations and Identifying New PatientsMakoto Ono, Don E Burgess, Elizabeth A Schroder, et al.
Circulation|January 25, 2006
Most LQT2 mutations reduce Kv11.1 (hERG) current by a class 2 (trafficking-deficient) mechanismCorey L Anderson, Brian P Delisle, Blake D Anson, et al.
American Journal of Physiology. Heart and Circulatory Physiology|October 18, 2005
Specific serine proteases selectively damage KCNH2 (hERG1) potassium channels and I(Kr)Sridharan Rajamani, Corey L Anderson, Carmen R Valdivia, et al.
Molecular Pharmacology|April 27, 2005
Intragenic suppression of trafficking-defective KCNH2 channels associated with long QT syndromeBrian P Delisle, Jessica K Slind, Jennifer A Kilby, et al.
American Journal of Physiology. Cell Physiology|July 19, 2013
Pharmacological correction of long QT-linked mutations in KCNH2 (hERG) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulumJennifer L Smith, Allison R Reloj, Parvathi S Nataraj, et al.
Circulation. Arrhythmia and Electrophysiology|March 17, 2021
Long QT Syndrome <i>KCNH2</i> Variant Induces hERG1a/1b Subunit Imbalance in Patient-Specific Induced Pluripotent Stem Cell-Derived CardiomyocytesLi Feng, Jianhua Zhang, ChangHwan Lee, et al.
Circulation. Arrhythmia and Electrophysiology|May 13, 2018
Functional Invalidation of Putative Sudden Infant Death Syndrome-Associated Variants in the <i>KCNH2</i>-Encoded Kv11.1 ChannelJennifer L Smith, David J Tester, Allison R Hall, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
International Journal of Molecular Sciences|July 9, 2022
Mutation-Specific Differences in Kv7.1 (<i>KCNQ1</i>) and Kv11.1 (<i>KCNH2</i>) Channel Dysfunction and Long QT Syndrome PhenotypesPeter M Kekenes-Huskey, Don E Burgess, Bin Sun, et al.
Biomolecules|August 8, 2020
Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 <i>KCNH2</i> (<i>hERG</i>) Mutations and Identifying New PatientsMakoto Ono, Don E Burgess, Elizabeth A Schroder, et al.
Circulation|January 25, 2006
Most LQT2 mutations reduce Kv11.1 (hERG) current by a class 2 (trafficking-deficient) mechanismCorey L Anderson, Brian P Delisle, Blake D Anson, et al.
American Journal of Physiology. Heart and Circulatory Physiology|October 18, 2005
Specific serine proteases selectively damage KCNH2 (hERG1) potassium channels and I(Kr)Sridharan Rajamani, Corey L Anderson, Carmen R Valdivia, et al.
Molecular Pharmacology|April 27, 2005
Intragenic suppression of trafficking-defective KCNH2 channels associated with long QT syndromeBrian P Delisle, Jessica K Slind, Jennifer A Kilby, et al.
American Journal of Physiology. Cell Physiology|July 19, 2013
Pharmacological correction of long QT-linked mutations in KCNH2 (hERG) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulumJennifer L Smith, Allison R Reloj, Parvathi S Nataraj, et al.
Circulation. Arrhythmia and Electrophysiology|March 17, 2021
Long QT Syndrome <i>KCNH2</i> Variant Induces hERG1a/1b Subunit Imbalance in Patient-Specific Induced Pluripotent Stem Cell-Derived CardiomyocytesLi Feng, Jianhua Zhang, ChangHwan Lee, et al.
Circulation. Arrhythmia and Electrophysiology|May 13, 2018
Functional Invalidation of Putative Sudden Infant Death Syndrome-Associated Variants in the <i>KCNH2</i>-Encoded Kv11.1 ChannelJennifer L Smith, David J Tester, Allison R Hall, et al.
Pageof 3