Gene · 3145
Papers3,427
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
381 to 400 of 3,427
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Porphyria: a case report. | J Med Case Rep | 2022 | 36575494 | PubTator, text mining | PubMed |
| Identification of optimal reference genes for gene expression normalization in human osteosarcoma cell lines under proliferative conditions. | Front Genet | 2022 | 36568365 | PubTator, text mining | PubMed |
| Simultaneous profiling of histone modifications and DNA methylation via nanopore sequencing. | Nat Commun | 2022 | 36566265 | PubTator, text mining | PubMed |
| Changes in the Cervical Microbiota of Women with Different High-Risk Human Papillomavirus Loads. | Viruses | 2022 | 36560678 | PubTator, text mining | PubMed |
| Mortality in Pedigrees with Acute Intermittent Porphyria. | Life (Basel) | 2022 | 36556425 | PubTator, text mining | PubMed |
| Circadian Genes Expression Patterns in Disorders Due to Enzyme Deficiencies in the Heme Biosynthetic Pathway. | Biomedicines | 2022 | 36551954 | PubTator, text mining | PubMed |
| Associations of Betatrophin/ANGPTL8 with Septic Dyslipidemia in Human Peritonitis: An Explorative Analysis. | Biomedicines | 2022 | 36551906 | PubTator, text mining | PubMed |
| The iron-modulating hormone hepcidin is upregulated and associated with poor survival outcomes in renal clear cell carcinoma. | Front Pharmacol | 2022 | 36532749 | PubTator, text mining | PubMed |
| The transcription factor DDIT3 is a potential driver of dyserythropoiesis in myelodysplastic syndromes. | Nat Commun | 2022 | 36494342 | PubTator, text mining | PubMed |
| Novel hydroxymethylbilane synthase gene mutation identified and confirmed in a woman with acute intermittent porphyria: A case report. | World J Clin Cases | 2022 | 36483813 | PubTator, text mining | PubMed |
| A Medical Conundrum in a Surgical Setting: Lessons Learned From an Atypical Case of Hyponatremia. | Cureus | 2022 | 36475216 | PubTator, text mining | PubMed |
| Functional characterization of 5p15.33 risk locus in uveal melanoma reveals rs452384 as a functional variant and NKX2.4 as an allele-specific interactor. | Am J Hum Genet | 2022 | 36459980 | PubTator, text mining | PubMed |
| SETD1A regulates transcriptional pause release of heme biosynthesis genes in leukemia. | Cell Rep | 2022 | 36450243 | PubTator, text mining | PubMed |
| First Case of Allochronic Onset of Two Primary Dermatofibrosarcoma Protuberans Lesions Proved by COL1A1-PDGFB Fusion Gene Analysis. | Acta Derm Venereol | 2022 | 36444562 | PubTator, text mining | PubMed |
| Recent Insights into the Pathogenesis of Acute Porphyria Attacks and Increasing Hepatic PBGD as an Etiological Treatment. | Life (Basel) | 2022 | 36430993 | PubTator, text mining | PubMed |
| Spontaneous Transformation of a p53 and Rb-Defective Human Fallopian Tube Epithelial Cell Line after Long Passage with Features of High-Grade Serous Carcinoma. | Int J Mol Sci | 2022 | 36430324 | PubTator, text mining | PubMed |
| USP7 Inhibitors in Cancer Immunotherapy: Current Status and Perspective. | Cancers (Basel) | 2022 | 36428632 | PubTator, text mining | PubMed |
| Gene-Level Associations in Patients With and Without Pathogenic Germline Variants in CDKN2A and Pancreatic Cancer. | JCO Precis Oncol | 2022 | 36409970 | PubTator, text mining | PubMed |
| BCG vaccinations drive epigenetic changes to the human T cell receptor: Restored expression in type 1 diabetes. | Sci Adv | 2022 | 36383663 | PubTator, text mining | PubMed |
| Acute Intermittent Porphyria as a Rare Challenging Neuro-Metabolic Disease; a Case Report. | Arch Acad Emerg Med | 2022 | 36381968 | 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/v1/3145/papers?page=20