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Edward C Cooper

Showing results (21-30 of 35) with videos related to

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International Journal of Molecular Sciences|July 13, 2019
Epileptic Encephalopathy In A Patient With A Novel Variant In The Kv7.2 S2 Transmembrane Segment: Clinical, Genetic, and Functional FeaturesMaria Virginia Soldovieri, Paolo Ambrosino, Ilaria Mosca, et al.
Experimental Neurology|June 12, 2022
Removal of KCNQ2 from parvalbumin-expressing interneurons improves anti-seizure efficacy of retigabineJunzhan Jing, Corrinne Dunbar, Alina Sonesra, et al.
Nature Neuroscience|November 3, 2014
Glial ankyrins facilitate paranodal axoglial junction assemblyKae-Jiun Chang, Daniel R Zollinger, Keiichiro Susuki, et al.
Epilepsia|November 19, 2016
Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variantJohn J Millichap, Francesco Miceli, Michela De Maria, et al.
Annals of Clinical and Translational Neurology|February 16, 2023
KCNA1 gain-of-function epileptic encephalopathy treated with 4-aminopyridinePeter Müller, Danielle S Takacs, Ulrike B S Hedrich, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|January 19, 2024
Phenotypic and functional assessment of two novel KCNQ2 gain-of-function variants Y141N and G239S and effects of amitriptyline treatmentAllan Bayat, Stefano Iavarone, Francesco Miceli, et al.
Plos One|March 24, 2015
Ion channel expression in the developing enteric nervous systemCaroline S Hirst, Jaime P P Foong, Lincon A Stamp, et al.
Frontiers in Physiology|October 5, 2020
A Novel Kv7.3 Variant in the Voltage-Sensing S<sub>4</sub> Segment in a Family With Benign Neonatal Epilepsy: Functional Characterization and <i>in vitro</i> Rescue by β-HydroxybutyrateFrancesco Miceli, Lidia Carotenuto, Vincenzo Barrese, 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.
Epilepsia|February 1, 2017
Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201HSarah B Mulkey, Bruria Ben-Zeev, Joost Nicolai, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

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Pageof 4
International Journal of Molecular Sciences|July 13, 2019
Epileptic Encephalopathy In A Patient With A Novel Variant In The Kv7.2 S2 Transmembrane Segment: Clinical, Genetic, and Functional FeaturesMaria Virginia Soldovieri, Paolo Ambrosino, Ilaria Mosca, et al.
Experimental Neurology|June 12, 2022
Removal of KCNQ2 from parvalbumin-expressing interneurons improves anti-seizure efficacy of retigabineJunzhan Jing, Corrinne Dunbar, Alina Sonesra, et al.
Nature Neuroscience|November 3, 2014
Glial ankyrins facilitate paranodal axoglial junction assemblyKae-Jiun Chang, Daniel R Zollinger, Keiichiro Susuki, et al.
Epilepsia|November 19, 2016
Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variantJohn J Millichap, Francesco Miceli, Michela De Maria, et al.
Annals of Clinical and Translational Neurology|February 16, 2023
KCNA1 gain-of-function epileptic encephalopathy treated with 4-aminopyridinePeter Müller, Danielle S Takacs, Ulrike B S Hedrich, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|January 19, 2024
Phenotypic and functional assessment of two novel KCNQ2 gain-of-function variants Y141N and G239S and effects of amitriptyline treatmentAllan Bayat, Stefano Iavarone, Francesco Miceli, et al.
Plos One|March 24, 2015
Ion channel expression in the developing enteric nervous systemCaroline S Hirst, Jaime P P Foong, Lincon A Stamp, et al.
Frontiers in Physiology|October 5, 2020
A Novel Kv7.3 Variant in the Voltage-Sensing S<sub>4</sub> Segment in a Family With Benign Neonatal Epilepsy: Functional Characterization and <i>in vitro</i> Rescue by β-HydroxybutyrateFrancesco Miceli, Lidia Carotenuto, Vincenzo Barrese, 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.
Epilepsia|February 1, 2017
Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201HSarah B Mulkey, Bruria Ben-Zeev, Joost Nicolai, et al.
Pageof 4