Gene · 6103
Papers1,847
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
261 to 280 of 1,847
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Identification of a novel splice site mutation in the DNAAF4 gene of a Chinese patient with primary ciliary dyskinesia. | Asian J Androl | 2023 | 37147940 | PubTator, text mining | PubMed |
| Human pluripotent-stem-cell-derived organoids for drug discovery and evaluation. | Cell Stem Cell | 2023 | 37146581 | PubTator, text mining | PubMed |
| Mapping rhodopsin trafficking in rod photoreceptors with quantitative super-resolution microscopy. | bioRxiv | 2023 | 37131638 | PubTator, text mining | PubMed |
| IMI-Management and Investigation of High Myopia in Infants and Young Children. | Invest Ophthalmol Vis Sci | 2023 | 37126360 | PubTator, text mining | PubMed |
| Retinitis Pigmentosa: Current Clinical Management and Emerging Therapies. | Int J Mol Sci | 2023 | 37108642 | PubTator, text mining | PubMed |
| Plasma Exosomal Non-Coding RNA Profile Associated with Renal Damage Reveals Potential Therapeutic Targets in Lupus Nephritis. | Int J Mol Sci | 2023 | 37108249 | PubTator, text mining | PubMed |
| Functional Analysis of a Novel, Non-Canonical RPGR Splice Variant Causing X-Linked Retinitis Pigmentosa. | Genes (Basel) | 2023 | 37107692 | PubTator, text mining | PubMed |
| Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism. | Invest Ophthalmol Vis Sci | 2023 | 37097228 | PubTator, text mining | PubMed |
| Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature. | Acta Myol | 2023 | 37091526 | PubTator, text mining | PubMed |
| One person can make a difference: identification of people with a rare genetic lung disease. | ERJ Open Res | 2023 | 37077554 | PubTator, text mining | PubMed |
| Editorial: Identifying genetics-based mechanisms and treatments for neurodevelopmental and psychiatric disorders through data integration. | Front Genet | 2023 | 37077543 | PubTator, text mining | PubMed |
| Definition of the transcriptional units of inherited retinal disease genes by meta-analysis of human retinal transcriptome data. | BMC Genomics | 2023 | 37072692 | PubTator, text mining | PubMed |
| Driving with retinitis pigmentosa. | Ophthalmic Genet | 2023 | 37013444 | PubTator, text mining | PubMed |
| Morphologically intact airways in lung fibrosis have an abnormal proteome. | Respir Res | 2023 | 37005656 | PubTator, text mining | PubMed |
| Performance Assessment of Self-Healing Polymer-Modified Bitumens by Evaluating the Suitability of Current Failure Definition, Failure Criterion, and Fatigue-Restoration Criteria. | Materials (Basel) | 2023 | 36984369 | PubTator, text mining | PubMed |
| Primary Ciliary Dyskinesia in a Portuguese Bronchiectasis Outpatient Clinic. | Genes (Basel) | 2023 | 36980814 | PubTator, text mining | PubMed |
| The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population. | Biomedicines | 2023 | 36979683 | PubTator, text mining | PubMed |
| Recoding of Nonsense Mutation as a Pharmacological Strategy. | Biomedicines | 2023 | 36979640 | PubTator, text mining | PubMed |
| Progress of Wnt Signaling Pathway in Osteoporosis. | Biomolecules | 2023 | 36979418 | PubTator, text mining | PubMed |
| Genetic variation in cis-regulatory domains suggests cell type-specific regulatory mechanisms in immunity. | Commun Biol | 2023 | 36977773 | 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/v1/6103/papers?page=14