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.
621 to 640 of 2,266
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Genome-wide association studies of cardiac electrical phenotypes. | Cardiovasc Res | 2020 | 32428210 | PubTator, text mining | PubMed |
| Electron Paramagnetic Resonance as a Tool for Studying Membrane Proteins. | Biomolecules | 2020 | 32414134 | PubTator, text mining | PubMed |
| COVID-19, Clinical Trials, and QT-Prolonging Prophylactic Therapy in Healthy Subjects: First, Do No Harm. | J Am Coll Cardiol | 2020 | 32407770 | PubTator, text mining | PubMed |
| Genetic susceptibility for COVID-19-associated sudden cardiac death in African Americans. | Heart Rhythm | 2020 | 32380288 | PubTator, text mining | PubMed |
| Functional Consequences of the Variable Stoichiometry of the Kv1.3-KCNE4 Complex. | Cells | 2020 | 32370164 | PubTator, text mining | PubMed |
| Penalized logistic regression based on L1/2 penalty for high-dimensional DNA methylation data. | Technol Health Care | 2020 | 32364148 | PubTator, text mining | PubMed |
| When genetic burden reaches threshold. | Eur Heart J | 2020 | 32350504 | PubTator, text mining | PubMed |
| Generation of three iPSC lines (XACHi007-A, XACHi008-A, XACHi009-A) from a Chinese family with long QT syndrome type 5 with heterozygous c.226G>A (p.D76N) mutation in KCNE1gene. | Stem Cell Res | 2020 | 32344329 | PubTator, text mining | PubMed |
| Rottlerin: Structure Modifications and KCNQ1/KCNE1 Ion Channel Activity. | ChemMedChem | 2020 | 32338831 | PubTator, text mining | PubMed |
| Small-conductance Ca2+-activated K+ channels promote J-wave syndrome and phase 2 reentry. | Heart Rhythm | 2020 | 32333974 | PubTator, text mining | PubMed |
| Associations of Genetic Variation in Glyceraldehyde 3-Phosphate Dehydrogenase Gene with Noise-Induced Hearing Loss in a Chinese Population: A Case-Control Study. | Int J Environ Res Public Health | 2020 | 32331439 | PubTator, text mining | PubMed |
| Pro-Arrhythmic Signaling of Thyroid Hormones and Its Relevance in Subclinical Hyperthyroidism. | Int J Mol Sci | 2020 | 32325836 | PubTator, text mining | PubMed |
| Serine mutation of a conserved threonine in the hERG K+ channel S6-pore region leads to loss-of-function through trafficking impairment. | Biochem Biophys Res Commun | 2020 | 32321643 | PubTator, text mining | PubMed |
| The rs2236609 Polymorphism Is Related to Increased Risk Susceptibility of Atrial Fibrillation. | Public Health Genomics | 2020 | 32316011 | PubTator, text mining | PubMed |
| Targeted next generation sequencing revealed a novel deletion-frameshift mutation of KCNH2 gene in a Chinese Han family with long QT syndrome: A case report and review of Chinese cases. | Medicine (Baltimore) | 2020 | 32311972 | PubTator, text mining | PubMed |
| PITX2 upregulation increases the risk of chronic atrial fibrillation in a dose-dependent manner by modulating IKs and ICaL -insights from human atrial modelling. | Ann Transl Med | 2020 | 32309338 | PubTator, text mining | PubMed |
| Diagnostic and therapeutic applications of genomic medicine in progressive, late-onset, nonsyndromic sensorineural hearing loss. | Gene | 2020 | 32304785 | PubTator, text mining | PubMed |
| Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans. | PLoS Genet | 2020 | 32294086 | PubTator, text mining | PubMed |
| The unconventional biogenesis of Kv7.1-KCNE1 complexes. | Sci Adv | 2020 | 32270035 | PubTator, text mining | PubMed |
| Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes. | EBioMedicine | 2020 | 32268277 | 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=32