Associated Papers
HCN1 epilepsy: From genetics and mechanisms to precision therapies.
Bleakley LE et al.
Journal of Neurochemistry, 2024
Proteome-scale characterisation of motif-based interactome rewiring by disease mutations.
Kliche J et al.
Molecular Systems Biology, 2024
39009827 (PubMed )
Supplement: 44320_2024_55_MOESM5_ESM.xlsx › A-binding_peptides
The Contribution of HCN Channelopathies in Different Epileptic Syndromes, Mechanisms, Modulators, and Potential Treatment Targets: A Systematic Review.
Kessi M et al.
Frontiers in Molecular Neuroscience, 2022
Novel HCN1 Mutations Associated With Epilepsy and Impacts on Neuronal Excitability.
Xie C et al.
Frontiers in Molecular Neuroscience, 2022
Cardiac and neuronal HCN channelopathies.
Rivolta I et al.
Pflugers Archiv : European Journal of Physiology, 2020
Ion Channel Genes and Epilepsy: Functional Alteration, Pathogenic Potential, and Mechanism of Epilepsy.
Wei F et al.
Neuroscience Bulletin, 2017
In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery.
Oliver KL et al.
Neurology. Genetics, 2016
27066588 (PubMed )
Supplement: supp_2.1.e51_table_e-2.xlsx › table_e-2
Novel Genes of Early-Onset Epileptic Encephalopathies: From Genotype to Phenotypes.
Mastrangelo M
Pediatric Neurology, 2015
De novo mutations in HCN1 cause early infantile epileptic encephalopathy.
Nava C et al.
Nature Genetics, 2014
HCN1 Gain-Of-Function Mutations - A New Cause of Epileptic Encephalopathy.
Poduri A
Epilepsy Currents, 0
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