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.
401 to 420 of 2,266
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Deconvolution of multiplexed transcriptional responses to wood smoke particles defines rapid aryl hydrocarbon receptor signaling dynamics. | J Biol Chem | 2021 | 34520756 | PubTator, text mining | PubMed |
| Paediatric/young versus adult patients with long QT syndrome. | Open Heart | 2021 | 34518285 | PubTator, text mining | PubMed |
| Molecular mechanisms of activation and regulation of ANO1-Encoded Ca2+-Activated Cl- channels. | Channels (Austin) | 2021 | 34488544 | PubTator, text mining | PubMed |
| Myocardial ultrastructure can augment genetic testing for sporadic dilated cardiomyopathy with initial heart failure. | ESC Heart Fail | 2021 | 34486814 | PubTator, text mining | PubMed |
| The Prevalence, Risk Factors and Clinical Correlates of QTc Prolongation in Chinese Hospitalized Patients With Chronic Schizophrenia. | Front Psychiatry | 2021 | 34483996 | PubTator, text mining | PubMed |
| Advances in the Molecular Genetics of Catecholaminergic Polymorphic Ventricular Tachycardia. | Front Pharmacol | 2021 | 34483927 | PubTator, text mining | PubMed |
| Genome-wide association study identifies new loci associated with noise-induced tinnitus in Chinese populations. | BMC Genom Data | 2021 | 34482816 | PubTator, text mining | PubMed |
| Anion and Cation Permeability of the Mouse TMEM16F Calcium-Activated Channel. | Int J Mol Sci | 2021 | 34445284 | PubTator, text mining | PubMed |
| Molecular Autopsy of Sudden Cardiac Death in the Genomics Era. | Diagnostics (Basel) | 2021 | 34441312 | PubTator, text mining | PubMed |
| Sudden Unexpected Death Associated with Arrhythmogenic Cardiomyopathy: Study of the Cardiac Conduction System. | Diagnostics (Basel) | 2021 | 34441258 | PubTator, text mining | PubMed |
| Molecular autopsy and subsequent functional analysis reveal de novo DSG2 mutation as cause of sudden death. | Eur J Med Genet | 2021 | 34438094 | PubTator, text mining | PubMed |
| The Contribution of Known Familial Cardiovascular Disease Genes to Sudden Cardiac Death in Patients Undergoing Hemodialysis. | Cardiorenal Med | 2021 | 34433165 | PubTator, text mining | PubMed |
| Genetic testing hearing loss: The challenge of non syndromic mimics. | Int J Pediatr Otorhinolaryngol | 2021 | 34433113 | PubTator, text mining | PubMed |
| Update on human genetic susceptibility to COVID-19: susceptibility to virus and response. | Hum Genomics | 2021 | 34429158 | PubTator, text mining | PubMed |
| Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association. | Circ Genom Precis Med | 2021 | 34412507 | PubTator, text mining | PubMed |
| Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study. | BMC Med | 2021 | 34404389 | PubTator, text mining | PubMed |
| Genetic Susceptibility Study of Chinese Sudden Sensorineural Hearing Loss Patients with Vertigo. | Curr Med Sci | 2021 | 34403091 | PubTator, text mining | PubMed |
| Recurrent Pregnancy Loss and Concealed Long-QT Syndrome. | J Am Heart Assoc | 2021 | 34398675 | PubTator, text mining | PubMed |
| Early Identification of Prolonged QT Interval for Prevention of Sudden Infant Death. | Front Pediatr | 2021 | 34395343 | PubTator, text mining | PubMed |
| Interpretation of Incidental Genetic Findings Localizing to Genes Associated With Cardiac Channelopathies and Cardiomyopathies. | Circ Genom Precis Med | 2021 | 34384235 | 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=21