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.
381 to 400 of 2,325
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Multiple machine learning methods aided virtual screening of NaV 1.5 inhibitors. | J Cell Mol Med | 2023 | 36573431 | PubTator, text mining | PubMed |
| Bioinformatics and network pharmacology analysis of drug targets and mechanisms related to the comorbidity of epilepsy and migraine. | Epilepsy Res | 2023 | 36571905 | PubTator, text mining | PubMed |
| Detection of mosaic variants using genome sequencing in a large pediatric cohort. | Am J Med Genet A | 2023 | 36563179 | PubTator, text mining | PubMed |
| IMPROVE-DD: Integrating multiple phenotype resources optimizes variant evaluation in genetically determined developmental disorders. | HGG Adv | 2023 | 36561149 | PubTator, text mining | PubMed |
| The fates of internalized NaV1.7 channels in sensory neurons: Retrograde cotransport with other ion channels, axon-specific recycling, and degradation. | J Biol Chem | 2023 | 36539035 | PubTator, text mining | PubMed |
| Targeting aberrant dendritic integration to treat cognitive comorbidities of epilepsy. | Brain | 2023 | 36448426 | PubTator, text mining | PubMed |
| A Push-Pull Mechanism Between PRRT2 and β4-subunit Differentially Regulates Membrane Exposure and Biophysical Properties of NaV1.2 Sodium Channels. | Mol Neurobiol | 2023 | 36441479 | PubTator, text mining | PubMed |
| Riluzole and novel naphthalenyl substituted aminothiazole derivatives prevent acute neural excitotoxic injury in a rat model of temporal lobe epilepsy. | Neuropharmacology | 2023 | 36436594 | PubTator, text mining | PubMed |
| Genetic Diagnosis Impacts Medical Management for Pediatric Epilepsies. | Pediatr Neurol | 2023 | 36403551 | PubTator, text mining | PubMed |
| Using reported pathogenic variants to identify therapeutic opportunities for genetic diseases. | Mol Genet Genomic Med | 2023 | 36374045 | PubTator, text mining | PubMed |
| Structural Influence of Lone Pairs in GeP2 N4 , a Germanium(II) Nitridophosphate. | Angew Chem Int Ed Engl | 2023 | 36350660 | PubTator, text mining | PubMed |
| SCN1A gain-of-function mutation causing an early onset epileptic encephalopathy. | Epilepsia | 2023 | 36287100 | PubTator, text mining | PubMed |
| The genomic landscape across 474 surgically accessible epileptogenic human brain lesions. | Brain | 2023 | 36226386 | PubTator, text mining | PubMed |
| Cortical neuronal hyperexcitability and synaptic changes in SGCE mutation-positive myoclonus dystonia. | Brain | 2023 | 36204995 | PubTator, text mining | PubMed |
| Three-dimensional functional anatomy of the human sinoatrial node for epicardial and endocardial mapping and ablation. | Heart Rhythm | 2023 | 36113768 | PubTator, text mining | PubMed |
| Conserved patterns across ion channels correlate with variant pathogenicity and clinical phenotypes. | Brain | 2023 | 36036558 | PubTator, text mining | PubMed |
| YWHAZ variation causes intellectual disability and global developmental delay with brain malformation. | Hum Mol Genet | 2023 | 36001342 | PubTator, text mining | PubMed |
| Population pharmacokinetics of oxcarbazepine 10-monohydroxy derivative in Chinese adult epileptic patients. | Eur J Hosp Pharm | 2023 | 35787526 | PubTator, text mining | PubMed |
| Characterizing Genotypes and Phenotypes Associated with Dysfunction of Channel-Encoding Genes in a Cohort of Patients with Intellectual Disability. | Arch Iran Med | 2022 | 37543906 | PubTator, text mining | PubMed |
| Telehealth for patients with rare epilepsies. | Ther Adv Rare Dis | 2022 | 37180417 | 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=20