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.
1,361 to 1,380 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Impact of regulatory light chain mutation K104E on the ATPase and motor properties of cardiac myosin. | J Gen Physiol | 2021 | 33891674 | PubTator, text mining | PubMed |
| Prediction of Genotype Positivity in Patients With Hypertrophic Cardiomyopathy Using Machine Learning. | Circ Genom Precis Med | 2021 | 33890823 | PubTator, text mining | PubMed |
| Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease. | NPJ Genom Med | 2021 | 33888711 | PubTator, text mining | PubMed |
| Fast skeletal myosin-binding protein-C regulates fast skeletal muscle contraction. | Proc Natl Acad Sci U S A | 2021 | 33888578 | PubTator, text mining | PubMed |
| Maternal smoking during pregnancy aggravated muscle phenotype in FHL1-/y offspring mice similar to congenital clubfoot through P2RX7-mediated pyroptosis. | Toxicol Lett | 2021 | 33872746 | PubTator, text mining | PubMed |
| Subtypes identification on heart failure with preserved ejection fraction via network enhancement fusion using multi-omics data. | Comput Struct Biotechnol J | 2021 | 33868594 | PubTator, text mining | PubMed |
| Case Report: Novel Likely Pathogenic ACTN2 Variant Causing Heterogeneous Phenotype in a Korean Family With Left Ventricular Non-compaction. | Front Pediatr | 2021 | 33859969 | PubTator, text mining | PubMed |
| Mechanical dysfunction of the sarcomere induced by a pathogenic mutation in troponin T drives cellular adaptation. | J Gen Physiol | 2021 | 33856419 | PubTator, text mining | PubMed |
| Stress-dependent activation of myosin in the heart requires thin filament activation and thick filament mechanosensing. | Proc Natl Acad Sci U S A | 2021 | 33850019 | PubTator, text mining | PubMed |
| A rare cause of sudden unexpected death syndrome (SUDS) in the first year of life: endomyocardial fibroelastosis (EFE) due to two compound heterozygous MYBPC3 mutations. | BMC Cardiovasc Disord | 2021 | 33849460 | PubTator, text mining | PubMed |
| 11p11.12p12 duplication in a family with intellectual disability and craniofacial anomalies. | BMC Med Genomics | 2021 | 33836758 | PubTator, text mining | PubMed |
| International Evidence Based Reappraisal of Genes Associated With Arrhythmogenic Right Ventricular Cardiomyopathy Using the Clinical Genome Resource Framework. | Circ Genom Precis Med | 2021 | 33831308 | PubTator, text mining | PubMed |
| Gender- and age-related differences in distinct phenotypes of hypertrophic cardiomyopathy-associated mutation MYBPC3-E334K. | Heart Vessels | 2021 | 33830315 | PubTator, text mining | PubMed |
| Special Issue "Cardiovascular Genetics". | Genes (Basel) | 2021 | 33810227 | PubTator, text mining | PubMed |
| Left Ventricular Noncompaction-A Systematic Review of Risk Factors in the Pediatric Population. | J Clin Med | 2021 | 33809657 | PubTator, text mining | PubMed |
| Novel CRISPR-Cas Systems: An Updated Review of the Current Achievements, Applications, and Future Research Perspectives. | Int J Mol Sci | 2021 | 33805113 | PubTator, text mining | PubMed |
| Emerging Medical Treatment for Hypertrophic Cardiomyopathy. | J Clin Med | 2021 | 33804412 | PubTator, text mining | PubMed |
| Plasma Proteomic Profiling in Hypertrophic Cardiomyopathy Patients before and after Surgical Myectomy Reveals Post-Procedural Reduction in Systemic Inflammation. | Int J Mol Sci | 2021 | 33804404 | PubTator, text mining | PubMed |
| Phenotypic Diversity of Cardiomyopathy Caused by an MYBPC3 Frameshift Mutation in a Korean Family: A Case Report. | Medicina (Kaunas) | 2021 | 33803538 | PubTator, text mining | PubMed |
| Genetic Cardiomyopathies: The Lesson Learned from hiPSCs. | J Clin Med | 2021 | 33803477 | 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/v1/4607/papers?page=69