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.
761 to 780 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Comparison of In Silico Tools for Splice-Altering Variant Prediction Using Established Spliceogenic Variants: An End-User's Point of View. | Int J Genomics | 2022 | 36275637 | PubTator, text mining | PubMed |
| Single muscle fibre contractile function with ageing. | J Physiol | 2022 | 36268622 | PubTator, text mining | PubMed |
| Identification and verification of IGFBP3 and YTHDC1 as biomarkers associated with immune infiltration and mitophagy in hypertrophic cardiomyopathy. | Front Genet | 2022 | 36267414 | PubTator, text mining | PubMed |
| NIMA-related kinase 9 regulates the phosphorylation of the essential myosin light chain in the heart. | Nat Commun | 2022 | 36266340 | PubTator, text mining | PubMed |
| Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General Population. | Circ Genom Precis Med | 2022 | 36264615 | PubTator, text mining | PubMed |
| Clinical Implication of Genetic Testing in Dilated Cardiomyopathy. | Int J Heart Fail | 2022 | 36262197 | PubTator, text mining | PubMed |
| Contemporary Therapies and Future Directions in the Management of Hypertrophic Cardiomyopathy. | Cardiol Ther | 2022 | 36243823 | PubTator, text mining | PubMed |
| Single Nucleus RNA-sequencing Reveals Altered Intercellular Communication and Dendritic Cell Activation in Nonobstructive Hypertrophic Cardiomyopathy. | Cardiol Cardiovasc Med | 2022 | 36237479 | PubTator, text mining | PubMed |
| Deciphering the Basis of Molecular Biology of Selected Cardiovascular Diseases: A View on Network Medicine. | Int J Mol Sci | 2022 | 36232723 | PubTator, text mining | PubMed |
| Effects of Noonan Syndrome-Germline Mutations on Mitochondria and Energy Metabolism. | Cells | 2022 | 36231062 | PubTator, text mining | PubMed |
| Hypertrophic cardiomyopathy: Mutations to mechanisms to therapies. | Front Physiol | 2022 | 36225299 | PubTator, text mining | PubMed |
| Identification and functional analysis of variants of MYH6 gene promoter in isolated ventricular septal defects. | BMC Med Genomics | 2022 | 36209093 | PubTator, text mining | PubMed |
| Genetic screening of relatives of decedents experiencing sudden unexpected death: medical examiner's office referrals to a multi-disciplinary cardiogenetics program. | J Community Genet | 2022 | 36203036 | PubTator, text mining | PubMed |
| Functional Assays Reclassify Suspected Splice-Altering Variants of Uncertain Significance in Mendelian Channelopathies. | Circ Genom Precis Med | 2022 | 36197721 | PubTator, text mining | PubMed |
| Sarcomere maturation: function acquisition, molecular mechanism, and interplay with other organelles. | Philos Trans R Soc Lond B Biol Sci | 2022 | 36189811 | PubTator, text mining | PubMed |
| Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort: The Use of Genetic Testing in Risk Stratification. | Circ Genom Precis Med | 2022 | 36178741 | PubTator, text mining | PubMed |
| Genomic findings of hypertrophic and dilated cardiomyopathy characterized in a Thai clinical genetics service. | PLoS One | 2022 | 36166435 | PubTator, text mining | PubMed |
| The «Amish» NM_000256.3:c.3330+2T>G splice variant in MYBPC3 associated with hypertrophic cardiomyopathy is an ancient Swiss mutation. | Eur J Med Genet | 2022 | 36162733 | PubTator, text mining | PubMed |
| Thin filament cardiomyopathies: A review of genetics, disease mechanisms, and emerging therapeutics. | Front Cardiovasc Med | 2022 | 36158814 | PubTator, text mining | PubMed |
| Haploinsufficiency of syncoilin leads to hypertrophic cardiomyopathy. | Genes Dis | 2022 | 36157493 | 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=39