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.
361 to 380 of 1,745
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| CDH1 overexpression predicts bladder cancer from early stage and inversely correlates with immune infiltration. | BMC Urol | 2022 | 36131343 | PubTator, text mining | PubMed |
| Determining the Likelihood of Disease Pathogenicity Among Incidentally Identified Genetic Variants in Rare Dilated Cardiomyopathy-Associated Genes. | J Am Heart Assoc | 2022 | 36129056 | PubTator, text mining | PubMed |
| Plasma microRNAs as potential biomarkers in early Alzheimer disease expression. | Sci Rep | 2022 | 36114255 | PubTator, text mining | PubMed |
| Transcriptional comparison of adult human primary Retinal Pigment Epithelium, human pluripotent stem cell-derived Retinal Pigment Epithelium, and ARPE19 cells. | Front Cell Dev Biol | 2022 | 36092714 | PubTator, text mining | PubMed |
| Overexpression of PYGO1 promotes early cardiac lineage development in human umbilical cord mesenchymal stromal/stem cells by activating the Wnt/β-catenin pathway. | Hum Cell | 2022 | 36085540 | PubTator, text mining | PubMed |
| The general law of plasma proteome alterations occurring in the lifetime of Chinese individuals reveals the importance of immunity. | Aging (Albany NY) | 2022 | 36084955 | PubTator, text mining | PubMed |
| Gene Ontology (GO)-Driven Inference of Candidate Proteomic Markers Associated with Muscle Atrophy Conditions. | Molecules | 2022 | 36080280 | PubTator, text mining | PubMed |
| Identification and functional characterization of BICD2 as a candidate disease gene in an consanguineous family with dilated cardiomyopathy. | BMC Med Genomics | 2022 | 36068540 | PubTator, text mining | PubMed |
| Clinical significance of genetic variation in hypertrophic cardiomyopathy: comparison of computational tools to prioritize missense variants. | Front Cardiovasc Med | 2022 | 36061567 | PubTator, text mining | PubMed |
| Ventricular arrhythmia and sudden cardiac death in hypertrophic cardiomyopathy: From bench to bedside. | Front Cardiovasc Med | 2022 | 36061538 | PubTator, text mining | PubMed |
| Left ventricular noncompaction: a disorder with genotypic and phenotypic heterogeneity-a narrative review. | Cardiovasc Diagn Ther | 2022 | 36033229 | PubTator, text mining | PubMed |
| Mutational Assessment in NKX2-5 and ACTC1 Genes in Patients with Congenital Cardiac Septal Defect (CCSD) from Ethnic Kashmiri Population. | Int J Environ Res Public Health | 2022 | 36011517 | PubTator, text mining | PubMed |
| Different Phenotypes of Sarcomeric MyBPC3-Cardiomyopathy in the Same Family: Hypertrophic, Left Ventricular Noncompaction and Restrictive Phenotypes (in Association with Sarcoidosis). | Genes (Basel) | 2022 | 36011256 | PubTator, text mining | PubMed |
| Spectrum of Rare and Common Genetic Variants in Arrhythmogenic Cardiomyopathy Patients. | Biomolecules | 2022 | 36008935 | PubTator, text mining | PubMed |
| Genetic Analysis of Cardiac Syncope-Related Genes in Korean Patients with Recurrent Neurally Mediated Syncope. | J Cardiovasc Dev Dis | 2022 | 36005429 | PubTator, text mining | PubMed |
| Single-cell analysis and functional characterization uncover the stem cell hierarchies and developmental origins of rhabdomyosarcoma. | Nat Cancer | 2022 | 35982179 | PubTator, text mining | PubMed |
| A novel missense mutation in obscurin gene in a Chinese consanguineous family with left ventricular noncompaction. | J Geriatr Cardiol | 2022 | 35975021 | PubTator, text mining | PubMed |
| Modulating biomolecular condensates: a novel approach to drug discovery. | Nat Rev Drug Discov | 2022 | 35974095 | PubTator, text mining | PubMed |
| Arrhythmogenic Cardiomyopathy: Exercise Pitfalls, Role of Connexin-43, and Moving beyond Antiarrhythmics. | Int J Mol Sci | 2022 | 35955883 | PubTator, text mining | PubMed |
| The Protective Action of Metformin against Pro-Inflammatory Cytokine-Induced Human Islet Cell Damage and the Mechanisms Involved. | Cells | 2022 | 35954309 | 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=19