Gene · 540
Papers3,770
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 3,770
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Clinical application value of preconception and prenatal carrier screening in Yinchuan. | Front Genet | 2026 | 42598284 | PubTator, text mining | PubMed |
| Ferroptosis, DNA damage repair, and transporter proteins: associated with platinum sensitivity and prognosis in epithelial ovarian cancer. | Mol Biol Rep | 2026 | 42593694 | PubTator, text mining | PubMed |
| Targeted degradation of ATP7B via a novel autophagy-targeting chimera promotes cuproptosis to potentiate anti-tumor immunity in clear cell renal cell carcinoma. | Free Radic Biol Med | 2026 | 42580537 | PubTator, text mining | PubMed |
| Referral-spectrum Effect in Hypercupriuric Referrals for Suspected Wilson Disease: Diagnostic Implications for Ceruloplasmin and 24-hour Urinary Copper Excretion. | J Clin Transl Hepatol | 2026 | 42559006 | PubTator, text mining | PubMed |
| Copper homeostasis and cuproptosis: New perspectives on the diagnosis and treatment of metabolic diseases. | J Trace Elem Med Biol | 2026 | 42551357 | PubTator, text mining | PubMed |
| Ceruloplasmin and neurodegeneration: A link between copper dysregulation, iron imbalance, and neuronal damage. | J Trace Elem Med Biol | 2026 | 42501667 | PubTator, text mining | PubMed |
| The utility of whole exome sequencing in diagnosing Wilson disease: A case report. | JPGN Rep | 2026 | 42499731 | PubTator, text mining | PubMed |
| Itching for a diagnosis: Dysesthesias as an atypical presentation of Wilson disease in an adolescent-Case report. | JPGN Rep | 2026 | 42499713 | PubTator, text mining | PubMed |
| Prognosis of pediatric hepatic Wilson disease with ATP7B loss of function variants. | Clin Exp Pediatr | 2026 | 42442737 | PubTator, text mining | PubMed |
| WC1/WC2-Sre1 Transcriptional Cascade Controls Predation and Chlamydospore Formation in the Nematode-Trapping Fungus Arthrobotrys flagrans. | Microb Biotechnol | 2026 | 42427068 | PubTator, text mining | PubMed |
| Mechanisms of multi-organ damage in Wilson disease from the gut-liver-brain axis perspective: copper metabolism, gut microbiota, and metabolite communication. | Front Microbiol | 2026 | 42416017 | PubTator, text mining | PubMed |
| Analysis of end-stage renal disease mediated by cuproptosis-related genes. | Clin Nephrol | 2026 | 42383521 | PubTator, text mining | PubMed |
| Age-associated clinical characteristics and ATP7B mutation landscape in pediatric Wilson's disease: a study from southwest China. | Front Genet | 2026 | 42376281 | PubTator, text mining | PubMed |
| Corrigendum to "Nuances in ATP7B Genetic Testing and Interpretation in India" [J Clin Exp Hepatol 16 (1) (2026) 103205]. | J Clin Exp Hepatol | 2026 | 42375647 | PubTator, text mining | PubMed |
| Pathogenic variation distribution of ACMG 3.2 list genes in 11 ethnic groups in southwest China. | BMC Genomics | 2026 | 42288740 | PubTator, text mining | PubMed |
| [Polydatin attenuates high copper induced damage in Atp7b knockout neural stem cells by regulating PPARG mediated ferroptosis]. | Zhejiang Da Xue Xue Bao Yi Xue Ban | 2026 | 42260313 | PubTator, text mining | PubMed |
| Pediatric Wilson Disease in Sudan: A Rare Case, Sudan Conflict and Diagnostic Challenges. | Clin Case Rep | 2026 | 42256941 | PubTator, text mining | PubMed |
| Diagnostic efficiency of whole exome sequencing in the search for genetic causes of hereditary diseases in Yugra (West Siberia, Russia). | Vavilovskii Zhurnal Genet Selektsii | 2026 | 42253454 | PubTator, text mining | PubMed |
| Clinical characteristics and genetic features of patients with Wilson's disease in southwestern China. | Orphanet J Rare Dis | 2026 | 42237336 | PubTator, text mining | PubMed |
| Prevalence of pre-existing neutralizing antibodies to AAV5 and AAV8 in patients with Wilson's disease. | Mol Ther Adv | 2026 | 42222354 | 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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