HCN ion channels and accessory proteins in epilepsy: genetic analysis of a large cohort of patients and review of the literatureScreening and Identification of Cardioprotective Compounds From Wenxin Keli by Activity Index Approach and in vivo Zebrafish Model.HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyondA novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitabilityA Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability.Modulation of the intrinsic neuronal excitability by multifunctional liposomes tailored for the treatment of Alzheimer’s disease.A synthetic peptide that prevents cAMP regulation in mammalian Hyperpolarization-activated Cyclic Nucleotide-regulated (HCN) channels.Effects of repeated sprints training on fracture risk-associated miRNAGeneration of human induced pluripotent stem cells (EURACi001-A, EURACi002-A, EURACi003-A) from peripheral blood mononuclear cells of three patients carrying mutations in the CAV3 gene.Preferential myofibroblast differentiation of cardiac mesenchymal progenitor cells in the presence of atrial fibrillation.Structure-guided design of a cell penetrating peptide preventing cAMP modulation of HCN channelsMammalian γ2 AMPK regulates intrinsic heart rate.The expression of the rare caveolin-3 variant T78M alters cardiac ion channels function and membrane excitability.Bone turnover response is linked to both acute and established metabolic changes in ultra-marathon runners.A Traditional Chinese Medicine Drug (TMYX) Controls Heart Rate by Modulation of the Pacemaker (F) Channels

HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond

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Mammalian γ2 AMPK regulates intrinsic heart rate.

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