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.
1,601 to 1,620 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy. | Circ Genom Precis Med | 2020 | 32885985 | PubTator, text mining | PubMed |
| Novel homozygous variant in WISP3 in a family with unrecognized progressive pseudorheumatoid dysplasia. | Clin Case Rep | 2020 | 32884773 | PubTator, text mining | PubMed |
| Heart Failure in Humans Reduces Contractile Force in Myocardium From Both Ventricles. | JACC Basic Transl Sci | 2020 | 32875169 | PubTator, text mining | PubMed |
| Myocardial Fibrosis in Heart Failure: Anti-Fibrotic Therapies and the Role of Cardiovascular Magnetic Resonance in Drug Trials. | Cardiol Ther | 2020 | 32862327 | PubTator, text mining | PubMed |
| Characterization and validation of a preventative therapy for hypertrophic cardiomyopathy in a murine model of the disease. | Proc Natl Acad Sci U S A | 2020 | 32859761 | PubTator, text mining | PubMed |
| Diurnal Differences in Human Muscle Isometric Force In Vivo Are Associated with Differential Phosphorylation of Sarcomeric M-Band Proteins. | Proteomes | 2020 | 32859009 | PubTator, text mining | PubMed |
| RBM20 mutations in left ventricular non-compaction cardiomyopathy. | Pediatr Investig | 2020 | 32851345 | PubTator, text mining | PubMed |
| Whole-exome sequencing reveals two de novo variants in the RBM20 gene in two Chinese patients with left ventricular non-compaction cardiomyopathy. | Pediatr Investig | 2020 | 32851336 | PubTator, text mining | PubMed |
| CRISPR Gene Therapy: Applications, Limitations, and Implications for the Future. | Front Oncol | 2020 | 32850447 | PubTator, text mining | PubMed |
| Spatial and Functional Distribution of MYBPC3 Pathogenic Variants and Clinical Outcomes in Patients With Hypertrophic Cardiomyopathy. | Circ Genom Precis Med | 2020 | 32841044 | PubTator, text mining | PubMed |
| Lifelong Clinical Impact of the Presence of Sarcomere Gene Mutation in Japanese Patients With Hypertrophic Cardiomyopathy. | Circ J | 2020 | 32830170 | PubTator, text mining | PubMed |
| Combined PTPN11 and MYBPC3 Gene Mutations in an Adult Patient with Noonan Syndrome and Hypertrophic Cardiomyopathy. | Genes (Basel) | 2020 | 32824488 | PubTator, text mining | PubMed |
| Emerging role of genetic analysis for stratification of sudden cardiac death risk in dilated cardiomyopathy: An illustrative case. | HeartRhythm Case Rep | 2020 | 32817827 | PubTator, text mining | PubMed |
| Genetic Studies of Hypertrophic Cardiomyopathy in Singaporeans Identify Variants in TNNI3 and TNNT2 That Are Common in Chinese Patients. | Circ Genom Precis Med | 2020 | 32815737 | PubTator, text mining | PubMed |
| Burden of premature ventricular contractions beyond nonsustained ventricular tachycardia is related to the myocardial extracellular space expansion in patients with hypertrophic-cardiomyopathy. | Clin Cardiol | 2020 | 32815161 | PubTator, text mining | PubMed |
| SVAD: A genetic database curates non-ischemic sudden cardiac death-associated variants. | PLoS One | 2020 | 32813752 | PubTator, text mining | PubMed |
| Identification of Undetected Monogenic Cardiovascular Disorders. | J Am Coll Cardiol | 2020 | 32792077 | PubTator, text mining | PubMed |
| Causal Genetic Variants in Stillbirth. | N Engl J Med | 2020 | 32786180 | PubTator, text mining | PubMed |
| SELAdb: A database of exonic variants in a Brazilian population referred to a quaternary medical center in São Paulo. | Clinics (Sao Paulo) | 2020 | 32785571 | PubTator, text mining | PubMed |
| Downregulation of the let-7 family of microRNAs may promote insulin receptor/insulin-like growth factor signalling pathways in pancreatic ductal adenocarcinoma. | Oncol Lett | 2020 | 32782579 | 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=81