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.
281 to 300 of 4,098
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Identification of a rare [Gγ(Aγδβ)0] -thalassemia using tandem mass spectrometry. | Proteomics | 2024 | 38212249 | 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 |
| SCN4A-related congenital myopathy in a Han Chinese patient: A case report and literature review. | Heliyon | 2024 | 38187266 | PubTator, text mining | PubMed |
| Possibilities and limitations of antisense oligonucleotide therapies for the treatment of monogenic disorders. | Commun Med (Lond) | 2024 | 38182878 | PubTator, text mining | PubMed |
| Nav1.7 as a chondrocyte regulator and therapeutic target for osteoarthritis. | Nature | 2024 | 38172636 | PubTator, text mining | PubMed |
| FDA Patient-Focused Drug Development Guidances: Considerations for Trial Readiness in Rare Developmental and Epileptic Encephalopathies | Neurology | 2024 | 38165374 | PubTator, text mining | PubMed |
| Neurodevelopmental outcomes in a cohort of Australian families with self-limited familial epilepsy of neonatal/infantile onset. | Seizure | 2024 | 38160512 | PubTator, text mining | PubMed |
| Distinctive In Vitro Phenotypes in iPSC-Derived Neurons From Patients With Gain- and Loss-of-Function SCN2A Developmental and Epileptic Encephalopathy. | J Neurosci | 2024 | 38148154 | PubTator, text mining | PubMed |
| Prioritizing de novo potential non-canonical splicing variants in neurodevelopmental disorders. | EBioMedicine | 2024 | 38113761 | PubTator, text mining | PubMed |
| Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene. | Eur J Hum Genet | 2024 | 38097767 | PubTator, text mining | PubMed |
| Biallelic pathogenic variants of PARS2 cause developmental and epileptic encephalopathy with spike-and-wave activation in sleep. | Mol Genet Genomic Med | 2024 | 38087948 | PubTator, text mining | PubMed |
| Common genes and recurrent causative variants in 957 Asian patients with pediatric epilepsy. | Epilepsia | 2024 | 38073125 | PubTator, text mining | PubMed |
| What does better look like in individuals with severe neurodevelopmental impairments? A qualitative descriptive study on SCN2A-related developmental and epileptic encephalopathy. | Qual Life Res | 2024 | 38064015 | PubTator, text mining | PubMed |
| Rapid haemoglobin A and S quantification using Tosoh HLC-723G8 in variant mode for patients with sickle cell disease. | Biomed Chromatogr | 2024 | 38041149 | PubTator, text mining | PubMed |
| A structural atlas of druggable sites on Nav channels. | Channels (Austin) | 2024 | 38033122 | PubTator, text mining | PubMed |
Voluntary running wheel exercise induces cognitive improvement post traumatic brain injury in mouse model through redressing aberrant excitation regulated by voltage-gated sodium channels 1.1, 1.3, and 1.6. | Exp Brain Res | 2024 | 37994916 | PubTator, text mining | PubMed |
| Prediction of molecular phenotypes for novel SCN1A variants from a Turkish genetic epilepsy syndromes cohort and report of two new patients with recessive Dravet syndrome. | Clin Transl Sci | 2024 | 37955180 | PubTator, text mining | PubMed |
| Characterization of Na+ currents regulating intrinsic excitability of optic tectal neurons. | Life Sci Alliance | 2024 | 37918964 | PubTator, text mining | PubMed |
| Inversed Effects of Nav1.2 Deficiency at Medial Prefrontal Cortex and Ventral Tegmental Area for Prepulse Inhibition in Acoustic Startle Response. | Mol Neurobiol | 2024 | 37650965 | PubTator, text mining | PubMed |
| Identification of common core ion channel genes in epilepsy and Alzheimer's disease. | Ir J Med Sci | 2024 | 37477849 | 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
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