Gene · 6326
Papers4,098
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
381 to 400 of 4,098
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| The dysregulation of miRNAs in epilepsy and their regulatory role in inflammation and apoptosis. | Funct Integr Genomics | 2023 | 37653173 | PubTator, text mining | PubMed |
| Epilepsy phenotype and gene ontology analysis of the 129 genes in a large neurodevelopmental disorders cohort. | Front Neurol | 2023 | 37645600 | PubTator, text mining | PubMed |
| Deep brain stimulation for status dystonicus in a toddler with SCN2A-related disorder. | Childs Nerv Syst | 2023 | 37642686 | PubTator, text mining | PubMed |
| An integrated approach for early in vitro seizure prediction utilizing hiPSC neurons and human ion channel assays. | Toxicol Sci | 2023 | 37632788 | PubTator, text mining | PubMed |
| Voltage-Gated Na+ Channels in Alzheimer's Disease: Physiological Roles and Therapeutic Potential. | Life (Basel) | 2023 | 37629512 | PubTator, text mining | PubMed |
| Store-Operated Ca2+ Entry as a Putative Target of Flecainide for the Treatment of Arrhythmogenic Cardiomyopathy. | J Clin Med | 2023 | 37629337 | PubTator, text mining | PubMed |
| Genotype-Phenotype Analysis of Children with Epilepsy Referred for Whole-Exome Sequencing at a Tertiary Care University Hospital. | Children (Basel) | 2023 | 37628333 | PubTator, text mining | PubMed |
Correlation of Transfusion Dependence and Its Associated Sequelae to Hematological and Biochemical Parameters in Patients With Sickle Cell Disease and Beta Thalassemia Major in Khobar: A Retrospective Study. | Cureus | 2023 | 37602131 | PubTator, text mining | PubMed |
| Challenge in diagnosis of hemoglobin E/beta thalassemia during pregnancy: A case report. | Int J Surg Case Rep | 2023 | 37597431 | PubTator, text mining | PubMed |
Generation of an iPSC line (FINi001-A) from a girl with developmental and epileptic encephalopathy due to a heterozygous gain-of-function p.R1882Q variant in the voltage-gated sodium channel Nav1.2 protein encoded by the SCN2A gene. | Stem Cell Res | 2023 | 37597357 | PubTator, text mining | PubMed |
| Phenotypic and genetic characteristics of 24 cases of early infantile epileptic encephalopathy in East China, including a rare case of biallelic UGDH mutations. | Mol Genet Genomic Med | 2023 | 37593999 | PubTator, text mining | PubMed |
| Landscape of genetic infantile epileptic spasms syndrome-A multicenter cohort of 124 children from India. | Epilepsia Open | 2023 | 37583270 | PubTator, text mining | PubMed |
| Epilepsy-associated SCN2A (NaV1.2) variants exhibit diverse and complex functional properties. | J Gen Physiol | 2023 | 37578743 | PubTator, text mining | PubMed |
| Comparative yield of molecular diagnostic algorithms for autism spectrum disorder diagnosis in India: evidence supporting whole exome sequencing as first tier test. | BMC Neurol | 2023 | 37543562 | PubTator, text mining | PubMed |
| A Rare Cause of Paroxysmal Movement Disorder Associated with TBC1D24 Gene Mutation in Two Siblings. | Ann Indian Acad Neurol | 2023 | 37538433 | PubTator, text mining | PubMed |
| Cold and warmth intensify pain-linked sodium channel gating effects and persistent currents. | J Gen Physiol | 2023 | 37531097 | PubTator, text mining | PubMed |
| An Uncommon Case of Recurrent Hypoglycemic Episodes in a Healthy Non-diabetic Male: Insulin Autoimmune Syndrome. | Cureus | 2023 | 37525774 | PubTator, text mining | PubMed |
| Editorial: Non-coding RNAs in neurodegenerative diseases. | Front Neurosci | 2023 | 37521693 | PubTator, text mining | PubMed |
| Genetic Modulation of the Erythrocyte Phenotype Associated with Retinopathy of Prematurity-A Multicenter Portuguese Cohort Study. | Int J Mol Sci | 2023 | 37511576 | PubTator, text mining | PubMed |
| Brevetoxin versus Brevenal Modulation of Human Nav1 Channels. | Mar Drugs | 2023 | 37504927 | 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/v1/6326/papers?page=20