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.
801 to 820 of 4,098
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Human iPSC Modeling of Genetic Febrile Seizure Reveals Aberrant Molecular and Physiological Features Underlying an Impaired Neuronal Activity. | Biomedicines | 2022 | 35625812 | PubTator, text mining | PubMed |
| Pathophysiological Responses to Conotoxin Modulation of Voltage-Gated Ion Currents. | Mar Drugs | 2022 | 35621933 | PubTator, text mining | PubMed |
| Recessive PKD1 Mutations Are Associated With Febrile Seizures and Epilepsy With Antecedent Febrile Seizures and the Genotype-Phenotype Correlation. | Front Mol Neurosci | 2022 | 35620448 | PubTator, text mining | PubMed |
| A Narrative Review on Axonal Neuroprotection in Multiple Sclerosis. | Neurol Ther | 2022 | 35610531 | PubTator, text mining | PubMed |
| Origins of direction selectivity in the primate retina. | Nat Commun | 2022 | 35606344 | PubTator, text mining | PubMed |
| Cross-Talk Between Histone Methyltransferases and Demethylases Regulate REST Transcription During Neurogenesis. | Front Oncol | 2022 | 35600406 | PubTator, text mining | PubMed |
| ATP6V0C Is Associated With Febrile Seizures and Epilepsy With Febrile Seizures Plus. | Front Mol Neurosci | 2022 | 35600075 | PubTator, text mining | PubMed |
| Whole exome sequencing and co-expression analysis identify an SCN1A variant that modifies pathogenicity in a family with genetic epilepsy and febrile seizures plus. | Epilepsia | 2022 | 35592948 | PubTator, text mining | PubMed |
| The Bradycardic Agent Ivabradine Acts as an Atypical Inhibitor of Voltage-Gated Sodium Channels. | Front Pharmacol | 2022 | 35586063 | PubTator, text mining | PubMed |
A Triple-Heterozygous β-Thalassemia Patient Demonstrated an Unusual Electrophoresis Pattern Due to a Novel β0 Mutation [an IVS-II-654 (C>T) mutation with a Hb Zürich-Langstrasse (HBB: c.151A>T) mutation in cis]. | Hemoglobin | 2022 | 35575165 | PubTator, text mining | PubMed |
| Paradoxical Hyperexcitability in Disorders of Neurodevelopment. | Front Mol Neurosci | 2022 | 35571370 | PubTator, text mining | PubMed |
| Genetic and Phenotype Analysis of a Chinese Cohort of Infants and Children With Epilepsy. | Front Genet | 2022 | 35571021 | PubTator, text mining | PubMed |
| Small RNA sequencing and identification of papaya (Carica papaya L.) miRNAs with potential cross-kingdom human gene targets. | Mol Genet Genomics | 2022 | 35570207 | PubTator, text mining | PubMed |
| SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility. | Acta Neuropathol | 2022 | 35551471 | PubTator, text mining | PubMed |
| Assessment of functional shunting in patients with sickle cell disease. | Haematologica | 2022 | 35548868 | PubTator, text mining | PubMed |
| Surface-engineered extracellular vesicles for targeted delivery of therapeutic RNAs and peptides for cancer therapy. | Theranostics | 2022 | 35547755 | PubTator, text mining | PubMed |
| Patient with Dravet syndrome: A case report. | Clin Case Rep | 2022 | 35540719 | PubTator, text mining | PubMed |
| A predictive study of metabolism reprogramming in cervical carcinoma. | Ann Transl Med | 2022 | 35530966 | PubTator, text mining | PubMed |
| Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions. | Front Pediatr | 2022 | 35529330 | PubTator, text mining | PubMed |
| [HemoTypeSC screening for sickle cell disease in the Democratic Republic of Congo (DRC): a case from the city of Kindu]. | Pan Afr Med J | 2022 | 35519159 | 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=41