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.
741 to 760 of 2,266
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Cardiac Arrest Associated with Both an Anomalous Left Coronary Artery and KCNE1 Polymorphism. | Int Heart J | 2019 | 31308327 | PubTator, text mining | PubMed |
| Linkage Evidence for a Two-Locus Inheritance of LQT-Associated Seizures in a Multigenerational LQT Family With a Novel KCNQ1 Loss-of-Function Mutation. | Front Neurol | 2019 | 31293497 | PubTator, text mining | PubMed |
| Understanding the Beat-to-Beat Variations of P-Waves Morphologies in AF Patients During Sinus Rhythm: A Scoping Review of the Atrial Simulation Studies. | Front Physiol | 2019 | 31275161 | PubTator, text mining | PubMed |
| The research of ion channel-related gene polymorphisms with atrial fibrillation in the Chinese Han population. | Mol Genet Genomic Med | 2019 | 31270966 | PubTator, text mining | PubMed |
| Gating modulation of the KCNQ1 channel by KCNE proteins studied by voltage-clamp fluorometry. | Biophys Physicobiol | 2019 | 31236320 | PubTator, text mining | PubMed |
| Disease-linked mutations alter the stoichiometries of HCN-KCNE2 complexes. | Sci Rep | 2019 | 31235733 | PubTator, text mining | PubMed |
| Human-induced pluripotent stem cell-derived cardiomyocytes have limited IKs for repolarization reserve as revealed by specific KCNQ1/KCNE1 blocker. | JRSM Cardiovasc Dis | 2019 | 31217965 | PubTator, text mining | PubMed |
| Regulatory Role of lncRNA NONHSAT089447 in the Dopamine Signaling Pathway in Schizophrenic Patients. | Med Sci Monit | 2019 | 31180069 | PubTator, text mining | PubMed |
| Di-(2-ethylhexyl)-phthalate induces apoptosis via the PPARγ/PTEN/AKT pathway in differentiated human embryonic stem cells. | Food Chem Toxicol | 2019 | 31163220 | PubTator, text mining | PubMed |
| Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies. | Front Genet | 2019 | 31156706 | PubTator, text mining | PubMed |
| ORVAL: a novel platform for the prediction and exploration of disease-causing oligogenic variant combinations. | Nucleic Acids Res | 2019 | 31147699 | PubTator, text mining | PubMed |
| Ion Transporters, Channelopathies, and Glucose Disorders. | Int J Mol Sci | 2019 | 31137773 | PubTator, text mining | PubMed |
| Cases in Precision Medicine: Genetic Assessment After a Sudden Cardiac Death in the Family. | Ann Intern Med | 2019 | 31083726 | PubTator, text mining | PubMed |
| TREML4 mRNA Expression and Polymorphisms in Blood Leukocytes are Associated with Atherosclerotic Lesion Extension in Coronary Artery Disease. | Sci Rep | 2019 | 31076644 | PubTator, text mining | PubMed |
| Emerging roles for multifunctional ion channel auxiliary subunits in cancer. | Cell Calcium | 2019 | 31071485 | PubTator, text mining | PubMed |
| The Polymorphic Analysis of the Human Potassium Channel KCNE Gene Family in Meniere's Disease-A Preliminary Study. | J Int Adv Otol | 2019 | 31058602 | PubTator, text mining | PubMed |
| Functional and pharmacological characterization of an S5 domain hERG mutation associated with short QT syndrome. | Heliyon | 2019 | 31049424 | PubTator, text mining | PubMed |
| Recurrent idiopathic polymorphic ventricular tachycardia/ventricular fibrillation successfully treated by cardiac sympathetic denervation. | HeartRhythm Case Rep | 2019 | 30997341 | PubTator, text mining | PubMed |
| Investigating the Complex Arrhythmic Phenotype Caused by the Gain-of-Function Mutation KCNQ1-G229D. | Front Physiol | 2019 | 30967788 | PubTator, text mining | PubMed |
| Optical Recording of Action Potentials in Human Induced Pluripotent Stem Cell-Derived Cardiac Single Cells and Monolayers Generated from Long QT Syndrome Type 1 Patients. | Stem Cells Int | 2019 | 30956674 | 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=38