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.
881 to 900 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Modeling Nonischemic Genetic Cardiomyopathies Using Induced Pluripotent Stem Cells. | Curr Cardiol Rep | 2022 | 35657495 | PubTator, text mining | PubMed |
| Circulating S-Glutathionylated cMyBP-C as a Biomarker for Cardiac Diastolic Dysfunction. | J Am Heart Assoc | 2022 | 35656993 | PubTator, text mining | PubMed |
| Metabolite Signature in the Carriers of Pathogenic Genetic Variants for Cardiomyopathy: A Population-Based METSIM Study. | Metabolites | 2022 | 35629941 | PubTator, text mining | PubMed |
| Signal-to-Noise Analysis Can Inform the Likelihood That Incidentally Identified Variants in Sarcomeric Genes Are Associated with Pediatric Cardiomyopathy. | J Pers Med | 2022 | 35629155 | PubTator, text mining | PubMed |
| Technical Performance of a 430-Gene Preventative Genomics Assay to Identify Multiple Variant Types Associated with Adult-Onset Monogenic Conditions, Susceptibility Loci, and Pharmacogenetic Insights. | J Pers Med | 2022 | 35629091 | PubTator, text mining | PubMed |
| Transmission Distortion of MCT1 rs1049434 among Polish Elite Athletes. | Genes (Basel) | 2022 | 35627255 | PubTator, text mining | PubMed |
| Inferring Potential Cancer Driving Synonymous Variants. | Genes (Basel) | 2022 | 35627162 | PubTator, text mining | PubMed |
| The Genetic Architecture of Hypertrophic Cardiomyopathy in Hungary: Analysis of 242 Patients with a Panel of 98 Genes. | Diagnostics (Basel) | 2022 | 35626289 | PubTator, text mining | PubMed |
| A Comprehensive Assessment of Cardiomyopathies through Cardiovascular Magnetic Resonance: Focus on the Pediatric Population. | Diagnostics (Basel) | 2022 | 35626178 | PubTator, text mining | PubMed |
| Significance of α-Myosin Heavy Chain (MYH6) Variants in Hypoplastic Left Heart Syndrome and Related Cardiovascular Diseases. | J Cardiovasc Dev Dis | 2022 | 35621855 | PubTator, text mining | PubMed |
| What Aspects of Phenotype Determine Risk for Sudden Cardiac Death in Pediatric Hypertrophic Cardiomyopathy? | J Cardiovasc Dev Dis | 2022 | 35621835 | PubTator, text mining | PubMed |
| Arrhythmias as Presentation of Genetic Cardiomyopathy. | Circ Res | 2022 | 35617362 | PubTator, text mining | PubMed |
| Clinical genetic testing in four highly suspected pediatric restrictive cardiomyopathy cases. | BMC Cardiovasc Disord | 2022 | 35614389 | PubTator, text mining | PubMed |
| Dysfunctional sarcomeric relaxation in the heart. | Curr Opin Physiol | 2022 | 35603011 | PubTator, text mining | PubMed |
| Nanosurfer assay dissects β-cardiac myosin and cardiac myosin-binding protein C interactions. | Biophys J | 2022 | 35591788 | PubTator, text mining | PubMed |
| Clinical Features and Natural History of Preadolescent Nonsyndromic Hypertrophic Cardiomyopathy. | J Am Coll Cardiol | 2022 | 35589160 | PubTator, text mining | PubMed |
| Controversial molecular functions of CBS versus non-CBS domain variants of PRKAG2 in arrhythmia and cardiomyopathy: A case report and literature review. | Mol Genet Genomic Med | 2022 | 35588295 | PubTator, text mining | PubMed |
| Prognosis of Adults With Isolated Left Ventricular Non-Compaction: Results of a Prospective Multicentric Study. | Front Cardiovasc Med | 2022 | 35586644 | PubTator, text mining | PubMed |
| Rare and Common Genetic Variation Underlying the Risk of Hypertrophic Cardiomyopathy in a National Biobank. | JAMA Cardiol | 2022 | 35583889 | PubTator, text mining | PubMed |
| BRG1 is a biomarker of hypertrophic cardiomyopathy in human heart specimens. | Sci Rep | 2022 | 35581268 | 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=45