Pages that link to "Q37787324"
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The following pages link to Sodium channel SCN1A and epilepsy: mutations and mechanisms (Q37787324):
Displaying 50 items.
- Altered cardiac electrophysiology and SUDEP in a model of Dravet syndrome (Q21089741) (← links)
- Genetic neurological channelopathies: molecular genetics and clinical phenotypes (Q26777559) (← links)
- Pathogenesis and new candidate treatments for infantile spasms and early life epileptic encephalopathies: A view from preclinical studies (Q27308052) (← links)
- Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome (Q27308208) (← links)
- Exaggerated Nighttime Sleep and Defective Sleep Homeostasis in a Drosophila Knock-In Model of Human Epilepsy (Q27318390) (← links)
- Design of Bioactive Peptides from Naturally Occurring -Conotoxin Structures (Q27670677) (← links)
- The C-terminal helical bundle of the tetrameric prokaryotic sodium channel accelerates the inactivation rate (Q27678721) (← links)
- Understanding Genotypes and Phenotypes in Epileptic Encephalopathies (Q28080066) (← links)
- On the multiple roles of the voltage gated sodium channel β1 subunit in genetic diseases (Q28080803) (← links)
- Nav1.1 modulation by a novel triazole compound attenuates epileptic seizures in rodents (Q28235994) (← links)
- A monoclonal antibody that targets a NaV1.7 channel voltage sensor for pain and itch relief (Q28240662) (← links)
- Major channels involved in neuropsychiatric disorders and therapeutic perspectives (Q28290639) (← links)
- Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. (Q29417109) (← links)
- An Scn1a epilepsy mutation in Scn8a alters seizure susceptibility and behavior. (Q30366738) (← links)
- Naturally occurring carboxypeptidase A6 mutations: effect on enzyme function and association with epilepsy. (Q30422925) (← links)
- Preferential inactivation of Scn1a in parvalbumin interneurons increases seizure susceptibility (Q30542513) (← links)
- Knock-in model of Dravet syndrome reveals a constitutive and conditional reduction in sodium current (Q30585940) (← links)
- Identifying and Analyzing Novel Epilepsy-Related Genes Using Random Walk with Restart Algorithm (Q30838585) (← links)
- Seizures and epilepsy: an overview for neuroscientists (Q33165796) (← links)
- The genetic relationship between epilepsy and hemiplegic migraine (Q33621149) (← links)
- Structure-based assessment of disease-related mutations in human voltage-gated sodium channels (Q33729032) (← links)
- Progressive myoclonic epilepsy-associated gene KCTD7 is a regulator of potassium conductance in neurons. (Q34196045) (← links)
- Epilepsy and epileptic syndrome. (Q34260757) (← links)
- Mechanisms of epileptogenesis: a convergence on neural circuit dysfunction. (Q34339959) (← links)
- Regulation of membrane excitability: a convergence on voltage-gated sodium conductance. (Q35024719) (← links)
- Novel HCN2 mutation contributes to febrile seizures by shifting the channel's kinetics in a temperature-dependent manner (Q35063727) (← links)
- Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform (Q35079979) (← links)
- Transcriptome analysis of the hippocampus in novel rat model of febrile seizures (Q35148980) (← links)
- Genetics and function of neocortical GABAergic interneurons in neurodevelopmental disorders (Q35173644) (← links)
- Cellular plasticity induced by anti-α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor encephalitis antibodies (Q35194421) (← links)
- Alternative splicing modulates inactivation of type 1 voltage-gated sodium channels by toggling an amino acid in the first S3-S4 linker (Q35378377) (← links)
- Novel carboxypeptidase A6 (CPA6) mutations identified in patients with juvenile myoclonic and generalized epilepsy (Q35393646) (← links)
- Large-Scale Phenotype-Based Antiepileptic Drug Screening in a Zebrafish Model of Dravet Syndrome(1,2,3). (Q35805872) (← links)
- Benchmarking the stability of human detergent-solubilised voltage-gated sodium channels for structural studies using eel as a reference (Q36018140) (← links)
- Pathophysiological role of omega pore current in channelopathies (Q36022793) (← links)
- Incidence of Dravet Syndrome in a US Population (Q36210601) (← links)
- Seizure control through genetic and pharmacological manipulation of Pumilio in Drosophila: a key component of neuronal homeostasis (Q36244251) (← links)
- Clemizole and modulators of serotonin signalling suppress seizures in Dravet syndrome (Q36245909) (← links)
- Investigation of TBR1 Hemizygosity: Four Individuals with 2q24 Microdeletions (Q36323609) (← links)
- A knock-in model of human epilepsy in Drosophila reveals a novel cellular mechanism associated with heat-induced seizure (Q36350607) (← links)
- Disruption of polycystin-L causes hippocampal and thalamocortical hyperexcitability (Q36514620) (← links)
- Mining integrated semantic networks for drug repositioning opportunities (Q36532112) (← links)
- Understanding the physical mechanism of transition to epileptic seizures (Q36694630) (← links)
- Novel GABRG2 mutations cause familial febrile seizures (Q36738596) (← links)
- Model systems for studying cellular mechanisms of SCN1A-related epilepsy (Q36760270) (← links)
- Fgf13 Identified as a Novel Cause of GEFS. (Q36771164) (← links)
- Genetic variations and associated pathophysiology in the management of epilepsy. (Q36925220) (← links)
- Effects of an epilepsy-causing mutation in the SCN1A sodium channel gene on cocaine-induced seizure susceptibility in mice (Q36961849) (← links)
- CRMP2 protein SUMOylation modulates NaV1.7 channel trafficking (Q37112626) (← links)
- A deleterious Nav1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patients (Q37127359) (← links)