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COOPER, EDWARD

One or more keywords matched the following items that are connected to COOPER, EDWARD

Item Type	Name
Academic Article	KCNQ2 is a nodal K+ channel.
Academic Article	Expression and localization of K channels KCNQ2 and KCNQ3 in the mammalian cochlea.
Academic Article	Made for "anchorin": Kv7.2/7.3 (KCNQ2/KCNQ3) channels and the modulation of neuronal excitability in vertebrate axons.
Academic Article	Identification by mass spectrometry and functional characterization of two phosphorylation sites of KCNQ2/KCNQ3 channels.
Academic Article	A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon.
Academic Article	KCNQ2 Potassium Channel Epileptic Encephalopathy Syndrome: Divorce of an Electro-Mechanical Couple?
Academic Article	A KCNQ channel opener for experimental neonatal seizures and status epilepticus.
Academic Article	M-channels: neurological diseases, neuromodulation, and drug development.
Academic Article	Exploiting the other inhibitory ion: KCNQ potassium channels and regulation of excitability in developing and mature brain.
Academic Article	Functional significance of axonal Kv7 channels in hippocampal pyramidal neurons.
Concept	Potassium Channels, Voltage-Gated
Concept	KCNQ Potassium Channels
Concept	Potassium
Concept	KCNQ3 Potassium Channel
Concept	Potassium Channels
Concept	KCNQ2 Potassium Channel
Academic Article	Heteromeric Kv7.2/7.3 channels differentially regulate action potential initiation and conduction in neocortical myelinated axons.
Academic Article	Channel-anchored protein kinase CK2 and protein phosphatase 1 reciprocally regulate KCNQ2-containing M-channels via phosphorylation of calmodulin.
Academic Article	Axonal Kv7.2/7.3 channels: caught in the act.
Academic Article	Cholinergic afferent stimulation induces axonal function plasticity in adult hippocampal granule cells.
Academic Article	An Ankyrin-G N-terminal Gate and Protein Kinase CK2 Dually Regulate Binding of Voltage-gated Sodium and KCNQ2/3 Potassium Channels.
Academic Article	Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variant.
Academic Article	Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201H.
Grant	KCNQ2 Epileptic Encephalopathy: Overcoming Hurdles to Effective Disease-Modifying Therapy
Grant	Proteomic Dissection of M-channel Phosphorylation
Grant	MODULATION OF HIPPOCAMPAL K+ CHANNELS BY PHOSPHORYLATION
Grant	KCNQ channel opener efficacy for neonatal seizures
Academic Article	Autism and developmental disability caused by KCNQ3 gain-of-function variants.
Academic Article	Epileptic Encephalopathy In A Patient With A Novel Variant In The Kv7.2 S2 Transmembrane Segment: Clinical, Genetic, and Functional Features.
Academic Article	Characteristics of KCNQ2 variants causing either benign neonatal epilepsy or developmental and epileptic encephalopathy.
Academic Article	High-throughput evaluation of epilepsy-associated KCNQ2 variants reveals functional and pharmacological heterogeneity.
Academic Article	Removal of KCNQ2 from parvalbumin-expressing interneurons improves anti-seizure efficacy of retigabine.
Academic Article	KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism.
Academic Article	Phenotypic and functional assessment of two novel KCNQ2 gain-of-function variants Y141N and G239S and effects of amitriptyline treatment.

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Potassium