Associated Papers
The Background K+ Channel TRESK in Sensory Physiology and Pain.
Andres-Bilbe A et al.
International Journal of Molecular Sciences, 2020
Ion channelopathies and migraine pathogenesis.
Albury CL et al.
Molecular Genetics and Genomics : Mgg, 2017
Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes.
Domitrz I et al.
Human Genomics, 2016
Properties, regulation, pharmacology, and functions of the K₂p channel, TRESK.
Enyedi P et al.
Pflugers Archiv : European Journal of Physiology, 2015
KCNK18 (TRESK) genetic variants in Italian patients with migraine.
Rainero I et al.
Headache, 2014
Nonmigraine-associated TRESK K+ channel variant C110R does not increase the excitability of trigeminal ganglion neurons.
Guo Z et al.
Journal of Neurophysiology, 2014
Functional analysis of missense variants in the TRESK (KCNK18) K channel.
Andres-Enguix I et al.
Scientific Reports, 2012
A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura.
Lafrenière RG et al.
Nature Medicine, 2010
Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.
Ryu GM et al.
Nucleic Acids Research, 2009
19139070 (PubMed )
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