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.
41 to 60 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Prognostic Value of MRI-Based Left Ventricular Trabecular Complexity for Sudden Cardiac Death in Hypertrophic Cardiomyopathy. | J Magn Reson Imaging | 2026 | 42276847 | PubTator, text mining | PubMed |
| Cardiovascular and Clinical Manifestations of Marfan Syndrome and Other Inherited Connective Tissue Disorders with Coexisting Genetic Variants. | Cells | 2026 | 42274593 | PubTator, text mining | PubMed |
| A large-scale single-nucleus resource reveals a cardiomyocyte-like fibroblast and stage-specific remodeling across cardiomyopathies. | BMC Med | 2026 | 42243863 | PubTator, text mining | PubMed |
| Dynamics of the β-cardiac myosin auto-inhibited state explain cardiomyopathy pathogenesis. | Nat Commun | 2026 | 42243087 | PubTator, text mining | PubMed |
| Can Systemic Sarcoidosis and Genetic Cardiomyopathy Coexist? | JACC Case Rep | 2026 | 42233912 | PubTator, text mining | PubMed |
| Subsarcomeric regulation of thin and thick filaments in skeletal muscle myofibrils. | Proc Natl Acad Sci U S A | 2026 | 42228534 | PubTator, text mining | PubMed |
| [Immunoglobulin-Like Domains Are the Key to Understanding Amyloid Aggregation]. | Mol Biol (Mosk) | 2026 | 42227123 | PubTator, text mining | PubMed |
| A Novel Splice Site Mutation in the RASA1 Gene Causing Rare Diffuse Gastrointestinal Vascular Malformations: A Case Report and Literature Review. | Am J Med Genet A | 2026 | 42215316 | PubTator, text mining | PubMed |
| Population-Based Analysis of Rare Genetic Variants in Sudden Cardiac Arrest. | JACC Clin Electrophysiol | 2026 | 42159526 | PubTator, text mining | PubMed |
| EPAS1 is associated with human muscle fiber composition and endurance phenotypes. | Physiol Rep | 2026 | 42157436 | PubTator, text mining | PubMed |
| Sarcopenia and chronic pain: Identification of shared genetic determinants and therapeutic implication. | Medicine (Baltimore) | 2026 | 42152289 | PubTator, text mining | PubMed |
| Variable cMyBP-C expression from cell to cell in a MYBPC3c.927-2 A>G hiPSC-CM model recapitulates HCM patient phenotype. | Stem Cell Res Ther | 2026 | 42152135 | PubTator, text mining | PubMed |
| Cardiomyopathy phenotypes caused by a heterozygous MYBPC3 mutation revealed in different hiPSC cardiac models. | Exp Cell Res | 2026 | 42144094 | PubTator, text mining | PubMed |
| Are clinical trajectories in obstructive hypertrophic cardiomyopathy mutation-specific? A systematic review and meta-analysis of MYH7 vs. MYBPC3. | Front Cardiovasc Med | 2026 | 42136721 | PubTator, text mining | PubMed |
| Diffuse hypertrophic obstructive cardiomyopathy complicated by apical ventricular aneurysm and excessive left ventricular trabeculation: a case report. | Front Cardiovasc Med | 2026 | 42124931 | PubTator, text mining | PubMed |
| Proteomic profiling identifies molecular subtypes and unveils mechanistic insights into clinical features of hypertrophic cardiomyopathy. | J Transl Med | 2026 | 42116078 | PubTator, text mining | PubMed |
| Cardiac magnetic resonance findings in two cases of hypertrophic cardiomyopathy with MYH7 and MYBPC3 variants: Limitations of genotype-based phenotypic prediction. | J Cardiol Cases | 2026 | 42112275 | PubTator, text mining | PubMed |
| Comparing cryo-EM structures of the vertebrate cardiac muscle thick filament. | Biophys Rev | 2026 | 42005345 | PubTator, text mining | PubMed |
| Yield of Postmortem Genetic Testing in Sudden Arrhythmic Death Syndrome: A Systematic Review and Meta-Analysis. | Circ Genom Precis Med | 2026 | 41979508 | PubTator, text mining | PubMed |
| Generation of two induced pluripotent stem cell lines from hypertrophic cardiomyopathy patients carrying MYBPC3 mutations. | Stem Cell Res | 2026 | 41946259 | 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=3