Gene · 5318
Papers2,073
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
101 to 120 of 2,073
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Adeno-associated virus-mediated PKP2 gene therapy confers robust exercise tolerance in a murine model of arrhythmogenic cardiomyopathy. | Heart Rhythm | 2025 | 40355016 | PubTator, text mining | PubMed |
| Arrhythmogenic Cardiomyopathy PKP2-Related: Clinical and Functional Characterization of a Pathogenic Variant Detected in Two Italian Families. | Genes (Basel) | 2025 | 40282378 | PubTator, text mining | PubMed |
| A novel mitochondrial quality regulation gene signature for anticipating prognosis, TME, and therapeutic response in LUAD by multi-omics analysis and experimental verification. | Cancer Cell Int | 2025 | 40211263 | PubTator, text mining | PubMed |
| Computational Modeling of Effects of PKP2 Gene Therapy on Ventricular Conduction Properties in Arrhythmogenic Cardiomyopathy. | Circ Arrhythm Electrophysiol | 2025 | 40201954 | PubTator, text mining | PubMed |
| Preclinical efficacy and safety of AAVrh10-based plakophilin-2 gene therapy (LX2020) as a treatment for arrhythmogenic cardiomyopathy. | NPJ Regen Med | 2025 | 40175378 | PubTator, text mining | PubMed |
| The Future of Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-Cas9 Gene Therapy in Cardiomyopathies: A Review of Its Therapeutic Potential and Emerging Applications. | Cureus | 2025 | 40130092 | PubTator, text mining | PubMed |
| Whole-Exome Sequencing Followed by dPCR-Based Personalized Genetic Approach in Solid Organ Transplantation: A Study Protocol and Preliminary Results. | Methods Protoc | 2025 | 40126245 | PubTator, text mining | PubMed |
| Natural History and Clinical Outcomes of Patients With DSG2/DSC2 Variant-Related Arrhythmogenic Right Ventricular Cardiomyopathy. | Circulation | 2025 | 40123482 | PubTator, text mining | PubMed |
| Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk. | Nat Genet | 2025 | 40050430 | PubTator, text mining | PubMed |
| Predicted Risk of Ventricular Arrhythmias in a Genome-First Population With Genetic Risk for Arrhythmogenic Right Ventricular Cardiomyopathy. | Circ Arrhythm Electrophysiol | 2025 | 39989366 | PubTator, text mining | PubMed |
| Genetics in arrhythmogenic cardiomyopathies: where are we now and where are we heading to? | Eur Heart J Suppl | 2025 | 39980788 | PubTator, text mining | PubMed |
| [A case of biventricular involvement of arrhythmogenic right ventricular cardiomyopathy associated with PKP2 gene variation]. | Zhonghua Xin Xue Guan Bing Za Zhi | 2025 | 39965856 | PubTator, text mining | PubMed |
| The impact of plakophilin-2 deficiency on the atrial myocardium: electrophysiological insights and therapeutic implications. | J Physiol | 2025 | 39888069 | PubTator, text mining | PubMed |
| Identification of Biomarkers of Arrhythmogenic Cardiomyopathy (ACM) by Plasma Proteomics. | Medicina (Kaunas) | 2025 | 39859087 | PubTator, text mining | PubMed |
| Coexistence of cardiac sarcoidosis and arrhythmogenic cardiomyopathy-associated genetic variants: a multicentre case-control study. | Heart | 2025 | 39837597 | PubTator, text mining | PubMed |
| Immunohistochemical study of ATP1A3 and plakophilin 2 as new potential markers in the diagnosis of myocardial ischemia. | Leg Med (Tokyo) | 2025 | 39733715 | PubTator, text mining | PubMed |
| Heritable Burden of Community Sudden Death by Autopsy and Molecular Phenotyping for Precision Genotype Correlation. | JACC Clin Electrophysiol | 2025 | 39708038 | PubTator, text mining | PubMed |
| Performance of ARVC Risk Calculators in (Likely) Pathogenic Plakophilin-2 Variant Carriers Without Definite ARVC Diagnosis. | Circ Arrhythm Electrophysiol | 2025 | 39670315 | PubTator, text mining | PubMed |
| Arrhythmogenic Cardiomyopathy: Towards Genotype Based Diagnoses and Management. | J Cardiovasc Electrophysiol | 2025 | 39623588 | PubTator, text mining | PubMed |
| The phenotype of necrotizing enterocolitis correlates with distinct changes of intestinal junctional proteins. | Pathol Res Pract | 2025 | 39579526 | 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
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