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.
61 to 80 of 1,847
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Panel-Based Genetic Testing in a Consecutive Series of Individuals with Inherited Retinal Diseases in Australia: Identifying Predictors of a Diagnosis. | Genes (Basel) | 2025 | 40869936 | PubTator, text mining | PubMed |
| RSPH4A-PCDx: An Index to Predict Lung Function Decline in Primary Ciliary Dyskinesia. | Adv Respir Med | 2025 | 40862699 | PubTator, text mining | PubMed |
| Addressing Challenges in Developing Treatments for Inherited Retinal Diseases: Recommendations From the Third Monaciano Symposium. | Transl Vis Sci Technol | 2025 | 40862658 | PubTator, text mining | PubMed |
| C28-aldehyde (n-octacosanal) modulates stage-specific temporal expression of effector genes in the wheat powdery mildew fungus. | Microbiol Res | 2025 | 40840036 | PubTator, text mining | PubMed |
| Spatial regulation of ARL3 and GSF-mediated lipidated cargo trafficking in the primary cilium. | FEBS Lett | 2025 | 40836900 | PubTator, text mining | PubMed |
| Chimerolectins: Classification, structural architecture, and functional perspectives. | Protein Sci | 2025 | 40815298 | PubTator, text mining | PubMed |
| Multi-proteomic profiling of the varicella-zoster virus-host interface reveals host susceptibilities to severe infection. | Nat Microbiol | 2025 | 40739040 | PubTator, text mining | PubMed |
| Whole exome sequencing reveals pathogenic variants in CNGA3, CACNA1F, and RPGRIP1 in consanguineous Pakistani families with diverse retinal phenotypes. | PLoS One | 2025 | 40737315 | PubTator, text mining | PubMed |
| Genotype-specific retinal and choroidal perfusion patterns in inherited retinal diseases: an SS-OCTA analysis. | Int J Retina Vitreous | 2025 | 40702517 | PubTator, text mining | PubMed |
| Improved epigenetic age prediction models by combining sex chromosome and autosomal markers. | Epigenetics Chromatin | 2025 | 40665390 | PubTator, text mining | PubMed |
| Analysis of choriocapillaris vascular density in patients with retinitis pigmentosa caused by RPGR gene mutations. | BMC Ophthalmol | 2025 | 40597960 | PubTator, text mining | PubMed |
| Tapetal-like reflex in X-linked RPGR-associated retinopathy. | Ophthalmic Genet | 2025 | 40583321 | PubTator, text mining | PubMed |
| Characterisation and prevalence of inherited retinal diseases in the Finnish population reveals enrichment of population-specific phenotypes and causative variants. | Br J Ophthalmol | 2025 | 40571344 | PubTator, text mining | PubMed |
| Induced Pluripotent (iPSC) and Mesenchymal (MSC) Stem Cells for In Vitro Disease Modeling and Regenerative Medicine. | Int J Mol Sci | 2025 | 40565081 | PubTator, text mining | PubMed |
| Early-Onset Cone Photoreceptor Degeneration Is Associated With High Myopia in RPGR-Related Retinal Dystrophy. | J Ophthalmol | 2025 | 40535564 | PubTator, text mining | PubMed |
| Systematic mapping of registered interventional studies addressing the top 10 research priorities in Barrett's oesophagus and gastro-oesophageal reflux disease. | BMJ Open Gastroenterol | 2025 | 40527525 | PubTator, text mining | PubMed |
| Female Simplex Carriers of X-Linked Retinal Dystrophies: A Case Series. | Case Rep Ophthalmol | 2025 | 40510754 | PubTator, text mining | PubMed |
| Nonsyndromic Retinitis Pigmentosa With Pathogenic CEP290 Mutations. | Ophthalmic Surg Lasers Imaging Retina | 2025 | 40407606 | PubTator, text mining | PubMed |
| The Impacts of Caregiving for Patients with X-Linked Retinitis Pigmentosa (XLRP): Findings from the EXPLORE XLRP-2 Study. | Adv Ther | 2025 | 40299280 | PubTator, text mining | PubMed |
| The Exponential Constriction Model of the Ellipsoid Zone in Taiwanese Individuals With RPGR-Related X-Linked Retinitis Pigmentosa. | Invest Ophthalmol Vis Sci | 2025 | 40257782 | 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=4