Gene · 5789
Papers1,768
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
21 to 40 of 1,768
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Epigenetic dysregulation of B‑cells in autoimmune diseases and lymphomas (Review). | Int J Mol Med | 2026 | 41574706 | PubTator, text mining | PubMed |
| Prospective tumour mutation burden and neoantigen profiling predicts immunotherapy response in metastatic melanoma. | NPJ Precis Oncol | 2026 | 41571736 | PubTator, text mining | PubMed |
| DNA variants affecting chromatin structure are key to the genetic architecture of obsessive compulsive disorder. | Epigenetics Chromatin | 2026 | 41555428 | PubTator, text mining | PubMed |
| Genotype subtyping approach to identify unnoticed variants in diseases from GWAS data. | BioData Min | 2026 | 41519843 | PubTator, text mining | PubMed |
| Single‑cell mapping of neutrophil extracellular trap signatures in lung adenocarcinoma reveals immune landscapes, prognostic potential, and therapeutic targets. | Transl Oncol | 2026 | 41496413 | PubTator, text mining | PubMed |
| Meta-analysis of differential gene expression in idiopathic pulmonary arterial hypertension. | Cardiovasc Pathol | 2026 | 41352442 | PubTator, text mining | PubMed |
| Genomic alteration correlates with programmed cell death ligand 1 (PD-L1) expression in 2750 Chinese non-small-cell lung cancer patients. | Clin Transl Oncol | 2026 | 40580408 | PubTator, text mining | PubMed |
| Development and validation of a glycosyltransferase-associated prognostic model for melanoma and characterization of the tumor immune microenvironment using single-cell sequencing data. | Biochem Biophys Rep | 2025 | 41542167 | PubTator, text mining | PubMed |
| Genetic and dietary determinants of gut microbiome-bile acid interactions in the BXD genetic reference population. | Nat Commun | 2025 | 41413047 | PubTator, text mining | PubMed |
| Decoding the Genetic Landscape of Postoperative Nausea and Vomiting in Cancer Surgery: A New Frontier in Personalized Medicine Driven by Genome-Wide Association Studies. | Indian J Surg Oncol | 2025 | 41283084 | PubTator, text mining | PubMed |
| Research on tracheal stenosis based on molecular biomarkers. | BMC Pulm Med | 2025 | 41272619 | PubTator, text mining | PubMed |
| Synaptic and Non-Synaptic Functions of PTPRD: A Receptor Tyrosine Phosphatase at the Crossroads of Neural Circuitry and Metabolism. | J Neurochem | 2025 | 41208653 | PubTator, text mining | PubMed |
| Identification of potential oncogenic miRNA clusters with a special focus on miR-106b/25 cluster-regulated networks and their clinical utility in hepatocellular carcinoma. | Discov Oncol | 2025 | 41196528 | PubTator, text mining | PubMed |
| Short Inverted Repeats as Mutational Hotspots and Putative Drivers of Genome Instability in Osteosarcoma. | Genes (Basel) | 2025 | 41153425 | PubTator, text mining | PubMed |
| Whole-genome sequencing reveals individual and cohort level insights into chromosome 9p syndromes. | Genome Med | 2025 | 41137173 | PubTator, text mining | PubMed |
| Deciphering genomic evolution of metastatic organotropism with 535 paired primary lung cancers and metastases. | Cell Rep | 2025 | 41100253 | PubTator, text mining | PubMed |
| Striae gravidarum in the Han Chinese pregnant population: identifying genetic markers and risk factors through a prospective cohort study. | BMC Pregnancy Childbirth | 2025 | 41083953 | PubTator, text mining | PubMed |
| Elucidate biomarkers and the molecular pathways associated with genetic variants that contribute to the etiology of Parkinson's disease. | Acta Neurol Belg | 2025 | 41026459 | PubTator, text mining | PubMed |
| Integrating genomic mutations and tumor-infiltrating lymphocytes improves prediction of response to trastuzumab-based adjuvant therapy in patients with HER2-positive breast cancer. | Cancer Drug Resist | 2025 | 41019979 | PubTator, text mining | PubMed |
| Distinct spatial transcriptomic patterns of substantia Nigra in Parkinson disease and Parkinsonian subtype of multiple system atrophy. | Acta Neuropathol Commun | 2025 | 40993824 | 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/v1/5789/papers?page=2