Gene · 6334
Papers2,325
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
161 to 180 of 2,325
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Impact on backpropagation of the spatial heterogeneity of sodium channel kinetics in the axon initial segment. | PLoS Comput Biol | 2024 | 38489374 | PubTator, text mining | PubMed |
| Machine learning models reveal distinct disease subgroups and improve diagnostic and prognostic accuracy for individuals with pathogenic SCN8A gain-of-function variants. | Biol Open | 2024 | 38466077 | PubTator, text mining | PubMed |
| Parvalbumin Interneuron Impairment Leads to Synaptic Transmission Deficits and Seizures in SCN8A Epileptic Encephalopathy. | bioRxiv | 2024 | 38464208 | PubTator, text mining | PubMed |
| Emergence of lingual dystonia and strabismus in early-onset SCN8A self-limiting familial infantile epilepsy. | Epileptic Disord | 2024 | 38436508 | PubTator, text mining | PubMed |
| Expanding the clinical and genetic landscape of (developmental) epileptic encephalopathy with spike-and-wave activation in sleep: results from studies of a Turkish cohort. | Neurogenetics | 2024 | 38388889 | PubTator, text mining | PubMed |
| Molecular Pharmacology of Selective NaV1.6 and Dual NaV1.6/NaV1.2 Channel Inhibitors that Suppress Excitatory Neuronal Activity Ex Vivo. | ACS Chem Neurosci | 2024 | 38359277 | PubTator, text mining | PubMed |
| [Clinical features and genetic analysis of five children with epilepsies due to variants of SCN8A gene]. | Zhonghua Yi Xue Yi Chuan Xue Za Zhi | 2024 | 38311555 | PubTator, text mining | PubMed |
| Reduced MUNC18-1 Levels, Synaptic Proteome Changes, and Altered Network Activity in STXBP1-Related Disorder Patient Neurons. | Biol Psychiatry Glob Open Sci | 2024 | 38298782 | PubTator, text mining | PubMed |
| Coupling of Slack and NaV1.6 sensitizes Slack to quinidine blockade and guides anti-seizure strategy development. | Elife | 2024 | 38289338 | PubTator, text mining | PubMed |
| Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study. | Int J Mol Sci | 2024 | 38279250 | PubTator, text mining | PubMed |
| Migraine - a borderland disease to epilepsy: near it but not of it. | J Headache Pain | 2024 | 38273253 | PubTator, text mining | PubMed |
| Feasibility of a reconfigured domestic violence and abuse training and support intervention responding to affected women, men, children and young people through primary care. | BMC Prim Care | 2024 | 38273231 | PubTator, text mining | PubMed |
| Functionally-selective inhibition of threshold sodium currents and excitability in dorsal root ganglion neurons by cannabinol. | Commun Biol | 2024 | 38263462 | PubTator, text mining | PubMed |
| An Overview of Cannabidiol as a Multifunctional Drug: Pharmacokinetics and Cellular Effects. | Molecules | 2024 | 38257386 | PubTator, text mining | PubMed |
| State-Dependent Blockade of Dorsal Root Ganglion Voltage-Gated Na+ Channels by Anethole. | Int J Mol Sci | 2024 | 38256108 | PubTator, text mining | PubMed |
| A Literature Review: The Mechanisms and Treatment of Neuropathic Pain-A Brief Discussion. | Biomedicines | 2024 | 38255308 | PubTator, text mining | PubMed |
| The interplay among individuals' distress, daily activities, and perceptions of COVID-19 and neighborhood cohesion: A study using network analysis. | PLoS One | 2024 | 38236893 | PubTator, text mining | PubMed |
| Expanding the genotype-phenotype spectrum in SCN8A-related disorders. | BMC Neurol | 2024 | 38233770 | PubTator, text mining | PubMed |
| Atypical absence seizures and gene variants: A gene-based review of etiology, electro-clinical features, and associated epilepsy syndrome. | Epilepsy Behav | 2024 | 38232560 | PubTator, text mining | PubMed |
Development and application of a multiple reaction monitoring method for the simultaneous quantification of sodium channels Nav 1.1, Nav 1.2, and Nav 1.6 in solubilized membrane proteins from stable HEK293 cell lines, rodents, and human brain tissues. | Rapid Commun Mass Spectrom | 2024 | 38211346 | PubTator, text mining | PubMed |
gene-search-2026-11-11-0.2.0
Sources 12
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- EMBL-EBI's patent proteinsNo added restrictions. Attribution expected
- GenBank's patent filesNo restrictions from NCBI. Submitters may hold rights
- HGNCCC0
- NCBI GenePublic domain (US government)
- NIH's project files and grant-paper linksPublic domain
- Open TargetsCC0 1.0
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- EMBL-EBI's patent proteinsEMBL-EBI's patent protein files from the EPO, JPO, KIPO and USPTO. EMBL-EBI: "EMBL-EBI itself places no additional restrictions on the use or redistribution of the data available via its Data Resources and Tools other than those provided by the original data owners" and "EMBL-EBI expects attribution (e.g. in publications, services or products) for the use of any of its Data Resources and Tools." Read on 11 Nov 2026 at https://www.ebi.ac.uk/about/terms-of-use
- GenBank's patent filesGenBank's patent files. NCBI: "NCBI places no restrictions on the use or distribution of the GenBank data. However, some submitters may claim patent, copyright, or other intellectual property rights in all or a portion of the data they have submitted." Read on 11 Nov 2026 at https://www.ncbi.nlm.nih.gov/genbank/about/
- HGNCCC0: https://www.genenames.org/about/license/
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH's project files and grant-paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/genes/v1/6334/papers?page=9