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.
901 to 920 of 2,266
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Function of Adenylyl Cyclase in Heart: the AKAP Connection. | J Cardiovasc Dev Dis | 2018 | 29367580 | PubTator, text mining | PubMed |
| Targeted next generation sequencing in a young population with suspected inherited malignant cardiac arrhythmias. | Eur J Hum Genet | 2018 | 29343803 | PubTator, text mining | PubMed |
| Heterogeneous Contributing Factors in MPM Disease Development and Progression: Biological Advances and Clinical Implications. | Int J Mol Sci | 2018 | 29342862 | PubTator, text mining | PubMed |
| A C-terminal nonsense mutation links PTPRQ with autosomal-dominant hearing loss, DFNA73. | Genet Med | 2018 | 29309402 | PubTator, text mining | PubMed |
| Effect of GRM7 polymorphisms on the development of noise-induced hearing loss in Chinese Han workers: a nested case-control study. | BMC Med Genet | 2018 | 29301492 | PubTator, text mining | PubMed |
| Ion channels as part of macromolecular multiprotein complexes : Clinical significance. | Herzschrittmacherther Elektrophysiol | 2018 | 29214349 | PubTator, text mining | PubMed |
Using the genome aggregation database, computational pathogenicity prediction tools, and patch clamp heterologous expression studies to demote previously published long QT syndrome type 1 mutations from pathogenic to benign. | Heart Rhythm | 2018 | 29197658 | PubTator, text mining | PubMed |
| Review: The past, present and future challenges in epilepsy-related and sudden deaths and biobanking. | Neuropathol Appl Neurobiol | 2018 | 29178443 | PubTator, text mining | PubMed |
| Application of Multigene Panel Sequencing in Patients with Prolonged Rate-corrected QT Interval and No Pathogenic Variants Detected in KCNQ1, KCNH2, and SCN5A. | Ann Lab Med | 2018 | 29071820 | PubTator, text mining | PubMed |
| Sudden death: Neurogenic causes, prediction and prevention. | Eur J Prev Cardiol | 2018 | 29053016 | PubTator, text mining | PubMed |
| Recurrent variants in OTOF are significant contributors to prelingual nonsydromic hearing loss in Saudi patients. | Genet Med | 2018 | 29048421 | PubTator, text mining | PubMed |
| Re-evaluating pathogenicity of variants associated with the long QT syndrome. | J Cardiovasc Electrophysiol | 2018 | 28988457 | PubTator, text mining | PubMed |
| Cardiac Potassium Channels: Physiological Insights for Targeted Therapy. | J Cardiovasc Pharmacol Ther | 2018 | 28946759 | PubTator, text mining | PubMed |
| Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group. | Pharmacogenomics J | 2018 | 27958378 | PubTator, text mining | PubMed |
| Brugada syndrome: a fatal disease with complex genetic etiologies - still a long way to go. | Forensic Sci Res | 2017 | 30483629 | PubTator, text mining | PubMed |
| Breast Cancer Clinical Trial of Chemotherapy and Trastuzumab: Potential Tool to Identify Cardiac Modifying Variants of Dilated Cardiomyopathy. | J Cardiovasc Dev Dis | 2017 | 29367538 | PubTator, text mining | PubMed |
| Action Potential Recording and Pro-arrhythmia Risk Analysis in Human Ventricular Trabeculae. | Front Physiol | 2017 | 29354071 | PubTator, text mining | PubMed |
| Tailoring Mathematical Models to Stem-Cell Derived Cardiomyocyte Lines Can Improve Predictions of Drug-Induced Changes to Their Electrophysiology. | Front Physiol | 2017 | 29311950 | PubTator, text mining | PubMed |
| Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death. | Biology (Basel) | 2017 | 29278359 | PubTator, text mining | PubMed |
| Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP. | PLoS One | 2017 | 29261713 | 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=46