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.
2,001 to 2,020 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Large next-generation sequencing gene panels in genetic heart disease: yield of pathogenic variants and variants of unknown significance. | Neth Heart J | 2019 | 30847666 | PubTator, text mining | PubMed |
| Large next-generation sequencing gene panels in genetic heart disease: challenges in clinical practice. | Neth Heart J | 2019 | 30847665 | PubTator, text mining | PubMed |
| Therapeutic Genome Editing in Cardiovascular Diseases. | JACC Basic Transl Sci | 2019 | 30847427 | PubTator, text mining | PubMed |
| Myofilament Ca2+ sensitivity correlates with left ventricular contractility during the progression of pressure overload-induced left ventricular myocardial hypertrophy in rats. | J Mol Cell Cardiol | 2019 | 30844361 | PubTator, text mining | PubMed |
| Recent developments in genetic/genomic medicine. | Clin Sci (Lond) | 2019 | 30837331 | PubTator, text mining | PubMed |
| Myosin heavy chain mutations that cause Freeman-Sheldon syndrome lead to muscle structural and functional defects in Drosophila. | Dev Biol | 2019 | 30826400 | PubTator, text mining | PubMed |
| Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. | Nat Genet | 2019 | 30820047 | PubTator, text mining | PubMed |
| Transcriptomics of cardiac biopsies reveals differences in patients with or without diagnostic parameters for heart failure with preserved ejection fraction. | Sci Rep | 2019 | 30816197 | PubTator, text mining | PubMed |
| Thickness and Ratio of Noncompacted and Compacted Layers of the Left Ventricular Myocardium Evaluated in 56 Normal Fetuses by Two-Dimensional Echocardiography. | Biomed Res Int | 2019 | 30809538 | PubTator, text mining | PubMed |
| Shared genetic architecture between metabolic traits and Alzheimer's disease: a large-scale genome-wide cross-trait analysis. | Hum Genet | 2019 | 30805717 | PubTator, text mining | PubMed |
| Impaired Right Ventricular Mechanics at Rest and During Exercise Are Associated With Exercise Capacity in Patients With Hypertrophic Cardiomyopathy. | J Am Heart Assoc | 2019 | 30798647 | PubTator, text mining | PubMed |
| Differential expression of circulating miRNAs as a novel tool to assess BAG3-associated familial dilated cardiomyopathy. | Biosci Rep | 2019 | 30792263 | PubTator, text mining | PubMed |
| Exosome in Cardiovascular Diseases: A Complex World Full of Hope. | Cells | 2019 | 30781555 | PubTator, text mining | PubMed |
| Identification of whole blood mRNA and microRNA biomarkers of tissue damage and immune function resulting from amphetamine exposure or heat stroke in adult male rats. | PLoS One | 2019 | 30779732 | PubTator, text mining | PubMed |
| Genetic basis and outcome in a nationwide study of Finnish patients with hypertrophic cardiomyopathy. | ESC Heart Fail | 2019 | 30775854 | PubTator, text mining | PubMed |
| Extra energy for hearts with a genetic defect: ENERGY trial. | Neth Heart J | 2019 | 30767167 | PubTator, text mining | PubMed |
| Three perspectives on the molecular basis of hypercontractility caused by hypertrophic cardiomyopathy mutations. | Pflugers Arch | 2019 | 30767072 | PubTator, text mining | PubMed |
| Non-familial cardiomyopathies in Lebanon: exome sequencing results for five idiopathic cases. | BMC Med Genomics | 2019 | 30764827 | PubTator, text mining | PubMed |
| Fatal neonatal hypertrophic cardiomyopathy caused by compound heterozygous truncating MYBPC3 mutation. | Neth Heart J | 2019 | 30742251 | PubTator, text mining | PubMed |
| Altered force generation and cell-to-cell contractile imbalance in hypertrophic cardiomyopathy. | Pflugers Arch | 2019 | 30740621 | 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=101