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Alfred L George

Showing results (221-230 of 296) with videos related to

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Cell Reports|June 2, 2023
Scanning mutagenesis of the voltage-gated sodium channel Na<sub>V</sub>1.2 using base editingJuan Lorenzo B Pablo, Savannah L Cornett, Lei A Wang, et al.
Circulation|May 25, 2005
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotypeLi Zhang, D Woodrow Benson, Martin Tristani-Firouzi, et al.
Circulation|October 26, 2005
Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder populationPaul A Brink, Lia Crotti, Valerie Corfield, et al.
The European Journal of Neuroscience|August 26, 2011
Nav 1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndromeLinda Volkers, Kristopher M Kahlig, Nienke E Verbeek, et al.
Journal of the American College of Cardiology|November 20, 2012
Vagal reflexes following an exercise stress test: a simple clinical tool for gene-specific risk stratification in the long QT syndromeLia Crotti, Carla Spazzolini, Alessandra P Porretta, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2026
Excitatory Dysfunction and Phenotypic Rescue in a Human Neuronal Model of <i>SCN2A</i> -Related DisordersSashmita Panda, Diana Jazmin Ixmatlahua Ribera, Luis A Williams, et al.
Science Advances|September 15, 2016
Structural basis for KCNE3 modulation of potassium recycling in epitheliaBrett M Kroncke, Wade D Van Horn, Jarrod Smith, et al.
Clinical Pharmacology and Therapeutics|February 3, 2018
Clinical Pharmacogenetics Implementation Consortium Guideline for HLA Genotype and Use of Carbamazepine and Oxcarbazepine: 2017 UpdateElizabeth J Phillips, Chonlaphat Sukasem, Michelle Whirl-Carrillo, et al.
JCI Insight|February 1, 2022
High-throughput evaluation of epilepsy-associated KCNQ2 variants reveals functional and pharmacological heterogeneityCarlos G Vanoye, Reshma R Desai, Zhigang Ji, et al.
Human Molecular Genetics|April 13, 2022
Cellular and behavioral effects of altered NaV1.2 sodium channel ion permeability in Scn2aK1422E miceDennis M Echevarria-Cooper, Nicole A Hawkins, Sunita N Misra, et al.
Pageof 30

Showing results (221-230 of 296) with videos related to

Sort By:
Pageof 30
Cell Reports|June 2, 2023
Scanning mutagenesis of the voltage-gated sodium channel Na<sub>V</sub>1.2 using base editingJuan Lorenzo B Pablo, Savannah L Cornett, Lei A Wang, et al.
Circulation|May 25, 2005
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotypeLi Zhang, D Woodrow Benson, Martin Tristani-Firouzi, et al.
Circulation|October 26, 2005
Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder populationPaul A Brink, Lia Crotti, Valerie Corfield, et al.
The European Journal of Neuroscience|August 26, 2011
Nav 1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndromeLinda Volkers, Kristopher M Kahlig, Nienke E Verbeek, et al.
Journal of the American College of Cardiology|November 20, 2012
Vagal reflexes following an exercise stress test: a simple clinical tool for gene-specific risk stratification in the long QT syndromeLia Crotti, Carla Spazzolini, Alessandra P Porretta, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2026
Excitatory Dysfunction and Phenotypic Rescue in a Human Neuronal Model of <i>SCN2A</i> -Related DisordersSashmita Panda, Diana Jazmin Ixmatlahua Ribera, Luis A Williams, et al.
Science Advances|September 15, 2016
Structural basis for KCNE3 modulation of potassium recycling in epitheliaBrett M Kroncke, Wade D Van Horn, Jarrod Smith, et al.
Clinical Pharmacology and Therapeutics|February 3, 2018
Clinical Pharmacogenetics Implementation Consortium Guideline for HLA Genotype and Use of Carbamazepine and Oxcarbazepine: 2017 UpdateElizabeth J Phillips, Chonlaphat Sukasem, Michelle Whirl-Carrillo, et al.
JCI Insight|February 1, 2022
High-throughput evaluation of epilepsy-associated KCNQ2 variants reveals functional and pharmacological heterogeneityCarlos G Vanoye, Reshma R Desai, Zhigang Ji, et al.
Human Molecular Genetics|April 13, 2022
Cellular and behavioral effects of altered NaV1.2 sodium channel ion permeability in Scn2aK1422E miceDennis M Echevarria-Cooper, Nicole A Hawkins, Sunita N Misra, et al.
Pageof 30