Gene · 3785
Papers2,279
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
261 to 280 of 2,279
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Benzydamine plays a role in limiting inflammatory pain induced by neuronal sensitization. | Mol Pain | 2023 | 37710969 | PubTator, text mining | PubMed |
| A cross-species proteomic map reveals neoteny of human synapse development. | Nature | 2023 | 37704727 | PubTator, text mining | PubMed |
Advances for pediatricians in 2022: allergy, anesthesiology, cardiology, dermatology, endocrinology, gastroenterology, genetics, global health, infectious diseases, metabolism, neonatology, neurology, oncology, pulmonology. | Ital J Pediatr | 2023 | 37679850 | PubTator, text mining | PubMed |
Generation of three induced pluripotent stem cell lines from a patient with KCNQ2 developmental and epileptic encephalopathy as a result of the pathogenic variant c.881C > T; p.Ala294Val (NUIGi059-A, NUIGi059-B, NUIGi059-C) and 3 healthy controls (NUIGi060-A, NUIGi060-B, NUIGi060-C). | Stem Cell Res | 2023 | 37659345 | PubTator, text mining | PubMed |
| iPSC motor neurons, but not other derived cell types, capture gene expression changes in postmortem sporadic ALS motor neurons. | Cell Rep | 2023 | 37651231 | PubTator, text mining | PubMed |
| Dehydroepiandrosterone Sulfate (DHEAS) Is an Endogenous Kv7 Channel Modulator That Reduces Kv7/M-Current Suppression and Inflammatory Pain. | J Neurosci | 2023 | 37648450 | 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 |
| Editorial: Ion-channels in epilepsy. | Front Neurol | 2023 | 37638194 | 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 |
| 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 |
| Epigenetic m6A RNA Modification Reader YTHDF1 in Merkel Cell Carcinoma. | Cancers (Basel) | 2023 | 37627103 | PubTator, text mining | PubMed |
| TDP-43-regulated cryptic RNAs accumulate in Alzheimer's disease brains. | Mol Neurodegener | 2023 | 37605276 | 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 |
| Retracted: Clinical and genetic evaluations of rare childhood epilepsies in Turkey's national cohort. | Epileptic Disord | 2023 | 37584621 | 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 |
| 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 |
| At-Risk Genomic Findings for Pediatric-Onset Disorders From Genome Sequencing vs Medically Actionable Gene Panel in Proactive Screening of Newborns and Children. | JAMA Netw Open | 2023 | 37523181 | PubTator, text mining | PubMed |
| Trends and hotspots in gene research of epilepsy in children: A review and bibliometric analysis from 2010 to 2022. | Medicine (Baltimore) | 2023 | 37505157 | PubTator, text mining | PubMed |
| Clinical analysis and functional characterization of KCNQ2-related developmental and epileptic encephalopathy. | Front Mol Neurosci | 2023 | 37497102 | 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.
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