Gene · 4607
Papers3,985
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
1,541 to 1,560 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Familial Arrhythmogenic Cardiomyopathy: Clinical Determinants of Phenotype Discordance and the Impact of Endurance Sports. | J Clin Med | 2020 | 33238575 | PubTator, text mining | PubMed |
| Identifying transcriptomic correlates of histology using deep learning. | PLoS One | 2020 | 33237966 | PubTator, text mining | PubMed |
| Gene expression responses to Zika virus infection in peripheral blood mononuclear cells from pregnant and non-pregnant women. | Microbiologyopen | 2020 | 33211409 | PubTator, text mining | PubMed |
| An interesting Mybpc3 heterozygous mutation associated with bicuspid aortic valve. | Transl Pediatr | 2020 | 33209723 | PubTator, text mining | PubMed |
| Apical hypertrophic cardiomyopathy, are low-risk patients really at low risk? A case report. | Eur Heart J Case Rep | 2020 | 33204988 | PubTator, text mining | PubMed |
| Role of Non-Coding Variants in Brugada Syndrome. | Int J Mol Sci | 2020 | 33202810 | PubTator, text mining | PubMed |
| Natural Biomaterials for Cardiac Tissue Engineering: A Highly Biocompatible Solution. | Front Cardiovasc Med | 2020 | 33195451 | PubTator, text mining | PubMed |
| Ventricular Arrhythmia in Septal and Apical Hypertrophic Cardiomyopathy: The French-Canadian Experience. | Front Cardiovasc Med | 2020 | 33195448 | PubTator, text mining | PubMed |
| A case report of congenital myasthenic syndrome caused by a mutation in theCHRNE genein the Iranian population. | Iran J Child Neurol | 2020 | 33193787 | PubTator, text mining | PubMed |
| Multi-Omics Analysis Detects Novel Prognostic Subgroups of Breast Cancer. | Front Genet | 2020 | 33193681 | PubTator, text mining | PubMed |
| Genetic Dilated Cardiomyopathy Due to TTN Variants Without Known Familial Disease. | Circ Genom Precis Med | 2020 | 33190517 | PubTator, text mining | PubMed |
| Hypothesis: Single Actomyosin Properties Account for Ensemble Behavior in Active Muscle Shortening and Isometric Contraction. | Int J Mol Sci | 2020 | 33182367 | PubTator, text mining | PubMed |
| Color Data v2: a user-friendly, open-access database with hereditary cancer and hereditary cardiovascular conditions datasets. | Database (Oxford) | 2020 | 33181822 | PubTator, text mining | PubMed |
| Unraveling the Genotype-Phenotype Relationship in Hypertrophic Cardiomyopathy: Obesity-Related Cardiac Defects as a Major Disease Modifier. | J Am Heart Assoc | 2020 | 33174505 | PubTator, text mining | PubMed |
| Identification of circulating hub long noncoding RNAs associated with hypertrophic cardiomyopathy using weighted correlation network analysis. | Mol Med Rep | 2020 | 33174017 | PubTator, text mining | PubMed |
| Basic Cardiovascular Sciences Scientific Sessions 2020: Emerging Opportunities in Cardiovascular Diseases. | Circ Res | 2020 | 33151800 | PubTator, text mining | PubMed |
| Heme-Induced Oxidation of Cysteine Groups of Myofilament Proteins Leads to Contractile Dysfunction of Permeabilized Human Skeletal Muscle Fibres. | Int J Mol Sci | 2020 | 33142923 | PubTator, text mining | PubMed |
| The Egyptian Collaborative Cardiac Genomics (ECCO-GEN) Project: defining a healthy volunteer cohort. | NPJ Genom Med | 2020 | 33110626 | PubTator, text mining | PubMed |
| Mixed Hypertrophic and Dilated Phenotype of Cardiomyopathy in a Patient With Homozygous In-Frame Deletion in the MyBPC3 Gene Treated as Myocarditis for a Long Time. | Front Pharmacol | 2020 | 33101033 | PubTator, text mining | PubMed |
| Weighted gene co-expression network analysis revealed key biomarkers associated with the diagnosis of hypertrophic cardiomyopathy. | Hereditas | 2020 | 33099311 | 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/v1/4607/papers?page=78