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.
581 to 600 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Homozygous TNNI3 Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the Literature. | Genes (Basel) | 2023 | 36981019 | PubTator, text mining | PubMed |
| Identification of Two Homozygous Variants in MYBPC3 and SMYD1 Genes Associated with Severe Infantile Cardiomyopathy. | Genes (Basel) | 2023 | 36980931 | PubTator, text mining | PubMed |
| Dilated Cardiomyopathy: A Comprehensive Approach to Diagnosis and Risk Stratification. | Biomedicines | 2023 | 36979813 | PubTator, text mining | PubMed |
| Transcriptome Profile Reveals Differences between Remote and Ischemic Myocardium after Acute Myocardial Infarction in a Swine Model. | Biology (Basel) | 2023 | 36979032 | PubTator, text mining | PubMed |
| Hypertrophic Cardiomyopathy. | J Cardiovasc Dev Dis | 2023 | 36975870 | PubTator, text mining | PubMed |
| A Novel Nonsense Pathogenic TTN Variant Identified in a Patient with Severe Dilated Cardiomyopathy. | Curr Issues Mol Biol | 2023 | 36975527 | PubTator, text mining | PubMed |
| Impaired Reorganization of Centrosome Structure Underlies Human Infantile Dilated Cardiomyopathy. | Circulation | 2023 | 36970983 | PubTator, text mining | PubMed |
| Identification of circRNA-miRNA-mRNA regulatory network and its role in cardiac hypertrophy. | PLoS One | 2023 | 36952519 | PubTator, text mining | PubMed |
| Is haploinsufficiency a sufficient mechanism for MYBPC3 truncating mutations? | J Gen Physiol | 2023 | 36946992 | PubTator, text mining | PubMed |
| Sex and gender differences in myocarditis and dilated cardiomyopathy: An update. | Front Cardiovasc Med | 2023 | 36937911 | PubTator, text mining | PubMed |
| Feline myocardial transcriptome in health and in hypertrophic cardiomyopathy-A translational animal model for human disease. | PLoS One | 2023 | 36928240 | PubTator, text mining | PubMed |
| Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. | Nat Commun | 2023 | 36918541 | PubTator, text mining | PubMed |
| In situ FRET-based localization of the N terminus of myosin binding protein-C in heart muscle cells. | Proc Natl Acad Sci U S A | 2023 | 36913580 | PubTator, text mining | PubMed |
| Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age. | Adv Genet (Hoboken) | 2023 | 36910592 | PubTator, text mining | PubMed |
| Transcriptomic profiling and differential analysis reveal the renal toxicity mechanisms of mice under cantharidin exposure. | Toxicol Appl Pharmacol | 2023 | 36907384 | PubTator, text mining | PubMed |
| Multi-Omics Profiling of Hypertrophic Cardiomyopathy Reveals Altered Mechanisms in Mitochondrial Dynamics and Excitation-Contraction Coupling. | Int J Mol Sci | 2023 | 36902152 | PubTator, text mining | PubMed |
| Epigenetics in LMNA-Related Cardiomyopathy. | Cells | 2023 | 36899919 | PubTator, text mining | PubMed |
| Insights into the Role of a Cardiomyopathy-Causing Genetic Variant in ACTN2. | Cells | 2023 | 36899856 | PubTator, text mining | PubMed |
| Genetically determined cardiomyopathies at autopsy: the pivotal role of the pathologist in establishing the diagnosis and guiding family screening. | Virchows Arch | 2023 | 36897369 | PubTator, text mining | PubMed |
| Mechanisms of pathogenicity in the hypertrophic cardiomyopathy-associated TPM1 variant S215L. | PNAS Nexus | 2023 | 36896133 | 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=30