Gene · 70
Papers1,745
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
601 to 620 of 1,745
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Expression of cell type incongruent alpha-cardiac actin 1 subunit in medulloblastoma reveals a novel mechanism for cancer cell survival and control of migration. | Neurooncol Adv | 2021 | 34337410 | PubTator, text mining | PubMed |
| Genetics of Cardiomyopathy: Clinical and Mechanistic Implications for Heart Failure. | Korean Circ J | 2021 | 34327881 | PubTator, text mining | PubMed |
| Cardiomyopathies: An Overview. | Int J Mol Sci | 2021 | 34299342 | PubTator, text mining | PubMed |
| X Chromosome Inactivation in Carriers of Fabry Disease: Review and Meta-Analysis. | Int J Mol Sci | 2021 | 34299283 | PubTator, text mining | PubMed |
| Dilated Cardiomyopathy: New Variant in the Filamin-C Gene. | Arq Bras Cardiol | 2021 | 34287470 | PubTator, text mining | PubMed |
| Improving Risk Stratification for Pediatric Patients with Rhabdomyosarcoma by Molecular Detection of Disseminated Disease. | Clin Cancer Res | 2021 | 34285060 | PubTator, text mining | PubMed |
| Identification of genes associated with sudden cardiac death: a network- and pathway-based approach. | J Thorac Dis | 2021 | 34277054 | PubTator, text mining | PubMed |
| Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy. | Eur Heart J | 2021 | 34263907 | PubTator, text mining | PubMed |
| Burden of Cardiomyopathic Genetic Variation in Lethal Pediatric Myocarditis. | Circ Genom Precis Med | 2021 | 34228484 | PubTator, text mining | PubMed |
| Functional analysis of novel genetic variants of NKX2-5 associated with nonsyndromic congenital heart disease. | Am J Med Genet A | 2021 | 34214246 | PubTator, text mining | PubMed |
| Omics Approaches to Study Formation and Function of Human Placental Syncytiotrophoblast. | Front Cell Dev Biol | 2021 | 34211975 | PubTator, text mining | PubMed |
| Personalized Genetic Diagnosis of Congenital Heart Defects in Newborns. | J Pers Med | 2021 | 34208491 | PubTator, text mining | PubMed |
| Direct Reprogramming of Cardiac Fibroblasts to Repair the Injured Heart. | J Cardiovasc Dev Dis | 2021 | 34206355 | PubTator, text mining | PubMed |
| Noncompaction Cardiomyopathy-History and Current Knowledge for Clinical Practice. | J Clin Med | 2021 | 34206037 | PubTator, text mining | PubMed |
| High-Risk Clinicopathological and Genetic Features and Outcomes in Patients Receiving Neoadjuvant Radiochemotherapy for Locally Advanced Rectal Cancer. | Cancers (Basel) | 2021 | 34202891 | PubTator, text mining | PubMed |
| The Double Mutation DSG2-p.S363X and TBX20-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case Report. | Int J Mol Sci | 2021 | 34202524 | PubTator, text mining | PubMed |
| Clinical impact of re-evaluating genes and variants implicated in dilated cardiomyopathy. | Genet Med | 2021 | 34194005 | PubTator, text mining | PubMed |
Comprehensive high-throughput meta-analysis of differentially expressed microRNAs in transcriptomic datasets reveals significant disruption of MAPK/JNK signal transduction pathway in Adult T-cell leukemia/lymphoma. | Infect Agent Cancer | 2021 | 34187521 | PubTator, text mining | PubMed |
| Single-Cell Transcriptomics Reveals the Cellular Heterogeneity of Cardiovascular Diseases. | Front Cardiovasc Med | 2021 | 34179129 | PubTator, text mining | PubMed |
| Novel polygenetic variants evidenced in a patient with Jervell and Lange-Nielsen syndrome. | Cardiol J | 2021 | 34165182 | 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/v1/70/papers?page=31