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.
661 to 680 of 2,266
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Calmodulin Mutations Associated with Heart Arrhythmia: A Status Report. | Int J Mol Sci | 2020 | 32093079 | PubTator, text mining | PubMed |
| Hypoxia Produces Pro-arrhythmic Late Sodium Current in Cardiac Myocytes by SUMOylation of NaV1.5 Channels. | Cell Rep | 2020 | 32075761 | PubTator, text mining | PubMed |
| Clinical and functional reappraisal of alleged type 5 long QT syndrome: Causative genetic variants in the KCNE1-encoded minK β-subunit. | Heart Rhythm | 2020 | 32058015 | PubTator, text mining | PubMed |
| Sudden cardiac death in young patients with diabetes: a call to study additional causes beyond ischaemic heart disease. | Eur Heart J | 2020 | 32031598 | PubTator, text mining | PubMed |
| Two-stage electro-mechanical coupling of a KV channel in voltage-dependent activation. | Nat Commun | 2020 | 32015334 | PubTator, text mining | PubMed |
| Long QT Syndrome Type 1 in an Australian Indigenous Patient. | Circ Genom Precis Med | 2020 | 32004091 | PubTator, text mining | PubMed |
Cardiac arrest in a mother and daughter and the identification of a novel RYR2 variant, predisposing to low penetrant catecholaminergic polymorphic ventricular tachycardia in a four-generation Canadian family. | Mol Genet Genomic Med | 2020 | 31994352 | PubTator, text mining | PubMed |
| An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome. | Circulation | 2020 | 31983240 | PubTator, text mining | PubMed |
| Combining an in silico proarrhythmic risk assay with a tPKPD model to predict QTc interval prolongation in the anesthetized guinea pig assay. | Toxicol Appl Pharmacol | 2020 | 31981640 | PubTator, text mining | PubMed |
| Simple Derivatization of RAFT-Synthesized Styrene-Maleic Anhydride Copolymers for Lipid Disk Formulations. | Biomacromolecules | 2020 | 31961664 | PubTator, text mining | PubMed |
| A male infant with Xq22.2q22.3 duplication containing PLP1 and MID2. | Mol Genet Genomic Med | 2020 | 31951325 | PubTator, text mining | PubMed |
| The effects of the DNA Demethylating reagent, 5-azacytidine on SMCHD1 genomic localization. | BMC Genet | 2020 | 31941450 | PubTator, text mining | PubMed |
| An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition. | Circulation | 2020 | 31941373 | PubTator, text mining | PubMed |
| Longitudinal epigenome-wide association studies of three male military cohorts reveal multiple CpG sites associated with post-traumatic stress disorder. | Clin Epigenetics | 2020 | 31931860 | PubTator, text mining | PubMed |
| Characterization and functional roles of KCNQ-encoded voltage-gated potassium (Kv7) channels in human corpus cavernosum smooth muscle. | Pflugers Arch | 2020 | 31919767 | PubTator, text mining | PubMed |
| MELK promotes Endometrial carcinoma progression via activating mTOR signaling pathway. | EBioMedicine | 2020 | 31915116 | PubTator, text mining | PubMed |
| Functional phenotype variations of two novel KV 7.1 mutations identified in patients with Long QT syndrome. | Pacing Clin Electrophysiol | 2020 | 31899541 | PubTator, text mining | PubMed |
| Structural Basis of Human KCNQ1 Modulation and Gating. | Cell | 2020 | 31883792 | PubTator, text mining | PubMed |
| Systematic Review of the Genetics of Sudden Unexpected Death in Epilepsy: Potential Overlap With Sudden Cardiac Death and Arrhythmia-Related Genes. | J Am Heart Assoc | 2020 | 31865891 | PubTator, text mining | PubMed |
| Physical and functional interaction sites in cytoplasmic domains of KCNQ1 and KCNE1 channel subunits. | Am J Physiol Heart Circ Physiol | 2020 | 31834838 | 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.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/genes/v1/3753/papers?page=34