Gene · 3753
Papers2,266
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
1,041 to 1,060 of 2,266
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Atrial fibrillation: Therapeutic potential of atrial K+ channel blockers. | Pharmacol Ther | 2017 | 27742566 | PubTator, text mining | PubMed |
| Thorough QT study of the effect of intravenous amisulpride on QTc interval in Caucasian and Japanese healthy subjects. | Br J Clin Pharmacol | 2017 | 27618796 | PubTator, text mining | PubMed |
| Latent pathogenicity of the G38S polymorphism of KCNE1 K+ channel modulator. | Heart Vessels | 2017 | 27255646 | PubTator, text mining | PubMed |
| Epilepsy-related sudden unexpected death: targeted molecular analysis of inherited heart disease genes using next-generation DNA sequencing. | Brain Pathol | 2017 | 27135274 | PubTator, text mining | PubMed |
| Electrophysiological properties of iPS cell-derived cardiomyocytes from a patient with long QT syndrome type 1 harboring the novel mutation M437V of KCNQ1. | Regen Ther | 2016 | 31245483 | PubTator, text mining | PubMed |
| Genetic basis of atrial fibrillation. | Genes Dis | 2016 | 30258896 | PubTator, text mining | PubMed |
| Genomic-based diagnosis of arrhythmia disease in a personalized medicine era. | Expert Rev Precis Med Drug Dev | 2016 | 28944294 | PubTator, text mining | PubMed |
| Structural interplay of KV7.1 and KCNE1 is essential for normal repolarization and is compromised in short QT syndrome 2 (KV7.1-A287T). | HeartRhythm Case Rep | 2016 | 28491751 | PubTator, text mining | PubMed |
| Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3-specific calmodulinopathy. | HeartRhythm Case Rep | 2016 | 28491681 | PubTator, text mining | PubMed |
| Normalization of QT interval duration in a long QT syndrome patient during pregnancy and the postpartum period due to sex hormone effects on cardiac repolarization. | HeartRhythm Case Rep | 2016 | 28491674 | PubTator, text mining | PubMed |
| Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study. | PLoS One | 2016 | 28030616 | PubTator, text mining | PubMed |
| Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated with Congenital Complete Heart Block in the Thai Population. | Dis Markers | 2016 | 28018021 | PubTator, text mining | PubMed |
| Translational Prospects and Challenges in Human Induced Pluripotent Stem Cell Research in Drug Discovery. | Cells | 2016 | 28009813 | PubTator, text mining | PubMed |
| Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation. | PLoS One | 2016 | 27930701 | PubTator, text mining | PubMed |
| Modeling Inherited Arrhythmia Disorders Using Induced Pluripotent Stem Cell-Derived Cardiomyocytes. | Circ J | 2016 | 27916777 | PubTator, text mining | PubMed |
| Epidemiology and genetics of ventricular fibrillation during acute myocardial infarction. | J Geriatr Cardiol | 2016 | 27899944 | PubTator, text mining | PubMed |
| A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family Study. | Front Genet | 2016 | 27877193 | PubTator, text mining | PubMed |
| TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT. | EMBO Mol Med | 2016 | 27861123 | PubTator, text mining | PubMed |
| Functional Studies and In Silico Analyses to Evaluate Non-Coding Variants in Inherited Cardiomyopathies. | Int J Mol Sci | 2016 | 27834932 | PubTator, text mining | PubMed |
| Receptor Species-dependent Desensitization Controls KCNQ1/KCNE1 K+ Channels as Downstream Effectors of Gq Protein-coupled Receptors. | J Biol Chem | 2016 | 27834678 | 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/v1/3753/papers?page=53