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.
141 to 160 of 1,847
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Retinitis Pigmentosa: From Pathomolecular Mechanisms to Therapeutic Strategies. | Medicina (Kaunas) | 2024 | 38276069 | PubTator, text mining | PubMed |
| Advanced Cellular Models for Rare Disease Study: Exploring Neural, Muscle and Skeletal Organoids. | Int J Mol Sci | 2024 | 38256087 | PubTator, text mining | PubMed |
| Inherited Retinal Degeneration Caused by Dehydrodolichyl Diphosphate Synthase Mutation-Effect of an ALG6 Modifier Variant. | Int J Mol Sci | 2024 | 38256083 | PubTator, text mining | PubMed |
| Whole genome sequencing enables new genetic diagnosis for inherited retinal diseases by identifying pathogenic variants. | NPJ Genom Med | 2024 | 38245557 | PubTator, text mining | PubMed |
| Quantitative comparison of nuclear transport inhibition by SARS coronavirus ORF6 reveals the importance of oligomerization. | Proc Natl Acad Sci U S A | 2024 | 38236733 | PubTator, text mining | PubMed |
| Spectrum of Genetic Variants in the Most Common Genes Causing Inherited Retinal Disease in a Large Molecularly Characterized United Kingdom Cohort. | Ophthalmol Retina | 2024 | 38219857 | PubTator, text mining | PubMed |
| Highly efficient capture approach for the identification of diverse inherited retinal disorders. | NPJ Genom Med | 2024 | 38195571 | PubTator, text mining | PubMed |
| N6-methyladenosine methylation in ophthalmic diseases: From mechanisms to potential applications. | Heliyon | 2024 | 38192819 | PubTator, text mining | PubMed |
| X-linked cone dystrophy with an uncommon tapetal-like sheen caused by a novel RPGR variant. | Can J Ophthalmol | 2024 | 38128582 | PubTator, text mining | PubMed |
| Interactome Analysis Reveals a Link of the Novel ALMS1-CEP70 Complex to Centrosomal Clusters. | Mol Cell Proteomics | 2024 | 38122899 | PubTator, text mining | PubMed |
| HIGH MYOPIA IS COMMON IN PATIENTS WITH X-LINKED RETINOPATHIES: Myopic Maculopathy Analysis. | Retina | 2024 | 38117582 | PubTator, text mining | PubMed |
| Gene Therapy for Inherited Retinal Diseases: From Laboratory Bench to Patient Bedside and Beyond. | Ophthalmol Ther | 2024 | 38113023 | PubTator, text mining | PubMed |
| Exome-wide benchmark of difficult-to-sequence regions using short-read next-generation DNA sequencing. | Nucleic Acids Res | 2024 | 38015437 | PubTator, text mining | PubMed |
| PREVALENCE AND CLINICAL FEATURES OF RADIAL FUNDUS AUTOFLUORESCENCE IN HIGH MYOPIC WOMEN. | Retina | 2024 | 37948743 | PubTator, text mining | PubMed |
| Visual Acuity by Decade in 139 Males with RPGR-Associated Retinitis Pigmentosa. | Ophthalmol Sci | 2024 | 37868789 | PubTator, text mining | PubMed |
| A SYSTEMATIC LITERATURE REVIEW OF DISEASE PROGRESSION REPORTED IN RPGR -ASSOCIATED X-LINKED RETINITIS PIGMENTOSA. | Retina | 2024 | 37683184 | PubTator, text mining | PubMed |
| Molecular genetic diagnostics for inherited retinal dystrophies in the clinical setting. | Can J Ophthalmol | 2024 | 37678418 | PubTator, text mining | PubMed |
| Clinical applications of the CRISPR/Cas9 genome-editing system: Delivery options and challenges in precision medicine. | Genes Dis | 2024 | 37588217 | PubTator, text mining | PubMed |
| Female carrier of RPGR mutation presenting with high myopia. | Ophthalmic Genet | 2024 | 37489109 | PubTator, text mining | PubMed |
| MANAGEMENT OF A UNIQUE CASE OF COATS'-LIKE X-LINKED RETINITIS PIGMENTOSA ASSOCIATED WITH AN RPGR VARIANT IN THE ERA OF ANTI-VASCULAR ENDOTHELIUM GROWTH FACTOR. | Retin Cases Brief Rep | 2024 | 36996441 | 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=8