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.
841 to 860 of 4,098
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| On the edge-A diagnostic odyssey. | Clin Case Rep | 2022 | 35425609 | PubTator, text mining | PubMed |
| Cellular and behavioral effects of altered NaV1.2 sodium channel ion permeability in Scn2aK1422E mice. | Hum Mol Genet | 2022 | 35417922 | PubTator, text mining | PubMed |
| SCN2A-related epilepsy of infancy with migrating focal seizures: report of a variant with apparent gain- and loss-of-function effects. | J Neurophysiol | 2022 | 35417276 | PubTator, text mining | PubMed |
| KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizures. | ASN Neuro | 2022 | 35414199 | PubTator, text mining | PubMed |
| Non-canonical endogenous expression of voltage-gated sodium channel NaV 1.7 subtype by the TE671 rhabdomyosarcoma cell line. | J Physiol | 2022 | 35413129 | PubTator, text mining | PubMed |
| Glucose increases the length and spacing of the lattice structure of the axon initial segment. | Microsc Res Tech | 2022 | 35411984 | PubTator, text mining | PubMed |
| New Insights into Hemopexin-Binding to Hemin and Hemoglobin. | Int J Mol Sci | 2022 | 35409149 | PubTator, text mining | PubMed |
| Functional Voltage-Gated Sodium Channels Are Present in the Human B Cell Membrane. | Cells | 2022 | 35406789 | PubTator, text mining | PubMed |
| Role of hemoglobin alpha and hemoglobin beta in non-small-cell lung cancer based on bioinformatics analysis. | Mol Carcinog | 2022 | 35394695 | PubTator, text mining | PubMed |
| A de novo PUM1 Variant in a Girl With a Dravet-Like Syndrome: Case Report and Literature Review. | Front Pediatr | 2022 | 35386260 | PubTator, text mining | PubMed |
| Gain-of-function and loss-of-function GABRB3 variants lead to distinct clinical phenotypes in patients with developmental and epileptic encephalopathies. | Nat Commun | 2022 | 35383156 | PubTator, text mining | PubMed |
| Characteristics of infantile convulsions and choreoathetosis syndrome caused by PRRT2 mutation. | Pediatr Investig | 2022 | 35382417 | PubTator, text mining | PubMed |
| [Association of SCN2A, ABCB1 and CYP2C19*3 with genetic susceptibility to major depressive disorder]. | Zhonghua Yu Fang Yi Xue Za Zhi | 2022 | 35381649 | PubTator, text mining | PubMed |
| Neonatal seizures: diagnostic updates based on new definition and classification. | Clin Exp Pediatr | 2022 | 35381171 | PubTator, text mining | PubMed |
| Druggability of Voltage-Gated Sodium Channels-Exploring Old and New Drug Receptor Sites. | Front Pharmacol | 2022 | 35370700 | PubTator, text mining | PubMed |
| Developmental pyrethroid exposure and age influence phenotypes in a Chd8 haploinsufficient autism mouse model. | Sci Rep | 2022 | 35365720 | PubTator, text mining | PubMed |
| Identification of epilepsy concomitant candidate genes recognized in Saudi epileptic patients. | Eur Rev Med Pharmacol Sci | 2022 | 35363364 | PubTator, text mining | PubMed |
| Do All Roads Lead to Rome? Genes Causing Dravet Syndrome and Dravet Syndrome-Like Phenotypes. | Front Neurol | 2022 | 35359639 | PubTator, text mining | PubMed |
| Modeling Epilepsy Using Human Induced Pluripotent Stem Cells-Derived Neuronal Cultures Carrying Mutations in Ion Channels and the Mechanistic Target of Rapamycin Pathway. | Front Mol Neurosci | 2022 | 35359577 | PubTator, text mining | PubMed |
| Commonalities and distinctions between two neurodevelopmental disorder subtypes associated with SCN2A and SCN8A variants and literature review. | Mol Genet Genomic Med | 2022 | 35348308 | 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.
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GET https://conductscience.org/api/genes/v1/6326/papers?page=43