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

Edward C Cooper

Showing results (1-10 of 35) with videos related to

Pageof 4
Sort By:
Seminars in Cell & Developmental Biology|October 14, 2010
Made for "anchorin": Kv7.2/7.3 (KCNQ2/KCNQ3) channels and the modulation of neuronal excitability in vertebrate axonsEdward C Cooper
The Journal of Biological Chemistry|May 23, 2015
An Ankyrin-G N-terminal Gate and Protein Kinase CK2 Dually Regulate Binding of Voltage-gated Sodium and KCNQ2/3 Potassium ChannelsMingxuan Xu, Edward C Cooper
Archives of Neurology|April 23, 2003
M-channels: neurological diseases, neuromodulation, and drug developmentEdward C Cooper, Lily Y Jan
Neuron|January 20, 2022
KCNQ channel PIP2 modulation: Two loose links, three rings, and a twistEdward C Cooper, Timothy Abreo, Baouyen Tran
The Journal of Biological Chemistry|March 15, 2014
Channel-anchored protein kinase CK2 and protein phosphatase 1 reciprocally regulate KCNQ2-containing M-channels via phosphorylation of calmodulinSeungwoo Kang, Mingxuan Xu, Edward C Cooper, et al.
Journal of Biomolecular Structure & Dynamics|February 11, 2026
Molecular dynamics of the pathogenic <i>KCNQ2</i> variant G256W reveals mechanisms of channel dysfunction in epileptic encephalopathyEmma C Thompson, Edward C Cooper, Bill R Miller
Biorxiv : the Preprint Server for Biology|December 18, 2025
Molecular dynamics of the pathogenic KCNQ2 variant G256W reveal mechanisms of channel dysfunction in epileptic encephalopathyEmma C Thompson, Edward C Cooper, Bill R Miller
Audiology & Neuro-Otology|October 2, 2008
Expression and localization of K channels KCNQ2 and KCNQ3 in the mammalian cochleaZhe Jin, Gui-Hua Liang, Edward C Cooper, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 6, 2004
KCNQ2 is a nodal K+ channelJérôme J Devaux, Kleopas A Kleopa, Edward C Cooper, et al.
Epilepsia|August 17, 2019
Characteristics of KCNQ2 variants causing either benign neonatal epilepsy or developmental and epileptic encephalopathyAyako Goto, Atsushi Ishii, Mami Shibata, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Seminars in Cell & Developmental Biology|October 14, 2010
Made for "anchorin": Kv7.2/7.3 (KCNQ2/KCNQ3) channels and the modulation of neuronal excitability in vertebrate axonsEdward C Cooper
The Journal of Biological Chemistry|May 23, 2015
An Ankyrin-G N-terminal Gate and Protein Kinase CK2 Dually Regulate Binding of Voltage-gated Sodium and KCNQ2/3 Potassium ChannelsMingxuan Xu, Edward C Cooper
Archives of Neurology|April 23, 2003
M-channels: neurological diseases, neuromodulation, and drug developmentEdward C Cooper, Lily Y Jan
Neuron|January 20, 2022
KCNQ channel PIP2 modulation: Two loose links, three rings, and a twistEdward C Cooper, Timothy Abreo, Baouyen Tran
The Journal of Biological Chemistry|March 15, 2014
Channel-anchored protein kinase CK2 and protein phosphatase 1 reciprocally regulate KCNQ2-containing M-channels via phosphorylation of calmodulinSeungwoo Kang, Mingxuan Xu, Edward C Cooper, et al.
Journal of Biomolecular Structure & Dynamics|February 11, 2026
Molecular dynamics of the pathogenic <i>KCNQ2</i> variant G256W reveals mechanisms of channel dysfunction in epileptic encephalopathyEmma C Thompson, Edward C Cooper, Bill R Miller
Biorxiv : the Preprint Server for Biology|December 18, 2025
Molecular dynamics of the pathogenic KCNQ2 variant G256W reveal mechanisms of channel dysfunction in epileptic encephalopathyEmma C Thompson, Edward C Cooper, Bill R Miller
Audiology & Neuro-Otology|October 2, 2008
Expression and localization of K channels KCNQ2 and KCNQ3 in the mammalian cochleaZhe Jin, Gui-Hua Liang, Edward C Cooper, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 6, 2004
KCNQ2 is a nodal K+ channelJérôme J Devaux, Kleopas A Kleopa, Edward C Cooper, et al.
Epilepsia|August 17, 2019
Characteristics of KCNQ2 variants causing either benign neonatal epilepsy or developmental and epileptic encephalopathyAyako Goto, Atsushi Ishii, Mami Shibata, et al.
Pageof 4