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.
241 to 260 of 2,266
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Cerebral Seizures in an Adolescent with Jervell and Lange-Nielsen Syndrome: It May Not Be Epilepsy. | Clin Pract | 2022 | 36136864 | PubTator, text mining | PubMed |
| GenOtoScope: Towards automating ACMG classification of variants associated with congenital hearing loss. | PLoS Comput Biol | 2022 | 36129964 | PubTator, text mining | PubMed |
| Profiling mouse cochlear cell maturation using 10× Genomics single-cell transcriptomics. | Front Cell Neurosci | 2022 | 36060279 | PubTator, text mining | PubMed |
| Time-regulated transcripts with the potential to modulate human pluripotent stem cell-derived cardiomyocyte differentiation. | Stem Cell Res Ther | 2022 | 36056380 | PubTator, text mining | PubMed |
| Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. | Nat Commun | 2022 | 36050321 | PubTator, text mining | PubMed |
| AAV8BP2 and AAV8 transduce the mammalian cochlear lateral wall and endolymphatic sac with high efficiency. | Mol Ther Methods Clin Dev | 2022 | 36034771 | PubTator, text mining | PubMed |
| Genetic Analysis of Cardiac Syncope-Related Genes in Korean Patients with Recurrent Neurally Mediated Syncope. | J Cardiovasc Dev Dis | 2022 | 36005429 | PubTator, text mining | PubMed |
| Long QT syndrome and left ventricular non-compaction in a family with KCNH2 mutation: A case report. | Front Pediatr | 2022 | 35989994 | PubTator, text mining | PubMed |
| Sporadic Creutzfeldt-Jakob disease VM1: phenotypic and molecular characterization of a novel subtype of human prion disease. | Acta Neuropathol Commun | 2022 | 35978418 | PubTator, text mining | PubMed |
| Two small-molecule activators share similar effector sites in the KCNQ1 channel pore but have distinct effects on voltage sensor movements. | Front Physiol | 2022 | 35957984 | PubTator, text mining | PubMed |
| Placental DNA methylation in pregnancies complicated by maternal diabetes and/or obesity: State of the art and research gaps. | Epigenetics | 2022 | 35950598 | PubTator, text mining | PubMed |
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases. | J Arrhythm | 2022 | 35936045 | PubTator, text mining | PubMed |
| Pharmacological activation of the hERG K+ channel for the management of the long QT syndrome: A review. | J Arrhythm | 2022 | 35936037 | PubTator, text mining | PubMed |
| Exercise Testing Using Sprint Protocol vs Bruce Protocol in Catecholaminergic Polymorphic Ventricular Tachycardia. | JACC Case Rep | 2022 | 35935149 | PubTator, text mining | PubMed |
| 1029 genomes of self-declared healthy individuals from India reveal prevalent and clinically relevant cardiac ion channelopathy variants. | Hum Genomics | 2022 | 35932045 | PubTator, text mining | PubMed |
| Genetics of hyperuricemia and gout: Insights from recent genome-wide association studies and Mendelian randomization studies. | Tzu Chi Med J | 2022 | 35912057 | PubTator, text mining | PubMed |
| Disruption of a Conservative Motif in the C-Terminal Loop of the KCNQ1 Channel Causes LQT Syndrome. | Int J Mol Sci | 2022 | 35887302 | PubTator, text mining | PubMed |
| A Panel of Eight miRNAs Is Deregulated in HTLV-2 Infected PBMCs and BJABGu Cell Line. | Int J Mol Sci | 2022 | 35886938 | PubTator, text mining | PubMed |
| RNA-seq-driven expression analysis to investigate cardiovascular disease genes with associated phenotypes among atrial fibrillation patients. | Clin Transl Med | 2022 | 35875838 | PubTator, text mining | PubMed |
| Purification and membrane interactions of human KCNQ1100-370 potassium ion channel. | Biochim Biophys Acta Biomembr | 2022 | 35870481 | 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
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