Gene · 7399
Papers2,630
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
1,041 to 1,060 of 2,630
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Development of a novel transcription factors-related prognostic signature for serous ovarian cancer. | Sci Rep | 2021 | 33785763 | PubTator, text mining | PubMed |
| Viruses, cancer and non-self recognition. | Open Biol | 2021 | 33784856 | PubTator, text mining | PubMed |
| Genetic investigation of 211 Chinese families expands the mutational and phenotypical spectra of hereditary retinopathy genes through targeted sequencing technology. | BMC Med Genomics | 2021 | 33781268 | PubTator, text mining | PubMed |
| Congenital Deafness and Recent Advances Towards Restoring Hearing Loss. | Curr Protoc | 2021 | 33780161 | PubTator, text mining | PubMed |
| Comprehensive Analysis of Ferroptosis Regulators in Lung Adenocarcinomas Identifies Prognostic and Immunotherapy-Related Biomarkers. | Front Mol Biosci | 2021 | 33778001 | PubTator, text mining | PubMed |
| R-locus for roaned coat is associated with a tandem duplication in an intronic region of USH2A in dogs and also contributes to Dalmatian spotting. | PLoS One | 2021 | 33755696 | PubTator, text mining | PubMed |
| Panel-based genetic testing for inherited retinal disease screening 176 genes. | Mol Genet Genomic Med | 2021 | 33749171 | PubTator, text mining | PubMed |
| Autosomal Recessive Rod-Cone Dystrophy Associated With Compound Heterozygous Variants in ARL3 Gene. | Front Cell Dev Biol | 2021 | 33748123 | PubTator, text mining | PubMed |
| On the Wrong Track: Alterations of Ciliary Transport in Inherited Retinal Dystrophies. | Front Cell Dev Biol | 2021 | 33748110 | PubTator, text mining | PubMed |
| Birthweight DNA methylation signatures in infant saliva. | Clin Epigenetics | 2021 | 33741061 | PubTator, text mining | PubMed |
| Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases. | Front Genet | 2021 | 33737949 | PubTator, text mining | PubMed |
| Descriptive Study of a Cohort of 488 Patients with Inherited Retinal Dystrophies. | Clin Ophthalmol | 2021 | 33727790 | PubTator, text mining | PubMed |
| Targeted next-generation sequencing of deaf patients from Southwestern China. | Mol Genet Genomic Med | 2021 | 33724713 | PubTator, text mining | PubMed |
| A novel missense mutation in SMPX causes a rare form of X-linked postlingual sensorineural hearing loss in a Chinese family. | Transl Pediatr | 2021 | 33708524 | PubTator, text mining | PubMed |
| Human cytomegalovirus infection: A considerable issue following allogeneic hematopoietic stem cell transplantation. | Oncol Lett | 2021 | 33692850 | PubTator, text mining | PubMed |
| Direct Priming of CD8+ T Cells Persists in the Face of Cowpox Virus Inhibitors of Antigen Presentation. | J Virol | 2021 | 33692206 | PubTator, text mining | PubMed |
| Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration. | BMC Med Genomics | 2021 | 33691693 | PubTator, text mining | PubMed |
| Clinical and genetic findings in Italian patients with sector retinitis pigmentosa. | Mol Vis | 2021 | 33688152 | PubTator, text mining | PubMed |
| Genomic and Transcriptomic Analyses Reveals ZNF124 as a Critical Regulator in Highly Aggressive Medulloblastomas. | Front Cell Dev Biol | 2021 | 33681213 | PubTator, text mining | PubMed |
| Comprehensive Analysis of Tumor Microenvironment Identified Prognostic Immune-Related Gene Signature in Ovarian Cancer. | Front Genet | 2021 | 33679883 | 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/v1/7399/papers?page=53