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Jamie I Vandenberg

Showing results (81-90 of 126) with videos related to

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Plos One|January 21, 2011
The N-terminal tail of hERG contains an amphipathic α-helix that regulates channel deactivationChai Ann Ng, Mark J Hunter, Matthew D Perry, et al.
Heart Rhythm|September 27, 2019
High-throughput phenotyping of heteromeric human ether-à-go-go-related gene potassium channel variants can discriminate pathogenic from rare benign variantsChai-Ann Ng, Matthew D Perry, Whitney Liang, et al.
The Journal of Biological Chemistry|November 11, 2008
The pore domain outer helix contributes to both activation and inactivation of the HERG K+ channelPengchu Ju, Guilhem Pages, R Peter Riek, et al.
The American Journal of Psychiatry|October 21, 2015
Differential Response to Risperidone in Schizophrenia Patients by KCNH2 Genotype and Drug Metabolizer StatusJuliane Heide, Fengyu Zhang, Kristin L Bigos, et al.
The Journal of Biological Chemistry|December 26, 2007
Substrate specificity of platypus venom L-to-D-peptide isomeraseParamjit S Bansal, Allan M Torres, Ben Crossett, et al.
American Journal of Human Genetics|June 10, 2022
A massively parallel assay accurately discriminates between functionally normal and abnormal variants in a hotspot domain of KCNH2Chai-Ann Ng, Rizwan Ullah, Jessica Farr, et al.
Nature Communications|October 11, 2023
Structural basis of promiscuous substrate transport by Organic Cation Transporter 1Yi C Zeng, Meghna Sobti, Ada Quinn, et al.
Journal of Molecular and Cellular Cardiology|September 25, 2016
Convergence of models of human ventricular myocyte electrophysiology after global optimization to recapitulate clinical long QT phenotypesStefan A Mann, Mohammad Imtiaz, Annika Winbo, et al.
Basic Research in Cardiology|August 30, 2002
Lentiviral vectors for delivery of genes into neonatal and adult ventricular cardiac myocytes in vitro and in vivoJing Zhao, Gavin J Pettigrew, Joan Thomas, et al.
The Journal of Physiology|March 10, 2016
Rescue of protein expression defects may not be enough to abolish the pro-arrhythmic phenotype of long QT type 2 mutationsMatthew D Perry, Chai Ann Ng, Kevin Phan, et al.
Pageof 13

Showing results (81-90 of 126) with videos related to

Sort By:
Pageof 13
Plos One|January 21, 2011
The N-terminal tail of hERG contains an amphipathic α-helix that regulates channel deactivationChai Ann Ng, Mark J Hunter, Matthew D Perry, et al.
Heart Rhythm|September 27, 2019
High-throughput phenotyping of heteromeric human ether-à-go-go-related gene potassium channel variants can discriminate pathogenic from rare benign variantsChai-Ann Ng, Matthew D Perry, Whitney Liang, et al.
The Journal of Biological Chemistry|November 11, 2008
The pore domain outer helix contributes to both activation and inactivation of the HERG K+ channelPengchu Ju, Guilhem Pages, R Peter Riek, et al.
The American Journal of Psychiatry|October 21, 2015
Differential Response to Risperidone in Schizophrenia Patients by KCNH2 Genotype and Drug Metabolizer StatusJuliane Heide, Fengyu Zhang, Kristin L Bigos, et al.
The Journal of Biological Chemistry|December 26, 2007
Substrate specificity of platypus venom L-to-D-peptide isomeraseParamjit S Bansal, Allan M Torres, Ben Crossett, et al.
American Journal of Human Genetics|June 10, 2022
A massively parallel assay accurately discriminates between functionally normal and abnormal variants in a hotspot domain of KCNH2Chai-Ann Ng, Rizwan Ullah, Jessica Farr, et al.
Nature Communications|October 11, 2023
Structural basis of promiscuous substrate transport by Organic Cation Transporter 1Yi C Zeng, Meghna Sobti, Ada Quinn, et al.
Journal of Molecular and Cellular Cardiology|September 25, 2016
Convergence of models of human ventricular myocyte electrophysiology after global optimization to recapitulate clinical long QT phenotypesStefan A Mann, Mohammad Imtiaz, Annika Winbo, et al.
Basic Research in Cardiology|August 30, 2002
Lentiviral vectors for delivery of genes into neonatal and adult ventricular cardiac myocytes in vitro and in vivoJing Zhao, Gavin J Pettigrew, Joan Thomas, et al.
The Journal of Physiology|March 10, 2016
Rescue of protein expression defects may not be enough to abolish the pro-arrhythmic phenotype of long QT type 2 mutationsMatthew D Perry, Chai Ann Ng, Kevin Phan, et al.
Pageof 13