Associated Papers
Comparison of K+ Channel Families.
Taura J et al.
Handbook of Experimental Pharmacology, 2021
The Background K+ Channel TRESK in Sensory Physiology and Pain.
Andres-Bilbe A et al.
International Journal of Molecular Sciences, 2020
A causal role for TRESK loss of function in migraine mechanisms.
Pettingill P et al.
Brain : a Journal of Neurology, 2019
Ion channelopathies and migraine pathogenesis.
Albury CL et al.
Molecular Genetics and Genomics : Mgg, 2017
Genetics of Migraine: Insights into the Molecular Basis of Migraine Disorders.
Sutherland HG et al.
Headache, 2017
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
The molecular pathogenesis of migraine: new developments and opportunities.
Zameel Cader M
Human Molecular Genetics, 2013
Analysis of 3 common polymorphisms in the KCNK18 gene in an Australian Migraine case-control cohort.
Maher BH et al.
Gene, 2013
Identification of novel genes involved in migraine.
Lafrenière RG et al.
Headache, 2012
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
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