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.
721 to 740 of 2,266
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Characterization of a novel LQT3 variant with a selective efficacy of mexiletine treatment. | Sci Rep | 2019 | 31506521 | PubTator, text mining | PubMed |
| Antitumor profiles and cardiac electrophysiological effects of aurora kinase inhibitor ZM447439. | Korean J Physiol Pharmacol | 2019 | 31496876 | PubTator, text mining | PubMed |
| Cochlear histopathology in human genetic hearing loss: State of the science and future prospects. | Hear Res | 2019 | 31493568 | PubTator, text mining | PubMed |
| The C-terminal HCN4 variant P883R alters channel properties and acts as genetic modifier of atrial fibrillation and structural heart disease. | Biochem Biophys Res Commun | 2019 | 31481236 | PubTator, text mining | PubMed |
| Towards Precision Medicine With Human iPSCs for Cardiac Channelopathies. | Circ Res | 2019 | 31465267 | PubTator, text mining | PubMed |
| Regulation of IKs Potassium Current by Isoproterenol in Adult Cardiomyocytes Requires Type 9 Adenylyl Cyclase. | Cells | 2019 | 31461851 | PubTator, text mining | PubMed |
| Genetic Mosaicism in Calmodulinopathy. | Circ Genom Precis Med | 2019 | 31454269 | PubTator, text mining | PubMed |
| [Jervell and Lange-Nielsen syndrome]. | Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi | 2019 | 31446697 | PubTator, text mining | PubMed |
| Long QT Syndrome: Genetics and Future Perspective. | Pediatr Cardiol | 2019 | 31440766 | PubTator, text mining | PubMed |
| Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairment. | Exp Mol Med | 2019 | 31434872 | PubTator, text mining | PubMed |
| Comprehensive analysis of syndromic hearing loss patients in Japan. | Sci Rep | 2019 | 31427586 | PubTator, text mining | PubMed |
| Differential coexpression networks in bronchiolitis and emphysema phenotypes reveal heterogeneous mechanisms of chronic obstructive pulmonary disease. | J Cell Mol Med | 2019 | 31419013 | PubTator, text mining | PubMed |
| Beyond the One Gene-One Disease Paradigm: Complex Genetics and Pleiotropy in Inheritable Cardiac Disorders | Circulation | 2019 | 31403841 | PubTator, text mining | PubMed |
| Clinical implications of sarcomere and nonsarcomere gene variants in patients with left ventricular noncompaction cardiomyopathy. | Mol Genet Genomic Med | 2019 | 31397097 | PubTator, text mining | PubMed |
| Phenotype-Based High-Throughput Classification of Long QT Syndrome Subtypes Using Human Induced Pluripotent Stem Cells. | Stem Cell Reports | 2019 | 31378668 | PubTator, text mining | PubMed |
| Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths. | Forensic Sci Int Genet | 2019 | 31376648 | PubTator, text mining | PubMed |
| Neuropathic pain and Kv7 voltage-gated potassium channels: The potential role of Kv7 activators in the treatment of neuropathic pain. | Mol Pain | 2019 | 31342847 | PubTator, text mining | PubMed |
| Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy. | BMC Cardiovasc Disord | 2019 | 31337358 | PubTator, text mining | PubMed |
| ML277 specifically enhances the fully activated open state of KCNQ1 by modulating VSD-pore coupling. | Elife | 2019 | 31329101 | PubTator, text mining | PubMed |
| A Rare Case of the Digenic Inheritance of Long QT Syndrome Type 2 and Type 6. | Case Rep Med | 2019 | 31320904 | 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=37