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.
441 to 460 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| The Molecular Role of Immune Cells in Dilated Cardiomyopathy. | Medicina (Kaunas) | 2023 | 37512058 | PubTator, text mining | PubMed |
| Phosphorylation Mimetic of Myosin Regulatory Light Chain Mitigates Cardiomyopathy-Induced Myofilament Impairment in Mouse Models of RCM and DCM. | Life (Basel) | 2023 | 37511838 | PubTator, text mining | PubMed |
| Recommendations for the Management of Cardiomyopathy Mutation Carriers: Evidence, Doubts, and Intentions. | J Clin Med | 2023 | 37510821 | PubTator, text mining | PubMed |
| The Novel Variant NP_00454563.2 (p.Glu259Glyfs*77) in Gene PKP2 Associated with Arrhythmogenic Cardiomyopathy in 8 Families from Malaga, Spain. | Genes (Basel) | 2023 | 37510372 | PubTator, text mining | PubMed |
| A Family with Myh7 Mutation and Different Forms of Cardiomyopathies. | Biomedicines | 2023 | 37509704 | PubTator, text mining | PubMed |
| Septal radioablation therapy for patients with hypertrophic obstructive cardiomyopathy: first-in-human study. | Eur Heart J Open | 2023 | 37503357 | PubTator, text mining | PubMed |
| Identification of variants in genes associated with hypertrophic cardiomyopathy in Mexican patients. | Mol Genet Genomics | 2023 | 37498360 | PubTator, text mining | PubMed |
| A Cadaveric Evaluation of Hypertrophic Obstructive Cardiomyopathy. | Cureus | 2023 | 37489192 | PubTator, text mining | PubMed |
| MYH7 p.(Arg1712Gln) is pathogenic founder variant causing hypertrophic cardiomyopathy with overall relatively delayed onset. | Neth Heart J | 2023 | 37488328 | PubTator, text mining | PubMed |
| Age and Sex Differences in the Genetics of Cardiomyopathy. | J Cardiovasc Transl Res | 2023 | 37477868 | PubTator, text mining | PubMed |
| Clinically Indicated Genomic Sequencing of Children in Foster Care: Legal and Ethical Issues. | J Pediatr | 2023 | 37468037 | PubTator, text mining | PubMed |
| Deep learning-derived 12-lead electrocardiogram-based genotype prediction for hypertrophic cardiomyopathy: a pilot study. | Ann Med | 2023 | 37467172 | PubTator, text mining | PubMed |
| The Definition of Sarcomeric and Non-Sarcomeric Gene Mutations in Hypertrophic Cardiomyopathy Patients: A Multicenter Diagnostic Study Across Türkiye. | Anatol J Cardiol | 2023 | 37466024 | PubTator, text mining | PubMed |
| Sudden Infant Death Syndrome: Risk Factors and Newer Risk Reduction Strategies. | Cureus | 2023 | 37465778 | PubTator, text mining | PubMed |
| Microstructural and Microvascular Phenotype of Sarcomere Mutation Carriers and Overt Hypertrophic Cardiomyopathy. | Circulation | 2023 | 37463608 | PubTator, text mining | PubMed |
| Preserving mitochondria to treat hypertrophic cardiomyopathy: From rare mitochondrial DNA mutation to heart failure therapy? | J Clin Invest | 2023 | 37463442 | PubTator, text mining | PubMed |
| A novel mutation in the TTN gene resulted in left ventricular noncompaction: a case report and literature review. | BMC Cardiovasc Disord | 2023 | 37460987 | PubTator, text mining | PubMed |
| Prognosis of patients with familial hypertrophic cardiomyopathy: A single-center cohort study with ten-year follow-up by propensity score matching analysis. | Heliyon | 2023 | 37455958 | PubTator, text mining | PubMed |
| RAS-dependent RAF-MAPK hyperactivation by pathogenic RIT1 is a therapeutic target in Noonan syndrome-associated cardiac hypertrophy. | Sci Adv | 2023 | 37450595 | PubTator, text mining | PubMed |
| Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland. | J Am Heart Assoc | 2023 | 37449562 | 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=23