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.
901 to 920 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Diagnostic yield of genetic testing in heart transplant recipients with prior cardiomyopathy. | J Heart Lung Transplant | 2022 | 35581137 | PubTator, text mining | PubMed |
| The prevalence of Fabry disease among 1009 unrelated patients with hypertrophic cardiomyopathy: a Russian nationwide screening program using NGS technology. | Orphanet J Rare Dis | 2022 | 35578305 | PubTator, text mining | PubMed |
| Identification of Phosphorylation and Other Post-Translational Modifications in the Central C4C5 Domains of Murine Cardiac Myosin Binding Protein C. | ACS Omega | 2022 | 35573219 | PubTator, text mining | PubMed |
| Implication of a novel truncating mutation in titin as a cause of autosomal dominant left ventricular noncompaction. | J Geriatr Cardiol | 2022 | 35572216 | PubTator, text mining | PubMed |
| A Rare Case of Isolated Right Ventricular Non-compaction With the Novel TTN Mutation. | Front Cardiovasc Med | 2022 | 35571204 | PubTator, text mining | PubMed |
| Identification of Potential Muscle Biomarkers in McArdle Disease: Insights from Muscle Proteome Analysis. | Int J Mol Sci | 2022 | 35563042 | PubTator, text mining | PubMed |
| Cellular Heterogeneity of the Heart. | Front Cardiovasc Med | 2022 | 35548426 | PubTator, text mining | PubMed |
| Genetic Testing for Early-Onset Atrial Fibrillation-Is It Time to Personalize Care? | JAMA Cardiol | 2022 | 35544088 | PubTator, text mining | PubMed |
| Mortality Among Patients With Early-Onset Atrial Fibrillation and Rare Variants in Cardiomyopathy and Arrhythmia Genes. | JAMA Cardiol | 2022 | 35544069 | PubTator, text mining | PubMed |
| Association of Pathogenic DNA Variants Predisposing to Cardiomyopathy With Cardiovascular Disease Outcomes and All-Cause Mortality. | JAMA Cardiol | 2022 | 35544052 | PubTator, text mining | PubMed |
| Defects in the Proteome and Metabolome in Human Hypertrophic Cardiomyopathy. | Circ Heart Fail | 2022 | 35543134 | PubTator, text mining | PubMed |
| Identification of clinically actionable secondary genetic variants from whole-genome sequencing in a large-scale Chinese population. | Clin Transl Med | 2022 | 35538921 | PubTator, text mining | PubMed |
| Trovafloxacin drives inflammation-associated drug-induced adverse hepatic reaction by changing macrophage polarization. | Toxicol In Vitro | 2022 | 35537566 | PubTator, text mining | PubMed |
| Population Prevalence of Premature Truncating Variants in Plakophilin-2 and Association With Arrhythmogenic Right Ventricular Cardiomyopathy: A UK Biobank Analysis. | Circ Genom Precis Med | 2022 | 35536239 | PubTator, text mining | PubMed |
| Dilated cardiomyopathy caused by a pathogenic nucleotide variant in RBM20 in an Iranian family. | BMC Med Genomics | 2022 | 35527250 | PubTator, text mining | PubMed |
| Genotype-Driven Pathogenesis of Atrial Fibrillation in Hypertrophic Cardiomyopathy: The Case of Different TNNT2 Mutations. | Front Physiol | 2022 | 35514357 | PubTator, text mining | PubMed |
| Aging Alters the Aortic Proteome in Health and Thoracic Aortic Aneurysm. | Arterioscler Thromb Vasc Biol | 2022 | 35510553 | PubTator, text mining | PubMed |
| Identification of an elusive spliceogenic MYBPC3 variant in an otherwise genotype-negative hypertrophic cardiomyopathy pedigree. | Sci Rep | 2022 | 35508642 | PubTator, text mining | PubMed |
| Ingenuity pathway analysis of the human cardiac cell Atlas identifies differences between right and left ventricular cardiomyocytes. | Pulm Circ | 2022 | 35506094 | PubTator, text mining | PubMed |
| Post-translational modification patterns on β-myosin heavy chain are altered in ischemic and nonischemic human hearts. | Elife | 2022 | 35502901 | 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=46