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.
181 to 200 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Hydroxychloroquine Cardiotoxicity and Sarcomeric Hypertrophic Cardiomyopathy. | JACC Case Rep | 2025 | 40514126 | PubTator, text mining | PubMed |
| Scaled multidimensional assays of variant effect identify sequence-function relationships in hypertrophic cardiomyopathy. | bioRxiv | 2025 | 40501845 | PubTator, text mining | PubMed |
| Principles and functional consequences of plasmid chromatinization in mammalian cells. | bioRxiv | 2025 | 40501650 | PubTator, text mining | PubMed |
| Genetic landscape of hypertrophic cardiomyopathy in Hong Kong Chinese population. | Front Genet | 2025 | 40453736 | PubTator, text mining | PubMed |
| MYBPC3 c.2309-2A>G: exploring a founder variant in Italian hypertrophic cardiomyopathy patients. | Eur J Hum Genet | 2025 | 40450116 | PubTator, text mining | PubMed |
| Application of RNA-seq for single nucleotide variation identification in a cohort of patients with hypertrophic cardiomyopathy. | Sci Rep | 2025 | 40442228 | PubTator, text mining | PubMed |
| Disparate Molecular Properties of Two Hypertrophic Cardiomyopathy-Associated cMyBP-C Mutants Reveal Distinct Pathogenic Mechanisms Beyond Haploinsufficiency. | Biomedicines | 2025 | 40426840 | PubTator, text mining | PubMed |
| ANMCO position paper 'Hypertrophic cardiomyopathy: from diagnosis to treatment'. | Eur Heart J Suppl | 2025 | 40385469 | PubTator, text mining | PubMed |
| Investigating the dual role of mitochondrial and nuclear genome variants in pediatric cardiomyopathies. | Sci Rep | 2025 | 40369053 | PubTator, text mining | PubMed |
| Mavacamten Inhibits the Effect of the N-Terminal Fragment of Cardiac Myosin-Binding Protein C with the L352P Mutation on the Actin-Myosin Interaction at Low Calcium Concentrations. | Biochemistry (Mosc) | 2025 | 40367081 | PubTator, text mining | PubMed |
| Advancing Non-Invasive Prenatal Screening: A Targeted 1069-Gene Panel for Comprehensive Detection of Monogenic Disorders and Copy Number Variations. | Genes (Basel) | 2025 | 40282387 | PubTator, text mining | PubMed |
| Generation of induced pluripotent stem cell lines from five individuals from two families carrying a pathogenic Dutch MYBPC3 founder variant with variable degrees of hypertrophic cardiomyopathy. | Stem Cell Res | 2025 | 40250125 | PubTator, text mining | PubMed |
| Prognostic role of novel variables in sudden cardiac death risk associated to hypertrophic cardiomyopathy. | An Pediatr (Engl Ed) | 2025 | 40221256 | PubTator, text mining | PubMed |
| Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum. | Nat Genet | 2025 | 40195560 | PubTator, text mining | PubMed |
| Genotype and arrhythmic risk in patients with apical hypertrophic cardiomyopathy. | Heart | 2025 | 40194828 | PubTator, text mining | PubMed |
| A Proposal for Research Involving New Biomarkers of Hypertension, Lifestyle, and Environmental Exposure. | Curr Issues Mol Biol | 2025 | 40136460 | PubTator, text mining | PubMed |
| Case report: Severe arrhythmogenic cardiomyopathy in a young girl with compound heterozygous DSG2 and MYBPC3 variants with a 6-year follow-up. | Front Genet | 2025 | 40115818 | PubTator, text mining | PubMed |
| Brain and blood transcriptome-wide association studies identify five novel genes associated with Alzheimer's disease. | J Alzheimers Dis | 2025 | 40111921 | PubTator, text mining | PubMed |
| Myocardial dysfunction caused by MyBPC3 P459fs mutation in hypertrophic cardiomyopathy: evidence from multi-omics approaches and super-resolution imaging. | Front Cardiovasc Med | 2025 | 40083819 | PubTator, text mining | PubMed |
| Impact of catheter ablation on atrial fibrillation outcomes in various cardiomyopathies: findings from LGE-MRI quantified atrial fibrosis analysis. | J Interv Card Electrophysiol | 2025 | 40056366 | 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=10