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Functional Evaluation of a Kcnt1 Variant Associated with Epilepsy in Rat
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/acn3.50822openalex-extracted
Encephalopathies with KCNC1 variants: genotype‐phenotype‐functional correlations
inferredcites →https://doi.org/10.1002/ana.24128openalex-extracted
KCNT1gain of function in 2 epilepsy phenotypes is reversed by quinidine
inferredcites →https://doi.org/10.1007/s11064-013-1037-9openalex-extracted
Hippocampal Gene Expression Profiling in a Rat Model of Posttraumatic Epilepsy Reveals Temporal Upregulation of Lipid Metabolism-Related Genes
inferredcites →https://doi.org/10.1007/s13311-019-00739-yopenalex-extracted
Treatment Responsiveness in KCNT1-Related Epilepsy
inferredcites →https://doi.org/10.1016/j.celrep.2014.11.015openalex-extracted
Human Slack Potassium Channel Mutations Increase Positive Cooperativity between Individual Channels
inferredcites →https://doi.org/10.1016/j.celrep.2020.108303openalex-extracted
Reduced GABAergic Neuron Excitability, Altered Synaptic Connectivity, and Seizures in a KCNT1 Gain-of-Function Mouse Model of Childhood Epilepsy
inferredcites →https://doi.org/10.1016/j.eplepsyres.2010.02.004openalex-extracted
Role of GRM4 in idiopathic generalized epilepsies analysed by genetic association and sequence analysis
inferredcites →https://doi.org/10.1016/j.gpb.2021.10.007openalex-extracted
Exploration of Target Spaces in the Human Genome for Protein and Peptide Drugs
inferredcites →https://doi.org/10.1016/j.neuron.2024.02.013openalex-extracted
Glial KCNQ K+ channels control neuronal output by regulating GABA release from glia in C. elegans
inferredcites →https://doi.org/10.1016/j.scr.2020.101711openalex-extracted
Generation of a human induced pluripotent stem cell line from an epilepsy patient carrying mutations in the PIK3R2 gene
inferredcites →https://doi.org/10.1016/j.yebeh.2019.02.029openalex-extracted
PTZ-induced seizures in mice require a revised Racine scale
inferredcites →https://doi.org/10.1016/j.ymgme.2017.12.433openalex-extracted
Characterization of a novel variant in siblings with Asparagine Synthetase Deficiency
inferredcites →https://doi.org/10.1074/jbc.m114.624056openalex-extracted
Identification and Pharmacological Inactivation of the MYCN Gene Network as a Therapeutic Strategy for Neuroblastic Tumor Cells
inferredcites →https://doi.org/10.1080/15384101.2018.1562286openalex-extracted
Dynorphin activation of kappa opioid receptor protects against epilepsy and seizure-induced brain injury via PI3K/Akt/Nrf2/HO-1 pathway
inferredcites →https://doi.org/10.1093/bioinformatics/btv300openalex-extracted
GOplot: an R package for visually combining expression data with functional analysis
inferredcites →https://doi.org/10.1093/brain/awz123openalex-extracted
Altered inhibitory synapses in de novo GABRA5 and GABRA1 mutations associated with early onset epileptic encephalopathies
inferredcites →https://doi.org/10.1093/cercor/bhad535openalex-extracted
Regional GABA levels modulate abnormal resting-state network functional connectivity and cognitive impairment in multiple sclerosis
inferredcites →https://doi.org/10.1093/hmg/ddu030openalex-extracted
Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis
inferredcites →https://doi.org/10.1093/nar/gkab447openalex-extracted
KOBAS-i: intelligent prioritization and exploratory visualization of biological functions for gene enrichment analysis
inferredcites →https://doi.org/10.1093/nar/gkab612openalex-extracted
Three human RNA polymerases interact with TFIIH via a common RPB6 subunit
inferredcites →https://doi.org/10.1093/nar/gkac1000openalex-extracted
The STRING database in 2023: protein–protein association networks and functional enrichment analyses for any sequenced genome of interest
inferredcites →https://doi.org/10.1101/cshperspect.a040675openalex-extracted
Physical Nature of Chromatin in the Nucleus
inferredcites →https://doi.org/10.1111/epi.17648openalex-extracted
Functional evaluation of epilepsy‐associated KCNT1 variants in multiple cellular systems reveals a predominant gain of function impact on channel properties
inferredcites →https://doi.org/10.1186/s12883-017-1001-4openalex-extracted
Isolated and repeated stroke-like episodes in a middle-aged man with a mitochondrial ND3 T10158C mutation: a case report
inferredcites →https://doi.org/10.1186/s12964-024-01528-7openalex-extracted
Impairments of GABAergic transmission in hippocampus mediate increased susceptibility of epilepsy in the early stage of Alzheimer’s disease
inferredcites →https://doi.org/10.1186/s13041-016-0273-8openalex-extracted
Personalized medicine approach confirms a milder case of ABAT deficiency
inferredcites →https://doi.org/10.1212/wnl.0000000000004762openalex-extracted
Clinical and molecular characterization of KCNT1 -related severe early-onset epilepsy
inferredcites →https://doi.org/10.1371/journal.pgen.1002405openalex-extracted
Age-Related Neuronal Degeneration: Complementary Roles of Nucleotide Excision Repair and Transcription-Coupled Repair in Preventing Neuropathology
inferredcites →https://doi.org/10.1523/jneurosci.1628-18.2019openalex-extracted
An Epilepsy-Associated KCNT1 Mutation Enhances Excitability of Human iPSC-Derived Neurons by Increasing Slack KNa Currents
inferredcites →https://doi.org/10.3109/17435390.2015.1107142openalex-extracted
In vitroscreening of metal oxide nanoparticles for effects on neural function using cortical networks on microelectrode arrays
inferredcites →https://doi.org/10.7150/thno.81981openalex-extracted
Extracellular vesicles improve GABAergic transmission in Huntington's disease iPSC-derived neurons
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